Quality Engineer Iii, Design Assurance
By Boston Scientific At Mississauga, Ontario, Canada
Apply technical skills including sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.
Utilize standard statistical analysis and problem-solving techniques to determine product acceptance and evaluate process capabilities.
3+ years of relevant work experience
Demonstrated interpersonal skills with ability to work within a team environment
Experience in the medical device industry
Training experience to FDA regulations or ISO standards
Quality Engineer Ii, Design Assurance
By Boston Scientific At Mississauga, Ontario, Canada
Apply technical skills including sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.
Utilize standard statistical analysis and problem-solving techniques to determine product acceptance and evaluate process capabilities.
3+ years of relevant work experience
Demonstrated interpersonal skills with ability to work within a team environment
Experience in the medical device industry
Training experience to FDA regulations or ISO standards
Design Quality Engineer Jobs
By Verv Technologies At Sudbury, Ontario, Canada
·Provide management with status updates on assigned responsibilities and goals and escalate issues in a timely fashion.
·Lead product risk management activities.
·Coordinate team with respect to project demands and facilitating program management functions.
commensurate with education and experience. This is an ESOP eligible role.
We are seeking an experienced
·Ensuring project requirements are clearly identified and stakeholders are kept informed of project status.
Sterility Assurance Lead Jobs
By Baxter International Inc. At Mississauga, Ontario, Canada
Knowledge and application of computer systems for word processing, reporting, data analysis and NCR/CAPA, and Change Control Management
Manage the Environmental Monitoring program and ensure compliance with applicable regulatory and corporate requirements.
Lead cross-functional teams in performing Environmental Performance Qualifications, Process Failure Modes and Effect Analysis, and Real Time Risk Assessment per requirements
Investigate all Sterility Assurance related exceptions (e.g. Micro OOLs, Particulate Matter OOLs, Qualification failures); coordinate and document follow-up actions
Manage audit readiness for Sterility Assurance, and host/participate in internal and external inspections
Ensure local SOPs are up to date and aligned with requirements and applicable regulatory standards