Role Description In this exciting role as Supplier Quality Engineer II, you will be responsible for the management of our strategic Contract Manufacturers (CMs) and Original Equipment Manufacturers (OEMs) at Medtronic, with accountability to support changes to existing supplied products and processes, as well as oversight of performance and improvement activities. While partnering with our CMs and OEMs, including sub-tier suppliers as required, this position is responsible for maintaining necessary controls and driving improvements relating to finished medical device/component quality in conjunction and within our suppliers’ quality systems. The individual is expected to be proficient in communication, project management, and troubleshooting complex medical devices involving mechanical, electrical, and software interactions. Hands-on experience with schematics, system diagnostics, and root cause analysis is required. Familiarity with medical device quality standards (ISO 13485, IEC 60601, IEC 62304) and structured problem-solving in a regulated environment is essential. Responsibilities may include the following and other duties may be assigned: - Ensures that suppliers deliver quality parts, materials, and services. - Qualifies suppliers according to company standards and may administer a Certified Supplier Program in receiving inspection to ensure cost effectiveness. - Monitors parts from acquisition through the manufacturing cycle and communicates and resolves supplier-related problems as they occur. - Develops and prioritizes an auditing schedule to ensure that designated suppliers are audited on a regular basis to ensure good manufacturing practices (GMP) and quality standards are met. - Evaluates suppliers' internal functions to assess their overall performance and provides feedback in assessment of their operation. - Provides Pre-Market Quality Engineering support to New Product Development (NPD) working in partnership with the Component Engineering and Post-Market Supplier Quality Teams. - Provides technical guidance and quality compliance for Supplier Quality engagement throughout the NPD lifecycle on newly qualified parts from NPD. - Collaborates with Component Engineers to develop and deliver the Product Acceptance Sampling Strategy, Approved Supplier List coordination, Supplier Owned Quality deployment, and Control Plans for new products. - Defines Receiving Inspection requirements as required and associated test method validation for all internal Medtronic Test Methods. Qualifications - Strong technical background in medical device mechanical assembly processes. - Experience with injection molded components, tooling considerations, and molding-related defect analysis. - Strong knowledge of metrology & measurement techniques; statistical analysis (Ppk/Cpk, standard deviation, etc.) in Minitab, measurement uncertainty, GD&T, Gauge Repeatability & Reproducibility. - Experience with sterile barrier packaging, package integrity considerations, and packaging-related validation support. - Hands-on experience with root cause analysis, nonconformance investigation, and structured problem-solving. - Familiarity with medical device quality systems and regulated product development/manufacturing environments, including ISO 13485. - Ability to work cross-functionally with design, manufacturing, quality, supplier, and packaging engineering teams. - Strong interpersonal, organizational and project management skills. - Demonstrated communication skills, both verbal and written. - Computer skills in MS Office and ERP systems desirable. - ASQ CQE, CQA and/or CSQP certification. - First Time Quality Coach (FTQ) / Six Sigma/ DFSS / Lean Green Belt or Black Belt certified. - Demonstrated track record of effectively influencing and negotiating with others and leading effective/successful change initiatives. Requirements - Requires a Baccalaureate degree and minimum of 2 years of relevant experience OR Master's degree with a minimum of 0 years relevant experience. Benefits - Medtronic offers a competitive Salary and flexible Benefits Package. - A commitment to our employees lives at the core of our values. - Wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. - This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

