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Validation - Engineer III/Lead - Project Farma

Newperkinelmer

Customer Site - IN | Customer Site - KS | Customer Site - MO, US$80k – $115konsite

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About this 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 Validation - Engineer III/Lead - Project Farma Location(s) Customer Site - IL, Customer Site - IN, Customer Site - KS, Customer Site - MO, Customer Site - OH Job Description Role Summary  

This is a   full-time salaried position with   Project Farma,   a PerkinElmer company. The successful candidate will   reside   in one of Project Farma's primary markets 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 .  

The   Validation   Lead   Engineer   is an advanced individual contributor with   demonstrated   depth in their technical discipline and a growing record of leading complex workstreams. This role applies strong   subject  matter   expertise   to solve   high  impact   technical and operational challenges, supports technical   decision  making , and contributes to the evolution of standards, methods, or best practices within their area. The   Lead   Engineer works with a high degree of independence, mentors junior and peer engineers, and partners closely with project and people leaders—while   remaining   focused on technical delivery rather than formal people management.  

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 member s 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.  

• 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 tool s    

• 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.  

• Create alignment with cross-functional client departments including but not limited to Validation, Manufacturing, Quality, Supply Chain, Engineering and Project Controls  

• Maintain internal site tools such as site dashboards, deliverable trackers, etc.  

• Continually develop technical aptitude of Project Farma’s core services within the life science space including but not limited to: Capital Project Management, Tech Transfers, Validation Life Cycles including CQV and Computer system Validation, Quality, Regulatory and Compliance,   GxP   Automated Systems, and Quality Control including clinical and commercial.    

• Analyze complex project data and then deliver clear,   articulate   and concise messages in a compelling manner to support decision making  

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  

Resource Management  

• Provide inp

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