Validation Engineer

The Validation Engineer must have thorough knowledge of global regulatory requirements for validation, including ERES (Part 11 and Annex 11) & current GAMP5 guidelines. Support all aspects of the Validation Life Cycle from design through operation & maintenance to retirement. Responsible for the preparation of site validation documentation such as qualification protocols, validation master plans, risk assessments & periodic reviews. Prepare reports using data from Process Validation, In-process Manufacturing testing In-process QC testing & Finished Product QC testing. Ensure validation testing performed by vendors is complete & accurate; work w/ vendors for issue resolution & validation deviation reporting. Support the revalidation program. Ensure site alignment with corporate standards & cGxP guidelines. Authoring & revising standard operating procedures within the electronic documentation management system. Technically independent & maintains up-to-date knowledge of validation standards & regulatory compliance requirements.

According to JobzMall, the average salary range for a Validation Engineer in 145 N Brandywine St, West Chester, PA 19380, USA is $58,348 to $97,564 per year. This salary range is based on the salary data of JobzMall, which has gathered information from various sources, including job postings, third-party market research, and user-submitted salary data.

Teva Pharmaceutical Industries Ltd., also known as Teva Pharmaceuticals, is an American Israeli pharmaceutical company with dual headquarters in Petah Tikva, Israel and Parsippany, New Jersey, U.S. Teva Pharmaceutical Industries Ltd. engages in the provision of pharmaceutical services. It operates through the following business divisions: Generic, Specialty Medicine, and Over-the-Counter (OTC).