Quality Control Supervisor

MSN Laboratories; Jakarta Pusat; On-site; IDR 200,000,000 - 420,000,000; Full time

Job summary

MSN Laboratories is seeking a qualified Quality Control Supervisor to oversee daily QC and laboratory activities in Jakarta. You will ensure materials and finished products meet quality standards and review test results.

The role requires a Bachelor's in Chemistry/Analytical Chemistry/Pharmacy with at least 3 years in QC, supervisory experience preferred, and strong knowledge of GMP/GLP and ISO standards. Excellent leadership and communication are essential.

Qualifications

• Candidate holds a Bachelor's degree in Chemistry, Analytical Chemistry or Pharmacy (Apoteker) and has at least 3 years in Quality Control.
• Experience supervising QC in pharmaceutical industries is preferred.
• Strong knowledge of quality control systems, testing, and analytical methods.
• Familiar with laboratory instruments and testing procedures.
• Solid understanding of ISO standards, GMP, GLP and quality management systems.
• Demonstrated leadership, problem solving and decision-making skills.
• Excellent communication and team management abilities.
• Ability to work independently and manage multiple priorities.

Responsibilities

• Supervise and coordinate daily Quality Control and laboratory activities.
• Ensure materials and finished products meet established quality standards.
• Review and approve laboratory test results and QC documentation.
• Monitor laboratory performance and ensure SOP compliance.
• Lead investigations related to OOS/OOT, customer complaints, and quality issues.
• Ensure calibration, maintenance and validation of laboratory equipment.
• Develop and improve QC procedures and laboratory performance.
• Lead, guide and evaluate QC team members.

Skills

Quality control

Laboratory testing

Analytical methods

Leadership

Communication

Team management

Independent work

GMP/GLP knowledge

Education

Bachelors in Chemistry/Analytical Chemistry/Pharmacy

Tools

Laboratory instruments

Job description

• 1. Bachelor's degree (S1) in Chemistry, Analytical Chemistry, Pharmacy (Apoteker)
• 2. Minimum 3 years of experience in Quality Control, preferably with supervisory experience in pharmaceutical industries.
• 3. Strong knowledge of quality control systems, laboratory testing, and analytical methods.
• 4. Familiar with laboratory instruments and testing procedures.
• 5. Good understanding of ISO standards, GMP, GLP, and quality management systems.
• 6. Strong leadership, problem-solving, and decision-making skills.
• 7. Excellent communication and team management abilities.
• 8. Able to work independently and manage multiple priorities.

B. Key Responsibilities:

• 1. Supervise and coordinate daily Quality Control and laboratory activities.
• 2. Ensure raw materials, in-process materials, and finished products meet established quality standards.
• 3. Review and approve laboratory test results and QC documentation.
• 4. Monitor laboratory performance and ensure compliance with SOPs and quality requirements.
• 5. Lead investigations related to OOS, OOT, customer complaints, and quality issues.
• 6. Ensure proper calibration, maintenance, and validation of laboratory equipment.
• 7. Develop and improve QC procedures and laboratory performance.
• 8. Lead, guide, and evaluate QC team members