- 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)
- **Job Description** The Director of Biologics Potency in Analytical Research & Development is responsible for providing strategic and technical leadership for a ... portion of the Biologics portfolio from candidate selection through launch. The successful...to build a culture of innovation and inclusion. The Director reports to the Executive Director , Cell… more
- Bristol Myers Squibb (Devens, MA)
- …Summary:** Reporting to Senior Director of the IT Site Lead, the Associate Director , Automation Control Systems defines and delivers the automation control ... project portfolio and operational support activities to enable and sustain fully automated biologics manufacturing at the BMS Devens site. He or she contributes to… more
- Merck (Rahway, NJ)
- **Job Description** The Associate Director of Scientific Nomenclature and Reference Data is responsible for assigning accurate chemical nomenclature to small ... molecules and biologics , as well as creating and maintaining reference data...excellent communications skills, and project management skills to derive high- quality reference data to meet the diverse needs of… more
- Merck (Rahway, NJ)
- …Reporting to a Technology Director in Global Engineering Solutions (GES), the Associate Director will be part of a high performing team, accountable for ... growing portfolio of Large Molecule, Small Molecule, and Animal Health work. The Associate Director participates in project activities ranging from business case… more
- Bristol Myers Squibb (Summit, NJ)
- …than here at BMS with our Cell Therapy team. The Associate Director , Drug Product External Manufacturing QA provides Quality oversight to Contract ... This role will partner cross functionally with Global Product Quality (GPQ), External Manufacturing (ExM), Manufacturing Science & Technology (MS&T/CTTO),… 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
- AbbVie (Barceloneta, PR)
- …Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director of Quality Control Laboratories is ... in science and 10 + years of relevant experience in quality /regulatory in pharma, biologics , or equivalent regulated industry or Master's degree and 8+ years… 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
- Merck (West Point, PA)
- …Description** Seeking candidates for a leadership position in our company's Biologics Pilot Plant Process Operations Team. This individual will provide technical ... on downstream unit operations in Good Manufacturing Practice manufacture of bulk biologics , vaccines, and adjuvant clinical supplies. Candidate is expected work in a… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Associate Director of Training **Grade:** L3-2 **About the Job** The Sanofi Genzyme ** Associate Director of Field Learning and ... the Sanofi Director of Field Learning (Foundations and Emerging Therapies). The Associate Director of Field Learning and Development role is based in… more
- Merck (West Point, PA)
- …candidates for a leadership position in our Research & Development Division Biologics Pilot Plant (BPP) Operations Team. The individual will lead campaign teams ... focusing on GMP manufacture of bulk biologics (vaccines and therapeutic proteins) clinical supplies. Candidate is expected work in a team atmosphere in close… more
- Merck (Millsboro, DE)
- …etc.) of animal facilities and program reviews is required. **Purpose** This Associate Director will report to the Site Quality Head/ Director of ... **Job Description** Our company seeks to add an Associate Director . Veterinarian Services at our...facilitating communication between the Animal Services team and the Quality organization. This position will work in close coordination… more
- Fujifilm (College Station, TX)
- **Position Overview** The Director Quality Systems is responsible for developing, implementing, and maintaining individual sub-systems of the Pharmaceutical ... practices. + Ability to serve as deputy for Senior Director Quality Systems. + Any other duties...regulations for the production of drug substance, drug product, biologics , vaccine, and/or advanced therapy products. **_Working Conditions &… more
- Merck (West Point, PA)
- …Reporting to the Director of Packaging Commercialization, the Associate Director , Engineering, Packaging Commercialization will lead packaging development ... prior experience developing and commercializing new products on cross-functional teams. The Associate Director will be accountable for the definition and… more
- Regeneron Pharmaceuticals (Rensselaer, NY)
- We are currently looking to fill an Associate Director of GMP Compliance & Inspections position. This position will work with cross-functional teams to drive ... and ensure we are performing with in compliance. The Director will also provide support during regulatory inspections and...quality driven organization + Have an understanding of biologics manufacturing operations To be considered for this role… more
- CSL Behring (King Of Prussia, PA)
- …biotherapies used to treat serious and often rare conditions. Could you be our next Associate Director , Global Regulatory Affairs? The job is located in our King ... Prussia PA office. This is a hybrid position. You will report to the Director of Global Regulatory Affairs. **Responsibilities:** You are a member of a Regional… more
- Novo Nordisk (Plainsboro, NJ)
- …for a living. Are you ready to make a difference? The Position The Associate Director , Regulatory Affairs - Advertising & Promotion will provide strategic ... strong and positive working relationship with OPDP reviewers. Report to Senior Director , Regulatory Affairs - Advertising & Promotion. Essential Functions + Provide… more
- Rhythm Pharmaceuticals (Boston, MA)
- …overcome barriers, together. Opportunity Overview Rhythm Pharmaceuticals is seeking an Associate Director , Non-Clinical Research to join the Translational ... to overall company strategy. This role will report into the Sr. Director , Non-Clinical Development. Responsibilities and Duties + Support and oversee Rhythm's… more
- Amneal Pharmaceuticals (Piscataway, NJ)
- Description: Subject matter expert in the area of Biologics . Promotes and develops initiatives to continually improve working relationships within and across ... Formulate and lead global CMC and clinical regulatory strategies for Biologics , Biosimilars, and Small Molecules.Ensure alignment with regulatory trends, innovation,… more
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