QA - QA Expert Systems & Compliance

WACKER; Amsterdam; Hybrid; EUR 65,000 - 85,000; Full time

Benefits offered by this job

Attractive salary

30 days of vacation

Flexible working hours

Job summary

WACKER is seeking a QA Expert Systems & Compliance in Amsterdam to manage quality assurance activities and ensure compliance with regulations. You will review qualification documents and participate in multidisciplinary projects. Candidates should have at least a Bachelor's degree in a related field and 3 years of experience in the pharmaceutical industry.

The position offers flexible working hours, a competitive salary, and various development opportunities, promoting a diverse culture.

Qualifications

• Minimum Bachelor degree in the orientation of Analytical Chemistry or related field.
• A minimum of 3 years experience in the pharmaceutical industry.
• Profound knowledge of Dutch and English language, verbal and written.

Responsibilities

• Reviews and approves qualification and validation documents.
• Participates as a QA delegate in multidisciplinary project groups.
• Investigates reported deviations after a quality issue.

Skills

Analytical Chemistry

Microbiology

Biochemistry

Pharmaceutical Sciences

FDA compliance

Education

Bachelor degree in relevant field

Tools

MS Office (Word, Excel, PowerPoint)

Veeva

SAP

Job description

Job Title

QA - QA Expert Systems & Compliance

Location

Amsterdam, NLD, 1105 BJ

Date Posted

Posting Start Date: 6/16/26

Job Description

Apply for the role in Amsterdam: QA - QA Expert Systems & Compliance (Focus: Qualification/Validation). The QA Expert Systems & Compliance reviews qualification/validation documents and coordinates and conducts QA activities.

Job Responsibilities

• Reviews and approves qualification and validation documents in order to prepare the final QA release of equipment, systems, processes and computer systems;


• Ensures, in cooperation with the responsible employees that errors in the documentation are corrected;


• Participates as a QA delegate in multidisciplinary project groups for the purchase, qualification and (re)validation of equipment, systems, processes and computerized systems;


• Reviews protocols, reports, test documents and other relevant documents in order to facilitate the final QA release of equipment, systems, processes and computerized systems;


• Register, calculate, check and assess data as needed to review relevant documentation;


• Participates in research and corrective actions related to quality issues at the request of QA management;


• Carries out spot audits and formulates the follow‑up in collaboration with the relevant departments;


• Participates in external GMP audits and inspections of supply companies, customers and government agencies;


• Investigates reported deviations after a quality issue within production or QC. Coordinates follow‑up;


• Assists in the preparation of annual reports and provides statistical overviews of the release data for the actual release;


• Participates in special interdisciplinary task forces where QA input is desired;


• Supports QA management with regard to all developments in the field of quality, GMP and legal guidelines and plays an important role in further and wider integration of quality in the company.

Qualifications Required

• Minimum Bachelor degree in the orientation of Analytical Chemistry, (Micro)Biology, Biochemistry or Pharmaceutical Sciences;


• A minimum of 3 years experience in the pharmaceutical industry in the field of equipment qualification and related topics;


• Ability to work with tight deadlines and handle multiple tasks;


• Computer fluency in MS Office, e.g. Word, Excel, PowerPoint. Knowledge of Veeva and SAP is a plus;


• Experience with FDA compliance is a plus;


• Profound knowledge of Dutch and English language, verbal and written;


• You reside in and are eligible to work in The Netherlands (valid work permit).

What do we offer?

• Employment: A challenging and international position in a professional and informal working environment;


• Compensation: Attractive salary, holiday allowance, home‑office travel allowance, participation in the company's success, subsidized pension plan;


• Work‑life balance: Flexible working hours (where possible), 30 days of vacation;


• Versatile development opportunities: Support for professional development, access to online learning platform GoodHabitz.

As an international company, we welcome the diversity of people. We consciously promote equal opportunities and a diverse, inclusive culture in our teams – this is what makes us successful.

We look forward to receiving your application!

Reference Code: 31168