1,571 Quality Assurance Specialist jobs in Singapore

About No deviation

At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation.

We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That's why we foster a culture of collaboration, inclusion, and continuous development empowering our team members to grow personally and professionally.

Position Overview

We are seeking a motivated and detail-oriented Junior Quality Assurance (QA) Specialist to support our manufacturing operations. This role ensures that products are manufactured in compliance with Good Manufacturing Practices (GMP), internal quality standards, and regulatory requirements. The successful candidate will collaborate closely with production, engineering, and quality teams to maintain a culture of quality and continuous improvement.

Key Responsibilities

• Review and approve batch records, standard operating procedures (SOPs), and deviations related to manufacturing operation.
• Support timely documentation and ensure adherence to GDP (Good Documentation Practices).
• Participate in internal audits and support regulatory inspection.
• Provide on-the-floor QA presence to oversee manufacturing activities and ensure compliance with GMP.
• Assist in the investigation of deviations, non-conformances, and complaints.

Required Qualifications

• Diploma or Bachelors degree in Life Sciences, Pharmaceutical Science, Chemistry, Biotechnology, or a related discipline.
• 1 to 3 years of relevant experience in pharmaceutical/biotech manufacturing or quality assurance.
• Strong attention to detail and ability to follow procedures accurately
• Good communication and interpersonal skills to work effectively with cross-functional teams

Why join us?

• Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated.
• Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career.

How to apply

Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you're passionate about making an impact, we want you on our team

Please submit your resume, outlining your qualifications and experience relevant to the role, here.

• MNC
• Basic $4500 - $5800 + AWS + Variable Bonus
• Excellent Welfare and Benefits + Career progression
• Working location : Jurong Island (Transport Provided)
• Working days : Monday to Friday
• Working hours : 8am to 4.30pm

Job Responsibilities:

• Manage and maintain the quality management system compliance with designated management standards that include ISO , ISO and IATF14969
• Report the status of the quality management system to site leadership periodically
• Management of the corrective action request system to improve quality performance and ensure compliance with ISO9001, ISO14001 and IATF14969
• Schedule, manage and assist the internal audit program and third-party certification audits
• Maintain all documentation for the Quality Management System
• Manage timely response to customer quality management system questionnaires
• Facilitate formal Root Cause Analysis of quality and other incidents periodically
• Coordinate the corrective action request system to improve quality performance and ensure compliance with quality standards, customers, and organization's QMS
• To perform any other duties or assignments as assigned by superiors

Requirements:

• Bachelor's degree in Engineering
• Minimum of 3 years of relevant experience in a manufacturing environment and quality assurance activities (Audits, CARs, RCA)
• Excellent working knowledge of relevant quality management standards (ISO9001, ISO14001, IATF16949) and related management systems

Candidates are encouraged to apply this position via Apply Now button 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.

THIEN CHING MEI (R

EA Recruitment Pte Ltd

EA License No: 21C0492

Responsibilities:

• Ensure adherence to the Change Control management systems and processes.
• Develop competency and proficiency in the QA Change Control process and the associated tools, supporting the delivery of training for change users as needed.
• Evaluate Change Control requests for process, validation, regulatory and product impact.
• Coordinate the review and approval process of change requests to ensure timely execution of changes.
• Ensure all site changes are managed appropriately to meet the expectation of the global change control board (if applicable) and meets site project timelines.
• Participate in cross functional and cross site change management forums.
• Collaborate with departments to ensure change control activities are executed efficiently and effectively, to provide supporting assistance to stakeholders in the process.
• Ensure completion of required change control actions prior to lifting lot disposition restrictions.
• Assist in the development and delivery of training materials and qualifications for Change Control processes and Change Management applications.
• Perform Change Records review in support of Annual Product Review activities.
• Ensure maintenance and continuous improvement of change control and processes.
• Support regulatory inspections and provide audit support with team, which may include presentations and facility, utility, equipment documentation review.
• Compliance with cGMP and site safety & security regulations at all times
• Any other duties as assigned by supervisor or manager.

