665 Quality Assurance Specialist jobs in Singapore

Job Responsibilities:

• Contribute to Life Science projects for Antaes Asia clients.
• Perform detailed reviews of raw materials, intermediate products, and finished products for compliance with quality specifications.
• Manage the release process by ensuring all quality checks are completed before approving materials and products for use or distribution.
• Ensure that all batch records and associated documentation are reviewed and meet regulatory requirements before product release.
• Provide on-site quality oversight during the manufacturing process, ensuring that all operations comply with Good Manufacturing Practices (GMP) and company quality standards.
• Collaborate with manufacturing teams to address any quality-related issues that arise during production and ensure prompt resolution.
• Conduct regular GEMBA (on-site workplace observation) and GMP (Good Manufacturing Practice) walk-throughs of the manufacturing floor to identify potential quality risks, ensure compliance, and promote a culture of continuous improvement.
• Document findings from walk-throughs and collaborate with the relevant teams to implement corrective actions where necessary.
• Review, revise, and approve Standard Operating Procedures (SOPs), forms, and Manufacturing Batch Records to ensure they are up to date and compliant with current regulations and company policies.
• Ensure that all documentation aligns with current industry standards and best practices in pharmaceutical manufacturing.
• Contribute to the promotion of Antaes services on top of assistance provided to clients.

Job Requirements:

• Bachelor’s degree in Biotechnology, Pharmaceutical or related field.
• 3-5 years of experience in quality assurance within the pharmaceutical or biotechnology industry.
• Experience with product and raw material release processes and related documentation.
• Strong knowledge of GMP (Good Manufacturing Practices) and regulatory compliance.
• Hands-on experience in conducting GEMBA or GMP walk-throughs and identifying quality risks.
• Proficient in reviewing and approving procedures such as SOPs, forms, and batch records.
• Strong attention to detail and ability to work in a fast-paced, regulated environment.
• Excellent communication and collaboration skills to work with cross-functional teams.
• Good communication and problem-solving skills.

CDI

Job Description:

• Contribute to Life Science projects for Antaes Asia clients
• Perform detailed reviews of raw materials, intermediate products, and finished products for compliance with quality specifications.
• Manage the release process by ensuring all quality checks are completed before approving materials and products for use or distribution.
• Ensure that all batch records and associated documentation are reviewed and meet regulatory requirements before product release.
• Provide on-site quality oversight during the manufacturing process, ensuring that all operations comply with Good Manufacturing Practices (GMP) and company quality standards.
• Collaborate with manufacturing teams to address any quality-related issues that arise during production and ensure prompt resolution.
• Conduct regular GEMBA (on-site workplace observation) and GMP (Good Manufacturing Practice) walk-throughs of the manufacturing floor to identify potential quality risks, ensure compliance, and promote a culture of continuous improvement.
• Document findings from walk-throughs and collaborate with the relevant teams to implement corrective actions where necessary.
• Review, revise, and approve Standard Operating Procedures (SOPs), forms, and Manufacturing Batch Records to ensure they are up to date and compliant with current regulations and company policies.
• Ensure that all documentation aligns with current industry standards and best practices in pharmaceutical manufacturing.
• Contribute to the promotion of Antaes services on top of assistance provided to clients.

Job Requirements:

• Bachelor’s degree in Biotechnology, Pharmaceutical or related field
• 3-5 years of experience in quality assurance within the pharmaceutical or biotechnology industry
• Experience with product and raw material release processes and related documentation
• Strong knowledge of GMP (Good Manufacturing Practices) and regulatory compliance
• Hands-on experience in conducting GEMBA or GMP walk-throughs and identifying quality risks
• Proficient in reviewing and approving procedures such as SOPs, forms, and batch records
• Strong attention to detail and ability to work in a fast-paced, regulated environment
• Excellent communication and collaboration skills to work with cross-functional teams
• Good communication and problem-solving skills

Our positions are open to people who have been recognized as disabled workers. T&S Group promotes diversity and equality in the workplace. All qualified M/F candidates are considered for employment on an equal basis.

