Pharmaceutical Validation Engineer Position

Embark on a rewarding career with LAPORTE as a Senior Pharmaceutical Validation Engineer in a hybrid setting. Contribute to quality assurance and compliance through protocol execution.

LAPORTE is looking for a Senior Engineer with a minimum of 5 years of experience in pharmaceuticals. Ideal candidates will demonstrate thorough knowledge of Good Manufacturing Practices (GMP) and pharmaceutical manufacturing processes. You will engage with client QA teams and oversee various validation efforts.

Key Responsibilities:

• Draft and execute master validation documents and risk assessments

• Carry out equipment and process qualification protocols

• Maintain compliance with GMP during validation phases

• Collaborate with QA teams on CAPA and change notices

• Develop and manage client accounts for validation initiatives

Requirements:

• Bachelor’s or master’s degree in a relevant field

• Minimum 5 years of experience in the pharmaceutical industry

• Strong understanding of GMP and regulatory standards

• Willingness to travel for site validation tasks

• Expertise in pharmaceutical manufacturing processes

Utilize your validation skills and knowledge to make an impact at LAPORTE.
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