FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Validation Engineer I/II
PerkinElmer. Execute specific technical tasks within projects and ensure high-quality deliverables .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in executing technical tasks, ensuring compliance with FDA/GMP regulatory requirements, and developing essential documentation such as SOPs and testing protocols. Strong ability to collaborate with teams and maintain client relationships while achieving billable targets.
Highest-signal resume keywords
CQV TasksProtocol DevelopmentGxP Best PracticesFDA/GMP ComplianceProject 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
Technical DocumentationSystem ValidationProcess ValidationEquipment TestingRequirements Specifications
Soft Skills
Team CollaborationProfessional CommunicationRelationship Building
Industry Keywords
Life ScienceEngineeringPharmaCGMPCapExOpEx
About the role
Key responsibilities & impact- Execute specific technical tasks within 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
- Ensure work meets client specifications, FDA/GMP regulatory requirements, and industry standards
- Author SOPs, requirements specifications, testing protocols, summary reports, and other technical documents
- Execute system and process validation protocols using GxP best practices
- Meet monthly billable targets and maintain 100% individual billability
- Identify and close knowledge gaps with support from team members and leads
- Share technical knowledge and support team collaboration
- Build internal and external relationships and present Project Farma services to clients
- Communicate professionally with clients and escalate feedback, opportunities, roadblocks, and skill gaps
- Maintain relationships with project team members and client points of contact to facilitate task completion
- 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
- 0–2 years in consulting and/or engineering services
- Willingness to travel up to 100% or as required for client projects
- Authorized to work in the United States on a full-time basis
- No current or future work visa sponsorship
- Valid driver's license required; the employer cannot employ anyone with an invalid driver's license
Benefits
Comp & perks- Full-time salaried position
- Equal opportunity employment
- Diverse and culturally diverse workforce commitment