- 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
- AbbVie (North Chicago, IL)
- …on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description As an Associate Director , Operations Strategy and Pipeline Leadership (OSPL) within the ... for potential license or acquisition, ensuring both the viability of the program itself and AbbVie's ability to execute it post-acquisition. This role demands… 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
- Regeneron Pharmaceuticals (Cambridge, MA)
- We are seeking an enthusiastic ** Associate Director , Program & Portfolio Management** to drive programs forward at Regeneron Cell Medicines (RCM) through ... In this role, you'll be a leader on cross-functional program teams (spanning research, clinical, CMC , quality,...in IND-enabling studies through clinical study execution. **As an Associate Director , Program & Portfolio… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …company that will inspire you and empower you to shine? Join us as an Associate Director , Global Program Management in our Cambridge, MA office. At ... have responsibility for line management of Sr. Manager and/or Associate Director level GPMs as well as...related functions (eg Clinical Science, Clinical Operations, Research, Regulatory, CMC , Marketing) + Minimum of 5 years program… 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
- Abeona (Cleveland, OH)
- The Associate Director Quality Control (QC) will lead QC activities associated with the GMP production. Such products include Adeno-associated Viral Vectors ... operation of the QC Microbiology and Transport functions. The Director is responsible for supporting the QC testing, utility...+ Implement and manage a GMP compliant laboratory control program in adherence to current FDA Guidelines, ICH, and… more
- Merck (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
- Magellan Health Services (San Diego, CA)
- …levels within HAI-CA. Interact with HAI-CA CMC Chief Clinical Officer, Medical Director and Associate Medical Director , Physician Advisors or Chief ... follow up issues log and interact with clinical team on Physician Liaison program status as well as functioning as administrative/clinical resource as appropriate. +… more
- Merck (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
- Merck (West Point, PA)
- …Description** We are seeking a highly motivated individual for the role of Associate Director , Tech Transfer Leader in Large Molecule Technology Transfer within ... scope includes Drug Substance and Drug Product for all large molecules. The Associate Director is expected to contribute to ongoing business process improvements… more
- University of Maryland, Baltimore (Baltimore, MD)
- …of the Department of Pharmaceutical Sciences with teaching responsibility to the Graduate Program Director and Associate Dean for Graduate Programs. ... activities such as student/alumni events and regulatory agency site visits. This program covers all major areas of drug product and biologics regulatory science,… more
- ThermoFisher Scientific (Providence, RI)
- …pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. Reporting to the Associate Director , CMC QC Stability, will be ... as required. + Support continuous improvement activities for VCGT stability program + Provide support to applicable stability sections of regulatory submissions… more
- State of Georgia (GA)
- …for continuous student improvement and success and submits results to the program director . Requires strong computer skills, communication skills, and ability ... Coder (CPC), Certified Coding Specialist (CCS), Certified Medical Coder ( CMC ), Registered Health Information Administrator (RHIA), or Registered Health Information… more
