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Nominate & AttendRegulatory Specialist for a leading multinational coatings company based in the North Lancashire area.Company: Leading coatings manufacturer, which owns some of the largest and most recognisable brands in the UK and the rest of the world. Profits from the organisation go towards education funds and other worthwhile causes.Hours of work:...
Role - QA/RA Senior SpecialistLocation - LondonHours 40 hours Monday to FridaySalary £50,000 to £60,000OverviewWe are seeking a highly skilled QA/RA Senior Specialist to join our clients team. To succeed in this role, you will bring extensive experience in Quality Assurance and Regulatory Affairs within the Medical Device industry, with...
Quality Assurance & Regulatory Affairs SpecialistLocation: BuckinghamshireSalary: £40,000-£60,000 (dependent on experience)Our client is an established life sciences business based in Buckinghamshire. They distribute and manufacture high-quality and innovative products, including in-vitro diagnostics, laboratory reagents, and biological materials, across the European life sciences market.An opportunity has become available for an experienced...
Selexa Life Sciences are delighted to partner with a leading Medical Device manufacturer in the search for a Regulatory Affairs Specialist to join their high-performing RA team based onsite in Cheltenham.Reporting into the Group Regulatory & Quality Director, as an RA Specialist you will be responsible for the assurance of...
Regulatory Affairs Assistant - Devon - up to £25,000 + Bonus + Benefits - REF 1935I am currently recruiting for a Regulatory Affairs Assistant to work for a leading engineering organisation based in Devon. Salary up to £25,000 + Bonus + Benefits.The company are leaders within their field of expertise...
Quality Assurance and Regulatory Engineer – HomebasedOpportunity:Do you have experience in quality assurance and regulatory affairs for medical devices? Do you have experience of working to ISO 13485, ISO 14971 and UK MDR, Regulation (EU) 2017/745, MDSAP, ISO 9001 standards? Want to work for an innovative medical device manufacturing company?...
Quality Assurance and Regulatory Engineer – HomebasedOpportunity:Do you have experience in quality assurance and regulatory affairs for medical devices? Do you have experience of working to ISO 13485, ISO 14971 and UK MDR, Regulation (EU) 2017/745, MDSAP, ISO 9001 standards? Want to work for an innovative medical device manufacturing company?...
Cure Talent are delighted to be recruiting for an experienced Validation Specialist to join a leading engineering function in the pharmaceutical and life sciences industry. This is a fantastic opportunity to apply your technical validation expertise in a dynamic and regulated environment focused on delivering high quality manufacturing solutions.As a...
Overview: Working alongside our client, a leading medical device manufacturer we are experienced Quality Engineer to join their team.Benefits:27 days annual leave + bank holidaysEligible for a 5% performance bonusPersonal development plans available for career progressionSalary sacrifice pension scheme3x life insurance coverFree refreshments including tea, coffee & fresh fruitFree on-site...
Job Role: Project Manager / Project CoordinatorLocation: Southampton (Germany and Singapore)Salary: £80,000 - £120,000 Per Annum (Or Day Rate if that is Preferred)Duration: 12 - 18 Month ProjectProactive are currently in search of an experienced Project Manager / Coordinator to start work in Southampton as soon as possible. This is...
Engineering Physicist - Sensors - CambridgeAn exciting opportunity has arisen for an experienced engineering physicist to join a new team in Cambridge to work on their revolutionary sensor technologies.This company are at the forefront of innovation and are developing a potentially disruptive product for their market.As an Engineering Physicist, you...
Production Quality Engineer - Medical DevicesNewton Colmore is working with a medical technology company near Lichfield, and we are assisting them with their search for a key quality hire to work closely with their production team.The role as an experienced quality engineer will give you the opportunity to work on...
Internal Auditor - Public Sector Services - Cannock - HomebasedDue to recent expansion, a growing Internal Auditing Organisation is currently looking for a few Internal Auditors to help with their growing workload. The offices are based in Cannock, but the company offer hybrid working meaning you will only need to...
Job Title: Regulatory Affairs Submission AssociateLocation: MaidenheadContract: 12 monthsHours: 37.5 hoursRates: £20-22p/hJob DescriptionSRG are looking for a regulatory affairs submission associate for a pharmaceutical company based in maidenhead. You will be responsible for establishing and maintaining submission content planners and associated timelines, facilitates tactical submission team meetings, prepares content planners...
Are you an experienced Regulatory Affairs Manager looking to make a impact in the chemical manufacturing industry? We are seeking a proactive and detail-oriented professional to lead the regulatory strategy and ensure full compliance across site operations.As a Regulatory Affairs Manager , you will play a critical role in navigating...
