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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.

Verify (SPV) analytical data of other analysts within the lab as requested.

•Accurately and safely perform analytical test methods or related support activities as per procedures or protocols. Uses technical knowledge in the review and interpretation of data for conformance to procedures, standards and protocols and/or real-time recognition of aberrant data and results.

•Perform data entry and reviews own work for accuracy in accordance with laboratory procedures, standards and GMP requirements.

•May perform holistic review of data for release of data from the laboratory.

•Recognizes when a deviation from procedures, etc has occurred and initiates and participates in a Root Cause Investigation.

•Performs investigations for deviations.

•Troubleshoot equipment and methods as required.

•Assist in improvement of quality systems by creating or revising worksheets and other lab documentation systems.

•Identifies and communicates opportunities for improvement initiatives in daily work activities.

•Contribute to development of PQEs.

•Reviews SOPs for executable as written.

•Shares technical information and best practice within plant sites or group.

•Write protocols for non-routine testing or validation with appropriate guidance.

•Develops equipment qualification protocols with appropriate guidance.

•Perform routine equipment calibrations or maintenance through execution of well- defined protocols.

•Comply with and implement safety standards.

•Executes notification to management when required by procedures or standards.

•Initiate change controls and deviations.

•Train and mentoring others. Develop training materials.

•Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals.

The ideal candidate would possess:

+ Strong computer, scientific, and organizational skills

+ Excellent communication (oral and written) and attention to detail

+  Ability to work independently and as part of a team with internal and external clients, self‑motivation, adaptability, and a positive attitude

+ Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies

+ Proficiency in IT related skills such as Microsoft excel, word, PowerPoint etc

+ Bachelor's degree

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

May be required to have a company phone off shift and respond to operational issues.

Position is 12-hour nights 6 PM - 6 AM -  3 on, 2 off, 2 on, 3 off schedule.  Overtime as needed.

Initial training may be 8 am-5 pm Monday - Friday.

Candidates currently living within a commutable distance of Indianapolis, IN  are encouraged to apply.

+ 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

+ #LI-EB1

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

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.