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 62,000 staff across a network of more than 1000 independent companies in over 62 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. In 2025, Eurofins generated total revenues of EUR € 7.296 billion and has been among the best performing stocks in Europe over the past 20 years.

Eurofins BioPharma Product Testing Australia / New Zealand provides contract GMP testing to human and animal pharmaceutical, biotechnology, medical device, cosmetic, and complimentary medicine manufactures, both in-vitro and in-vivo in accordance with a range of local and international standards. The range of testing includes microbiological and chemistry on raw materials, in process and finished products. We operate out of sites in Sydney, Melbourne, and Auckland, which are all GMP licensed by local regulators and are accredited to ISO 17025.

Are you an experienced Quality professional looking for a flexible part-time role in a regulated laboratory environment?

Eurofins BioPharma Product Testing NZ is seeking a QA Site Coordinator to lead and maintain our Quality Management System while supporting a culture of quality, compliance, and continuous improvement across our laboratory operations. The role is based in Penrose, Auckland.

Reporting to the Head of Quality AU/NZ and working closely with the Business Unit Manager, you will be responsible for maintaining and enhancing the site's quality systems, ensuring compliance with GMP, quality standards, and regulatory requirements.

This is a part-time position, ideally suited to someone looking to work shorter hours from Monday to Friday, with flexibility to schedule hours within normal business hours. The exact hours can be discussed with the successful candidate.

Responsibilities for this role will include but are not limited to:

• Maintain and continually improve the site's Quality Management System.
• Coordinate client, supplier, and regulatory audits.
• Lead investigations relating to deviations, incidents, complaints, OOS and OOT results.
• Oversee internal audit programs and proficiency testing activities.
• Manage approved supplier qualification and technical quality agreements.
• Support staff training, quality awareness, and compliance activities.
• Review and approve quality documents, procedures, and controlled records.
• Monitor compliance with GMP, laboratory quality standards, and internal procedures.
• Participate in management reviews, risk assessments, and continuous improvement initiatives.
• Liaise with clients and internal stakeholders on quality-related matters.
• Undertake other duties and special project as directed by the Head of Quality -AU/NZ and the Business Unit Manager.

• A degree in Microbiology, Life Sciences, Quality, or a related discipline.

About you:

• Experience working within GMP, GLP, pharmaceutical, medical device, or laboratory quality environments.
• Experience managing or coordinating quality systems, audits, investigations, and compliance programs.
• Strong written and verbal communication skills.
• Excellent organisational skills and attention to detail.
• Confidence working independently and managing multiple priorities.
• Proficiency in Microsoft Office applications.
• A collaborative and practical approach to problem-solving.

This opportunity is only open to candidates who are eligible to work in New Zealand, and already have work rights or an appropriate working visa.

If you feel that you can bring outstanding skills and a great attitude to our team, please submit a cover letter, curriculum vitae and be able to provide at least two recent professional references.  Applications will be treated with the strictest confidence. Due to the volume of responses we may only contact shortlisted candidates.

Please note: Current Eurofins employees should first speak with their Business Unit Manager before submitting an application for this position.