- Bristol Myers Squibb (Devens, MA)
- …or Black belt is preferred but not required + Expert understanding of cGMP regulations and/or business and documentation processes. + Expert in root cause analysis, ... people with disabilities can excel through a transparent recruitment process , reasonable workplace accommodations/adjustments and ongoing support in their roles.… more
- Lilly (Indianapolis, IN)
- …robotics integrators across the portfolio. + Manage aspects of the project delivery process for the deployment of Global Robotics Program platform systems. + Develop ... experience managing initiatives with aggressive timelines. + Thorough knowledge/experience in cGMP , ICH, USP, and other applicable regulations. + Six Sigma Green… more
- Kelly Services (South San Francisco, CA)
- Kelly(R) Science & Clinical is seeking an Associate Director / Director of Drug Substance Manufacturing for a direct hire opportunity with a leading ... Senior Director , $275,000 - $320,000 **Overview** As Associate Director / Director , Drug...you will be a strategic leader in drug substance process development, technology transfer, and external partnership management across… more
- Merck (Durham, NC)
- …drive strategic maintenance and reliability projects. The Mechanical Services Engineer Associate Director (AD) position will ensure reliable performance of ... timing commitments + Lead in the identification and implementation of process improvement projects, productivity initiatives and corrective actions while focusing on… more
- Fujifilm (College Station, TX)
- **Position Overview** The Director Quality Systems is responsible for developing, implementing, and maintaining individual sub-systems of the Pharmaceutical Quality ... and maintain the risk-based PQS sub-systems to meet all CGMP regulatory requirements for phase-appropriate clinical and commercial bulk...practices. + Ability to serve as deputy for Senior Director Quality Systems. + Any other duties as assigned.… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. #WeAreLilly **Responsibilities:** The Associate Director - Quality Assurance (QA) is responsible for managing ... (API) manufactured within Indianapolis Active Pharmaceutical Ingredient (IAPI) manufacturing site. The Associate Director - QA is primarily responsible for the… more
- Fujifilm (Holly Springs, NC)
- **Position Overview** The Director , Drug Substance Manufacturing (DSM) plays a critical role in the design, execution, and leadership of DSM Operations strategy for ... and successful delivery of life changing therapies for patients. The Director , DSM guides leaders, develops high-performing teams, and works cross-functionally to… more
- Lilly (Indianapolis, IN)
- …issues + Performance management and development of staff, in partnership with Executive Director - Parenteral Technical Services and Associate Vice President - ... and rigorous quality standards. Lilly Manufacturing strives for excellence in its process , standards, procedures and behaviors to develop medicines with safety first… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …The QA Training Associate will manage new hire onboarding training for CGMP and GDP. The QA Training Associate will maintain the Instructor-led training ... college, freelance instructors, and others as designated by the Director of ACT/QABR. The QA Training Associate ...steps to reduce wastages and losses in the analysis process and build improved efficiency. OPERATIONAL EXCELLENCE: + Assist… more
- Lilly (Lebanon, IN)
- …(and per delegation procedure), in the absence of the Associate Director -Manufacturing provide continuity to the Process Team activities and operational ... Operations Associate , your responsibilities will include:** + Assisting the Process Team Leaders with leading the Process Teams, specifically focusing… more