R&D Test Engineer - Sensor TechnologyA growing instrumentation technology inventor in Cambridge is searching for a research and development test engineer to join their in-house testing team.As a R&D Test Engineer within this organisation, you will be utilising your experience to determine the performance and reliability of brand-new physical sensors...
Title: QA Officer - ClinicalLocation: Greater ManchesterSalary: £41,000About the RoleSRG are recruiting for a QA Officer with GcP experience to join an innovative company whose technologies form an integral to the advancement of Life science & Healthcare research all over the world.Based at their site in Greater Manchester, you will...
Job Title: Regulatory Affairs AssociateIndustry: Medical DevicesLocation: PlymouthPosition Type: PermanentAbout The CompanyA world-leading developer and manufacturer of tissue-healing technology, this company focuses on quality patient outcomes and value for payers. Its surgical products include tissue adhesives, sutures, haemostats, fixation devices, and sealants. Since 2019, it has acquired seven companies specialising...
Regulatory Affairs Associate - Devon -Up to £40,000 pa + benefits - Ref 1894Hybrid or remote working£30,000 - £40,000 pa + company benefits + bonusI am currently recruiting for a Regulatory Affairs Associate to work for a multi-national medical device organisation. Salary up to £40,000 pa + benefitsOn a day-to-day...
Working for an SME Medical Device manufacturer, you will be responsible for the delivery of the company's development regulatory roadmap. This will be achieved through leading the regulatory elements of the company's product development efforts and compliance programme as well as supporting its customers' regulatory requirements and projects.Key competence /...
Are you passionate about regulatory affairs and eager to help life-changing medical products reach the market? Our client is looking for a Regulatory Affairs Officer to support their team in guiding pharmaceutical, medical device and life sciences companies through complex regulatory landscapes.Key ResponsibilitiesAssist in preparing and submitting regulatory documents for...
CK Group are recruiting for a CMC Regulatory Affairs Consultant to join a company in the Pharmaceutical industry at their site based in High Wycombe on a on a contract basis for 6 months.Salary:£45-£62.93 per hour PAYE or £65-84.55 per hour UmbrellaCMC Regulatory Affairs Consultant Role:Responsible for the development of...
The company is involved with the design, development and manufacture of a range of diesel, hybrid and hydrogen powered engines for various applications and sell them Worldwide.The role will involve working with trade associations (government bodies, etc) on new engine emissions legislation and supporting the company in order to enable...
CK Group are working with a very well backed biotechnology company, with a strong pipeline who are looking for an Associate Director, Regulatory Affairs, for a six-month contract. The role will be in support of their expanding Oncology portfolio, extensive Oncology experience is an absolute must, radiopharmaceuticals experience would be...
Regulatory Affairs Associate (Hybrid Working) - Cheshire -Up to £40,000 pa + benefits - REF 1900Hybrid working (1 or 2 days in office)£30,000 - £40,000 pa + company benefits + bonusI am currently recruiting for a Regulatory Affairs Associate to work for a multi-national medical device organisation. Salary up to...
Regulatory & Specification Manager (Fully Remote, UK)Location: UK (Fully Remote, with occasional travel)Salary: £50,000 - £60,000 per annumJob Type: Full-time, PermanentAre you an experienced regulatory and compliance professional with a background in food specifications? We're recruiting for a Regulatory & Specification Manager to lead a team of experts delivering high-quality...
We are seeking a Dossier Manager to join a leading global organization in the regulatory sciences industry. This role is essential in managing and publishing key regulatory submissions to Health Authorities, ensuring compliance, accuracy, and timely delivery.Key Responsibilities:Manage the preparation, build, and publishing of regulatory dossiers for global submissions.*Ensure regulatory...
Specification Team Leader (12-Month FTC) - Fully RemoteLocation: UK (Fully Remote)Salary: £40,000 - £45,000 per annumJob Type: Full-time, 12-Month Fixed Term ContractThe OpportunityAre you an experienced compliance or regulatory professional looking for a fully remote role with a leading organization? We're looking for a Specification Team Leader to manage a...
We are seeking an experienced Qualified Person (QP) with IMP experience to join a leading pharmaceutical company in Greater London. This is a fantastic opportunity to play a key role in ensuring the highest standards of compliance and product quality within a dynamic and growing organisation.Key Responsibilities:Act as a QP...
CK Group are recruiting for a Quality Oversight and Compliance Manager to join a company in the pharmaceutical industry on a contract basis for 6 months initially.Salary:PAYE £23.39 - £28.59 per hour or UMB £26.21 - £32 per hour (inside IR35).Quality Oversight & Compliance Manager role:Responsible for driving improvements to...
