988 Manufacturing Quality jobs in Singapore

Imagine how your ideas and expertise can change a patient’s life. Our Quality teams help shape the development of groundbreaking technologies to ensure each stage of our innovation process is held to the highest standards of integrity and safety. You’ll bring your passion for problem solving and partner with various teams to influence decision-making for a product’s entire lifecycle. Your work will involve you optimizing product development to impact patients around the world with pioneering technology.

How you will make an impact:
• Investigate basic manufacturing product quality and compliance issues (e.g, CAPA, non-conformances, audit observations) for all production processes prior to final product release based on engineering principles; analyze results, make recommendations and develop reports
• Optimize Manufacturing processes using engineering methods (e.g., SIX Sigma and LEAN methods) for design for manufacturing and for continuous process improvement. Identify opportunities for re-design/design of basic equipment, tools, fixtures, etc. to improve manufacturing processes, and reduce risk
• May develop, update, and maintain technical content of risk management files
• Develop training and documentation materials for production (e.g., work instructions) to enable the seamless knowledge transfer of project and manufacturing processes
• Assign support tasks; gives instruction to technicians on conducting tests; trains technicians and provides feedback; and may coordinates technician work
• Other incidental duties assigned by Leadership

What you'll need (Required):
• Bachelor's Degree in in Engineering or Scientific field or Master's Degree or equivalent in in Engineering or Scientific field

What else we look for (Preferred):
• Good computer skills in usage of MS Office Suite; CAD experience preferred
• Basic documentation, communication and interpersonal relationship skills
• Basic understanding of statistical techniques
• Previous experience working with lab/industrial equipment preferred
• Good understanding and knowledge of principles, theories, and concepts relevant to Engineering
• Good problem-solving, organizational, analytical and critical thinking skills
• Good understanding of processes and equipment used in assigned work
• Knowledge of and adherence to Quality systems
• Strict attention to detail
• Ability to interact professionally with all organizational levels
• Ability to manage competing priorities in a fast paced environment
• Must be able to work in a team environment, including immediate supervisor and other team members in the section or group
• Ability to build stable working relationships internally
• Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control

Imagine how your ideas and expertise can change a patient’s life. Our Quality teams help shape the development of groundbreaking technologies to ensure each stage of our innovation process is held to the highest standards of integrity and safety. You’ll bring your passion for problem solving and partner with various teams to influence decision-making for a product’s entire lifecycle. Your work will involve you optimizing product development to impact patients around the world with pioneering technology.
How you will make an impact:
• Investigate basic manufacturing product quality and compliance issues (e.g, CAPA, non-conformances, audit observations) for all production processes prior to final product release based on engineering principles; analyze results, make recommendations and develop reports
• Optimize Manufacturing processes using engineering methods (e.g., SIX Sigma and LEAN methods) for design for manufacturing and for continuous process improvement. Identify opportunities for re-design/design of basic equipment, tools, fixtures, etc. to improve manufacturing processes, and reduce risk
• May develop, update, and maintain technical content of risk management files
• Develop training and documentation materials for production (e.g., work instructions) to enable the seamless knowledge transfer of project and manufacturing processes
• Assign support tasks; gives instruction to technicians on conducting tests; trains technicians and provides feedback; and may coordinates technician work
• Other incidental duties assigned by Leadership
What you'll need (Required):
• Bachelor's Degree in in Engineering or Scientific field or Master's Degree or equivalent in in Engineering or Scientific field
What else we look for (Preferred):
• Good computer skills in usage of MS Office Suite; CAD experience preferred
• Basic documentation, communication and interpersonal relationship skills
• Basic understanding of statistical techniques
• Previous experience working with lab/industrial equipment preferred
• Good understanding and knowledge of principles, theories, and concepts relevant to Engineering
• Good problem-solving, organizational, analytical and critical thinking skills
• Good understanding of processes and equipment used in assigned work
• Knowledge of and adherence to Quality systems
• Strict attention to detail
• Ability to interact professionally with all organizational levels
• Ability to manage competing priorities in a fast paced environment
• Must be able to work in a team environment, including immediate supervisor and other team members in the section or group
• Ability to build stable working relationships internally
• Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control #J-18808-Ljbffr

As a seasoned quality assurance professional, you will be responsible for leading a high-performing Quality team to ensure compliance with food safety, quality, and hygiene standards.

• Develop and implement robust Quality frameworks and Standard Operating Procedures (SOPs) to drive business excellence.
• Conduct thorough risk assessments and implement corrective actions to mitigate risks and prevent non-conformities.
• Drive projects and initiatives to ensure compliance with regulatory requirements, fostering a culture of continuous improvement.
• Schedule and coordinate internal/external quality audits, ensuring seamless execution and effective communication.
• Analyze data and prepare insightful reports for submission to Senior Management, providing actionable recommendations for growth and optimization.

• Strong understanding of SFA, FSSC 22000, HACCP, and GMP regulations, with the ability to apply this knowledge effectively in a dynamic environment.
• Hands-on experience in the food manufacturing industry, with a proven track record of delivering results-driven solutions.
• Excellent leadership, analytical, and communication skills, with the ability to motivate and inspire high-performing teams.
• Demonstrates problem-solving and independent working capabilities, with a strong focus on quality and customer satisfaction.

• Bachelor's degree in Food Science or Technology, or equivalent qualification, with a strong emphasis on quality management and control.
• Minimum 8 years of experience in the food manufacturing industry, with a proven history of delivering high-quality products and services.

