US Regulatory Affairs Lead - Personal Care Category SCOPE OF RESPONSIBILITIES: He/She will be accountable to support regulatory for Personal Care Brands in NA Consumer Healthca…
Job Title: Sr. Specialist, Regulatory Affairs Location: Columbus, OH Job Type: Full time Req ID: 5929 About Us: As a developer, manufacturer, and supplier of essential me…
Responsibilities: This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe, support of internatio…
Responsibilities: Well versed in performing CMC compliance activities including Gap Analysis, CMC comparison and validation for the quality reports Experienced in authoring of a…
The Regulatory Affairs Manager will create, evaluate and execute domestic and/or international regulatory tasks related to the following: global submissions, technical file compila…
Responsibilities Entering and monitoring of complaints in conjunction with the international team Review of all US marketing materials including patient and health care provide…
Consultant, GPV Case Management Product Specialist, Pharmaceuticals Summary Our growing, mid-sized pharmaceutical client has engaged GForce Life Sciences to provide a GPV Submi…
Roche fosters diversity, equity and inclusion, representing the communities we serve. When dealing with healthcare on a global scale, diversity is an essential ingredient to succes…
Terumo Medical Corporation (TMC) develops, manufactures, and markets a complete, solutions-based portfolio of high-quality medical devices used in a broad range of applications for…
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About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From healt…
Now Hiring! Customs/Foreign Trade Management/Senior Specialist Florham Park, NJ - Local telecommuting permitted. Up to 5% domestic travel required. The world needs creative s…