Quality & Regulatory Manager

The Company:

Year on Year growth.



Great career opportunity.



Part of a larger group.



Established for over 25 years.





Benefits of the Quality And Regulatory Manager

£65k-£75k



Pension



Private healthcare



Mobile



Laptop



25 days’ annual leave + bank holiday





The Role of the Quality And Regulatory Manager

Our client sells a range of advanced wound care dressings, absorbents, skin protectants, peak flow meters, gloves, & surgical tapes.



The QA/RA Manager will be responsible for ensuring continued compliance of the Company’s Quality Management System with the relevant Medical Device Directives, Medical Device Regulations, International Standards, and Customer Requirements and provide knowledge and support to the company to enable it to operate within all the applicable Regulatory Guidelines.



The QA/RA Manager will act as the person responsible for regulatory compliance within the definition of the EUMDR 2017/745.



Lead and mentor the QA team: Manage, train, and develop the QA/RA team, including hiring, performance reviews, and fostering a collaborative, results-driven environment.



Allocate resources: efficiently manage the team's workload, budget, and resources to meet project timelines and quality goals.

Maintain frequent contact with external sub-contract manufacturers and suppliers.



Ensuring that process validations and other activities are in a state of control.



Resolving quality issues.



Identify issues and minimise regulatory risks.



Promote a quality culture within the organisation.



Maintain a personal knowledge of the current Quality Management System and applicable Regulatory Requirements.



Managing a team of 3.





The Ideal Person for the Quality And Regulatory Manager

The QA/RA Manager will have a tertiary qualification in life sciences or engineering (BSc, or BEng).



The QA /RA manager will have a minimum of 4 years of experience in a regulatory compliance role in the medical device industry.



Ideally experience of managing a small team.



Specific experience in regulatory affairs and submissions in the UK, European Canadian and American markets is required.



Experience in dermatology products is desirable.



Qualification or experience as a microbiologist is desirable.





If you think the role of Quality And Regulatory Manager is for you, apply now!



Consultant: Rio Barclay

Email: riob@otrsales.co.uk

Tel no.

0208 397 4114

Candidates must be eligible to work and live in the UK.



About On Target

At On Target, we specialise in sales, technical and commercial jobs in the Engineering, Construction, Building Services, Medical & Scientific, and Commercial & Industrial Solutions sectors, enabling our consultants to become experts in their market sector.

We place all levels of personnel, up to Director across the UK and internationally.