918 Quality Assurance Manager jobs in Singapore

Job Responsibilities

1. Lead the company's quality and compliance activities, including directing resources, setting objectives, serving as the SPOC for clients, delivering quality tasks, and reporting performance directly to the Global QA Director.
2. Manage quality and compliance activities and oversee the compliance aspects of operational activities carried out by the service provider for the pharma client.
3. Perform audits of all GxP services provided by the internal FM service provider to pharma/manufacturing companies in Singapore. These services include Distribution and Logistics, Document Solutions, GMP cleaning, Pest control, Lab services, Records services, Technical lab services, Contract management, Waste disposal, Lab instrument services, and Facilities management (e.g., buildings/equipment maintenance, calibration, qualification).
4. Execute special audits as required by the Group, Chief Operating Officers, or other Sodexo senior executives to investigate specific issues.
5. Assist with the management, development, and continuous improvement of the Global Quality Management System for the pharma site.
6. Collaborate with the client and internal teams to investigate root causes and implement corrective actions for GxP deficiencies. Coach and influence senior management to ensure robust quality systems are in place.
7. Present quality-related topics to local and group senior management.
8. Conduct investigations and special projects as required by the Global Quality & Compliance Executive.
9. Maintain communication with key Sodexo and client personnel.
10. Provide guidance and assistance to Quality and Compliance staff (both company and client).
11. Conduct site visits to implement quality systems and ensure regulatory and client expectations are met.
12. Conduct training on GxP and QMS topics for the wider company operations team.
13. Advise clients and the company of any legislative changes that may impact the business.

• Lead and guide moderately complex projects, managing time and resources effectively, and apply skills and discipline knowledge to departmental work
• Make decisions to resolve complex problems, develop new options guided by policies, and operate independently in ambiguous situations
• Support the development of quality strategic initiatives, lead continuous inspection readiness, and drive effective management of quality issues and CAPAs
• Ensure reference standard testing is conducted in a manner consistent with cGMPs, Pfizer policies, site procedures and regulatory guidance.
• Review/approve various types of laboratory documentation. These documents would include (but are not limited to) laboratory investigation reports, deviation reports, change control documentation, certificate of results, laboratory instrument qualification/calibration, laboratory procedures, memorandums and quality alerts according to procedure requirements.
• Create, track and approve corrective/preventative action items to help ensure they are completed with the agreed timeframes.
• Provide QA approval of Reference Standard Materials in the Reference Standard Database.
• Perform internal audits or host external audits as needed and provide timely feedback during the audit process. Assure adequate follow-up and resolution of external or internal audit findings.
• Provide support with the training and document management systems within SLS.
• Leading and participating on limited duration teams to achieve specific objectives.
• Managing assigned tasks/projects within agreed upon timeframes.
  
  

• Bachelor's Degree in Chemistry, Biology or Other Health Science
• 15+ years' experience working in the Pharmaceutical Industry or other GMP setting with an emphasis in Quality Assurance.
• Thorough knowledge and understanding of the technical and commercial aspects of a Corporate Reference Standard Program, Current Good Manufacturing Practices {part of GxP}, validation principles, and applicable regulations
• Demonstrated record of successful interaction with global regulatory and other internal and external auditing groups
• Experience in conducting GMP system audits.
• Strong understanding of QA requirements and is aware of industry trends
• Experience in preparing and negotiating Quality Agreements with contract sites
• Good understanding of the principles and application of quality risk management
• Ability to manage multiple projects simultaneously typically involving cross functional teams.
• Excellent verbal and written communication skills with the ability to share vision, direction, and data with colleagues across all levels and in a wide range of different work groups
  
  

• Experience in Quality Systems in pharmaceutical, medical device, or combination product industry
• Knowledge or exposure to data science
• Strong leadership and team management skills
• Ability to work under pressure and meet tight deadlines
• Ability to influence and negotiate with stakeholders
• Advanced computer skills in MS office applications and good knowledge of enterprise systems, such as PDM, EQMS, Documentum platforms
  
  

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.

To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.

Pfizer Global Supply proudly shoulders the responsibility of manufacturing and distributing our wide-ranging pharmaceutical products.

Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.

Transforming Delivery of high quality products

Pfizer, We are one

PGS - Manufacture the Future

Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are involved in development, maintenance, compliance, or analysis through research programs, your contribution directly impacts patients.

What You Will Achieve

In this role, you will:

• Lead and guide moderately complex projects, managing time and resources effectively, and apply skills and discipline knowledge to departmental work
• Make decisions to resolve complex problems, develop new options guided by policies, and operate independently in ambiguous situations
• Support the development of quality strategic initiatives, lead continuous inspection readiness, and drive effective management of quality issues and CAPAs
• Ensure reference standard testing is conducted in a manner consistent with cGMPs, Pfizer policies, site procedures and regulatory guidance.
• Review/approve various types of laboratory documentation. These documents would include (but are not limited to) laboratory investigation reports, deviation reports, change control documentation, certificate of results, laboratory instrument qualification/calibration, laboratory procedures, memorandums and quality alerts according to procedure requirements.
• Create, track and approve corrective/preventative action items to help ensure they are completed with the agreed timeframes.
• Provide QA approval of Reference Standard Materials in the Reference Standard Database.
• Perform internal audits or host external audits as needed and provide timely feedback during the audit process. Assure adequate follow-up and resolution of external or internal audit findings.
• Provide support with the training and document management systems within SLS.
• Leading and participating on limited duration teams to achieve specific objectives.
• Managing assigned tasks/projects within agreed upon timeframes.

Here Is What You Need (Minimum Requirements)

• Bachelor's Degree in Chemistry, Biology or Other Health Science
• 15+ years' experience working in the Pharmaceutical Industry or other GMP setting with an emphasis in Quality Assurance.
• Thorough knowledge and understanding of the technical and commercial aspects of a Corporate Reference Standard Program, Current Good Manufacturing Practices {part of GxP}, validation principles, and applicable regulations
• Demonstrated record of successful interaction with global regulatory and other internal and external auditing groups
• Experience in conducting GMP system audits.
• Strong understanding of QA requirements and is aware of industry trends
• Experience in preparing and negotiating Quality Agreements with contract sites
• Good understanding of the principles and application of quality risk management
• Ability to manage multiple projects simultaneously typically involving cross functional teams.
• Excellent verbal and written communication skills with the ability to share vision, direction, and data with colleagues across all levels and in a wide range of different work groups

Bonus Points If You Have (Preferred Requirements)

• Experience in Quality Systems in pharmaceutical, medical device, or combination product industry
• Strong leadership and team management skills
• Ability to work under pressure and meet tight deadlines
• Ability to influence and negotiate with stakeholders
• Advanced computer skills in MS office applications and good knowledge of enterprise systems, such as PDM, EQMS, Documentum platforms

Non-Standard Working schedule, Tavel or Environment Requirements:

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Use Your Power for Purpose

Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are involved in development, maintenance, compliance, or analysis through research programs, your contribution directly impacts patients.

What You Will Achieve

In this role, you will:

• Lead and guide moderately complex projects, managing time and resources effectively, and apply skills and discipline knowledge to departmental work
• Make decisions to resolve complex problems, develop new options guided by policies, and operate independently in ambiguous situations
• Support the development of quality strategic initiatives, lead continuous inspection readiness, and drive effective management of quality issues and CAPAs
• Ensure reference standard testing is conducted in a manner consistent with cGMPs, Pfizer policies, site procedures and regulatory guidance.
• Review/approve various types of laboratory documentation. These documents would include (but are not limited to) laboratory investigation reports, deviation reports, change control documentation, certificate of results, laboratory instrument qualification/calibration, laboratory procedures, memorandums and quality alerts according to procedure requirements.
• Create, track and approve corrective/preventative action items to help ensure they are completed with the agreed timeframes.
• Provide QA approval of Reference Standard Materials in the Reference Standard Database.
• Perform internal audits or host external audits as needed and provide timely feedback during the audit process. Assure adequate follow-up and resolution of external or internal audit findings.
• Provide support with the training and document management systems within SLS.
• Leading and participating on limited duration teams to achieve specific objectives.
• Managing assigned tasks/projects within agreed upon timeframes.

