Senior QA Associate - 28263BR - EI in St Leonards at Stryker Corporation

Date Posted: 5/5/2018

Job Snapshot

Job Description

We help to change and save people’s lives through teamwork, dedication and innovative technology. We care about our customers, patients and each other which is why we are consistently recognised as a great place to work. Our continued success means we are expanding our team.

We are looking for exceptional people who truly want to make a difference…. because at Stryker we do!! Working for Australia’s #1 best place to work is rewarding. We help to change and saves people’s lives every single day. We are high achievers who know how to work hard and have fun.

The main objective of this role is to be the subject matter expert for quality management systems within Stryker South Pacific.

Main responsibilities include:
  • Responsible for overall certification process and maintenance
  • Ownership of identified core processes of Quality Management System
  • Lead auditor for internal (head office and branch), and external supplier audits including OEMs
  • Ensure compliance of all suppliers to corporate RAQA requirements and relevant regulations
  • SME representing Quality for Merger & Acquisition activities
  • Responsible for partnering with areas of business to ensure activities are in compliance with Quality System
  • Provide mentoring, assistance and training to core quality management system processes where required
  • Provide mentoring and assistance to junior members of Quality team
  • Monitoring and reporting of quality activity ensuring management is informed in a timely manner of changes/trends that could affect SSPs quality system
  • Reporting of SSPs audit performance and results to executive leadership corporate RAQA
  • Ensure compliance of documents to corporate RAQA policies and incorporate into SSP Quality Management System
  • Ensure SSP maintains an exemplary record of compliance and commitment to relevant quality standards by working with, and influencing all departments
  • Identify areas for process improvement and implement actions accordingly.
As the successful candidate, you will have:
  • Ideally 5+ years’ experience in the Medical Device Quality Systems
  • Experience in implementing and maintaining quality systems
  • Experience in the development of training material & facilitation
  • Knowledge and understanding of applicable external regulatory standards
  • Strong interpersonal and project management skills, must be able to interact effectively at all levels of the company and handle confidential and sensitive information appropriately
If you want a change in pace, some excitement in your work and to feel a sense of satisfaction that you are helping make healthcare better for customers, then apply below. Or to find out more about this or any other potential role within our business, please visit to view our current vacancies.

Job Requirements

As above

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