Regulatory Affairs Specialist

ConvaTec Group; United Kingdom; Remote; GBP 30,000 - 45,000; Full time

Job summary

A leading medical products company is seeking a Regulatory Affairs Specialist to ensure compliance and manage regulatory projects. The role involves writing regulatory submissions, advising on product strategies, and fostering knowledge of regulatory principles within the organization. Ideal candidates will have a degree in a relevant field and experience in regulatory affairs.

Qualifications

• 1-2 years relevant experience in regulatory affairs.
• Understanding of medical device regulations.
• Experience with Class I, II, and III devices.

Responsibilities

• Ensure regulatory compliance for Convatec products.
• Write and submit regulatory dossiers.
• Advise on strategies for product development.

Skills

Time Management

Problem Solving

Interpersonal Skills

Analytical Skills

Communication Skills

Education

Bachelor’s degree in Science, Engineering, Medical Technology, or Nursing

Regulatory Affairs Certification (RAC)

Tools

Microsoft Office

Adobe Acrobat

Job description

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Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2024 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about Convatec, please visit http://www.convatecgroup.com

Our search for better is changing the lives of our customers. It’s changing the careers of our people too – creating new challenges and opportunities all the time. We’re a business that never stands still. Join us on our journey to #ForeverCaring

The role:

The primary responsibilities of the position are to ensure regulatory compliance of a defined group of Convatec products, drive regulatory processes and activities (such as regulatory strategy, product registration, change control, review of marketing materials, etc) and continue to develop strong working relationships with internal and external customers. The person will be responsible for the management of global and regional regulatory projects, including, but not limited to, the regulatory aspects of new product development, product life cycle and changes to existing products.

Key Responsibilities:

• Advise on strategies and registration requirements for product development and marketed products
• Write and submit regulatory dossiers (e.g., US FDA submissions, EU CE marking and UKCA Technical Documentation), and interface with authorities during the review process
• Lead regulatory assessment and actions for changes to product and QMS processes
• Ensure Regulatory compliance to maintain market approvals
• Foster thorough knowledge of regulatory principles and compliance with regulatory policies throughout the organization through training and mentorship
• Regulatory support to enquiries from customers and authorities
• Provide guidance to business partners and junior regulatory staff regarding regulatory requirements including indications of risk and approximate timing for approval for planning purposes. Supports both new product development and currently marketed product portfolio
• Review, interpret and communicate FDA/EU/international regulations and guidance documents to ensure complete and scientifically sound product submissions
• Support base business activities, such as Annual Reports, Supplements, Labeling reviews, UDI
• Identify and support or lead process improvement projects to streamline current activities and increase department efficiencies, including the update, enhancement, creation of new internal policies and procedures, and maintenance of existing procedures
• Supports regulatory compliance to QSR, ISO, MDSAP, CE and other worldwide regulatory requirements as appropriate through customer complaints, internal and external audits, and training systems
• Regulatory review and approval of documents supporting the QMS and product registrations
• Participates as an active member of Industry, Regulatory or Scientific Committees, as appropriate
• This position serves as a delegate for the line manager stated on this job description
  
  
  

Skills & Experience:

• Preferred 1-2 years relevant experience, preferably in a regulatory affairs role in the life science industry
• Understanding of the regulatory framework for medical devices.
• Understanding of the Quality System Regulations ISO 13485:2016 including preparation and
• implementation of standard operating procedures
• Experience with Class I, II, and III sterile medical devices.
• Preferred experience dealing directly with Notified Bodies, Competent Authorities, and/or the US FDA
• Experience with US/EU submissions preferred.
• Good time management and problem-solving skills.
• Strong interpersonal and collaborative skills.
• Ability to execute both reactively and proactively and in a timely manner.
• Ability to conduct thorough research of regulatory requirements and related issues to identify potential
• solutions and available options.
• Experience supporting change control and new product development projects
• Strong analytical skills with good judgment-making capabilities.
• Demonstrated organizational skills.
• Strong oral and written communication skills.
• Proficiency with Microsoft Office (Excel, Word, PowerPoint), Adobe Acrobat, and Internet-based
• regulatory resources, Trackwise, Documentum etc.
  
  
  

Qualifications/Education:

• A minimum of a bachelor’s degree in Science, Engineering, Medical Technology, or Nurse required.
• An advanced degree and/or Regulatory Affairs Certification (RAC) is preferred.
  
  
  

Travel Requirements

• Not more than 25% of work time.
• There may be some business-related travel associated with this role dependent on project and / or local market and UK / US / EU travel associated with this role because some team members are home based and face-to-face contact with line manager and peers may be required.
• Attendance of relevant training and development events would be required.
• Some destinations may involve overnight stay(s).
  
  
  

Languages

• Speaking: English
• Writing/Reading: English
  
  
  

Working Conditions

This position is remote based, with occasional travel to the office. The office location for this role is Deeside UK

Our transformation will change your career. For good. You’ll be pushed to think bigger and aim for excellence. Your ideas will be heard, and you’ll be supported to bring them to life. There’ll be challenges. But, stretch yourself and embrace the opportunities, and you could make your biggest impact yet. This is stepping outside of your comfort zone.

This is work that’ll move you.

Remote

Beware of scams online or from individuals claiming to represent Convatec

A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.

If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at [e-mail].

Equal opportunities

Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.

Notice to Agency and Search Firm Representatives

Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Already a Convatec employee?

If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Legal

• Industries

  Medical Equipment Manufacturing

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