Quality Control Technician

Analyst I (Quality Control Technician III)

Quality Analytical Laboratory (QAL) | Teva Haarlem | 24/5 Shift Schedule

Position Summary

As an Analyst I (Quality Control Technician III), you will be part of a multi-skilled analytical team performing GMP-regulated testing across several laboratory areas, including In-Process Control, environmental monitoring, raw material testing, release testing, stability testing, and validation-related testing.

In this role, you will perform analytical testing, review and document results, troubleshoot laboratory equipment when needed, and contribute to timely product release in support of Teva's manufacturing operations.

Key Responsibilities

• Perform in-process control testing using techniques such as (U)HPLC, GC, PSD, and other chemical methods.

• Perform daily environmental monitoring testing, including conductivity, TOC, and wet chemical analyses.

• Perform non-routine testing, including finished product release, stability, raw material, and validation-related testing.

• Evaluate, document, and verify analytical results in accordance with GMP requirements and applicable laboratory procedures.

• Support laboratory investigations, deviations, equipment troubleshooting, and analytical problem-solving where required.

• Contribute to effective daily laboratory operations, reliable sample flow, and continuous improvement initiatives.

Analytical Techniques and Systems

Work may include (U)HPLC, GC, UV/VIS, TOC, PSD, conductivity measurements, and various wet chemical tests.

Experience with laboratory systems such as LabWare LIMS v7 and Empower 3 is preferred.

Shift Pattern

The QAL organization includes day-shift activities and a three-shift pattern. This position follows a 24/5 rotating shift schedule aligned with Teva's production schedule. The three-week rotation is repeated continuously:

• Week 1: Sunday to Thursday night shifts, 23:00 to 07:30. Each shift ends the following day.

• Week 2: Monday to Friday evening shifts, 15:00 to 23:30.

• Week 3: Monday to Friday morning shifts, 07:00 to 15:30.

Required Qualifications

• MLO or HLO degree in Analytical Chemistry, Chemistry, Life Sciences, or a related discipline.

• Willingness and ability to work a 24/5 rotating shift schedule.

• Strong attention to detail and a clear focus on quality and compliance.

• Hands-on team player with a practical, solution-oriented approach.

• Fluent spoken and written English.

• Flexible and effective in a changing laboratory and manufacturing environment.

Preferred Experience

• Experience working in a GMP-regulated laboratory environment.

• Experience with chromatographic techniques such as HPLC, UPLC, or GC.

• Experience using LabWare LIMS v7, Empower 3, or comparable laboratory systems.

Let op: vacaturefraude

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* Wij zullen nooit via WhatsApp of in een videogesprek vragen om jouw persoonlijke gegevens (zoals een kopie van je ID, bankgegevens of BSN).
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Important: job fraud

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* We will never ask for personal information (such as a copy of your ID, bank details, or social security number) via WhatsApp or during a video call.
* If you're unsure whether a vacancy or contact person is legitimate, please reach out to us directly using the official contact details on our website.