Pharmagend Global Medical Services Pte Ltd Hiring! Full Time Quality Control Laboratory Manager in - Ricebowl

Job Summary – QC Laboratory Manager / QC Manager:

The QC Laboratory Manager is responsible for leading Quality Control laboratory operations to ensure compliance with GMP, regulatory requirements (FDA, USP, EP, ICH, ChP), and company quality standards. The role oversees raw and packaging material testing, laboratory quality systems, instrument lifecycle management, documentation, audits, team leadership, and continuous improvement to support pharmaceutical manufacturing.

Key Responsibilities:

• Lead daily QC laboratory operations, including raw material sampling, testing, release, inventory, and laboratory purchasing.
• Support new product introductions, analytical method validation/transfer, and preparation of specifications and testing procedures.
• Ensure compliance with GMP, regulatory requirements, SOPs, and data integrity standards.
• Lead laboratory investigations, CAPA, change controls, and quality event management.
• Manage laboratory instruments throughout their lifecycle, including qualification, calibration, maintenance, and CAPEX planning.
• Prepare, review, and maintain laboratory documentation, SOPs, validation documents, and training records.
• Ensure audit readiness and support internal, customer, and regulatory inspections.
• Develop and lead the QC team through training, performance management, competency development, and resource planning.
• Support laboratory budgeting and maintain a safe working environment in accordance with EHS requirements.

Qualifications:

• Bachelor's degree or higher in Chemistry, Pharmaceutical Science, Analytical Chemistry, Material Science, or a related field.
• Minimum 8 years of pharmaceutical Quality Control or GMP laboratory experience.
• Minimum 3 years of supervisory or management experience in a GMP-regulated environment.
• Experience in raw material and packaging material testing, method validation/transfer, laboratory investigations, instrument qualification, and audit support is highly preferred.

Core Competencies:

• GMP & regulatory compliance
• Pharmaceutical Quality Control
• Analytical testing and laboratory operations
• Method validation and transfer
• Laboratory investigations & CAPA
• Instrument qualification and lifecycle management
• Documentation & data integrity
• Audit and inspection readiness
• Leadership, coaching, and people development
• Project, budget, and resource management
• EHS and laboratory safety compliance

To apply:

Candidates are encouraged to apply this position via email to ************* with the following information in the resume.

• Work experiences and job responsibilities.
• Current and Expected salary
• Reason for leaving.
• Date of availability
• Education background

We regret that only shortlisted candidates will be contacted.