Job Title: Quality Assurance Specialist

The primary responsibility of the Quality Assurance Specialist is to ensure that products meet the required quality standards. This involves leading a team of inspectors, implementing and maintaining quality control policies, and overseeing sampling and inspections.

Key Responsibilities:

• Lead a team of inspectors to achieve quality goals.
• Develop and implement quality control procedures.
• Conduct regular audits to identify areas for improvement.
• Collaborate with production teams to resolve quality issues.
• Maintain accurate records and provide regular reports to management.

Required Skills and Qualifications:

• At least 1-2 years of experience in manufacturing quality assurance.
• Familiarity with quality control tools and equipment.
• Excellent communication and leadership skills.

Benefits:

• A permanent role with opportunities for professional growth.
• A competitive salary package.
• The chance to work in a dynamic and fast-paced environment.

How to Apply:

• Submit your application by clicking the 'Apply' button.
• Email your resume to

Job Title: Quality Assurance Specialist

We are seeking a highly skilled Quality Assurance Specialist to join our team. The successful candidate will be responsible for planning, coordinating and performing inspection works on newly installed and existing equipment under maintenance contracts.

Key Responsibilities:

• Assist the management/senior engineer in technical aspects of the equipment
• Carry out inspections on newly installed equipment and equipment under maintenance
• Attend to safety and performance-related breakdowns of equipment
• Plan and implement new measures to improve performance of equipment
• Investigate and submit reports on the technical failures of equipment
• Act as calibration committee member when assigned by senior manager and ensure all instruments within the department are properly documented and calibrated
• Assist in technical training of subordinates within the department
• Perform any other duties as assigned by superior

Requirements:

• Experience in lift industry is advantageous
• Degree in Electrical Engineering or equivalent qualification

This role requires strong analytical skills, attention to detail, excellent communication and interpersonal skills. You must be able to work effectively in a team environment and have a positive attitude towards continuous learning and improvement.

About This Job:

This is an exciting opportunity for a motivated and experienced Quality Assurance Specialist to take on a key role in our organization. If you have a passion for quality assurance and a desire to make a real difference, we encourage you to apply.

What We Offer:

• A competitive salary package
• Ongoing professional development opportunities
• A dynamic and supportive work environment
• The chance to work with a talented team

Quality Assurance Specialist

We are seeking a highly motivated Quality Assurance Specialist to join our team. The successful candidate will be responsible for ensuring the highest quality standards are met in all aspects of our operations.

• Develop and implement quality control procedures to ensure compliance with industry standards.
• Conduct regular audits and inspections to identify areas for improvement.
• Collaborate with cross-functional teams to resolve quality-related issues.
• Implement corrective actions to prevent recurrence of quality issues.

• At least 1-3 years of quality assurance experience.
• Min. Diploma / Degree in a relevant field.
• Able to perform overtime when necessary.

• Competitive salary range: SGD $2500 - $3500.
• Opportunities for professional growth and development.
• A dynamic and supportive work environment.

If you are a motivated and detail-oriented individual looking for a challenging role, please submit your application.

The role of Senior Quality Control Analyst is a pivotal position within the laboratory team.

The incumbent will be responsible for performing and reviewing analytical testing and results, ensuring adherence to test methods, site Standard Operating Procedures (SOPs), and relevant protocols, all in accordance with ALCOA principles and Data Integrity requirements.

This includes documenting analytical testing accurately and collaborating with cross-functional teams to drive flawless execution.

Additional responsibilities include participating in 5S initiatives, practicing good housekeeping, and upholding Pfizer's code of conduct and values.

An ideal candidate will possess effective problem-solving skills, demonstrated ability to perform in a team environment, knowledge of cGMPs and ALCOA principles, and a can-do attitude.

Bonus points are awarded for candidates with a minimum of one year of QC experience in an analytical laboratory.

