Quality Assurance & Validation Specialist

☞ Vivid Resourcing

View: 86

Update day: 10-12-2025

Location: Ghent East Flanders

Category: High Technology Quality Assurance / Quality Control

Industry: Engineering Services Pharmaceutical Manufacturing

Position: Mid-Senior level

Job type: Full-time

Loading ...

Job content

Location: Ghent, Belgium

Company: Global leader in production for biomedical, pharmaceutical, food, and technical industries

Salary: Up to €7,000 + Premium Belgium Package

My client are seeking a Quality Assurance & Validation Specialist to help ensure that all biomedical products are manufactured, packaged, stored, and distributed in full compliance with current Good Manufacturing Practices (cGMPs).

You’ll join a collaborative team and report to the Quality and Compliance Manager Biomedical to uphold quality and drive improvements across our operations.

AREA OF RESPONSIBILITY AND RELATED TASKS:

• Quality Assurance

· Disposition of finished product batches & preparation of certificates of analysis

· Incoming release of materials and packaging components

· Investigation and resolution of non-conformances, deviations, and complaints

· Approval of change controls and supplier qualifications

· Management of specifications, QMS documentation and training program

· Performing internal audits

· Support during customer and authority audits, including CAPA follow-up

· Documentation support towards customers

• Validation

· Development of validation masterplans, protocols (IQ/OQ/PQ) and related documentation

· Execution of validation tests and coordination with external partners

· Oversight of process validation activities and QC results

· Ownership of re-qualifications and centralized validation archive

· Contribution to risk assessments (FMEA)

PROFILE

· 2+ years of experience in the (bio)pharmaceutical industry with working knowledge of GMP (EU & US)

· Skilled in root cause analysis and structured problem-solving

· Strong communicator with the ability to influence and collaborate across teams

· Proficient in Dutch and English

Organized, detail-oriented, and proactive

WE OFFER THE OPPORTUNITY AND CHALLENGE

· Impact: Your expertise will directly shape product quality and validation, fueling innovation in life sciences.

· Growth in a Global Leader: Be part of an international organization recognized for its pioneering role for biomedical applications.

· Learning That Lasts: Expand your skill set in GMP compliance, Quality Management Systems and validation technologies in a supportive environment.

If the role sounds interesting and you feel you have the necessary experience please do get in touch with me:

trishan.patel@vividresourcing.com

033180074

Loading ...
Loading ...

Deadline: 09-01-2026

Click to apply for free candidate

Apply

Report job
Loading ...

SIMILAR JOBS

Loading ...
Loading ...