Quality Management Systems Consultant

BaxMed – Quality Management Systems Consultant

Led by Stuart Baxter, a seasoned professional with a distinguished career in Regulatory Affairs, BaxMed Regulatory Ltd is an exciting early-stage organisation formed to provide Regulatory and Quality Compliance Services for the global Medical Device / healthcare sector. With a core ethos and commitment to simplifying the complexities of Regulatory Affairs, BaxMed offers a comprehensive range of services tailored to guide organisations to success in the highly regulated medical device and in vitro diagnostic space.

Role - Quality Management Systems Consultant

Brightwork is delighted to be supporting BaxMed as they seek to recruit a Quality Management Systems Consultant. Supporting a highly varied client base, start-up / early stage to well established, you will have a varied and interesting role, your duties and responsibilities including;

• Assessing, developing, implementing and managing quality management standards for diverse clients across various industries.
• Supporting clients in developing and implementing quality management systems specific to industry, sector and regulatory standards / requirements
• Collaborating on internal and external client audits
• Ensuring quality management systems meet bespoke company and industry regulatory requirements
• Supporting clients in training and development of internal staff in relation to quality management systems
• Identifying and developing new service offerings to meet evolving client needs.

Ideally degree qualified, you will have a wealth of experience in assessment, development and management of quality systems and ideally within Medical Device, Pharma and associated Life Sciences sectors. You will have first class communication skills, both verbal and written, and be well versed in developing highly effective client relationships to provide tailored quality management systems.

BaxMed Regulatory Ltd is poised to become a trusted name in the medical device sector, offering a full suite of services that span quality management systems, regulatory strategy development, in vitro diagnostic regulatory affairs, companion diagnostics regulatory affairs, medical device regulatory affairs and clinical affairs.

For further information on this excellent opportunity within an exciting early-stage organisation, please call Ian Grant on or email