1,566 Quality Systems jobs in the Philippines
Quality Management Systems
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About the role
This is a full-time position at TRI-DIMENSION METAL FABRICATION, located in Binan City Laguna. As a Quality Management Systems professional, you will be responsible for developing, implementing, and maintaining the company's quality management systems and processes to ensure the production of high-quality products that meet industry standards and customer requirements.
What you'll be doing
- implementing, and continuously improving quality management systems, including quality control procedures, inspection processes, and documentation
- Conducting regular quality audits to identify areas for improvement and implementing corrective actions
- Collaborating with production teams to identify and resolve quality issues, and implementing preventive measures
- Analyzing quality data and generating reports to track performance and identify trends
- Ensuring compliance with relevant industry regulations and standards
- Providing training and guidance to production staff on quality management practices
- Collaborating with cross-functional teams to continuously improve quality and efficiency
What we're looking for
- Degree in a relevant field, such as Quality Assurance, Manufacturing Engineering, or a related discipline
- 1+ years of experience in a quality management or quality assurance role within the Metal Fabrication industry
- Proficient in data analysis and quality control tools and techniques
- Strong problem-solving, critical-thinking, and decision-making skills
- Excellent communication and collaboration skills to work effectively with cross-functional teams
- Proactive, detail-oriented, and committed to continuous improvement
quality systems officer
Posted today
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Job Specification:
- Preferably Graduate of any 4 year course
Prefereably with training in ISO 9001:2015 Standards and in IATF 16949:2016 Standards
With at least One Year background in QUALITY MANAGEMENT SYSTEM (QMS) including knowledge in ISO 9000:2015, IATF 16949:2016 and ISO 1400:2015
with at least One Year experience in Quality Assurance of a Manufacturing company including implementation.
JOB RESPONSIBILITY:
A. Simulation and designing of system.
Acquires new requirements in QMS and EMS pertinent to customer, regulatory, management or organizational needs.
B. ISO and IATF Coordination
Support imlementation and monitors IATF and ISO related activities or requirements on the assigned division.
C. Implementation and Continual Improvement of the QMS and EMS
Job Types: Full-time, Permanent
Benefits:
- Additional leave
- Company events
- Free parking
- Life insurance
- On-site parking
- Opportunities for promotion
- Pay raise
- Staff meals provided
- Transportation service provided
Work Location: In person
Application Deadline: 10/30/2025
Expected Start Date: 10/30/2025
Quality Systems Specialist
Posted today
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Job Description
QUALITY SYSTEMS SPECIALIST
Job Qualifications:
- Candidate must be a graduate of Bachelor's degree in Chemistry, Chemical Engineering, Biology, Food Engineering, Food Technology or any related course and preferably a licensed.
- With at least 1 year work experience in Quality Assurance in the manufacturing industry but fresh graduate are welcome to apply.
- Preferably knowledgeable in GMP, GLP, HACCP, ISO 9001 or QMS
- Proficiency in Microsoft Office (Excel, PowerPoint, Word) and email software.
- Excellent communication skills, both written and verbal
- Good analytical ability and technical skills
No. of vacancy: 1
Place of assignment : Gate Technology Avenue Biñan, Laguna Technopark , Brgy. Biñan City of Biñan, Laguna
Note: All your questions and inquiries will be answered upon interview.
Quality Systems Specialist
Posted 1 day ago
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**A Day in the Life**
This position is an exciting opportunity to work with Medtronic's Diabetes business. Medtronic has announced its intention to separate the Diabetes division to promote future growth and innovation within the business and reallocate investments and resources across Medtronic, subject to applicable information and consultation requirements. This separation provides our team with a bold opportunity to unleash our potential, enabling us to operate with greater speed and agility. As a separate entity, we anticipate leveraging increased investments to drive meaningful innovation and enhance our impact on patient care.
**Responsibilities may include the following and other duties may be assigned:**
+ Supports the development and maintenance of quality programs, systems, processes and procedures that ensure compliance with policies and that the performance and quality of services conform to established internal and external standards and guidelines.
+ Conduct quality reviews of Change Orders for Quality Management System documents and records.
+ Provides expertise and guidance to stakeholders in interpreting policies, regulatory and/or governmental regulations, and internal regulations to assure compliance.
