- Texas A&M University System (College Station, TX)
- Job Title Postdoctoral Research Associate Agency Texas A&M Agrilife Research Department Institute for Advancing Health through Agriculture-Project Management ... the fields: plant biology/ genetics, human nutrition, physiology, nutritional epidemiology, biotechnology , genetics, or food systems, or other closely related fields… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …years of experience in a microbiology/virology role within the pharmaceutical or biotechnology industry, with a focus on sterile manufacturing and advanced therapies ... years of experience in a microbiology/virology role within the pharmaceutical or biotechnology industry, with a focus on sterile manufacturing and advanced therapies… more
- Gilead Sciences, Inc. (Oceanside, CA)
- …years of progressive experience in Quality Assurance within the pharmaceutical or biotechnology industry, with a significant focus on quality systems management in a ... years of progressive experience in Quality Assurance within the pharmaceutical or biotechnology industry, with a significant focus on quality systems management in a… more
- Charles River Laboratories (Northridge, CA)
- …unique challenges. Our client base includes global pharmaceutical and biotechnology companies, government agencies, and hospitals and academic institutions around ... the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work… more
- Novo Nordisk (West Lebanon, NH)
- …equivalent with two (2) years of experience preferred + Pharmaceutical or biotechnology experience strongly preferred + Knowledge, Skills, and Abilities + Requires ... functional understanding of cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines + Ability to understand and execute established written instructions is essential + Organizational skills and an… more
- Takeda Pharmaceuticals (Thousand Oaks, CA)
- …experience in a manufacturing or quality operations function in a biotechnology , biologics, or pharmaceutical manufacturing facility + Minimum 5 years previous ... leadership, supervisory or management experience required **More about us:** At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company… more
- ManpowerGroup (Milwaukee, WI)
- Our client, a leading organization in the Biotechnology sector, is seeking a Quality Assurance Project Specialist to join their team. As a Quality Assurance Project ... Specialist, you will be part of the Quality Assurance department supporting various teams. The ideal candidate will have system experience- Mango, Trackwise, SAP, MS Suite, ISO - 9001, strong problem-solving skills, excellent communication abilities, and a… more
- AbbVie (North Chicago, IL)
- …budgetary activities. Qualifications + More than 5 years of direct biotechnology / pharmaceutical industry experience and/or payer experience. + Relevant global ... payer and access experience* Education: BA/BS required; Advanced degree (PharmD, MBA, PhD) in a scientific or economic area nice to have. Preferred Competencies: + Strong leadership, intrapersonal, critical thinking, and analytical skills to work with a… more
- Bristol Myers Squibb (San Diego, CA)
- …lives. Read more: careers.bms.com/working-with-us . **Background** RayzeBio is a dynamic biotechnology company headquartered in San Diego, CA. Launched in late 2020 ... and recently acquired by Bristol Myers Squibb (BMS) as a wholly owned subsidiary, the company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio will operate as a standalone entity within the BMS… more
- Fresenius Medical Center (Waltham, MA)
- …five (5) years of regulatory operations experience in the pharmaceutical or biotechnology industry, with a strong emphasis on global regulatory submissions. + Proven ... expertise in the preparation, compilation, publishing, and validation of eCTD submissions in support of US (FDA), Canada (Health Canada), EU (EMA, MHRA), and Asia-Pacific (PMDA, TGA, NMPA, etc.) regulatory requirements. + In-depth knowledge of electronic… more