Metrologist: 2nd or 3rd shift at Eurofins

Lancaster, Pennsylvania, United States -

Full Time

Start Date

Immediate

Expiry Date

13 May, 26

Salary

0.0

Posted On

12 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

GMP, GLP, Instrument Maintenance, Troubleshooting, Repair, Preventative Maintenance, Validation Testing, Documentation, Quality Systems Compliance, Productivity Metrics, Process Improvement, Teamwork, Coaching, PC Skills, Instrumentation Theory

Industry

Medical and Diagnostic Laboratories

Description

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 Organization 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 Organizations. It also has a rapidly developing presence in highly specialized 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 decentralized 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. Job Description Essential Duties and Responsibilities: Applies GMP/GLP in all areas of responsibility, as appropriate Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration Performs other duties as assigned Subject Matter Expert (SME) - Maintain routine instruments in a validated state at all times. Perform assessment, trouble-shooting, repair. Ensure completion of preventative maintenance, routine testing, and assigned validation testing. Compliance - Ensure all activities are completed on time, accurately documented, and in compliance with existing quality systems. Ensure that the quality policy program is understood, implemented and maintained at all times. Productivity - Organize schedule in a manner such that higher priority projects and tasks are completed in a timely manner. Ensure completion of all assigned tasks according to company and department stated TAT's. Innovation - Active involvement with process improvement initiatives Teamwork - Foster teamwork internally and with technical groups to increase overall quality. Take responsibility for group success by assisting and supporting team members. Training - Provide guidance and coaching within a team environment Qualifications Associates degree/Certification in physical science, engineering, or information technology; combination of college and related technical experience will be considered (e.g. Certificate program with 1 year experience). Experience performing and documenting instrument trouble shooting, non-routine events, and/or validations. Strong PC skills and experience. Experience with GMP-compliant work practices and systems Strong understanding of instrumentation theory Authorization to work in the United States indefintely without restriction or sponsorship Additional Information Working schedule will be Full-Time, 2nd shift: Monday to Friday 3pm to 11pm or 3rd shift (Four 10s) Monday 11pm to Friday 9am. Candidates currently living within a commutable distance of 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.

Responsibilities

The role involves applying GMP/GLP standards while maintaining routine instruments in a validated state, which includes assessment, troubleshooting, repair, and ensuring completion of preventative maintenance and validation testing. Responsibilities also include meeting quality and productivity metrics, ensuring timely completion of tasks, and actively participating in process improvement initiatives.