- Merck & Co. (North Wales, PA)
- …the Director/Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the review and approval of all US ... promotional materials and serving as the promotional regulatory expert with marketing, legal, and medical teams to ensure that promotional practices are consistent… more
- Merck & Co. (Rahway, NJ)
- …experience in Regulatory AffairsNOTICE FOR INTERNAL APPLICANTSIn accordance with Managers' Policy - Job Posting and Employee Placement , all employees subject to ... Job DescriptionWe are seeking a Senior Director (Sr. Principal Scientist) Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can help… more
- Merck & Co. (Rahway, NJ)
- …optimize product labeling and obtain shortest time to approval by global regulatory agencies.Reports to Associate Vice President, Executive Director, or Senior ... Job DescriptionWe are seeking a Director (Principal Scientist), Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can help advance our… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Director of Method Development & Testing is responsible for leading a Center of Excellence (CoE) focused on developing and validating ... GMP testing nodes in support of clinical and PPQ supplies. Additionally, the Associate Director leads, manages, and develops a team responsible for providing routine… more
- Merck & Co. (Millsboro, DE)
- …Delaware seeks to add an Attending Veterinarian in the role of Associate Director.This position will have overall responsibility for oversight and administration of ... documentation, and other information as needed for annual reports to Federal regulatory agencies. Leadership for internal and external regulatory inspections… more
- Merck & Co. (Rahway, NJ)
- …drug products.Our team is looking for a candidate for the position of Associate Principal Scientist (R4) supporting the Biologics formulation team within Sterile and ... packaging, compatibility characterization for processing and administration, and supporting regulatory filings.Build deep fundamental knowledge around the drug product… more
- Novo Nordisk Inc. (Los Angeles, CA)
- 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 health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting… more
- Novo Nordisk Inc. (Boulder, CO)
- …analytical and process development, the CMC team works alongside Quality, Regulatory , Technical Operations and RNAi Early Development professionals at our Boulder, ... driving change. Are you ready to make a difference? The Position The Associate Director, Process Chemistry will be responsible for the design, development and… more
- Merck & Co. (Rahway, NJ)
- …to addressing privacy and data protection on a global scale.-The Associate Director, Global Privacy Operations, Data Subject Requests (DSR) position oversees ... from individuals around the world.The future incumbent of this position ensures regulatory compliance and operational excellence by managing the DSR process through… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …project under the direction of the GPT CDx representative while keeping abreast of regulatory and policy updates in the external environment and by tracking and ... Science Leads, Clinical Biomarker Leads, Biosample Operations, Clinical Leads and Regulatory Liaisons to ensure successful implementation of CDx and data… more
- Merck & Co. (North Wales, PA)
- …us to deliver a personalized customer experience and drive performance.The Associate Director, Commercial Model Innovation is responsible for driving innovation in ... of work consistent with Quality standards (meets legal & regulatory requirements & maintains compliance technology standards where appropriate)Delivery of… more
- Merck & Co. (North Wales, PA)
- Job DescriptionWe are currently recruiting for an Associate Director, US Oncology Marketing - Head & Neck Cancers. The position will report to the US Oncology ... sales leadership, etc.)Oncology marketing experienceExperience bringing materials through legal, regulatory , and clinical reviewExperience leading development of strategic/tactical plans… more
- Merck & Co. (Rahway, NJ)
- …both analytical experimental design and biotherapeutic pipeline programs. Finally, this Associate Principal Scientist will be a partner in problem solving, building ... protein analysis.Represent the mass spectrometry group in project teams.Author regulatory submission sections and responses, technical reports and scientific… more
- Eisai, Inc (Providence, RI)
- …you. The New England territory includes: CT, MA, RI, NH, VT & METhe Associate Director, Regional Thought Leader Liaison (RTLL), AD Marketing will lead and execute ... of brand plansStrong communication and presentation skillsUnderstanding of legal and regulatory issues impacting pharmaceutical product marketing as well as the… more
- Merck & Co. (Rahway, NJ)
- …teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing ... when necessary, through formal or informal presentations-Stays current in technology and regulatory changes both within and outside of our companies that may impact… more
- Merck & Co. (Rahway, NJ)
- …are deployed in support of clinical trials. The candidate for this Associate Principal Scientist position should have strong technical expertise in Liquid ... validation, collaborating with project teams, biomarker leaders, clinical operations and regulatory affairs on the implementation of these assays in clinical trials.… more
- Merck & Co. (North Wales, PA)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The incumbent is responsible for… more
- Merck & Co. (South San Francisco, CA)
- …approaches in drug safetyStay abreast with new AI approaches and regulatory landscape in the field of predictive toxicologyQualifications:Education:Ph.D. (with 4+ ... and other healthcare sectorsNOTICE FOR INTERNAL APPLICANTSIn accordance with Managers' Policy - Job Posting and Employee Placement, all employees subject to… more
- Merck & Co. (Rahway, NJ)
- …Modalities, and lead a team comprised of 10-15 experienced senior and associate scientists.- The main responsibilities include leading the small molecule parenteral ... to support formulation and process development and document technical reports and regulatory filings. The successful candidate will be key in implementing strategy,… more
- Merck & Co. (Durham, NC)
- …systems)Required Experience and Skills: Required Experience and Familiarity of regulatory requirements in accordance with GMP manufacturing operations Preferred ... Experience and Skills: Associate Degree in Industrial Systems, Mechanical, Electronics, Electrical or InstrumentationExperience working in a clean room or… more
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