Sterling Life Sciences Regulatory Affair

Sr. Manager, Regulatory Affairs (Maryland)

Sun, 28 Jun 2009

Message by Our client is a publicly traded biopharmaceutical company headquartered in Maryland which is focused in the development and commercialization of vaccines and treatments to help the immune system prevent diseases. The company has an experienced management team, a robust pipeline of products and an empowering corporate culture that is focused on the long-term professional development of its employees. on Sun, 28 Jun 2009 EST

Director of Regulatory Affairs (Michigan)

Thu, 25 Jun 2009

Regional Regulatory Affairs Director (Durham, NC)

Thu, 18 Jun 2009

Message by Our client is a leading global supplier of solutions for the biopharma, forensic and diagnostic industries The company is a leader in the development, production and distribution of advanced automation and detection solutions for the world�s leading life science laboratories Our client is a strong partner in laboratory automation on Thu, 18 Jun 2009 EST

Associate Regulatory Affairs Specialist (Wisconsin)

Tue, 16 Jun 2009

Message by Our client is a biopharmaceutical company based in Wisconsin. They are a leading global supplier of high quality active pharmaceutical ingredients for nearly three decades. The company has premier investors, an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of it's employees. on Tue, 16 Jun 2009 EST

Regulatory and Quality Manager (New Jersey)

Fri, 29 May 2009

Message by Our client is a world leader in the development, manufacture and distribution of generic and branded pharmaceuticals. The company has a world class management team, an excellent track record of steady growth and a robust portfolio containing some of the industry�s most reputable products. This is a unique opportunity for someone that wants to put their drive and initiative to work! on Fri, 29 May 2009 EST

Director Quality and Regulatory Affairs (Piscataway, NJ)

Thu, 14 May 2009

Message by Our client is a small start up company. They are partnered with a pharmaceutical firm and are venture backed. They have money for the next two years. Great situation for someone who is entrepreneurial and wants to have a sense of accomplishment. on Thu, 14 May 2009 EST

Senior Director, Regulatory Affairs (Winston-Salem, NC)

Sun, 10 May 2009

Message by Our client is a publicly traded clinical stage biopharmaceutical company based in North Carolina which is focused in the development of therapeutics for the treatment of central nervous system diseases and disorders. The company has an experienced management team, multiple compounds in clinical trials, and an empowering corporate culture that is focused on the long-term professional development of it's employees. on Sun, 10 May 2009 EST

Regulatory Affairs Project Manager (Florida)

Mon, 4 May 2009

Message by Our client designs and makes products for arthroscopic and orthopedic surgery. They distribute more than 3,000 products to hospitals and surgeons throughout the US and in around 70 other countries. They also offer training in a variety of surgical skills. on Mon, 4 May 2009 EST

Regulatory Associate (Illinois)

Mon, 4 May 2009

Message by Our client is a privately owned company based in Illinois which is a leading producer of personal care products. The company has an experienced management team, an innovative line of products and an empowering corporate culture that is focused on the long-term professional development of it's employees. on Mon, 4 May 2009 EST

Sr. Regulatory Affairs Specialist (Memphis, TN)

Mon, 23 Mar 2009

Message by Our client is a global Medical Device company with a 50 year history of success in the industry. With over 1000 employees, the organization boasts an experienced management team, strong momentum in their various product lines and an empowering corporate culture that is focused on the professional development of it's employees. This is a strong opportunity for someone that wants to put their drive and initiative to work! on Mon, 23 Mar 2009 EST

Director of Regulatory Affairs (North Brunswick, NJ)

Thu, 12 Mar 2009

Message by Our Client is a biotechnology company focused on developing multiple platform approaches to the treatment of several cancers and HIV. Their lead products in development represent a market potential in excess of $10 billion. With a highly experienced management team and several products in their pipeline, this is an exciting opportunity for the right person to join a fast paced environment on Thu, 12 Mar 2009 EST

Director of Compliance and Regulatory Affairs (Louisville, KY)

Tue, 3 Mar 2009

Message by Our client is a publicly traded healthcare services company headquartered in Virginia with a 100-year track record of success in serving their customers. The company has an experienced management team and exceptional financial fundamentals, including recording both record revenue and earnings in 2008. This is a great situation for an executive that is interested in an opportunity to have a visible impact on a rapidly growing organization. on Tue, 3 Mar 2009 EST

Sr. Director/VP of Regulatory Affairs (Brisbane, CA)

Tue, 3 Mar 2009

Message by Our client is a publicly traded pharmaceutical company located in southern California that specializes in development and commercialization of Pulmonology and Hepatology therapeutics. The organization has an experienced management team, a world-class corporate culture and an established reputation for being a leading innovator in the field. on Tue, 3 Mar 2009 EST

Director of Compliance and Regulatory Affairs (Bohemia NY)

Tue, 24 Feb 2009

Message by Our Client is a medical device company located in Bohemia NY. They focus on orthodontic systems, services, software and support for medical professionals. With over 40 years of experience, they are leaders in innovative patient care. This is an excellent opportunity for the right candidate to join a fast paced environment! on Tue, 24 Feb 2009 EST

Regulatory Affairs Manager (Atlanta, GA)

Sun, 22 Feb 2009

Message by Our client is a rapidly growing specialty pharmaceutical company that is focused on the development and commercialization of women�s health and gastroenterology products. The company has an experienced management team, excellent revenue momentum and offers equity to all employees. This is a unique opportunity for someone that wants to put their drive and to work for an entrepreneurial organization that rewards initiative with true ownership on Sun, 22 Feb 2009 EST

VP Quality and Regulatory Affairs (Crown Point, IN)

Tue, 17 Feb 2009

Message by Our client is dedicated to the development of diagnostic and therapeutic radiopharmaceuticals for use in rare diseases. The company's vision is to transfer technologies to those most in need. The company's subtle leadership has resulted in four initial products or chemical entities in various stages of development or under licensing discussions at this time. The company's goal is to elucidate opportunities that will enable the diagnosis and treatment of rare diseases that will be designated as Orphan Drugs. on Tue, 17 Feb 2009 EST

Vice President, Quality and Regulatory Affairs (Utah)

Fri, 13 Feb 2009

Message by Our client is a rapidly expanding medical device firm headquartered in Utah that carries the distinction of being the first orthopedic focused outsourcing company that provides a complete portfolio of services ranging from product innovation, to contract manufacturing and supply chain management. The organization has an experienced management team, a world-class corporate culture and an established reputation for being a leading innovator in the field. This is a unique opportunity for an executive that wants to put their drive and entrepreneurial initiative to work! on Fri, 13 Feb 2009 EST

Regulatory Affairs Specialist (Houston TX)

Wed, 11 Feb 2009

Message by Our client is a publicly traded medical device company headquartered in Texas that is focused on the development and commercialization of innovative therapies for neurological disorders.The company has an experienced management team, excellent momentum with their target market and have grown both revenue and profitability significantly during the past year. This is a unique opportunity for someone that wants to put their drive and initiative to work! on Wed, 11 Feb 2009 EST

Director of Regulatory Affairs (Lewisberry, PA)

Mon, 9 Feb 2009

Message by Our client is a rapidly growing medical device company headquartered in Pennsylvania that is focused on the development and commercialization of innovative Class I & II products. The company has an experienced management team, strong financing and excellent momentum due to securing a highly sought after exclusive licensing partnership with a world-class pharmaceutical firm. on Mon, 9 Feb 2009 EST

Regulatory Affairs Manager (Irvine CA - South)

Thu, 5 Feb 2009

Message by Our client is a young venture-backed medical device company headquartered in Southern California that is focused on the development and commercialization of innovative drug delivery and surgical wound care products. The company has an experienced management team, strong financing and a robust pipeline of products in development with excellent momentum. This is a unique opportunity for someone that wants to put their drive and initiative to work! on Thu, 5 Feb 2009 EST

Regulatory Affairs Representative (Wisconsin)

Thu, 29 Jan 2009

Message by Our client is the medical device division of a world leading biopharmaceutical company. They are a highly profitable, publicly traded company whose products are currently being sold in over 60 countries worldwide. This is a great opportunity for someone to join a company which offers a great corporate culture and is focused on the long-term development of its employees. on Thu, 29 Jan 2009 EST

Director of Regulatory Affairs (Kansas)

Wed, 28 Jan 2009

Message by Our client is a rapidly growing development-stage pharmaceutical company that is focused on the commercialization of therapeutics for patients with unmet needs that are suffering from respiratory disorders. With offices in 20 countries worldwide, the company boasts a world-class management team with unparalleled expertise in this area, a varied selection of cutting-edge protocols and an empowering corporate culture that is focused on the long-term professional development of its employees. on Wed, 28 Jan 2009 EST

Regulatory Affairs Manager (Ohio)

Wed, 21 Jan 2009

Message by Our client, a biopharmaceutical company, focuses on developing therapeutic products, for the medical needs of patients with debilitating conditions and life-threatening diseases. With numerous revolutionary products in the development and pre-clinical development stage, this is a great opportunity for someone to join a company, which offers a great corporate culture and is focused on the long-term development of its employees. on Wed, 21 Jan 2009 EST

Director of Regulatory Affairs (Illinois)

