1,121 Qc Supervisor jobs in Singapore

Location: 15 Joo Koon Circle

Job Summary:

In this role, you will

• Be accountable for day-to-day performance of team/s safety, quality, delivery, cost and productivity

• Manage teams of QC Technicians & Team Leads in execution of QC processes, schedule and personnel to ensure smooth operational activities work-flow and work compliance

• Promote better quality mindset through inter-department collaborations

Essential Duties and Responsibilities:

• Oversee resource management and team schedules for smooth execution of daily operational tasks in QC while meeting daily inspection targets and support Work In Progress (WIP) controls within team/s

• Ensure proper product release and rework activities per procedures to support delivery requirements

• Lead product characteristics trend monitoring with effective escalation and follow-ups

• Demonstrate leadership, teamwork, and problem-solving support to resolve escalated operational issues collaboratively and ensure proper batch segregation

• Define goals, clearly communicate these objectives and monitor/correct/recognize work performance respectively. Coach and counsel QC employees

• Manage and resolve QC employee's relation issues and disputes

• Manage onboarding activities for new QC employees for training and qualification

• Manage ongoing activities for existing QC employees for training and requalification

• Identify future training needs and enhance QC employees career opportunities

• Responsible to review SOI revisions to enhance improvements for better workflow

• Manage Deviation/Out-of-Spec report closures, batch dispositions while ensuring proper root cause analysis and CAPA identification

• Accountable for on time operational updates for Tier 1, Tier 2, Tier 2.5 & Tier 3 of the LDMS system

• Attend Tier 2, Tier 2.5 as QC representative, and facilitate Tier 1 (Shift Start Up) within QC

• Promote and support site initiatives including safety programs, lean initiatives, training programs and consistently interpret and apply policies, procedures among employees

• Manage non-routine requests from departments (eg validations, investigations, improvements, projects, product transfers, non-routine testings, non-conformance reports, etc)

• Other duties as assigned by superior

Basic Qualifications:

• Academic qualification of bachelor's degree in engineering or relevant fields

• Computer literate and good grasp of Microsoft Office

• Preferably 8 years work experience in QA/QC related activities

• Added advantage with SAP, cGMP, Basic Lean and/or ISO working experience

• Preferably with exposure to medical device, pharmaceutical or related manufacturing environment

• Preferably minimum 5 years work experience managing a QC team

• Able to work independently with minimum supervision

Preferred Knowledge, Skills and Abilities:

• Able to be aware of all relevant standard operating procedures as per Company policy

• Support and contribute to Lean Sigma programs and activities towards delivery of the set target

  • Minimize waste, always ensure efficient work execution by continuous improvements

• Able to comply with the company’s safety policy at all times

  • Ensure use of Personal Protective Equipment (PPE) in respective work environments for all members within the shift/s

  • Report unsafe conditions or acts to responsible persons for corrections and improvements

  • Ensure risk assessment control practices are adopted per HIRA for all members within the shift/s

  • Ensure all legal licenses required for the proper usage of QC equipment are effective for all members within the shift/s

• Able to comply with the company’s quality policy at all times

  • Lead monitoring / improvement activities to enhance operational support activities

  • Participate in establishment and maintenance of documented procedure

• Excellent communication & teamwork skills

• Self-motivated and positive thinking

• Ability to remain calm and professional under pressure

• Proficiency in workplace English for work applications and interfaces

• Time management skills

Physical and Mental Requirements:

• Manufacturing environment with rotating working shift patterns

• Overtime and being on-call are required. Occasionally required to work on different shift patterns

• 20/30 Vision minimum, at near and/or far with at least one eye with or without corrective lenses and no color deficiency

Job Duties and Responsibilities:

Quality Functions:

• Responsible for the operations of the Quality Control Lab.
• Ensure that all lab analyses (starting materials, packaging materials, intermediates and finished products, stability samples etc.) are done in a timely manner, according to established test method and to provide accurate results.
• Prepare or revise Standard Operating Procedures (SOPs) relevant to product quality.
• Prepare or revise Specifications, Test Methods and Quality Control Procedures for all starting materials, intermediates and finished products.
• Ensure the maintenance of reference and retention samples
• Ensure that on-going stability studies are conducted for finished products as per cGMP requirements
• Perform sampling and testing of Starting Materials (Packaging) in accordance with Standard Operating Procedures (SOPs) in a timely manner.
• Perform Product testing in accordance with Standard Operating Procedures (SOPs) in a timely manner.
• Perform Analytical Method Validation and Cleaning Method Validation
• Assist in validation or revalidation of manufacturing processes
• Handle installation, operation, calibration and maintenance of lab instruments.
• Maintain good lab practice, lab safety, inventories and housekeeping programs.
• Participate in the investigation of product complaint in evaluation of returned goods relating to product quality.
• Perform supplier qualification.
• Conduct and coordinate Out-Of-Specification/Deviations/atypical results investigation.
• Review Changes, Deviations, Corrective and /or Preventive Actions as Area/Process Owner.
• Ensure that the required initial and continued training is carried out to quality control personnel.
• Maintain all Quality Control documents and records.

