Laboratory Instrument System Administrator

Company DescriptionEurofins 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 is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. Eurofins 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 Organizations. The Group also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

Job DescriptionCoordinating Capillary Electrophoresis, iCE, CD, and MFI instrument maintenance and qualificationServing as technical expert for both instrument hardware and software Supporting new and existing systems through installation, configuration, validation, procedure development/review, training, troubleshooting and software/firmware managementAssist validation personnel in determining approach to validate new technologies, providing technical and/or regulatory support; Research instrumentation with information obtained from vendors, manuals, industry resources, and other staff performing similar functions; Work with validation group and assist in writing validation protocols, test scripts, and related documentation in accordance with established validation program; review and assess documents written by validation personnel for approach, GMP compliance, consistency, and thoroughness, consistent with internal validation procedures; Coordinate installation and execution of validation testing, document results, assess documentation generated by vendors or other validation personnel and summarize results obtained identifying compliance with the test plan; Perform instrument trouble-shooting and operational training when required QualificationsBasic Minimum QualificationsMust have a BSc in Science (Chemistry, Biology, Physics or Similar), Engineering Degree, or BSc in Computer Sciences with exposure/experience in the

LIFE SCIENCES

 Authorization to work in the United States indefinitely without restriction or sponosorshipAdditional InformationPosition is full-time, Monday-Friday, 8:00 a.m.-5:00 p.m. with additional hours, as needed. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply. We offer excellent full-time benefits including:

Comprehensive medical coverage,Life and disability insurance,401(k) with company match,Paid holidays and vacation, Dental and vision options. Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.