Life Sciences Validation Engineer & Lead (cGMP)

PerkinElmer; North Carolina; Hybrid; USD 60,000 - 105,000; Full time

Job summary

PerkinElmer is seeking a Validation Engineer/Lead (cGMP) for Project Farma with 1–8+ years of life sciences or engineering experience. The role will be based on-site with travel up to 100% to client projects in Charlotte, Huntsville, Raleigh, and surrounding areas, contributing to CQV and validation activities across projects.

The successful candidate will mentor teams, own deliverables, and collaborate across cross-functional groups, ensuring compliance with FDA/GMP and client specifications

Qualifications

• Bachelor's degree in Life Science, Engineering, or related discipline.
• 0-8 years of experience in consulting and/or engineering services.
• Willingness to travel as required for client project assignments.

Responsibilities

• Execute technical tasks within a project, delivering high-quality results.
• Perform CQV tasks, such as protocol development or equipment testing, under guidance.
• Report technical issues to the Site Lead and support resolution efforts.
• Ensure tasks meet client specifications, regulatory requirements (FDA, GMP).
• Author technical documents: SOPs, requirements specifications, testing protocols, reports.

Education

Bachelor's Degree in Life Science, Engineering, or related discipline

Job description

PerkinElmer is seeking a Validation Engineer/Lead (cGMP) for Project Farma with 1–8+ years of life sciences or engineering experience. The role will be based on-site with travel up to 100% to client projects in Charlotte, Huntsville, Raleigh, and surrounding areas, contributing to CQV and validation activities across projects.

The successful candidate will mentor teams, own deliverables, and collaborate across cross-functional groups, ensuring compliance with FDA/GMP and client specifications