Molecular Templates, a clinical-stage drug discovery company currently has an opening for a full-time Director of Quality who will direct Quality Control (QC) efforts and manage Quality Assurance (QA) efforts related to cGMP manufacturing of...
South San Francisco, CA,
* Key, multi-faceted, PhD-level, CLIA lab technical and operational leadership role for a high-complexity clinical laboratory-experienced director within an established, pioneering, diagnostic-focused biotech company that has expanded its domestic...
Sanaria Inc., a Rockville, MD based biotechnology company, offers a unique and challenging opportunity to join a world-class team to work on the development and commercialization of a live sporozoite-based malaria vaccine. Sanaria is now conducting...
Miltenyi Biotec, Inc.
Are you a quality assurance expert who would thrive in a GMP environment? Are your organization and documentation skills always geared for audits? If yes, then come and join our team as a…
Senior Quality Assurance Specialist
As a member...
The Quality Assurance (QA) Manager is expected to bring in-depth experience in drug substance and drug product manufacturing. Reporting to the Director, Quality Assurance, the QA Manager will provide Quality oversight and support to the Operations...
South San Francisco ,
As part of a talented and multi-disciplinary team advancing an exciting novel approach to drug development, the QA Validation Manager will support equipment/systems validation, method validation and process validation for the Company’s GMP facility...
Leidos Biomedical Research, Inc.
Leidos Biomedical Research, Inc. (LBRI), a wholly owned subsidiary of Leidos, operates the Frederick National Laboratory for Cancer Research (FNLCR). FNLCR is a Federally Funded Research and Development Center (FFRDC) sponsored by...
Recro Gainesville LLC
The QA Associate III will be responsible for a product line(s) as assigned by management. This includes responsibility for the release of materials in accordance with cGMPs and Standard Operating Procedures, review of validation documents, change...
Insmed understands that its most valuable resource is its employees. We place great value on the unique skills, talents and qualities that each of our employees brings to our company. We are building a world-class team with a focus on innovation,...
The Production Quality Engineer will assist in the development, improvement, and implementation of documentation requirements under the direction of Operations Management. This includes reviewing executed production batch...