Here Is What You Need (Minimum Requirements)

• Bachelor's Degree in Chemistry, Biology or Other Health Science
• 15+ years' experience working in the Pharmaceutical Industry or other GMP setting with an emphasis in Quality Assurance.
• Thorough knowledge and understanding of the technical and commercial aspects of a Corporate Reference Standard Program, Current Good Manufacturing Practices {part of GxP}, validation principles, and applicable regulations
• Demonstrated record of successful interaction with global regulatory and other internal and external auditing groups
• Experience in conducting GMP system audits.
• Strong understanding of QA requirements and is aware of industry trends
• Experience in preparing and negotiating Quality Agreements with contract sites
• Good understanding of the principles and application of quality risk management
• Ability to manage multiple projects simultaneously typically involving cross functional teams.
• Excellent verbal and written communication skills with the ability to share vision, direction, and data with colleagues across all levels and in a wide range of different work groups

Bonus Points If You Have (Preferred Requirements)

• Experience in Quality Systems in pharmaceutical, medical device, or combination product industry
• Knowledge or exposure to data science
• Strong leadership and team management skills
• Ability to work under pressure and meet tight deadlines
• Ability to influence and negotiate with stakeholders
• Advanced computer skills in MS office applications and good knowledge of enterprise systems, such as PDM, EQMS, Documentum platforms

Non-Standard Working schedule, Tavel or Environment Requirements:

Some after hour/weekend work maybe required

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Research confirms what intuition tells us: that purpose-driven companies perform better, are more innovative, attract and retain the best people, and know how to unleash the power of those people. Pfizer’s purpose—Breakthroughs that change patients' lives—fuels everything we do and reflects our passion for building on our legacy as one of the greatest contributors of good to the world.

Each word in our purpose has meaning and reflects the value we strive to bring to patients and society:

“Breakthroughs” - These are the innovations, scientific and commercial, that we seek to deliver every day. All colleagues, regardless of role, level or location, strive for breakthroughs every day.

“Change” - We want to do more than simply improve patients’ medical conditions; we want to dramatically change their lives for the better.

“Patients’ lives” - We consider not only patients, but everyone they touch—including their families, caregivers, and friends—and everything they love to do. It’s an intentionally holistic view.

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Every decision we make and every action we take is done with the patient in mind—and to nurture an environment where breakthroughs can thrive.

To fully realize Pfizer’s purpose, we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.

The “how” is represented by four simple, powerful values—courage, excellence, equity, and joy—that define our company and our culture.

Courage: Breakthroughs start by challenging convention, especially in the face of uncertainty or adversity. This happens when we think big, speak up, and are decisive.

Excellence: We can only change patients’ lives when we perform at our best together. This happens when we focus on what matters, agree who does what, and measure our outcomes.

Equity: We believe that every person deserves to be seen, heard, and cared for. This happens when we are inclusive, act with integrity, and reduce healthcare disparities.

Joy: We give ourselves to our work, but it also gives to us. We find joy when we take pride, recognize one another, and have fun.

Pfizer Global Supply proudly shoulders the responsibility of manufacturing and distributing our wide-ranging pharmaceutical products.

With an unwavering commitment to ensuring the availability and accessibility of these life-saving medications, we play a pivotal role in reaching patients, healthcare professionals, and markets across the globe.

Our network of state-of-the-art manufacturing facilities, strategically located distribution centers , and streamlined logistics systems enables us to deliver Pfizer's medicines with utmost efficiency and reliability, making a tangible difference in patients' lives worldwide.

Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues. Our Pay for Performance Philosophy and Practices reward colleagues based on the contributions they make to our business.