Wed, 21 Jan 2009

Message by Our client, a global biopharmaceutical company, focuses on developing therapeutic products, for the medical needs of patients with debilitating conditions and life-threatening diseases. With numerous revolutionary products in the development and pre-clinical development stage, this is a great opportunity for someone to join a company which offers a great corporate culture and is focused on the long-term development of its employees. on Wed, 21 Jan 2009 EST

Director of Regulatory Affairs and Compliance (Georgia)

Wed, 21 Jan 2009

Message by Our client, a biopharmaceutical company, focuses on developing therapeutic products, for the medical needs of patients with debilitating conditions and life-threatening diseases. With numerous revolutionary products in the development and pre-clinical development stage, this is a great opportunity for someone to join a company which offers a great corporate culture and is focused on the long-term development of its employees. on Wed, 21 Jan 2009 EST

Senior Director, Regulatory Affairs (New York)

Thu, 15 Jan 2009

Message by Our client has an established presence in all global AIDS crisis zones including East and South Africa. They also recently opened a 36,000 square foot state-of-the-art lab in New York. Exceptional management team and board, the Vice President of Vaccine Development is former Global Vice President of Process Development at Sanofi Pasteur, the largest vaccine company worldwide.World class corporate (i.e. Pfizer, Bristol-Meyers, Google) and foundation (i.e. Bill and Melinda Gates Foundation) financing. on Thu, 15 Jan 2009 EST

Regulatory Affairs Project Manager (New Jersey)

Thu, 15 Jan 2009

Message by Our client is a global medical device company with operations in over 60 countries. They have a leadership position in their targeted markets and have established a reputation for having the dynamic environment and innovation focus of a small company, with the resources and brand presence of a large company. This is a great opportunity for the right candidate! on Thu, 15 Jan 2009 EST

Senior Director of Regulatory Affairs (Port Washington, New York)

Thu, 8 Jan 2009

Message by Our client is a global pharmaceutical company headquartered in New York. They lead the market with filtration, separation and purification products being their specialization. The company has an experienced management team, an unmatched product portfolio and an empowering corporate culture that is focused on the long-term professional development of it's employees. on Thu, 8 Jan 2009 EST

Regulatory Affairs Supervisor (Massachusetts)

Thu, 8 Jan 2009

Message by Our client is a leading private label health and beauty care company. The company has marketed products, an experienced management team and an empowering corporate culture that is focused on the professional development of its employees. This is a great opportunity for the right candidate. on Thu, 8 Jan 2009 EST

Director of Regulatory Affairs (Georgia)

Wed, 7 Jan 2009

Message by Our client is a rapidly growing development-stage pharmaceutical company that is focused on the commercialization of therapeutics for patients with unmet needs that are suffering from respiratory disorders. With offices in 20 countries worldwide, the company boasts a world class management team with unparalleled expertise in this area, a varied selection of cutting-edge protocols and an empowering corporate culture that is focused on the long-term professional development of its employees. on Wed, 7 Jan 2009 EST

Director of Regulatory Affairs (Pennsylvania)

Tue, 23 Dec 2008

Message by Our client is a publicly traded life sciences company that is recognized as a leader in the parenteral packaging technology and components sector. The organization is highly profitable and boasts both an experienced management team and a global customer base. They have also developed an industry-wide reputation for their commitment to quality and innovation. This is a strong opportunity for someone that wants to put their drive and initiative to work! on Tue, 23 Dec 2008 EST

Regulatory Affairs Specialist (Pennsylvania)

Tue, 23 Dec 2008

Director of Regulatory Affairs and Compliance (Massachusetts)

Thu, 18 Dec 2008

Message by Our client is a biopharmaceutical company focusing on developing therapeutic products, for the medical needs of patients with debilitating conditions and life-threatening diseases. With numerous revolutionary products in the development and pre-clinical development stage, this is a great opportunity for someone to join a company which offers a great corporate culture and is focused on the long-term development of its employees. on Thu, 18 Dec 2008 EST

Director of Regulatory Affairs (Massachusetts)

Thu, 18 Dec 2008

Message by Our client is a global biopharmaceutical company focusing on therapeutic products for the medical needs of patients with debilitating conditions and life-threatening diseases. With numerous revolutionary products in the development and pre-clinical development stage, this is a great opportunity for the right candidate! on Thu, 18 Dec 2008 EST

Regulatory Affairs Manager (Massachusetts)

Wed, 17 Dec 2008

Message by Our client is a biopharmaceutical company focused on developing therapeutic products for the medical needs of patients with debilitating conditions and life threatening diseases. With numerous revolutionary products in the development and pre-clinical development stage, this is a great opportunity for someone to join a company which offers a great corporate culture and is focused on the long-term development of its employees. on Wed, 17 Dec 2008 EST

Senior Regulatory Affairs Manager (North Carolina)

Thu, 11 Dec 2008

Message by Our client is a world leading medical device company that is focused on the development and commercialization of minimally invasive medical devices and procedures. They aim to meet the needs of patients with debilitating conditions and life threatening diseases. on Thu, 11 Dec 2008 EST

Regulatory Affairs Representative (Illinois)

Wed, 10 Dec 2008

Message by Our client is the medical device division of a global biopharmaceutical company. They are a highly profitable, publicly traded company whose products are currently being sold in over 60 countries worldwide. This is a great opportunity for someone to join a company, which offers a great corporate culture and is focused on the long-term development of its employees. on Wed, 10 Dec 2008 EST

Director of Regulatory Affairs (San Jose, California)

Thu, 4 Dec 2008

Message by Our client is a rapidly expanding generic pharmaceutical company based in San Jose, California. The company has an experienced management team, a dynamic pipeline and an empowering corporate culture that is focused on the professional development of its employees. on Thu, 4 Dec 2008 EST

Director of Regulatory Affairs (San Jose, California)

Wed, 26 Nov 2008

Message by Our client is the world�s biggest medical device organization committed to less-invasive medicine. They lead the market in minimally-invasive medical devices delivering over 13,000 products to health professionals in close to fifty countries. These technologies offer alternatives to major surgery and other medical procedures that are typically traumatic to the body. The procedure usually involves inserting the device into the body through natural openings or small incisions and then guiding it to most areas of the anatomy to diagnose and treat a wide range of medical problems. on Wed, 26 Nov 2008 EST

Regulatory Affairs Manager (New Jersey)

Tue, 25 Nov 2008

Message by Our client is a leading medical device company based in New Jersey. They focus on the design, development and manufacturing of solutions to improve the safety, delivery and effectiveness of patient healthcare. This is a great opportunity for someone looking for personal growth and a challenge. on Tue, 25 Nov 2008 EST

Director of Regulatory Affairs (Massachusetts)

Wed, 19 Nov 2008

Message by Our client is a rapidly growing biotech company headquartered in Massachusetts that is focused on the development and commercialization of novel monoclonal antibody drugs targeted towards diseases of the immune system. The company has a world class CEO, exceptional venture capital backing and a deep pipeline with multiple products entering late-stage clinical trials. This is an excellent time to join an organization that is on the verge of delivering several ground breaking therapies in the market. on Wed, 19 Nov 2008 EST

Senior Program Manager, Regulatory Affairs (New Jersey)

Mon, 17 Nov 2008

Message by Our client is a top 10 pharmaceutical company that has established a reputation as one of the most desirable organizations to work for in North America. With a demonstrated commitment to ongoing scientific innovation and an empowering corporate culture that is focused on rewarding top performers, this is a strong opportunity for the right candidate! on Mon, 17 Nov 2008 EST

Associate Director of Regulatory Affairs (New Jersey)

Mon, 17 Nov 2008

Senior Regulatory Affairs Specialist (Southern California)

Thu, 13 Nov 2008

Message by Our client is a rapidly growing medical device company headquartered in Southern California that is focused on the development and commercialization of innovative drug delivery systems. The organization has grown significantly over the past few years, spurred by the guidance of an experienced Management Team and relatively few real competitors. This is a strong opportunity for someone that wants to put their drive and initiative to work! on Thu, 13 Nov 2008 EST

Director of Regulatory Affairs and Compliance (Washington)

Wed, 12 Nov 2008

Message by Our client is one of the world's leading pharmaceutical companies. They are a highly profitable, publicly traded company whose products are currently being sold in over 50 countries globally. This is a great opportunity for someone to join a company that offers a great corporate culture and is focused on the long-term development of its employees. on Wed, 12 Nov 2008 EST

Associate Director of Regulatory Affairs (Tarrytown, New York)

Tue, 11 Nov 2008

Message by Our client is a biopharmaceutical company based in Tarrytown, New York. They focus on the development and commercialization of innovative therapeutic products to treat the unmet medical needs of patients with debilitating conditions and life-threatening diseases. Their clinical programs are focused in gastroenterology, virology and oncology. Our client has a strong pipeline of products and boasts revenues for the third quarter of 2008 totaling $17.5M. Due to expansion, they are seeking an experienced Associate Director of Regulatory Affairs to join their Team. This is an exciting opportunity for the right candidate to be part of a successful company. on Tue, 11 Nov 2008 EST

Regulatory Compliance Specialist (Allendale, New Jersey)

Fri, 31 Oct 2008

Message by Our client is one of the world's leading medical device providers. They are a highly profitable, publicly traded company whose products are currently being sold in over 120 countries worldwide. This is a great opportunity for someone to join a company, which offers a great corporate culture and is focused on the long-term development of its employees. on Fri, 31 Oct 2008 EST

