Data Reviewer

About the company

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 just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.

In 2019, Eurofins generated total revenues of EUR € 4.56 billion, and has been among the best performing stocks in Europe over the past 20 years.

Your tasks

Position Summary We are seeking a Data Reviewer to support medical devices microbiology team for data review/QC. This role sits at the intersection of science and communication, ensuring that scientific documentation is complete, consistent, timely, and publication‑ or audit‑ready.

Review laboratory data packages for accuracy, completeness, and compliance with approved procedures.

 Verify calculations, transcriptions, and data entries for correctness.

 Primary focus on sterility by membrane filtration studies

 Review test documentation to ensure all required information is present and properly documented.

 Identify discrepancies, documentation errors, and potential compliance concerns and escalate as appropriate.

 Confirm that investigations, deviations, and corrections are adequately documented.

 Ensure test results are supported by raw data and meet applicable acceptance criteria.

 Maintain timely review and release of data to support client turnaround times.

 Collaborate with laboratory personnel to resolve data review findings and improve documentation practices.

Ensure document outputs meet internal quality standards and external regulatory requirements

Requirements

Candidates may come from roles such as Experience in CROs, GMP laboratories, or regulated scientific environments is strongly preferred.

Preferred Qualifications (M.Sc Microbiology with 1-2 years of experience)

-Familiarity with regulated environments (GMP, GxP, clinical research, or equivalent)

-Strong written communication skills with attention to detail and consistency

-Demonstrated ability to manage multiple deliverables and competing priorities

Abilities and/or Skills

• Honest, Dependable, Demonstrated Ability to Self-Manage
• Detail Oriented, Accurate, Precise
• Strong Math Skills
• Strong Organizational Skills
• Logical Thinking, Good Reasoning Ability
• Strong communication including verbal, writing, and presentation skills
• Dedication to quality, ethics, and customer service
• Ability to handle personal stress
• Mental and emotional stability and maturity
• Motivation to excel
• Should able to sit for long periods as per role requirement