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


    • 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


    Project Management

    Sub Function

    General Management

    Reports To

    Head of QC Analytical Laboratory

    Already Working @TEVA?

    If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

    The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

    Open Positions from Teva Pharmaceuticals
    Related positions