- Bristol Myers Squibb (Devens, MA)
- …. **Summary:** Bristol Myers Squibb is seeking an experienced and strategic Associate Director to lead the MES (Manufacturing Execution Systems) and ... cell therapy manufacturing operations. + Ensure compliance with relevant regulatory requirements (GMP, GxP, 21 CFR Part 11) and...plans then in effect and may include the following: Medical , pharmacy, dental and vision care. Wellbeing support such… more
- Takeda Pharmaceuticals (Brooklyn Park, MN)
- …**Job Description** About the role: As the Environmental, Health and Safety, Associate Director , you will establish and foster strategic partnerships across ... of strong environmental, health and safety programs in alignment with legal, regulatory , corporate requirements and industry best practice. + Support business growth… more
- Lilly (Lebanon, IN)
- …clinical trial medicines, while also reducing costs and environmental impact. The Associate Director Small Molecule Process Engineering provides leadership and ... approval for documents as appropriate, including investigations, change controls, regulatory submissions, expert opinions, validations, annual product reviews, manufacturing… more
- RTX Corporation (East Hartford, CT)
- …**What You Will Do:** We have an exciting opportunity for a highly motivated ** Associate Director of Global Trade** to join our team! **Key Responsibilities:** + ... capable and effective Global Trade professionals operating across a complex global regulatory and operational landscape for the P&W Commercial Engines business; +… more
- Lilly (Durham, NC)
- …are determined to make life better for people around the world. The Associate Director - Quality Engineering is responsible for demonstrating leadership, ... teamwork, and quality and regulatory knowledge to lead the Quality Engineering team to...in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical , dental, vision and prescription drug benefits; flexible benefits… more
- AbbVie (North Chicago, IL)
- …medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's ... Irvine, South San Francisco, Worcester MA, Waltham, MA Leads global regulatory dossier preparation activities for novel biologics by coordinating cross-functional… more
- J&J Family of Companies (Jacksonville, FL)
- …more at https://www.jnj.com/medtech **We are searching for the best talent for an** Associate Director , North America Professional Education - Myopia to be based ... impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Medical Affairs Group **Job Sub** **Function:** Professional Medical Education… more
- Taiho Oncology (Princeton, NJ)
- …and medical materials review committees. Position Summary: The Associate Director , Promotional Materials will provide guidance to the Promotional ... Review Committee (PRC) and Medical -Legal Review (MLR) process by interpreting and applying relevant...communications strategy and planning. + Review and approve the regulatory content of materials created for product promotion, corporate,… more
- Organon & Co. (Jersey City, NJ)
- …**The Position** The Associate Principal Scientist ( Associate Director ) is responsible for developing and implementing Regulatory Chemistry, ... in accordance with global regulations and guidances, and Organon procedures. The Associate Principal Scientist will lead the preparation and submission of CMC… more
- Blue Cross Blue Shield of Massachusetts (Boston, MA)
- …help us transform healthcare? Bring your true colors to blue. What we need The Associate Director of Clinical Data Management will be a key leader in executing ... data management standards, processes, and procedures to ensure compliance with regulatory requirements and company policies. + Ensure the accuracy, completeness, and… more