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

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