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      • Saint-Laurent, Québec
      • Contract
      Role: Supplier Quality Engineer Status: Full time Location: Saint-Laurent We are looking for a supplier Quality Engineer to join our client based in Ville Saint-Laurent for a 1 year contract. The Supplier Quality Engineer will be responsible for the following; Provides supplier quality performance data to ensure a meaningful supplier performanceevaluationInteract with Customer Facing businesses to investigate potential Product Non conformanceLead supplier root cause investigations and corrective actions through Problem Resolutionprocess.Conduct improvement projects to Quality and Delivery performance improvementInvestigate and resolve manufacturing capability issues within the supply chain to ensurebusiness continuityIdentify and support Cost reduction opportunities through interaction with the SupplyChain/StrategyAudit existing and potential suppliers to determine capability of manufacturing and ensurequality systems are in place. Develop supplier capability to meet current and futurerequirementsLead and/or facilitate improvement projects to satisfy problems and improve performance ofsuppliers by applying appropriate LEAN / Quality improvement toolsTrain and coach suppliers to improve aspects of their business performanceLead Product validation through PPQ processQualificationsMinimum of 5 years of experience in a similar role Advanced knowledge of lean Sigma quality tools methods Leadership or project management experience Vous devez avoir le droit de travailler au Canada Please send your resume to à melina.guemiri@randstad.caRESPONSIBILITIESQUALIFICATIONS
      Role: Supplier Quality Engineer Status: Full time Location: Saint-Laurent We are looking for a supplier Quality Engineer to join our client based in Ville Saint-Laurent for a 1 year contract. The Supplier Quality Engineer will be responsible for the following; Provides supplier quality performance data to ensure a meaningful supplier performanceevaluationInteract with Customer Facing businesses to investigate potential Product Non conformanceLead supplier root cause investigations and corrective actions through Problem Resolutionprocess.Conduct improvement projects to Quality and Delivery performance improvementInvestigate and resolve manufacturing capability issues within the supply chain to ensurebusiness continuityIdentify and support Cost reduction opportunities through interaction with the SupplyChain/StrategyAudit existing and potential suppliers to determine capability of manufacturing and ensurequality systems are in place. Develop supplier capability to meet current and futurerequirementsLead and/or facilitate improvement projects to satisfy problems and improve performance ofsuppliers by applying appropriate LEAN / Quality improvement toolsTrain and coach suppliers to improve aspects of their business performanceLead Product validation through PPQ processQualificationsMinimum of 5 years of experience in a similar role Advanced knowledge of lean Sigma quality tools methods Leadership or project management experience Vous devez avoir le droit de travailler au Canada Please send your resume to à melina.guemiri@randstad.caRESPONSIBILITIESQUALIFICATIONS
      • Cambridge, Ontario
      • Permanent
      Our client, a new manufacturing facility in the Cambridge area, has partnered with Randstad Engineering in their search for a Quality Engineer to join their growing team! As a Quality Engineer, you would be hands on, ensuring proper documentation, implementation, and application of the Quality Management Systems (QMS) to ensure high quality products reach their customers.In this role, responsibilities would include:•Maintain and enhance company quality standards•Perform finished goods audit according to inspection protocols and sampling procedures•Inspection and testing of raw materials, work in process, finished goods to ensure adherence to quality standards and product specifications•Document evidence of the manufacturing process to ensure continued quality•Lead functional area responses to CAPA and NCR •Participate in production meetings with the manufacturing team•Continuously review processes, systems and products to determine where improvements can be made•Propose changes in specifications, materials, or products using evidence based analysisAs a qualified candidate, you meet the following requirements: •5+ years of quality engineering experience•Previous experience in an ISO 13485 environment •CQE would be considered an asset•Post secondary education in related field•Attention to detail and ability to find defects in product streams•Ability to work in a start up like environment with growth and evolution on the horizon.If you are interested in this opportunity, apply today! Only qualified candidates will be contacted.RESPONSIBILITIESQUALIFICATIONS
      Our client, a new manufacturing facility in the Cambridge area, has partnered with Randstad Engineering in their search for a Quality Engineer to join their growing team! As a Quality Engineer, you would be hands on, ensuring proper documentation, implementation, and application of the Quality Management Systems (QMS) to ensure high quality products reach their customers.In this role, responsibilities would include:•Maintain and enhance company quality standards•Perform finished goods audit according to inspection protocols and sampling procedures•Inspection and testing of raw materials, work in process, finished goods to ensure adherence to quality standards and product specifications•Document evidence of the manufacturing process to ensure continued quality•Lead functional area responses to CAPA and NCR •Participate in production meetings with the manufacturing team•Continuously review processes, systems and products to determine where improvements can be made•Propose changes in specifications, materials, or products using evidence based analysisAs a qualified candidate, you meet the following requirements: •5+ years of quality engineering experience•Previous experience in an ISO 13485 environment •CQE would be considered an asset•Post secondary education in related field•Attention to detail and ability to find defects in product streams•Ability to work in a start up like environment with growth and evolution on the horizon.If you are interested in this opportunity, apply today! Only qualified candidates will be contacted.RESPONSIBILITIESQUALIFICATIONS