About You:

• Bachelor's degree or higher in Biologics, Pharmacy, Pharmaceutical Engineering, Bioengineering, or other relevant fields.
• 3+ years of experience in a GMP-regulated biopharmaceutical or pharmaceutical
• manufacturing environment.

Job Type: Contract

Contract length: 12 months

Pay: $4, $8,000.00 per month

Experience:

• Change Control management systems: 3 years (Preferred)
• biopharmaceutical or pharmaceutical: 3 years (Preferred)
• qualifications for Change Control processes: 3 years (Preferred)

Responsibilities:

• Ensure adherence to the Change Control management systems and processes.
• Develop competency and proficiency in the QA Change Control process and the associated tools, supporting the delivery of training for change users as needed.
• Evaluate Change Control requests for process, validation, regulatory and product impact.
• Coordinate the review and approval process of change requests to ensure timely execution of changes.
• Ensure all site changes are managed appropriately to meet the expectation of the global change control board (if applicable) and meets site project timelines.
• Participate in cross functional and cross site change management forums.
• Collaborate with departments to ensure change control activities are executed efficiently and effectively, to provide supporting assistance to stakeholders in the process.
• Ensure completion of required change control actions prior to lifting lot disposition restrictions.
• Assist in the development and delivery of training materials and qualifications for Change Control processes and Change Management applications.
• Perform Change Records review in support of Annual Product Review activities.
• Ensure maintenance and continuous improvement of change control and processes.
• Support regulatory inspections and provide audit support with team, which may include presentations and facility, utility, equipment documentation review.
• Compliance with cGMP and site safety & security regulations at all times
• Any other duties as assigned by supervisor or manager.

About You:

• Bachelor's degree or higher in Biologics, Pharmacy, Pharmaceutical Engineering, Bioengineering, or other relevant fields.
• 3+ years of experience in a GMP-regulated biopharmaceutical or pharmaceutical manufacturing environment.

Duration: 12-months contract role

About No deviation

At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation.

We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That's why we foster a culture of collaboration, inclusion, and continuous development – empowering our team members to grow personally and professionally.

Position Overview

We are seeking a motivated and detail-oriented Junior Quality Assurance (QA) Specialist to support our manufacturing operations. This role ensures that products are manufactured in compliance with Good Manufacturing Practices (GMP), internal quality standards, and regulatory requirements. The successful candidate will collaborate closely with production, engineering, and quality teams to maintain a culture of quality and continuous improvement.

Key Responsibilities

• Review and approve batch records, standard operating procedures (SOPs), and deviations related to manufacturing operation.
• Support timely documentation and ensure adherence to GDP (Good Documentation Practices).
• Participate in internal audits and support regulatory inspection.
• Provide on-the-floor QA presence to oversee manufacturing activities and ensure compliance with GMP.
• Assist in the investigation of deviations, non-conformances, and complaints.

Required Qualifications

• Diploma or Bachelors degree in Life Sciences, Pharmaceutical Science, Chemistry, Biotechnology, or a related discipline.
• 1 to 3 years of relevant experience in pharmaceutical/biotech manufacturing or quality assurance.
• Strong attention to detail and ability to follow procedures accurately
• Good communication and interpersonal skills to work effectively with cross-functional teams

Why join us?

• Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs.
• Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company.
• Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated.
• Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career.

How to apply

Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you're passionate about making an impact, we want you on our team

Please submit your resume, outlining your qualifications and experience relevant to the role, here.

About the Role

As a Quality Assurance Specialist, you will champion quality standards and process integrity across machining and surface treatment operations. You will develop and implement quality systems, conduct internal audit inspections, and ensure compliance with customer and industry standards. This role is critical in strengthening customer trust by preventing quality escapes and driving root cause corrective actions.

Key Responsibilities

· Develop and maintain QA systems, inspection methods, and testing protocols across machining and surface treatment processes.

· Perform in-process checks and final inspections of parts/products before delivery to customers.

· Investigate and document non-conformances, perform root cause analysis, and implement corrective and preventive actions (CAPA).

· Work closely with production and engineering teams to reinforce quality standards from the start of the process until completion.

· Support quality certifications (e.g., ISO 9001) and ensure compliance with customer-specific requirements.

