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Morrisville, North Carolina, United States · On-site
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Raleigh, North Carolina, United States · On-site
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Raleigh, North Carolina, United States • On-site
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Execute technical CQV tasks, including protocol development and equipment testing, ensuring compliance with FDA and GMP standards. Author technical documentation and provide hands-on troubleshooting for manufacturing processes throughout the engineering life cycle.
Requires a Bachelor's degree in Life Science, Engineering, or equivalent experience with 1-5 years in consulting or engineering services. Must be authorized to work in the US and be willing to travel up to 100% to client sites.
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.
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 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 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.
Years of Experience: 1-5 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.
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.
For 85 years, we have pushed the boundaries of science with a clear purpose – to help our customers achieve theirs.
For 85 years, PerkinElmer has pushed the boundaries of science in our food, industrial, life science and environmental markets. In addition to innovative laboratory technologies, our OneSource services division delivers a highly trained, experienced, and collaborative team of service engineers with solutions scalable and customizable to serve laboratory needs. We’ve always pursued science with a clear purpose – to help our customers achieve theirs. Our expert team brings technology and intangibles, like creativity, empathy, diligence, and a spirit of collaboration, in equal measure, to fulfill our customers’ desire to work better, innovate better, and create better. PerkinElmer is a leading, global provider of technology and service solutions that help customers measure, quantify, detect, and report in ways that help ensure the quality, safety, and satisfaction of their products. Science with Purpose. Learn more at www.perkinelmer.com.
Offices: 710 Bridgeport Avenue, Shelton, CT 06484, US
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