Quality Consultant (Fixed – Term Contract)

Job description

1. Perform QMS and regulatory compliance assessments across the product lifecycle.
2. Strengthen key quality systems including deviations, CAPA, change control, and data integrity.
3. Improve manufacturing, validation, laboratory, and warehouse quality processes.
4. Lead risk management activities and maintain an effective site risk register.
5. Drive audit readiness through audits, training, and timely, robust CAPA closure.

Requirements

1. Proven experience as a quality consultant / quality lead in regulated manufacturing environments (FMCG / pharma / healthcare).
2. Strong working knowledge of GMP, GLP, GDP, data integrity, and validation requirements.
3. Hands-on expertise in QMS implementation, audit management, and continuous improvement.
4. Ability to work on-site at least 3 days per week and support corporate quality audits.
5. Willingness to sign NDA and participate in weekly review meetings with management, delivering clear documentation and reports.

When applying

Submit your resume.