Spirit Health Group
- Extremely Competitive Package
- Up to 39 days available leave (FTE)
- Fabulous Employee Benefits Package
- Share Option Scheme
- Career Progression
- Work Life Balance
- Work Satisfaction
- Making a Difference
Are you passionate about ensuring medical devices meet and exceed global regulatory standards? We are seeking a dedicated regulatory compliance specialist to take charge of our ISO13485 and relevant global standards adherence.
We are a rapidly growing family of healthcare companies and offer an exceptional package and progression for the right person. These are exciting times – come and join us!
Spirit Health Group is a fabulous place to work. We genuinely do things differently! We are like no other healthcare company and only employ exceptional people who embrace and encourage change. We innovate. We simplify. We inspire. We look at things from a new perspective, and we genuinely care about patients and our people. We live by our values of brilliance, vigour and family – that’s how we roll.
We’re more than just an award-winning family; we’ve been voted the best health and social care company to work for in the UK! In addition to this recognition, we’ve achieved an impressive #16 in the national league tables, surpassing last year’s ranking of #88. Our outstanding levels of engagement have won us recognition from Best Companies in 2021 and 2022, and we are also proud winners of the Business Culture Awards.
Our people are pivotal in:
- Saving the NHS millions of pounds with a rapidly growing range of cost-effective healthcare products and devices.
- Implementing medicines optimisation and prescribing programmes, brilliantly
- Building innovative digital remote monitoring solutions for people with long-term health conditions.
- Providing patients with high-quality education services.
- Dispensing NHS prescriptions through our friendly pharmacy that has a passion for diabetes.
Our massive growth plans will help us save the NHS £1 million and touch the lives of millions more patients.
As our Head of Regulatory Affairs, you’ll lead in our journey to meet and exceed ISO13485 and global standards. You’ll lead the charge, ensuring our Quality Management Systems are in perfect harmony with ISO13485, MDR, MDD, and other critical ISO benchmarks. But that’s not all – you’ll also conduct internal audits, become the guru of MDD, MDR, QMS, and ISO13485, and train our teams in the art of compliance.
This role is the guardian of Risk Management Files and Clinical Evaluation reports for each Technical file, putting SaaS expertise to work in the Medical Device environment, with a special focus on our product, Clinitouch. And when it comes to international markets, you’ll support our Senior Leadership Team with rigorous research and actionable advice.
A full Job Description is available.
You will be driven by passion for regulatory excellence and thrive in a dynamic, fast paced, collaborative environment. You will have a degree (or equivalent) in law, medicine, engineering, or a life science discipline along with proven experience in overseeing regulatory compliance and quality management systems . You are highly motivated and dedicated to providing a brilliant service across the businesses, whilst committed to our goals and values.
Interested? Apply below by sending us your CV. Come and join the Spirit Family and be part of driving our (and your) success forward.
Closing date for applications is 30 November 2023.
Successful applicants will be subject to pre-employment checks including a successful disclosure at an appropriate level from the Disclosure and Barring Service (DBS), Access NI or Disclosure Scotland.
We are an equal opportunities employer