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April

Quality Assurance Coordinator

Job Search - Collingwood, VIC

Biotech, R&D, Science
Source: uWorkin

JOB DESCRIPTION

Our vision is focused on premium nutrition and lifetime wellness; to inspire and achieve this vision we bring together seven international brands as we strive to make people around the world healthier and happier. We have established market positions in more than 12 countries in Asia-Pacific, Europe, North America and Oceania with more than 2,800 employees working across the globe. We are excited about our future as we expand these premium, proven and aspirational brands to new markets, greeting consumers in all life stages.

Life at H&H Group is nothing short of extraordinary. By being true to our mission and vision, living our values and choosing our mindset, we create an environment where we can be first and fast in all we do. Our commitment to innovation means you'll be encouraged to exercise your imagination to generate big idea thinking.

Your role within the team

The Quality Assurance Coordinator monitors the Quality Management System in compliance with the PIC/S Guide to Good Manufacturing Practice for Medicinal Products in all facility and inspection areas in consultation with the Quality Manager.

Specifically, the Quality Assurance Coordinator inspects materials, processes and products ensuring compliance with existing quality standards and regulations, implementing quality management actions, and contributing to the development of company policies and procedures.

Key responsibilities include:

  • Supporting Quality Control key functions, including performing release testing of incoming goods, bulk and finished product and activities associated with this testing.
  • Supporting Quality Management Systems (QMS) Document Control, Training, Trending of Quality Control data and Product Quality Reviews (PQRs)
  • Assist Quality Team and wider Swisse Team with Compliance and GxP projects.
  • Perform routine release testing (physical testing by visual inspection) of Incoming Goods, Bulk and Finished Product according to approved Test Methods based on international pharmacopial methods (BP, USP, PhEur)
  • Organising external contract testing (e.g. chemical and micro testing) by approved Contract Testing Laboratories.
  • Compilation of Product Quality Reviews for review by the Quality Assurance Manager.
  • Adherence to all Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), Good Documentation Practice (GDP) and Good Housekeeping Practice (GHP) requirements with a basic understanding of TGA regulations.

What you will need

We look for people who have what it takes to make an impact; who can challenge us to go further while pushing themselves to deliver exciting and ambitious results.

To make sure we’re setting new starters up for success, we ask that you meet a few criteria relevant to the role to be considered for this opportunity:

  • A relevant tertiary qualification in a Science discipline or at least 2 years working in a similar pharmaceutical or regulated medical company.
  • Expertise in working in a Quality Control laboratory
  • Proficiency in Microsoft Office (Word and Excel) and Quality Management Systems
  • Excellent written, verbal and presentation skills
  • Excellent organisational and follow-up skills
  • Competent in problem solving, team building, planning and decision making

How to Apply:

If you have what it takes, please apply via the online portal and a member of our Talent Team will be in touch over the coming weeks.

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