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Sr. Validation Engineer; cGMP - Project Farma

Job in Raleigh, Wake County, North Carolina, 27601, USA
Listing for: PerkinElmer
Full Time position
Listed on 2026-07-01
Job specializations:
  • Engineering
    Quality Engineering, Systems Engineer, Operations Engineer, Electrical Engineering
Job Description & How to Apply Below
Position: Sr. Validation Engineer (cGMP) - Project Farma

Sr. Validation Engineer (cGMP) - Project Farma

When joining Perkin Elmer, 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 One Source services.

This is a full-time salaried position with Project Farma, a Perkin Elmer 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
  • 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.
  • General understanding of Earned Value Analysis (EVA) and project management tools
  • May be requested to assist with Project Controls and Scheduling to include;
    Budget estimates, detailed project schedules and milestones, feasibility estimates, risks, forecasts and scenario analysis and project cost reports and analysis.
Talent Development
  • Focus on professional development and support team collaboration under the Site Leads guidance.
  • Share technical knowledge with peers to support project delivery. Mentor less experienced team members.
  • Participate in Project Farma internal qualification training program.
Site Strategy
  • Support the execution of site strategy under the direction of the Site Lead, contributing to specific project tasks that align with Project Farma's services.
  • Perform assigned tasks to meet strategic objectives, such as preparing and executing CQV Protocols
  • Identify and reports client needs or project challenges to the Site Lead for further action.
  • Maintain professional relationships with project team members and client POCs at the operational level (e.g., technicians, engineers) to facilitate task completion
Business Growth & Development
  • Contribute to project-level success by delivering high-quality work that supports business growth opportunities.
  • Build meaningful internal and external relationships.
  • Present Project Farma as a service to clients as needed.
  • Communicate with clients in a professional manner.
  • Ensure any client feedback or opportunities identified are being escalated properly.
  • Provides data or insights (e.g., project progress, risks) to the Site Lead for inclusion in dashboards or expansion discussions.
  • Participate in project tasks that support extensions or proposals, such as preparing deliverables for clients.
Operational Performance & Billability
  • Maintain 100% individual billability by completing assigned project tasks.
  • Escalate any roadblocks on achieving billable targets to the Site Lead.
Attributes for Success
  • Technical Delivery:
    Applies advanced technical knowledge and…
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