Senior Validation Engineer at LAPORTE

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 GMP regulations

• Willingness to travel for client site visits

• Expertise in pharmaceutical manufacturing processes

Utilize your validation expertise working with LAPORTE's dynamic team.
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