ResMed

Quality Auditor

ResMed$68K — $102K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in Engineering or Science
  • Strong communication skills (listening, verbal, written)
  • Experience with Quality Systems in regulated industries
  • Moderate experience in auditing
  • Preferred: 3+ years in quality assurance, ideally in the medical field
  • Preferred: Formal training in Quality Systems audits
  • Preferred: Knowledge of ISO 13485 and FDA regulations

Responsibilities

  • Support and implement supplier and internal audit programs
  • Provide management with reports on audit and CAPA program status
  • Project manage corrective actions from internal audit findings
  • Review audit observations and CAPA evidence for closure
  • Assist in external audit preparation and facilitation
  • Recommend improvements for the audit system
  • Collaborate with QA teams globally for quality systems alignment
  • Support ongoing monitoring of QA suppliers
  • Perform other QA project and ad hoc tasks
  • Travel approximately 10% of the time

Benefits

  • Comprehensive medical, vision, and dental insurance
  • Life, AD&D, short-term and long-term disability insurance
  • Sleep care management support
  • Health Savings Account (HSA) and Flexible Spending Account (FSA)
  • Commuter benefits and 401(k) plan
  • Employee Stock Purchase Plan (ESPP)
  • Employee Assistance Program (EAP)
  • Tuition assistance and three weeks Paid Time Off (PTO) the first year
  • 11 paid holidays and 3 floating days
  • 14 weeks primary caregiver or 2 weeks secondary caregiver leave for new family members
Full Job Description

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

ResMed’s products and our design and manufacturing operations must comply with the regulatory requirements applicable to medical devices for the markets in which they are sold. This includes, but is not limited to, the Food and Drug Administration (FDA) in the United States of America and the relevant competent authorities in Europe as well as applicable international standards such as ISO 13485 and those requirements prescribed in the Medical Device Single Audit Program (MDSAP) and European Union Regulations. The role will interact with stakeholders including suppliers, external auditors and internal ResMed departmental managers. Also, the role will be responsible for all aspects of auditing to ensure regulation compliance, quality best practice, process improvements and development of supplier quality systems. Providing broad business technical support around QA systems and processes to the organization. Supporting and implementing quality projects across the business and also creating and improving quality and business processes for compliance and Continuous improvement.

Let’s talk about Responsibilities

  • Support preparation of and implement a comprehensive supplier and internal audit program that meets the requirements of the business and applicable external regulatory bodies.
  • Provide reports to management on the status of the audit and CAPA programs and provide an assessment of the possible resulting business impact.
  • ​Project manage the activities resulting from observations and non-conformances raised during internal audits and as part of CAPA investigations. Liaise with stakeholders and drive these findings to effective and timely closure.
  • Review and interpret audit observation activities and CAPA evidence for completeness prior to closure
  • As required, support and represent ResMed in external audit situations through audit preparation, facilitation and acting as a direct auditee when required, including supporting the preparation of formal responses to external audits ready for management review prior to submission.
  • Recommend opportunities for the continual improvement of the audit system in accordance with best practice and individual analysis of specific ResMed needs and support implementation.
  • Work with corresponding QA teams in other parts of ResMed to ensure that the audit, CAPA and general Quality Systems are aligned to facilitate global deployment where appropriate.
  • Support the maintenance of QA supplier management and ongoing monitoring activities to facilitate effective supply chain management and ensure external regulatory compliance requirements are met.
  • Undertake other QA project and ad hoc activities as required
  • Travel as needed, approximately 10%


Let’s talk about Qualifications and Experience

Required:

  • Bachelor Degree in Engineering or Science
  • Strong listening, verbal and written communication skills.
  • Experience with Quality Systems within a Medical or similarly regulated industry
  • Moderate audit experience

Preferred:

  • Minimum 3 years applied professional quality assurance experience ideally including the medical industry or similar regulated industry.
  • Formal Training in Quality Systems audits.
  • Formal Six Sigma and analytical problem-solving training and application experience
  • Knowledge and coverage of ISO13485 and FDA 21 CFR Part 820 requirements.
  • Acting as lead or experienced supporting auditor for internal and supplier audits, covering a range of relevant processes and supplier types.

We are shaping the future at ResMed, and we recognize the need to build on and broaden our existing skills and continue to attract and retain the world’s best talent. We work hard to offer holistic benefits packages, provide flexible work arrangements, cultivate a workforce culture that allows employees to grow personally and professionally, and deliver competitive salaries to our team members. Employees scheduled to work 30 or more hours per week are eligible for benefits. This position qualifies for the following benefits package:  comprehensive medical, vision, dental, and life, AD&D, short-term and long-term disability insurance, sleep care management, Health Savings Account (HSA), Flexible Spending Account (FSA), commuter benefits, 401(k), Employee Stock Purchase Plan (ESPP), Employee Assistance Program (EAP), and tuition assistance. Employees accrue three weeks Paid Time Off (PTO) in their first year of employment, receive 11 paid holidays plus 3 floating days and are eligible for 14 weeks of primary caregiver or two weeks of secondary caregiver leave when welcoming new family members.

Individual pay decisions are based on a variety of factors, such as the candidate’s geographic work location, relevant qualifications, work experience, and skills.  

At ResMed, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current salary range for this position is: $68,000 to $102,000

About ResMed

ResMed is a global leader in the development, manufacturing, and marketing of medical devices and software solutions for the treatment of sleep apnea, chronic obstructive pulmonary disease (COPD), and other respiratory disorders. The company's products include continuous positive airway pressure (CPAP) machines, masks, and accessories, as well as ventilators and other respiratory care devices. ResMed serves patients and healthcare providers in more than 140 countries worldwide. The company was founded in 1989 and is headquartered in San Diego, California.
Learn more about ResMed
Size
7,970 employees
Market Cap
$30.4 billion
Industry
Net Income
$698.8 million
Founded
1989
5 Year Trend
+11.6%
Revenue
$3 billion
NASDAQ

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