- Novo Nordisk Inc. (Boulder, CO)
- …are driving change. Are you ready to make a difference? The Position The Associate Director , Process Chemistry will be responsible for the design, development ... development and scaling of small molecules, oligonucleotide intermediates and API's. The Associate Director is expected to implement novel strategies towards… more
- 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)
- …company is seeking a highly motivated candidate for the position of Director , Small Molecule Development within the Mixed Modalities, Sterile Product Development ... for parenteral drug products within the small molecule and synthetic modality pipeline.The Director will report to the Executive Director of Sterile Product… more
- Merck & Co. (Rahway, NJ)
- …oral and non-oral portfolio. Within Biologics and Biopharmaceutics, the Biopharmaceutics Director will influence the strategy, lead activities, and develop a team ... portfolio and influence bridging strategies across the portfolio. The Biopharmaceutics Director will work with their direct reports to proactively develop and… more
- Takeda Pharmaceuticals (Boston, MA)
- …best of my knowledge. **Job Description** Takeda Development Center Americas, Inc. is seeking an Associate Director , CMC Program Lead, Cell Therapies in ... pre-IND briefing book packages and IND filings; Represent Cell Therapy CMC teams in technical, program , and governance forums and drive program strategy and… more
- AbbVie (Worcester, MA)
- …Instagram, YouTube and LinkedIn. Job Description Position will be responsible for CMC leadership and project management for existing and new biologics projects from ... the drug substance perspective. Responsibilities: *Develop comprehensive project plans, budgets, timelines and strategy; biologics projects at all stages of development are included, from phase I through commercial. *Must present technical information… more
- Lilly (Indianapolis, IN)
- …determined to make life better for people around the world. **Position Summary:** The Associate Director , CMC Project Management will provide strategic and ... CMC team, who are accountable for technical deliverables. CMC Project Management is the program and...strategy optimization at both project and portfolio level. The Associate Director , CMC Project Management… more
- Regeneron Pharmaceuticals (Troy, NY)
- …preferably related to health, environment or politics or related degree and: + Associate Director : 15+ years of related experience in regulated industry or ... The Director of CMC Industry and Regulatory...The Director of CMC Industry and Regulatory Intelligence is responsible for...include the following + Provides oversight on the IOPS CMC intelligence program + Collaborates with the… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …academic community. **Description** The Goizueta Business School is in search of an Associate Director - Graduate Student Advising and Programming to join the ... Management Center team. This position will report to the Director of Specialized Master's Programs at the Goizueta Business...of Finance) Programs served by the Career Management Center ( CMC ). + Develops the overall student advising strategy and… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , Outsourcing & Vendor Management Pleasanton, CA, USA * Princeton, NJ, USA Req #385 Friday, August 16, 2024 Looking for a chance to make a ... dynamic and expanding mid-size company in the role of Associate Director , Outsourcing and Vendor Management. Your...Proposal (RFP) through contract execution for clinical studies and CMC projects as well as ongoing governance with key… more
- Merck (Rahway, NJ)
- …clinical development teams and the operational/executional arms within the business. The Program Clinical Supplies Project Manager ( Program CSPM) serves as the ... spokesperson at clinical and development related meetings. Working independently, the Program CSPM designs strategic and operational plans for all clinical supply… more
- Merck (Rahway, NJ)
- …Operations. We are seeking a highly motivated individual for the role of Associate Director , Tech Transfer Leader in Large Molecule Technology Transfer within ... end-to-end scope includes Drug Substance and Drug Product for all large molecules. Associate Director is expected to contribute to ongoing business process… 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 ... team performance in line with Pharmaceutical Sciences' strategy to deliver on program strategy and initiatives. The individual is expected to have acquired expertise… 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
- Takeda Pharmaceuticals (Boston, MA)
- …within related functions (eg Clinical Science, Clinical Operations, Research, Regulatory, CMC , Marketing) + 3-5 years program management experience leading ... into an efficiently executable plan; predicting and planning solutions to achieve program goals and objectives; driving clarity and removing barriers to ensure team… 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
- Lilly (Philadelphia, PA)
- …global health by accelerating the development of new medicines. **Responsibilities:** The Associate Director of Contract Manufacturing is responsible for leading ... review meetings as appropriate) to ensure timely deliverables to meet development program requirements. + Proactively solve potential supply chain issues for the… more
- Frontier Medicines (Boston, MA)
- Reporting to the Head of Research, the Associate Director will serve as a bridge, operationally linking our Research & Development organizations. The successful ... new operational strategies, prioritize and drive short-term and long-term program and company goals + Partner with Finance to...value and balancing risk) of vendors for activities in CMC , tox studies etc. What are we looking for?… 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
