Analyst 3 – Quality Assurance

Location:

Beerse – Flanders, Belgium

Salary:

market rate

Type:

Contract

Start Date: 

As Soon As Possible

Contract Period: 

To be confirmed.

Main Industry:

Search Health, Nursing & Social Services Jobs

Advertiser:

SEC Recruitment Ltd

Job ID:

132726178

Posted On: 

25 February 2026

Quality Assurance Engineer – Contract

Assignment Overview

The QA Engineer will support the Quality Assurance Engineering function in ensuring that all qualification-related regulatory and procedural requirements are fulfilled throughout the full lifecycle of manufacturing systems (concept, project, operational, and retirement phases).

The role focuses on maintaining compliance and quality standards within a pharmaceutical manufacturing environment.

Key Responsibilities

Qualification & Compliance Oversight

* Review and approve qualification documentation and quality records, including:

* SOPs
* User Requirements Specifications (URS)
* Impact and risk assessments
* Test plans and test scripts
* Change controls
* CAPAs

* Ensure continued compliance with applicable regulations, guidelines, and internal quality standards.

Project & Engineering Support

* Participate in cross-functional engineering teams for the introduction of new or upgraded systems and processes.
* Provide guidance and support in preparing qualification activities.
* Safeguard cGMP compliance throughout project execution.

Deviation & Quality Management

* Address and follow up on deviations occurring during qualification activities.
* Support investigation and resolution processes to maintain compliance standards.

Stakeholder Communication

* Communicate quality, compliance, and planning status updates to QA Qualification team members.
* Collaborate effectively with cross-functional teams across departments.

Candidate Profile

Knowledge & Experience

* Experience in the chemical and/or pharmaceutical industry, specifically in equipment qualification.
* Strong knowledge of cGMP regulations and industry guidelines.
* Ability to translate complex technical information into clear communication suitable for all organizational levels.
* Sound judgement in assessing urgency, criticality, and impact of decisions.
* Ability to manage multiple projects simultaneously.
* Comfortable working independently as well as within cross-functional teams.
* Strong communication and interpersonal skills.

Technical Expertise

* Experience with manufacturing systems in pharmaceutical or chemical environments.
* Familiarity with:

* Problem reporting and change request systems (e.g., TrackWise, Comet)
* Document Management Systems (e.g., TruVault)
* Qualification and test management tools (e.g., Kneat)

Languages

* Fluent in English and Dutch (written and spoken)

Assignment Details

* Start Date: 23 February 2026
* End Date: 31 December 2026
* Business Unit: Pharmaceutical Quality Control (non-IT)
* Location: Geel, Belgium

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