Our Competitive Benefits Programs help our colleagues by:

• Promoting Health and Wellness to help colleagues maintain and improve their physical and mental wellbeing . Pfizer offerings include health and disability insurance, preventative health programs, medical screenings, free or reduced-cost vaccinations, discounts on Pfizer products, mental health support, nutrition and fitness counseling and more.
• Strengthening Colleagues’ Financial Security by providing company contributions to retirement plans, life insurance and financial planning education to help colleagues achieve their financial goals.
• Providing Benefits and Time off for the Moments that Matter to ensure Pfizer colleagues have the time away from the office to recharge, recover and return to work as the best version of themselves. Vacation, Holiday time and Sick time are just the beginning, with a 12 week parental leave policy for both parents of a new born, 10 day of caregiver leave for those times when your family needs you whether it’s a child, spouse or parent, bereavement leave, and additional country-specific programs.
• And so much more , depending on your country and site, Pfizer offers childcare facilities or discount programs, on-site health and/or fitness centers , movement and mindfulness solutions, “Log in for your Day” work flexibility and so much more.
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Join to apply for the Quality Assurance Manager role at Thales

Join to apply for the Quality Assurance Manager role at Thales

Location: Singapore, Singapore

Thales is a global technology leader trusted by governments, institutions, and enterprises to tackle their most demanding challenges. From quantum applications and artificial intelligence to cybersecurity and 6G innovation, our solutions empower critical decisions rooted in human intelligence. Operating at the forefront of aerospace and space, cybersecurity and digital identity, we’re driven by a mission to build a future we can all trust.

In Singapore, Thales has been a trusted partner since 1973, originally focused on aerospace activities in the Asia-Pacific region. With 2,000 employees across three local sites, we deliver cutting-edge solutions across aerospace (including air traffic management), defence and security, and digital identity and cybersecurity sectors. Together, we’re shaping the future by enabling customers to make pivotal decisions that safeguard communities and power progress.

The opportunity:

The QAM role for project and bid, is focused on assuring that the supplied and processes implemented are in accordance with the requirements of the customer and the Thales Group, as well as with statutory regulations.

This includes taking a risk-based approach to defining and implementing quality assurance activities, assuring compliance, identifying deficiencies, certifying products, and evaluating and minimizing potential quality related risk and raising Alerts and enforcing Veto for quality issues when necessary. It also includes facilitating continuous quality improvement, and ensuring the Business Management System (called Chorus 2.0) is implemented and effective in delivering quality across all areas of their business.

The primary challenges of this position are:

• Ensuring quality is owned by everyone not only the quality function
• Reduction of quality risks and minimization of Cost of Non-Quality through active support of operational areas.
• Assuring that the commitments we make to our customers are met indeed and in intent while balancing the cost and schedule constraints.
  
  
  

• Provide a point of contact for the customer on quality matters and developing a good working relationship with counterparts in the customer’s organization to ensure timely resolution of issues that may arise.
• Identify risks with a proactive approach, implement mitigations actions and collaborate with Project & Bid teams in resolving problems
• Provide insightful advice and stimulate actions based on independent assessment of performance
• Build trusted relationships and influence project & bid teams to focus on delivering Customer satisfaction
• Confirm Customer’s technical and non-technical requirements are well understood and managed efficiently by all members of the project & bid team
• Ensure deliverables comply with the applicable regulations and standards
• Support project & bid team to ensure objectives/criteria for each of the engineering project gates are achieved
• Support the project & bid teams in applying processes, identifying risks and developing problem solving mindset
• Assure that teams capitalize on lessons learnt
• Provide visibility to the management and alert when necessary; raise a veto in case of non-compliance not properly addressed or in case of a critical event/situation generating a major risk for the project / bid or for the company.
• Adjust Quality Assurance activities with a risk-driven mindset, anticipating risks, considering the maturity of the Bid/Project team, and focusing on core Quality value-added activities
  
  
  

• Tertiary Qualifications in a project/bid management, an engineering or related technical discipline.
• Audit Qualifications background or qualifications is desirable.
• Minimum of 5 years of experience in Engineering (i.e. systems engineering or SW) with a good understanding of systems and software development principles’ and lifecycles
• Experience in quality management, preferably in a system’s engineering organisation, or other relevant technically orientated discipline.
• Knowledge of the requirements of ISO 9001:2015 Quality Management System is desirable.
• Strategic influencing skills including the ability to promote improvement at all levels and across all areas of the organisation.
• Analytical and problem-solving skills, including the ability to understand and critique requirements. Expertise in applying problem solving tools, such as 8D is desirable
• Good communication & interpersonal skills, including ability to prepare and present reports.
• Ability to work well in a multi-disciplinary team.
• Diplomacy skills, including the ability to withstand pressures and say 'no' when quality is insufficient, or processes are not being adhered to.
  
