- Merck & Co. (Rahway, NJ)
- …portfolio. Within Biologics and Biopharmaceutics, the large molecule product development Director will influence the strategy, lead activities, and develop a team ... with key stakeholders across the organizations such as Quality, Regulatory CMC , and technical functions, to ensure timebound progression of portfolio, initiatives… more
- Merck & Co. (Rahway, NJ)
- …of regulatory submissions. -Under the general scientific and administrative direction of Director in the CCFS group and working in conjunction with internal and ... partners, this individual will support late stage and commercial large molecule program activities within CCFS. The individual will be responsible for leading a… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …integrity, and timelines for assigned studies and escalates issues to the Associate Director of Medical Coding to gain resolution. Functional Expertise:Study ... conventions. Reviews and submits DS Medical Coding synonym list update requests to the Associate Director of Medical Coding to ensure accuracy and consistency of… more
- Takeda Pharmaceuticals (Boston, MA)
- …possible in order to bring life-changing therapies to patients worldwide. Join Takeda as the Associate Director , CMC Program Lead in Allogeneic Cell ... program regulatory filings, critical cross-functional capability building, etc.). + Represent CMC team in technical, program and governance discussions. +… more
- UTMB Health (Dickinson, TX)
- …patients. Works under the supervision of a Psychologist, Mental Health Manager and/or Program Director . **_ESSENTIAL JOB FUNCTIONS_** **:** + Contributes to the ... Mental Health Clinician - CMC - Carole Young **Dickinson, Texas, United States**...or eligibility for licensure as a Professional Counselor, Psychological Associate , or Social Worker. Salary is commensurate with years… more
- Otsuka America Pharmaceutical Inc. (Rockville, MD)
- **Job Summary** Associate Director , Quality Control, Biologics is responsible for late development stage through commercial biologic products including product ... ability to understand and communicate impact of technical risks on CMC program timelines. + Review and interpret complex data, communicating clearly to… more
- Lilly (Indianapolis, IN)
- …of the scorecards with the 3rd parties. The key responsibilities for a business/operations Associate Director or Director may include: + Works with BRD, ... create RFP's and communication plan with vendors. + Manage program budgets, POs and invoices from vendors by effective...from vendors by effective communication between vendor, finance and CMC PM teams. + Manage the collection of performance… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- We are seeking an ** Associate Director ** within the Formulation Development Group of Regeneron Pharmaceutical Inc. at Tarrytown, NY. This role will lead clinical ... Regeneron functions and stakeholders including Therapeutic Focus Areas, Pre-clinical Development, CMC and Manufacturing (DS and DP), Program Management,… 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- ... products, in compliance with current Good Manufacturing Practices (cGMP). As the Associate Director of Process Development, the individual will be responsible… 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
