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, 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 for supporting clinical studies. In addition, Eurofins is one of the leading global emerging players in specialty clinical diagnostic testing.

In 2018, Eurofins generated 4.2 billion Euro proforma turnover in 800 laboratories across 47 countries, employing about 45.000 staff.

The principal purpose of this role is to assist the Senior Quality Officer and Director Quality Assurance and Regulatory Affairs to ensure that the appropriate quality standards and systems are maintained and adhered to in order to satisfy regulatory requirements for work performed on behalf of external sponsors.

Duties and Responsibilities:

• To assist the Senior Quality Officer and Director of Quality Assurance & Regulatory Affairs in performing and reporting quality assurance audits on data generated in support of Sponsor validation and sample analysis studies.
• To perform internal facility and procedural audits and to track completion of corrective and preventative actions to ensure regulatory compliance.
• To assist in the review of documentation for the validation of software and the qualification of equipment.
• To maintain a library of relevant regulatory documentation and to ensure that management are kept up to date with changes in regulatory requirements.
• To assist in Sponsor and regulatory audits and to assist in coordinating responses and completion of actions arising.
• To help maintain company accreditation to an appropriate quality scheme.
• To assist in providing training in regulatory compliance and quality systems to other members of staff.
• To maintain controlled company documents
• To audit suppliers to assess appropiateness for use.
• To write and review company SOPs.

• Degree qualified within a relevant field (ideally Quality or Biological)
• Proficient within audit procedures, quality systems and processes.
• Proven experience within a Regulated Quality environment.

In return you can expect a competitive salary, 25 days holiday plus bank holidays, good team and working environment, life assurance and other benefits such as Perkbox, car parking and employee assistance programme.

Please note that this is a part time role, working around 20hrs per week.