QMS Coordinator

Company Description

The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

If you’re looking for a rewarding career, a place to call home, apply with us today!  

Job Description

• Perform documentation review to ensure consistency (e.g. language, formatting, etc.) within the Redesign Team and across the Clinical Supply network
• Serve as communication channel between WP site personnel and RY / WAG site personnel
• Assist with the coordination and collection of project metrics to support monthly Operations review and project progress
• Assist with project management activities in support of various QMS topics.
• Assist and support other client department projects

Qualifications

• Strong computer, scientific, and organizational skills
• Excellent communication (oral and written) and attention to detail
• Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
• Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
• Experience directly related to Quality Assurance or Quality Control
• Experience directly related to the development of Quality Standards and core requirements for Market Supply and / or Clinical Supply
• Experience defining, generating and reporting Operational metrics 

  Minimum Qualifications:

• B.S. in Biology, Cell Biology, Bio/chemical Engineering, or related science
• Minimum of three years’ experience in the Pharmaceutical or equivalent industry
• Authorization to work in the United States indefinitely without restriction or sponsorship

Additional Information

Position is full-time, 1st shift role with overtime as needed. Candidates currently living within a commutable distance of West Point, PA are encouraged to apply.

What we offer:

• Excellent full time benefits including comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays

Eurofins Lancaster Laboratories Professional Scientific Services® (PSS) is a global, award-winning insourcing solution that places our people at our clients’ site dedicated to running and managing laboratory services while eliminating headcount, co-employment and project-management worries.

We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.

To learn more about Eurofins Lancaster Laboratories, please explore our website www.eurofinsus.com.

Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.