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Quality Control Analyst - Method Implementation & Transfer

Date: Sep 25, 2021

Location: Haarlem, NL, 2031 GA

Company: Teva Pharmaceuticals

Our company


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!

Your role


The QC analyst is responsible to develop & validate analytical methods to obtain reliable and robust  release testing procedures. Furthermore, the research analyst is involved in non-routine analyses to support investigations as well as the support of submission –related activities for new product introductions into the production department.  Taking into account the experience with complex product testing it is considered that the QC analyst may act as key-expert in trouble-shooting  analytical challenges with this type of products. 

Your responsibilities


  • Perform complex testing 
  • Development, validation, verification and/or remediation of analytical methods 
  • Writing of protocols &reports 
  • Maintain adherence to corporate policies and appropriate regulations through actions and decisions
  • Active participation in advanced problem solving, root cause analysis, troubleshooting, interpretation/consultation, verification of quality and test results discussions
  • First-line Troubleshooting  of laboratory equipment
  • Active participation in changes or act as change owner as part of continuous improvement

Your profile


  • Bachelor  degree in analytical chemistry/pharmacy or equivalent experience
  • Knowledge and familiarity with the use of Pharmacopoeia methods
  • A strong analytical oriented mindset
  • Experience with working in a pharmaceutical environment 
  • Experience with  development/validation or verification of analytical methods for complex drug products like liposomal or protein coated drugs 
  • Experience with UPLC, CD, PSD, FFF is a preference
  • Good knowledge of Pharmaceutical quality systems and production processes
  • Team player
  • Strong can-do mentality

Pre-employment screening


Teva will carry out appropriate verification and legally permitted vetting prior to the confirmation of any offer of employment. More information on this verification and vetting will be provided if you reach this stage of the application process.

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.