Eurofins BioPharma Product Testing North America · 9 hours ago
Associate Project Manager: Biopharmaceutical Product Testing
Lancaster, PA
Full-time
Onsite
Mid LevelEurofins Scientific is an international life sciences company providing a unique range of analytical testing services. The Associate Project Manager is responsible for planning and overseeing GMP-compliant testing projects, ensuring timely delivery and adherence to regulatory standards while maintaining effective communication with clients and internal teams.
Biotechnology
No H1B
Responsibilities
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
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
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
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
Collaborate with cross-functional teams (Operations, QA, Sample Registration, Pricing, Business Development)
Collaborate with partner Eurofins sites and subcontractors as required
Qualification
Required
Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or related field
Strong background in pharmaceutical sciences, analytical chemistry, or biologics
Experience in GMP lab operations, especially in CMC testing
Proven ability to manage complex projects and cross-functional teams
Familiarity with regulatory requirements and quality standards
Excellent communication and client management skills
Knowledge of GMP regulations (21 CFR Part 210/211, EU GMP)
Excellent organizational and time-management skills
Proficiency in project management tools (MS Project, Smartsheet)
Strong communication and stakeholder management abilities
Authorization to work in the United States indefinitely without restriction or sponsorship
Benefits
Comprehensive medical coverage
Life and disability insurance
401(k) with company match
Paid holidays and vacation
Dental and vision options
Company
Eurofins BioPharma Product Testing North America
Eurofins BioPharma Product Testing is the largest network of harmonized bio/pharmaceutical GMP product testing laboratories worldwide providing comprehensive laboratory services for the world's largest pharmaceutical, biopharmaceutical and medical device companies.
1001-5000 employees
Funding
Current Stage
Late StageCompany data provided by crunchbase