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PerkinElmer is seeking a Project Controls - Engineer III / Lead Engineer for Project Farma across multiple U.S. sites. The role focuses on developing and maintaining detailed project schedules, cost models, and performance reports while coordinating with clients, vendors, and site teams.
Domestic travel is required to meet project requests. Ideal candidates hold a technical degree with 2–7 years in project controls, strong Excel skills, and familiarity with MS Project, Primavera P6 or
When joining PerkinElmer, you select an experienced and trusted leader in scientific solutions, with the support of a global service network and distribution centres, 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 TitleProject Controls - Engineer III / Lead Engineer - Project Farma
Location(s) Boulder, CO, Customer Site - CA, Customer Site - OR, Customer Site - TX, Houston, TX, LosAngeles, CA, Pasadena, CA, SanDiego, CA, South San Francisco, CA
Job Description 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 Project Controls - Engineer III / 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 Principal 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.
Analysis of complex project data and then deliver clear, articulate and concise messages in a compelling manner to support decision making. Communicate project information internally in a timely manner and relay in-field project decisions to highlight long‑range, down‑stream project and team impacts. Independently prepare project controls reports, dashboards, and management summaries. Utilize inputs from Project Coordinators, field teams, and other disciplines while retaining accountability for final project controls outputs. Provide hands‑on support and troubleshooting for clients navigating the engineering life cycle of cutting‑edge equipment and manufacturing processes. Maintain project tools such as site dashboards, detailed schedules, deliverable trackers, etc. Perform due diligence and quality checks on subject domains to generate high‑quality project deliverables. Proactively identify and escape roadblocks and utilize critical thinking skills and knowledge of problem‑solving skills to identify creative solutions to those problems and roadblocks. Create alignment with cross‑functional client departments including but not limited to Design, Construction, Validation, Manufacturing, Quality, Supply Chain, and Engineering groups. Continually develop a technical aptitude of project controls services within the life‑science space including but not limited to: Capital project management (CAPEX) for new/existing facility builds Facility shutdowns/turnarounds Technology transfers Enterprise system integrations Validation Life Cycle, including Commissioning and Qualification, Process Validation, Computer System Validation, etc. Quality, Regulatory, and Compliance GxP Automated Systems Quality Control, including commercial and construction Operational readiness
Prepare and issue weekly, monthly, and ad‑hoc internal and external project controls reports. Develop and maintain project dashboards and performance metrics aligned with project and corporate requirements. Conduct in‑depth analysis of schedule, cost, and performance data to support proactive decision‑making
Implement and maintain approved project controls systems, coding structures, and procedures on the project. Ensure accuracy, consistency, and integrity of all project controls data across systems and reports. Provide guidance to project teams on project controls processes, data requirements, and reporting standards. Support continuous improvement of project‑level controls workflows and reporting efficiency
Bachelor’s Degree (and/or Masters) in technical Sciences, Engineering, Regulatory or related discipline OR a combination of equivalent experience project controls, general construction, cGMP facility start‑up, project management and/or comparable military experience. Advanced experience with Microsoft Excel; Microsoft Project, Oracle Primavera P6, and/or Smartsheet a plus. 2-7 Years of Experience required Willingness to travel as required for client project assignments. Other Preferred
Project Management Professional (PMP) Certification
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 $(74,000) to $(113,000). 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. PerkinElmer 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. Are you ready to help improve the lives of millions of people and create a healthier world? When you work at PerkinElmer, that’s exactly what you’ll do. From our dedicated scientists and world‑class operations employees to our innovative R&D professionals and committed sales and service groups, we’re a unique team of 5,000+ global colleagues who come to work every day knowing we’re making a difference. Through innovation, collaboration, and believing in our mission, we strive to create an inspiring and inclusive culture for our employees, so that they can be their best and, together, create a better tomorrow.