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Jobs - QA and Regulatory Director, Medical Devices
Hexoskin is looking for a QA Director to join its development team.
Work environment
The QA Director is in charge of the Hexoskin Quality System, its implementation, control and maintenance. She/he works closely with...
Medical device
Vena Medical - Regulatory Affairs Specialist
About Us: Vena Medical is at the forefront of revolutionizing stroke treatment through cutting-edge... ...crucial role in successfully navigating our cutting-edge medical devices through regulatory pathways, ensuring they meet all...
Medical device
Full time
Flexible hours
...Lead a team of auditors in performing medical device audits, in conformance with the SGS Global... ...requirements of ISO 9001, ISO 13485 and other regulatory requirements for access into Canada, EU,... ...and development
~ Global Regulatory Affairs background, including MDD / IVDD.
~...
Medical device
Full time
Local area
Relocation
Shift work
...quality system (CAPA program, NCMRs, etc.) and acts as the representative for Straumann Canada with respect to the Quality System and Regulatory Affairs functions as the liaison to Health Canada.
Job Responsibilities
This position is responsible for, but not limited to, the...
Suggested
Full time
Local area
...regulations and rules. Provide responses to regulatory agencies. Stay apprised of regulatory... ...Canada. Reporting to the Director, Regulatory Affairs as part of the NRG Regulatory Affairs... ...Benefits on the first day of employment - Medical, Dental, Vision, Life Insurance, and...
Suggested
Holiday work
Contract work
Temporary work
Work from home
Flexible hours
...progressing – whatever your ambitions.
About the role
The Regulatory Affairs Senior Associate supports the Manager, Regulatory Affairs in... ...will include:
Plan, organize, assemble and file medical device license applications and regulatory dossiers to Health Canada...
Medical device
Worldwide
Flexible hours
...and effective products at a fast-growing medical technology company!
Type of Position:... .... We are seeking a Quality Assurance & Regulatory Affairs (QARA) Analyst to join our QARA team to... ...sale of Intellijoint Surgical medical devices in a regulated environment. As an integral...
Medical device
Full time
Internship
3 days per week
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..., for the first time in their lives. The device is currently being used by hundreds of families... ..., and comprehensive documentation for medical device for a small to midsize company and... ...to suit various audiences, including regulatory agencies, customers, or production employee...
Medical device
Contract work
Remote job
Part time
Relocation package
...Requisition ID: 182413
Career Group: Corporate Office Careers
Job Category: Food Safety Regulatory Affairs
Travel Requirements: 0 - 10%
Job Type: Full-Time
Country: Canada (CA)
Province: Québec
City: Montréal
Location: Bureau de Montréal-...
Suggested
Full time
Internship
...and effective products at a fast-growing medical technology company!
Type of Position:... .... We are seeking a Quality Assurance & Regulatory Affairs (QA/RA) Coordinator to join our Quality... ....
~ Experience working in a medical device environment (ISO 13485, FDA QSR, EU MDD/...
Medical device
Full time
Internship
3 days per week
...why more people from across the globe are moving here.
About the Opportunity
Reporting to the Manager and Supervisor of the Medical Device Reprocessing Department and in accordance with the established vision and values of the organization, this position performs a series...
Medical device
Holiday work
Permanent employment
Full time
Shift work
Night shift
Weekend work
...the globe.
Position Summary
The mission of the STERIS Regulatory Affairs function is to standardize and optimize regulatory activities... ...and maintaining Canadian market authorization of STERIS’s medical devices, biocides and chemical products, determining Canadian submission...
Medical device
Holiday work
Contract work
Work experience placement
Local area
...maintenance and continual improvement of the company’s quality systems (ISO 13485:2016, MDSAP (FDA/Canada), EU (MD).
Communicate with regulatory agencies regarding potential regulatory pathways, compliance requirements, or clarification and follow-up of regulatory filings or...
Suggested
Contract work
Flexible hours
...community that values bold ideas, professional growth and employee wellness, we want you on the Bell team.
Summary
BCE’s Regulatory Affairs department furthers the business interests of BCE’s business units through interactions with government departments and...
Suggested
Full time
Flexible hours
...Position Title: Regulatory Affairs Associate
Status: Full-time Contract, 6 months
Location: Mississauga, ON
Schedule: Must be willing... ...international affiliates.
Maintains pertinent Canadian medical device regulations to ensure submission requirements are current,...
Medical device
Full time
Contract work
For contractors
Local area
...Field of work: Regulatory & Medical
Posting Date: 17 Apr 2024
Application deadline:
Location: Toronto M2H 3S8, , Canada
Contract type... ...approval
~Coordination and execution of day-to-day Regulatory Affairs processes and deliverables
Role & Responsibilities:...
Permanent employment
Full time
Contract work
Local area
...the dynamics of sterilization and an ability to operate any sterilization system in use within the department including preparing the device for a particular sterilization technique, operating the sterilizer, and processing monitoring readings, error codes and quality assurance...
Medical device
Shift work
...Position Number: 20018232
Posting End Date: May 15, 2024
City: Winnipeg
Employer: Shared Health
Department / Unit: Medical Device Reprocessing 2 - HSC
Job Stream: Clinical Support
Union: CUPE
Anticipated Start Date - End Date: 06/07/2024 -...
Medical device
Shift work
Weekend work
...Req ID: 179848
Company: Nova Scotia Health
Location: Northern Zone, Aberdeen Hospital
Department: OPNZ PERI Medical Device Reprocess ARH
Type of Employment: Casual Casual Relief (3% FTE) x 2 position(s)
Status: CUPE Support Position
Posting...
Medical device
Casual work
Relief
Shift work
Weekend work
...delivery and those customer requirements are met while adhering to SGS Policies, procedures, and processes.
As a member of the Global Medical Device office (MDO) to minimize risks associated with medical device certification. Act as a support/leader to the defined group in terms...
Medical device
Full time
Work alone
