Project Engineer, PF Project Delivery

TheProject Engineer is a fully billable role thatwill workclients, vendors,,biomanufacturing across the entireengineeringlifecycle. TheProject Engineer isresponsible forformingandmaintainingvaluable,long-term relationships with ourclients, and continually strengthening theirtechnical and industry knowledge.TheywillmaintainProject Farma’sPatient FocusedPeople First. _Essential Functions:_ **Site Strategy** * Supportthe execution of site strategy under the direction of theSite Lead,Project Farma’s * Perform assigned tasks to meet strategicobjectives, such as preparingand executing CQV Protocols * IdentifySite Lead * Maintain professional relationships with project team members and client POCs at the operational level (e.g., technicians, engineers) tofacilitate **Business Growth & Development** * Contribute to project-level success by delivering high-quality work that supports business growth opportunities. * Provides data or insights (e.g., project progress, risks) to theSite Lead. * Participate in project tasks that support extensions or proposals, such as preparing deliverablesclients. * Build meaningful internal and external relationships. * Possess a solidunderstanding of theindustry and our position within it. * Present Project Farma as a service to clients as needed. * Attendeventswithin the industry. * Communicate with clients in a professional manner. * Ensure identified **Talent Development** * Focus on professional development and support team collaboration under theSite Leads * Seek mentorship fromleaders * Share technical knowledge with peers to support project delivery. * Report personal career goals or retention concerns to theSite Lead **Resource Management** * Provide input on task-level resource needs to theSite Lead * Report workload or skill gaps within assigned tasks. * Assistmaintaining **Te chnicalDelivery** * Create alignmentwith cross-functionalclientdepartments includingbut not limited toValidation, Manufacturing, Quality, Supply Chain, Engineering * Communicate updatesinternallyin a timely mannerandrelay in-field project decisions to highlight long-range,down-stream project and team impacts. * Provide hands-on supportand troubleshootingfor clientsnavigating theengineeringlife cycle ofcutting-edge. * Perform due diligencesystem and subject domains to generate. * Execute specific technical tasks within a project, ensuring high-quality deliverables. * Perform CQV tasks, such as protocol development or equipment testing, under theSite Lead’sguidance. * Report technical issues to theSite Lead * Ensure tasks meet client specifications, regulatory requirements (e.g., FDA, GMP), and industry standards. * Author technical documents such as SOPs,requirements specifications, testingprotocols, summary reports, etc. * Identify individual. * Execute system and process validation protocolsGxP. * Proactivelyidentifyand escalateroadblocks andutilizeidentify * Support forecasted. * Maintain internal site tools such as site dashboards, deliverable trackers, etc. * Continually develop technical aptitude ofProject Farma’sservicesincluding but not limited to:Capital Project Management, Facility Builds, Tech Transfers, Validation Life Cycles including CQVGxP * GeneralarnedValueAnalysis(EVA)and PO management tool * Analyze complex project data and then deliver clear,articulate * MayassistProject Controlsand Schedulinginclude; 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 thesite **Leadership and Philanthropy** * Contributeto andembody**Patient Focused****People First** missionic. * Activelyseek outProject Farma’sculture,support internal initiatives, andbegin todevelop servant * Seeksopportunities to supportthe team and leadership. * Actively request continuous feedbackin order toseek out **Qualifications:** _Education and Experience Required:_ * 0-1years experienceconsulting and/or engineering services. * Bachelor’s Degree in Life Science, Engineering, or related discipline (OR a combination of equivalent work experience in CQV engineering, cGMP facility start-up, projectmanagement. _Other Required:_ * Full time on-site * Willingness to travel up to 100% or asrequired. _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 annual compensation range for this full-time position is $61,000 - 68,000. 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._