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Dudley

    Specialist Analytical Chemist - Dudley, West Midlands, United Kingdom - Sterling Pharma Solutions

    Sterling Pharma Solutions
    Sterling Pharma Solutions Dudley, West Midlands, United Kingdom

    3 weeks ago

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    Description

    As the Analytical Chemist, you will perform analysis and related activities of substances and materials in accordance with safety and compliance regulations such as current Good Manufacturing Practice (cGMP).

    Reporting directly to the QC Department Manager you will be based at our Cramlington site in Northumberland and would welcome applications from graduates with some relevant industry experience.

    Sterling's facility in Cramlington, Northumberland is based 8 miles outside of Newcastle upon Tyne and boasts amazing countryside, alongside stunning beaches and more than 70 castle sites.

    With a wide range of housing from countryside and beachside to city living and village life, our site at Dudley offers a location with something for everyone.

    We are a fast-growing global pharmaceutical CDMO (Contract Development and Manufacturing Organisation), with more than 50 years' experience in developing and manufacturing Active Pharmaceutical Ingredients (APIs).

    We are a proven and trusted partner to some of the world's most innovative biotechs and leading pharmaceutical companies and are widely recognised for our expertise in complex and hazardous chemistry.

    We are a dynamic business, employing more than 1300 talented and passionate people in the UK, US and Europe who together support our customers in bringing new medicines to market, improving and saving the lives of patients.

    We support our customers through the full product lifecycle from pre-clinical development right up to full scale commercial manufacturing and today we are proud to have built a culture of excellence in science and unrivalled service.

    Performing analysis and reporting results in accordance with cGMP requirements.
    Organising the calibration and maintenance of analytical laboratory equipment.
    Performing routine auditing of laboratory areas.
    Carrying out SAP transactions in a timely and accurate manner.
    Characterising reference materials for use in cGMP analysis.
    Liaising with manufacturing, technical, and operational quality personnel on relevant aspects of compliance and analytical atypicality.
    Must have a degree in Chemistry or other relevant scientific discipline.
    Previous laboratory experience is essential, ideally in a GMP environment.
    Must be flexible and able to manage changing priorities.
    Previous experience with Chromatography Data Systems is essential, preferably Chromeleon.

    We also run a variety of programmes across our sites to promote health, wellbeing and work life balance, in addition to supporting causes and charities close to our employees' hearts, encouraging volunteering within the communities we are part of and even arranging socials, through our global social committees, to encourage team building and reward our team's hard work.

    We offer a competitive compensation and benefits package including bonus, pension scheme, private healthcare, Engagement Hub, cycle to work scheme, death in service coverage, on-site health and wellbeing support including medical consultations and physiotherapy, 24/7 employee assistance programme, employee referral scheme, sports and social club as well as opportunity for training and further career development.


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