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Biberach an der Riß

    Pharmacist (m/f/d) - Biberach, Deutschland - GULP – experts united

    GULP – experts united
    GULP – experts united Biberach, Deutschland

    vor 3 Wochen

    GULP - Experts United background
    TEMP_JOB
    Beschreibung

    Are you a scientist or pharmaceutical technician looking for a career change? Is professional security just as important to you as a responsible job and a variety of tasks that you can manage and take responsibility for independently thanks to your experience and expertise? Trust our expertise - we have the right position for you in the pharmaceutical sector : We are currently looking for a Specialist Final Release at our Biberach site. Apply directly online now We value equal opportunities and welcome applications from people with disabilities, whose inclusion is of particular concern to us.

    Here's what we offer

  • Attractive salary package with Christmas and vacation bonuses
  • Reimbursement of travel expenses
  • Vacation entitlement of up to 30 days per year
  • Contribution to company pension scheme after end of probationary period
  • Monthly changing employee offers, e.g. for technology, fashion, cars, etc.

    • Your tasks

  • Support of the qualified person (QP) for investigational medicinal products
  • Reviewing the release documentation for investigational medicinal products
  • Supporting the subsequent certification of the investigational medicinal products by the Qualified Person
  • Documentation of the results of the review and the associated KPIs
  • Contribute to the continuous improvement and optimization of the release process and the systems used in this process
  • Work together with internal and external interfaces in an efficient and goal-oriented manner to jointly resolve open issues
  • Responsible for the assignment and documentation of the batch status, including maintenance of batch-related data in CTSS in accordance with the applicable internal instructions

    • Your profile

  • Completed Master's degree in a scientific program or completed professional training in a pharmaceutical environment
  • Several years of professional experience in one or more of the following fields: Pharmaceutical development, manufacturing, packaging and/or testing
  • Approval in the field of clinical trials or quality assurance
  • Strong knowledge of national and international regulatory requirements for investigational medicinal products and clinical trials as well as the current requirements for good manufacturing practice (cGMP) and quality assurance
  • Very good PC skills (MS Office); knowledge of SAP applications desirable
  • Good written and spoken German and English skills
  • A strong sense of responsibility and ability to work in a team
  • Ability to handle complex contexts successfully, efficiently and carefully
  • Excellent communication skills in local and international teams
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