The successful candidate will contribute to the continuous improvement activities in the QC laboratory or cross-functional teams as nominated.

This role is accountable for executing quality control analyses in compliance with laboratory and analytical methods, ensuring adherence to quality standards, regulatory requirements, and environmental best practices.

• Evaluate and perform analytical testing in accordance with specifications, analytical methods, laboratory procedures, and pharmacopoeia guidelines.
• Monitor the calibration and maintenance schedule for laboratory instruments/equipment to ensure compliance with established protocols.
• Qualify laboratory equipment and validate analytical methods to guarantee accuracy and reliability.
• Ensure that analyses are conducted and reported in accordance with Good Laboratory Practices (GLP) and completed on time, aligning with business objectives.
• Investigate out-of-specification (OOS) and atypical results to identify root causes and implement corrective actions.
• Review and report test results to stakeholders.
• Develop and implement quality testing schedules to ensure cGMP-compliant documentation and timely completion of tasks.
• Prepare laboratory reagents in accordance with GLP and laboratory standard operating procedure (SOP) requirements.
• SOURCE high-quality reagents/laboratory consumables while adhering to departmental budget constraints.
• Collaborate with the team as required and contribute to other functions such as preparation of SOPs and documentation.

• Possess a year's hands-on experience in analytical testing within a lab environment from the pharmaceutical industry.
• Familiarity with analytical equipment (e.g., HPLC, GC).
• Ability to work flexible shifts on a rotational basis.
• Analytical, methodical, and quality-focused.
• Good knowledge of FDA regulations and current Good Manufacturing Practices (cGMP).
• Possession of a diploma in chemistry/chemical process technology/bio-process technology or an ITE graduate qualification is preferred.

Job Title: Quality Assurance Specialist

About the Role:

• In charge of implementing and maintaining Quality Management System standards and ensuring adherence to regulatory oversight.
• Responsible for conducting internal quality audits, external vendor QMS audits, and managing vendor qualification into an approved vendor list.
• Liaise with assigned aviation authorities for certifications, approvals, and inspections.
• Take charge of assigned customer audits.
• Manage the quality and safety of assigned workshops.
• Conduct investigations for incidents and accidents, and warranty claims.
• Support the development, review, and improvement of quality management procedures.

Requirements:

• Minimum Diploma in aerospace engineering or a related field.
• Minimum 3 years of experience in QMS in the aerospace industry.
• Qualified auditor required.

Key Responsibilities:

1. Implement and maintain Quality Management System standards.
2. Ensure adherence to regulatory oversight.
3. Conduct internal and external audits.
4. Liaise with aviation authorities.
5. Manage vendor qualification.
6. Conduct customer audits.
7. Manage workshop quality and safety.
8. Investigate incidents and accidents.
9. Support quality procedure development.

This is an exciting opportunity to join our team as a Quality Assurance Specialist. In this role, you will be responsible for ensuring that all products meet the highest standards of quality.

The ideal candidate will have at least 1-3 years of experience in QA and hold a minimum diploma/degree. You should be able to perform overtime when necessary and be adaptable to changing circumstances.

• Responsible for QA documentation and data control.
• Conduct analysis and reporting of internal/external quality performance.
• Identify and initiate actions to prevent nonconformity relating to internal process and product.
• Implement control on Reject area for nonconforming material/product.

Key Responsibilities:

• Handle customer complaints and ensure that they are resolved satisfactorily with necessary countermeasures to prevent recurrence.
• Assist QA Manager in coordinating Engineering Change/Production Part Approval Process.
• Supervise generation of QA Work Instruction/Procedure and Part Inspection Plan.

Required Skills and Qualifications:

• At least 1-3 years of QA experience
• Min. Diploma / Degree
• Able to perform overtime when necessary

What We Offer:

• Opportunity to work in a dynamic environment
• Competitive salary and benefits package
• Ongoing training and development opportunities