  
  

• Seniority level Not Applicable

• Employment type Full-time

• Job function Quality Assurance
• Industries Aviation and Aerospace Component Manufacturing and Defense and Space Manufacturing

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South East Community Development Council, Singapore 4 days ago

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Job Description

The opportunity:

The QAM role for project and bid, is focused on assuring that the supplied and processes implemented are in accordance with the requirements of the customer and the Thales Group, as well as with statutory regulations.

This includes taking a risk-based approach to defining and implementing quality assurance activities, assuring compliance, identifying deficiencies, certifying products, and evaluating and minimizing potential quality related risk and raising Alerts and enforcing Veto for quality issues when necessary. It also includes facilitating continuous quality improvement, and ensuring the Business Management System (called Chorus 2.0) is implemented and effective in delivering quality across all areas of their business.

The primary challenges of this position are:

• Ensuring quality is owned by everyone not only the quality function
• Reduction of quality risks and minimization of Cost of Non-Quality through active support of operational areas.
• Assuring that the commitments we make to our customers are met indeed and in intent while balancing the cost and schedule constraints.

Responsibilities:

• Provide a point of contact for the customer on quality matters and developing a good working relationship with counterparts in the customer’s organization to ensure timely resolution of issues that may arise.
• Identify risks with a proactive approach, implement mitigations actions and collaborate with Project & Bid teams in resolving problems
• Provide insightful advice and stimulate actions based on independent assessment of performance
• Build trusted relationships and influence project & bid teams to focus on delivering Customer satisfaction
• Confirm Customer’s technical and non-technical requirements are well understood and managed efficiently by all members of the project & bid team
• Ensure deliverables comply with the applicable regulations and standards
• Support project & bid team to ensure objectives/criteria for each of the engineering project gates are achieved
• Support the project & bid teams in applying processes, identifying risks and developing problem solving mindset
• Assure that teams capitalize on lessons learnt
• Provide visibility to the management and alert when necessary; raise a veto in case of non-compliance not properly addressed or in case of a critical event/situation generating a major risk for the project / bid or for the company.
• Adjust Quality Assurance activities with a risk-driven mindset, anticipating risks, considering the maturity of the Bid/Project team, and focusing on core Quality value-added activities

Requirements:

• Tertiary Qualifications in a project/bid management, an engineering or related technical discipline.
• Audit Qualifications background or qualifications is desirable.
• Minimum of 5 years of experience in Engineering (i.e. systems engineering or SW) with a good understanding of systems and software development principles’ and lifecycles
• Experience in quality management, preferably in a system’s engineering organisation, or other relevant technically orientated discipline.
• Knowledge of the requirements of ISO 9001:2015 Quality Management System is desirable.
• Strategic influencing skills including the ability to promote improvement at all levels and across all areas of the organisation.
• Analytical and problem-solving skills, including the ability to understand and critique requirements. Expertise in applying problem solving tools, such as 8D is desirable
• Good communication & interpersonal skills, including ability to prepare and present reports.
• Ability to work well in a multi-disciplinary team.
• Diplomacy skills, including the ability to withstand pressures and say 'no' when quality is insufficient, or processes are not being adhered to.

1 month ago Be among the first 25 applicants

Summary

The Quality Assurance Manager is responsible for overseeing all aspects of quality assurance, food safety, and regulatory compliance. This role ensures that all food products meet national standards, customer specifications, and company policies. The Quality Assurance Manager leads internal and external audits, maintains ISO and Halal certifications, and provides guidance to the Quality Assurance (QA) team. The role also involves staff training, process improvement, and supplier quality assessment.

Summary

The Quality Assurance Manager is responsible for overseeing all aspects of quality assurance, food safety, and regulatory compliance. This role ensures that all food products meet national standards, customer specifications, and company policies. The Quality Assurance Manager leads internal and external audits, maintains ISO and Halal certifications, and provides guidance to the Quality Assurance (QA) team. The role also involves staff training, process improvement, and supplier quality assessment.

