Pharmaceutical Data Review Scientist

Eurofins US Network; Portage (MI); Presencial; USD 55.000 - 75.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical, dental, vision

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Descripción de la vacante

Eurofins USA BioPharma Services in Portage, MI is seeking a full-time data reviewer to ensure client data aligns with GLP/GMP standards. You will review laboratory data for accuracy and clarity across multiple areas and generate clear written reports.

Ideal candidates hold a chemistry degree, possess strong analytical and communication skills, and can work independently within a team. Monday–Friday work with comprehensive benefits is provided.

Formación

• Bachelor's degree in chemistry or related field, or equivalent directly-related experience.
• Authorization to work in the United States indefinitely without restriction or sponsorship.
• Experience reviewing data following GLP/GMP requirements in a laboratory setting.

Responsabilidades

• Review laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations.
• Review data across three or more areas according to SOPs; read and understand analytical procedures; ensure work follows GLP/GMP requirements.
• Perform analysis of proteins and 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 quality following all method, industry, and client requirements where applicable.
• Diagnose problems, solve simple problems, and perform complex calculations.
• Troubleshoot method and instrumentation problems.
• Use office and instrumentation specific computer software.
• Produce written reports (e.g., SOP, OMC, client reports)

Conocimientos

Analytical skills

Attention to detail

Communication skills

Organizational skills

Independent work

Team player

Problem solving

Documentation

Adaptability

Educación

Bachelor's degree in chemistry

Herramientas

Office software

Descripción del empleo

Portage, MI, USA

Full-time

Company 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 Organization 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 Organizations. It also has a rapidly developing presence in highly specialized 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 decentralized 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.

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.

Job Description

• 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 position Monday - Friday, 8:00am - 5:00pm.

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.