Imagine how your ideas and expertise can change a patient’s life. Our Quality teams help shape the development of groundbreaking technologies to ensure each stage of our innovation process is held to the highest standards of integrity and safety. You’ll bring your passion for problem solving and partner with various teams to influence decision-making for a product’s entire lifecycle. Your work will involve you optimizing product development to impact patients around the world with pioneering technology.
How you will make an impact:

• Investigate basic manufacturing product quality and compliance issues (e.g, CAPA, non-conformances, audit observations) for all production processes prior to final product release based on engineering principles; analyze results, make recommendations and develop reports
• Optimize Manufacturing processes using engineering methods (e.g., SIX Sigma and LEAN methods) for design for manufacturing and for continuous process improvement. Identify opportunities for re-design/design of basic equipment, tools, fixtures, etc. to improve manufacturing processes, and reduce risk
• May develop, update, and maintain technical content of risk management files
• Develop training and documentation materials for production (e.g., work instructions) to enable the seamless knowledge transfer of project and manufacturing processes
• Assign support tasks; gives instruction to technicians on conducting tests; trains technicians and provides feedback; and may coordinates technician work
• Other incidental duties assigned by Leadership

What you'll need (Required):
• Bachelor's Degree in in Engineering or Scientific field or Master's Degree or equivalent in in Engineering or Scientific field
What else we look for (Preferred):

• Good computer skills in usage of MS Office Suite; CAD experience preferred
• Basic documentation, communication and interpersonal relationship skills
• Basic understanding of statistical techniques
• Previous experience working with lab/industrial equipment preferred
• Good understanding and knowledge of principles, theories, and concepts relevant to Engineering
• Good problem-solving, organizational, analytical and critical thinking skills
• Good understanding of processes and equipment used in assigned work
• Knowledge of and adherence to Quality systems
• Strict attention to detail
• Ability to interact professionally with all organizational levels
• Ability to manage competing priorities in a fast paced environment
• Must be able to work in a team environment, including immediate supervisor and other team members in the section or group
• Ability to build stable working relationships internally
• Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control
• #J-18808-Ljbffr

Job Title: Manufacturing Quality Control Specialist

We are seeking a seasoned professional to oversee quality control systems, manage inspection teams, and ensure compliance with industry standards.

• Develop and maintain robust quality management systems for manufactured products.

• Lead inspection teams and implement testing methods to guarantee product quality and specifications.

• Analyze customer feedback and resolve quality-related issues in a timely manner.

• Drive continuous improvement in production processes and maintain quality records.

• Maintain proficiency in relevant certifications and train staff on best practices.

• Conduct audits to evaluate quality management systems and make recommendations for improvement.

Requirements:

• Diploma in Engineering or a related field.

• Relevant certifications in Quality Management (e.g., ISO 9001).

• A minimum of 3 years' experience in quality management, preferably in the manufacturing industry.

• Proven track record of leading a team and managing budgets.

• Knowledge of quality standards and testing methodologies.

• Proficiency in computer software.

What We Offer:

• A competitive salary package.

• Opportunities for professional growth and development.

• A dynamic and supportive work environment.

How to Apply:

• Email your resume to us with the job title in the subject line.

This key role requires a team player to work closely with Process Engineers and the Engineering team to ensure quality standards are met.

• Documenting inspection criteria and quality plans is crucial for success in this position
• Collaborating with QA, Process, and Product teams on corrective actions for quality issues
• Working with the Process team on in-process audits and FQC audits

• A diploma in Manufacturing/Quality Engineering or relevant field is required
• At least 1 year of experience in Electronics Product Manufacturing is essential
• Control of Supplier Quality Assurance (SQA) skills are necessary
• Knowledge of ISO 9001, 14001, 13485 & 45001, as well as FDA requirements, is a must

Quality Assurance Specialist

The role involves ensuring the highest quality standards are met across manufacturing operations. It requires collaborating with teams to develop and implement quality control procedures.

• Perform routine quality checks and inspections on all incoming products.
• Conduct checks on production raw materials, production, and company trucks.
• Generate reports and maintain quality assurance records.
• Ensure product adherence to food regulations.
• Report non-conformances to the QA manager for investigation and corrective action.

• Three to five years of experience in a quality assurance or quality control role.
• Strong understanding of quality management systems and techniques.

• Five and a half working days per week: Monday to Friday 8:15am to 5pm, Saturday 8:15am to 12:15pm.
• Location: Senoko.

We regret to inform that only shortlisted candidates will be notified.

We are seeking a Quality Systems Specialist to join our team. The successful candidate will be responsible for maintaining ISO 9001/14001/13485 documentation, ensuring audit readiness and compliance.

• Maintain accurate records of audits and corrective actions to drive quality improvement.
• Lead internal and external audits, managing non-conformities to ensure compliance.
• Oversee supplier quality performance, implementing strategies for continuous improvement.
• Coordinate equipment calibration and maintenance programs to minimize downtime.
• Responsible for resolving production and customer quality issues using root cause analysis techniques.

• Bachelor's degree in Engineering, Quality, or Manufacturing from a recognized institution.
• A minimum of 3-5 years' experience in ISO audit/documentation within manufacturing, with a strong understanding of ISO standards.
• Familiarity with PFMEA, Control Plans, and GR&R principles is essential.
• Proven experience in supplier management and problem-solving methodologies.