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PerkinElmer · 4 hours ago

Senior Project Engineer II, PF Services

Sacramento, CA

Full-time

Onsite

Mid, Senior Level

$70K/yr - $80K/yr

2+ years exp

PerkinElmer is a company focused on biomanufacturing and engineering services. They are seeking a Senior Project Engineer II to collaborate with clients and manage projects throughout the engineering lifecycle, ensuring high-quality deliverables and maintaining strong client relationships.

HardwareHealth Care

No H1B

U.S. Citizen Only

Responsibilities

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

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 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

Possess a solid understanding of the industry and our position within it

Present Project Farma as a service to clients as needed

Attend networking events within the industry

Communicate with clients in a professional manner

Ensure any client feedback or opportunities identified are being escalated properly

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

Seek mentorship from leaders to improve technical and professional skills

Share technical knowledge with peers to support project delivery

Report personal career goals or retention concerns to the Site Lead

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

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 such as SOPs, requirements specifications, testing protocols, summary reports, etc

Identify and close individual knowledge gaps with support from other team members, leads, or resources as needed

Execute system and process validation protocols by using GxP best practices

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

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 including CQV and 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 in a compelling manner 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

Maintain 100% individual billability by completing assigned project tasks

Escalate any roadblocks on achieving billable targets to the site lead

Contribute to and embody our Patient Focused and People First mission through the involvement in professional development and philanthropic opportunities

Actively seek out opportunities to enhance Project Farma’s culture, support internal initiatives, and begin to develop servant leadership skills

Seeks opportunities to support the team and leadership

Actively request continuous feedback in order to develop and seek out opportunities for improvement

Qualification

CQV ProtocolsCGMP Facility Start-upProject ManagementValidation Life CyclesQuality ControlTechnical DocumentationAccountabilityCustomer FocusedProblem SolvingTeamworkCollaborationInitiativeFlexibilityAdaptabilityIntegrity

Required

2-3 years' experience in consulting 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, project management and/or comparable military experience)

Full-time on-site client presence

Willingness to travel up to 100% or as required