Senior Pharmaceutical Validation Engineer

Elevate your career with LAPORTE as a Senior Pharmaceutical Validation Engineer. Contribute to compliance and quality assurance through validation plan drafting and protocol execution in a hybrid work environment.

LAPORTE is a leading consulting engineering firm specializing in pharmaceutical and industrial processes. We are seeking a skilled Senior Engineer with a minimum of 5 years of experience in the pharmaceutical sector. The ideal candidate will demonstrate strong knowledge of Good Manufacturing Practices (GMP) and pharmaceutical manufacturing processes.

Your role will involve collaborating with client QA teams and managing validation activities effectively.

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 relevant discipline

• At least 5 years’ pharmaceutical industry experience

• Strong knowledge of GMP regulations

• Willingness to travel for client site visits

• Expertise in pharmaceutical manufacturing processes

Maximize your expertise in validation and compliance with LAPORTE's dynamic team.
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