Job Properties
  • Job Type
    Full-time Position
  • Background
    Other Science and Tech
  • Languages
    English
  • Experience Required
    1 - 2 Years
  • Degree Required
    Bachelor
    • Province
      3,321 reviews
    • Date Posted
      February 12,2021
    • VISA
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    • internship package

    QC Technician

    QUALITY CONTROL TECHNICIAN RAW MATERIALS

    Thermo Fisher Scientific Inc. is the world leader in serving science with annual revenue exceeding $ 25 billion.

    Our mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life science research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing productivity in their laboratories, we are here to support them. Our global team of more than 75.000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon. For more information, please visit WWW.thermofisher.com.

    The Mission

    Within Patheon, part of Thermo Fisher Scientific in Tilburg, we are responsible for the development and production of commercial medicines in dosed forms (soft gel capsules). You can think of products such as Paracetamol, Ibuprofen, but also various supplements. The soft gel capsules are available at pharmacies and drug stores but also on a doctor’s prescription. Because everyone contributes to the development and production of out soft gel capsules, we are all responsible to make the world healthier, cleaner and safer.

    Position

    The Raw Material section is a part of the Quality Control Department and ensures that the release testing of Raw Materials is on time to ensure timely production.

    Within the Raw Material section, a width range of tests is performed. Technics which are used are for example:

    HPLC, GC, UV/VIS spectrophotometry, FTIR, Titrimetry.

    Your tasks and responsibilities will be:

    • Analysis of raw materials according to approved regulations according European and United States Pharmacopeia.
    • Accurately recording all activities performed in the laboratory in various logbooks and using computer software, in accordance with GMP guidelines.
    • Support in verification of methods
    • Responsible for analytical equipment
    • Support and maintaining of procedures and working instructions
    • Investigations of deviations and complaints

    Education

    • A completed education MLO/HLO (Analytical/Chemical)

    Knowledge, skills, abilities

    We are looking for a colleague who has:

    • Preferable, a minimum of three-year experience within the pharmaceutical industry (GMP)
    • Good communicating skills (in writing and verbal) in English and Dutch
    • Good knowledge of Microsoft Office

    You are also able to:

    • Plan and organize
    • Work carefully and accurately
    • Collaborate

    What we offer

    We offer you to work in an enthusiastic, young and dynamic team with good training opportunities and personal development. Next to this we offer good secondary employment conditions.

    Job Summary

    • Position

    Quality Control Technician

    • Job Type

    Full-Time

    • Job Location

    Tilburg, Netherlands

     
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