Requirements:

• Candidate must possess a Degree in a relevant Science field or related discipline
• Lab experience in a Chemistry related field
• Hands-on experience in GC
• Must have experience in Analytical Method Validation
• Knowledge of GLP
• Meticulous, Independent, takes initiative and able to multi-task
• Good communication skills.

This position may have to undertake some of the responsibilities of the QA in his/her absence.

Job Duties and Responsibilities:

Quality Functions:

• Responsible for the operations of the Quality Control Lab.
• Ensure that all lab analyses (starting materials, packaging materials, intermediates and finished products, stability samples etc.) are done in a timely manner, according to established test method and to provide accurate results.
• Prepare or revise Standard Operating Procedures (SOPs) relevant to product quality.
• Prepare or revise Specifications, Test Methods and Quality Control Procedures for all starting materials, intermediates and finished products.
• Ensure the maintenance of reference and retention samples
• Ensure that on-going stability studies are conducted for finished products as per cGMP requirements
• Perform sampling and testing of Starting Materials (Packaging) in accordance with Standard Operating Procedures (SOPs) in a timely manner.
• Perform Product testing in accordance with Standard Operating Procedures (SOPs) in a timely manner.
• Perform Analytical Method Validation and Cleaning Method Validation
• Assist in validation or revalidation of manufacturing processes
• Handle installation, operation, calibration and maintenance of lab instruments.
• Maintain good lab practice, lab safety, inventories and housekeeping programs.
• Participate in the investigation of product complaint in evaluation of returned goods relating to product quality.
• Perform supplier qualification.
• Conduct and coordinate Out-Of-Specification/Deviations/atypical results investigation.
• Review Changes, Deviations, Corrective and /or Preventive Actions as Area/Process Owner.
• Ensure that the required initial and continued training is carried out to quality control personnel.
• Maintain all Quality Control documents and records.

Requirements:

• Candidate must possess a Degree in a relevant Science field or related discipline
• Lab experience in a Chemistry related field
• Hands-on experience in GC
• Must have experience in Analytical Method Validation
• Knowledge of GLP
• Meticulous, Independent, takes initiative and able to multi-task
• Good communication skills.

This position may have to undertake some of the responsibilities of the QA in his/her absence.

Location: 15 Joo Koon Circle

Job Summary:

In this role, you will

• Be accountable for day-to-day performance of team/s safety, quality, delivery, cost and productivity

• Manage teams of QC Technicians & Team Leads in execution of QC processes, schedule and personnel to ensure smooth operational activities work-flow and work compliance

• Promote better quality mindset through inter-department collaborations

Essential Duties and Responsibilities:

• Oversee resource management and team schedules for smooth execution of daily operational tasks in QC while meeting daily inspection targets and support Work In Progress (WIP) controls within team/s

• Ensure proper product release and rework activities per procedures to support delivery requirements

• Lead product characteristics trend monitoring with effective escalation and follow-ups

• Demonstrate leadership, teamwork, and problem-solving support to resolve escalated operational issues collaboratively and ensure proper batch segregation

• Define goals, clearly communicate these objectives and monitor/correct/recognize work performance respectively. Coach and counsel QC employees

• Manage and resolve QC employee's relation issues and disputes

• Manage onboarding activities for new QC employees for training and qualification

• Manage ongoing activities for existing QC employees for training and requalification

• Identify future training needs and enhance QC employees career opportunities

• Responsible to review SOI revisions to enhance improvements for better workflow

• Manage Deviation/Out-of-Spec report closures, batch dispositions while ensuring proper root cause analysis and CAPA identification

• Accountable for on time operational updates for Tier 1, Tier 2, Tier 2.5 & Tier 3 of the LDMS system

• Attend Tier 2, Tier 2.5 as QC representative, and facilitate Tier 1 (Shift Start Up) within QC

• Promote and support site initiatives including safety programs, lean initiatives, training programs and consistently interpret and apply policies, procedures among employees

• Manage non-routine requests from departments (eg validations, investigations, improvements, projects, product transfers, non-routine testings, non-conformance reports, etc)

