QC Leader / Engineer | Chemical MNC | Tuas South

Jobscope:

• Quality Control Oversight – Ensure raw materials, in-process materials, and finished products meet quality standards through inspections and testing.
• QC Laboratory Management – Plan and manage daily QC lab operations, including staffing, scheduling, and resource allocation.
• Data Analysis & Continuous Improvement – Analyze test data to identify trends, improve production processes, and enhance quality systems.
• Product Acceptability Assessment – Review test results and approve only products that meet required specifications.
• Non-Conforming Product Management – Evaluate non-conforming products and collaborate with other departments to implement corrective actions.
• Customer Complaint Handling – Assist in investigating and resolving product quality complaints by identifying root causes and corrective measures.
• QC Reporting – Compile and issue accurate quality control reports for internal review and customer documentation.
• Work Method & Inspection Plan Review – Regularly assess and optimize inspection plans and testing methods for continuous process improvement.
• New Product & Equipment Testing – Oversee testing of new products and ensure proper setup and calibration of laboratory equipment.

Requirements:

• Minimum Honours Degree in a relevant science discipline
• Preferably with 3-5 years of relevant experience in QA/QC functions in chemical, pharmaceutical or similar industry
• Experience in laboratory management
• Possess strong analytical thinking skills and good attention to details

To find out more about this opportunity, please contact Fiona at [email protected]
We regret that only shortlisted candidates will be notified.

GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Fiona Koh | Registration No: R1109239

Jobscope:

• Quality Control Oversight – Ensure raw materials, in-process materials, and finished products meet quality standards through inspections and testing.
• QC Laboratory Management – Plan and manage daily QC lab operations, including staffing, scheduling, and resource allocation.
• Data Analysis & Continuous Improvement – Analyze test data to identify trends, improve production processes, and enhance quality systems.
• Product Acceptability Assessment – Review test results and approve only products that meet required specifications.
• Non-Conforming Product Management – Evaluate non-conforming products and collaborate with other departments to implement corrective actions.
• Customer Complaint Handling – Assist in investigating and resolving product quality complaints by identifying root causes and corrective measures.
• QC Reporting – Compile and issue accurate quality control reports for internal review and customer documentation.
• Work Method & Inspection Plan Review – Regularly assess and optimize inspection plans and testing methods for continuous process improvement.
• New Product & Equipment Testing – Oversee testing of new products and ensure proper setup and calibration of laboratory equipment.

Requirements:

• Minimum Honours Degree in a relevant science discipline
• Preferably with 3-5 years of relevant experience in QA/QC functions in chemical, pharmaceutical or similar industry
• Experience in laboratory management
• Possess strong analytical thinking skills and good attention to details

To find out more about this opportunity, please contact Fiona at [email protected]
We regret that only shortlisted candidates will be notified.

GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Fiona Koh | Registration No: R1109239