· Drive internal quality audit processes and lead continuous improvement projects to enhance quality management systems.

· Prepare production and operations staff for annual customer and supplier audits, coordinating documentation and readiness activities.

· Report directly to the CEO, provide regular updates on quality issues, audit findings, and progress on corrective actions.

Requirements

· Diploma/Degree in Mechanical, Materials, or Industrial Engineering or equivalent or a minimum of 5 years of quality assurance or quality engineering experience in precision machining, metal finishing, surface treatment, or related sectors in lieu of academic qualifications will be considered

· In-depth knowledge of QA tools and methodologies such as FMEA, SPC, CAPA, and root cause analysis.

· Hands-on experience with measuring tools, gauges, and understanding of GD&T.

· Strong communication skills for cross-department coordination and customer interfacing.

· Experience in MNC manufacturing/engineering environment preferred, with ability to implement structured QA practices in an SME setup.

As a Quality Assurance Specialist, you will champion quality standards and process integrity across machining and surface treatment operations. You will develop and implement quality systems, conduct internal audit inspections, and ensure compliance with customer and industry standards. This role is critical in strengthening customer trust by preventing quality escapes and driving root cause corrective actions

Key Responsibilities

· Develop and maintain QA systems, inspection methods, and testing protocols across machining and surface treatment processes.

· Perform in-process checks and final inspections of parts/products before delivery to customers.

· Investigate and document non-conformances, perform root cause analysis, and implement corrective and preventive actions (CAPA).

· Work closely with production and engineering teams to reinforce quality standards from the start of the process until completion.

· Support quality certifications (e.g., ISO 9001) and ensure compliance with customer-specific requirements.

· Drive internal quality audit processes and lead continuous improvement projects to enhance quality management systems.

· Prepare production and operations staff for annual customer and supplier audits, coordinating documentation and readiness activities.

· Report directly to the CEO, provide regular updates on quality issues, audit findings, and progress on corrective actions.

Requirements

· Diploma/Degree in Mechanical, Materials, or Industrial Engineering or equivalent or a minimum of 5 years of quality assurance or quality engineering experience in precision machining, metal finishing, surface treatment, or related sectors in lieu of academic qualifications will be considered

· In-depth knowledge of QA tools and methodologies such as FMEA, SPC, CAPA, and root cause analysis.

· Hands-on experience with measuring tools, gauges, and understanding of GD&T.

· Strong communication skills for cross-department coordination and customer interfacing.

· Experience in MNC manufacturing/engineering environment preferred, with ability to implement structured QA practices in an SME setup.

Title:

Quality Assurance Specialist

Job Responsibilities:

• Provides specialized technical expertise in support of the Quality program, including specialized inspection and testing techniques, quality training, statistical methods, audits, quality tools for problem solving and assessment.
• Creates inspection reports stating the conditions of a work area to ensure requirements are met. Makes recommendations for corrective action.
• Applies knowledge of quality systems and tools to validate and verify contractually required standards for project execution.
• Implements principles of performance evaluation and prediction methods are used to improve product systems safety, reliability, and maintainability.
• Responsible for maintaining quality standard of products and the procedures and materials that go into work scope.
• Aligns quality management function with the performance needs of product lines.
• Under general supervision, and occasional direct supervision, performs assignments requiring experience and knowledge of standard concepts within their field.
• Displays core job competencies by analyzing possible solutions using standard procedures while developing advanced skills.
• Manages interface between various regulatory bodies and verification bodies on behalf of the organization

Job Requirements:

• Bachelor's degree in engineering preferably in Materials, Mechanical, Electrical, Welding from an accredited university with minimum 2 years of experience
• Quality Management experience in Oil & Gas industries
• Experience in design projects for Offshore (FPSO/Platforms) and Onshore (Refineries, LNG facilities, Storage terminal etc)
• Familiarity in Oil and Gas EPC is preferred
• Have a detailed knowledge of ISO 9001 standard
• Have working knowledge of ISO 14001 and ISO 45001 standards
• Strong understanding and familiarity with industry codes & regulations
• Candidate shall be good team Player, problem solver and possess good communication skills
• Certified ISO Lead Auditor (preferred)