Stability Protocol Writer / Study Builder - Specialist

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 detail‑oriented and highly organized Stability Protocol Writer / Study Builder to join our team. This role is critical in supporting our stability program operations by transforming client requirements and Eurofins‑generated quotes into accurate, compliant protocols and complete study builds within the LIMS system.

The ideal candidate is comfortable navigating complex technical documents, working with cross‑functional teams, and ensuring all study components are aligned with Good Manufacturing Practices (GMP) and internal quality standards.

Key Responsibilities

• Translate Eurofins‑generated quotes into fully developed, compliant stability protocols within the LIMS system.
• Build stability studies based on client‑provided protocols, ensuring all parameters are configured accurately.
• Collaborate with Project Management, Study Management, and Laboratory teams to ensure protocols and studies reflect correct requirements and timelines.
• Verify that protocol content aligns with regulatory expectations, internal SOPs, and client specifications.
• Maintain meticulous documentation and version control throughout protocol creation and study build processes.
• Identify and communicate any discrepancies or missing information to internal stakeholders or clients.
• Support continuous process improvements related to protocol writing, workflow efficiency, and system utilization.
• Ensure daily work complies with GMP, data integrity expectations, and Eurofins quality standards.

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 working within a regulated environment (GMP/GLP/GDP).
• Ability to interpret scientific protocols, quotes, and technical documents.
• Comfortable working with electronic systems such as LIMS or other laboratory informatics tools.
• Strong written and verbal communication skills, including the ability to convey technical information clearly.
• Proven attention to detail and strong organizational skills.

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