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        • 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
        • Ottawa, Ontario
        • Permanent
        Are you a Senior Planner / Project Manager looking for a challenging role where you will have the opportunity to make a huge impact with an industry leader?Do you have a passion for both Public and Private sector projects?Are you a specialist in Planning, Landscape Architecture and Urban Design?If so, this role may be for you!The details of this role that will help you decide if it’s the right move for you…• Location: Ottawa, ON• Competitive pay and an attractive benefits package• Ability to make an impact on the world around you• Excellent workplace cultureIn this role you will be responsible for...• Preparing planning policy and zoning reviews for municipal and development clients;• Municipal planning documents such as official plans, zoning by-laws, secondary plans, community improvement plans;• Research and presentation of planning analysis• Providing mentoring and guidance to other members of the team• You will obtain planning and development approvals• Take the lead on public engagement processes• Managing projects of various sizes• Act as a brand ambassador for the company brand and demonstrate guiding principles;• Be part of the business development practiceYou’re an ideal candidate for this role because you bring…• A degree in Planning or related studies;• Full membership in the Ontario Professional Planners Institute and the Canadian Institute of Planners;• A minimum of 10 years of planning experience• Familiarity with the planning policy framework in Ontario and has familiarity with Ottawa and Eastern Ontario;• Demonstrated skills in project management, including management of multi-disciplinary teams;• A high attention to detail;• Excellent technical, analytical, research and problem-solving skills;• Excellent writing and verbal communication skills;• Bilingual capabilities will be considered an asset.• A valid Ontario Driver’s License.If this role sounds like a good fit for you please APPLY ONLINE or submit your resume directly to Brian Roach at brian.roach@randstad.caOnly qualified candidates will be contacted.Please visit www.randstad.ca for a complete list of available positionsRESPONSIBILITIESQUALIFICATIONS
        Are you a Senior Planner / Project Manager looking for a challenging role where you will have the opportunity to make a huge impact with an industry leader?Do you have a passion for both Public and Private sector projects?Are you a specialist in Planning, Landscape Architecture and Urban Design?If so, this role may be for you!The details of this role that will help you decide if it’s the right move for you…• Location: Ottawa, ON• Competitive pay and an attractive benefits package• Ability to make an impact on the world around you• Excellent workplace cultureIn this role you will be responsible for...• Preparing planning policy and zoning reviews for municipal and development clients;• Municipal planning documents such as official plans, zoning by-laws, secondary plans, community improvement plans;• Research and presentation of planning analysis• Providing mentoring and guidance to other members of the team• You will obtain planning and development approvals• Take the lead on public engagement processes• Managing projects of various sizes• Act as a brand ambassador for the company brand and demonstrate guiding principles;• Be part of the business development practiceYou’re an ideal candidate for this role because you bring…• A degree in Planning or related studies;• Full membership in the Ontario Professional Planners Institute and the Canadian Institute of Planners;• A minimum of 10 years of planning experience• Familiarity with the planning policy framework in Ontario and has familiarity with Ottawa and Eastern Ontario;• Demonstrated skills in project management, including management of multi-disciplinary teams;• A high attention to detail;• Excellent technical, analytical, research and problem-solving skills;• Excellent writing and verbal communication skills;• Bilingual capabilities will be considered an asset.• A valid Ontario Driver’s License.If this role sounds like a good fit for you please APPLY ONLINE or submit your resume directly to Brian Roach at brian.roach@randstad.caOnly qualified candidates will be contacted.Please visit www.randstad.ca for a complete list of available positionsRESPONSIBILITIESQUALIFICATIONS
        • Ottawa, Ontario
        • Contract
        Under the supervision of the Manager, Chemical Preparation Operations; the Chemical Preparation Lab Technician, Level I is responsible for is responsible for preparation of sensor print mixes, stock solutions, or other chemical mixtures for sensor and test card assembly processes.Duties and Responsibilities•Follow written procedures for each mixture, and maintain appropriate records for each activity•Accurate and timely preparation of chemical mixes for sensor and test card assembly processes•Maintain Chemical Preparation room cleanliness and organization•Preparation of changeover chemicals, calibration fluid, stock solutions, and emulsionsADVANTAGESKey Contacts•Reports directly to Manager, Chemical Preparation Operations.•Follow daily schedule direction from Chemical Preparation Lead Hand.•Regularly interacts with process engineers, equipment technicians, clinical services lab and assembly operators to ensure adequate supply of chemical mixtures throughout the shift. Also works in close proximity with all personnel in Chem Prep lab.RESPONSIBILITIESJob Demands•Flexibility to work overtime, on-call and/or on different/rotating shifts as required•Routine, detailed nature of chemical preparations•Proven ability to work effectively in a team environment while satisfying personal responsibilities•Physical oManual dexterityoAbility to distinguish between coloursQUALIFICATIONSSkills & Qualifications (Education and Experience)•Technical diploma, or BSc in chemistry and/or an equivalent combination of education and technical experience acceptable•Experience in a regulated industry is an assetSUMMARYIf this role sounds like a good fit for you please APPLY ONLINE or submit your resume directly to Ariel at ariel.rodello@randstad.caThank you for applying to the role. We’ll review your application and connect shortly if you meet all the requirements.Good luck!
