Coordinating Capillary Electrophoresis, iCE, CD, and MFI instrument maintenance and qualification Serving 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 management Assist 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
Basic Minimum Qualifications Must 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 sponosorship
Position is full-time, working Monday-Friday, 8:00 a.m.-5:00 p.m., plus any additional hours as needed. Candidates currently living within commutable distance to Lancaster, 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 USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.