Manager of Regulatory Affairs (Utica, New York)

Thu, 30 Oct 2008

Message by Our client is a well established global brand in the area of medical device manufacturing, with 11 facilities and over 3000 employees. on Thu, 30 Oct 2008 EST

Director of Regulatory Affairs (Utica, New York)

Thu, 30 Oct 2008

Message by Our client is a well-established global brand in the area of medical device manufacturing with 11 facilities and over 3000 employees. on Thu, 30 Oct 2008 EST

Regulatory Compliance Specialist (Southborough, Massachusetts)

Mon, 27 Oct 2008

Message by Our client is a medical device company based in Southborough MA. They were recently purchased by an international opto-digital technology company. Together, they focus on the design, development and manufacturing of devices that allow medical professionals to perform safe and invasive free surgery. Their comprehensive product portfolio includes instruments designed for advanced visualization and for providing rapid, accurate tissue management that is less traumatic to the patient. With over 100 employees based in Southborough and many locations overseas, this is an excellent opportunity for the right person to join a fast paced environment! on Mon, 27 Oct 2008 EST

International Regulatory Affairs Specialist (Southborough, Massachusetts)

Mon, 27 Oct 2008

Regulatory Affairs Manager (Beaverton, Oregon)

Wed, 22 Oct 2008

Message by Our client is a rapidly growing biotech company that focuses on wound care and infection control therapeutics. The company has an experienced management team, a varied selection of interesting protocols and an empowering corporate culture that is focused on the long-term professional development of it's employees. on Wed, 22 Oct 2008 EST

Regulatory Strategy Specialist (Montreal, Quebec)

Thu, 16 Oct 2008

Message by Our client is a rapidly growing pharmaceutical company headquartered in Montreal that is focused on the manufacturing and distribution of various generic brand therapeutics. The company has some of the strongest financial indicators in the industry, an experienced management team, and a robust pipeline. They also offer an empowering corporate culture that is focused on the professional development and advancement of clinical team members. on Thu, 16 Oct 2008 EST

Regulatory Affairs Specialist (New Jersey)

Fri, 10 Oct 2008

Message by Our client is a global leader in processing human bone and connective tissue for relocation and an innovator in developing, manufacturing and marketing biologic, biomaterial and device systems for musculoskeletal surgery. With an exacting focus on spinal, trauma and total joint revision procedures, their current and development-stage technologies address needs within numerous musculoskeletal discipline. on Fri, 10 Oct 2008 EST

Regulatory Affairs Manager (Sunrise, Florida)

Mon, 6 Oct 2008

Message by Our client is a global pharmaceutical company based in Sunrise, Florida. They focus on the development of generic therapeutics. The company has premier investors, an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. on Mon, 6 Oct 2008 EST

Regulatory Affairs Manager (Cypress, California)

Fri, 3 Oct 2008

Message by Our client is a diagnostics company based in California, with their head office in New York. They offer products and services used by the industry to assist with the diagnosis, treatment and management of infectious diseases. The company has an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. on Fri, 3 Oct 2008 EST

Senior Regulatory Affairs Specialist (Santa Clara, California)

Thu, 2 Oct 2008

Message by Our client is a medical device company based in Santa Clara, California. They are a worldwide leader in medical and aesthetic lasers and light-based technology. They have installed over 70,000 leading-edge systems in doctors� offices, clinics and hospitals in more than 100 countries worldwide. They also boast of 250 patents. The company offers an empowering corporate culture that is focused on the professional development and advancement of all team members. on Thu, 2 Oct 2008 EST

Regulatory Affairs Specialist (Eden Prairie, Minnesota)

Thu, 2 Oct 2008

Message by Our client is a medical device company based in Minnesota. They design, develop and manufacture imaging systems for vascular angiography procedures. Over 2000 of their systems are installed worldwide and more than 4 million people have had cardiovascular angiographic procedures using their system. The company has marketed products, an experienced management team and an empowering corporate culture that is focused on the professional development of its employees. This is a great opportunity for the right candidate. on Thu, 2 Oct 2008 EST

Regulatory Affairs Specialist (Hudson, New Hampshire)

Thu, 2 Oct 2008

Message by Our client is a leading medical device company based in Hudson, New Hampshire. They specialize in developing technologies for the treatment of cardiovascular diseases, such as coronary stents and state-of-the-art hernia repair. They have offices in Australia and The Netherlands too and boasts a demand of over 2 million sterile medical products to over 60 countries every year. With emphasis placed on personal development of employees, this is a great opportunity for the right candidate. on Thu, 2 Oct 2008 EST

Regulatory Affairs Specialist (Valencia, California)

Thu, 2 Oct 2008

Message by Our client is a medical device company based in Valencia, California. They offer award-winning medical devices designed to benefit people with stroke, multiple sclerosis, traumatic brain injury, cerebral palsy and spinal cord injury. These products use electrical stimulation to help people regain mobility and independence, to improve quality of life and productivity. on Thu, 2 Oct 2008 EST

Chief Operating Officer (Southern California)

Wed, 1 Oct 2008

Message by Our client is a rapidly growing contract manufacturing firm that has developed a reputation for excellence in the development and production of peptide-based APIs. The company has a very strong financial track record, an experienced management team and a loyal customer base. This is a strong opportunity for someone that wants to put their drive and initiative to work. on Wed, 1 Oct 2008 EST

Regulatory Affairs Supervisor (St. Louis, Michigan)

Fri, 19 Sep 2008

Message by Our client is the country�s oldest family owned private label health and beauty care company. It serves retailers in all states across the USA. They have produced and manufactured their own private label beauty products for the last 90 years, as well as distributing branded products. The company has marketed products, an experienced management team and an empowering corporate culture that is focused on the professional development of its employees. This is a great opportunity for the right candidate. on Fri, 19 Sep 2008 EST

Assistant Global Regulatory Manager Strategy (New Jersey)

Thu, 18 Sep 2008

Message by Our client is a top 10 pharmaceutical company that has established a reputation as one of the most desirable companies to work for in North America. With operations around the globe and an empowering corporate culture that is focused on the professional development of its employees, this is a strong opportunity for the right candidate. on Thu, 18 Sep 2008 EST

Director, Regulatory Intelligence (New Jersey)

Thu, 18 Sep 2008

Regulatory Affairs Specialist (Baltimore, Maryland)

Fri, 12 Sep 2008

Message by Our client is the medical devices and diagnostics division of a Fortune 500 company that is renowned for being one of America's top employers and one of the most elite brands in the world. on Fri, 12 Sep 2008 EST

Complaint System Specialist (New Jersey)

Fri, 5 Sep 2008

Message by Our client is a global leader in the processing of human bone and connective tissue for transplantation and an innovator in the development, manufacturing and marketing of biologic, biomaterial and device systems for musculoskeletal surgery. With a particular focus on spinal, trauma, and total joint revision procedures, the company's current and development-stage technologies address needs within numerous musculoskeletal disciplines. on Fri, 5 Sep 2008 EST

Clinical Compliance and Training Manager (Southern California)

Thu, 4 Sep 2008

Message by Our client is the biotech division of a world-leading healthcare company that has developed a reputation for successfully bringing complex products to market in a variety of therapeutic areas. With an experienced clinical team and empowering corporate culture that is focused on the professional development of its employees, this is a great opportunity for the right candidate. on Thu, 4 Sep 2008 EST

Vice President of Regulatory Affairs (Southern California)

Thu, 4 Sep 2008

Controlled Substances Manager (Miami, Florida)

Fri, 29 Aug 2008

Message by Our client is a publicly traded biopharmaceutical company that is dedicated to the development and commercialization of drug delivery therapies. The company has marketed products, an experienced management team and an empowering corporate culture that is focused on the professional development of its employees. This is a great opportunity for the right candidate. on Fri, 29 Aug 2008 EST

International Regulatory Affairs and Quality Specialist (Prairie du Sac, Wisconsin)

Thu, 28 Aug 2008

Message by Our client is a sports medicine product distributor that focuses on innovative products that are changing the way companies view the sports medicine industry. Their long line of products include support wraps and braces for joint injuries, as well as mouth guards and other sports accessories. Our client values teamwork and creative thinking and rewards employees with a competitive compensation package. This is a challenging opportunity for the right candidate. on Thu, 28 Aug 2008 EST

Vice President, Quality and Regulatory Affairs (Tuscon, Arizona)

Wed, 27 Aug 2008

Message by Our client is a global leading developer and manufacturer of medical diagnostic instrument and reagent systems. They focus on providing leading-edge automation technology for use in slide-based diagnosis of cancer and infectious disease. With their 40-acre campus HQ based in Tuscan, AZ, our client boasts a financial and intellectual capital to partner successfully with the healthcare community. Their products are found in hospital-based histology laboratories, independent reference laboratories and the drug discovery laboratories of some of the world�s largest pharmaceutical and biotechnology companies, government labs and medical research centers. This is an exciting opportunity for the right person to join a world leader. on Wed, 27 Aug 2008 EST

Regulatory Product Manager (Bloomsbury, New Jersey)

Wed, 27 Aug 2008

Message by Our client is a biopharmaceutical company focused on the discovery, development and potential commercialization of fully human antibody-based therapeutics to treat life- threatening and debilitating diseases including cancer, inflammation, autoimmune and infectious diseases. on Wed, 27 Aug 2008 EST