        Under the supervision of the Manager, Chemical Preparation Operations; the Chemical Preparation Lab Technician, Level I is responsible for is responsible for preparation of sensor print mixes, stock solutions, or other chemical mixtures for sensor and test card assembly processes.Duties and Responsibilities•Follow written procedures for each mixture, and maintain appropriate records for each activity•Accurate and timely preparation of chemical mixes for sensor and test card assembly processes•Maintain Chemical Preparation room cleanliness and organization•Preparation of changeover chemicals, calibration fluid, stock solutions, and emulsionsADVANTAGESKey Contacts•Reports directly to Manager, Chemical Preparation Operations.•Follow daily schedule direction from Chemical Preparation Lead Hand.•Regularly interacts with process engineers, equipment technicians, clinical services lab and assembly operators to ensure adequate supply of chemical mixtures throughout the shift. Also works in close proximity with all personnel in Chem Prep lab.RESPONSIBILITIESJob Demands•Flexibility to work overtime, on-call and/or on different/rotating shifts as required•Routine, detailed nature of chemical preparations•Proven ability to work effectively in a team environment while satisfying personal responsibilities•Physical oManual dexterityoAbility to distinguish between coloursQUALIFICATIONSSkills & Qualifications (Education and Experience)•Technical diploma, or BSc in chemistry and/or an equivalent combination of education and technical experience acceptable•Experience in a regulated industry is an assetSUMMARYIf this role sounds like a good fit for you please APPLY ONLINE or submit your resume directly to Ariel at ariel.rodello@randstad.caThank you for applying to the role. We’ll review your application and connect shortly if you meet all the requirements.Good luck!
        • Ottawa, Ontario
        • Contract
        Under the supervision of the Clinical Lab Lead Hand; the Finishes Goods Quality Control Laboratory Technician is responsible for: Duties and Responsibilities•Testing of cards •Testing of Readers •Testing of Capillary tubes•Routine performance checks including Adaptive Process Control, linearity, lifetimes, and validations •Assistance with testing requirements for Process Engineering, Test Engineering and R&D experimentsAssisting in routine upkeep and operational tasks related to the Clinical Lab ADVANTAGESKey tasks and activities will be completed with guidance and supervision from a higher-level technician or team leader:•Testing for various purposes (using written instructions) of card lots/readers/capillary tubes coming from the assembly departments. •Carries out routine maintenance and basic troubleshooting of clinical lab testing equipment and records these activities in maintenance logs with assistance and guidance form a higher-level technician.•Ability to track inventory of clinical lab supplies and replace what is in house and communicate to responsible personnel reorder points.•Participates in testing process and equipment improvement efforts, including experimental testing. Maintains appropriate records for testing.Percent of TimeFrequencyActivity50DailyProduction card Lot, Reader and Capillary tube testing, Analysis45DailyExperimental Lot Testing5Daily / WeeklyTest Equipment Maintenance / PhlebotomyRESPONSIBILITIESDemands•Routine, detailed nature of testing•Flexibility required for varied nature of testing•Regular and reoccurring exposure to blood from screened donors•Flexibility with adjusting work hours to follow up with overnight shifts as scheduled•Attention to detail is vital•Proven ability to work and communicate effectively in a team environment while satisfying personal responsibilities•Ability to function in a fast-paced environment•Ability to organize and prioritize responsibilities and multi-task•Ability to assess and troubleshoot computers, software applications and equipment•Ready to speak up about concerns•Satisfaction derived from solid completion of tasks •Clear understanding of health and safety in a lab environment•PhysicaloManual dexterity oAbility to distinguish between coloursoCombination of sitting and standingoExtended periods of detailed visual inspectionoInvolves regular and recurring exposure to blood from screened donorsoWork involves inventorying and processing cards, which requires