      • Calgary, Alberta
      • Permanent
      Scope of Work: Are you looking for fast-paced, challenging role where you can put your top-notch process and quality engineering skills to use? Do you have experience in an automated manufacturing environment? We have the perfect Process and Quality Engineer role for you: The Process and Quality Engineer is focused on resolving production problems, optimizing process and product reliability.Why do you want this job?-Job security, this is a permanent, full-time position, with a career path-Paid relocation for new employees-Make OT pay as a Manager!-Accessible Calgary, AB location-Flexible schedule-Work in a multi-disciplinary team with other manufacturing experts-Opportunities to advance into second level management roles-Opportunities to train in the newest, most exciting manufacturing methodologies-Work on exciting or fulfilling work/projects-Make great products and create iconic brands-Above average compensation-Tons of great employee perks, like an optional pension program, comprehensive benefits, bonuses, and more (employer pays for long term disability entirely)-Casual office culture – no need to wear suits and ties to work every day-Generous paid vacation allotment-Free parking-Opportunities to relocate-Training and development programs-Chance to work with a great manager/mentor-Work with a financially stable, established/recognizable, industry-leading brand.Main Duties:-Maintain and improve Quality Management System, Product Audits/Process Audits – facilitate and ensure Corrective Actions applied-Implement Quality program CTQ/SPC/Error Proofing Controls at every level-Conduct Root Cause Countermeasure activities, fish bone diagrams etc. to help identify Root Causes for defects and failures-Implement sound corrective and preventive actions to quality incidents-Standardize best practices in processes across the network by updating relevant SOP’s, Work Instructions, and more-Track, manage and effectively close Process Improvement/CI projects in a timely manner-Support New Product Development in performing process and material trials in conjunction with Plant Supervisors and other Engineers to verify proposed changes-Support new product introduction activities-Manage Deviation Notices, CAPA’s, Root Cause Counter Measures, Engineering Change Orders, Monthly Quality Reports, and Quality Alerts.-Organizing and ensuring all quality critical documentation is updated and maintained in Sharepoint-Prepare and compile any required testing and validation plan with completed testing reports.-Liaise and stay updated with Quality initiatives with SSB US and standardize where appropriate for SSB Calgary.-Ensure Plant Quality metrics and Dashboard are updated as required; manage Plant Quality Reviews.-Ensure all key stakeholders remain informed of all critical quality incidents-As required, support the plant supervision team during periods of vacation, absence, and more-Support Kaizen activities to drive quality, safety, productivity and cost improvements.ADVANTAGES-Job security, this is a permanent, full-time position, with a career path-Paid relocation for new employees-Make OT pay as a Manager!-Accessible Calgary, AB location-Flexible schedule-Work in a multi-disciplinary team with other manufacturing experts-Opportunities to advance into second level management roles-Opportunities to train in the newest, most exciting manufacturing methodologies-Work on exciting or fulfilling work/projects-Make great products and create iconic brands-Above average compensation-Tons of great employee perks, like an optional pension program, comprehensive benefits, bonuses, and more (employer pays for long term disability entirely)-Casual office culture – no need to wear suits and ties to work every day-Generous paid vacation allotment-Free parking-Opportunities to relocate-Training and development programs-Chance to work with a great manager/mentor-Work with a financially stable, established/recognizable, industry-leading brand.RESPONSIBILITIES-Responsible for applying methods to resolve production problems and to optimize process and product reliability.-Implement best practices and standardize while achieving SQDC metrics.-Perform material/product/process testing to ensure product quality and durability.QUALIFICATIONS-Bachelor of Engineering – Mechanical/Industrial-Five years of job related experience-Training background in use of Quality tools and methods, Lean manufacturing techniques-Experience in mechanical test methods, experimental design, and documentation of test results and analysis-Experience in developing process and plant layouts-Good knowledge of or ability to learn Quality Systems-Effective project management knowledge and experience -Strong written, oral, analytical, and organizational skills-Proficient in AutoCAD and MS Office/Sharepoint-Professional engineering designation SUMMARYAre you looking for fast-paced, challenging role where you can put your top-notch process and quality engineering skills to use? Do you have experience in an automated manufacturing environment? We have the perfect Process and Quality Engineer role for you: The Process and Quality Engineer is focused on resolving production problems, optimizing process and product reliability.
