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Jobs in Ardwick, greater manchester, united kingdom
Quality and Regulatory Consultant - Medical Devices - Contract
linkupArdwick, UKGeneral Manager In Training
Mitchells & ButlersMitchells and Butlers – North West, Manchester M60 7RA, UKHead of Finance
HousrManchester, GB-ENG, GBCare Co-ordinator
Voyage CareArdwick, UK- Promoted
Senior Software Engineers
GCHQLongsight, England, United Kingdom- Promoted
AVON Representatives wanted in Ardwick, Manchester, England – start today
Reps.co.ukArdwick, Greater Manchester, United KingdomKey Account Manager - Sector Specialist
ENWLGreater Manchester & Lancashire, UKAccount Executive
Blink PaymentManchester, GB-ENG, GBSenior Accountant
Modern MilkmanManchester, GB-ENG, GBRetail & Fashion / Merchandising Merchandiser – Womens young fast fashion
Success TalentGreater Manchester UK North West ManchesterAssistant Manager Retail
BootsManchester, Piccadilly StationEstate Officer
Your Housing GroupGrove Village, Ardwick, Manchester , United KingdomPrimary Tutor
Prospero TeachingThornton-Cleveleys, Greater Manchester, North West, EnglandRecruitment and Training Manager – ML564
MetrolineManchester, M12 4AHDuty Manager - Burger King
SSPManchester, GB, M60 7RA, UKCustomer Service OOH Agent
MearsManchester, Devonshire St N- Promoted
Driving Instructor Trainee - Work from home
My Four WheelsArdwick, Greater ManchesterCosmosDB and .NET Lead Technology Developer (temporary for 2 years, with a possibility the role may become permanent)
Office for Standards in Education, Children's Services and SkillsPiccadilly Gate ManchesterBack of House Nandoca
nando'sManchester, Piccadilly, ManchesterTesco Colleague - Beswick Express
TescoManchester, BeswickQuality and Regulatory Consultant - Medical Devices - Contract
linkupArdwick, UK- Full-time
Medical Device Quality and Regulatory Consultant - Contract Opportunity Location : Greater Manchester (Hybrid) Contract : 6 months initially Rate : Up to £500 per day (Outside IR35) Start Date : ASAP KO2's exclusive client is developing a life-changing Medical Device and is seeking an experienced QA / RA Consultant to support their Quality Assurance & Regulatory Affairs efforts. The Role : Lead QA / RA activities, ensuring compliance with Medical Device regulations Take ownership of QMS implementation and Technical Files Focus on FDA 510(k), ISO 13485, and IEC 62304 compliance Work on a multi-disciplinary Medical Device project (Electronics, Software, Mechanical, Clinical) Join a dynamic start-up where you can make a real impact on Quality Assurance & Regulatory Affairs This is a hands-on role in a growing business with a fantastic culture- where collaboration, respect, and motivation drive innovation. A one stage interview can be quickly arranged. ADZN1_UKTJ