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Regulatory Affairs Specialist
5 days ago
Vector Recruitment Limited Cambridge, United KingdomRegulatory 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 ...
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Regulatory Affairs Specialist
1 week ago
Hyper Recruitment Solutions Ltd Cambridgeshire, United KingdomWe 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 ...
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Regulatory Affairs Specialist
2 hours ago
Newton Colmore Consulting Ltd Cambridge, United KingdomRegulatory 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 ...
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Regulatory Affairs Specialist
1 week ago
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 ...
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Senior Regulatory Affairs Specialist
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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 ...
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Senior Reg Affairs Specialist
3 days ago
Thermo Fisher Scientific Cambridgeshire, United KingdomAt 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 ...
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Senior Regulatory Affairs Specialist
2 hours ago
Thermo Fisher Scientific Cambridgeshire, United KingdomAt 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 ...
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Regulatory Affairs Specialist Us Market
5 days ago
Vector Recruitment Limited Cambridge, United KingdomRegulatory 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 ...
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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 ...
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Regulatory Affair Specialist
5 days ago
Medicareplus International Ltd Wembley, Greater London, United KingdomJob 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 ...
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Regulatory Affair Specialist
4 days ago
Medicareplus International Ltd Wembley, United KingdomJob 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. · ...
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Regulatory Affairs Specialist
1 week ago
D R Newitt & Associates Welwyn Hatfield, Hertfordshire, United KingdomCompliance 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 ...
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Regulatory Affair Specialist
5 days ago
Medicareplus International Ltd Wembley, Greater London, United KingdomJob 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 ...
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Regulatory Affairs Specialist
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Cpl Life Sciences Buckinghamshire, United KingdomJob 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 ...
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Principal Regulatory Affairs Specialist
1 week ago
Werfen Bedford, United KingdomOverview · 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 ...
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Senior Regulatory Affairs Specialist
1 week ago
Werfen Bedford, United KingdomOverview · 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 ...
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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 ...
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Medicareplus International Ltd Wembley, Greater London, United KingdomJob 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. · ...
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Medicareplus International Ltd Wembley, Greater London, United KingdomRA 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 ...
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Origin Sciences Cambridge, United Kingdom Full timeOrigin 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 ...
Regulatory Affairs Specialist - North Hertfordshire, Hertfordshire, United Kingdom - Vector Recruitment
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.