Medical Device Regulatory Lead
1 month ago
Senior Quality Assurance Position
We are seeking an experienced Senior Quality Assurance Specialist to join our client's team as a key member of their senior leadership group. In this role, you will be responsible for ensuring the quality management system meets regulatory requirements and maintains excellence within the organization.
The successful candidate will have a strong background in quality assurance, regulatory affairs, and team leadership, with a proven track record in managing quality initiatives and projects. Experience working with ISO standards, particularly ISO 13485, is essential.
Responsibilities:
- Oversee the development and implementation of the quality management system, aligning it with regulatory demands and industry best practices.
- Provide guidance and support to the quality and regulatory team, promoting continuous improvement and process optimization.
- Liaise with stakeholders to ensure effective communication and collaboration across departments.
Requirements:
- Significant experience in quality assurance, regulatory affairs, or a related field.
- Demonstrable expertise in ISO 13485 and other relevant standards.
- Proven leadership skills, with experience in managing quality initiatives and projects.
Benefits:
- A salary range of £65,000 - £75,000, plus bonus and benefits.
- A comprehensive pension plan and hybrid vehicle allowance.
- Ongoing professional development opportunities.
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Morecambe, Lancashire, United Kingdom Ernest Gordon Recruitment Full timeCompany OverviewA global leader in filtration solutions seeks an experienced Regulatory & Quality Manager (Medical Devices) to join its Senior Leadership team. This is a unique opportunity to make a tangible impact on the growth and continued success of the business.This company operates within various sectors, including healthcare, life sciences,...
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