Make a Real Difference - Join a Global Leader in Health careAre you passionate about improving people's health and well being? Do you thrive working independently and have basic computer skills? If so, we have an exciting opportunity for you!Position: Receiving/Unpacking Investigator Location: Witney, Oxfordshire (OX29) Pay Rate: £15.29 per hour Shift Pattern: 4 on / 4 off, 7:00am - 7:00pmWe're hiring on behalf of a globally respected medical device and he
Make a Real Difference - Join a Global Leader in Health careAre you passionate about improving people's health and well being? Do you thrive working independently and have basic computer skills? If so, we have an exciting opportunity for you!Position: Receiving/Unpacking Investigator Location: Witney, Oxfordshire (OX29) Pay Rate: £15.29 per hour Shift Pattern: 4 on / 4 off, 7:00am - 7:00pmWe're hiring on behalf of a globally respected medical device and he
Are you passionate about quality and making a difference in health care? Do you enjoy working independently and have strong analytical skills?Complaints Investigator (Night Shift) - Join a Global Health care Leader in Witney!If so, we're looking for you! We're seeking Complaints Investigators to join our team at a leading global medical device and health care company based in Witney, Oxfordshire.What You'll Do:Investigate Product Returns: You'll play a cru
Are you passionate about quality and making a difference in health care? Do you enjoy working independently and have strong analytical skills?Complaints Investigator (Night Shift) - Join a Global Health care Leader in Witney!If so, we're looking for you! We're seeking Complaints Investigators to join our team at a leading global medical device and health care company based in Witney, Oxfordshire.What You'll Do:Investigate Product Returns: You'll play a cru
Are you an experienced Regulatory Affairs specialist or Medical Writer? Do you have experience in the writing / authoring of technical files? If so, we would love to speak with you! We are recruiting for a Regulatory Affairs Specialist to join our clients Infectious Disease business unit, preparing documentation for international product registrations. We are looking for someone with an RA or Medical Writing background, preferably within an IVD or medica
Are you an experienced Regulatory Affairs specialist or Medical Writer? Do you have experience in the writing / authoring of technical files? If so, we would love to speak with you! We are recruiting for a Regulatory Affairs Specialist to join our clients Infectious Disease business unit, preparing documentation for international product registrations. We are looking for someone with an RA or Medical Writing background, preferably within an IVD or medica
Laboratory Technician - Grade 4 (Microbiology Team)Title: Laboratory Technician - Grade 4Location: WokinghamStart Date: ASAPEnd Date: 31st January 2026Pay Rate: £13.30 per hourHours: 36 hours per week, 9am - 5pm, Thursday - MondayQualifications:You provide hands-on assistance to support the operation and goals of the laboratory by supporting experiments and projects under technical guidance. What you will bring:A desire to drive your future and accelerate
Laboratory Technician - Grade 4 (Microbiology Team)Title: Laboratory Technician - Grade 4Location: WokinghamStart Date: ASAPEnd Date: 31st January 2026Pay Rate: £13.30 per hourHours: 36 hours per week, 9am - 5pm, Thursday - MondayQualifications:You provide hands-on assistance to support the operation and goals of the laboratory by supporting experiments and projects under technical guidance. What you will bring:A desire to drive your future and accelerate
Do you thrive in a fast-paced, regulated environment and have a passion for detail?This is your opportunity to join a leading pharmaceutical and biotechnology company in Harwell, where you'll play a critical role in ensuring the integrity of documentation and training.As the QA Admin - Document Control & Training, you will:Maintain the heart of our documentation system: You'll oversee the entire lifecycle of controlled documents, including creation, mainte
Do you thrive in a fast-paced, regulated environment and have a passion for detail?This is your opportunity to join a leading pharmaceutical and biotechnology company in Harwell, where you'll play a critical role in ensuring the integrity of documentation and training.As the QA Admin - Document Control & Training, you will:Maintain the heart of our documentation system: You'll oversee the entire lifecycle of controlled documents, including creation, mainte
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