Third-Party Quality Lead: Supplier Oversight (GxP)

MindCapture BV; Belgique; On-site; EUR 60,000 - 85,000; Full time

Benefits offered by this job

Meal vouchers

Eco vouchers

Health insurance

Group insurance

Net expense allowance

Company car with charging or fuel card

Job summary

MindCapture BV is seeking a Medior Third Party Quality Specialist to ensure qualification, oversight and continuous improvement of external service providers within a regulated life sciences environment.

You will assess supplier compliance, manage quality agreements, and monitor performance, with a focus on computerised systems validation and regulatory expectations. On-site work with our client in Antwerp, with clear onboarding and ongoing support.

Qualifications

• Minimum 2 years in a GxP regulated environment with focus on third party quality management.
• Familiarity with FDA 21 CFR Part 11, EU Annex 11 and GAMP 5 is preferred.
• Strong supplier quality management and risk assessment capabilities.
• Excellent communication with internal stakeholders and external suppliers.
• Fluency in Dutch and English (written and spoken).
• Experience with computerised systems validation (CSV) is a plus.

Responsibilities

• Assess third party suppliers for suitability and compliance.
• Manage quality agreements and contractual quality clauses.
• Monitor supplier performance and maintain supplier database.
• Contracted on site and remote qualifications of external providers.
• Lead continuous improvement initiatives in supplier quality processes.

Skills

Regulatory knowledge

Supplier quality management

Risk assessment

Communication skills

Dutch language

English language

Documentation skills

CSV knowledge

Education

Bachelor’s or Master’s degree in Life Sciences/Engineering/CS

Job description

MindCapture BV is seeking a Medior Third Party Quality Specialist to ensure qualification, oversight and continuous improvement of external service providers within a regulated life sciences environment.

You will assess supplier compliance, manage quality agreements, and monitor performance, with a focus on computerised systems validation and regulatory expectations. On-site work with our client in Antwerp, with clear onboarding and ongoing support.