- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** The Associate Director , Biopharmaceutics will provide expert biopharmaceutical guidance on the pharmacokinetic performance ... for the general medicines portfolio of products marketed worldwide. The Associate Director , Biopharmaceutics will also be responsible for contributing… more
- CSL Behring (King Of Prussia, PA)
- The ** Associate Director , Field Reimbursement Manager Resourcing (FRM), US Portfolio,** is responsible for developing and implementing in office resources and ... care delivery and while advancing capabilities in field reimbursement + Advances process , standards and operational plans to advance CSLs capabilities of field… more
- Merck & Co. (Durham, NC)
- Job DescriptionThe Quality Associate Director /GMP Lead Site Auditor will have leadership responsibility for the site internal audit program, encompassing the ... agent related to culture and audit program performance Lead change and process improvement initiatives related to Auditing, Inspections, CAPA, and other compliance… more
- Amgen (San Francisco, CA)
- …yet we all use our unique contributions to serve patients. The Area Sales Director - Nephrology we seek is a motivated professional with these qualifications. Basic ... experience OR Bachelor's degree or AND 8 years of Sales/Marketing experience OR Associate 's degree and 10 years of Sales/Marketing experience Or High school diploma… more
- Otsuka America Pharmaceutical Inc. (Boise, ID)
- **Job Summary** The Associate Director , Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial products ... expectations and applicable cGMP/GDP quality standards. This role will direct Biologics Quality Assurance support, including oversight of upstream and downstream … more
- Lilly (Indianapolis, IN)
- … process control engineers and consultants that support the daily operations of the Biologics facility. The Associate Director is also responsible for the ... who are determined to make life better for people around the world. The Associate Director -Automation Engineering is responsible for the supervision of the… more
- J&J Family of Companies (Spring House, PA)
- …at https://www.jnj.com/innovative-medicine **We are searching for the best talent for an Associate Director , Biologics in Spring House, PA.** **Purpose:** ... then Johnson & Johnson Innovative Medicine is recruiting an Associate Director for the Expression Sciences team...identify and mitigate risks as part of our discovery process . Creatively identify drug developability trends by modeling large… more
- Lotte Biologics USA LLC (Syracuse, NY)
- …innovation, to reliably deliver benefits for patients worldwide. Position Summary The Associate Director , Project Management Office (PMO) will play a key ... risk management, and stage-gate governance. + Strong understanding of biologics manufacturing processes, analytical and process technical transfer,… more
- Lotte Biologics USA LLC (Syracuse, NY)
- …to reliably deliver benefits for patients worldwide. Position Summary The Associate Director of Antibody Drug Conjugate (ADC) Manufacturing Operations ... We are LOTTE BIOLOGICS ! Delivering Therapies That Enable a Healthier...services to external customers and internal programs, and the Associate Director will play a critical role… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Join Gilead and help create possible, together. **Job Description** The QC Microbiology Director is vital role for the success of Clinical and Commercial ... Biologics and Small Molecule Quality Control. This individual provides...methods for biological and small molecule product - includes in- process , release and stability + Support microbiology quality events.… more
- Lilly (Indianapolis, IN)
- …for clinical trial medicines, while also reducing costs and environmental impact. The Associate Director of Materials will lead the planning and procurement of ... direct materials supporting clinical supply manufacturing across small molecule, biologics , and peptides at the Lilly Medicine Foundry. This role ensures on-time… more
- University of Southern California (Los Angeles, CA)
- …of cell and gene therapies and other biological products for internal/external users. The Associate Director of Process Development (cGMP) is responsible for ... the current Good Manufacturing Practices (cGMP) laboratory, including manufacturing and process development activities, in order to ensure that project deliverables… more
- Fujifilm (Holly Springs, NC)
- **Position Overview** The Associate Director , Cleaning Validation is responsible for leading and executing Cleaning Validation (CV) activities for a large-scale ... biologics manufacturing facility in compliance with regulatory requirements, including...mitigate risks associated with the therapeutic product lifecycle. The Associate Director collaborates with cross-functional teams to… more
- Mallinckrodt Pharmaceuticals (Horsham, PA)
- Job Title Associate Director , Manufacturing Operations Requisition JR000015470 Associate Director , Manufacturing Operations (Open) Location Horsham, PA ... Additional Locations Job Description Summary Job Description The Associate Director , Manufacturing Operations will provide leadership and management of… more
- Sanofi Group (Framingham, MA)
- **Job Title:** Associate Director -CMC BioDPDM **Location** : Framingham, MA As Associate Director within CMC BioDPDM, you'll have the opportunity to lead ... could turn the impossible into possible for millions. The Associate Director role is a key leadership...modalities, experience in in-use study design principles, knowledge of biologics manufacturing and process development. + **Soft… more
- Teva Pharmaceuticals (West Chester, PA)
- Associate Director , Regulatory Affairs Date: Dec 2, 2025 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals Job Id: 65114 ... difference, and new people to make a difference with. **The opportunity** The Associate Director , Global Regulatory Affairs, will be responsible for providing… more
- AbbVie (North Chicago, IL)
- …Waltham, MA Leads global regulatory dossier preparation activities for novel biologics by coordinating cross-functional teams of subject matter experts, from ... and coordinate submission documentation for all phases of clinical development of biologics , with emphasis on later phase programs and marketing applications, often… more
- Gilead Sciences, Inc. (Frederick, MD)
- …trends and best practices in document control. + Identify opportunities for process improvement and innovation. + Implement changes to enhance the efficiency and ... PhD with 2+ years of related experience in a biologics or pharma organization OR + MS/MA with 8+...1990, applicants who require accommodation in the job application process may contact ###@gilead.com for assistance. For more information… more
- Takeda Pharmaceuticals (Boston, MA)
- …Science GMSci DP/PKG** **Location: Cambridge, MA** **About the role:** As a Process Scientist ( Associate Director ) - Global Manufacturing Science ... By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application… more
- Bristol Myers Squibb (Devens, MA)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The ** Associate Director , Supply Planning** will drive the Sales & Operations ... Planning Process (S&OP) including the Production Scheduling process in support of the Devens Biologics Manufacturing Site. The role will lead a team that… more
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