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Senior Post Market Specialist in St Leonards at Stryker Corporation

Date Posted: 5/2/2019

Job Snapshot

Job Description

Stryker - Proud to be recognised as one of Australia's Best Places to Work again in 2018!

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. We are looking for exceptional people who truly want to make a difference…. because at Stryker we do.

The Role:

In this exciting Senior Post Market Specialist role, you will partner with areas of business to ensure Stryker South Pacific (SSP) follows all Post-Market activities in accordance with Quality System, regulatory and corporate requirements.

Who We Want:

  • Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, information, use cases, and industry analyses to develop best practices.
  • Business-oriented evaluators. People who effectively interpret information to demonstrate the effects of business initiatives, regulation and industry trends for sales, management and leadership teams.
  • Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.
  • Self-starters. People who take ownership of their work and need no prompting to drive productivity, change, and outcomes.
  • Analytical problem solvers. People who go beyond just fixing to identify root causes, evaluate optimal solutions, and recommend comprehensive upgrades to prevent future issues.

What You Will Do:

  • Build relationships and liaise with key stakeholders from regulatory, operations, marketing and sales teams
  • Action complaint handling product holds and product fields
  • Ensure Stryker South Pacific's process reflect all corporate and regulatory requirements
  • Prepare and release regular reports associated with regulatory actions, and Post Market Surveillance
  • Develop quality systems that are contemporary with industry business best practices
  • Identify areas for process improvement and work with key stakeholder both locally and globally to implement actions accordingly.

What You Will Need:

  • 3+ years’ experience in the Health Industry in Regulatory Affairs and/or quality systems and standards such as ISO 9001 and ISO13485
  • Proven experience in post market activity
  • Proven ability to use initiative and drive to achieve results
  • Natural talent to influence and build relationships across an organisation
  • Knowledge and understanding of applicable external regulatory standards, including TGA, ISO 13485, FDA 820, AS/NZS3551
  • Highly developed communication skills and experience working with a diverse range of internal and external customers and clients

If this sounds like you, click apply now!

Work From Home: No

Travel Percentage: None

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