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Validation Engineer – Lead, cGMP
PerkinElmer. Execute technical tasks within life sciences projects and ensure high-quality deliverables .
Posted 9/23/2026full-timeRaleigh • North Carolina • United StatesSenior💰 $68,000 - $121,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in CQV tasks, including protocol development and equipment testing, while ensuring compliance with cGMP and GxP standards. Capable of managing project controls, mentoring team members, and maintaining client relationships to support business growth.
Highest-signal resume keywords
CQV Protocol DevelopmentSystem And Process ValidationCGMP And GxP KnowledgeProject Management ToolsTechnical Documentation
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 TestingSystem ValidationProcess ValidationTechnical DocumentationEarned Value AnalysisProject ManagementTroubleshootingSOP AuthoringRisk Identification
Soft Skills
CollaborationMentoringCommunicationProblem-SolvingClient Relationship Management
Industry Keywords
Life SciencesFDA RegulationsRegulatory RequirementsCapital Project EngineeringPharma cGMP FacilityCapEx/OpEx Project ManagementConsulting ServicesEngineering ServicesClient ProposalsBusiness Growth
About the role
Key responsibilities & impact- Execute technical tasks within life sciences projects and ensure high-quality deliverables
- Perform CQV tasks, including protocol development and equipment testing, under Site Lead guidance
- Report technical issues and support resolution efforts
- Author SOPs, requirements specifications, testing protocols, and summary reports
- Execute system and process validation protocols using GxP best practices
- Provide hands-on support and troubleshooting for equipment and manufacturing processes
- Identify and escalate roadblocks, workload gaps, and project risks
- Support project controls and scheduling, including budgets, schedules, milestones, forecasts, and cost reports
- Collaborate with cross-functional teams, project members, clients, and client points of contact
- Mentor less experienced team members and share technical knowledge
- Support site strategy and prepare and execute CQV protocols
- Contribute to client relationships, proposals, project extensions, and business growth
- Maintain 100% individual billability and report progress, risks, and opportunities to the Site Lead
- Travel domestically and provide full-time on-site client presence as required
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
- 1-7 years of experience in consulting and/or engineering services
- Willingness to travel as required for client project assignments, up to 100% or as required
- Must reside within 50 miles of Raleigh, NC
- Must be authorized to work in the United States on a full-time basis
- No current or future work visa sponsorship
- Valid driver's license required
- Knowledge of cGMP, GxP, FDA, and regulatory requirements
- Experience with CQV tasks, protocol development, equipment testing, system and process validation, and technical documentation
- General understanding of Earned Value Analysis and project management tools
Benefits
Comp & perks- Full-time employment
- Opportunity for professional development
- Project Farma internal qualification training program
- Mentoring and collaboration opportunities
- Equal opportunity and commitment to a diverse workforce