      Scope of Work: Are you looking for fast-paced, challenging role where you can put your top-notch process and quality engineering skills to use? Do you have experience in an automated manufacturing environment? We have the perfect Process and Quality Engineer role for you: The Process and Quality Engineer is focused on resolving production problems, optimizing process and product reliability.Why do you want this job?-Job security, this is a permanent, full-time position, with a career path-Paid relocation for new employees-Make OT pay as a Manager!-Accessible Calgary, AB location-Flexible schedule-Work in a multi-disciplinary team with other manufacturing experts-Opportunities to advance into second level management roles-Opportunities to train in the newest, most exciting manufacturing methodologies-Work on exciting or fulfilling work/projects-Make great products and create iconic brands-Above average compensation-Tons of great employee perks, like an optional pension program, comprehensive benefits, bonuses, and more (employer pays for long term disability entirely)-Casual office culture – no need to wear suits and ties to work every day-Generous paid vacation allotment-Free parking-Opportunities to relocate-Training and development programs-Chance to work with a great manager/mentor-Work with a financially stable, established/recognizable, industry-leading brand.Main Duties:-Maintain and improve Quality Management System, Product Audits/Process Audits – facilitate and ensure Corrective Actions applied-Implement Quality program CTQ/SPC/Error Proofing Controls at every level-Conduct Root Cause Countermeasure activities, fish bone diagrams etc. to help identify Root Causes for defects and failures-Implement sound corrective and preventive actions to quality incidents-Standardize best practices in processes across the network by updating relevant SOP’s, Work Instructions, and more-Track, manage and effectively close Process Improvement/CI projects in a timely manner-Support New Product Development in performing process and material trials in conjunction with Plant Supervisors and other Engineers to verify proposed changes-Support new product introduction activities-Manage Deviation Notices, CAPA’s, Root Cause Counter Measures, Engineering Change Orders, Monthly Quality Reports, and Quality Alerts.-Organizing and ensuring all quality critical documentation is updated and maintained in Sharepoint-Prepare and compile any required testing and validation plan with completed testing reports.-Liaise and stay updated with Quality initiatives with SSB US and standardize where appropriate for SSB Calgary.-Ensure Plant Quality metrics and Dashboard are updated as required; manage Plant Quality Reviews.-Ensure all key stakeholders remain informed of all critical quality incidents-As required, support the plant supervision team during periods of vacation, absence, and more-Support Kaizen activities to drive quality, safety, productivity and cost improvements.ADVANTAGES-Job security, this is a permanent, full-time position, with a career path-Paid relocation for new employees-Make OT pay as a Manager!-Accessible Calgary, AB location-Flexible schedule-Work in a multi-disciplinary team with other manufacturing experts-Opportunities to advance into second level management roles-Opportunities to train in the newest, most exciting manufacturing methodologies-Work on exciting or fulfilling work/projects-Make great products and create iconic brands-Above average compensation-Tons of great employee perks, like an optional pension program, comprehensive benefits, bonuses, and more (employer pays for long term disability entirely)-Casual office culture – no need to wear suits and ties to work every day-Generous paid vacation allotment-Free parking-Opportunities to relocate-Training and development programs-Chance to work with a great manager/mentor-Work with a financially stable, established/recognizable, industry-leading brand.RESPONSIBILITIES-Responsible for applying methods to resolve production problems and to optimize process and product reliability.-Implement best practices and standardize while achieving SQDC metrics.-Perform material/product/process testing to ensure product quality and durability.QUALIFICATIONS-Bachelor of Engineering – Mechanical/Industrial-Five years of job related experience-Training background in use of Quality tools and methods, Lean manufacturing techniques-Experience in mechanical test methods, experimental design, and documentation of test results and analysis-Experience in developing process and plant layouts-Good knowledge of or ability to learn Quality Systems-Effective project management knowledge and experience -Strong written, oral, analytical, and organizational skills-Proficient in AutoCAD and MS Office/Sharepoint-Professional engineering designation SUMMARYAre you looking for fast-paced, challenging role where you can put your top-notch process and quality engineering skills to use? Do you have experience in an automated manufacturing environment? We have the perfect Process and Quality Engineer role for you: The Process and Quality Engineer is focused on resolving production problems, optimizing process and product reliability.
