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Validation Engineer III – Lead
PerkinElmer. Execute technical tasks within validation and life sciences projects .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in CQV tasks, system and process validation, and technical documentation while ensuring compliance with FDA and GMP requirements. Capable of analyzing project data and effectively communicating insights to support decision-making and project management.
Highest-signal resume keywords
CQV TasksSystem And Process ValidationTechnical DocumentationFDA And GMP RequirementsProject Management
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Protocol DevelopmentEquipment TestingTroubleshootingData AnalysisSOP AuthoringValidation ProtocolsProject ControlsEarned Value AnalysisClient Specifications ComplianceGxP Best Practices
Soft Skills
CommunicationMentoringRelationship BuildingProblem-SolvingTeam Coordination
Tools & Technologies
Project Management ToolsDeliverable TrackersSite Dashboards
Certifications & Qualifications
Bachelor’s Degree In Life ScienceBachelor’s Degree In Engineering
Industry Keywords
Life SciencesPharmaCGMP Facility Start-UpCapital Project EngineeringOpEx Project Management
About the role
Key responsibilities & impact- Execute technical tasks within validation and life sciences projects
- Perform CQV tasks including protocol development and equipment testing under Site Lead guidance
- Report technical issues and support resolution efforts
- Ensure deliverables meet client specifications, FDA/GMP requirements, and industry standards
- Author SOPs, requirements specifications, testing protocols, and summary reports
- Execute system and process validation protocols using GxP best practices
- Provide hands-on troubleshooting for equipment and manufacturing processes
- Analyze project data and communicate concise insights for decision-making
- Support project controls, scheduling, budgets, milestones, forecasts, risks, and cost reports as requested
- Coordinate with Validation, Manufacturing, Quality, Supply Chain, Engineering, and Project Controls teams
- Maintain site dashboards and deliverable trackers
- Mentor junior and peer engineers and share technical knowledge
- Support site strategy and client project tasks
- Communicate resource needs, workload, and skill gaps to the Site Lead
- Build internal and external relationships and communicate professionally with clients
- Support extensions and proposals and identify cross-selling/up-selling opportunities
- Maintain 100% individual billability and escalate roadblocks
- Travel domestically to meet client project requests
Requirements
What you’ll need- Bachelor’s Degree in Life Science, Engineering, or related discipline, or 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
- Willingness to travel up to 100% or as required
- Applicants must be authorized to work in the United States on a full-time basis
- PerkinElmer will not sponsor current or future work visas
- Valid driver’s license required
- Full-time on-site client presence preferred
- Knowledge of CQV, system and process validation, GxP best practices, FDA and GMP requirements, technical documentation, project management tools, and Earned Value Analysis
Benefits
Comp & perks- Full-time salaried position
- Significant domestic travel opportunities