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HomeCompaniesConaviSenior Manufacturing Engineer

Senior Manufacturing Engineer

Conavi · Toronto, Ontario, M3B 2V1, Canada · Hybrid · Active · BambooHR

Job facts

FieldValue
CompanyConavi
TitleSenior Manufacturing Engineer
Normalized title-
Department / teamOperations
LocationToronto, Canada
Work modelHybrid / Hybrid
Employment typeFull Time
Salary-
Statusactive
ATS providerBambooHR
Posted / first seen2026-05-19 / 2026-05-30
Changed / last seen2026-05-30 / 2026-06-06

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PageWhat it containsOpen
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ATS provider jobsActive postings observed through BambooHR.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Toronto.Open
Department jobsActive postings in Operations.Open
Work model jobsActive Hybrid postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyConavi
Sourcea7c040d4-2d5d-4879-99c0-7413548dcd2e
ATS providerBambooHR

Description

Imagine your future at Conavi! Join our team in the design, manufacture, and sale of an innovative intravascular imaging system to improve cardiac care. Conavi Medical’s Novasight Hybrid System enables simultaneous imaging of a patient’s coronary arteries using both intravascular ultrasound (IVUS) and Optical Coherence Tomography (OCT) technologies. If you would like to be a part of a talented team that is making a difference in healthcare, we currently have a new opening   for a Senior Manufacturing Engineer to develop, validate, and optimize the manufacturing processes for Conavi’s medical device including the catheter-based products and durable electromechanical assemblies at our manufacturing partners ensuring that all devices are built to the highest standards of quality, cost, efficiency, and scalability. In this position, you will: Contribute to the development, optimization, and scale-up of manufacturing processes for new medical devices in collaboration with internal design teams and external manufacturing partners Support design transfer, pilot builds, manufacturing readiness, and commercialization activities in both disposable catheter and durable electromechanical systems including mechanical assemblies, PCBA, cable harnesses, sensors, motors, and power subsystems. Develop and execute IQ/OQ/PQ validations for catheter-based disposable products (e.g. bonding, coating, assembly, packaging, and testing) and durable electromechanical assemblies (e.g. consoles, power systems, imaging modules, and mechanical sub-assemblies). Design, qualify, and implement manufacturing equipment, fixtures, and tooling, focusing on efficiency improvements and ergonomic/safety enhancements Lead and execute key projects such as material qualification, tooling and fixture optimization, automation, and line balancing that drive Cost of Goods Sold (COGS) reduction and DFM improvements. Develop and monitor critical quality attributes (CQAs) using PFMEA, Control Plans, DOE, SPC, and capability analysis Lead root cause investigations, CAPA activities, and process troubleshooting efforts for issues related to product performance, reliability, and integration Coach and mentor other manufacturing engineers and provide technical leadership across cross-functional teams Participate in, and adhere to, health and safety initiatives and requirements You possess the following qualifications: Bachelor’s or above degree in engineering (Mechanical, Biomedical, Manufacturing, or related field) Significant manufacturing engineering experience ideally in the medical device industry. Practical experience in ISO (ideally 13485) and CGMP Demonstrated skills in the application of root cause analysis, and statistical process control Strong experience with process development, validation (IQ/OQ/PQ), and manufacturing transfer activities Skilled in preparing and updating mfg. documentation such as protocols and reports Proficiency in MS Office (Outlook, Word, Excel, Word, Visio, Access), Minitab, Solidworks, and ERP/MRP systems Competencies include teamwork, communication, organizational, attention to detail, and problem resolution Ability to travel to contract manufacturer and supplier sites across North America as required Conavi Medical values everyone and their contributions.  We value diversity and encourages applications from all qualified candidates.  Please let us know if you require accommodations on any of the grounds protected by the Ontario Human Rights Code during the recruitment process. Please submit a resume directly to Conavi Medical through the Careers section of our website at  www.conavi.com .  We thank all candidates for their interest but only those selected for an interview will be contacted.

