- Bristol Myers Squibb (Devens, MA)
- …lives. Read more: careers.bms.com/working-with-us . **Position Summary** This position supports Biologics Quality Control (QC) testing within the BioSeparations, ... Company SOPs. **Key Responsibilities** + Directs the daily operation of a biologics QC department testing and reporting of BioSeparations, STAT, BioAssay, and… more
- Gilead Sciences, Inc. (Foster City, CA)
- …countries worldwide, with headquarters in Foster City, California. ** Associate Director - Material Science** **(Pivotal & Commercial Biologics )** **Role ... various departments such as Pharmaceutical Development & Manufacturing (PDM), Quality , Supply Chain, Manufacturing, Regulatory Affairs CMC, Finance, and Technical… more
- Merck (Rahway, NJ)
- …Within Biologics and Biopharmaceutics, the large molecule product development Director will influence the strategy, lead activities, and develop a team whose ... environment with key stakeholders across the organizations such as Quality , Regulatory CMC, and technical functions, to ensure timebound...The Director will report to the Executive Director of Biologics and Biopharmaceutics, have 10-15… more
- Merck (Rahway, NJ)
- …as the biopharmaceutics support for the oral and non-oral portfolio. Within Biologics and Biopharmaceutics, the Biopharmaceutics Director will influence the ... in bioperformance of formulations The Director will report to the Executive Director of Biologics and Biopharmaceutics, have 8-10 direct reports composed of… more
- Takeda Pharmaceuticals (Boston, MA)
- …. As part of the Biologics Analytics team, you will report to the Associate Director and work with the Global Biologics organization. **How you will ... therapies to patients worldwide. Join Takeda as a Research Senior Associate where you will perform biotherapeutics and antigens characterization to support… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …database to address external questions regarding drug products. The CMC Regulatory Associate Director , Biologics is responsible for content development, ... compilation, maintenance, and review of the Quality Module for regulatory submissions to support ...meetings); and/or post-approval submissions. In this role, the GRS-CMC Associate Director , Biologics will serve… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director where you will help develop the vison, strategy, roadmap ... access to data insights. + Owns the data accuracy, quality & governance for Global Biologics ; accountable...data accuracy, quality & governance for Global Biologics ; accountable for supporting reporting, analytics and the user… more
- Catalent Pharma Solutions (Kansas City, MO)
- ** Associate Director - Continuous Improvement** **Position Summary:** Catalent is a global, high-growth, public company and a leading partner for the ... facility is home to our Clinical Delivery Services and Biologics Analytical Services businesses. The site provides a range...Pharma Solutions in Kansas City, MO is hiring an Associate Director , Continuous Improvement. This person will… more
- Merck (West Point, PA)
- **Job Description** **Position Description:** ** Associate Director , Quality Systems & Compliance** Our Quality Assurance group ensures every single ... on time, every time, across the globe. **Position Responsibilities:** + The Associate Director is responsible for performing comprehensive and detailed GMP… more
- Merck (Durham, NC)
- **Job Description** The Associate Director of Quality Systems provides leadership, focus, and governance to the Hilleman site in the following Quality ... Action Management, Annual Product Review Authoring, Quality Risk Management, and Quality Council), the Associate Director will be responsible for… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders. **Summary** The Associate Director , RACMC Portfolio Products, will be responsible for ... topics. **Responsibilities** - Supports CMC regulatory compliance activities for portfolio biologics to meet US, International Conference on Harmonization (ICH), and… more
- Bristol Myers Squibb (Devens, MA)
- …more: careers.bms.com/working-with-us . **PURPOSE AND SCOPE OF POSITION:** The Associate Director , CTF Digital Plant IT Quality at Devens Cell Therapy ... as it applies to Cell & Gene Therapy or Biologics manufacturing. + Demonstrated knowledge of Quality principles and QA methodologies including GAMP and ISO 9001.… more
- University of Southern California (Los Angeles, CA)
- cGMP Associate Director Process DevelopmentApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/cGMP- ... compliance with current Good Manufacturing Practices (cGMP). As the Associate Director of Process Development, the individual...of processes for the production of cell therapies and biologics in accordance with cGMP guidelines. + Create and… more
- Charles River Laboratories (Memphis, TN)
- …to MSAT leadership and the Site Leadership Team detailing scheduling adherence, quality , and safety of active technology transfers. + Performs feasibility assessment ... but not limited to, experience, skills, education, certifications, and location. **About Biologics Testing Solutions** With more than 50 years of experience and… more
- Bristol Myers Squibb (Summit, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . **Title: Associate Director , Cell Therapy Comparability** **Location: Summit, NJ or ... your career, and the ability to help patients are incredible. The ** Associate Director , Cell Therapy Comparability** will lead comparability programs and… more
- Merck (Millsboro, DE)
- …animal facilities and program reviews is required. **Purpose** The Associate Director /Attending Veterinarian will report to the Site Quality Head/ Director ... **Job Description** ** Associate Director , Animal Services** **About the...facilitating communication between the Animal Services team and the Quality organization. This position will work in close coordination… more
- Takeda Pharmaceuticals (Lexington, MA)
- …to the best of my knowledge. **Job Description** **Objective / Purpose:** As an Associate Director in Analytical Development, it is expected that the individual ... potentially across Pharmaceutical Sciences especially for Bioanalytics for late stage Biologics programs + Manage staff with accountability for performance and… more
- BeiGene (Hopewell, NJ)
- …International Regulations and BeiGene processes procedures. Develops and implements quality control processes and procedures and supports regulatory compliance ... of the job_** **_:_** + Establish, update, implement, and enforce Quality Control procedures, specifications and test methods (chemistry and biochemistry) consistent… more
- J&J Family of Companies (Titusville, NJ)
- Associate Director , Temperature Strategy & Execution - 2406177829W **Description** Johnson & Johnson Innovative Medicine Research & Development (JJIM R&D), part ... of the Johnson & Johnson Family of Companies, is recruiting for an Associate Director , Temperature Strategy & Execution within Clinical Supply Chain (CSC). The… more
- Merck (Rahway, NJ)
- …Dosage (Non-Sterile) team at the FLEx Center in Rahway is looking for an Associate Director - Process Engineer to lead clinical supply manufacturing, scientific ... and Experimentation (FLEx) Center is a multi-modality (small molecule, biologics , vaccine) Drug Product development and clinical manufacturing facility in… more