Compliance Audit Specialist (Bloomsbury, New Jersey)

Wed, 27 Aug 2008

Message by Our client is a biopharmaceutical company focused on the discovery, development and potential commercialization of fully human antibody-based therapeutics to treat life-threatening and debilitating diseases, including cancer, inflammation, autoimmune and infectious diseases. on Wed, 27 Aug 2008 EST

CMC Manager, Regulatory Affairs (Los Angeles, California)

Fri, 22 Aug 2008

Message by Our client is a publicly traded biotechnology company headquartered in Los Angeles that focuses on the development and commercialization of various oncology therapeutics. The company has an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. on Fri, 22 Aug 2008 EST

Director of Regulatory Affairs (Los Angeles, California)

Fri, 22 Aug 2008

Director of Regulatory Affairs (New Jersey)

Thu, 21 Aug 2008

Message by Our client is a dynamic and growing, independent contract drug development and consulting company. Employees at this company are experienced and highly qualified team players, essential to its success. on Thu, 21 Aug 2008 EST

Vice President of Regulatory Affairs (San Diego, CA)

Mon, 18 Aug 2008

Message by Our client is a developer of products to treat artery disease, which can occur throughout the body including the heart, neck, torso, and legs. At the core of this company lies a team of experts and successful medical device veterans that have developed a multi-use, proprietary catheter technology that identifies, selects and reduces atherosclerotic disease. The unique technology addresses the unique dynamics of arteries, utilizes well-known device procedures and does not require an implant, such as a stent. The company is initially targeting Peripheral Artery Disease (PAD), �probably the most under-diagnosed and least aggressively managed" of the three vascular beds.� on Mon, 18 Aug 2008 EST

Regulatory Affairs Specialist (Scottsdale, Arizona)

Mon, 11 Aug 2008

Message by Our client, based in Arizona, is a leading specialty pharmaceutical company focused on treating skin conditions. They are devoted to helping patients attain a healthy and youthful look and self-image. Our client has numerous leading branded prescription products in various therapeutic categories, like acne, fungal and skin infections. With a stable business in North America and an amazing track record of revenue, operating income growth and impressive gross profit margins, this is an exciting opportunity for someone to join a stable and profitable company. on Mon, 11 Aug 2008 EST

Regulatory Affairs Manager/Associate (Minneapolis, Minnesota)

Mon, 11 Aug 2008

Message by Our client is a rapidly expanding generic pharmaceutical company based in Minneapolis. They focus on the high-volume manufacturing of generic pharmaceuticals and OTC specialty products. Founded in 1977, they now have 250 employees, an 180,000 square feet facility and revenue of $120M this year alone. This is an excellent opportunity for the right person to join a stable, profitable and rapidly growing company! on Mon, 11 Aug 2008 EST

Director of Regulatory and Clinical Affairs (Bedford, Massachusetts)

Fri, 8 Aug 2008

Message by Our client is an leading diabetes management company based in Bedford MA. They focus on providing superior treatment options and lifelong health benefits for people with diabetes. Our client�s employees have extensive knowledge and experience in the diabetes and medical device industries. Their first marketable product is a new insulin blend. It brings together all of the functionality of a predictable insulin pump and blood glucose monitor into a system that features no tubing and automated cannula insertion. With a leading product on board and an experienced management team, this is an excellent opportunity for the right person to join a dynamic and rapidly growing company. on Fri, 8 Aug 2008 EST

Vice President of Scientific and Clinical Affairs (Cincinnati, Ohio)

Wed, 6 Aug 2008

Message by Our client is a leading provider of contracted drug development services to the pharmaceutical industry. Their services span from pre-clinical through manufacturing, clinical, regulatory and commercial phases of drug development. Our client�s executive team are accomplished leaders in the full spectrum of drug development and have extensive experience working in and with pharmaceutical, biotech and contract services organizations. on Wed, 6 Aug 2008 EST

Director and Subject Matter Expert (Cincinnati, Ohio)

Wed, 6 Aug 2008

Regulatory Affairs Manager (Pennsylvania)

Mon, 4 Aug 2008

Message by Our client is a publicly traded pharmaceutical company headquartered in Pennsylvania. The company develops generic therapeutics for the treatment of various diseases. The company has an excellent track record with regulatory agencies and an experienced management team. on Mon, 4 Aug 2008 EST

Director of Compliance (Long Island, New York)

Tue, 29 Jul 2008

Message by Our client is a New York-based cGMP facility with a strong pipeline. The company has an opportunity for growth. on Tue, 29 Jul 2008 EST

Director of Regulatory Affairs (Texas)

Tue, 22 Jul 2008

Director of Regulatory Affairs (East Coast, USA)

Mon, 21 Jul 2008

Message by Our client is a young venture-backed biotechnology company with several locations on the East Coast that focuses on the development and commercialization of devices for the orthopedic industry. The company has premier investors, an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. on Mon, 21 Jul 2008 EST

Clinical Affairs Manager (New Jersey)

Thu, 17 Jul 2008

Message by Our client is a leading medical device company. They have a leadership position in their targeted markets and an established reputation as a leading innovator in the field. The company has premier investors and a strong pipeline. This is a great opportunity for the right candidate. on Thu, 17 Jul 2008 EST

Regulatory Affairs Manager (Malvern, Pennsylvania)

Thu, 10 Jul 2008

Message by Our client is a life science company focused on the development of products that eliminate contagious pathogens. The company has an experienced management team, a varied selection of interesting protocols and an empowering corporate culture that is focused on the long-term development of it's employees. on Thu, 10 Jul 2008 EST

Director of Regulatory Affairs (Pennsylvania)

Wed, 9 Jul 2008

Message by Our client is a pharmaceutical company that develops, manufactures and markets pharmaceutical therapeutics for medical conditions requiring specialized treatment. The company�s prescription drugs are marketed both nationally and internationally. on Wed, 9 Jul 2008 EST

Regulatory Affairs Manager (Naples, Florida)

Tue, 8 Jul 2008

Message by Our client is a medical device company located in Naples, Florida. They focus on providing the finest quality engineered products and educational services for orthopedic surgeons. With over 3,000 products for arthroscopic and orthopedic surgical procedures (shoulder, knee/hip and small joint), our client has built up a strong customer base across the USA and in 60 countries worldwide. This is a great opportunity for the right candidate! on Tue, 8 Jul 2008 EST

Coordinator of CMC Services, Analytical (Cincinnati, Ohio)

Mon, 30 Jun 2008

Regulatory Affairs Manager (Massachusetts)

Fri, 27 Jun 2008

Message by Our client is a young venture-backed pharmaceutical company headquartered in Massachusetts that is using a science-driven approach to develop novel therapeutics to treat a number of large, poorly served dermatological disorders. The company has premier investors and an experienced management team that is committed to the highest standards of integrity and to improving the lives of patients and their families. This is a strong opportunity for someone that wants to put their drive and initiative to work! on Fri, 27 Jun 2008 EST

Director of Regulatory Affairs and Compliance (Connecticut)

Fri, 27 Jun 2008

Message by Our client is a leading global producer of active pharmaceutical ingredients. The company has demonstrated strong growth and profitability in recent years and brings a lengthy history of innovation to each of its products. With a profit sharing program and best-in-class benefits this is a great situation for a candidate that is pursuing a challenging and visible leadership opportunity. on Fri, 27 Jun 2008 EST

Senior Director, CMC Regulatory Affairs (San Diego, California)

Wed, 25 Jun 2008

Message by Our client is a biopharmaceutical company based in San Diego. They focus on in-licensing, developing and commercializing therapeutics for the treatment of cancer and infectious disease. Coupled with these is an experienced management team with significant product development, clinical, regulatory, finance and business management expertise. This is a great opportunity for the right individual to join a dynamic company! on Wed, 25 Jun 2008 EST

Senior Director of Global Regulatory Affairs (Vermont, New Jersey, New Hampshire, New York, California)

Fri, 27 Jun 2008

Message by Our client is an emerging biopharmaceutical company that is focused on the development and commercialization of next generation therapeutics for infectious diseases and cancer. With an experienced CEO and a strong, diverse pipeline, they present a great opportunity for the right candidate! on Fri, 27 Jun 2008 EST

Senior Director of Regulatory Affairs (Tampa, Florida)

Tue, 24 Jun 2008

Message by Our client is an ophthalmic biopharmaceutical company based in Florida. They focus on the discovery, development and commercialization of products to meet the medical needs for the preservation of eyesight. Their corporate headquarters are based in Tampa and they boast a state-of-the-art R&D center in San Diego. With an experienced management team, a robust pipeline and a �can do attitude�, this is a great opportunity for the right person to join a rapidly growing company! on Tue, 24 Jun 2008 EST

Director of Regulatory Affairs (California)

Tue, 24 Jun 2008

Message by Our client specializes in clinical research and is an expert in a variety of areas including trial design, quality of life and health economics. on Tue, 24 Jun 2008 EST

Associate Director of Regulatory Affairs (Westminster, Colorado)

Tue, 24 Jun 2008

Message by Our client is a biopharmaceutical company based in Westminster, Colorado. They focus on the development and commercialization of small molecule therapeutics for the treatment of cancer. Their team is dedicated to patients and the customers they serve. They want to attract, develop and retain world-class talent to build a high-performance organization. This is a great opportunity for the right candidate! on Tue, 24 Jun 2008 EST

