Lead Quality & Batch Release Expert (QP)

Anotech Energy company; Belgique; Remote; EUR 110,000 - 150,000; Full time

Job summary

Anotech Energy, a leading healthcare and pharmaceutical organization, seeks a Quality Control Manager/QP for its Belgium pharmaceutical manufacturing site. The role combines operational quality leadership, batch release, and project management with GMP compliance.

Reporting to the Pharmaceutical Affairs Director, you will act as the primary quality representative on site, lead a multidisciplinary quality team, supervise deviations and audits, and drive improvement across processes and analytical

Qualifications

• Master's Degree in Pharmacy or Pharmaceutical Sciences.
• Qualified Person (QP) certification is required.
• Minimum 8 years experience as a Qualified Person in pharma manufacturing.
• Strong GMP/GLP knowledge and CAPA experience.
• Proven leadership and people management capabilities.
• Fluent Dutch and English; French is a plus.

Responsibilities

• Act as the Qualified Person (QP) for pharmaceutical manufacturing operations.
• Ensure batch certification and release per GMP and marketing authorizations.
• Review and approve batch documentation and quality records.
• Lead, coach and develop a multidisciplinary quality team.
• Oversee deviations, CAPA, OOS investigations and product complaints.
• Coordinate internal and external audits and regulatory inspections.
• Lead site projects related to new products and processes.
• Ensure lab instruments and quality systems remain compliant and qualified.

Skills

Leadership

People management

Analytical skills

Problem solving

Dutch-English fluency

Education

Master's Degree in Pharmacy or Pharmaceutical Sciences

Qualified Person (QP) certification

8+ years QP experience

Job description

Anotech Energy, a leading healthcare and pharmaceutical organization, seeks a Quality Control Manager/QP for its Belgium pharmaceutical manufacturing site. The role combines operational quality leadership, batch release, and project management with GMP compliance.

Reporting to the Pharmaceutical Affairs Director, you will act as the primary quality representative on site, lead a multidisciplinary quality team, supervise deviations and audits, and drive improvement across processes and analytical