Duties And Responsibilities

• Manage the Quality Assurance department, ensuring compliance in the following areas:
• Quality, food safety, and Halal assurance of raw materials, in-process, and finished products.
• Hygiene and cleanliness of facilities, equipment, and personnel.
• Implementation and monitoring of microbiological quality standards.
• Ensure the establishment, implementation, maintenance, and continuous improvement of the Quality, Food Safety, and Halal Assurance Management System.
• Develop and maintain prerequisite programs (PRPs), operational prerequisite programs (OPRPs), and HACCP plans.
• Oversee the handling, storage, and distribution of food products in compliance with ISO/HACCP guidelines.
• Maintain and update the Quality & Food Safety Manual, standard operating procedures, and supporting documentation.
• Lead and manage internal and external audits, including ISO, Halal, and customer audits.
• Establish and monitor key performance indicators (KPIs) for quality and food safety, including audit pass rates, non-conformance reduction targets, and employee training completion.
• Conduct supplier risk assessments and audits to ensure raw material quality and safety.
• Investigate non-conformities, implement corrective/preventive actions, and monitor effectiveness.
• Ensure compliance with company policies, regulatory requirements, and industry standards.
• Conduct root cause analysis for customer complaints and food safety incidents, implementing corrective actions where necessary.
• Develop and oversee crisis management protocols, including food safety incident response, product recall procedures, and emergency handling.
• Develop and implement training programs on food hygiene, HACCP, and quality assurance for employees.
• Promote a culture of food safety awareness and hygiene compliance.
• Provide mentorship and development opportunities for junior QA staff.
• Collaborate with internal teams to identify and implement process improvements in quality and food safety management.
• Support additional tasks and projects as assigned by the immediate superior.
  

• Degree or Diploma in Food Science, Food Technology, Microbiology, or a related field.
• Minimum 10 years of experience managing quality assurance and food safety in the food manufacturing or catering industry.
• Strong knowledge and certifications in ISO 22000, ISO 9001, HACCP, and Halal audits.
• Experience in food safety audits conducted by customers, certification bodies, and government authorities.
• Knowledge of Halal certification processes, including new applications and renewals.
• Proficiency in SAP or other quality management systems is preferred.
• Leadership & Team Management – Ability to lead and develop the QA team to maintain high-quality standards.
• Food Safety & Compliance – Strong understanding of ISO, HACCP, and regulatory food safety requirements.
• Audit & Risk Management – Experience in conducting and managing audits, ensuring compliance with national and international standards.
• Problem-Solving & Decision-Making – Analytical skills to investigate quality issues and implement corrective actions.
• Training & Development – Ability to design and deliver food safety training for employees.
• Stakeholder Communication – Effective interaction with internal teams, suppliers, auditors, and regulatory authorities.
• Continuous Improvement – Commitment to identifying and implementing process enhancements.

• Seniority level Mid-Senior level

• Employment type Full-time

• Job function Quality Assurance
• Industries Airlines and Aviation

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Johor Baharu, Johore, Malaysia 4 days ago

South East Community Development Council, Singapore 1 week ago

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Job Description Summary

To manage and maintain an industry-leading quality and food safety management systems throughout the Inspire Brands International supply chain with focus on the APAC region, delivering quality (inclusive of food safety) and risk management, mitigation, and focused improvement. Ensuring the protection of our consumers, franchisees, and brands through execution of supplier and product approval based on risk assessment and measurement of ongoing performance to standards in assigned regions.

DUTIES AND RESPONSIBILITIES

• Maintain, implement, and execute systems for the management of supplier approval based on risk and quality and food safety performance in assigned region.

• Evaluate suppliers for QA qualification for the Inspire supply chain in accordance with Innovation to Market, New Market Entry and Supply Chain demands and project timelines.

• Ensure all suppliers are risk assessed and approved in accordance with Inspire policies and quality management system & standards requirements.

• Measure, analyze and report supplier risk, quality performance through systems audits, certifications, specification compliance, KPIs, complaints, defect rates and any other applicable performance measures.

• Establish supplier performance indicators and controls to mitigate risks.

