GMP Biopharma Testing Project Lead

Eurofins; Lancaster (Lancaster County); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Comprehensive medical coverage

Life and disability insurance

401(k) with company match

Paid holidays and vacation

Dental and vision options

Job summary

Eurofins USA BioPharma Services in Lancaster, PA is seeking a GMP Testing Project Manager to plan, coordinate and oversee GMP-compliant testing projects in a regulated laboratory. You will ensure timely delivery, regulatory adherence (FDA, EMA, ICH), and effective communication with internal teams and clients; collaborate with Operations, QA, Sample Registration, Pricing and Business Development.

Position is full-time with standard hours; benefits include comprehensive medical coverage, life and

Qualifications

• Bachelor’s degree required and strong background in pharmaceutical sciences and analytical chemistry.
• Experience with GMP lab operations and CMC testing.
• Ability to manage complex, cross-functional projects with regulatory awareness.
• Excellent communication and stakeholder management.

Responsibilities

• Lead GMP testing projects from initiation to closure.
• Maintain tracking tools, schedules, dashboards, and milestones.
• Identify risks and implement mitigation strategies.
• Ensure deliverables meet regulatory requirements and client expectations.
• Present status, KPIs and reports to clients and internal teams.
• Collaborate with Operations, QA, Sample Registration, Pricing and BD.

Skills

Pharmaceutical sciences

Analytical chemistry

Biologics

GMP knowledge

Regulatory compliance

Communication

Project management

MS Project

Smartsheet

Education

Bachelor’s degree in Chemistry, Biology, Pharmaceutical Sciences, or related field

Tools

MS Project

Smartsheet

Job description

Eurofins USA BioPharma Services in Lancaster, PA is seeking a GMP Testing Project Manager to plan, coordinate and oversee GMP-compliant testing projects in a regulated laboratory. You will ensure timely delivery, regulatory adherence (FDA, EMA, ICH), and effective communication with internal teams and clients; collaborate with Operations, QA, Sample Registration, Pricing and Business Development.

Position is full-time with standard hours; benefits include comprehensive medical coverage, life and