Lead Validation Engineer – Life Sciences CQV & Projects

PerkinElmer; Illinois; On-site; USD 80,000 - 115,000; Full time

Job summary

PerkinElmer is seeking a Validation - Engineer III/Lead for Project Farma to reside in one of Project Farma’s primary markets and travel domestically as needed. This full-time salaried role supports the life sciences project lifecycle with cross-functional collaboration to deliver high-quality validation services.

The role emphasizes technical delivery, patient-focused outcomes, and growth within a global service network.

Qualifications

• Bachelor’s Degree in Life Science, Engineering, or related discipline (OR a combination of equivalent work experience in capital project engineering, pharma cGMP facility start-up, CapEx/OpEx project management and/or comparable military experience).
• Years of Experience: 4-7 years in consulting and/or engineering services.
• Willingness to travel as required.

Responsibilities

• Execute specific technical tasks within a project, ensuring high-quality deliverables.
• Perform CQV tasks, such as protocol development or equipment testing, under the Site Lead’s guidance.
• Report technical issues to the Site Lead and support resolution efforts.
• Ensure tasks meet client specifications, regulatory requirements (e.g., FDA, GMP), and industry standards.
• Author technical documents: SOPs, requirements specifications, testing protocols, summary reports, etc.

Education

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

Job description

PerkinElmer is seeking a Validation - Engineer III/Lead for Project Farma to reside in one of Project Farma’s primary markets and travel domestically as needed. This full-time salaried role supports the life sciences project lifecycle with cross-functional collaboration to deliver high-quality validation services.

The role emphasizes technical delivery, patient-focused outcomes, and growth within a global service network.