Direct message the job poster from Salt Medical.
Reporting to the Director of Regulatory Affairs and Quality Assurance, responsibilities include:
* Working within the established document control / quality management system to ensure that quality management system documentation is accurate, controlled, transmitted, and archived for optimized tracking and retrieval.
* Responsibility for providing day-to-day document control activities for the company and its projects.
* Ensuring that all quality documentation and records are organized in accordance with company and project requirements.
* Expedite and ensure documentation control runs smoothly and efficiently at all times.
The successful candidate will have:
* A minimum of 5 years’ experience in the document control / quality field at the Engineer / Coordinator level.
* Demonstrated ability for operating and maintaining a Quality Management System based Document Control process, having prepared for and passed quality inspections from a recognized Notified Body.
* Established office operational skills, word processing, and other relevant administrative skills.
* Knowledge of the importance of operating and maintaining an adequate Document Control process within a regulated industry, preferably medical devices.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Engineering and Information Technology
Industries
Medical Equipment Manufacturing
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