Skip to main content
Post your CV and find your next job on Indeed!

Medical Pharmaceutical jobs

Sort by: -
    • 3+ years in the medical device industry in a similar Regulatory role.
    • This pivotal role involves overseeing regulatory compliance, ensuring that medical device…
    • A medical cash plan scheme.
    • As a Pharmaceutical Final Checker, you will be performing in-process checks and the final check of aseptically manufactured products…
    • A medical cash plan scheme.
    • Your work will include assisting with all aspects of Quality Control and Quality Assurance in relation to personnel, equipment and…
    • A medical cash plan scheme.
    • Experience in a microbiology laboratory, preferably in a pharmaceutical, biotechnology, or aseptic manufacturing environment.
    • Hours: Full Time - Permanent on a shift basis, 5 days our of 7 between 6am and 7pm.
    • Benefits: Private Medical Insurance - Subsidised On-site Gym - Enhanced…
  • View similar jobs with this employer
    • Experience of working in a pharmaceutical quality environment or equivalent.
    • Knowledge of analytical techniques and processes used in the determination of…
    • Pharmacy Technician – Medicines Management & Audit | East Midlands | Field-Based*.
    • Conduct medicines management audits across designated sites, ensuring…
    • ADDITIONAL BENEFITS: Relocation package of up to £2,000, generous yearly bonus (Profit Related Pay), company sick pay, 30 days holiday including bank holidays.
    • Undertake clinical decision-making based on patient-submitted information, medical history, and diagnostic results, ensuring all prescribing is appropriate,…
    • We are currently only looking for qualified Accuracy Checking Technicians (with NVQ Level 3 or equivalent) who are registered with the GPhC.
  • View similar jobs with this employer
    • PAY: £13.45 per hour increasing to £13.95 per hour after successful completion of 6-months probationary period*.
    • Attend training sessions appertaining to post.
    • The ideal candidate will play a crucial role in ensuring optimal patient care through the safe and effective use of medications.
    • We are currently recruiting for both full-time and part-time in-person roles.
    • Full-time roles involve working 40 hours per week, including participation in a…
  • View similar jobs with this employer
    • Focussing on providing a safe and secure medicines management service, ensuring patient medical records are maintained to the agreed standard at all times and…
    • Medical devices or pharmaceutical industries: 5 years (required).
    • Minimum of 5 years’ experience working in a manufacturing facility preferably within medical…

People also searched:

medical secretary
medical writer
pharmaceutical company
pharmaceutical manufacturing
pharmaceutical sales
pharmacist
pharmacy
quality assurance
regulatory affairs
scientist

Job Post Details

Senior Regulatory Professional - Medical Devices - job post

MCA Recruitment recruiting on behalf of our client
London
£55,000 - £58,000 a year - Permanent, Full-time

Job details

Pay

  • £55,000 - £58,000 a year

Job type

  • Permanent
  • Full-time

Shift and schedule

  • Monday to Friday

Location

London

Benefits

Pulled from the full job description

  • Sick pay
  • Company pension
  • Private medical insurance
  • Health & wellbeing programme
  • Company events
  • Transport links
  • On-site parking

Full job description

Job Summary

We are seeking an experienced Senior Regulatory Professional specialising in Medical Devices to join our clients dynamic team. This pivotal role involves overseeing regulatory compliance, ensuring that medical device products meet all necessary standards and regulations. The ideal candidate will possess a strong background in quality assurance and have a comprehensive understanding of medical device regulations across various markets. This position offers an excellent opportunity to contribute to innovative healthcare solutions within a collaborative and forward-thinking organisation.

Located in North London. Excellent transport links.

The hours 8.30am to 5pm, or you can do 8am to 4.30pm.Monday to Friday.

The Package

  • Salary £55,000 to £57,000 dependent on experience
  • Bonus
  • 25 days Holiday plus bank holidays
  • The company will support you with professional development, this is very important to them.
  • Private Healthcare
  • Online GP Services -Access to an online GP service

Experience

3+ years in the medical device industry in a similar Regulatory role.

  • Strong knowledge of EU MDR 2017/745, ISO 13485, and other relevant international regulatory frameworks and standards.
  • Proven ability to compile, maintain, and submit Technical Documentation, product registrations, and regulatory submissions to authorities and Notified Bodies.
  • Experienced in clinical evaluation activities, including Clinical Evaluation Plans/Reports, literature reviews, and post-market clinical follow-up.
  • Solid understanding of labelling compliance, product classification, intended use determination, and regulatory pathways during product development.
  • Skilled in post-market surveillance and vigilance activities, including adverse event reporting, PSURs, and field safety corrective actions.
  • Able to monitor, interpret and communicate regulatory changes to the business in language that is easy to understand.
  • Strong, pragmatic collaborator across Quality, Clinical, Marketing, R&D, and Operations, supporting product launches and ongoing compliance.
  • Familiarity with QMS processes and regulatory audits/Notified Body inspections, with exposure to sterile manufacturing environments considered a plus.

This role is ideal for professionals committed to advancing healthcare through rigorous regulatory oversight and quality assurance excellence.

Pay: £55,000.00-£58,000.00 per year

Benefits:

  • Company events
  • Company pension
  • Health & wellbeing programme
  • On-site parking
  • Private medical insurance
  • Sick pay

Application question(s):

  • Is your current location commutable to North London on a daily basis ?

Experience:

  • MDR 2017/745, ISO 13485 directives : 3 years (required)
  • submit Tech Docs, product regs, and regulatory submissions : 3 years (required)

Work authorisation:

  • United Kingdom (required)

Work Location: In person

Let Employers Find YouUpload Your Resume