- Novo Nordisk (Fremont, CA)
- …treat Type 1 Diabetes, Parkinson's disease, and chronical heart failure. The Senior Associate - Quality Control will perform day-to-day QC activities while ... cell research raises hopes for improved treatment of Type 1 Diabetes and for future treatments with cell transplantation...role will also support method verification as assigned. Relationships Senior Associate - Quality Control will work… more
- Actalent (West Greenwich, RI)
- …facilities equipment materials organization processes procedures and products follow cGMP practices and other applicable regulations. Performs review and approval ... of cGMP processes procedures documents and records. Review logbooks batch...Schedule: This position works a rotating shift schedule, Week 1 : Monday, Tuesday, Friday, Saturday Week 2: Sunday, Wednesday,… more
- WuXi AppTec (Philadelphia, PA)
- …'why' behind the regulations. * Identifies, communicates, addresses and improves complex cGMP compliance and regulatory gaps and issues across assigned programs and ... will not be discriminated against on the basis of disability (https://careers-wuxiapptec.icims.com/connect?back=intro&findajob= 1 &in\_iframe= 1 &hashed=-435740542) **Job Locations** _US-PA-Philadelphia_ **Job ID**… more
- Bristol Myers Squibb (Bothell, WA)
- …personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Senior Engineer I, Validation is responsible for supporting the production ... commercial supply at the BMS Manufacturing Plant (Jump), in Bothell, WA. The Senior Engineer I, Validation is responsible for ensuring the compliance of aseptic… more
- Teva Pharmaceuticals (Salt Lake City, UT)
- Senior Quality Engineer - SLE East Date: Apr 1 , 2024 Location: Salt Lake City, United States, Utah, 84108 Company: Teva Pharmaceuticals Job Id: 55087 **Who we ... Assurance direction to ensure a thorough and timely review and approval of cGMP documents. Any non-essential functions are assumed to be included in other related… more
- Merck (West Point, PA)
- …an entry-level, or early career, individual contributor. Under the supervision of a Senior Specialist or Associate Director, is responsible to provide day-to-day ... **DUTIES:** + Reports to and receives supervision from a Senior Specialist or Associate Director. On routine...Technology Degree **Required Experience and Skills:** + Minimum one ( 1 ) year of cGMP , technical/mechanical services experience.… more
- University of Michigan (Ann Arbor, MI)
- Research Lab Specialist Senior Apply Now **Summary** The Rajapakse Lab in the Department of Computational Medicine and Bioinformatics is seeking a Research ... Associate with cell and molecular biology experience, with a...results in compliance with applicable regulatory standards in a CGMP compliant manner, have the ability to work under… more
- Astrix Technology (Athens, GA)
- QA Associate III Quality Assurance Athens, GA, US Pay Rate Low: 28.00 | Pay Rate High: 30.00 + Added - 05/04/2024 Apply for Job Our client is a global, ... to date. The company is looking for a QA Associate to join the team. This is an amazing...cutting edge treatments and make a difference! **Schedule** : 1 st Shift **Pay:** $25-28/hr. 6 month development opportunity… more
- Novo Nordisk (Boulder, CO)
- …Colorado facility and works closely with our teams in Lexington, Massachusetts. Ranked the No. 1 Place to Live for the second consecutive year by US News & World ... cost & timely completion of all validation deliverables. Relationships Associate Director. Essential Functions + Perform, review & approve validation/revalidation.… more
- Merck (West Point, PA)
- …Development, Technical Services, Utilities and Validation. Under the supervision of a Senior Specialist or Associate Director, the Associate Specialist ... cost goals. **Position Responsibilities** + Reports to and receives supervision from a Senior Specialist or Associate Director. On routine process operations, is… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** The Associate Director is responsible for achieving and maintaining qualification/certification status through robust training ... receipt) meet established expectations. + Maintain a broad-based expertise of cGMP 's, Organon Policies, Procedures and Guidelines, regulatory requirements, etc. that… more
- Pfizer (Kalamazoo, MI)
- …the medicines they need, when they need them. **What You Will Achieve** As a Senior Associate , your knowledge and skills will contribute towards the goals and ... drug products. + Create and review Good Manufacturing Practices {also cGMP } documentation, including batch records, product specific cleaning assessments, and… more
- ICU Medical (Austin, TX)
- …of general aspects of the job and will work under the close direction of senior personnel in the functional area. Will be responsible to help maintain and service ... repairs and modifications to production equipment in line with cGMP requirements. Respond in a timely manner to demand...other mechanics. . Works under the close direction of senior personnel in the area. . Must be able… more
- Belcan (Thousand Oaks, CA)
- …Date: Right Away Keywords: #Engineering Job Description: HYBRID 3/4 days onsite, 1 -2 remote. USTO. Standard Business hours with some after-hours support on call ... site 3-4 days a week and may work remotely 1 -2 days a week (activities permitting). Ideal candidate: ...highly dynamic manufacturing facility. JOB RESPONSIBILITIES: Under guidance of senior staff, the Engineer performs the following: - Transfer… more