Project Engineer / Senior Project Engineer

Project Engineer / Senior Project Engineer

Trenton, New Jersey | Remote

Responsibilities

Location

Trenton, New Jersey, US

Job ID

REQ-056538

Project Engineers

(PE) and

Senior Project Engineers

(Senior PE) are fully billable roles that will work collaboratively with clients, vendors, contractors, and other Team Members to support projects related to biomanufacturing across the entire engineering lifecycle. PEs and Senior PEs are responsible for delivering high quality work, forming and maintaining valuable, long-term relationships with our clients, and continually strengthening their technical and industry knowledge. They will maintain a strong focus on Project Farma’s

Patient Focused

and

People First

mindset.

Key Responsibilities

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 report 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 to facilitate task completion.

Business Growth & Development

Contribute to project-level success by delivering high-quality work that supports business growth opportunities.

Provide data or insights 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.

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.

Talent Development

Focus on professional development and support team collaboration under the Site Leads guidance.

Share technical knowledge with peers to support project delivery.

Resource Management

Provide input on task-level resource needs to the Site Lead to support project delivery.

Report workload or skill gaps within assigned tasks.

Assist in maintaining project schedules by communicating resource constraints.

Technical Delivery

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

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.

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 using GxP best practices.

Proactively identify and elevate roadblocks and utilize critical thinking skills to identify creative solutions to problems and roadblocks.

Support necessary billables as forecasted by site dashboards on billable targets per month.

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, Facility Builds, Tech Transfers, Validation Life Cycles, CQV, Computer system Validation, Quality, Regulatory and Compliance, GxP Automated Systems, and Quality Control including clinical and commercial.

General understanding of Earned Value Analysis (EVA) and PO management tool.

Analyze complex project data and then deliver clear, articulate and concise messages to support decision making.

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.

Operational Performance & Billability

Maintain 100% individual billability by completing assigned project tasks.

Escalate any roadblocks on achieving billable targets to the site lead.

Experience Required

0-4 years’ experience in consulting and / or engineering services.

Bachelor’s Degree in Life Science, Engineering, or related discipline (or equivalent work experience in CQV engineering, cGMP facility start-up, project management, and / or comparable military experience).

Other Required

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. This position may require significant travel to support project and business needs. We cannot employ anyone with an invalid driver’s license.

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