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

• Coordination of lab equipment installation process including procurement approvals.


• Coordination of activities relating to the repair, calibration, and maintenance of laboratory equipment and related systems.


• Review repairand validation documents as needed.


• Scheduling and coordinating repair work performed by outside contractors (includes ensuring vendors are in compliance with site requirements prior to performing equipment-related services).


• Ensure repair activities are communicated to and scheduled with the affected QC functional area and that area management is informed.


• Review of vendor documentation in support of repair.


• Understand vendor specifications and track updates and critical bugs affecting hardware and software.


• Review and track, work records in BMRAM equipment database as needed.


• Support change control activities impacting QC equipment; provide impact assessments when required.


• Support investigations of equipment-related deviations as needed.


• Complies with all pertinent regulatory agency requirements.


• Writes and revises Equipment related SOPs as necessary.


• Working with Cross-function teams that will be supporting a long-term project.

• Bachelor's degree in Chemistry, Life Sciences, Engineering, or other science-related degree concentration, orequivalent directly-related experience


• Project management or coordination experience is preferred


• Strong computer, scientific, and organizational skills


• Authorization to work in the United States indefinitely without restriction or sponsorship

• 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


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