GMP Compliance Coordinator — Manufacturing

Lonza Group Ltd.; Geleen; On-site; EUR 41,000 - 58,000; Full time

Benefits offered by this job

Agile career culture

Inclusive workplace

Performance-based compensation

Global benefits

Job summary

Lonza Group Ltd. Geleen, Netherlands, is seeking a Manufacturing Compliance Coordinator to help maintain GMP readiness and support high-quality advanced therapy medicines.

You will work cross-functionally with Manufacturing, Quality Assurance and other teams to investigate quality events, revise GMP documentation, and drive continuous improvement on site. This fully site-based role emphasizes hands-on collaboration and precise execution to sustain regulatory compliance and safe, effective

Qualifications

• Bachelor's degree in Biotechnology or Life Sciences
• Up to four years of experience in manufacturing, pharmaceutical or biotech environments
• Good understanding of current Good Manufacturing Practice (cGMP) and regulated environments
• Strong written and verbal communication in English

Responsibilities

• Maintain readiness for routine GMP inspections and pre-approval inspections.
• Initiate, review and revise batch records, SOPs, protocols and GMP-related documentation.
• Investigate and manage quality events, including deviations, change controls and CAPAs.
• Collaborate with Manufacturing, QA and other stakeholders to resolve quality issues and ensure compliance.
• Support internal and external audits and drive continuous improvement on processes, planning and training.

Skills

Planning

Prioritisation

Problem-solving

Communication in English

Education

Bachelor's degree in Biotechnology or Life Sciences

Job description

Lonza Group Ltd. Geleen, Netherlands, is seeking a Manufacturing Compliance Coordinator to help maintain GMP readiness and support high-quality advanced therapy medicines.

You will work cross-functionally with Manufacturing, Quality Assurance and other teams to investigate quality events, revise GMP documentation, and drive continuous improvement on site. This fully site-based role emphasizes hands-on collaboration and precise execution to sustain regulatory compliance and safe, effective