Validation Engineers & Leads (cGMP) - Project Farma
$60k - $105kPerkinElmer
Project Farma is growing our Validation Services practice, and will consider candidates' ranging from 1-8+ years' relevant experience. The successful candidate will reside in Charlotte, NC; Huntsville, AL; Greenville, NC; or Raleigh, NC 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 Engineer is a technical leader who drives complex workstreams from planning through execution. This role applies technical expertise and strong understanding of project objectives to solve complex problems, influence technical direction, and deliver high-quality outcomes. They act as trusted advisors to project teams and stakeholders while demonstrating leadership through mentorship, quality ownership, and cross-functional collaborations. This role requires strategic problem-solving, sound judgement, and a high level of accountability in driving results. 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 cutting-edge equipment and manufacturing processes. Perform due diligence on system and subject domains to generate high-quality project deliverables. Proactively identify and elevate 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 professional expertise Innovation & Continuous Improvement : Seeks better ways, adapts to change and champions new ideas. Customer Focus & Professionalism : Represents PF with consistent professionalism, appropriate escalation and respect for internal stakeholders, even during high stress delivery situations Integrity & Humility : Demonstrates self-awareness and puts PF mission above ego Collaboration & Communication : Communicates clearly and proactively and drives transparent alignment with clients. Project Execution : Delivers reliably, manages priorities and drives for high quality outcomes Growth Mindset : Shows openness to new ideas, feedback and change Experience Required 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. undefined Years of Experience: 0-8 years in consulting and/or engineering services Willingness to travel as required for client project assignments. Other Preferred Full-time on-site client presence Willingness to travel up to 100% or as required. Project Farma is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability status, age, or veteran status or any other characteristics protected by applicable law. PerkinElmer is committed to a culturally diverse workforce. 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. The annualcompensation range for this full-time position is $60,000 - $105,000. The final base pay offered to the successful candidate will be determined by factors including internal equity, work location, as well as individual qualifications, such as job-related skills, experience, and relevant education or training. #J-18808-Ljbffr PerkinElmer
$111k - $219k
...services.Job TitleC&Q Validation Manager / Senior Manager - Project FarmaLocation(s)... ...DescriptionProject Farma’s purpose is to improve... ...is responsible for leading teams and... ...of high-quality GMP Engineering services that meet... ...in CQV engineering, cGMP facility start-up,...ProjectFull timeTemporary workLocal areaWork visa- Fresenius Kabi in the United States seeks a validation professional responsible for supporting operations through initial validation and... ...testing, critical area airflow testing, and ensuring adherence to cGMP and change control requirements. The incumbent provides...SuggestedFor contractors
$116k - $258k
...OneSource services.Job TitleSenior Automation Engineer (cGMP) - Project FarmaLocation(s)Customer Site - AL,... ...US Remote - NCJob DescriptionProject Farma will consider candidates' ranging from... ...Strategy Client Engagement & Delivery Lead medium sized projects or scope of work...ProjectFull timeRemote workWork visa- ...Position Summary The Cleaning Validation Engineer oversees the development,... ...commercialization, ensuring compliance with cGMP, FDA, and global regulatory... ...and contamination risk Lead CQV activities for CIP, COP,... ...Engineering & Facilities Project Management Regulatory...ProjectFull timeFor contractors
$94k - $203k
...Controls Manager - Project FarmaLocation(s)... ...DescriptionProject Farma’s purpose is to improve... ...responsible for leading teams and... ...across the entire engineering lifecycle. You will... ...system integrations Validation Life Cycle, including... ...general construction, cGMP facility start-up,...ProjectFull timeFor contractorsWork visa$90k - $175k
...services.Job TitleLead Process Engineers & Managers - Project FarmaLocation(s)Raleigh, NCJob DescriptionProject Farma is growing our... ...with Quality, Manufacturing, Validation, Regulatory, EHS, and Operations... ...project engineering, pharma cGMP facility start-up, CapEx/OpEx...ProjectFull timeFor contractorsWork experience placementWork visa$220k - $275k
...Practice Area Leader - Project FarmaLocation(s)... ...withProject Farma, a PerkinElmer company... ...responsible for leading a team and overseeing... ..., process validations, and facility fit... ...Supply Chain, and Engineering.Partner with technical... ...engineering, pharma cGMP facility start-up,...ProjectFull timeWork experience placementRemote workWork visa$200k - $250k
...Principal Consultant - Project FarmaLocation(s)Dallas,... ...executive responsible for leading the company’s most... ...Degree in Life Science, Engineering, or related discipline... ...experience in CQV engineering, cGMP facility start-up,... ....PerkinElmer/Project Farma is committed to creating...ProjectFull timeWork visa- ...Our client is seeking experienced Validation Engineers/Validation Specialists to support a large-scale pharmaceutical project portfolio at a GMP manufacturing site in the greater... ...and be capable of independently leading validation activities with minimal guidance...ProjectLong term contractCasual workAfternoon shift
- Project Farma seeks a Validation Engineer to lead complex validation tasks across the project lifecycle. The role focuses on technical delivery, CQV activities, and cross-functional collaboration to ensure high-quality, compliant outcomes. Qualifications include a life...Project
