QC Technician - Microbiology

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity

As QC Technician - Microbiology you will work in the Quality Microbiological laboratory.  You will have the opportunity to hold a varied position, because you will work on tasks like the execution and reviewing of routine and non-routine sample analyses, performing method validations for the purpose of analyses and providing support in the implementation of (validation) project as well as microbiological supervision of production departments, so that the quality requirements are met.

How you’ll spend your day

• Performing  Investigations (gDR), Root Cause Analysis (RCA), trending, Out of Specifications analyses (gLIR)
• Drafting and reviewing of SOP’s
• Advising the management regarding the feasibility of the analysis methods
• Compiling and checking the final microbiology reports
• Training and instructing the operators in the microbiological  activities, troubleshooting for microbiological issues and thereby contribute to improving Quality and GMP behavior.

Your experience and qualifications

You preferably have a bachelor degree in microbiology or life science and you bring experience and knowledge of GMP. Additional experience with identification of microorganisms or Environmental monitoring is expected.

We believe you are a highly motivated professional with experience in a highly regulated industry, preferred in the Pharmaceuticals/Biotech industry.

Fluency in English, Dutch will be an advantage.

On top of all of this you are a team player who want to contribute to laughter, support and work spirit in the team and organization.

What will we offer?

• 25 paid holidays with 11,5 extra days (based on fulltime) with option to use for other purposes like education, cycle plan, etc.
• Competitive salary
• A number of health benefits including like Accident Assurance and Income protection
• 9 weeks of fully paid parenteral leave
• Flexible working conditions with hybrid working policy
• Competitive Pension
• A very diverse International team

Reports To

Group Leader Microbiology

Contact person

Ivo Huijskens - Senior Recruiter Europe

Already Working @TEVA?

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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.

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. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.