Validation Engineering Senior at LAPORTE

Position: Validation Engineering Senior Role at LAPORTE
Elevate your expertise as a Validation Engineer with LAPORTE. This senior position in a hybrid work environment centers on compliance and quality through precise validation plan execution.

LAPORTE, a leader in consulting engineering focused on pharmaceutical processes, seeks a Senior Pharmaceutical Validation Engineer with a minimum of five years in the industry. You should possess a strong grasp of Good Manufacturing Practices (GMP) and experience in managing collaboration with client QA teams for efficient validation.

Key Responsibilities:

• Create master validation documents and perform risk analyses

• Implement equipment and process qualification protocols

• Ensure adherence to GMP standards during validations

• Support QA teams with change notice and CAPA processes

• Oversee client account management and development

Requirements:

• Bachelor’s or master’s degree in a related discipline

• Five years’ experience in the pharmaceutical industry

• Comprehensive understanding of GMP regulations

• Willingness to travel for client site interactions

• Expertise in pharmaceutical manufacturing processes

Maximize your compliance and validation skills with LAPORTE's expert team.
#J-18808-Ljbffr