Data Review – Specialist (Stability Protocol / Study Build Review)

Eurofins Scientific is an international life sciences company which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment and pharmaceutical 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, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the key emerging players in specialty clinical diagnostic testing in Europe and the USA.

Group's key figures are approx. 6.95 billion Euros turnover, over 950 laboratories across 60 countries and about 63,000 staff.

Position Summary: Eurofins Lancaster Laboratories is seeking a highly analytical and quality‑driven Data Reviewer Specialist to ensure accuracy and compliance of all stability protocols and study builds prior to client release. This position plays a crucial role in safeguarding data integrity and ensuring that client expectations are consistently met.

This role includes a structured training progression: the individual will be fully trained as a Stability Protocol Writer / Study Builder prior to performing protocol and study review responsibilities. This ensures a deep understanding of both the technical content and system workflows that impact the quality of client deliveries.

Key Responsibilities

Training Phase – Protocol Writing & Study Building

• Complete comprehensive training in protocol writing based on Eurofins‑generated quotes.
• Learn and practice building stability studies within the LIMS system following client‑provided protocols.
• Develop proficiency in interpreting client requirements, scientific documentation, and stability program workflows.

Primary Role – Data Review

• Perform detailed, independent review of stability protocols and study builds to ensure accuracy, completeness, and alignment with client expectations.
• Confirm that all protocol parameters (e.g., storage conditions, pull points, test plans) are correctly entered and consistent with both quotes and client-provided documents.
• Verify compliance with GMP, internal SOPs, and industry guidelines.
• Identify discrepancies, errors, or gaps and communicate effectively with Protocol Writers, Project Managers, and other stakeholders to resolve issues.
• Ensure documentation is traceable, audit-ready, and maintained in accordance with data integrity principles (ALCOA+).
• Support continuous improvements in review workflows, documentation standards, and system utilization.

Qualifications Required:

• Master’s degree in a scientific discipline (Chemistry, Biology, Pharmaceutical Sciences, or related field) or equivalent industry with 4-6 years of experience.
• Experience or familiarity with GMP, data integrity expectations, and regulated laboratory environments.
• Ability to learn and work effectively within LIMS or similar informatics systems.
• Strong scientific comprehension and ability to interpret technical protocols, quotes, and study plans.
• Exceptional attention to detail and commitment to data accuracy.
• Strong communication skills with the ability to constructively collaborate and provide clear feedback.

Key Candidate Attributes:

• Self-motivation; excellent quality of work and attention to detail
• Ability to communicate effectively with coworkers and internal/external clients
• Ability to learn new tasks quickly and to move easily from task to task
• Ability to handle prioritization and multiple tasks simultaneously
• Ability to use a personal computer and learn necessary programs
• Good communication skills (oral and written)
• Organizational ability and good judgement
• Science background/education and/or laboratory experience
• Strong Math Skills
• Logical Thinking, Good Reasoning Ability
• Motivation to excel
• Coaching/mentoring of peers