Company Description
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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description
- Initiate continuous improvement initiatives for Asset management and laboratory Operations and update impacted procedures
- Maintain and support best business practices for Asset management such as Share Point Asset management
- Work with managers, coordinators, and staff of labs to resolve instrumentation documentation issues
- Work with QA and compliance to initiate, investigate, and resolve quality issues
- Review QA’s monthly overdue work order list and research instrument service history and use to resolve documentation issues
- Review training documents to see which are coming due for their 3 year update
- Verify CAR-T data for regulatory submission and make SharePoint updates
- Verify regulatory submission needed, and make Share Point updates
- Facilitate change control closure and send out notifications to activity owners and approvers
- Make status updates to change control SharePoint
- Work directly with vendors to resolve instrumentation accuracy and inventory documentation issues
- Support inventory accuracy for laboratories in Malvern and Spring House sites
- Update Maximo/eCMMS to address inventory inaccuracies, and maintain eCMMs system’s accuracy
- Provide process improvement and instruction to decrease turn-around time for bringing instruments into service
- Research asset history for resolution of outstanding work orders
Qualifications
- BS/MS in a scientific field
- 1-5 years experience in a GMP environment
- Pharmaceutical industry experience
- Experience with SharePoint is preferred
- Ability to travel to Spring House site (10%)
- Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information
Position is full-time, Monday-Friday, generally 8 a.m. - 5 p.m., weekend work might be expected. Candidates currently living within a commutable distance of Malvern, PA are encouraged to apply. This role may require travel to the Spring House, PA site.
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 USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.