Jobs
>
Hitchin

    Regulatory Affairs Specialist - North Hertfordshire, Hertfordshire, United Kingdom - Vector Recruitment

    Vector Recruitment
    Vector Recruitment North Hertfordshire, Hertfordshire, United Kingdom

    2 weeks ago

    Default job background
    Description

    Compliance / Quality Administrator – Medical Devices We are looking for a Compliance / Quality Administrator to join a dynamic company developing an array of products for the medical and healthcare industry.

    The company is growing and offering many opportunities for personal career development in addition to a wide variety of new projects to work on.

    As the Compliance / Quality Administrator you will join their Product Management Team and will be responsible for document control in compliance with applicable regulatory standards.

    The job will suit a friendly, diligent and motivated individual with a background in Quality Assurance / Quality Management /Document Control or similar technical administration role within medical equipment sector.


    Compliance / Quality Administrator`s Responsibilities:
    Assist with quality control of products.

    Manage medical device technical files and documentation for new products, working closely with Sales and Purchasing to resolve technical questions.

    Experience in document control for ISO9001 Quality Management System and understanding of medical regulatory standards.
    Excellent computer literacy with proficiency in Microsoft Office products is essential (especially Word and Excel). Quality Data reporting and analysis.


  • Vector Recruitment Limited Cambridge, United Kingdom

    Regulatory Affairs Specialist · £45k-£55k (dep on exp) · Cambridge · We have a brand-new vacancy for a Regulatory Affairs Specialist to join a fascinating Cambridge based R&D technology company. This business is very well established and is undergoing rapid growth due to the impa ...


  • Hyper Recruitment Solutions Ltd Cambridgeshire, United Kingdom

    We are currently looking for a Regulatory Affairs Specialist to join a leading Medical Device company based in the Cambridgeshire area. · KEY DUTIES AND RESPONSIBILITIES: · Your duties as the Regulatory Affairs Specialist will be varied however the key duties and responsibilities ...


  • Newton Colmore Consulting Ltd Cambridge, United Kingdom

    Regulatory Affairs Specialist - Medical Devices - Cambridge · Newton Colmore is working with a medical devices company in Cambridge who are looking to hire an experienced regulatory affairs scientist/engineer to join their team. · This role will give you an opportunity to take le ...


  • GE Healthcare Chalfont Saint Giles, United Kingdom

    **Job Description Summary**: This role is an entry level role for those who are looking to start a career in Regulatory Affairs. As a Global Regulatory Affairs specialist you will be supporting Marketing Authorisation activities with varying levels of responsibility, autonomy and ...


  • SPD Development Company Ltd Bedford, United Kingdom

    **Senior Regulatory Affairs Specialist** · Swiss Precision Diagnostics (SPD) is a world leader in the research, design and supply of advanced consumer diagnostic products. SPD is a joint venture between **Procter & Gamble (P&G)** and **Abbott**; and our brand **Clearblue**, is re ...


  • Thermo Fisher Scientific Cambridgeshire, United Kingdom

    At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed ...


  • Thermo Fisher Scientific Cambridgeshire, United Kingdom

    At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed ...


  • Vector Recruitment Limited Cambridge, United Kingdom

    Regulatory Affairs Specialist - US Market · £45k-£55k (dep on exp) · Cambridge · We have a brand-new vacancy for a Regulatory Affairs Specialist to join a fascinating Cambridge based R&D technology company. This business is very well established and is undergoing rapid growth due ...


  • GSK Ware, United Kingdom

    **Site Name**: UK - Hertfordshire - Ware RD, USA - Pennsylvania - Upper Providence · **Posted Date**: Jan · **Devices Specialist, Global CMC Regulatory Affairs**: · We're combining the power of genetic and genomic insights into what causes disease, with the speed and scale of ar ...


  • Medicareplus International Ltd Wembley, Greater London, United Kingdom

    Job Description Job Summary · RA Specialist is responsible for ensuring continued compliance of the Quality Management System of the company with the relevant Medical Device Regulations, International Standards, and Customer Requirements and that this is maintained and implemen ...


  • Medicareplus International Ltd Wembley, United Kingdom

    Job Summary · RA Specialist is responsible for ensuring continued compliance of the Quality Management System of the company with the relevant Medical Device Regulations, International Standards, and Customer Requirements and that this is maintained and implemented accordingly. · ...


  • D R Newitt & Associates Welwyn Hatfield, Hertfordshire, United Kingdom

    Compliance Officer - Initital 12 Month Contract - Food Manufacture · * Laws / Regulations / Policies · * £38,000 - £40,000 + Great Bonus · * ASAP Start · * Hybrid working (3 days on site & 2 from home) · Purpose of job - To implement a culture of enterprise risk management and in ...


  • Medicareplus International Ltd Wembley, Greater London, United Kingdom

    Job SummaryRA Specialist is responsible for ensuring continued compliance of the Quality Management System of the company with the relevant Medical Device Regulations, International Standards, and Customer Requirements and that this is maintained and implemented accordingly.Respo ...


  • Cpl Life Sciences Buckinghamshire, United Kingdom

    Job Title: Regulatory Affairs Specialist Employment type: 6-Month Contract – Outside IR35Location: Buckinghamshire, UK – 2 days on-site per week. Rate: £84.50 Per Hour via Limited or Umbrella. An opportunity to join a global leading consumer health business and be responsible for ...


  • Werfen Bedford, United Kingdom

    Overview · Werfen · Werfen, founded in , is a worldwide developer, manufacturer and distributor of specialized diagnostic instruments, related reagents, automation workcells, and data management solutions for use primarily in hospitals and independent clinical laboratories. The ...


  • Werfen Bedford, United Kingdom

    Overview · Werfen · Werfen, founded in , is a worldwide developer, manufacturer and distributor of specialized diagnostic instruments, related reagents, automation workcells, and data management solutions for use primarily in hospitals and independent clinical laboratories. Th ...

  • The Institution of Engineering & Technology

    Public Affairs Manager

    23 hours ago


    The Institution of Engineering & Technology Stevenage, United Kingdom

    **Public Affairs Manager** · **Circa £45,000 per annum, dependent on experience** · **Permanent/Full-time** · **Stevenage, Hertfordshire (with Hybrid working)** · What if you worked for an organisation where you influenced policy development? · What if you were increasing the pro ...


  • Medicareplus International Ltd Wembley, Greater London, United Kingdom

    Job Summary RA Specialist is responsible for ensuring continued compliance of the Quality Management System of the company with the relevant Medical Device Regulations, International Standards, and Customer Requirements and that this is maintained and implemented accordingly. · ...


  • Medicareplus International Ltd Wembley, Greater London, United Kingdom

    RA Specialist is responsible for ensuring continued compliance of the Quality Management System of the company with the relevant Medical Device Regulations, International Standards, and Customer Requirements and that this is maintained and implemented accordingly. · Responsible ...


  • Origin Sciences Cambridge, United Kingdom Full time

    Origin Sciences is a start-up biotechnology company based in Granta Park, just south of Cambridge. We develop our own innovative medical devices, which we use in clinical trials to collect a biobank of mucus-based biospecimens. This biobank provides clinical material for our rese ...