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For Companies At a Glance
- Tasks: Lead and manage GMP testing projects, ensuring compliance and timely delivery.
- Company: Join Eurofins Scientific, a global leader in analytical testing services.
- Benefits: Enjoy comprehensive medical coverage, 401(k) match, and flexible hours.
- Why this job: Make a real impact in biopharmaceutical testing while growing your career.
- Qualifications: Bachelor's degree in relevant field and strong project management skills.
- Other info: Dynamic work environment with opportunities for professional development.
The predicted salary is between 40000 - 50000 £ per year.
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 relationships 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.
Education
- Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or related field.
Experience
- 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.
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.
Position Details
- Position is full‑time, Monday‑Friday, 8:00 a.m.-4:00 p.m. Hours are flexible.
- Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply.
Benefits
- Comprehensive medical coverage
- Life and disability insurance
- 401(k) with company match
- Paid holidays and vacation
- Dental and vision options
Associate Project Manager: Biopharmaceutical Product Testing in Jarrow employer: Eurofins Scientific
Contact Detail:
Eurofins Scientific Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Project Manager: Biopharmaceutical Product Testing in Jarrow
✨Tip Number 1
Network like a pro! Reach out to your connections in the biopharmaceutical field and let them know you're on the hunt for an Associate Project Manager role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on GMP regulations and project management tools. We recommend creating a cheat sheet of key terms and concepts that are relevant to the role. This will help you feel confident and ready to impress during those crucial conversations.
✨Tip Number 3
Showcase your communication skills! During interviews, be sure to highlight your experience in client communication and team collaboration. Use specific examples to demonstrate how you've successfully managed projects and kept stakeholders informed.
✨Tip Number 4
Don't forget to apply through our website! It's the best way to ensure your application gets noticed. Plus, it shows you're genuinely interested in joining our team at Eurofins and contributing to our mission of making life safer and healthier.
We think you need these skills to ace Associate Project Manager: Biopharmaceutical Product Testing in Jarrow
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter to highlight your experience in GMP testing and project management. We want to see how your skills align with the role, so don’t hold back on showcasing relevant projects you've managed!
Showcase Your Communication Skills: Since this role involves a lot of client interaction, it’s crucial to demonstrate your communication prowess. Use clear and concise language in your application, and maybe even share examples of how you’ve effectively communicated complex information in the past.
Highlight Your Regulatory Knowledge: Familiarity with GMP regulations is key for this position. Make sure to mention any specific experiences you have with regulatory compliance or quality management systems. We love seeing candidates who understand the importance of adhering to standards!
Apply Through Our Website: We encourage you to submit your application through our website for the best chance of being noticed. It’s super easy, and you’ll be able to track your application status directly. Let’s get your journey started with us!
How to prepare for a job interview at Eurofins Scientific
✨Know Your GMP Inside Out
Make sure you brush up on Good Manufacturing Practice (GMP) regulations, especially 21 CFR Part 210/211 and EU GMP. Being able to discuss these in detail will show that you understand the compliance landscape and can navigate it effectively.
✨Showcase Your Project Management Skills
Prepare examples of how you've successfully managed complex projects in the past. Highlight your experience with project management tools like MS Project or Smartsheet, and be ready to discuss how you track progress and manage risks.
✨Communicate Like a Pro
Since client communication is key in this role, practice articulating technical data clearly and concisely. Think of scenarios where you've had to explain complex information to non-experts and be prepared to share those experiences.
✨Demonstrate Team Collaboration
Be ready to talk about your experience working with cross-functional teams. Share specific examples of how you've collaborated with different departments to achieve project goals, as this will show your ability to work well in a team-oriented environment.