Project Manager

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.
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…