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    Analytical Chemist - United Kingdom - Kindeva Drug Delivery Company

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    Description

    Posted Monday, January 8, 2024 at 5:00 AM

    Kindeva is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch Technologies. We partner with our customers to improve patient outcomes around the world. Together, as One Team, we will manufacture many more tomorrows.

    We are currently looking for Analytical Chemist to join our R&D organisation in Loughborough, Charnwood Campus.

    Overall Mission

    The Kindeva Drug Delivery Ltd. site in Loughborough manufactures and packages pharmaceutical and medical products in various forms.

    This role will be working as part of a team responsible for the testing and development of new inhalation pharmaceutical products as part of a successful R&D organisation.

    Key Job Responsibilities

    Customer at the core

    • Coordinate, drive and carry out analytical testing compliant with GMP regulations, delivering to plan on time in full.
    • Input protocol design to deliver robust data and outcomes whilst working in a fast, flexible environment, with a strong focus on right first time.
    • Produce laboratory investigation reports (preliminary) and/or Quality incident reports
    • Represent the department as and when required, including greeting and interacting with both internal and external customers and regulators.

    Safety

    • Promote a "safety first" culture and environment
    • Raise and report any safety incident as required
    • Complete Corrective Action Preventative Action (CAPA) closures on time in full

    Knowledge & Skills

    • Experience in pharmaceutical product testing
    • Testing of pressurised metered dose inhalers is preferable
    • Method development and validation of analytical methods is desirable
    • Good understanding of GMP and GLP
    • Knowledge of Analytical Chemistry and its practical application
    • Working knowledge of Analytical instrumentation, preferably GC, MS, UPLC and UV. HPLC knowledge is essential.
    • Understanding of basic statistics and experimental design, desirable
    • Computer literate, familiar with Microsoft Word and Excel
    • Strong verbal and numerical aptitude skills
    • Strong team player with the ability to work independently

    Key Capabilities

    • Good organisational, interpersonal, and time management skills
    • Enthusiastic, flexible, conscientious and proactive in approach
    • To work efficiently with supervision or unsupervised as required
    • Take a positive approach to own training and development

    Qualifications

    • Ideally a degree (or higher) in a relevant scientific discipline with practical laboratory elements (or equivalent) or relevant previous experience
    #J-18808-Ljbffr

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