+ Supports audit and inspection preparation, resolution of audit and inspection findings and liaises with auditing groups and inspectors through all stages of the audits.
+ Prepares reports and/or necessary documentation, data analysis, etc. and provides to applicable stakeholders.
+ Co-ordinates implementation of enterprise changes within local quality management system.
+ Co-ordinates legal requests in support of government investigations or litigations.
+ Ensures the quality assurance programs and policies are maintained and modified regularly.
+ Facilitates uniform standards worldwide and enables best practice sharing, thereby fostering the achievement of company's mission globally.
+ Leads smaller quality projects and project teams, while facilitating larger quality projects in a variety of roles
**Required Knowledge and Experience:**
+ Bachelor's Degree in Pharmaceutical Sciences, Industrial Engineering, Biomedical Engineering, or field related experience
+ Experience with medical device industry Regulations, Standards and Quality Management Systems
+ Intermediate or better level of experience with Microsoft suite, including but not limited to Word, Excel, SharePoint, Teams, PowerPoint and Adobe
+ Experience with Oracle Agile, Trackwise and/or PowerBI systems
+ Experience in FDA, Certifying Body and/or Notified Body audits/inspections
+ Experience or training in project management
**Physical Job Requirements**
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
**Benefits & Compensation**
**Medtronic offers a competitive Salary and flexible Benefits Package**
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
**About Medtronic**
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
Learn more about our business, mission, and our commitment to diversity here ( lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
**We change lives** . Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.
**We build extraordinary solutions as one team** . With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.
**This life-changing career is yours to engineer** . By bringing your ambitious ideas, unique perspective and contributions, you will.
+ **Build** a better future, amplifying your impact on the causes that matter to you and the world
+ **Grow** a career reflective of your passion and abilities
+ **Connect** to a dynamic and inclusive culture that welcomes the challenge of life-long learning
These commitments set our team apart from the rest:
**Experiences that put people first** . Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.
**Life-transforming technologies** . No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.
**Better outcomes for our world** . Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.
**Insight-driven care** . Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in care
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
For sales reps and other patient facing field employees, going into a healthcare setting is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.
This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here ( .
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Quality Systems Improvement Staff
Posted today
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Completed 2 years in College/ Bachelor's Degree (Business Courses)
At least 3 years of experience in manufacturing improvement in Electronics/Semicon company.
Technical Competency:
Ensure that all activities, procedures, and processes comply with internal standards, as well as external regulatory requirements (e.g., ISO 9001, ISO 14001, and ISO 4500, IATF 16949, ISO 22301 and customer-specific requirements).
Support continuous improvement initiatives using methodologies such as Six Sigma, Lean, or Kaizen.
Support cross-functional teams to implement process improvements or corrective actions.
Documentation Management of all initiatives improvement are documented and up-to-date and validation of effective of improvement in manufacturing process.
Validation of effectiveness of improvement to manufacturing line or department.
Job Type: Full-time
Benefits:
- Additional leave
- Company Christmas gift
- Company events
- Free parking
- Health insurance
- Life insurance
- On-site parking
- Opportunities for promotion
- Staff meals provided
- Transportation service provided
Work Location: In person
Quality Systems Internal Auditor
Posted today
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Job Description
- Completed 2 years in College/ Bachelor's Degree (Business Courses)
- With 3 year experience in Quality Assurance/ Quality System or Production Manufacturing Auditor
- Certified Internal Audito
Technical Competence:
- Audit Programme/Audit Planning: Develops an audit programme/audit plan and scope to assess the effectiveness of the ISO.
- Data Collection: Gathers relevant information and documentation to evaluate the system's compliance with the relevant standards.
- Manufacturing Auditing: Conducts on-site audits by reviewing processes, interviewing staff, and observing operations to verify the implementation of the ISO.
- Identifying Non-Conformities: Identifies areas where the ISO is not in compliance or could be improved.
- Knowledge of ISO standards (ISO 9001, ISO 14001, ISO 45001, ISO 22301 and IATF 16949)
Job Type: Full-time
Benefits:
- Additional leave
- Company events
- Health insurance
- Life insurance
- Opportunities for promotion
Work Location: In person
Quality Systems Improvement Staff
Posted today
Job Viewed
Job Description
Completed 2 years in College/ Bachelor's Degree (Business Courses)
At least 3 years of experience in manufacturing improvement in Electronics/Semicon company.
