Senior Validation Engineer at LAPORTE

Join LAPORTE as a Senior Pharmaceutical Validation Engineer in a hybrid work environment. Drive compliance and quality assurance while executing validation plans and protocols.

This role requires a skilled engineer with at least 5 years of experience in the pharmaceutical industry. You will utilize your robust understanding of Good Manufacturing Practices (GMP) to effectively support and manage validation activities. Collaborating with client QA teams is a key aspect of this role.

Key Responsibilities:

• Draft and manage master validation documents and risk analyses

• Execute and oversee equipment and process qualification protocols

• Ensure adherence to GMP throughout validation processes

• Assist QA teams in handling change notices and CAPA

• Develop and maintain client accounts for ongoing projects

Requirements:

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

• At least 5 years of experience within the pharmaceutical sector

• Strong expertise in GMP regulations

• Ability to travel for client visits as required

• In-depth knowledge of pharmaceutical manufacturing processes

Leverage your skills in compliance and validation with LAPORTE's expert team.
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