Senior Regulatory Affairs Manager (Pennsylvania)

Tue, 24 Jun 2008

Message by Our client is a privately held biopharmaceutical company focused on the treatment of vascular disease. on Tue, 24 Jun 2008 EST

Vice President of Regulatory Affairs (Cambridge, Massachusetts)

Fri, 13 Jun 2008

Message by Our client is small private company that specializes in developing therapeutics for endocrinology, bone loss and neuromuscular disease. They have a strong pipeline as well as great leadership and culture. This opportunity is great for someone who is hands-on and is looking for a sense of ownership and accomplishment. on Fri, 13 Jun 2008 EST

Regulatory Affairs Manager/Associate (Kirkland, Washington)

Tue, 10 Jun 2008

Message by Our client is a privately owned medical device company that is focused on the treatment of vascular disease. The company has an experienced CEO and board, an exciting product candidate and a team that is committed to the highest standards of integrity and to improving the lives of patients and their families. on Tue, 10 Jun 2008 EST

Director of Regulatory Affairs (San Jose, California)

Tue, 10 Jun 2008

Message by Our client is a successful division of a world-leading medical device company that has developed a reputation for successfully bringing complex products to market in a variety of therapeutic areas. The company has some of the strongest financial indicators in the industry, an experienced management team and a robust pipeline. This is a strong opportunity for someone that wants to put their drive and initiative to work! on Tue, 10 Jun 2008 EST

Division Statistical Leader (Michigan)

Thu, 5 Jun 2008

Message by Our client is one of the world's leading medical device providers. They are a highly profitable, publicly traded company whose products are currently being sold in over 120 countries worldwide. This is a great opportunity for someone to join a company that offers a great corporate culture and is focused on the long-term development of its employees. on Thu, 5 Jun 2008 EST

Manager, ELISA Technology Lab (New York)

Thu, 5 Jun 2008

Message by Our client is a fast growing Contract Research Organization (CRO) located in Central New York State that focuses on conducting research and providing GLP/cGMP compliant analytical testing services for the development of various therapeutics for the Biotech/Pharmaceutical industry. The company has an experienced management team, a varied selection of interesting protocols and an empowering corporate culture that is focused on the long-term professional development of its employees. on Thu, 5 Jun 2008 EST

Regulatory Affairs Manager/Associate (Hudson, New Hampshire)

Wed, 4 Jun 2008

Message by Our client is a leading medical device company based in the Northeast. They specialize in developing technologies for the treatment of cardiovascular diseases, such as coronary stents and state-of-the-art hernia repair. The company has offices in Australia and The Netherlands and boasts a demand of over 2 million sterile medical products to over 60 countries every year. With emphasis placed on personal development of employees, this is a great opportunity for the right candidate! on Wed, 4 Jun 2008 EST

Regulatory Submissions Manager (The Woodlands, Texas)

Wed, 4 Jun 2008

Message by Our client is a rapidly growing biopharmaceutical company based in The Woodlands, Texas. Using their state of the art technology, they have discovered the physiological and behavioral functions of nearly 5,000 genes. They have an exciting goal of advancing 10 drug candidates into human clinical trials by the year 2010. This is a great opportunity for someone looking for personal growth and a challenge! on Wed, 4 Jun 2008 EST

Process Equipment Engineer (San Diego, Southern California)

Tue, 3 Jun 2008

Message by Our client is an acute care specialty pharma company based in San Diego. They specialize in a technology that provides sustained-release delivery of medications for post-surgical pain. Our client has two marketed products that are used by professionals in the healthcare industry. The company has premier investors, an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. on Tue, 3 Jun 2008 EST

Toxicologist (Lake Forest, Illinois)

Mon, 2 Jun 2008

Message by Our client is a global specialty pharma and medical device company located just outside of Chicago, IL. They focus on the design, development, and manufacturing of solutions to improve the safety, delivery and effectiveness of patient healthcare. on Mon, 2 Jun 2008 EST

Director of Pre-clinical Development/Toxicology (Lake Forest, Illinois)

Mon, 2 Jun 2008

Regulatory Affairs Project Manager (Toronto, Ontario)

Fri, 23 May 2008

Message by Our client is a top 10 pharmaceutical company that has established a reputation as one of the most desirable companies to work for in Canada. With operations around the globe and an empowering corporate culture that is focused on the professional development of its employees, this is a strong opportunity for the right candidate! on Fri, 23 May 2008 EST

Medical Products Manager (Honolulu, Hawaii)

Wed, 21 May 2008

Message by Our client is a rapidly growing company headquartered in Honolulu that is focused on tissue generation for people with illness. The company has an experienced management team and an empowering corporate culture that is focused on the professional development of its employees. on Wed, 21 May 2008 EST

Toxicologist (Illinois)

Thu, 15 May 2008

Message by Our client is a publicly traded provider of personal care products that has established a reputation as one of the best managed companies in North America. With operations in over 120 countries, over $1B in revenue, and an empowering corporate culture that is focused on the professional development of its employees, this is a strong opportunity for the right candidate! on Thu, 15 May 2008 EST

Director of Regulatory Affairs (West Coast)

Tue, 13 May 2008

Senior Manager, Regulatory Affairs (North Carolina)

Mon, 5 May 2008

Message by Our client is a well established biologics (allergy extract) located in beautiful Western North Carolina. The company, founded in 1904, is a leader in developing and providing allergy immunotherapy products/services for treatment of human beings and animals. In addition to their current product line, they have clinical trials also in process. on Mon, 5 May 2008 EST

Senior Regulatory Affairs Specialist (South California)

Mon, 28 Apr 2008

Associate Director of Regulatory Affairs (New Jersey)

Mon, 28 Apr 2008

Message by Our client is a publicly traded pharmaceutical company headquartered in NJ with over 10 years of success in the development and commercialization of OTC therapeutics. The company has some of the strongest financial indicators in the industry, an experienced management team and a robust pipeline. They also offer an empowering corporate culture that is focused on the professional development and advancement of clinical team members. on Mon, 28 Apr 2008 EST

Scientist, Regulatory Affairs (San Francisco, California)

Tue, 22 Apr 2008

Message by Our client is a leading drug company with close to $10B in sales and over 10,000 employees worldwide. The company has strong financials, an experienced management team and a loyal customer base. They have developed an industry-wide reputation for a positive work environment and an aggressive training program that ensures employees are up-to-date on current trends and best practices. This is a strong opportunity for someone that wants to put their drive and initiative to work! on Tue, 22 Apr 2008 EST

Director, Regulatory Affairs (New York)

Mon, 21 Apr 2008

Message by Our client is a leading medical device company specialized in ophthalmology and eye care products. They have over 13,000 employees globally and a reputation as a leading innovator in the field. With operations in 36 countries and a 150-year track record of success, this is a great situation for a candidate that is pursuing a challenging opportunity with a world-class employer. on Mon, 21 Apr 2008 EST

Regulatory Affairs Manager (Pennsylvania)

Thu, 17 Apr 2008

Message by Our client is a leading medical device company headquartered in Pennsylvania, which is focused on the development and commercialization of various fluid collection devices. The company has an experienced management team, a varied selection of interesting protocols and an empowering corporate culture that is focused on the long-term development of its employees. on Thu, 17 Apr 2008 EST

Manager Regulatory Affairs (North East, USA)

Wed, 16 Apr 2008

Message by Our client is a rapidly growing biotech company headquartered in the NE that is focused on the development and commercialization of various therapeutic for Cardiology. on Wed, 16 Apr 2008 EST

Regulatory Affairs Supervisor (New Jersey)

Wed, 16 Apr 2008

Message by Our client is a leading pharmaceutical company specialized in pain therapy. They have close to 5,000 employees globally and have a developed a reputation as a leading innovator in the field. With operations in approximately 30 countries and a 70-year track record of success, this is a great situation for a candidate that is pursuing a challenging opportunity with a world-class employer. on Wed, 16 Apr 2008 EST

Regulatory Affairs Supervisor (Minneapolis, Minnesota)

Tue, 15 Apr 2008

Message by Our client is a leading producer of medical device products with approximately 4,000 employees globally. The company has exceeded all growth expectations over the past few years and has demonstrated a stable history, recently celebrating their 50th anniversary! This is a great situation for a candidate that is pursuing a challenging and visible opportunity with a world-class employer. on Tue, 15 Apr 2008 EST

Regulatory Toxicologist (East Coast, USA)

Mon, 14 Apr 2008

Message by Our client is a world-leading specialty chemical and materials� company that has developed a reputation for successfully bringing impacting products to market. The company has marketed products, an experienced management team and an empowering corporate culture that is focused on the professional development of its employees; this is a great opportunity for the right candidate! on Mon, 14 Apr 2008 EST

Director/Senior Director of Regulatory Affairs (Lexington, Massachusetts)

Wed, 2 Apr 2008

Message by Our client is a global biopharmaceutical company headquartered in MA that is dedicated to the development and commercialization of therapeutics for the treatment of anti infective diseases.The company has marketed products, an experienced management team, and an empowering corporate culture that is focused on the professional development of its employees, this is a great opportunity for the right candidate! on Wed, 2 Apr 2008 EST

Associate Director of Regulatory Affairs (Southern California)

