Key Responsibilities

Manage and report all Quality Metrics for the Molecular Cell Biology team—including Exceptions, CAPAs, Change Controls, and SOPs—ensuring all actions are assigned, tracked, and closed in line with company compliance requirements.
Review and approve all relevant Quality documentation for the Molecular Cell Biology department, such as Exceptions, CAPAs, SOPs, and quality/technical agreements.
Lead and participate in cross‑functional risk assessments as required.
Support and lead problem‑solving activities within the department, ensuring effective collaboration across functions.
Ensure processes and systems are in place to complete Quality- and CAPA‑related project work and produce customer reports in a timely manner.
Provide continuous feedback to team members regarding customer expectations, quality requirements, and process changes.
Manage the completion of compendia update assessments for the department.
Support department leadership in maintaining the quality of daily laboratory work and collaborate with team members to resolve any quality-related issues.
Manage assigned customer queries, lead complaint investigations, and work with the team to identify and resolve root causes.
Support internal and external/regulatory audits, including preparation, participation, responding to audit queries, and driving corrective actions to closure.
Represent the Molecular Cell Biology department at Change Control Review Boards and equipment meetings, ensuring actions are assigned and tracked appropriately.
Approve and maintain up‑to‑date laboratory SOPs within your area of responsibility.
Identify opportunities to enhance quality, efficiency, and customer service, and support the implementation of continuous improvement initiatives.
Establish and monitor key metrics related to quality and customer satisfaction/delivery, ensuring targets are met and trends are proactively addressed.
Ensure all team documentation is accurate, complete, up to date, and compliant with company procedures.
Communicate regularly with the team and supporting departments to ensure effective information flow throughout the organisation.
Provide coaching and mentoring to improve understanding and compliance with quality standards.
Review data in accordance with regulatory requirements, analytical procedures, and documentation standards.
Review and accurately prepare reports for technological projects, ensuring confidentiality and timely delivery to clients.

Qualifications

Education / Qualifications

Primary degree or equivalent in a related life sciences discipline
At least 3 years’ experience in a laboratory GMP regulated environment
Working knowledge of pharmaceutical quality systems
Strong understanding of Biologics and Molecular Cell Biology
Ability to work independently or as part of a team.
Excellent report writing, communication and organisational skills.
Quality oriented with the ability to consistently work to industry and client standards.
Positive and tenacious approach to work.
Highly organised, methodical and systematic approach to work.
Passionate about quality and customer service.
Good communication skills both internally and externally. Ability to understand clients’ requirements and to be able to devise and articulate the most appropriate solutions

Additional Information

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 just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 61,000 staff across a network of more than 1000 independent companies in over 61 countries and operating more than 900 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.