• Support, enable, and execute quality requirements and verification of suppliers as part of oversight of licensee/franchisee local sourcing within Inspire QA policies.

• Lead continuous improvement, corrective and preventative actions, and other focused improvement with suppliers as necessary.

• Maintaining process and procedures for effectively reporting supplier of performance.

• Provide technical and subject matter expertise as required.

• Monitor, review, assign disposition communicate and resolve product/supplier related complaints and incidents.

• Support and/or lead supplier manufacturing plant start up and related start up activities as needed.

• Interface with supplier QA contacts, Franchisees and regulators for all quality and food safety matters.

• Identify and maintain such 3rd Party relationships and support providers, inclusive of identification, capability assessment, qualifications, ongoing performance, and calibration to brand standards and requirements.

• Maintain and execute product risk analysis and process and procedures for product approval.

• Execute process and procedures in accordance with Inspire policies and quality management systems for product approval.

• Monitor, risk assess, respond to and resolve product complaints in accordance with Inspire policies and procedures.

• Execute product quality evaluation and compliance verification processes and performance optimization and communication.

• Ensure quality role within the new market entry and innovation to market projects are executed right first time and on time.

• Lead quality by design within the innovation to market process

• Contribute to supply chain cost, capacity and contingency projects as required with supplier qualification processes and procedures.

• Maintain effective two-way dialogue to ensure teams/stakeholders are engaged and informed.

• Link with stakeholders to gain cross-functional support for product quality improvement initiatives.

• Execute supply chain interventions as necessary to ensure product related incidents are effectively managed.

• For locally sourced products execute systems and processes for Specification Life Cycle Management.

• Ensures systems are in place to manage and maintain current specifications with suppliers.

• Ensures the basis for managing product quality for key products are defined in product specifications.

• Ensures the process for specification creation, review and approval are executed and maintained.

• Ensures current specifications are communicated to and agreed with Suppliers.

• Ensure process and procedures specification change management is established and executed.

• Support local supplier quality systems and standards continuous improvement.

• Contribute to systems and standards landscape analysis and best practice discovery.

• Support and contribute to systems optimization initiatives and projects.

• Ensure standards, process and procedures are documented, communicated, and always maintained current.

• Support systems user training, calibration, and qualification.

Inspire Brands is a multi-brand restaurant company whose portfolio includes more than 32,000 Arby’s, Baskin-Robbins, Buffalo Wild Wings, Dunkin’, Jimmy John’s, and SONIC restaurants worldwide.

We’re made up of some of the world’s most iconic restaurant brands, but we’re much more than just a restaurant company. We’re a team of hundreds of thousands who individually and collectively are changing the way people eat, drink, and gather around the table. We know that food is much more than a staple—it’s an experience. At Inspire, that’s our purpose: to ignite and nourish flavorful experiences.

Quality Assurance Manager page is loadedQuality Assurance Manager Apply remote type Hybrid locations Singapore time type Full time posted on Posted Today job requisition id R0293560 Location: Singapore, Singapore

Thales is a global technology leader trusted by governments, institutions, and enterprises to tackle their most demanding challenges. From quantum applications and artificial intelligence to cybersecurity and 6G innovation, our solutions empower critical decisions rooted in human intelligence. Operating at the forefront of aerospace and space, cybersecurity and digital identity, we’re driven by a mission to build a future we can all trust.

The opportunity:

The QAM role for project and bid, is focused on assuring that the supplied and processes implemented are in accordance with the requirements of the customer and the Thales Group, as well as with statutory regulations.

This includes taking a risk-based approach to defining and implementing quality assurance activities, assuring compliance, identifying deficiencies, certifying products, and evaluating and minimizing potential quality related risk and raising Alerts and enforcing Veto for quality issues when necessary. It also includes facilitating continuous quality improvement, and ensuring the Business Management System (called Chorus 2.0) is implemented and effective in delivering quality across all areas of their business.

The primary challenges of this position are:

• Ensuring quality is owned by everyone not only the quality function
• Reduction of quality risks and minimization of Cost of Non-Quality through active support of operational areas.
• Assuring that the commitments we make to our customers are met indeed and in intent while balancing the cost and schedule constraints.

