Circa £45,000 - £60,000
Could this brand-new role be your chance to take over the technical function and lead from the front?
This high-growth multi-brand SME medical devices producer with many successful products and a strong history behind them are looking to bring a top-shelf QA/RA/Technical professional on board to look after regulatory affairs, quality assurance and product compliance.
Reporting straight into the Managing Director you will have full autonomy of the initially small quality & technical department which is destined for big growth over the next few years. It's likely to be a busy role and will require a truly hands-on individual!
You'll be tasked with ensuring production standards are up to the required legal, regulatory and customer compliance requirements and the business is armed with all the information it needs to ensure safe methods of production.
This could be a great step up for an existing QA/RA Manager in medical devices looking to take ownership of the function, or an existing technical manager who would be interested in working with a fast-growing SME which can provide total autonomy.
What will you need?
- Quality Assurance/Regulatory Affairs/Technical background within medical devices
- Ability to comfortably audit to ISO 13485
- Knowledge of legislative requirements within medical device manufacturing
- Capacity to work in a fast-paced SME environment
We are looking to shortlist immediately so please apply now!
For more information please contact The One Group's Technical Division on 01733 234000.
This isn't just recruitment, it's recruitment as it should be.