QMS Specialist

philips· NL3M Philips International BV
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📍 ShanghaiFull time

About this role

Job Title

QMS Specialist

Job Description

The QMS Specialist is responsible for supporting the establishment of a compliant and effective Quality Management System (QMS) for the activities in scope. The role participates in developing and revising QMS process documents, such as SOPs and quality manuals, ensuring their accuracy and currency. The role works under general supervision, and collaborates with cross-functional teams to resolve quality issues through root cause analysis and corrective actions. The role collects and reports data on QMS performance metrics and tracks non-conformance reports, contributing to continuous improvement activities.

Job Responsibilities

  • Participates in the effective deployment and continuous improvement of QMS processes in the assigned area/areas such as document control, training, and audits, by providing technical expertise and ensuring compliance with regulatory standards.

  • Collects, compiles, and reports data on QMS performance metrics, such as non-conformances, critical findings, and training completion rates, to support management in decision-making.

  • Contributes to continuous improvement initiatives by identifying opportunities for enhancing efficiency and compliance within existing QMS processes and providing support in implementing improvements.

  • Participates in the planning and organization of internal audits by preparing necessary documentation, assisting audit teams during audits, and ensuring follow-up actions are completed.

  • Ensures the proper maintenance, organization, and archiving of quality records in accordance with QMS procedures, regulatory requirements, and company policies to maintain audit readiness.

  • Collaborates with cross-functional teams and stakeholders to ensure effective communication and understanding of QMS processes, and provide basic guidance on compliance-related inquiries.

  • Participates in problem-solving sessions by providing data and insights related to quality processes, supporting the identification of root causes, and recommending potential corrective actions.

  • Works under general supervision and established processes, utilizing independent judgment to navigate and adhere to operational policies, ensuring compliance and optimal performance.

  • Engages in risk management activities, identifying potential risks to regulatory compliance, quality and QMS integrity, and proposing mitigation strategies to minimize impact.

  • Participates in training sessions to stay updated on quality standards and QMS procedures, actively engaging in learning opportunities to enhance understanding of industry regulations and best practices.

  • Develops professional expertise and applies comprehensive knowledge of company products and services to effectively address challenges and opportunities.

Education

Vocational Education/ Bachelor's Degree in Mechanical Engineering, Industrial Engineering, Science or equivalent.

Work Experience

No prior experience required with Bachelor's OR minimum 4 years of experience in Quality Management Systems, Quality Audits or equivalent in highly regulated environments/industries such as MD, Pharma, Automotive with Vocational Education.

Preferred Skills

  • Regulatory Requirements

  • Quality Management Systems (QMS)

  • Troubleshooting

  • KPI Monitoring and Reporting

  • Data Analysis & Interpretation

  • Process Improvements

  • Agile Methodology

  • User Training & Support

  • Training Content Development

  • Business Acumen


How we work together
We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week.
Onsite roles require full-time presence in the company’s facilities.
Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.
Indicate if this role is an office/field/onsite role.
About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
• Learn more about our business.
• Discover our rich and exciting history.
• Learn more about our purpose.
If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care here.

Frequently Asked Questions

Is the salary disclosed for the QMS Specialist position at philips?
The salary for this QMS Specialist role at philips is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the QMS Specialist position at philips located?
This QMS Specialist role at philips is based in Shanghai. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the QMS Specialist role at philips full-time or part-time?
This is listed as a Full time position. It is posted as a QMS Specialist role in the NL3M Philips International BV department at philips.
Which team or department does the QMS Specialist at philips belong to?
This QMS Specialist position is part of the NL3M Philips International BV department at philips. See the full job description for more information about the team structure and responsibilities.
How do I apply for the QMS Specialist position at philips?
Click the "Apply Now" button on this page. You will be redirected to philips's official application portal hosted on workday where you can submit your application directly.
When was the QMS Specialist job at philips posted?
This QMS Specialist position at philips was posted on Jul 3, 2026. Apply as soon as possible — early applications are often reviewed first.
QMS Specialist
philips
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