Regulatory Affairs Specialist (Worksop)

Regulatory Affairs Specialist (Worksop)

Worksop Full-Time Home office (partial)
Vernacare International

Regulatory Affairs Specialist

Location: Hybrid – Worksop (with occasional travel to Vernacare sites)

Reports to: Regulatory Affairs Manager

Join Vernacare and help shape the future of sustainable healthcare

At Vernacare, we’re committed to protecting people and the planet through innovative, sustainable healthcare solutions. As a Regulatory Affairs Specialist within our QARAC (Quality, Assurance, Regulatory Affairs & Compliance) team, you’ll play a critical role in ensuring our products meet the highest regulatory standards while supporting innovation and growth across our portfolio.

The Opportunity:

This is a key position within the QARAC team, responsible for supporting regulatory compliance across the full product lifecycle—from development through to post-market activities.

You’ll act as a subject matter expert on regulatory requirements, working closely with colleagues across R&D, Quality, Manufacturing and Commercial teams to ensure that products are compliant, competitive, and aligned to evolving regulatory frameworks.

This is a hybrid role, with flexibility built in, alongside occasional travel to Vernacare sites across the UK to support collaboration, audits and project activity.

What You’ll Be Doing:

Regulatory Compliance & Strategy

  • Support the development and implementation of regulatory strategies for new and existing products
  • Ensure compliance with applicable regulations including UKCA, CE marking (EU MDR) and other international requirements where applicable
  • Interpret regulatory requirements and provide clear, pragmatic guidance to the business

Technical Documentation & Submissions

  • Prepare, review and maintain technical files and regulatory documentation in line with regulatory expectations
  • Support product registrations, submissions and regulatory approvals across relevant markets
  • Ensure documentation is inspection-ready at all times

Product Lifecycle Management

  • Provide regulatory input into new product development (NPD) and design change activities
  • Support change control processes and assess regulatory impact of product or process changes
  • Contribute to post-market surveillance activities, including vigilance and reporting where required

Stakeholder & Authority Interaction

  • Act as a key contact for notified bodies, regulatory authorities and external partners
  • Support and participate in regulatory audits and inspections
  • Build strong relationships internally to ensure regulatory considerations are embedded early

Regulatory Intelligence & Continuous Improvement

  • Monitor changes in regulations, standards and guidance (e.g., MDR updates, UK regulations)
  • Assess impact to Vernacare’s products and processes, providing recommendations and action plans
  • Contribute to the continuous improvement of regulatory systems, processes and ways of working within QARAC

What We’re Looking For:

We’re looking for someone who combines technical regulatory expertise with a collaborative, solutions-focused mindset.

Experience & Knowledge

  • Proven experience in a Regulatory Affairs role within medical devices, healthcare or another highly regulated industry
  • Strong working knowledge of EU MDR, UKCA and CE marking requirements
  • Understanding of quality management systems (e.g., ISO 13485) and how regulatory and quality overlap
  • Experience supporting technical documentation, submissions and audits

Skills & Attributes

  • Excellent attention to detail with strong documentation and technical writing skills
  • Ability to interpret complex regulations and translate them into practical business guidance
  • Confident stakeholder management skills, with the ability to influence across functions
  • Strong organisational skills and ability to manage multiple priorities
  • Proactive, adaptable, and comfortable working in a changing regulatory environment

Why Join Vernacare?

  • Be part of a purpose-led business focused on sustainable healthcare solutions
  • Work within a collaborative and supportive QARAC team
  • Enjoy flexible hybrid working
  • Gain exposure across multiple UK sites and functions
  • Be part of a company that values innovation and continuous improvement

We offer a competitive benefits package designed to support your wellbeing and reward your contributions:

  • Life Insurance – 4x salary
  • 25 Days Annual Leave + Bank Holidays
  • Enhanced Sick Pay Scheme
  • EV & Cycle to Work Salary Sacrifice Schemes
  • Employee Assistance Programme – includes 24/7 GP access
  • Mental Health First Aiders
  • Refer a Friend Scheme – up to £1,000
  • Company Pension Scheme
  • Quarterly Impact Awards – up to £2,500
  • Manager Recognition Awards

Be the driving force behind Vernacare’s growth and work with a company committed to sustainability and innovation.

Interested?

If you’re looking for a role where your expertise will make a real impact, we’d love to hear from you.

Apply now and be part of Vernacare’s mission to create a more sustainable healthcare future.

Vernacare International

Contact Details:

Vernacare International Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Regulatory Affairs Specialist (Worksop)

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Some tips for your application 🫡

Show Your Understanding of Compliance:In the compliance-risk field, it's super important to showcase your understanding of regulations and risk management frameworks. Highlight any relevant coursework, certifications (like ICA or AML), or even projects that demonstrate your knowledge and commitment to this area. We want to see how you can navigate this complex landscape!

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How to prepare for a job interview at Vernacare International

Master the Regulations

Brush up on key compliance regulations relevant to the industry you're applying to. Familiarising yourself with specific laws and frameworks used in your field will give you an edge during technical questions. Show that you’re not just aware of them but can also apply them—think real-life scenarios!

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