Sr Supervisor, Quality Systems

Sr Supervisor, Quality Systems

Apply locations: Singapore
Time type: Full time
Posted on: Posted Yesterday
Job requisition id: Req-40127

Make a meaningful difference to patients around the world. At Edwards Lifesciences, our Manufacturing teams create the tools, technologies, and devices that transform patients’ lives. Your attention to detail and commitment to continuous improvement will help us turn innovative ideas into reality, leaving a lasting positive impact on patient lives.

How you’ll make an impact:

1. Supervise a team of QS related roles coordinators/associates and oversee daily activities, including establishing schedules, organizing and overseeing the execution of complex change efforts, ensuring staff is appropriately trained, and providing guidance and coaching.
2. Lead in the evaluation of current and new processes, identify opportunities, and implement solutions to improve efficiency within and between related functional areas. Identify technical and/or process problems to determine root causes, propose recommendations, and develop improvement strategies.
3. Act as a liaison between the corporate team and personnel for unresolved issues. Work with the global team to establish a common approach to compliance management and lead improvement initiatives across functional/global boundaries for QS related roles.
4. Ensure compliance with internal procedures, and that the change control process continuously meets EW Quality System requirements in compliance with regulatory requirements.
5. Serve as the Subject Matter Expert (SME) for Quality Systems. Provide training to employees across functions to ensure appropriate understanding and deployment of the system.
6. Review and analyze performance metrics. Share trend metrics with management.
7. Other incidental duties assigned by Leadership.

What you'll need (Required):

1. Bachelor's Degree in Engineering or related field.
2. 4 years of experience using a document product life cycle management system.
3. Previous experience with full responsibility for all personnel, including hire/fire authority and handling all aspects of employee relations in manufacturing, quality, and/or product development engineering.

What else we look for (Preferred):

1. Proven project management expertise.
2. Experience in the medical device industry.
3. Proven expertise in Microsoft Office Suite and Enterprise Resource Planning (ERP) systems, preferably JDE.
4. Excellent written and verbal communication, and interpersonal relationship skills.
5. Solid understanding of medical device documentation development activities.
6. Full understanding of quality procedures and the ability to analyze and solve problems.
7. Demonstrated ability to supervise teams and provide coaching and feedback.
8. Strong documentation, communication, and interpersonal relationship skills.
9. Ability to interact professionally with all organizational levels.
10. Ability to develop creative solutions to challenging problems.

About Us

Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations worldwide and currently employs over 15,000 individuals.

For us, helping patients is not a slogan - it's our life's work.