GMP Testing Project Manager — Regulated Lab Delivery

Eurofins BioPharma Product Testing North America; Lancaster (Lancaster County); On-site; USD 95,000 - 125,000; 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 seeks a GMP Testing Project Manager to plan, coordinate, and oversee GMP-compliant testing projects in a regulated lab. You will ensure timely delivery, regulatory adherence (FDA/EMA/ICH), and clear communication with clients and internal teams.

You will lead multiple projects, track milestones, manage budgets, and drive quality through QMS-compliant documentation. Strong GMP knowledge and client management are essential.

Qualifications

• Bachelor’s degree in Chemistry, Biology, Pharmaceutical Sciences, or related field.
• Strong GMP lab operations knowledge and regulatory familiarity.
• Experience coordinating cross-functional teams and projects.

Responsibilities

• Lead GMP testing projects from initiation to closure.
• Maintain tracking tools, dashboards and schedules for timely delivery.
• Coordinate client communications and present project updates.
• Monitor budgets, hours and cash flow to ensure financial performance.
• Support audits and ensure documentation meets QMS standards.

Skills

GMP regulations

Project management

Client communication

Regulatory knowledge

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 seeks a GMP Testing Project Manager to plan, coordinate, and oversee GMP-compliant testing projects in a regulated lab. You will ensure timely delivery, regulatory adherence (FDA/EMA/ICH), and clear communication with clients and internal teams.

You will lead multiple projects, track milestones, manage budgets, and drive quality through QMS-compliant documentation. Strong GMP knowledge and client management are essential.