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AccuBio Ltd

Primary Production Scientist

AccuBio Ltd Alva
32 - 40 hour


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    AccuBio Ltd

    Primary Production Scientist

    AccuBio Ltd Alva
    32 - 40 hour
    Status Open
    Apply now

    Apply on the employer's website


    What we ask

    Education

    No minimum education required

    What we offer

    Hours
    32 to 40 hours per week
    Employment type
    permanent

    Job description

    Primary Production Scientist
    Location: On-site, Alva, Clackmannanshire - FK12 5DQ
    Salary: £24,785 - £29,573 per annum (depending on experience) plus benefits
    Contract: Permanent, Full time
    Hours: Monday to Thursday 8.00am – 5.00pm and alternate Fridays 8.00am – 3.30pm
    At Accubio Ltd, we develop and produce innovative diagnostic technologies that make a real difference to global healthcare.
    We’re looking for a Primary Production Scientist to join our team in Alva, playing a hands-on role in manufacturing high-quality medical devices used worldwide.
    Why this role matters:
    As one of our Primary Production Scientists, you’ll play a key role in the production of our lateral flow devices, helping ensure we consistently deliver safe, high-quality medical devices used worldwide.
    You’ll be joining a collaborative and supportive team where quality, innovation, and continuous improvement are at the heart of everything we do.
    What you’ll be doing:
    Your day-to-day will be varied, working within our production laboratories. Key responsibilities include:
    • Manufacture of medical device reagents and components to strict quality standards and in line with planned manufacturing timelines and KPIs.
    • In-process testing of components to ensure compliance with defined parameters at all stages of manufacturing.
    • Operation, cleaning and routine maintenance of laboratory equipment associated with product manufacturing.
    • Completion of batch manufacturing records and associated documentation to the appropriate standard, in compliance with ISO13485 and GMP.
    • Support investigations of out of specification results or product failures where required.
    • Contribute to continuous improvement of documentation and processes.
    • Maintain compliance with QMS policies and procedures.
    • Maintain compliance with Health & Safety policies and procedures.
    What you bring:
    The ideal candidate will be educated to degree level and preferably have at least 1 years’ experience within a GMP based medical device manufacturing environment, or similar industry.
    Essential:
    • A relevant degree or equivalent qualification
    • Strong organisational and time management skills
    • Excellent attention to detail with a methodical approach
    • Clear written and verbal communication skills
    • Ability to work both independently and as part of a team
    Apply now

    Apply on the employer's website

    Apply now

    Apply on the employer's website


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