Mon, 31 Mar 2008

Message by Our client is a rapidly growing contract drug development and manufacturing company that provides complete solutions for API, prototype and final product, clinical supplies, as well as commercial production and distribution. The company has an experienced management team, a strong track record with its clients and an empowering corporate culture that is focused on the long-term professional development of its employees. on Mon, 31 Mar 2008 EST

Regulatory Affairs Operations Specialist IV (Irvine, California)

Fri, 28 Mar 2008

Message by Our client is a leading pharmaceutical company headquartered in California that is focused on the development and commercialization of various ophthalmology diseases therapeutics. The company has marketed products, an experienced management team, and an empowering corporate culture that is focused on the professional development of its employees; this is a great opportunity for the right candidate! on Fri, 28 Mar 2008 EST

Regulatory Affairs Operations Specialist I (Irvine, California)

Thu, 27 Mar 2008

Message by Our client is a leading pharmaceutical company headquartered in California that is focused on the development and commercialization of various ophthalmology disease therapeutics. The company has marketed products, an experienced management team, and an empowering corporate culture that is focused on the professional development of its employees; this is a great opportunity for the right candidate! on Thu, 27 Mar 2008 EST

Regulatory Affairs Specialist IV (Irvine, California)

Thu, 27 Mar 2008

Senior Regulatory Affairs Representative (North California)

Tue, 25 Mar 2008

Regulatory Affairs Representative (North California)

Wed, 26 Mar 2008

Senior Regulatory Affairs Specialist (Massachusetts)

Fri, 14 Mar 2008

Message by Our client is a leading medical device company, which is focused in the development and commercialization of less invasive medical devices and procedures. The company has an experienced management team, a varied selection of interesting protocols and an empowering corporate culture that is focused on the long-term professional development of its employees. on Fri, 14 Mar 2008 EST

Principle Specialist, Corporate Regulatory Affairs (Massachusetts)

Thu, 13 Mar 2008

Regulatory Affairs Manager (Endoscopy) (Massachusetts)

Thu, 13 Mar 2008

Regulatory Affairs Manager (Irvine, California)

Wed, 12 Mar 2008

Message by Our client is a publicly traded pharmaceutical company headquartered in Southern California that is dedicated to the development and commercialization of generic therapeutics for the treatment of various diseases. The company has an excellent track record with regulatory agencies, an experienced management team, and an empowering corporate culture that is focused on the professional development of its employees. on Wed, 12 Mar 2008 EST

Associate Director, Regulatory Affairs (Oncology) (New Jersey)

Mon, 10 Mar 2008

Message by Our client is a human health care company seeking innovative solutions in disease prevention, cure and care for the health and well being of people worldwide. on Mon, 10 Mar 2008 EST

Director Regulatory Affairs (Midwest, USA)

Mon, 10 Mar 2008

Message by Our client is a rapidly growing pharmaceutical company headquartered in the Midwest that is focused on the development and commercialization of therapeutic radio-pharmaceuticals for the US nuclear medicine market. The company has an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. on Mon, 10 Mar 2008 EST

Director of Monitoring Services (Home-Based) (East Coast, USA)

Fri, 7 Mar 2008

Message by Our client, a niche CRO with focus on oncology studies, has an opportunity for home-based Director of Monitoring Services. on Fri, 7 Mar 2008 EST

Regulatory Affairs Manager (Pennsylvania)

Wed, 5 Mar 2008

Message by Our client is a reputable R&D company based in PA. They focus on assisting pharmaceutical companies across the globe in product development. The company has an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. on Wed, 5 Mar 2008 EST

Director (Scientific and Regulatory Affairs) (Ohio)

Wed, 5 Mar 2008

Message by Our client is a privately owned specialty pharmaceutical company focused on the design, development and commercial manufacture of sterile, injectable, sustained release pharmaceuticals. Products of this class have extremely high commercial potential. Our client concentrates exclusively in this drug delivery space. They are advancing their lead products, and building successful partnerships with major and specialty pharmaceutical companies worldwide. on Wed, 5 Mar 2008 EST

Regulatory Affairs Manager (Bohemia, NY)

Mon, 18 Feb 2008

Message by Our client is a leading medical device company based in Bohemia, New York. The company has marketed products, an experienced management team, and an empowering corporate culture that is focused on the professional development of its employees. This is a great opportunity for the right candidate! on Mon, 18 Feb 2008 EST

Senior Director of Regulatory Affairs (Los Angeles, CA)

Thu, 14 Feb 2008

Message by Our client, a clinical site dedicated to oncology patients, has an immediate need of two experienced clinical research nurses. on Thu, 14 Feb 2008 EST

Senior Regulatory Affairs Specialist (Michigan)

Mon, 4 Feb 2008

Message by Our client is one of the world's leading medical device providers. They are highly profitable, publicly traded company whose products are currently being sold in over 120 countries worldwide. This is a great opportunity for someone to join a company that offers a great corporate culture and is focused on the long-term development of its employees. on Mon, 4 Feb 2008 EST

Reimbursement Manager (Redwood City, CA)

Fri, 1 Feb 2008

Message by Excellent opportunity to join a growing medical device company focused in the treatment of pulmonary diseases. on Fri, 1 Feb 2008 EST

Medical Writer (Houston, TX)

Wed, 9 Jan 2008

Message by Our client is a reputable, mid-size CRO that is experiencing unprecedented growth. The company has an experienced management team, a varied selection of interesting protocols and an empowering corporate culture that is focused on the long-term professional development of its employees. on Wed, 9 Jan 2008 EST

CMC Manager, Regulatory Affairs (Southeast USA)

Wed, 9 Jan 2008

Message by Our client is a publicly traded biopharmaceutical company that is dedicated to the development and commercialization of trans-dermal therapies. The company has marketed products, an experienced management team and an empowering corporate culture that is focused on the professional development of its employees; this is a great opportunity for the right candidate! on Wed, 9 Jan 2008 EST

Regulatory Affairs Manager (Southern California)

Fri, 4 Jan 2008

Message by Our client is the biotech division of a world leading healthcare company that has developed a reputation for successfully bringing complex products to market in a variety of therapeutic areas. With an experienced clinical team and empowering corporate culture that is focused on the professional development of its employees, this is a great opportunity for the right candidate! on Fri, 4 Jan 2008 EST

Senior Regulatory Affairs Associate (California)

Thu, 27 Dec 2007

Message by Our client is dedicated to improving and preserving human life by developing innovative pharmaceutical products. The company�s premier product has been developed for delaying/preventing renal flares. Treatment for various other autoimmune and inflammatory conditions have also been developed by the company. on Thu, 27 Dec 2007 EST

Associate Director, Regulatory Affairs (Colorado)

Thu, 27 Dec 2007

Message by Our client is a biopharmaceutical company dedicated to discovering, developing and commercializing orally active drugs that address significant unmet medical needs. Primarily focused on the treatment of cancer and inflammatory disease, their proprietary drug development pipeline includes several small molecule drug candidates designed to regulate targets in therapeutically important biologic pathways. This company aims to be the most efficient inventor of therapeutic products in the pharmaceutical industry. on Thu, 27 Dec 2007 EST

Regulatory Affairs Associate (San Diego, CA)

Thu, 27 Dec 2007

Message by Our client is a rapidly growing medical device company headquartered in San Diego that is known for innovative strides in the development and commercialization of minimally invasive therapies. The company has an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. on Thu, 27 Dec 2007 EST

Regulatory Affairs Manager (Florida)

Thu, 27 Dec 2007

Message by Our client is a specialty generic pharmaceutical company engaged in the formulation and commercialization of both controlled release (CR) and immediate release (IR) products utilizing their proprietary drug delivery technologies. By applying the technologies to selected generic prescription pharmaceuticals, they seek to duplicate the release characteristics of these drugs in order to manufacture and market versions that can be substituted for branded products. The company intends to develop and use their drug delivery technologies to commercialize a portfolio of generic pharmaceutical products. In the near future, they also plan to apply their drug delivery technologies to the development of proprietary branded drugs. on Thu, 27 Dec 2007 EST

Regulatory Affairs Analyst (Michigan)

Thu, 27 Dec 2007

Message by Our client supplies incorporated services in product development, manufacturing, packaging and logistics. The company is synergistic, focused and has a leading edge. It offers challenging opportunities by empowering people to their full potential. on Thu, 27 Dec 2007 EST

Director of Regulatory Affairs (Northern California)

Thu, 27 Dec 2007

Message by Our client is amongst the top servers of science and serves up to 35,000 customers in varied fields such as pharmaceutical and biotech companies, hospitals and clinical diagnostics labs, industrial process control settings, environmental settings, government agencies and also to universities and research institutes. The company has over 30,000 employees working for it in across 150 countries worldwide. They provide a complete range of high-end equipments, analytical instruments, reagents and consumables. They also provide software and services for research, analysis, discovery and diagnostics. on Thu, 27 Dec 2007 EST

Regulatory Affairs Manager (Northern California)

Thu, 27 Dec 2007

Message by Our client is amongst the top servers of science and serves up to 35,000 customers in varied fields such as pharmaceutical and biotech companies, hospitals and clinical diagnostics labs, industrial process control settings, environmental settings, government agencies and also to universities and research institutes. The company employs over 30,000 people across 150 countries worldwide and provides a total range of high-end equipments, analytical instruments, reagents and consumables. They also provide software and services for research, analysis, discovery and diagnostics. on Thu, 27 Dec 2007 EST

