Technician QC Protein Analytics (f/m/d)

WACKER; Amsterdam; On-site; EUR 40,000 - 60,000; Full time

Benefits offered by this job

Attractive salary

Holiday allowance

Home-office travel allowance

Participation in company success

Flexible working hours

30 days of vacation

Support for professional development

Access to online learning platform (GoodHabitz)

Job summary

WACKER, located in Amsterdam, is seeking a Technician QC Protein Analytics to perform laboratory testing and quality control in a GMP environment. The ideal candidate will possess strong analytical skills and be proficient in both Dutch and English.

The role offers an international working environment, flexible hours, 30 days of vacation, and support for professional development. Join us in contributing to the production of biopharmaceuticals with a 100-year legacy.

Qualifications

• Preferably experience in a pharmaceutical/GMP environment.
• Resident of the Netherlands with valid work permit.

Responsibilities

• Perform routine laboratory testing in accordance with SOPs and regulatory requirements.
• Test intermediates, drug substance and drug product using techniques such as HPLC, spectrophotometry, SDS‑PAGE and ELISA.
• Analyze utility samples weekly using TOC, nitrates and conductivity.
• Test raw materials with FTIR, GC and other pharmacopoeia methods when applicable.
• Participate in validation studies for product‑specific methods.
• Participate in stability studies.
• Conduct general laboratory controls, including equipment maintenance, calibration, data review and quality documentation.

Skills

Strong analytical skills

Good communication in Dutch and English

Flexibility

Education

Completed MLO education

Job description

Job Title: Technician QC Protein Analytics (f/m/d)

Job Location: Amsterdam, 1105 BJ, Netherlands

Posting Start Date: 6/2/26

We are WACKER – a leading, research‑intensive chemical company for over 100 years. Wacker Biotech, part of WACKER, specializes in the production of biopharmaceuticals and is the world's largest dedicated microbial CDMO. Our Amsterdam site focuses on GMP‑compliant microbial production of recombinant proteins, vaccines and live microbials.

Job Responsibilities

• Perform routine laboratory testing in accordance with SOPs and regulatory requirements.
• Test intermediates, drug substance and drug product using techniques such as HPLC, spectrophotometry, SDS‑PAGE and ELISA.
• Analyze utility samples weekly using TOC, nitrates and conductivity.
• Test raw materials with FTIR, GC and other pharmacopoeia methods when applicable.
• Participate in validation studies for product‑specific methods.
• Participate in stability studies.
• Conduct general laboratory controls, including equipment maintenance, calibration, data review and quality documentation.

Qualifications Required

• Completed MLO education.
• Preferably experience in a pharmaceutical/GMP environment.
• Strong analytical skills and flexibility.
• Good oral and written communication in Dutch and English.
• Resident of the Netherlands with valid work permit.

What We Offer

• International position in a professional and informal working environment.
• Attractive salary, holiday allowance, home‑office travel allowance and participation in company success.
• Flexible working hours where possible and 30 days of vacation.
• Support for professional development and access to an online learning platform (GoodHabitz).

As an international company, we welcome diversity. We consciously promote equal opportunities and an inclusive culture.

We look forward to receiving your application!

Reference Code: 31019