- ...Responsibilities: Client is seeking validation consultants to support a 9-month minimum onsite project in South Carolina. The... ...on validation strategies. The lead consultant should be able to drive... ...Requirements: Bachelor's degree in Engineering, Science, Life Sciences, or...Project
- ...Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on... ...C&Q activities in alignment with project schedules- Track and report progress of... ...Experience- Bachelor’s degree (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant...ProjectFull timeFor contractorsWorldwide
- ...Responsible for end-to-end power system studies, protection engineering, grid code compliance, quantitative reliability (RAM) modeling, and closed-loop validation for utility-grade and hyperscale microgrid projects. This role ensures microgrid solutions are safe,...ProjectFull timeWorldwide
- ...Alliance Biotech Solutions is currently hiring multiple Cleaning Validation Engineers to supports the execution and coordination of cleaning... ...functional teams to ensure validation activities align with project timelines and operational needs Author and review validation...ProjectFull timeTemporary workCurrently hiringFlexible hours
$71k - $105k
...Validation Engineer Eaton's ES AMER ESS division is currently seeking a Validation Engineer. This role is based out of Raleigh, NC. The... ..., engineering assessments, and technical documentation for project reviews and regulatory submissions. • Support UL, IEEE, IEC,...ProjectInternshipLocal area$135k - $185k
...Manager, Pharma GMP Sites - Project FarmaLocation(s)... ...position with Project Farma, a PerkinElmer company... ...Construction Manager will lead large-scale capital... ...with on-site engineering, design teams, system... ...commissioning/qualification, validation, and system turnover....ProjectFull timeLocal areaWork visa- ...Alliance Biotech Solutions has multiple openings for Validation Engineers to support the execution and coordination of commissioning, qualification... ..., and hands-on execution to ensure compliant, efficient project delivery within aggressive timelines. Requirements •...ProjectFull timeTemporary work
- ...experts. We’re one of the largest engineering and system integration firms... ...) to be responsible for leading or contributing to detailed... ...automation control systems projects. This includes defining architecture... ...designReview documentation/validation requirements with the...ProjectLocal area
- ...Summary We are seeking a detail-oriented Validation Specialist to support validation and... ...cross-functionally with Quality Assurance, Engineering, Manufacturing, Quality Control, and... ...ability to manage documentation and projects in a regulated environment. Key Responsibilities...ProjectFull timeWork at office
- ...Commissioning, Qualification, and Validation (CQV) Engineer This is a hands-on commissioning, qualification... .... You will work alongside our CQV Lead on facility, utility and equipment... ...regulator may read. Familiarity with cGMP under 21 CFR Parts 210 and 211, and with...Full timeMonday to Friday
$107.1k - $160.7k
...mission to become the world’s leading integrated design practice. Our architects, engineers, interior designers, consultants... ...innovative, sustainable approach to projects help us create buildings that... .... The Commissioning and Validation role provides crucial services...ProjectFull timeTemporary workPart timeCasual workWork at officeLocal areaImmediate startFlexible hours- ...Description: We are seeking a Computer System Validation (CSV) Engineer for a global pharmaceutical client. This role will work cross-functionally to lead and execute validation activities for... ..., and SOPs. Ensure compliance with cGMP, GxP, GAMP, SDLC regulations, 21 CFR...Remote work
$142.8k - $274.8k
...Hardware, and Infrastructure Engineering (SCHIE) is the team behind Microsoft... ...goal, the Verification & Validation team is instrumental in... ...responsibilities upon hire:Own or lead Formal verification of Fabric... ...working on or leading projects from beginning-to-end.5+ years...ProjectOngoing contractPermanent employmentWork at officeLocal areaWorldwide3 days per week$180k - $215k
...Director, Raleigh Project OperationsLocation... ...position with Project Farma, a PerkinElmer... ...partner with their Site Leads to proactively... ...assessment to validation and closeout, ensuring... ...in Life Science, Engineering, or related... ...CQV engineering, cGMP facility start-up,...ProjectFull timeLocal areaWork visa- ...a global provider of system validation and lifecycle services—provides... ...clients meet their capital project and lifecycle maintenance... ...validation initiative at a leading biopharmaceutical manufacturing... ...with Quality, Validation, Engineering, Manufacturing, and IT teams...ProjectImmediate start
$170k - $240k
...integrated architecture, engineering, construction, system... ...to help the world’s leading companies solve their... ...investment decisions.cGMP & Regulatory Compliance... ...phase on a wide range of projects from system... ...Maintenance, Quality, and Validation to ensure systems are...ProjectFull timeWork at officeFlexible hours- ...that enable high‑density, flexible power delivery for datacenters, renewable energy systems, and advanced microgrids The Validation Engineer is responsible for planning, executing, and owning system‑level validation activities for Solid‑State Transformer (SST)...Full timeWorldwideFlexible hours
- ...—a global provider of system validation and lifecycle services—provides... ...clients meet their capital project and lifecycle maintenance goals... ...therapies. Senior CQV Engineer (Cleaning Validation & Data... ...Kentucky. This consultant will lead validation activities...ProjectDaily paidContract workImmediate start
- ...- Pharmaceutical facilities - Utilities - Equipment 3. Project & Team Management - Plan and coordinate work - Direct small... ...Qualifications and Experience - Bachelor’s degree in a science or engineering field (or equivalent experience) - 2–4 years’ experience in...ProjectWorldwide
- ...We are seeking an experienced Senior Validation Specialist to lead qualification and validation activities... ...compliance with FDA, EMA, and cGMP regulations. Responsibilities: Lead... ...internal/external audits. Collaborate with Engineering, Quality Assurance, Manufacturing,...
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