Job Properties
  • Job Type
    Full-time Position
  • Background
    Biotech and Agricultural
    Engineering
    Medical and Healthcare
    Other Science and Tech
  • Languages
    English
  • Experience Required
    1 - 2 Years
  • Degree Required
    Bachelor
    • Province
      1,267 reviews
    • Date Posted
      January 19,2021
    • VISA
    • IMG_6430
    • IMG_6430
    • Career Consultation
    • COVERLETTER CHECK
    • CV CHECK
    • internship package

    Teamleader Analytical Laboratories Stability & Investigations

    1. Manage Stability & Investigation

    • Guide team in Stability & investigation strategies
    • Guide team in implementation of Pharmaceutical and Dossier compliance tasks
    • Manage the team in establishing and maintaining quality at the lab in accordance with Site SOP’s, regulatory guidelines and cGXP compliance requirements.
    • Maintain a culture of enhancing quality throughout the entire Laboratory. Performance of in-depth root cause analyses and problem solving
    • Act as SME during regulatory and internal audits.
    • Responsible for intercompany communication with external TEVA Global Analytical Stability Laboratory
    • Responsible for adherence to planning and execution of stability programs for commercial drug products.

    2. Manage Team and Resources

    • Manage own team through talent identification, active performance management, succession planning, employee development, mentoring and modeling behavior according to Teva values.
    • Run an efficient and effective QC Stability& Investigation team through managing the team budget and resources.

    3. Manage of Culture of Safety

    • Maintain a culture of enhancing safety throughout the entire Laboratory.
    • Review and provide options to meet business needs without compromising health & safety.

    Qualifications

    • Bachelor or Master degree in analytical chemistry/pharmacy or equivalent experience
    • Good Knowledge with the use of ICH guidelines and Pharmacopoeia methods
    • Excellent organizational skills and a strong analytical oriented mindset.
    • Experience with working in a pharmaceutical environment
    • Solid experience with equivalence, method validation or method verification studies
    • Management Experience is preferred (2-3 yrs)
    • Good knowledge of Pharmaceutical quality systems and production processes
    • Good scientific analytical attitude
    • Excellent written and verbal communication skills
    • Pro-active team player
    • Results oriented

    Function

    Project Management

    Sub Function

    General Management

    Reports To



    Head of QC Analytical Laboratory

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