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Stryker

Manufactures orthopedic and surgical medical devices

Quality Assurance

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeSingaporeNo salary listed

About the Job

Requirements

  • A minimum bachelor's degree in Pharmacy, Biomedical Sciences, or a related discipline is required.
  • Experience in the medical device, healthcare, or pharmaceutical industry is preferred.
  • Knowledge of quality management systems and applicable regulations or standards, such as ISO 13485, GDPMDS, or GDPMD, is preferred.
  • Strong attention to detail and a quality mindset are required.
  • Good communication skills are required.
  • Ability to work independently and manage multiple priorities is required.
  • Strong organizational skills are required.
  • Ability to work effectively across functions and cultures is required.

Responsibilities

  • Support implementation and maintenance of the East Asia Quality Management System (QMS) and continuous improvement activities.
  • Manage Product Complaints, Commercial Holds, Field Safety Corrective Actions (FSCAs), Product Field Actions (PFAs), and Adverse Event reporting with local teams and manufacturing divisions, ensuring timely execution and closure in accordance with internal and regulatory requirements.
  • Support regulatory reporting by providing quality-related information and documentation for submissions to local regulatory authorities.
  • Support document control activities, including document change management and training management, in accordance with established procedures.
  • Monitor and maintain quality key performance indicators (KPIs) and support periodic reporting as required.
  • Support preparation for internal and external audits as required.
  • Assist in maintaining compliance with QMS requirements and implementing quality process improvements.
  • Maintain awareness of applicable quality and regulatory requirements and support implementation of required actions.
  • Perform assigned quality activities as needs and opportunities arise.
  • Collaborate with cross-functional teams and the East Asia QA team to support effective QMS implementation.
  • Collaborate effectively with cross-functional teams to support quality objectives.

Desired Qualifications

  • Experience in the medical device, healthcare, or pharmaceutical industry.
  • Knowledge of quality management systems and applicable regulations or standards, such as ISO 13485, GDPMDS, or GDPMD.

About the Company

Stryker

Manufactures orthopedic and surgical medical devices

Stryker makes medical devices for hospitals, surgical centers and emergency responders, spanning joint implants, surgical instruments and patient transport equipment. Its Mako platform assists surgeons with joint replacement, while its neurotechnology products support brain and spine procedures and stroke treatment. Clinicians use its equipment during surgery and emergency care, and the company earns money by selling implants, disposable products and capital equipment through direct sales teams and distributors. The business also supplies training and technical support for healthcare providers using its devices. Stryker was founded in 1941 and is headquartered in Portage, Michigan.

Company size
10,001+
Company stage
IPO
Headquarters
Portage, MI
Founded
1941

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