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Validation Engineer III – Lead
PerkinElmerValidation Lead Engineer at PerkinElmer executing high-quality life sciences projects. Collaborating with cross-functional teams and focusing on client satisfaction and business growth.
About the role
Key responsibilities & impact- 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.
- Create alignment with cross-functional client departments including but not limited to Validation, Manufacturing, Quality, Supply Chain, Engineering and Project Controls.
Requirements
What you’ll need- 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.
- 4-7 years in consulting and/or engineering services
- Willingness to travel as required for client project assignments.
Benefits
Comp & perks- Health insurance
- Professional development opportunities
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
protocol developmentequipment testingcapital project engineeringproject managementcGMP facility start-upCapEx managementOpEx management
Soft Skills
communicationproblem-solvingcollaborationattention to detail
Certifications
Bachelor’s Degree in Life ScienceBachelor’s Degree in Engineering