Supplier Quality Engineer

Features:

• Opportunity to join a reputable medical device and pharmaceutical manufacturer with exposure to FDA, TGA and European Notified Bodies.
• Collaborative, respectful, and innovative company environment.
• Competitive Salary Package.
• Career progression opportunities.
• Onsite Parking.

Benefits
Gain exposure in both medical device and pharmaceutical operational activities whilst working in a company with a positive team culture.

About the company
With over 30 years’ experience in research and design, this medical device company brings an innovative and niche product to the healthcare industry. The Sydney-based device company is driven by enhancing and developing medical innovations for diagnostic imaging, specialising in lung health. This is an exciting time to join the organisation as they have obtained new market share and enhanced products.


About the opportunity
As the Supplier Quality Engineer, you will be required onsite daily overseeing all supplier-related aspects. This involves managing the existing supplier list, engaging with new suppliers, and performing supplier audits to ensure purchased materials meet compliance requirements. You will report directly to the Head of Quality and collaborate closely with other departments. To be successful in this role, you must possess excellent communication skills, a solution-driven mindset, and proactive initiative.

Duties

• Inspecting suppliers against specifications and reporting deviations.
• Conduct external audits when required.
• Management of the Vendor Qualification program.
• Liaising with new suppliers.
• Track and manage maintenance of Issues/Actions with supplier’s follow-up on actions such as non-conformances, deviations, design, development, post market.
• Providing solutions and ensuring corrective action aligns with the current standards.
• Ensuring all documents comply with the current requirements.
• Interstate travel required for supplier audits.

Skills and Experience

• Tertiary qualification in a Science, Engineering, or related field
• Minimum 2 years of experience in Quality Assurance or supplier management within a GMP-certified medical device or pharmaceutical environment.
• Knowledge and understanding of GMP, GDP environments and regulatory compliance requirements.
• Strong written and verbal communication skills.
• Great organizational and problem-solving skills.
• Strong interpersonal skills.
• Ability to work individually and as part of a team.

Culture
Collaborative team environment. This company values integrity, innovation, and quality whilst manufacturing and developing innovative technologies.


How to Apply
Click apply or email Tamara El Husseini, Recruitment Consultant on telhusseini@hpgconnect.com for a confidential discussion