Pharma QA Specialist – EU GMP & QMS Expert

Akkodis; Waals-Brabant; Hybrid; EUR 75,000 - 95,000; Full time

Benefits offered by this job

Permanent contract

13.92 months of salary

Company car or mobility budget

Flexible cafeteria plan

Training and development opportunities

Job summary

Akkodis is seeking a Quality Assurance expert in Belgium to lead GMP compliance and quality systems. You will review GMP documentation, manage deviations and CAPAs, and support supplier quality management across multiple functions in a fast-paced pharmaceutical setting.

Ideal candidates hold a strong background in EU GMP and regulatory expectations, with at least five years of QA experience in life sciences.

Qualifications

• 5+ years of Quality Assurance experience in pharma, biotech or life sciences.
• Strong knowledge of EU GMP, GDP and regulatory expectations.
• Experience approving GMP documentation and supporting validation activities.
• Experience with supplier quality management and audits.

Responsibilities

• Implement and maintain Pharmaceutical Quality System per EU GMP, GDP and company standards.
• Review and approve GMP documentation including SOPs and batch records.
• Manage deviations, CAPAs, change controls and investigations with timely closure.

Skills

QA experience

GMP knowledge

Regulatory knowledge

Stakeholder management

ALCOA+

Education

Master's or Bachelor's degree in Pharmacy, Chemistry, Biology, Biotechnology, Biomedical Sciences or related

Tools

eQMS systems

Job description

Akkodis is seeking a Quality Assurance expert in Belgium to lead GMP compliance and quality systems. You will review GMP documentation, manage deviations and CAPAs, and support supplier quality management across multiple functions in a fast-paced pharmaceutical setting.

Ideal candidates hold a strong background in EU GMP and regulatory expectations, with at least five years of QA experience in life sciences.