Sr. Validation Engineer (cGMP) - Project Farma
PerkinElmerAbout the role
When joining PerkinElmer, you select an experienced and trusted leader in scientific solutions, with the support of a global service network and distribution centers, providing the right solution, at the right time, to meet critical customer needs. With over an 80+ year legacy of advancing science and a mission of innovating for a healthier world, our dedicated team collaborates closely with commercial, government, academic and healthcare customers to deliver our broad portfolio of analytical solutions, and OneSource services.
Job Title
Sr. Validation Engineer (cGMP) - Project Farma
Location(s)
Customer Site - AL, Raleigh, NCJob Description
This is a full-time salaried position with Project Farma, a PerkinElmer company. The successful candidate will reside within 50 miles of Raleigh, NC - Greenville, NC - or Huntsville, AL and be willing to travel domestically to meet client project requests.
Project Farma’s purpose is to improve patient lives by accelerating the delivery of life-changing therapies. We accomplish this through the successful execution of high-quality life sciences projects across the full project lifecycle. Project Farma (PF) team members collaborate with cross-functional teams to build trusted client relationships, deliver an exceptional customer experience, and contribute to business growth by identifying opportunities and applying data-driven insights to support project planning, cost, schedule, and performance management.
All team members are expected to embody Project Farma’s values by being curious, personable, and unselfish, while maintaining a strong commitment to a Patient Focused and People First mindset.
Key Responsibilities
Technical Delivery
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
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