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The Manager of GMP Manufacturing for Upstream Processing is responsible to lead a team of professionals while overseeing the GMP manufacturing process
This position will support Manufacturing Operations in the successful transfer and startup of clinical drug substance and drug product.
The Sr. Validation Engineer will work in an FDA regulated environment responsible for validation bio process equipment and GMP utilities.
Be part of the Theravance Strategic Sourcing team, manage a wide range of sourcing activities, including stakeholder and supplier engagement...
The Statistical Programming Associate Director will be responsible for multiple therapeutic areas or therapeutic indications...
Now we’re looking for a Product Transfer Scientist to join our Genomics Operations team. And if you’re the right person, we’d like to make you a deal.
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader ...
The Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research...
Fate Therapeutics is currently seeking a talented and highly motivated molecular biologist with strong genetic engineering background to join a mul...
The Senior Clinical Program Manager is the primary operational contact for the study...
Join a company that’s making a difference in the fight against cancer. Astex Pharmaceuticals, www.astx.com...
Check out our new Process Validation Engineer position with Lentigen Technology!
Are you a process development associate who is an expert in downstream activities? If so, join us at Lentigen Technology
Are you a technical professional who enjoys working with and servicing scientific instruments used in the biotech and Life Science Research fields?
Company Description: Molecular Templates (MTEM) is a clinical stage biopharmaceutical company targeting a variety of cancers through development of...
This position is a team leader responsible for planning and executing HCEI messaging, tools and initiatives that support all priority products within
The Director Segment Marketing will leverage business acumen, a strong knowledge of the US Market Access Customer Base, and market access research/VAP
Position Summary:Serves as a point of contact for processes, systems and controls for Standard Operating Procedures (SOPs), Trial Master Files (TMF),
This position will support drug discovery and drug development programs in the area of immuno-oncology. The area of responsibility will include, bu...
To provide support and expertise in developing effective clinical contractual agreements, forecast, budgets and actively manage clinical financial ...