Regulatory Affairs Manager (California)

Thu, 27 Dec 2007

Message by Our client is a publicly traded pharmaceutical company headquartered in Southern California that is dedicated to the development and commercialization of generic therapeutics for the treatment of various diseases. The company has an excellent track record with regulatory agencies, an experienced management team and an empowering corporate culture that is focused on the professional development of its employees. on Thu, 27 Dec 2007 EST

Senior Manager/Associate Director of Regulatory Affairs (Los Angeles, California)

Thu, 27 Dec 2007

Message by Our client is a privately owned biopharmaceutical company headquartered in Los Angeles that is dedicated to the development and commercialization of protein and antibody-based therapeutics for the treatment of various diseases. They have an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. on Thu, 27 Dec 2007 EST

Regulatory Affairs Associate (Maryland)

Thu, 27 Dec 2007

Message by Our client is a company dealing in the biopharmaceutical sector, developing novel gene-based therapeutic drugs and vaccines. These products help in the production of proteins directly at the site of disease by the genes it delivers. All gene-based therapies use the same patent protected technology. on Thu, 27 Dec 2007 EST

Regulatory Affairs Specialist � I (New Jersey)

Thu, 27 Dec 2007

Message by Our client is in the field of human bone and connective tissue processing for transplants and is a world leader in their field. They are also an innovator in the development, manufacturing, and marketing of biological, biometrical, and device systems for musculoskeletal surgery. The company�s present and development-stage technologies address the needs within many musculoskeletal disciplines. on Thu, 27 Dec 2007 EST

Senior Regulatory Affairs Specialist (New Jersey)

Thu, 27 Dec 2007

Senior Manager of Regulatory Affairs (Ontario)

Thu, 27 Dec 2007

Message by Our client is an innovative drug development company. The firm develops pain reliever and acne treatment formulas. It uses advanced drug delivery technologies to create novel molecule formulations, which can be commercialized and are currently marketed by the company. They currently have three late-stage drugs in their clinical expansion channel. on Thu, 27 Dec 2007 EST

Director of Regulatory Affairs (Pennsylvania)

Thu, 27 Dec 2007

Message by Our client is a pharmaceutical company and works to develop, manufacture and market pharmaceutical therapies indicated for diseases/medical conditions requiring specialized treatment. The company�s prescription drugs are marketed both nationally and internationally. It caters to therapeutic categories of antiviral and anti-fungal agents. on Thu, 27 Dec 2007 EST

Associate Director of Regulatory Affairs (New York)

Thu, 27 Dec 2007

Message by Our client, a biopharmaceutical company, focuses on developing therapeutic products, for the medical needs of patients with debilitating conditions and life threatening diseases. The programmes of the company are intended for gastroenterology as well as treating HIV infection and cancer. The company has many products in the development and pre-clinical development stage. on Thu, 27 Dec 2007 EST

Regulatory Affairs Manager (New York)

Thu, 27 Dec 2007

Director of Regulatory Affairs (New Jersey)

Thu, 27 Dec 2007

Message by Our client is a leading privately held pharmaceutical company with operations in over 40 countries. With marketed products, an experienced management team, and an empowering corporate culture that is focused on the professional development of its employees, this is a great opportunity for the right candidate! on Thu, 27 Dec 2007 EST

Regulatory Affairs Specialist (Montreal, Quebec)

Thu, 27 Dec 2007

Message by Our client is a biotechnology company focused on developing new treatments for under-served markets in oncology and infectious diseases. on Thu, 27 Dec 2007 EST

Associate/Director of Regulatory Affairs (Maryland)

Thu, 27 Dec 2007

Message by Our client is a rapidly growing biotech company headquartered in Maryland that is focused on the development and commercialization of various therapeutics for disorders of the nervous system. The company has an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. on Thu, 27 Dec 2007 EST

Director of Regulatory Affairs (California)

Thu, 27 Dec 2007

Message by Our client is into brand and generic pharmaceutical products. It develops, manufactures, markets and distributes such products. The Corona-based specialty pharmaceutical company has one of the broadest product offerings in the US generics industry and a track record of service excellence. It is well known as a reliable and low-cost provider of quality pharmaceutical products. on Thu, 27 Dec 2007 EST

Regulatory Affairs Manager (Northern California)

Thu, 27 Dec 2007

Message by Our client is into brand and generic pharmaceutical products. It develops, manufactures, markets and distributes such products. The Corona-based specialty pharmaceutical company has one of the broadest product offerings in the U.S. generics industry and a track record of service excellence. It is well known as a reliable and low-cost provider of quality pharmaceutical products. on Thu, 27 Dec 2007 EST

Director of Regulatory Affairs (California)

Thu, 27 Dec 2007

Message by Our client is a medical device company that designs, develops and markets products for restoring blood flow in patients who have suffered ischemic strokes, resulting from blood clots in the vessels of the brain. on Thu, 27 Dec 2007 EST

Manager, Regulatory Affairs (New Jersey)

Fri, 28 Dec 2007

Message by Our client is a bio pharmaceutical company with four licensed products, two manufacturing sites and a strong program in research and development. on Fri, 28 Dec 2007 EST

Regulatory Affairs Manager (California)

Fri, 28 Dec 2007

Message by Our client is a leading biopharmaceutical company based in San Francisco. The company focuses on the discovery, development and marketing of cardiovascular and anti-cancer therapies. Founded by cell biology pioneers working to create a unique and powerful approach to drug discovery, their mission is to translate cell biology into novel pharmaceuticals and technologies. The company�s exceptional approach has created two cancer drug candidates, one heart failure drug candidate and numerous other research programs addressing a variety of disease areas. Its development programs are based on a mechanistic understanding of the biology underlying their interests in cell cycle control and contractility. on Fri, 28 Dec 2007 EST

Regulatory Affairs Manager (New Jersey)

Fri, 28 Dec 2007

Message by Our client is a biopharmaceutical company dedicated to the development and commercialization of therapeutics to treat patients with cancer and other life-threatening diseases. The company has an experienced management team, a strong pipeline and multiple products currently on the market. on Fri, 28 Dec 2007 EST

Regulatory Affairs Manager (San Diego, California)

Fri, 28 Dec 2007

Message by Our client is a biopharmaceutical company based in San Diego. The company focuses on in-licensing, developing and commercializing products pharmaceuticals to meet the needs of hospitalized patients and their care givers. Since their inception in 2004, they have in-licensed rights to two Phase III products, both of which have been studied in previous Phase III clinical trials conducted by their licensors. on Fri, 28 Dec 2007 EST

Regulatory Affairs Manager (East Coast, USA)

Fri, 28 Dec 2007

Message by Our client is a biopharmaceutical company. From treating life-threatening and incapacitating diseases (including cancer, autoimmune and infectious diseases), the company is focused on the discovery, development and potential commercialization of therapeutics. These are fully human antibody-based therapeutics. on Fri, 28 Dec 2007 EST

Director of Regulatory Affairs (Washington)

Sun, 30 Dec 2007

Message by Our client is committed to developing, acquiring, and commercializing innovative treatments for cancer. The company pursues making cancer more treatable. They are developing a diversified portfolio of oncology products focused on identifying new, less toxic and more effective cancer therapies. on Sun, 30 Dec 2007 EST

Director of Regulatory Affairs (Kansas)

Thu, 3 Jan 2008

Message by Our client is a premier biopharmaceutical company. The company is focused on the discovery, development, and commercialization of novel small molecule drugs. on Thu, 3 Jan 2008 EST

Director of Regulatory Affairs (Washington)

Sun, 30 Dec 2007

Message by Our client is located in Kirkland Lake, Washington, and was founded in late �80s. The company is into designing, developing and manufacturing innovative medical devices intended for the treatment of arterial disease. The company's primary focus is on peripheral artery disease (PAD). on Sun, 30 Dec 2007 EST

Manager Regulatory Affairs and Compliance (Virginia)

Sun, 30 Dec 2007

Message by Our client is a rising biopharmaceutical company engaged in the research and development of therapeutic products for transdermal delivery. The company�s task is to use their own technology to develop and commercialize products to overcome therapeutic barriers, and raise the standard of care for certain chronic conditions. on Sun, 30 Dec 2007 EST

Regulatory Affairs Manager (Dallas, Texas)

Sun, 30 Dec 2007

Message by Our client is a manufacturer of dietary supplements and personal care products. The company follows Good Manufacturing Practices (GMPs), product formulation standards and product labeling standards of the countries that it does business with. on Sun, 30 Dec 2007 EST

Regulatory Affairs Manager (Saskatchewan)

Thu, 3 Jan 2008

Message by Our client is a leading biomedical company focused on enhancing patient care. on Thu, 3 Jan 2008 EST

Regulatory Affairs Manager (Arkansas)

Thu, 3 Jan 2008

Message by Our client is a leading biomedical company focused on enhancing patient care. on Thu, 3 Jan 2008 EST

Clinical Trial Manager (Newfoundland and Labrador)

Thu, 3 Jan 2008

Message by Our client is a publicly traded biotechnology company. The company has an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. on Thu, 3 Jan 2008 EST

Clinical Trial Manager (Delaware)

Thu, 3 Jan 2008

Message by Our client is a biopharmaceutical company focused on development and commercialization of therapeutic products. on Thu, 3 Jan 2008 EST

