Entry Level Associate Project Manager: Biopharmaceutical Product Testing

Eurofins

Lancaster, PA, United States Posted November 3, 2026

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On-site Full-time Entry level
Job Description

Role Overview

The GMP Testing Project Manager is responsible for planning, coordinating, and overseeing Good Manufacturing Practice (GMP)-compliant testing projects within a regulated laboratory environment. This role ensures timely delivery of testing services, adherence to regulatory standards (FDA, EMA, ICH), and effective communication with internal teams and external clients.

Key Responsibilities

  • Project Management
    • Lead and manage multiple GMP testing projects from initiation to closure.
    • Establish and maintain comprehensive tracking tools for projects, including schedules, action trackers and dashboards to enforce accountability and timely delivery.
    • Monitor progress, identify risks, and implement mitigation strategies.
    • Ensure all deliverables meet client expectations and regulatory requirements.
    • Prepare and present project updates and reports to internal and external stakeholders.
    • Track, manage and report turnaround time metrics and schedule variance. 
  • Client Communication
    • Serve as the primary point of contact for clients, ensuring clear communication and accurate interpretation of technical data across functional teams.
    • Organize and facilitate planned and ad hoc project meetings including:  project kick off, recurring project status calls, client technical visits, and project closure meetings.
    • Prepare and present project status and performance KPIs in client Business Review Meetings.
  • Financial Management
    • Work closely with the Business Development team to grow client relationship and revenue through cross selling and managing assigned projects to provide exemplary customer experience and value
    • Track financial performance - including FTE utilization, planned vs actual hours, budget variance, and cash flow. 
  • Compliance & Quality
    • Ensure testing activities comply with GMP, GLP, and relevant regulatory guidelines.
    • Maintain accurate documentation in accordance with Quality Management Systems (QMS).
    • Support audits and inspections by regulatory authorities and clients.
    • Drive investigations to timely closure.
  • Team Collaboration
    • Collaborate with cross-functional teams (Operations, QA, Sample Registration, Pricing, Business Development).
    • Collaborate with partner Eurofins sites and subcontractors as required.
Required Skills
project management testing manufacturing communication KPIs business development compliance audit collaboration cross-functional collaboration quality assurance
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