• Other duties as assigned by superior

Basic Qualifications:

• Academic qualification of bachelor's degree in engineering or relevant fields

• Computer literate and good grasp of Microsoft Office

• Preferably 8 years work experience in QA/QC related activities

• Added advantage with SAP, cGMP, Basic Lean and/or ISO working experience

• Preferably with exposure to medical device, pharmaceutical or related manufacturing environment

• Preferably minimum 5 years work experience managing a QC team

• Able to work independently with minimum supervision

Preferred Knowledge, Skills and Abilities:

• Able to be aware of all relevant standard operating procedures as per Company policy

• Support and contribute to Lean Sigma programs and activities towards delivery of the set target

  • Minimize waste, always ensure efficient work execution by continuous improvements

• Able to comply with the company’s safety policy at all times

  • Ensure use of Personal Protective Equipment (PPE) in respective work environments for all members within the shift/s

  • Report unsafe conditions or acts to responsible persons for corrections and improvements

  • Ensure risk assessment control practices are adopted per HIRA for all members within the shift/s

  • Ensure all legal licenses required for the proper usage of QC equipment are effective for all members within the shift/s

• Able to comply with the company’s quality policy at all times

  • Lead monitoring / improvement activities to enhance operational support activities

  • Participate in establishment and maintenance of documented procedure

• Excellent communication & teamwork skills

• Self-motivated and positive thinking

• Ability to remain calm and professional under pressure

• Proficiency in workplace English for work applications and interfaces

• Time management skills

Physical and Mental Requirements:

• Manufacturing environment with rotating working shift patterns

• Overtime and being on-call are required. Occasionally required to work on different shift patterns

• 20/30 Vision minimum, at near and/or far with at least one eye with or without corrective lenses and no color deficiency

Job Description

· Control and communicate with batching plant for concrete works.

· Site quality inspection for any on-going works at all locations for concrete works.

· Off-site and On-site quality inspection for Structural Steel works.

· Lead and supervise QC inspectors providing guidance and support to meet quality standards while overseeing daily QC inspection activities.

· Maintenance and calibration of measuring equipment.

· Document inspection results by completing reports and logs.

· Summarizing rework and waste.

· Inputting data into a quality database.

· Maintain a safe and healthy working environment by following standards and procedures; and complying with legal regulations

· Perform any other related duties as assigned by QAQC Manager.

Requirements

· Certificate/ITE/NITEC/ Higher NITEC in QC/ Precision Engineering or equivalent.

· Minimum 5 years relevant experience in QC Civil & Structural for LTA projects

· Ability to read and interpret drawings with a good understanding of geometric dimension and tolerance.

· Team player with a dependable attitude.

Job Highlight

• Location: Tuas Crescent MRT
• Salary: Up to S$3,500 + Variable Bonus
• Working Hours: 7.45 a.m. – 4.45 p.m. (Monday – Friday)

About the Role

Our client is looking for a motivated and detail-oriented QC Supervisor to join our team. You will lead and guide the QC laboratory team, ensuring quality standards are upheld throughout raw material checks, in-process inspections, and finished product testing. This role offers career stability in a regulated manufacturing environment with opportunities to support continuous improvement.

Key Responsibilities

• Supervise and coach QC lab technicians, providing guidance and support.
• Inspect incoming raw materials for compliance with standards.
• Conduct periodic checks and analysis on work-in-progress (WIP) materials.
• Retain and test finished product samples to ensure compliance.
• Assist QA in failure analysis, CAPA (Corrective & Preventive Actions), and response to customer complaints.
• Support GMP audits, validation, qualification, and change control processes.
• Assist in maintaining Product Quality and Technical Files.
• Prepare reports, technical papers, and specifications for products, processes, and tests.

Requirements

• Diploma in Chemical Process Technology, Biotechnology, or related field; or Bachelor's Degree in Chemistry / Quality Assurance.
• Minimum 1 year of supervisory experience in QC.
• Strong understanding of quality standards in a GMP-regulated environment.

What We Offer

Career stability in a growing manufacturing company

Variable bonus and benefits

Opportunities to build your expertise in QC and QA functions

Interested candidate may submit full resume to 6990 0434 (WhatsApp - Miya) and only shortlisted candidate will be notified.

By submitting your personal data and/or resume, you give consent to collection, use and disclosure of your personal data and/or resume by the company (or its agent) for the purpose of the processing and administration by the company relating to this job application.

Kuan Mei Yang

Registration Number: R24124509

EA License No: 06C2859 (MCI Career Services Pte Ltd)