      • Ottawa, Ontario
      • Contract
      Are you a Senior quality assurance engineer with experience in the medical device industry?We have an amazing opportunity with a global manufacturer of medical devices!As a leading global healthcare company, the client develops innovations that support better patient outcomes with greater efficiencies, giving providers the confidence, they need to meet the clinical, operational, and financial challenges of a changing healthcare landscape. As a leader in medical imaging, laboratory diagnostics, and healthcare information technology, we have a keen understanding of the entire patient care continuum – from prevention and early detection to diagnosis and treatment. Under the supervision of the Manager, Quality Assurance, the Senior Quality Assurance Engineer is responsible for the following:Job Demands•Independent collaborative self-starter with the ability to make appropriate quality-related decisions in real-time•Proven ability to manage projects, achieve timelines and stay within budget•Process-orientated, logical, analytical, meticulous, highly organized and able to analyze data & implement solutions•Proven ability to work effectively within a team environment while satisfying individual responsibilities and objectives•Excellent high level oral & written communications skills enabling incumbent to act as a facilitator and/or educator with strong leadership skills•Adaptable and willing to take on multiple new tasks and responsibilities•Ability to understand a technically complex product•Prioritizing multiple tasks within a dynamic work environment with tight timelines and limited resources•Ensuring compliance while meeting business objectives•Physical requirements: Extended periods of sitting/computer useADVANTAGESDuties and Responsibilities•Technical Expert support of Operations and R&D to provide guidance and direction on activities necessary to comply with the Epocal quality system and with ISO13485, FDA Quality System Regulation, Health Canada Medical Device Regulations and other international requirements as applicable•Support new product introduction initiatives as the Quality delegate by participating on project teams and providing independent technical review of designs and providing input into required Verification and Validation activities. •Work with change initiators to support change initiatives by providing guidance on required verifications and validations. Approve change packages and associated verifications and validations.•Guides Quality Incident (non-conformance) and CAPA investigational activities ensuring thorough root cause analysis and appropriate corrective actions. Approve Quality Incidents (disposition product) and CAPAs, ensuring they are technically accurate, compliant to procedure and complete.•Develop quality plans and recommendations for improvement •Implement changes to the Quality System ensuring continuous improvement to ensure the effective and efficient operation of the quality system •Oversee key quality systems and maintain and improve quality system documentation, i.e. policies and procedures to ensure ongoing compliance with quality system standards and requirements.•Maintain and supports quality systems that assure product conformance and customer satisfaction•Collect and analyzes data from quality processes and generate reports.•Develop training materials and conduct quality system training, as required.•Support internal and external audit processes by leading, coordinating and/or conducting quality system audits, as requiredNote: Duties are not limited to those listed above. Additional duties may be assigned as required. However, reasonable accommodations will be made if all possible under business conditions.RESPONSIBILITIESKey Contacts•Reports directly to Manager, Quality Assurance•Regularly interacts with all departments (Operations / R&D) at all levels and with some key customers/suppliers QUALIFICATIONSJob Demands•Independent collaborative self-starter with the ability to make appropriate quality-related decisions in real-time•Proven ability to manage projects, achieve timelines and stay within budget•Process-orientated, logical, analytical, meticulous, highly organized and able to analyze data & implement solutions•Proven ability to work effectively within a team environment while satisfying individual responsibilities and objectives•Excellent high level oral & written communications skills enabling incumbent to act as a facilitator and/or educator with strong leadership skills•Adaptable and willing to take on multiple new tasks and responsibilities•Ability to understand a technically complex product•Prioritizing multiple tasks within a dynamic work environment with tight timelines and limited resources•Ensuring compliance while meeting business objectives•Physical requirements: Extended periods of sitting/computer useSkills & Qualifications (Education and Experience)•University Degree (preferably BSc or Engineering) and/or an equivalent combination of education and technical experience acceptable to Epocal•5 – 10 years of industry experience in operations, R&D or QA within an ISO registered manufacturing environment •ISO13485 and FDA Quality System Regulation (QSR) experience preferred•ASQ certified designation: Certified Quality Auditor (CQA), Certified Quality Manager (CQM) or Certified Quality Engineer (CQE) preferred•High-level computer literacy; including Microsoft 365 tools and Adobe Acrobat SUMMARYIf this is the position for you, APPLY ONLINE or email your resume to Ariel Rodello at ariel.rodello@randstad.caOnly qualified candidates will be contacted.Please visit www.randstad.ca for a complete list of opportunities
