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Sterling Life Sciences, Specialists in Pharmaceuticals, Healthcare and BioTech Recruitment
Career Opportunities

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Position: Location:
Senior Regulatory Affairs Representative
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.
North California
Regulatory Affairs Representative
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.
North California
Senior Regulatory Affairs Specialist
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.
Massachusetts
Principle Specialist, Corporate Regulatory Affairs
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.
Massachusetts
Regulatory Affairs Manager (Endoscopy)
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.
Massachusetts
Regulatory Affairs Manager
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.
Irvine, California
Associate Director, Regulatory Affairs (Oncology)
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.
New Jersey
Director Regulatory Affairs
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.
Midwest, USA
Director of Monitoring Services (Home-Based)
Our client, a niche CRO with focus on oncology studies, has an opportunity for home-based Director of Monitoring Services.
East Coast, USA
Regulatory Affairs Manager
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.
Pennsylvania
Director (Scientific and Regulatory Affairs)
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.
Ohio
Regulatory Affairs Manager
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!
Bohemia, NY
Senior Director of Regulatory Affairs
Our client, a clinical site dedicated to oncology patients, has an immediate need of two experienced clinical research nurses.
Los Angeles, CA
Senior Regulatory Affairs Specialist
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.
Michigan
Reimbursement Manager
Excellent opportunity to join a growing medical device company focused in the treatment of pulmonary diseases.
Redwood City, CA
Medical Writer
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.
Houston, TX
CMC Manager, Regulatory Affairs
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!
Southeast USA
Regulatory Affairs Manager
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!
Southern California
Senior Regulatory Affairs Associate
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.
California
Associate Director, Regulatory Affairs
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.
Colorado
Regulatory Affairs Associate
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.
San Diego, CA
Regulatory Affairs Manager
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.
Florida
Regulatory Affairs Analyst
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.
Michigan
Director of Regulatory Affairs
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.
Northern California
Regulatory Affairs Manager
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.
Northern California
Regulatory Affairs Manager
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.
California
Senior Manager/Associate Director of Regulatory Affairs
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.
Los Angeles, California
Regulatory Affairs Associate
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.
Maryland
Regulatory Affairs Specialist – I
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.
New Jersey
Senior Regulatory Affairs Specialist
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.
New Jersey

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