Role Description As a Technical Specialist within Supplier and Distribution Quality, this role is responsible for ensuring suppliers, third-party logistics providers (3PLs), distributors, and service providers consistently deliver quality products and services that meet company, regulatory, and customer requirements. The position leads supplier qualification, auditing, performance monitoring, and corrective action activities while driving continuous improvement across the supply chain. Key responsibilities include: - Supporting new product development by providing pre-market quality engineering expertise. - Collaborating with component engineering teams on supplier selection, product acceptance strategies, control plans, and receiving inspection requirements. - Ensuring suppliers are qualified and compliant throughout the product lifecycle. - Serving as a subject matter expert for distribution quality, focusing on onboarding and qualifying 3PL and distributor activities. - Managing complex quality issues and influencing cross-functional stakeholders. - Implementing process improvements to enhance product quality, reliability, and compliance. - Leading projects, mentoring team members, and providing strategic recommendations. - Building consensus across internal and external partners to achieve organizational objectives and strengthen overall supplier quality performance. This is a fully remote opportunity with flexibility required to support North America, EMEA, and LATAM as needed. Responsibilities may include the following and other duties may be assigned: - Ensures that suppliers (including 3PL and distributors) deliver quality parts, materials, and services. - Qualifies suppliers (including 3PLs and distributors) according to company standards and may administer a Certified Supplier Program in receiving inspection to ensure cost effectiveness. - Monitors parts (or services) from acquisition through the manufacturing cycle and communicates and resolves supplier-related problems as they occur. - Develops and prioritizes an auditing schedule to ensure that designated suppliers are audited on a regular basis to ensure quality standards are met. - Evaluates suppliers' internal functions to assess their overall performance and provides feedback in assessment of their operation. - Provides Pre-Market Quality Engineering support to New Product Development (NPD) working in partnership with the Component Engineering and Post-Market Supplier Quality Teams. - Supports the qualification of Value Added Service activities (packaging and labeling) at DCs and 3PLs. - Provides technical guidance and quality compliance for Supplier Quality engagement throughout the NPD lifecycle. - Collaborates with Component Engineers to develop and deliver the Product Acceptance Sampling Strategy, Approved Supplier List coordination, Supplier Owned Quality deployment, and Control Plans for new products. - Defines Receiving Inspection requirements as required and associated test method validation for all internal Medtronic Test Methods. Qualifications - Bachelor’s degree with 4+ years of relevant experience, or Advanced degree with 2+ years of relevant experience. Requirements - Must have a strong understanding of quality assurance processes and supplier management. - Ability to work independently and lead projects with minimal supervision. - Excellent communication and interpersonal skills to influence cross-functional teams. Benefits - Competitive salary and flexible benefits package. - Health, dental, and vision insurance. - Access to a Health Savings Account and Healthcare Flexible Spending Account. - Life insurance and long-term disability leave. - Dependent daycare spending account. - Incentive plans and a 401(k) plan with company match. - Paid time off and holidays. - Participation in the Employee Stock Purchase Plan. - Access to the Employee Assistance Program. - Eligibility for Non-qualified Retirement Plan Supplement and Capital Accumulation Plan.

• Create, review, and execute manual test cases based on requirements and user stories. • Develop, maintain, and run automated test scripts for web applications. • Perform functional, regression, integration, smoke, exploratory, and UAT testing. • Test APIs using tools such as Postman or similar tools. • Identify, document, and track bugs using Jira, Azure DevOps, or similar tools. • Work closely with developers and product managers to clarify requirements and resolve issues. • Support release testing and provide clear test reports. • Help improve test processes, test coverage, and automation practices. • Participate in Agile ceremonies such as daily stand-ups, sprint planning, and retrospectives.

Role Description At SMG, we turn our patented DAFUZ system to create award-winning titles including LEGO Party!, Moving Out, Thumb Drift, and One More Line. We love building fun first games and we don’t take ourselves too seriously. We are seeking a detail-oriented Junior QA Tester to join us on a 1-year fixed term contract. This role offers flexible, project-based work, testing various software applications. We offer remote working, but have offices in Sydney, Melbourne, Brisbane, Perth, and Adelaide you could work from depending on you having full Australian working rights. If you're on top of your game (or would like to be) and care about your work, then let’s talk! - Execute test cases across various software applications and platforms - Create clear, detailed test cases based on project requirements - Document and report bugs using JIRA, including steps to reproduce, expected results - Collaborate remotely with development teams to verify bug fixes - Adapt to different project requirements and maintain testing documentation Qualifications - An understanding of software testing principles and methodologies - Strong attention to detail and analytical mindset - Ability to work independently and manage time effectively - Experience with JIRA or similar bug tracking systems Benefits - The opportunity to give back with dedicated volunteer leave and our whole-company event, One Day for Change. - 5 weeks annual leave after 2 years of service and 3 whole company Wellness days off per year for you to switch off and take your day, your way. - Career Development and Learning & Development opportunities, including access to our global online dentsu University. - Become a champion for meaningful progress: Our diverse and inclusive culture enables our employees to bring their whole selves to work and be proud of doing so. - We encourage applications from people with disabilities, and of all ages, nationalities, backgrounds, and cultures. - If you want to belong to a one global network where opportunities are limitless – we look forward to welcoming you. Company Description Location: Sydney Brand: Smg Studio Time Type: Full time Contract Type: Fixed Term Contract (Fixed Term)