Intertek Group

Auditor - Medical Devices, Quebec

Intertek Group$80K — $95K *
Healthcare
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Minimum 6-10 years in a medical device related industry.
  • 4-year degree in a science or technical field or equivalent experience.
  • In-depth knowledge of quality management systems relevant to medical devices.
  • Strong communication and interpersonal skills are essential.
  • Excellent computer literacy and writing abilities.
  • Sound organizational, analytical, and judgment skills.
  • Proven ability to manage time effectively and travel extensively.

Responsibilities

  • Audit client management systems for regulatory compliance and industry standards.
  • Assist clients with audit-related inquiries and certification processes.
  • Act as Lead Auditor or team member during assessments.
  • Coordinate audit activities effectively with team members.
  • Document compliance evidence and prepare audit reports.
  • Review and discuss audit results with clients and certification boards.
  • Support corrective actions and continuous improvement initiatives.

Benefits

  • Medical, dental, and vision coverage.
  • Life and disability insurance.
  • Registered Retirement Savings Plan (RRSP) with company match.
  • Generous vacation and sick leave (PTO).
  • Tuition reimbursement for continuing education costs.
  • Paid holidays and flexible working arrangements.
Full Job Description
Job Description

The Auditor, Medical Devices will support the Business Assurance business by leading and/or participating as an assessor during all phases of a client's management system, in accordance with the company's accredited certification program. The Auditor is the primary interface with the client before and during the process of all auditing activities. Additionally, the Auditor will help train low graded Auditors through witness audits, technical support, and education of both client and sales force as needed. We're looking for somebody with a minimum of 6-10 years of full time work experience in a medical device related industry. This will be a full-time/home-based position, with extensive travel to client sites required.

DUTIES:
  • Audit client management systems for compliance with established standards, client, and/or industry requirements, government regulations, and other relevant standards, specifically ISO 13485,
  • regulatory requirements for the US, Canada, Japan, Australia, and/or Brazil, and/or GMP regulatory requirements related to the medical device, pharmaceutical and/or cosmetic industry.
  • Assist clients with questions relevant to the audit and/or certification process.
  • Act as Lead Auditor or team member.
  • Coordinate audit activity with team members.
  • Liaison with client regarding audit activity.
  • Review client's quality management system documentation
  • Verify and document evidence of compliance and non-compliance.
  • Prepare audit report.
  • Review audit results with coordinator and other assessment team members. Make presentations to clients and/or certification board concerning audit results, when required.
  • Assist with corrective action requirements resulting from assessments.
  • Participate in audit meetings.
  • Review audit reports and provide technical assistance to the medical team.
  • Support management in areas of continuous improvement and different Medical program projects.
  • Provide management with updates on status of work, initiatives, and projects, as required.
  • Travel will include overnight/multiple days, to various worksites and client locations.


Qualifications
REQUIREMENTS:
  • In-depth knowledge of quality management systems in the medical device industry sector, demonstrated through a combination of education and experience (minimum 2 years in Quality or controlled environment in medical device industry).
  • 4 year college/university degree in a science or technical field (biology or microbiology; chemistry or biochemistry; computer and software technology; electrical, electronic, mechanical or bioengineering; human physiology; medicine; pharmacy; physics or biophysics) or equivalent combination of relevant education and work experience.
  • A minimum of 4+ years work experience in a medical device or related industry.
  • Strong communication and interpersonal skills.
  • Sound judgment, organizational, and analytical skills.
  • Excellent computer and writing skills.
  • Ability to define problems, collect data, establish facts, and draw valid conclusions.
  • Ability to exercise effective time management skills in completion of assignments.
  • Must be willing and able to travel extensively. Primarily domestic travel, some international travel may be needed.


PREFERRED:
  • Related 3rd party auditing industry management systems experience.
  • Completed Lead Auditor training for any standard (preferably ISO 13485), but will train if needed.
  • Working/Training knowledge of relevant regulatory requirements for medical devices and pharmaceuticals in the EU, USA, Australia, Japan, Brazil, and/or Canada.
  • Experience implementing/auditing to ISO 13485, ISO 14971, and medical device and /or pharmaceutical regulatory requirements.
  • Specific experience/training on processes used in the relevant industry's design, manufacturing, testing or clinical use (ex. sterilization, design and development of electro-mechanical or passive medical device, plastic injection molding or extrusion, training/experience in quality tools (Kaizen, lean manufacturing, etc.).
  • Working experience in a wide range of medical devices is preferred.


PHYSICAL REQUIREMENTS:

This role requires the ability to:
  • Ascend or descend ladders, stairs, ramps, and the like, using feet and legs and/or hands and arms. Body agility is emphasized.
  • Stand, for sustained periods of time.
  • Walk, moving on foot to accomplish tasks and to move from one work location to another.
  • Communicate well, thru spoken word, conveying detailed accurate information & instructions to others.
  • Hear well, perceiving sounds with or without correction, including the ability to receive information thru oral communications.
  • Exert up to 10 pounds of force occasionally and/or negligible amounts of force frequently to lift, carry, push, pull or otherwise move objects.
  • Have close visual acuity to perform an activity such as preparing & analyzing data, viewing a computer monitor, reading, report writing, visual inspection, and use of measurement devises.


Salary & Benefits Information

When working with Intertek, you can expect salary and benefit package competitively placed within the local market, including medical, dental, vision, life, disability, Registered Retirement Savings Plan (RRSP) with company match, generous vacation/sick time (PTO), tuition reimbursement and more. Intertek employees are eligible for a variety of benefits including paid holidays.

Please apply online at Intertek Canada Careers (oraclecloud.com)

Bilingualism is needed for this role as the incumbent would need to deal with internal and external clients and employee's that work outside of Quebec.

*Intertek does not accept unsolicited approaches from agencies and will not pay a fee for any placement resulting from the receipt of an unsolicited resume.

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About the Team

The Business Assurance group of Intertek provides a full range of business process audit and support services, including management systems certification, sustainability and responsible sourcing audits, risk management, and training. Our range of bespoke auditing, performance benchmarking and supply chain solutions provide insight into every aspect of operations, allowing clients to make informed decisions about their business while ensuring their workforce competencies are current and relevant.

About Intertek Group

Intertek Group plc is a British multinational assurance, inspection, product testing and certification company headquartered in London, United Kingdom. It is listed on the London Stock Exchange and is a constituent of the FTSE 100 Index. Intertek operates in over 100 countries and has more than 46,000 employees. The company provides services such as testing, inspection, auditing, certification, quality assurance, advisory, and outsourcing services to various industries such as aerospace, construction, consumer goods, food, healthcare, and more.
Learn more about Intertek Group
Size
46,000 employees
Industry
Founded
1996

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