- Merck & Co. (Rahway, NJ)
- …responsible for serving as the quality representative for, and providing quality oversight of, contractors performing various GMP activities supporting the ... associated with deviations, negotiation of site and global Technical and Quality Agreements, maintenance and accuracy of the Development Approved Vendor Listing,… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …and productivity.Key Responsibilities Co-Lead Deviation Investigations: Collaborate closely with the Quality Associate Director to co-lead the deviation ... in the treatment of multiple myeloma. Legend Biotech is seeking an Associate Director for Operations Compliance and Investigations Managementas part of… more
- Merck & Co. (Millsboro, DE)
- …of animal facilities and program reviews is required.PurposeThe Associate Director /Attending Veterinarian will report to the Site Quality Head/ Director ... Millsboro Delaware seeks to add an Attending Veterinarian in the role of Associate Director .This position will have overall responsibility for oversight and… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionFLEx is a set of multi-modality Drug Product development and GMP clinical manufacturing assets being constructed in the Rahway, New Jersey site, to ... across two co-leader roles, and includes operations that support end-to-end GMP clinical supply manufacture and product/process development, as well as oversight… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …other research areas centered around rare diseases and immune disorders.Summary The Associate Director , RACMC Portfolio Products, will be responsible for ... that CMC documentation is complete, well organized, scientifically sound, of a high quality , aligned with the current regulations, and presented in a manner that… more
- Merck & Co. (Rahway, NJ)
- …fast-paced job that provides both technical and project management responsibility. The Associate Specialist - Manufacturing Automation position will report to the ... Director , Engineering, Automation Lead position and will be a...production, utility systems and associated infrastructure.- Responsibilities of the Associate Specialist - Manufacturing Automation include the following: Small… more
- Merck & Co. (Durham, NC)
- …policies, procedures and business plan; receives guidance and oversight from Operations Associate Director and Director ;Interprets client and/or customer ... Regulatory Agency, and State and Local code requirements for quality , good manufacturing practices ( GMP ), equal employment...and any action plans to address gaps to the Associate Director and/or Director .- Identify,… more
- Merck & Co. (Durham, NC)
- …support for business area applications. Working Relationships Reports to the Associate Director Manufacturing Automation Frequent interaction with employees from ... embrace an empowered team culture including significant interaction with manufacturing, quality , IT, and engineering groups. - The Senior Specialist for… more
- Novo Nordisk Inc. (Boulder, CO)
- …, cost & timely completion of all validation deliverables. Relationships Associate Director . Essential Functions Perform, review & approve ... to support analytical and process development, the CMC team works alongside Quality , Regulatory, Technical Operations and RNAi Early Development professionals at our… more
- FUJIFILM Holdings America Corporation (Holly Springs, NC)
- …Holly Springs, North Carolina, United States. External US About The RoleThe Associate Director , Analytical Development, is responsible for directing and ... and method transfer of analytical methods from external clients to FDBN Quality Control (QC) teams to support drug substance and drug product manufacturing.… more
- FUJIFILM Holdings America Corporation (College Station, TX)
- …area.The QC Supervisor of Drug Product Operations under general direction from the Associate Director , Contamination Control, will be required to oversee all ... and environmental procedures. Adhere to and enforce the standards of quality ruled by current GMP and the company Quality Policies and site SOPs.Identify… more
- Sumitomo Pharma (Columbus, OH)
- ** Associate Director , GMP Quality Control** Sumitomo Pharma America (SMPA) is focused on delivering therapeutic and scientific breakthroughs in areas of ... highly motivated, and experienced individual for the position of Associate Director of GMP Quality Control, who oversees GMP compliance of… more
- Regeneron Pharmaceuticals (Troy, NY)
- We are currently looking to fill an Associate Director of Quality Auditing position. This position will be responsible for providing professional expertise, ... leadership, oversight and planning for the Regeneron Quality Auditing function, with primary emphasis on GMP , IT and Quality audits that may impact GMP … more
- Regeneron Pharmaceuticals (Rensselaer, NY)
- …preferably in the pharmaceutical or biotech industries or related field, for each level: + Associate Director - 10+ years + Director - 12+ years May ... We are currently looking to fill a Director of GMP Compliance & Inspections...well as procedures and processes. + Collaborate with customer/partner quality organizations. + Participates on internal committees/teams, as required.… more
- Lilly (Philadelphia, PA)
- …people who are determined to make life better for people around the world. The Associate Director , Supplier Quality Management, Avid leads quality ... role establishes and maintains standard operating procedures in alignment with corporate quality standards and current GMP expectations. In collaboration with QA… more
- Lilly (Indianapolis, IN)
- …is a wholly owned subsidiary of Eli Lilly and Company. **Position Summary:** The Associate Director of Quality Engineering and Computer System Validation ... to POINTs Engineering and Computer System Validation processes. The Associate Director of Engineering and CSV will...and systems are designed, established, and operated in a GMP manner. + Overall accountability for Quality … more
- Merck (Columbus, OH)
- …patients on time, every time, across the globe. **Position Responsibilities:** + The Associate Director is responsible for performing comprehensive and detailed ... **Job Description** Our Quality Assurance group ensures every single material inside...forums. + Prior experience at a health authority performing GMP inspections. + Demonstrated ability to establish and maintain… more
- Lilly (Lebanon, IN)
- …startup into GMP manufacturing operations. **Position Description:** The Associate Director Engineering - Utilities provides leadership and direction ... engineering team responsible for plant and environmental control utilities. The Associate Director Engineering Utilities ensures that engineering deliverables… more
- Merck (West Point, PA)
- …responsible for serving as the quality representative for, and providing quality oversight of, contractors performing various GMP activities supporting the ... associated with deviations, negotiation of site and global Technical and Quality Agreements, maintenance and accuracy of the Development Approved Vendor Listing,… more
- Lilly (Indianapolis, IN)
- …people who are determined to make life better for people around the world. The Associate Director - Quality Control is responsible for managing the ... activities of Quality Control personnel. The Assoc. Director Quality Control must balance coaching a...implement the technical agenda, site business plan objectives, and GMP Quality Plan objectives + Interact with… more
