ASSOCIATE DIRECTOR MANUFACTURING GMP jobs in UNITED STATES, United Kingdom #4

) to receive an alert: × Select how often (in days) to receive an alert: Associate Director - Chemical Development Facility... manufacturing in early- to late-stage development. Relationships The selected individual will report to the head of Chemical...

Novo Nordisk

The Associate Director/Director of Quality Assurance, reporting to VP of Quality & Regulatory, will be responsible... Flexible paid time off $150,000 - $200,000 a year The posted range covers Associate Director to Director leveling...

Synthego

Job Description As a key team leader in the Manufacturing Sciences & Technology function, the Associate Director... will participate in high-impact cross-functional initiatives, lead the resolution of complex analytical/manufacturing issues, provide...

Vertex Pharmaceuticals

Frontier Medicines is seeking a highly motivated individual for a newly created Associate Director role in Process... development, scale up, and manufacturing for GLP studies and GMP manufacturing at CDMOs Develop manufacturing processes...

Frontier Medicines

Associate Director, Quality – US Consumer Healthcare (CHC) Location: Morristown, NJ Remote Work: Hybrid Travel... closely/hand-in-hand with the Industrial Affairs Quality Team at the Chattanooga manufacturing & development site...

Sanofi

, drug product manufacturing process, and process tech transfer to GMP manufacturing sites. Associate Director is a key... responsibilities. The Associate Director is responsible for drug product development for Teva biologics products to ensure project...

Teva Pharmaceuticals

Associate Director/Director, Clinical Operations Job Overview We are looking for a talented and highly motivated... Clinical Operations professional to join our client's fast-paced biotech startup. Under the direction of the Executive Director...

The Steely Group

Job Description: ASSOCIATE DIRECTOR , GLOBAL TRADE COMPLIANCE JOB DESCRIPTION Summary The Associate Director..., implement and monitor a metrics performance package General knowledge of GMP and/or GCP Proficient knowledge of trade...

Alkermes

others. Position Overview The Associate Director, Bioinformatics is largely self-driven, working in collaboration... with others on one or more projects which are extremely complex in scope. The Associate Director, Bioinformatics is responsible for successfully leading...

Exact Sciences Corporation

:INS SF:HERC SF:DIV SF:LJN SF:IHE Director of Cell Therapies, Assistant/Associate Professor, Hoxworth Blood Center... Medical Director and Processing Facility Director. This is an open rank, open track, faculty position but is expected...

University of Cincinnati

/Cellular Therapies Medical Director and Processing Facility Director. This is an open rank, open track, faculty position... but is expected to be at the Assistant or Associate Professor level. HBC and the UC-CoM offer many opportunities for collaborative...

University of Cincinnati

Overview The Associate Director, Process Analytics is the system owner for this function, focusing on the drug... substance manufacturing at FDBN. This role sets up and maintains informatics systems for process analytics purposes, leads...

Fujifilm

Job Description The Small Scale Organics (SSO) Pilot Plant is a Good Manufacturing Practices (GMP) facility...-up of clinical supplies manufacturing, demonstration of new manufacturing technology/processes, training opportunities...

MSD

, manufacturing, and commercialization. Provide review of and input to development plans. When appropriate, provide guidance... of ICH Guidelines regarding GMP/GCP, ICH Guidelines for CTD/eCTD, and CBER and/or CDER requirements for the drug approval process...

Replimune

in support of our late clinical stage manufacturing. This role is crucial to ensuring compliance with regulatory... requirements and maintaining the integrity of our manufacturing processes. The ideal candidate will have a strong background in...

Cartesian Therapeutics

. Familiarity with Good Manufacturing Practices (GMP) requirements, quality procedures, and Standard Operating Procedure (SOP... is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed...

MSD

Major Duties/Responsibilities · Lead drug product formulation and formulation process development in a GMP, CDMO... drug products and ultimate technical transfer(s), as applicable, of the manufacturing process to commercial manufacturing...

AL Solutions