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Validation Engineer I / II
PerkinElmer. Support project execution through technical contribution, analysis, and problem-solving within defined scope and guidance .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in executing system and process validation protocols using GxP best practices, along with strong technical writing skills for authoring SOPs, requirements specifications, and testing protocols. Capable of collaborating effectively with cross-functional teams and maintaining professional client relationships to support project execution and business growth.
Highest-signal resume keywords
System Validation ProtocolsProcess Validation ProtocolsTechnical Document AuthoringGxP Best PracticesClient Relationship 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
CQV TasksProtocol DevelopmentEquipment TestingProject ManagementTechnical Analysis
Soft Skills
Problem-SolvingCollaborationCommunication
Industry Keywords
FDA/GMP Regulatory RequirementsLife ScienceEngineeringPharmaCGMP Facility Start-Up
About the role
Key responsibilities & impact- Support project execution through technical contribution, analysis, and problem-solving within defined scope and guidance
- Execute technical tasks and deliver high-quality project deliverables
- Perform CQV tasks, including protocol development and equipment testing, under Site Lead guidance
- Report technical issues and support resolution efforts
- Author technical documents including SOPs, requirements specifications, testing protocols, and summary reports
- Execute system and process validation protocols using GxP best practices
- Meet monthly billable targets and escalate workload, skill gaps, or roadblocks
- Collaborate with cross-functional teams and share technical knowledge with peers
- Build internal and external relationships and communicate professionally with clients
- Present Project Farma services to clients as needed
- Escalate client feedback and business opportunities
- Maintain relationships with project team members and client points of contact to facilitate task completion
- Support professional development and contribute to project-level business growth
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
- 0–2 years in consulting and/or engineering services
- Willingness to travel up to 100% or as required for client projects
- Must be authorized to work in the United States on a full-time basis
- PerkinElmer will not sponsor current or future work visas
- Cannot be employed with an invalid driver's license
- Ability to meet client specifications, FDA/GMP regulatory requirements, and industry standards
- Ability to execute system and process validation protocols using GxP best practices
- Ability to author SOPs, requirements specifications, testing protocols, and summary reports
Benefits
Comp & perks- Full-time employment
- Equal opportunity employer
- Diverse and culturally diverse workforce
- Domestic travel opportunities to support client projects