Register
Recruit Create CV

Quality Assurance Regulatory Affairs Coordinator Jobs

Regulatory Coordinator Jobs
By Skeena Resources Limited At Vancouver, British Columbia, Canada
Promotion of Tahltan management and governance related to environmental matters.
Exceptional written and verbal communication skills to support communication of permitting requirements across the organization.
Experience embedding environmental design requirements into engineering design and construction execution plans.
Facilitate the exchange of technical data to/from the mine in meeting compliance and permitting requirements.
Demonstrated success working within multi-discipline environmental programs and regulatory submissions to meet timelines and technical requirements.
Strong organization skills, managing, tracking, and recording multiple tasks and a heavy workload.
Vp Food Safety/ Quality Assurance/ Regulatory Affairs
By Donald's Fine Foods At Langley, British Columbia, Canada
Strong experience with HACCP, GMPs, animal care practices, regulatory submissions, SFCR documentation, and other relevant management systems.
Experience with crisis management, recall processes, ethical sourcing audits, regulatory inspections, and SFCR assessments.
Provide guidance, training, and performance management to ensure team members are equipped to meet their objectives.
Ensure compliance with industry standards (e.g., BRC/GFSI), animal welfare certifications, CFIA regulations, SFCR requirements, and customer-specific mandates.
Ensure alignment with industry best practices, evolving regulatory requirements, SFCR, and animal welfare standards.
In-depth knowledge of food safety regulations, quality standards, animal welfare principles, ethical sourcing practices, CFIA regulations, and the SFCR.
Quality Assurance And Regulatory Affairs Analyst
By Intellijoint Surgical Inc. At Kitchener, Ontario, Canada
Experience working within a Quality Management System (QMS)
Strong organizational, time management, and prioritization skills.
Support system administration of Quality Management System software.
Skills and Experience to Enable Success:
A continuous learner that builds on their existing knowledge of medical device and biomedical technology regulations
Collaborate with cross-functional teams and interface with external parties to meet quality requirements within project timelines.
Regulatory Affairs & Quality Specialist
By Endocision At Montreal, Quebec, Canada
Maintain all Quality Management meeting documentation.
Maintain and issue training requirements to company.
Maintain working knowledge of ISO 13485 and ISO 14971.
Maintain in depth knowledge of regulatory guidance documents.
Experience in documentation for Class II/III or IV medical devices, experience with 510(k) or De Novo Submissions a plus.
Experience with ISO 13485 or ISO 9001, experience with ISO 14971 a plus.
Coordinator - Quality Assurance
By Ocean / Océan At Quebec, Canada
Keep welding procedures up to date with certification requirements;
Participate and support the activities of the Health, Safety and Environment Management System.
Ensure the application and maintenance of ISO certification in collaboration with the various teams;
Support project managers and foremen in the execution of projects to ensure work compliance;
Plan, prepare and carry out, in collaboration with the project manager – quality, external inspections carried out by Transport Canada;
Minimum of five (5) years of experience in a similar role;
Quality Assurance Coordinator Jobs
By Biomed International Products Corp. At Vancouver, British Columbia, Canada

Looking for new work? Quality Assurance Coordinator at Biomed in South Burnaby. Are you driven to succeed? Do you have strong attention for details? Are you passionate about Natural Health Products? ...

Quality Assurance Coordinator Jobs
By Canada Goose At Montreal, Quebec, Canada
Excellent common sense, decision-making abilities, interpersonal and analytical skills
Support development and implementation of processes using advanced knowledge of industry standards
2 years of experience in Garment Industries
Excellent written and verbal French and English skills
Strong knowledge of garment construction and patternmaking
Audit Finished Goods at end of line and report issues to Production
Quality Assurance/Regulatory Affairs Specialist (14M Mat Leave Contract)
By DIVA At Kitchener, Ontario, Canada
Support maintenance of Diva’s ISO 13485 certification and Quality Management System as a whole.
Experience in the maintenance of Quality Management Systems, e.g., ISO 13485 and FDA QSR for medical devices;
Report on performance of the QMS to top management
Proficient in MS Office applications, quality management software & tools, and the ability to learn new software as required;
Prepare, upkeep and manage FDA, Health Canada, and other worldwide regulatory submissions as well as other regulatory related documents;
Ensure compliance with applicable regulatory standards/requirements;
Quality Assurance Regulatory Affairs Coordinator
By CPG Executive Search Inc. At Caledon, Ontario, Canada
· Organize and planning skills to effectively manage the flow of stock
· Ability to have the right mindset and attitude to freely share knowledge, knowhow, and skills
· Manages internal label documents ensuring only current and up-to-date labels are circulated.
· 4-7 years of regulatory experience in a regulatory, preferably in manufacturing environment
· Detail oriented, accurate and excellent record keeping skills
· Knowledge of Canadian and US Food Labelling Regulations is required