QA Specialist

About the role

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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.

Responsibilities

• Maintain the Quality Management system
• Perform document control activities.
• Provide quality support in writing, reviewing, revising, and maintaining standard operating procedures (SOPs), forms, presentations, and other business documents.
• Assure documents capture the current process, provide sufficient detail to perform the process, and comply with internal procedures for generating documents.
• Support the training program, such as creating training files and ensuring that they are updated and current as appropriate.
• Provide training sessions.
• Host meetings and/or scribe meeting minutes.
• Follow up on CAPA and Change Control systems, as appropriate.
• Perform internal audits to ensure compliance is maintained within the organization. May provide audit reports to the applicable audited function/area management.
• Cooperate in the preparation of study files prior to and during all client audits and regulatory inspections.
• Attend meetings and participate on multi-disciplinary teams, as required, to provide routine status updates related to their functional area and/or to provide quality guidance.
• Become a subject matter expert (SME) in a particular quality system (i.e. documentation, supplier quality, other) depending on experience, skill set, and business needs.
• Conduct QA reviews of study data generated when required.
• Generate QA statements for study reports when required

Qualifications

• Ability to follow instructions and deliver complete and accurate results.