Digital Batch Records QA Specialist

Mindcapture-; Belgique; On-site; EUR 60,000 - 80,000; 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 is seeking a QA Specialist to support the digitalisation of batch records in a multi-product pharmaceutical facility. The role focuses on converting paper records to electronic batch records, ensuring cGMP compliance, and collaborating with manufacturing, quality and project stakeholders.

You will contribute to documentation quality, deviation prevention and risk assessments, while supporting operations across clinical and commercial manufacturing within a consultancy on site at a

Qualifications

• Master’s degree in a scientific discipline or equivalent experience.
• 3–5 years in a GMP-regulated environment, preferably QA roles.
• Strong understanding of cGMP requirements and regulatory standards.

Responsibilities

• Support electronic batch record implementation and transition from paper records.
• Review and approve electronic master batch records within MES.
• Prepare, review and maintain project quality documentation and records.

Skills

GMP knowledge

Electronic Batch Records

Quality Assurance

Documentation skills

Attention to detail

Independent worker

Communication skills

English proficiency

Education

Master’s degree in science

Tools

MES system

Job description

MindCapture is seeking a QA Specialist to support the digitalisation of batch records in a multi-product pharmaceutical facility. The role focuses on converting paper records to electronic batch records, ensuring cGMP compliance, and collaborating with manufacturing, quality and project stakeholders.

You will contribute to documentation quality, deviation prevention and risk assessments, while supporting operations across clinical and commercial manufacturing within a consultancy on site at a