Internal & Supplier Quality Auditor
KeyMed (Medical & Industrial Equipment) Ltd. (OKM) | Chief Quality Officer
A global leader in the medical device and technology industry, for more than 100 years Olympus has focused on making people's lives healthier, safer, and more fulfilling. Our products and solutions help to diagnose, prevent, and treat illnesses, further scientific research and keep people safe.
The role
- Define, manage and lead an internal audit programme for the UK & Ireland quality management system and complete audits according to the plan
- Ensure actions as a consequence of audits are completed within specified timescales
- Ensure continued regulatory compliance to international regulations and standards
- Provide internal auditor training
- Provide and present regular detailed management reports.
- Lead and Support other Olympus entity audits (ISO, MDR, MDSAP)
- Represent the company during external audits e.g. FDA, Notified Body
Your responsibilities
- What You'll Be Doing
- Support external audits and regulatory inspections, including ISO 13485, MDSAP, MDR and FDA assessments.
- Lead and evolve the internal audit programme, ensuring robust audit planning, delivery and follow-up across the business.
- Develop and communicate audit schedules that keep teams aligned, informed and inspection-ready.
- Conduct impactful audits, delivering clear, actionable findings and driving accountability for outcomes.
- Partner with stakeholders to resolve non-conformities, implement corrective actions and prevent recurrence.
- Analyse audit data and trends to identify risks, highlight opportunities and provide insight to senior leadership.
- Champion continuous improvement initiatives, supporting quality enhancement projects across the wider Olympus organisation.
- Promote best practice by sharing learnings, success stories and improvement opportunities across the business.
- Drive enhancements to audit processes, implementing local and global improvements that increase effectiveness and compliance.
- Build quality awareness and foster a culture of excellence throughout the organisation.
- Collaborate with global process owners to strengthen audit methodologies and deliver consistent standards worldwide.
- Ensure all activities are carried out in line with regulatory, quality, health, safety and environmental requirements.
- Qualifications
The Ideal candidate for this role will combine strong technical and regulatory expertise with a collaborative, improvement-focused mindset. Comfortable challenging the status quo, you'll use your auditing experience and quality knowledge to identify risks, drive meaningful improvements and help maintain the highest standards of quality and compliance across the business.
- Proven experience within Quality Assurance and/or Regulatory Affairs in a manufacturing environment, ideally within the Medical Device or Pharmaceutical sectors.
- An exceptional communicator with the ability to influence stakeholders at all levels, both verbally and in writing.
- Strong expertise in Quality Management Systems (QMS), quality engineering principles, and regulatory compliance requirements.
- Experienced in planning, conducting and reporting audits against multiple standards and regulations, with a strong focus on quality management systems.
- Self-motivated and confident working independently, with the ability to prioritise workloads and make informed decisions.
- Qualified Internal or Lead Auditor through an IRCA-recognised programme (or equivalent), with knowledge of ISO 9001 and ISO 13485 standards. Candidates willing to undertake formal auditor training will also be considered.
- Good understanding of MDSAP requirements and the regulatory landscape within the medical device industry.
- A proactive problem-solver who is passionate about continuous improvement, compliance excellence and driving quality culture.
- Degree-qualified in a technical discipline such as Engineering, Electronics, Biomedical Science or Manufacturing (Bachelor's or Master's level).
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- Patient Focus - We put patients at the heart of everything
- Integrity - We do the right thing
- Innovation - We look for new ways to make things better
- Impact - We take accountability and get things done
- Empathy - We care for one another and work together
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In addition to a competitive salary, you will receive a generous annual leave entitlement
- You will be eligible to receive private medical cover
- Comprehensive company pension scheme
- You will receive an annual health check with BUPA, funded by us
- Employee Assistance Program to support your health, mental and emotional-wellbeing
- At our HQ, we have a subsidised staff restaurant and free parking
- Other benefits include discounted gym and wellness memberships, cashback and discounts with major UK retailers
Further information
We value the diversity of individuals, perspectives, and lifestyles, and prioritise inclusion and mutual respect. We are committed to fostering a non-discriminatory, inclusive work environment where everyone feels a sense of belonging. Empathy and unity are core to our company culture, empowering employees to contribute fully and flourish.
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Internal & Supplier Quality Auditor employer: OLYMPUS EUROPA SE & CO. KG
KeyMed (Medical & Industrial Equipment) Ltd. is an exceptional employer, offering a dynamic work environment in the heart of West Sussex, Hampshire, Berkshire, Cheltenham, and Gloucestershire. With a strong focus on patient care and employee well-being, we provide comprehensive benefits including private medical cover, a generous pension scheme, and wellness programmes, all while fostering a culture of integrity, innovation, and empathy. Our commitment to diversity and inclusion ensures that every team member feels valued and empowered to grow within their role.
Contact Details:
OLYMPUS EUROPA SE & CO. KG Recruitment Team