Latest Managed Services Jobs

Test Engineer

This role involves designing and implementing quality test procedures for both software and hardware components of medical devices. Responsibilities include attending design meetings, writing test plans, analyzing opportunities for automated testing, and ensuring compliance with regulatory standards.

Quality Start Walsall, West Midlands (county), United Kingdom £30,000 – £35,000 pa

On-site Permanent

Business Development Director

£75,000 - £80,000 per annum + 20% Bonus + Car AllowanceOffice is based in Hampshire, close to the Surrey borderFull Time | PermanentRegular UK Travel requiredOur client is an established international manufacturing and engineering business supplying innovative material solutions to...

HR Dept (Recruitment Agency) Farnborough, Hampshire, GU14 7JT, United Kingdom £75,000 – £80,000 pa

Product Design Engineer ( Manufacturing )

Product Design Engineer ( Manufacturing )£70,000 - £75,000 + Bonus + Excellent Company Benefits + Training into MedicalWarrington (Commutable from Manchester, Liverpool, Wigan, St Helens, Widnes, Runcorn, Northwich, Leigh & surroundingareas)Are you an experienced Design Engineer with a background in...

Rise Technical Recruitment Warrington, Cheshire, United Kingdom £70,000 – £75,000 pa

Document Controller

Job Title:Document Control SpecialistLocation:ThornabySalary:£30,000 - £35,000 DOEBenefits:* Competitive salary* Excellent benefits package* Ongoing training and development* Career progression opportunities* Collaborative and supportive working environment* Opportunity to work within a highly regulated manufacturing environmentThe Company:Our client is a leading manufacturer operating...

Theo James Recruitment Thornaby-on-Tees, North Yorkshire, TS17 9BT, United Kingdom £30,000 – £35,000 pa

Test Quality Assurance Engineer

This role involves designing and implementing quality test procedures for both software and hardware in medical device products. Responsibilities include attending design meetings, writing test plans, and ensuring compliance with regulatory standards.

Quality Start Walsall, West Midlands (county), United Kingdom £30,000 – £35,000 pa

On-site Permanent

Global Labelling Director (Team Lead), Content

This role involves leading a team of labelling professionals, developing global labelling strategies, and ensuring compliance with regulatory requirements. The Director will collaborate with cross-functional partners and drive continuous improvement in labelling processes.

Novartis London, United Kingdom

Hybrid Permanent

Scientist I, Molecular and Cell Biology

This role involves conducting cutting-edge research in molecular and cell biology, focusing on cell health and rejuvenation. Responsibilities include designing and executing experiments, developing new assays, and collaborating with multidisciplinary teams to advance translational projects and validate therapeutic targets.

Altos Labs Cambridge, United Kingdom £51,500 – £67,700 pa

On-site Permanent

Regulatory Affairs Specialist

This role involves preparing and managing regulatory submissions for medical devices, ensuring compliance with EU MDR and ISO 13485 standards. The specialist will maintain technical documentation, support clinical evaluations, and collaborate with cross-functional teams throughout the product lifecycle. A key focus is staying current with global regulatory changes and ensuring continuous market access through timely renewals and post-market surveillance.

SRG Perivale, London, UB6 8DD, United Kingdom £50,000 – £60,000 pa

On-site Permanent

Technician Project Lead

Lead technical project workstreams in medical device development from concept to manufacturing transfer, coordinating cross-functional teams and ensuring compliance with quality systems. Drive project timelines, resolve technical issues, and support verification and industrialisation activities within a regulated environment. Engage with suppliers, manufacturing partners, and stakeholders to ensure on-time, in-scope delivery.

Cranleigh Scientific Cambridge, Cambridgeshire, United Kingdom £60,000 – £70,000 pa

On-site Permanent

Head of Marketing

Head of MarketingLocation: West SussexSalary: Up to £70,000, Plus BenefitsDrive the marketing function for a respected manufacturer supplying global organisations. This is a hands‑on Head of Marketing role ideal for a commercially minded marketer who enjoys both strategy and execution.About...

OM Search Consultants LTD Haywards Heath, West Sussex, United Kingdom £60,000 – £70,000 pa

Global Development Lead, Early Clinical Development, Internal Medicine

The Global Development Lead will drive clinical research for cardiometabolic diseases, creating early clinical development strategies and leading the execution of research projects. They will translate pre-clinical observations into clinical experiments, manage clinical trial data, and collaborate with cross-functional teams to ensure medical and scientific excellence.

Pfizer United Kingdom

On-site Permanent

Global Development Lead, Early Clinical Development, Internal Medicine

The Global Development Lead will drive clinical research for cardiometabolic diseases, creating and executing early clinical development strategies. They will work closely with cross-functional teams to translate pre-clinical observations into clinical experiments, ensuring medical and scientific excellence in Phase 1/2 studies and regulatory submissions.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent

Clinical Research Associate

This role involves managing and monitoring clinical trial sites remotely, ensuring compliance with Good Clinical Practice and Pfizer standards. The Clinical Research Associate serves as the primary point of contact for investigator sites, conducting remote and on-site monitoring, supporting patient safety, resolving protocol issues, and driving site activation and recruitment. The position emphasizes strong collaboration with study teams and site staff to maintain data quality and regulatory compliance throughout the trial lifecycle.

Pfizer United Kingdom

Remote Permanent

Global Regulatory Associate Director, Life Cycle Management

Manages regulatory maintenance for a high-complexity pharmaceutical portfolio, ensuring compliance and timely submissions to global health authorities. Develops strategic input on safety reports, variations, and renewals, while leading responses to regulatory queries and supporting cross-functional initiatives. Plays a key role in lifecycle management of innovative medicines, requiring strong scientific interpretation and stakeholder collaboration.

Novartis £67,900 – £126,100 pa

Hybrid Permanent

VMG Access Technology & Operations Lead

This role involves leading the advancement of AI, digital tools, and operational capabilities across VMG Access at Pfizer. Responsibilities include driving technology strategy, implementing AI and automation, shaping GTCS-related changes, enabling data-driven decision-making, and ensuring compliance and risk management.

Pfizer Spain

On-site Permanent Flexible