cGMP Lab Specialist: Projects, Validation & Quality

West Pharmaceutical Services; Kinston (NC); On-site; USD 64,000 - 88,000; Full time

Job summary

West Pharmaceutical Services in Kinston, NC seeks a Laboratory Specialist to execute and support laboratory projects in a high‑quality, regulated environment. You will work on equipment qualifications, method transfers, method validation, investigations, and documentation updates to maintain cGMP compliance.

You will collaborate with Quality, Operations, Engineering, and global teams while maintaining data integrity and safety standards.

Qualifications

• Masters degree in science-related discipline required or preferred.
• 3–5 years lab experience in pharmaceutical/medical device settings.
• Experience with electronic document management systems and validations.

Responsibilities

• Plan and execute local laboratory projects including quality and safety initiatives.
• Coordinate internal equipment qualifications, methods transfers and validations.
• Support routine laboratory testing and review documentation for accuracy and compliance.

Skills

English proficiency

Project management

Data analysis

Communication skills

Adaptability

Education

Masters degree in Science related discipline

Tools

Electronic Document Management Systems

Job description

West Pharmaceutical Services in Kinston, NC seeks a Laboratory Specialist to execute and support laboratory projects in a high‑quality, regulated environment. You will work on equipment qualifications, method transfers, method validation, investigations, and documentation updates to maintain cGMP compliance.

You will collaborate with Quality, Operations, Engineering, and global teams while maintaining data integrity and safety standards.