Lead Validation Engineer, cGMP Life Sciences

RiseMe; North Carolina; On-site; USD 68,000 - 121,000; Full time

Job summary

PerkinElmer in Raleigh, NC is seeking a Validation Engineer / Lead (cGMP) for Project Farma. The role combines technical delivery, CQV tasks on client projects, and domestic travel as needed.

You will author SOPs and specifications, support project planning and cost/schedule control, and collaborate with cross-functional teams to ensure regulatory compliance and high-quality outcomes.

Qualifications

• 1-7 years in consulting and/or engineering services.
• Bachelor’s Degree in Life Science, Engineering, or related discipline.
• Willingness to travel to client sites.

Responsibilities

• Execute technical tasks within a project and deliver high-quality results.
• Perform CQV tasks and document protocols under Site Lead guidance.
• Report issues and support resolution; ensure regulatory adherence (FDA, GMP).
• Create SOPs, requirements specs, testing protocols, and reports.
• Identify knowledge gaps and support risk and change management.
• Collaborate with cross-functional teams to support project planning and cost control.
• Maintain 100% billability and support project dashboards.

Skills

1-7 years experience in consulting/eng

Education

Bachelor’s Degree in Life Science/Engineering

Job description

PerkinElmer in Raleigh, NC is seeking a Validation Engineer / Lead (cGMP) for Project Farma. The role combines technical delivery, CQV tasks on client projects, and domestic travel as needed.

You will author SOPs and specifications, support project planning and cost/schedule control, and collaborate with cross-functional teams to ensure regulatory compliance and high-quality outcomes.