Data Review Specialist

3 weeks ago

Indianapolis, United States Eurofins USA PSS Insourcing Solutions Full time
Job DescriptionJob DescriptionCompany 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

Data Reviewer responsibilities include, but are not limited to, the following:

  • Reviews simple routine and non-routine laboratory data for one or more areas according to departmental, corporate and client Standard Operating Procedures, Work Instructions, and/or Forms; read and understand analytical procedures; make sure all work is performed according to ISO17025 guidelines, GLP Regulatory, and GMP Regulatory requirements; Independent auditing of laboratory data to ensure continous compliance to both the quality system and regulatory requirements
  • Maintain the highest level of proficiency in terms of those duties and responsibilities as required by auditors/data reviewers.
  • Perform mathematical calculations as part of data review.
  • Interact both directly and indirectly with laboratory staff members to ensure all data review are appropriately and efficiently corrected and documented
  • Responsible for ensuring the integrity of laboratory data. 
  • Communicate in writing and in person with laboratory personnel and/or with the client in an intelligent and clear manner.
  • May assist in conducting laboratory investigations, exceptions, planned deviations, and/or corrective and preventative actions.
  • May assist in training of laboratory personnel
  • May assist with Quality and Regulatory Audits and interact directly with auditors.
  • May assist with Technical Writing and/or Report Writing
Qualifications

  • Bachelor’s degree in chemistry, biology, or other related degree concentration, or equivalent directly-related experience (2 years of directly related industry experience is equivalent to1 full-time year of college in related major).
  • Minimum of 2 years of experience in laboratory chromatography analyses, Quality, Regulatory, or related experience
  • Experience in a cGMP and/or ISO 17025 environment
  • 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, 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
  • Authorization to work in the United States indefinitely without restriction or sponsorship


Additional Information

 

Position is Monday- Friday 8:00 am- 5:00 pm. Overtime as needed.  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 is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

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