Info
Portage (MI)
Portage (MI), USA
Eurofins
Eurofins
Regular Full Time
Regular Full Time
Scientific and Research Fellow, Quality Control (QC), Software
Scientific and Research Fellow, Quality Control (QC), Software

Pharmaceutical Data Review Scientist

Inactive
Eurofins - Career

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 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 believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 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 2025, Eurofins generated total revenues of EUR 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years.

Pharmaceutical Data Review Scientist

  • Ensure that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations
  • Review simple and complex routine and non-routine data (for three or more areas) according to departmental, corporate, and client SOPs; read and understand analytical procedures; ensure all work is performed according to GLP/GMP requirements and apply GLP/GMP in all areas of responsibility as appropriate
  • Perform analysis of proteins and the impurities or raw materials associated with their production using various analytical techniques
  • Determine if data is compliant and defendable based on industry regulations and methodology
  • Verify data is of sound quality following all method, industry, and client requirements where applicable
  • Diagnose problems, solve simple problems, and suggest solutions to complex problems in professional area; perform complex calculations
  • Troubleshoot method and instrumentation problems
  • Use office and instrumentation specific computer software
  • Produce written reports (e.g., SOP, OMC, client reports)

Qualifications

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, 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
Minimum Qualifications:
  • Bachelor's degree in chemistry or other related degree concentration, or equivalent directly-related experience
  • Authorization to work in the United States indefinitely without restriction or sponsorship

Additional Information

Position is full-time, first shift Monday - Friday 8:00am - 5:00pm. Candidates currently living within a commutable distance of Portage, MI 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

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

 

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