Responsibilities:

• Provide a point of contact for the customer on quality matters and developing a good working relationship with counterparts in the customer’s organization to ensure timely resolution of issues that may arise.
• Identify risks with a proactive approach, implement mitigations actions and collaborate with Project & Bid teams in resolving problems
• Provide insightful advice and stimulate actions based on independent assessment of performance
• Build trusted relationships and influence project & bid teams to focus on delivering Customer satisfaction
• Confirm Customer’s technical and non-technical requirements are well understood and managed efficiently by all members of the project & bid team
• Ensure deliverables comply with the applicable regulations and standards
• Support project & bid team to ensure objectives/criteria for each of the engineering project gates are achieved
• Support the project & bid teams in applying processes, identifying risks and developing problem solving mindset
• Assure that teams capitalize on lessons learnt
• Provide visibility to the management and alert when necessary; raise a veto in case of non-compliance not properly addressed or in case of a critical event/situation generating a major risk for the project / bid or for the company.
• Adjust Quality Assurance activities with a risk-driven mindset, anticipating risks, considering the maturity of the Bid/Project team, and focusing on core Quality value-added activities

Requirements:

• Tertiary Qualifications in a project/bid management, an engineering or related technical discipline.
• Audit Qualifications background or qualifications is desirable.
• Minimum of 5 years of experience in Engineering (i.e. systems engineering or SW) with a good understanding of systems and software development principles’ and lifecycles
• Experience in quality management, preferably in a system’s engineering organisation, or other relevant technically orientated discipline.
• Knowledge of the requirements of ISO 9001:2015 Quality Management System is desirable.
• Strategic influencing skills including the ability to promote improvement at all levels and across all areas of the organisation.
• Analytical and problem-solving skills, including the ability to understand and critique requirements. Expertise in applying problem solving tools, such as 8D is desirable
• Good communication & interpersonal skills, including ability to prepare and present reports.
• Ability to work well in a multi-disciplinary team.
• Diplomacy skills, including the ability to withstand pressures and say 'no' when quality is insufficient, or processes are not being adhered to.

At Thales, we’re committed to fostering a workplace where respect, trust, collaboration, and passion drive everything we do. Here, you’ll feel empowered to bring your best self, thrive in a supportive culture, and love the work you do. Join us, and be part of a team reimagining technology to create solutions that truly make a difference – for a safer, greener, and more inclusive world.

ACTIVELY HIRINGQuality Assurance Manager Fairgrowth Management Consultants Pvt. Ltd.

As the Quality Assurance Specialist at our company, you will play a crucial role in ensuring the implementation of all quality norms as per the company standards and reviewing quality specifications along with technical designs. Your responsibilities will include material testing, including third-party testing, maintaining all quality-related records, analyzing data, and proposing alternate solutions when necessary. Additionally, you will be responsible for providing training to site teams on quality aspects and actively engaging in problem-solving and troubleshooting activities.Your profile will require you to have a strong understanding and hands-on experience in implementing quality norms aligned with company standards. Proficiency in material testing, including third-party testing, and the ability to maintain quality-related records, analyze data, and propose effective solutions are essential for success in this role. Furthermore, your expertise in imparting training to site teams on quality aspects and your problem-solving skills will be crucial in fulfilling the responsibilities of this position.This role is located in Thane Estate, providing an opportunity to contribute significantly to the company's commitment to maintaining high-quality standards and ensuring operational excellence. Join us in this dynamic environment where your skills and expertise will make a meaningful impact on our quality assurance processes and overall success.,

• Recruiter Details Fairgrowth Management Consultants Pvt. Ltd.
• Job Tags business process quality, quality assurance
• Job Type Full time

• Implementation of all quality norms as per Company standards
• Material testing including thirdparty testing
• Maintain all qualityrelated records
• Analyse data
• suggest alternate solutions as may be required
• Impart training to site teams on quality aspects
• Problemsolving
• Troubleshooting

About RecruiterFairgrowth Management Consultants Pvt. Ltd. All India

Fairgrowth Management Consultants Pvt. Ltd.

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• Strong understanding of quality control standards