Lab Equipment Specialist

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

The Quality Analytical Laboratory is responsible for all analytical testing to support the production of Cytotoxic and Inhalation drug products. The laboratory executes various analytical test packages to test APIs, excipients, packaging materials, and drug products for release and stability purposes. The department is also responsible for the transfer, validation, and verification of analytical methods for testing new drug products. A variety of analytical techniques is used (GC, UPLC/HPLC, FT-IR, and UV-VIS). To expand and strengthen this responsibility, the Quality Analytical Laboratory is searching for an Lab Equipment Specialist.

How you’ll spend your day

• Perform daily maintenance and troubleshooting to address issues related to analytical equipment functionality (HPLC, GC, FT-IR, UV-VIS, etc.).
• Analyze root cause of recurring problems and implement corrective actions, ensuring timely response to maintenance and calibration related incidents. 
• Coordinate maintenance & calibration activities to maintain compliance with industry standards, monitoring and optimizing downtime during this tasks.
• Serve as point of contact for external service providers, requesting quotes and managing procurement process for spare parts and services, ensuring vendors performance aligns with organizational quality and safety standards.
• Collaborate with cross-functional teams to prioritize and align facility needs.
• Draft and review Standard Operating Procedures (SOPs) and technical reports for equipment operation in English.
• Manage equipment access rights and perform periodic reviews to maintain data integrity.
• Provide support during internal and regulatory audits.
   

Your experience and qualifications

• A minimum of HBO in chemistry or related fields.
• Experience with scientific analytical approaches.
• Good knowledge of analytical laboratory equipment is required.
• Experience in the Pharmaceutical industry or an equivalent GMP environment for 3-4 years and familiarization with CFR Part 11, and current regulatory guidelines related to instrument calibration. 
• Strong troubleshooting, organizational and communication capabilities are part of your nature.
• Team player with problem-solving and critical thinking approach.
• Ability to multitask and prioritize in a fast-paced environment.
• Proficiency in English is required, both written and spoken.
   

Contact person

Ivo Huijskens - Senior Recruiter 

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.

Reports To

Group Leader QC Analytical 

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

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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.