Job Description
Advance your profession with LAPORTE as a Senior Validation Engineer. This hybrid role focuses on compliance and quality assurance through drafting validation plans and executing protocols.
LAPORTE is a renowned consulting engineering firm in the pharmaceutical sector. We are searching for a seasoned Senior Engineer with a minimum of five years of experience. The role demands a robust understanding of Good Manufacturing Practices (GMP) and the ability to collaborate with client QA teams while managing validation activities efficiently.
Key Responsibilities: • Draft master validation documents and risk analyses • Execute equipment and process qualification protocols • Ensure compliance with GMP during validation activities • Support QA teams in change notices and CAPA processes • Manage and develop client accounts
Requirements: • Bachelor’s or master’s degree in a relevant discipline • Minimum of five years in the pharmaceutical industry • Strong knowledge of ...
LAPORTE is a renowned consulting engineering firm in the pharmaceutical sector. We are searching for a seasoned Senior Engineer with a minimum of five years of experience. The role demands a robust understanding of Good Manufacturing Practices (GMP) and the ability to collaborate with client QA teams while managing validation activities efficiently.
Key Responsibilities: • Draft master validation documents and risk analyses • Execute equipment and process qualification protocols • Ensure compliance with GMP during validation activities • Support QA teams in change notices and CAPA processes • Manage and develop client accounts
Requirements: • Bachelor’s or master’s degree in a relevant discipline • Minimum of five years in the pharmaceutical industry • Strong knowledge of ...
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