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Teamleader Analytical Laboratories Stability & Investigations

Date: Jan 14, 2021

Location: Haarlem, NL, 2031 GA

Company: Teva Pharmaceuticals

Company Info

Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

Job Description

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.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.