Senior Quality Assurance Engineer - Audits

Posted 10 Days Ago
Be an Early Applicant
Sydney, New South Wales, AUS
In-Office
Senior level
Healthtech
The Role
Leads internal, supplier, and external quality systems audits; coordinates CAPA investigations and corrective actions; prepares audit responses; mentors auditors; reports audit-program status; improves audit processes; and supports global quality-system deployment. The role requires extensive medical-device quality assurance experience, lead-auditor training, and knowledge of ISO 13485, 21 CFR Part 820, QMSR, and related regulatory frameworks. Travel is required for audits.
Summary Generated by Built In

Job Summary

The primary role of the Quality Assurance – Quality Systems function is to ensure that management systems are established and maintained to enable business compliance with multiple regulatory frameworks and support the design, development and manufacture of products that meet customer quality requirements.

The function supports all aspects of the audit program to ensure regulatory compliance, quality best practice, process improvement and the development of supplier quality systems. It provides broad technical support across the business for QA systems and processes, supports and implements significant quality projects, and creates and improves quality and business processes.

Let’s talk about Responsibilities

  • Prepare a comprehensive internal and supplier audit program that meets business requirements and applicable external regulatory body expectations.
  • Support the global internal quality auditor program, including mentoring and coaching less-experienced auditors in their internal audit assignments.
  • Work with business and process stakeholders to effectively implement the audit program and coordinate CAPA investigations with CAPA owners, as required.
  • Ensure internal audits are conducted and followed up through effective corrective action implementation.
  • Review audit findings for adequacy and the effectiveness of actions prior to closure.
  • Project-manage activities required to prepare for external audits and address findings raised during external audits.
  • Prepare formal responses to external audits for management review prior to submission.
  • Review quality audit processes, policies and tools on an ongoing basis to ensure they remain relevant and valuable to the business.
  • Provide management with reports on the status of the audit program, including an assessment of potential business impact.
  • Develop and implement strategies for the continual improvement of the audit system, aligned with recognised best practice and informed by analysis of specific Resmed needs.
  • Work with corresponding QA teams in other parts of Resmed to ensure audit systems are aligned and suitable for global deployment, where appropriate.
  • Travel as required to conduct supplier and internal audits, and to support external audits.

Let’s talk about Qualifications and Experience

Required (Qualifications/experiences that are an absolute must for the position)

  • Bachelor’s degree in science or engineering.
  • Experience with ISO 13485 and 21 CFR Part 820 requirements.
  • Minimum of 8 years applied professional quality assurance experience, ideally including experience in the medical device industry.
  • Formal training and experience as a lead auditor for Quality Systems audits.
  • Knowledge of Quality System requirements and their practical application in medical device manufacturing and development, including but not limited to QMSR, ISO 9001 and ISO 13485.

Preferred (Qualifications/experiences that are preferred for the position)

  • Experience in a regulated industry associated with manufacturing or design, including ISO, MDSAP, FDA CFR, EU MDR and TGA requirements.
  • Knowledge of Environmental Management Systems, including but not limited to ISO 14001.
  • Experience in conducting supplier audits.
  • Knowledge and application of Six Sigma, Lean methodologies, 8D and other problem-solving techniques.
  • Moderate statistical analysis skills and experience applying AI tools or techniques.
  • Strong listening, verbal, and written communication skills.
  • Change management skills.
  • The ability to identify linkages and dependencies between processes.
  • Ability to think clearly and critically, assess information and evidence, and make informed, timely decisions.
  • Agility to adapt and respond quickly, with resilience to overcome obstacles.

Joining us is more than saying “yes” to making the world a healthier place. It’s discovering a career that’s challenging, supportive and inspiring. Where a culture driven by excellence helps you not only meet your goals, but also create new ones. We focus on creating a diverse and inclusive culture, encouraging individual expression in the workplace and thrive on the innovative ideas this generates. If this sounds like the workplace for you, apply now! We commit to respond to every applicant.

Skills Required

  • Bachelor's degree in science or engineering
  • Experience with ISO 13485 requirements
  • Experience with 21 CFR Part 820 requirements
  • At least 8 years of applied professional quality assurance experience
  • Experience in the medical device industry is preferred within the required QA experience
  • Formal training and experience as a lead auditor for Quality Systems audits
  • Knowledge and practical application of quality system requirements in medical device manufacturing and development
  • Knowledge of QMSR, ISO 9001, and ISO 13485
  • Experience in a regulated manufacturing or design industry
  • Experience with ISO, MDSAP, FDA CFR, EU MDR, and TGA requirements
  • Knowledge of Environmental Management Systems, including ISO 14001
  • Experience conducting supplier audits
  • Knowledge of Six Sigma, Lean, 8D, and other problem-solving methodologies
  • Moderate statistical analysis skills and experience applying AI tools or techniques
  • Strong listening, verbal, and written communication skills
  • Change management skills
  • Ability to identify process linkages and dependencies
  • Ability to critically assess information and evidence and make timely decisions
  • Adaptability, agility, and resilience

ResMed Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about ResMed and has not been reviewed or approved by ResMed.

  • Strong & Reliable Incentives Bonuses are considered a meaningful component of total compensation and are paid regularly. Annual payouts and performance incentives are frequently highlighted alongside base pay.
  • Healthcare Strength Health coverage is described as comprehensive, including medical, dental, and vision plans that are viewed favorably. Wellbeing resources and flexibility around care reinforce the overall strength of the offering.
  • Equity Value & Accessibility An employee stock purchase plan is broadly available and regarded as a valuable ownership benefit. Equity elements are positioned as accessible parts of total rewards across many roles.

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The Company
HQ: San Diego, CA
5,300 Employees
Year Founded: 1989

What We Do

ResMed provides medical equipment for treating, diagnosing, and managing sleep-disordered breathing and other respiratory disorders.

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