Full job record

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Org ID665f8852-3b41-42a0-bdf5-fa463894006a
Source IDa7c040d4-2d5d-4879-99c0-7413548dcd2e
Board IDa7c040d4-2d5d-4879-99c0-7413548dcd2e
Providerbamboohr
Provider Job Key166
TitleSenior Manufacturing Engineer
Normalized Title
Statusactive
Activeyes
Location TextToronto, Ontario, M3B 2V1, Canada
DepartmentOperations
Team
Employment Typefull_time
Workplace Typehybrid
Remote Policyhybrid
CountryCanada
Region
CityToronto
Salary Raw
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://conavi.bamboohr.com/careers/166
Apply URLhttps://conavi.bamboohr.com/careers/166
First Seen At2026-05-30 06:01:29Z
Last Seen At2026-06-06 10:28:55Z
Last Checked At2026-06-06 10:28:55Z
Last Changed At2026-05-30 06:01:29Z
Inactive At
Source Posted At2026-05-19 00:00:00Z
Source Updated At
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Parsed Structured
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Extensions
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    "description": "<p>Imagine your future at Conavi!</p>\n<p><br></p>\n<p>Join our team in the design, manufacture, and sale of an innovative intravascular imaging system to improve cardiac care.</p>\n<p> </p>\n<p>Conavi Medical’s Novasight Hybrid System enables simultaneous imaging of a patient’s coronary arteries using both intravascular ultrasound (IVUS) and Optical Coherence Tomography (OCT) technologies.  </p>\n<p> </p>\n<p>If you would like to be a part of a talented team that is making a difference in healthcare, we currently have a new opening<span style=\"font-weight: bold\"> </span>for a Senior Manufacturing Engineer to develop, validate, and optimize the manufacturing processes for Conavi’s medical device including the catheter-based products and durable electromechanical assemblies at our manufacturing partners ensuring that all devices are built to the highest standards of quality, cost, efficiency, and scalability. </p>\n<p> </p>\n<p>In this position, you will:  </p>\n<ul>\n<li><span>Contribute to the development, optimization, and scale-up of manufacturing processes for new medical devices in collaboration with internal design teams and external manufacturing partners </span></li>\n<li><span>Support design transfer, pilot builds, manufacturing readiness, and commercialization activities in both disposable catheter and durable electromechanical systems including mechanical assemblies, PCBA, cable harnesses, sensors, motors, and power subsystems.</span></li>\n<li><span>Develop and execute IQ/OQ/PQ validations for catheter-based disposable products (e.g. bonding, coating, assembly, packaging, and testing) and durable electromechanical assemblies (e.g. consoles, power systems, imaging modules, and mechanical sub-assemblies).</span></li>\n<li><span>Design, qualify, and implement manufacturing equipment, fixtures, and tooling, focusing on efficiency improvements and ergonomic/safety enhancements </span></li>\n<li><span>Lead and execute key projects such as material qualification, tooling and fixture optimization, automation, and line balancing that drive Cost of Goods Sold (COGS) reduction and DFM improvements.</span></li>\n<li><span>Develop and monitor critical quality attributes (CQAs) using PFMEA, Control Plans, DOE, SPC, and capability analysis </span></li>\n<li><span>Lead root cause investigations, CAPA activities, and process troubleshooting efforts for issues related to product performance, reliability, and integration</span></li>\n<li><span>Coach and mentor other manufacturing engineers and provide technical leadership across cross-functional teams </span></li>\n<li>Participate in, and adhere to, health and safety initiatives and requirements</li>\n</ul>\n<p><br></p>\n<p>You possess the following qualifications:</p>\n<ul>\n<li><span>Bachelor’s or above degree in engineering (Mechanical, Biomedical, Manufacturing, or related field) </span></li>\n<li><span>Significant manufacturing engineering experience ideally in the medical device industry. </span></li>\n<li><span>Practical experience in ISO (ideally 13485) and CGMP</span></li>\n<li><span>Demonstrated skills in the application of root cause analysis, and statistical process control</span></li>\n<li><span>Strong experience with process development, validation (IQ/OQ/PQ), and manufacturing transfer activities</span></li>\n<li><span>Skilled in preparing and updating mfg. documentation such as protocols and reports</span></li>\n<li><span>Proficiency in MS Office (Outlook, Word, Excel, Word, Visio, Access), Minitab, Solidworks, and ERP/MRP systems </span></li>\n<li><span>Competencies include teamwork, communication, organizational, attention to detail, and problem resolution </span></li>\n<li>Ability to travel to contract manufacturer and supplier sites across North America as required</li>\n</ul>\n<p><br></p>\n<p>Conavi Medical values everyone and their contributions.  We value diversity and encourages applications from all qualified candidates.  Please let us know if you require accommodations on any of the grounds protected by the Ontario Human Rights Code during the recruitment process.  </p>\n<p><br></p>\n<p>Please submit a resume directly to Conavi Medical through the Careers section of our website at <a href=\"http://www.conavi.com\" target=\"_blank\" rel=\"noopener noreferrer\">www.conavi.com</a>.  We thank all candidates for their interest but only those selected for an interview will be contacted.</p>",
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