      Are you a Senior quality assurance engineer with experience in the medical device industry?We have an amazing opportunity with a global manufacturer of medical devices!As a leading global healthcare company, the client develops innovations that support better patient outcomes with greater efficiencies, giving providers the confidence, they need to meet the clinical, operational, and financial challenges of a changing healthcare landscape. As a leader in medical imaging, laboratory diagnostics, and healthcare information technology, we have a keen understanding of the entire patient care continuum – from prevention and early detection to diagnosis and treatment. Under the supervision of the Manager, Quality Assurance, the Senior Quality Assurance Engineer is responsible for the following:Job Demands•Independent collaborative self-starter with the ability to make appropriate quality-related decisions in real-time•Proven ability to manage projects, achieve timelines and stay within budget•Process-orientated, logical, analytical, meticulous, highly organized and able to analyze data & implement solutions•Proven ability to work effectively within a team environment while satisfying individual responsibilities and objectives•Excellent high level oral & written communications skills enabling incumbent to act as a facilitator and/or educator with strong leadership skills•Adaptable and willing to take on multiple new tasks and responsibilities•Ability to understand a technically complex product•Prioritizing multiple tasks within a dynamic work environment with tight timelines and limited resources•Ensuring compliance while meeting business objectives•Physical requirements: Extended periods of sitting/computer useADVANTAGESDuties and Responsibilities•Technical Expert support of Operations and R&D to provide guidance and direction on activities necessary to comply with the Epocal quality system and with ISO13485, FDA Quality System Regulation, Health Canada Medical Device Regulations and other international requirements as applicable•Support new product introduction initiatives as the Quality delegate by participating on project teams and providing independent technical review of designs and providing input into required Verification and Validation activities. •Work with change initiators to support change initiatives by providing guidance on required verifications and validations. Approve change packages and associated verifications and validations.•Guides Quality Incident (non-conformance) and CAPA investigational activities ensuring thorough root cause analysis and appropriate corrective actions. Approve Quality Incidents (disposition product) and CAPAs, ensuring they are technically accurate, compliant to procedure and complete.•Develop quality plans and recommendations for improvement •Implement changes to the Quality System ensuring continuous improvement to ensure the effective and efficient operation of the quality system •Oversee key quality systems and maintain and improve quality system documentation, i.e. policies and procedures to ensure ongoing compliance with quality system standards and requirements.•Maintain and supports quality systems that assure product conformance and customer satisfaction•Collect and analyzes data from quality processes and generate reports.•Develop training materials and conduct quality system training, as required.•Support internal and external audit processes by leading, coordinating and/or conducting quality system audits, as requiredNote: Duties are not limited to those listed above. Additional duties may be assigned as required. However, reasonable accommodations will be made if all possible under business conditions.RESPONSIBILITIESKey Contacts•Reports directly to Manager, Quality Assurance•Regularly interacts with all departments (Operations / R&D) at all levels and with some key customers/suppliers QUALIFICATIONSJob Demands•Independent collaborative self-starter with the ability to make appropriate quality-related decisions in real-time•Proven ability to manage projects, achieve timelines and stay within budget•Process-orientated, logical, analytical, meticulous, highly organized and able to analyze data & implement solutions•Proven ability to work effectively within a team environment while satisfying individual responsibilities and objectives•Excellent high level oral & written communications skills enabling incumbent to act as a facilitator and/or educator with strong leadership skills•Adaptable and willing to take on multiple new tasks and responsibilities•Ability to understand a technically complex product•Prioritizing multiple tasks within a dynamic work environment with tight timelines and limited resources•Ensuring compliance while meeting business objectives•Physical requirements: Extended periods of sitting/computer useSkills & Qualifications (Education and Experience)•University Degree (preferably BSc or Engineering) and/or an equivalent combination of education and technical experience acceptable to Epocal•5 – 10 years of industry experience in operations, R&D or QA within an ISO registered manufacturing environment •ISO13485 and FDA Quality System Regulation (QSR) experience preferred•ASQ certified designation: Certified Quality Auditor (CQA), Certified Quality Manager (CQM) or Certified Quality Engineer (CQE) preferred•High-level computer literacy; including Microsoft 365 tools and Adobe Acrobat SUMMARYIf this is the position for you, APPLY ONLINE or email your resume to Ariel Rodello at ariel.rodello@randstad.caOnly qualified candidates will be contacted.Please visit www.randstad.ca for a complete list of opportunities

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