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Qa tester • port colborne on
- Promoted
Junior QA Engineer
Welland Medical LtdWelland, Niagara Region, CASenior Project Manager - Utilities Construction
Black & McDonaldON, CASenior Highway Engineer
McIntosh PerryOntario, CAJPC - 1414 - Senior Project Manager
ITS GlobalOntario- Port Moody, BC (from $ 105,750 to $ 172,500 year)
- Halifax, NS (from $ 75,282 to $ 150,150 year)
- Bradford West Gwillimbury, ON (from $ 106,848 to $ 136,580 year)
- Quinte West, ON (from $ 106,848 to $ 136,580 year)
- Old toronto, ON (from $ 97,500 to $ 136,500 year)
- Toronto, ON (from $ 95,063 to $ 136,500 year)
- Calgary, AB (from $ 78,000 to $ 132,978 year)
- North Bay, ON (from $ 107,406 to $ 131,625 year)
- Thunder Bay, ON (from $ 122,683 to $ 131,625 year)
- Richmond, BC (from $ 57,500 to $ 126,977 year)
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Junior QA Engineer
Welland Medical LtdWelland, Niagara Region, CA- Full-time
Welland Medical brings to market the best and most innovative products that enhance the lives of people living with a stoma across the world. Investing in the most talented people, collaborating to create world‑class, ground‑breaking products and services devoted to improving peoples’ lives. We are passionate about making a difference in the world. Our reputation is based on a tradition of improvement, ethical leadership, and total commitment to quality and safety.
Welland Medical, established in 1988, is part of the CliniMed Group, and has over 250 colleagues committed to enhancing people’s lives.
Main Duties and Responsibilities
As a Junior QA Engineer, your main responsibilities and duties will include :
- Ensure the QMS is adhered to and that ISO standard requirements are met and maintained
- Calibrate Production Equipment as necessary in a timely manner and maintain the calibration database Maintain and report on quality metrics
- Support Manufacturing to ensure quality and material issues are dealt with and closed out in a timely manner.
- Assist with new material, Equipment, CSV, and Process validation as necessary
- Assist in the improvements of QMS against ISO 13485
- Support training to site staff on Quality System procedures as required
- Assist with Corrective and Preventive Actions (CAPAs) and support CAPA teams as necessary
- Assisting the business in closing CAPA and Non – Conformances
- Providing QA support and approval of CAPA and Non‑Conformances
- Assist in Quality Audits (Internal, Supplier) against ISO 13485
- Support for logging, monitoring, and closing audit actions, Internal, and Supplier
- Work with manufacturing teams (Operations, Engineering and Planning Departments) in driving through the focus, teamwork and support required to ensure the delivery of all key manufacturing KPI’s.
- Support with customer complaints and complaint reporting
- Assist Incoming Inspection sampling and analysis of raw materials
- Support in post market surveillance (PMS) and post market clinical follow up (PMCF) activities
- Contribute to Lean Manufacturing Projects and communicate progress to CI Management with regards to key KPIs.
A degree of flexibility is needed, and the job holder may be required to perform work not specifically referred to above and which will be appropriate to the level of the role.
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