Medical Device Regulatory Assistant
By Surgmed Group At Montreal, Quebec, Canada
Minimum College education or Accredited Certificate program preferred, with certifications in ISO 13485, MDSAP, CE, and/or FDA regulations.
Participate in internal and external audits to ensure compliance with regulatory requirements.
Keep abreast of changes in regulatory guidelines and requirements, communicating these changes to the relevant teams.
Previous work experience in regulatory affairs within ISO certified companies is mandatory.
Minimum of 2 years of relevant experience in a similar role.
Medical device experience is necessary; understanding of medical device classifications and regulations is essential.
Travel Medical Laboratory Tech (Mlt)
By Anders Group, LLC At St Thomas, Ontario, Canada
Additional requirements may also be provided during interview
Graduate from an accredited school
State License required/registration where applicable
Medical Device Risk Manager- Remote
By Varian At Canada
At least 3 years of relevant experience in medical device risk management
Leads Risk Management efforts, processes and process improvements for the Varian Products, with a main focus on Varian Digital Oncology.
Develops and maintains Risk Management Files that include risk management plans, hazard analyses and risk assessments
Keeps abreast of changes to regulations and standards as they bear on risk management
Minimum Required Skills And Knowledge
Bachelor’s degree in Science or Engineering with several years of related experience
Medical Device Sales Specialist
By Moscovich MedTech Inc. At Kelowna, British Columbia, Canada
Identify prospects, set appointments, make effective qualifying sales calls, and manage sales cycle to develop new business
Continuing development of product knowledge
1+ years of sales experience preferred
Maintain/developing working relationships with existing customers to ensure that they receive exceptional service and to identify potential new sales opportunities
Develop and execute effective business developments plans
Training and case support for operating room staff
Medical Device Logistics Analyst 1
By IQVIA At Montreal, Quebec, Canada
Knowledge of Medical Devices and Regulatory Requirements
Advise Project Management on correct shipping materials and documentation to order for global studies
Liaise closely with Project Management to ensure accurate address details in QLIMS
plays a key role in the ordering, management, and collection of worldwide field medical devices.
1-3 years of strong Global Shipping and Logistics experience is Required, preferably from another CRO or pharma company
Knowledge of Customs and International Shipping Regulations/Restrictions for Import/Export
Medical Device Logistics Analyst 2
By IQVIA At Halifax, Nova Scotia, Canada
Knowledge of Medical Devices and Regulatory Requirements
Participate in local vendor management meetings, promoting continuous improvement
Thorough knowledge of and current certification in international and domestic air transport regulations.
plays a key role in the ordering, management, and collection of worldwide field medical devices.
3-4 years of strong Global Shipping and Logistics experience is Required, preferably from another CRO or pharma company
Knowledge of Customs and International Shipping Regulations/Restrictions for Import/Export
Medical Device Sales Representative
By Tribe Medical, Arthrex agency partner At Lethbridge, Alberta, Canada
SURGICAL TECHNOLOGY SPECIALIST, hiring in: LETHBRIDGE, ALBERTA
We provide a base pay, monthly auto, cell & parking allowances, commission, bonus and more.
If you wish to be considered for our team, please send your resume to:
Medical Device Reprocessing Techician
By University of Alberta At Edmonton, Alberta, Canada
Knowledge of Infection Control Protocol; sterilization procedures for dental instruments and equipment and inventory management an asset
Moves carts as required between the Dispensaries, Central Sterilization and Materials Management
High School Diploma and Medical Device Reprocessing Technician (MDRT) certification
One year experience with medical or dental instruments preferred
Experience working with specialized dental or sterilization software
Excellent verbal and written communication skills

Are you looking for a job that will make a real difference in people's lives? Become a Medical Device Reprocess Tech and help ensure that medical devices are safe and ready for use! Join a team of dedicated professionals and make a positive impact in the healthcare industry.

Overview:

Medical Device Reprocess Techs are responsible for the safe and effective reprocessing of medical devices used in healthcare facilities. They must ensure that all medical devices are properly cleaned, disinfected, and sterilized in accordance with established protocols and standards. They must also inspect and test the devices to ensure they are in good working order. Medical Device Reprocess Techs must be knowledgeable of the various types of medical devices and their proper use and maintenance. They must also be familiar with the safety protocols and procedures associated with the reprocessing of medical devices.