Clinical Trial Manager (Michigan)

Thu, 3 Jan 2008

Message by Our client is a biopharmaceutical company focused on development and commercialization of therapeutic products. on Thu, 3 Jan 2008 EST

Clinical Operations Manager (New Brunswick)

Thu, 3 Jan 2008

Message by Our client is a leading drug discovery company dedicated to the discovery and development of therapeutics across various therapy areas. on Thu, 3 Jan 2008 EST

Senior Regulatory Affairs Manager (Texas)

Sun, 30 Dec 2007

Message by Our client represents one of the most significant market opportunities in the medical device industry today. Their aim is to develop, manufacture, and market advanced products such as spinal cord stimulation (SCS) to improve the quality of life for people who suffer with disabling pain or nervous system disorders. on Sun, 30 Dec 2007 EST

Regulatory Affairs Manager (San Diego, California)

Sun, 30 Dec 2007

Message by Our client is a rapidly growing biotech company headquartered in San Diego that is focused on the development and commercialization of various oncology and infectious disease therapeutics. The company has an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. on Sun, 30 Dec 2007 EST

Manager of Regulatory Affairs (New Jersey)

Mon, 31 Dec 2007

Message by Our client is an international pharmaceutical company headquartered in New Jersey with a 60-year history of service in the development and commercialization of various oncology and CNS therapeutics. The company has an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. on Mon, 31 Dec 2007 EST

Senior Manager Regulatory Affairs/Biologics (New York)

Mon, 31 Dec 2007

Message by Our client focuses on the development of therapeutic products and has programs aimed at treating gastroenterology, cancer and HIV infection. The company�s products are used to treat patients with life-threatening diseases and incapacitating conditions. It has several products candidates � both in clinical and preclinical development. on Mon, 31 Dec 2007 EST

Manager of Regulatory Affairs (New Jersey)

Mon, 31 Dec 2007

Senior Director of Global Regulatory Affairs (California)

Mon, 31 Dec 2007

Message by Our client is an emerging biopharmaceutical company that is focused on the development and commercialization of next generation therapeutics for infectious diseases and cancer. The company has an established revenue stream, experienced management staff, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. on Mon, 31 Dec 2007 EST

Associate Director of Regulatory Affairs (California)

Mon, 31 Dec 2007

Message by Our client is an emerging biopharmaceutical company that is focused on the development and commercialization of next generation therapeutics for infectious diseases and cancer. The company has an established revenue stream, experienced management staff, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. on Mon, 31 Dec 2007 EST

Associate Director/Director, Medical Regulatory Writing (Pennsylvania)

Mon, 31 Dec 2007

Message by Our client has pioneered a company focused on meeting the growing demand for credible evidence as it believes that this evidence can make a difference when trying to bring a drug to market and that it can enhance healthcare by defining patient requirements, clarifying therapeutic options, and providing patients with appropriate access to the medicines that they need. The company�s comprehensive services cover early-stage product planning through post-approval development. Its depth of industry expertise and a unique operational capability enables the company to demonstrate clinical benefit, manage safety, and minimize risk. The company helps document the economic value of medicines, and develop the evidence that is necessary to secure appropriate coverage and reimbursement. on Mon, 31 Dec 2007 EST

Senior Regulatory Affairs Specialist (Northern California)

Mon, 31 Dec 2007

Message by Our client is a successful molecular diagnostics business with powerful genomic and proteomic discovery platforms that have identified and validated new drug targets and biomarkers. The company is dedicated to advance the practice of Targeted Medicine. It develops and sells a growing number of molecular diagnostic products with a strategic alliance partner. The company is developing new molecular diagnostics and pharmacogenomic tests, and is also creating additional value through collaborations based on its genomic discoveries, including new druggable targets, new indications for existing drugs, and pharmacogenomic markers for predicting therapy response. The company is also using its high-throughput proteomics discovery platform to identify and validate novel targets in cancer. on Mon, 31 Dec 2007 EST

Senior Manager, Regulatory Affairs (Northern California)

Mon, 31 Dec 2007

Senior Manager, Regulatory Affairs (Northern California)

Mon, 31 Dec 2007

Regulatory Affairs Associate (Ohio)

Mon, 31 Dec 2007

Message by Our client is a contract drug development company that has established relationships with many pharmaceutical and biotechnology companies in over 17 countries. The company�s services include, early-stage development and trials through late-stage development and trials, CMC and CMO, pharmacokinetics, and CRO services. The company also assists its clients with regulatory consulting, review, and submissions via eCTD. on Mon, 31 Dec 2007 EST

Clinical Compliance Associate (New York)

Mon, 31 Dec 2007

Message by Our client is a leading global health-care supplier and the world�s largest manufacturer of over-the-counter (OTC) pharmaceutical and nutritional products for the store-brand market. The company also develops and manufactures generic prescription (Rx) drugs, active pharmaceutical ingredients (API), and consumer products. on Mon, 31 Dec 2007 EST

Senior Project Manager (New York)

Mon, 31 Dec 2007

Message by Our client is a leading global healthcare supplier and the world�s largest manufacturer of Over-the-Counter (OTC) pharmaceutical and nutritional products for the store-brand market. The company also develops, manufactures, and markets generic prescription (Rx) drugs, Active Pharmaceutical Ingredients (API), and consumer products. on Mon, 31 Dec 2007 EST

Director of Regulatory Affairs and Quality Assurance (Georgia)

Mon, 31 Dec 2007

Message by Our client is a leading medical device company that engineers and markets safe medication delivery systems. The company is also a champion in its quest to protect healthcare workers, patients, and the environment with innovative medical devices. Our client has developed a patented syringe that offers enhanced infection control and protection for needle-stick injuries. on Mon, 31 Dec 2007 EST

Senior Regulatory Affairs Manager (West Coast, USA)

Mon, 31 Dec 2007

Message by Our client is a medical device company committed to developing innovative medical technologies that restore function and quality of life to people who suffer from stroke and other neurological disorders. on Mon, 31 Dec 2007 EST

Regulatory Affairs Manager (Maryland)

Mon, 31 Dec 2007

Message by Our client is a biopharmaceutical company focused on the development, manufacture, and commercialization of biopharmaceutical products such as vaccines and immune globulins that induce the body's immune system to prevent or treat disease. The company operates in two business segments: biodefense and commercial. In its biodefense business the company develops and commercializes immunobiotics for use against biological agents that are potential biological weapons. In its commercial business, the company develops immunobiotics for use against infectious diseases with significant unmet or underserved medical needs. on Mon, 31 Dec 2007 EST

Regulatory Affairs Manager (Maryland)

Mon, 31 Dec 2007

Director of Regulatory Affairs (Southeast USA)

Mon, 31 Dec 2007

Message by Our client is a Contract Research Organization (CRO), which manages individual as well as entire development programs for its clients. Using its fully validated systems, the company can customize and accelerate the processing and reporting of clinical data. on Mon, 31 Dec 2007 EST

Deputy Director of Regulatory Affairs (Pennsylvania)

Mon, 31 Dec 2007

Message by Our client is a leading producer of vaccines. The company employs over 8500 people and has a presence in 150 countries. on Mon, 31 Dec 2007 EST

Deputy Director of Regulatory Affairs (Pennsylvania)

Mon, 31 Dec 2007

Message by Our client is a leading producer of vaccines. The company employs over 8500 people and has a presence in 150 countries. on Mon, 31 Dec 2007 EST

Regulatory Affairs Manager (California)

Mon, 31 Dec 2007

Message by Our client is a premier molecular diagnostics business that uses proprietary genomics and proteomics discovery platforms to identify and validate novel diagnostic markers. The company develops diagnostic products based on these as well as other known markers. on Mon, 31 Dec 2007 EST

Director of Regulatory Affairs (California)

Mon, 31 Dec 2007

Message by Our client creates, distributes, and sells topical skin care as well as restoration products. These include prescription creams and liquids for photodamage, hyperpigmentation, wrinkles, and other skin imperfections. The company has more than 70 employees, but is planning to grow its employee strength to 145. on Mon, 31 Dec 2007 EST

Regulatory Affairs Manager (Maryland)

Mon, 7 Jan 2008

Message by Our client is a leader in the development of compounds used in a variety of clinical indications. Established in 1950s, the company offers the stability of a well-established organization along with the flexibility of a startup. Priding themselves on their aggressive pipeline, the small North American office provides a family environment allowing each individual to be a contributing member of the team. on Mon, 7 Jan 2008 EST

Contract Regulatory Affairs Associate (New Jersey)

Mon, 7 Jan 2008

Message by Our client is dedicated to developing and commercializing novel therapeutic products in the field of oncology. on Mon, 7 Jan 2008 EST

Director of Regulatory Affairs (New York City, New York)

Mon, 7 Jan 2008

Message by Our client is a biopharmaceutical company focused on the development of drugs to treat leukemia, multiple myeloma and osteolytic bone disease. on Mon, 7 Jan 2008 EST

Regulatory Affairs Manager (Dublin, Ohio)

Mon, 7 Jan 2008

Message by Our client is a leading biomedical company focused on enhancing patient care and improving patient outcome by meeting the physicians� critical intraoperative diagnostic information needs and patients� therapeutic treatment needs. on Mon, 7 Jan 2008 EST