Technical Competency:
Ensure that all activities, procedures, and processes comply with internal standards, as well as external regulatory requirements (e.g., ISO 9001, ISO 14001, and ISO 4500, IATF 16949, ISO 22301 and customer-specific requirements).
Support continuous improvement initiatives using methodologies such as Six Sigma, Lean, or Kaizen.
Support cross-functional teams to implement process improvements or corrective actions.
Documentation Management of all initiatives improvement are documented and up-to-date and validation of effective of improvement in manufacturing process.
Validation of effectiveness of improvement to manufacturing line or department.
Job Type: Full-time
Benefits:
- Additional leave
- Company Christmas gift
- Company events
- Health insurance
- Life insurance
- Opportunities for promotion
Work Location: In person
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Quality Systems Internal Auditor
Posted today
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Job Description
- Completed 2 years in College/ Bachelor's Degree (Business Courses)
- With 3 year experience in Quality Assurance/ Quality System or Production Manufacturing Auditor
- Certified Internal Audito
Technical Competence:
- Audit Programme/Audit Planning: Develops an audit programme/audit plan and scope to assess the effectiveness of the ISO.
- Data Collection: Gathers relevant information and documentation to evaluate the system's compliance with the relevant standards.
- Manufacturing Auditing: Conducts on-site audits by reviewing processes, interviewing staff, and observing operations to verify the implementation of the ISO.
- Identifying Non-Conformities: Identifies areas where the ISO is not in compliance or could be improved.
- Knowledge of ISO standards (ISO 9001, ISO 14001, ISO 45001, ISO 22301 and IATF 16949)
Job Type: Full-time
Quality Systems and Processes Specialist
Posted today
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Job Description
Company Description
Aboitiz Foods
is an integrated regional food and agribusiness company dedicated to creating a high-performance culture anchored on our time-honored values of Integrity, Teamwork, Innovation, and Responsibility. Through the collective strengths of our subsidiaries, Pilmico and Gold Coin, we believe in sustainably feeding Asia's growth from mill to meal.
We are constantly improving and optimizing our processes by integrating the value chain around Asia. We leverage our sector expertise and capabilities to deliver quality every time. With our world-class technology and culture of constant innovation, we devote ourselves to serving you better.
At Aboitiz Foods, we embrace change and inspire innovation, leading the way in food and agribusiness solutions. Join us as we shape the future of food in Asia and build a culture where, together, we nourish the future.
Job Description
The
Quality Systems and Processes Specialist
spearheads programs and initiatives in ensuring that the implementation of the Company's systems and processes are regularly monitored, analyzed and improved for its efficient and effective operations. He/She reports the development of his/her outputs to the QSP Supervisor.
Provides assistance to QSP Supervisor in ensuring that the company's guidelines & policies for systems and processes as well as External Interested Parties (e.g. customer and legal requirements) are implemented and up to date.
- Coordinates with the departments on their compliance to the established systems and processes, ensuring that overall performance are reported, recorded and monitored.
- Gives assistance to QSP Supervisor in ensuring that objectives of established systems and processes are aligned to the Context & Strategic direction of the organization through regular review
- Ensures that requirements of the Food Safety System Certification and HACCP are implemented, maintained and regularly reviewed. Gives assistance to Quality Management System & HALAL Assurance System requirements.
- Ensures that resources needed for the Food Safety/HACCP and QMS Certifications are provided and made available.
- Supports stakeholders to contribute to the effectiveness of the Food Safety systems and processes.
- Supports QSP Supervisor in promoting improvements of the established Food Safety and Quality systems and processes to other teams.
- Performs QMS/HACCP and other relevant audits for various business processes.
- Ensures that departmental issues regarding Food Safety systems and processes are resolved effectively and without undue delays.
- Conducts training on food safety systems & processes to all relevant stakeholders.
- Supports QSP Supervisor in providing assistance to suppliers and service providers audits.
- Participates and contributes to the department's scheduled meetings & discussions.
Other Responsibilities
- Keep abreast with the new developments and advances on industry practices, quality management technology through attending seminars and conferences, networking with local and foreign quality experts and liaison with other quality institutions / organizations.
