Are you a seasoned Quality Leader looking to join a forward-thinking team where your leadership will shape quality and compliance excellence in a regulated environment? What You’ll Do Lead as the ISO 13485 Management Representative, driving quality benchmarks and improvements.
Make sure to apply with all the requested information, as laid out in the job overview below.
Oversee the integrated Quality Management System (eQMS), maintaining ISO 13485, ISO 9001, 14001, 27001, and FSC certifications.
Ensure GDP compliance and manage the MHRA WDA license.
Tackle quality challenges, oversee audits, and ensure processes align with industry standards.
Collaborate with leadership to promote continuous improvement and regulatory compliance.
What You’ll Bring 10 years in Quality Management, ideally within the medical device and healthcare industry.
Expert knowledge of ISO 13485 and related standards.
Proven leadership and problem-solving skills, with a proactive approach.
Strong communication and relationship management abilities.
Why This Role? This is your chance to make a real impact, driving quality and compliance while working with an innovative and supportive team.