walking, bending, stretching and occasionally lifting boxes of up to 20lbsQUALIFICATIONSSkills & Qualifications (Education and Experience)•Post-secondary education in a field of Science or related field, and/or combination of education and technical experience acceptable to Epocal•Proficient in using MS Office Suite (i.e. Excel, Word, PowerPoint) and capable in troubleshooting basic technological issues•Clinical laboratory experience such as blood testing, use of pipettes, centrifuges, and table-top analyzers is an asset•Some working knowledge of GMP and Good lab practices•Knowledge of basic statistics is preferred•Trained phlebotomist is considered an assetSUMMARYIf this role sounds like a good fit for you please APPLY ONLINE or submit your resume directly to Ariel at ariel.rodello@randstad.caThank you for applying to the role. We’ll review your application and connect shortly if you meet all the requirements.Good luck!
        Under the supervision of the Clinical Lab Lead Hand; the Finishes Goods Quality Control Laboratory Technician is responsible for: Duties and Responsibilities•Testing of cards •Testing of Readers •Testing of Capillary tubes•Routine performance checks including Adaptive Process Control, linearity, lifetimes, and validations •Assistance with testing requirements for Process Engineering, Test Engineering and R&D experimentsAssisting in routine upkeep and operational tasks related to the Clinical Lab ADVANTAGESKey tasks and activities will be completed with guidance and supervision from a higher-level technician or team leader:•Testing for various purposes (using written instructions) of card lots/readers/capillary tubes coming from the assembly departments. •Carries out routine maintenance and basic troubleshooting of clinical lab testing equipment and records these activities in maintenance logs with assistance and guidance form a higher-level technician.•Ability to track inventory of clinical lab supplies and replace what is in house and communicate to responsible personnel reorder points.•Participates in testing process and equipment improvement efforts, including experimental testing. Maintains appropriate records for testing.Percent of TimeFrequencyActivity50DailyProduction card Lot, Reader and Capillary tube testing, Analysis45DailyExperimental Lot Testing5Daily / WeeklyTest Equipment Maintenance / PhlebotomyRESPONSIBILITIESDemands•Routine, detailed nature of testing•Flexibility required for varied nature of testing•Regular and reoccurring exposure to blood from screened donors•Flexibility with adjusting work hours to follow up with overnight shifts as scheduled•Attention to detail is vital•Proven ability to work and communicate effectively in a team environment while satisfying personal responsibilities•Ability to function in a fast-paced environment•Ability to organize and prioritize responsibilities and multi-task•Ability to assess and troubleshoot computers, software applications and equipment•Ready to speak up about concerns•Satisfaction derived from solid completion of tasks •Clear understanding of health and safety in a lab environment•PhysicaloManual dexterity oAbility to distinguish between coloursoCombination of sitting and standingoExtended periods of detailed visual inspectionoInvolves regular and recurring exposure to blood from screened donorsoWork involves inventorying and processing cards, which requires walking, bending, stretching and occasionally lifting boxes of up to 20lbsQUALIFICATIONSSkills & Qualifications (Education and Experience)•Post-secondary education in a field of Science or related field, and/or combination of education and technical experience acceptable to Epocal•Proficient in using MS Office Suite (i.e. Excel, Word, PowerPoint) and capable in troubleshooting basic technological issues•Clinical laboratory experience such as blood testing, use of pipettes, centrifuges, and table-top analyzers is an asset•Some working knowledge of GMP and Good lab practices•Knowledge of basic statistics is preferred•Trained phlebotomist is considered an assetSUMMARYIf this role sounds like a good fit for you please APPLY ONLINE or submit your resume directly to Ariel at ariel.rodello@randstad.caThank you for applying to the role. We’ll review your application and connect shortly if you meet all the requirements.Good luck!

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