- Insmed Incorporated (Bridgewater, NJ)
- …in the biopharma industry, come to Insmed to accelerate your career. RecognitionsNamed Science 's Top Employer in 2021, 2022, and 2023Insmed is dedicated to creating ... where our team can thrive. Every day, our employees turn their passion for science and research into innovative solutions for patients. That's why we were named the… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally ... by leveraging our world-class science and technology. With more than 100 years of...across functions on key regulatory topics, particularly relating to biologics and Oncology, incl. coordinating Reg Intelligence & Policy… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally ... by leveraging our world-class science and technology. With more than 100 years of...centered around rare diseases and immune disorders.Summary The Senior Director , Global Oncology Medical Affairs is responsible for developing… more
- Merck & Co. (North Wales, PA)
- Job DescriptionReports to the Director /Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the ... promotional materials are aligned with US promotional regulations, corporate standards and policies and business objectives.Actively- participate in labeling and… more
- Insmed Incorporated (Bridgewater, NJ)
- …in the biopharma industry, come to Insmed to accelerate your career.RecognitionsNamed Science 's Top Employer in 2021, 2022, and 2023Insmed is dedicated to creating ... where our team can thrive. Every day, our employees turn their passion for science and research into innovative solutions for patients. That's why we were named the… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally ... by leveraging our world-class science and technology. With more than 100 years of...centered around rare diseases and immune disorders.Summary The Associate Director , RACMC Portfolio Products, will be responsible for regulatory… more
- Merck & Co. (North Wales, PA)
- …requirements and industry trends as described in worldwide regulations and industry standards , and trend reporting. Maintain a subject matter expert level of ... and Health Authority GMP expectations. Required: Bachelor's degree in Life Science Field, Engineering field or a related relevant discipline.-Minimum of ten… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally ... by leveraging our world-class science and technology. With more than 100 years of...centered around rare diseases and immune disorders.Summary The Senior Director , Global Oncology Medical Affairs is responsible for developing… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …The Position Manage and oversee all assigned projects/products/processes. Assist the Director /Associate Director in assuring Novo Nordisk compliance with ... regulatory agencies. Supervise designated personnel. Relationships Report to the Director /Associate Director /Lead Regulatory Scientist/Sr. Manager Regulatory Affairs.… more
- Gilead Sciences, Inc. (Foster City, CA)
- …impact. Join Gilead and help create possible, together. **Job Description** The Senior Director of Materials Science will spearhead the technical support for ... **Responsibilities:** + Building, leading and mentoring a best-in-class Materials Science function within Gilead's Biologics Technical Development organization… more
- Gilead Sciences, Inc. (Foster City, CA)
- …countries worldwide, with headquarters in Foster City, California. **TITLE:** **Senior Director , Analytical Lifecycle Management - Biologics Quality Control ... biologics drug substances and drug products. The Senior Director collaborates with cross-functional teams, fosters a culture of continuous improvement,… more
- Astellas Pharma (Northbrook, IL)
- …more than 70 countries around the world. We are committed to turning innovative science into medical solutions that bring value and hope to patients and their ... in remote work are encouraged to apply. **Purpose and Scope:** The Director , Global Clinical Pharmacology will have ultimate responsibility and accountability for… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …Sigma tools + Operations experience in pharmaceutical manufacturing to cGMP standards including extensive knowledge of regulatory guidelines and validation practices ... operations problems. + Ability to effectively transfer complex knowledge regarding science and engineering procedures. + Demonstrated team leadership skills and… more
- Catalent Pharma Solutions (Bloomington, IN)
- **Job Title: Sr. Director , Technical Services** **Location: Bloomington, IN** **Position Summary:** Catalent Biologics is a fast-growing business within Catalent ... new state-of-the-art biomanufacturing facility in Madison, WI, and our market leading biologics analytical services in Kansas City, MO and Research Triangle Park,… more
- Boehringer Ingelheim (Ridgefield, CT)
- …regulatory science and global regulatory requirements, guidelines, developments, and standards , allowing for informed comments and input to a broad spectrum of ... programs reflect Boehringer Ingelheim's high regard for our employees. The Director , Global Regulatory Strategy Lead will provide strategic regulatory guidance and… more
- Merck (North Wales, PA)
- **Job Description** Reports to the Director /Senior Director in the Office of Promotion and Advertising Review (OPAR) The Associate Director is responsible ... ensure promotional materials are aligned with US promotional regulations, corporate standards and policies and business objectives. Actively participate in labeling… more
- Bristol Myers Squibb (Seattle, WA)
- …external and internal manufacturing partners, process engineering and establishing manufacturing standards to enable a robust and scalable global cell therapy ... manufacturing network. We are looking for a director to join our Process Robustness team within the...Chemical Engineering, or equivalent area of related experience in biologics upstream manufacturing: Master's degree with 12+ years or… more
- Astellas Pharma (Westborough, MA)
- …the site to manufacture clinical and commercial products to the highest standards of cGMP manufacturing. **Organizational Context:** The Director , Manufacturing ... ** Director , Manufacturing Operations** Do you want to be...around the world. We are committed to turning innovative science into medical solutions that bring value and hope… more
- Teva Pharmaceuticals (Parsippany, NJ)
- Director , Quality System Compliance Date: Apr 10, 2024 Location: Parsippany, United States, New Jersey, 07054 Company: Teva Pharmaceuticals Job Id: 55102 **Who we ... a difference, and new people to make a difference with. **The opportunity** The Director of Global Quality Systems Compliance plays a critical role in overseeing and… more
- Sanofi Group (Bridgewater, NJ)
- …in the development and monitoring of the global regulatory environment and updating of standards and processes related to drug and biologics regulations + Ensure ... degree (PharmD, PhD, MD or DVM or MSc in Biology, Life Science , or related field) preferred **Experience/Professional requirements:** + US regulatory expertise in… more