- Participates in all Company initiatives and programs as well as provide support whenever necessary
- Performs other job-related duties as assigned.
Qualifications
- Graduate of Industrial Engineering, Food Technology, Chemistry, Chemical Engineering, or any Science and Technology course.
- Preferably with at least 1-2 years' experience in related work
- Excellent communication skills and fluent in English both written and spoken.
- Knowledge and understanding to Food Safety/HACCP and Quality Management System
- Training and presentation skills.
- Competent in the use of Microsoft Office programs and Google Suite (familiarity with Looker Studio is preferrable).
- Ability to establish interpersonal relationships.
- Proactive and able to act on his or her own initiative.
- Ability to handle, motivate and influence people.
- Progressive thinking
- Above average leadership skill
- Good planning skills
- Able to translate standard requirements to operations people
Additional Information
- Willing to be based in Capas, Tarlac
Quality Systems and Processes Specialist
Posted today
Job Viewed
Job Description
Company Description
Aboitiz Foods is an integrated regional food and agribusiness company dedicated to creating a high-performance culture anchored on our time-honored values of Integrity, Teamwork, Innovation, and Responsibility. Through the collective strengths of our subsidiaries, Pilmico and Gold Coin, we believe in sustainably feeding Asia's growth from mill to meal.
We are constantly improving and optimizing our processes by integrating the value chain around Asia. We leverage our sector expertise and capabilities to deliver quality every time. With our world-class technology and culture of constant innovation, we devote ourselves to serving you better.
At Aboitiz Foods, we embrace change and inspire innovation, leading the way in food and agribusiness solutions. Join us as we shape the future of food in Asia and build a culture where, together, we nourish the future.
Job Description
The Quality Systems and Processes Specialist spearheads programs and initiatives in ensuring that the implementation of the Company's systems and processes are regularly monitored, analyzed and improved for its efficient and effective operations. He/She reports the development of his/her outputs to the QSP Supervisor.
Provides assistance to QSP Supervisor in ensuring that the company's guidelines & policies for systems and processes as well as External Interested Parties (e.g. customer and legal requirements) are implemented and up to date.
- Coordinates with the departments on their compliance to the established systems and processes, ensuring that overall performance are reported, recorded and monitored.
- Gives assistance to QSP Supervisor in ensuring that objectives of established systems and processes are aligned to the Context & Strategic direction of the organization through regular review
- Ensures that requirements of the Food Safety System Certification and HACCP are implemented, maintained and regularly reviewed. Gives assistance to Quality Management System & HALAL Assurance System requirements.
- Ensures that resources needed for the Food Safety/HACCP and QMS Certifications are provided and made available.
- Supports stakeholders to contribute to the effectiveness of the Food Safety systems and processes.
- Supports QSP Supervisor in promoting improvements of the established Food Safety and Quality systems and processes to other teams.
- Performs QMS/HACCP and other relevant audits for various business processes.
- Ensures that departmental issues regarding Food Safety systems and processes are resolved effectively and without undue delays.
- Conducts training on food safety systems & processes to all relevant stakeholders.
- Supports QSP Supervisor in providing assistance to suppliers and service providers audits.
- Participates and contributes to the department's scheduled meetings & discussions.
Other Responsibilities
- Keep abreast with the new developments and advances on industry practices, quality management technology through attending seminars and conferences, networking with local and foreign quality experts and liaison with other quality institutions / organizations.
- Participates in all Company initiatives and programs as well as provide support whenever necessary
- Performs other job-related duties as assigned.
Qualifications
- Graduate of Industrial Engineering, Food Technology, Chemistry, Chemical Engineering, or any Science and Technology course.
- Preferably with at least 1-2 years' experience in related work
- Excellent communication skills and fluent in English both written and spoken.
- Knowledge and understanding to Food Safety/HACCP and Quality Management System
- Training and presentation skills.
- Competent in the use of Microsoft Office programs and Google Suite (familiarity with Looker Studio is preferrable).
- Ability to establish interpersonal relationships.
- Proactive and able to act on his or her own initiative.
- Ability to handle, motivate and influence people.
- Progressive thinking
- Above average leadership skill
- Good planning skills
- Able to translate standard requirements to operations people
Additional Information
- Willing to be based in Capas, Tarlac