You will develop and deliver conceptual, preliminary, and detailed design packages through to CQV for GMP-compliant integrated process equipment and u..Share
Are you a driven validation professional looking to make an immediate impact on a major GMP facility expansion? A leading global pharmaceutical compan..Share
Senior Automation Engineer (GMP). SCADA systems, industrial automation, IT development, and GMP compliance. This is a hands-on technical role for an e..Share
Build and oversee cGMP Quality Management Systems, Batch Review and Release, Quality Control testing activities and disposition of packaging products ..Share
You will develop and deliver conceptual, preliminary, and detailed design packages through to CQV for GMP-compliant integrated process equipment and u..Share
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Seasonal Warehouse Worker UPS Quick Apply Applying for this role online is quick and easy – and you could even schedule your first day of work within ..Share
Are you a driven validation professional looking to make an immediate impact on a major GMP facility expansion? A leading global pharmaceutical compan..Share
United Pharma in the United States is seeking an experienced Technical Writer with a strong chemistry and pharmaceutical laboratory background. You wi..Share
Director, GMP QA (CMC/Development) – Permanent – New York. In this role, you will be responsible for the hands-on oversight of all Quality Assurance (..Share
The purpose of the Review Panel is to hear oral representations, in accordance with the legislation, from licence holders who disagree with a proposed..Share
Seeking motivated individuals to participate in National Focus Groups and Clinical Trial studies. Earn up to $750/week in your spare time. Must regist..Share
Customs and Border Protection Officer (CBPO) With more than 69,000 employees, U.S. Customs and Border Protection (CBP) is one of the world's largest l..Share
Good Manufacturing Practices (GMP), Equipment Validation. Are you a driven validation professional looking to make an immediate impact on a major GMP ..Share
You will develop and deliver conceptual, preliminary, and detailed design packages through to CQV for GMP-compliant integrated process equipment and u..Share
Are you a driven validation professional looking to make an immediate impact on a major GMP facility expansion? A leading global pharmaceutical compan..Share