FREE ACCESS
5,000–10,000 jobs/day
See all jobs on JobTailor
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Senior Validation Engineer – cGMP
PerkinElmerValidation Engineer managing life sciences projects at Project Farma. Focused on technical delivery and client relationship building while ensuring project success.
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.
- Author technical documents: SOPs, requirements specifications, testing protocols, summary reports, etc.
- Identify and close individual knowledge gaps with support from other team members or leads as needed.
- Execute system and process validation protocols by using GxP best practices.
- Support necessary billables as forecasted by site dashboards on billable targets per month.
- Report workload or skill gaps within assigned tasks.
- Communicate updates internally in a timely manner and relay in-field project decisions to highlight long-range, down-stream project and team impacts.
- Provide hands-on support and troubleshooting for clients navigating the engineering life cycle of cutting-edge equipment and manufacturing processes.
- Perform due diligence on system and subject domains to generate high-quality project deliverables.
- Proactively identify and escalate roadblocks and utilize critical thinking skills and knowledge of problem-solving skills to identify creative solutions to those problems and roadblocks.
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)
- 1-5 years in consulting and/or engineering services
- Willingness to travel as required for client project assignments.
- Full-time on-site client presence
- Applicants must be authorized to work in the United States on a full-time basis. We will not sponsor applicants for current or future work visas for this position.
- This position may require significant travel to support project and business needs.
- We cannot employ anyone with an invalid driver's license.
Benefits
Comp & perks- Health insurance
- Retirement plans
- Flexible work arrangements
- Professional development
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 testingtechnical documentationsystem validationprocess validationGxP best practicesproblem-solvingcritical thinkingproject managementcapital project engineering
Soft Skills
communicationteam collaborationtroubleshootingclient supporttime managementadaptabilityproactive identification of issuesescalation of roadblockscreative solutionsreporting