Senior Data Review Specialist – Chemistry (LC-MS/MS Data Review)
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.
Senior Data Review Specialist – Chemistry (LC-MS/MS Data Review)
Position Summary: Ensure the client receives quality data in a timely manner by reviewing laboratory documentation, generated data, calculated results, and final reports for accuracy, clarity, and adherence to GMP and/or GLP regulations, and evaluating problems/system failures to achieve efficiency gains
Essential Duties and Responsibilities:
- Applies GMP/GLP in all areas of responsibility, as appropriate
- Demonstrate and promote the company vision
- Regular attendance and punctuality
- Review simple and complex routine and non-routine data (for 3 or more areas) according to departmental, corporate, and client SOPs; read and understand analytical procedures; make sure all work is performed according to GLP/GMP requirements; perform complex calculations
- Communication in writing and in person with laboratory personnel in an intelligent and clear manner
- Exercise discretion and independent judgment with respect to matters of significance directly related to the management or general business operations through the data review process
- Perform review of scientific data, including, but not limited to standard preparation, calibrations, methodology, QC, sample data, integration review, compound evaluation, and other subjective review based on testing performed; perform complex calculations to verify results
- Verify the data is of sound quality and determine if data is compliant and defendable based on industry regulations and methodology
- May serve as technical advisor for analysts with regard to QA/QC of data
- Diagnose problems; solve simple problems, and suggest solution to complete problems in professional area
- Keep oneself and peers abreast of current developments and trends in professional area by reading and understanding internal procedures, attending/providing training sessions, by writing/revising SOPs (as required), and by assisting Group Leader / Principal Specialists in training new and existing employees
- Use MS Windows applications such as Excel, Word, Access, Outlook email; create complex Excel worksheets and formulas
- Communicate with internal clients to discuss any findings and notify them of any necessary rework or compliance/regulatory concerns
- Conducts all activities in a safe and efficient manner
- Performs other duties as assigned
Qualifications
Basic Minimum Qualifications (BMQ):
To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements below are representative of the knowledge, skill or ability required.
Education/Experience (BMQ):
Master’s degree in a science-related field with at least 7-10 years of experience in Bio/Pharmaceutical Chemistry drug product/substance testing with knowledge of regulatory requirements and some data review responsibilities
Experience with analytical techniques data review such as Chromatography and Mass Spectrometry (HPLC/UPLC, LC-MS/MS, GC, GC-MS/MS, IC…etc.), knowledge of analytical method validation, USP/EP compendia, and laboratory software applications such as Waters Empower software, LIMS, Electronic Notebook is preferred. AB Sciex LC-MS/MS experience will be an added advantage.
Additional Information
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 be able to sit for long periods as per role requirement
- Team Lead experience
