LAPORTE Senior Validation Engineer

Position: LAPORTE Senior Validation Engineer Role
Advance your career with LAPORTE as a Senior Pharmaceutical Validation Engineer in a hybrid setting. This role focuses on compliance, quality assurance, and validation protocol execution.

LAPORTE, a leading consulting engineering firm, is seeking a Senior Engineer with over 5 years in the pharmaceutical sector. Candidates should possess strong knowledge of Good Manufacturing Practices (GMP) and a solid foundation in pharmaceutical manufacturing processes. You will collaborate with client QA teams and manage various validation activities effectively.

Key Responsibilities:

• Draft master validation documents and perform risk analyses

• Execute protocols for equipment and process qualification

• Ensure compliance with GMP during all validation activities

• Support QA teams on change notices and CAPA processes

• Manage and develop client accounts for validation projects

Requirements:

• Bachelor's or master's degree in a relevant discipline

• Minimum of 5 years of experience in the pharmaceutical industry

• Expertise in GMP regulations and compliance

• Willingness to travel for client site assessments

• Strong understanding of pharmaceutical manufacturing processes

Bring your validation and compliance expertise to LAPORTE's innovative team.
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