Quality Engineer II

Medtronic; Singapore; On-site; SGD 60,000 - 90,000; Full time

Benefits offered by this job

Medtronic Incentive Plan (MIP)

Competitive benefits

Job summary

Medtronic in Singapore is hiring a Quality Engineer II to support QA/QE activities across manufacturing operations. You will investigate quality issues, implement corrective actions, and drive continuous improvement in a fast-paced medical device environment.

The role requires collaboration with engineering and manufacturing teams, ensuring compliance with quality systems and regulatory requirements while maintaining product quality and reliability.

Qualifications

• Experience with quality investigations and problem-solving methodologies.
• Knowledge of CAPA, SPC, and FMEA.
• Experience with process validation and equipment qualification.

Responsibilities

• Supports quality assurance and quality engineering activities across operations.
• Investigates quality issues and collaborates with cross-functional teams.
• Implements corrective actions and drives continuous improvement.
• Maintains compliance with quality systems and regulatory requirements.
• Develops, updates and revises Quality Management System documents.

Skills

Quality investigations

Data analysis

CAPA / SPC / FMEA

Process validation support

Equipment qualification

Education

Bachelor's in Quality/Engineering

Master's degree (optional)

Job description

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.

A Day in the Life

Medtronic's Neuroscience portfolio is dedicated to helping people regain function, reduce pain, and improve quality of life through innovative therapies. Within Neuroscience, the Pelvic Health Operating Unit develops minimally invasive neuromodulation solutions that help patients manage bladder and bowel control conditions and achieve greater independence and confidence.

The Medtronic Singapore Operations (MSO) is responsible for delivering high-quality products through robust manufacturing, quality, and operational excellence processes. Within the Quality function, this role supports product and process quality activities across manufacturing operations to ensure compliance with quality system and regulatory requirements.

Located at Medtronic's headquarters in Minneapolis, MN, this role is onsite four days per week. Travel is not required for this role.

This position is based in Singapore and is an onsite role.

As a Quality Engineer II, you will support quality assurance and quality engineering activities to ensure products, materials, and manufacturing processes meet established quality standards. You will partner with cross-functional teams to investigate quality issues, implement corrective actions, and drive continuous improvement initiatives.

Primary Responsibilities

• Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product.
• Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
• Evaluate internal manufacturing processes upon receiving customer complaints.
• Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
• Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.
• Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
• May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality
• Develop, update and revise Quality Management System Document and ensuring compliance with standards, internal policies and regulations established by regulatory bodies.

Required Qualifications

• Bachelor's degree and 2+ years of experience in Quality Engineering, Quality Assurance, or Manufacturing Engineering; OR Master's degree with no experience required.
• Experience working with engineering and manufacturing teams
• Experience with quality investigations, data analysis, and problem-solving methodologies.
• Knowledge of quality systems and documentation requirements.
• Experience in the medical device, pharmaceutical, or life sciences industry.
• Knowledge of Corrective and Preventive Action (CAPA), Statistical Process Control (SPC), or Failure Mode and Effects Analysis (FMEA).
• Experience supporting process validation, equipment qualification, or product reliability activities.

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).