Quality Assurance And Regulatory Affairs Manager
Eli
About usEli Health is making continuous hormone monitoring possible, helping users support their daily and long-term health. No more waiting days to track key biomarkers—get results you can use within minutes. Eli’s flagship product, Hormometer®, is the first instant hormone monitoring platform to deliver results from saliva to mobile app—anytime, anywhere.
Developed over six years of R&D, over 2,000 product iterations, and backed by a dozen patent-pending innovations, Eli’s award-winning platform turns hormones into measurable signals you can track and improve. Just as the thermometer and glucometer have transformed health for millions, Eli’s platform is poised to be the next major evolution in tracking changes in stress, endurance, sleep, and more.
About the roleEli is looking for a QA/RA Manager to own our quality management system end-to-end. Eli's QMS is built to comply with FDA 21 CFR Part 820: running and updating core processes, keeping the system audit-ready, and making quality work at the pace of a company bringing a novel diagnostic to market. You will work closely with manufacturing and regulatory. Your primary responsibilities will be to:
Own and run the core QMS processes on a defined cadence: document control, change control, non-conformances, CAPA, training records, and equipment management.
Maintain and improve our electronic QMS while keeping it practical for the teams who use it daily.
Keep design and production documentation up to date as the product evolves, including the Design History File and Device Master Record.
Own supplier qualification and supplier quality — audits, agreements, and documentation.
Support internal audits and coordinate Eli through external audits.
Train new and existing employees on the QMS and applicable regulations, and follow through until records are complete.
Work with the CTO to define, communicate, and meet quality policies and objectives.
This description is not exhaustive. We are looking for someone who wants to own a quality system, not administer one corner of someone else’s.
About you
You have 3-5 years of QA/RA experience in medical devices, diagnostics, or another regulated industry where records are part of the work rather than paperwork after it.
You think about regulation from first principles. You go back to what a standard actually requires and why, rather than reproducing the system you used elsewhere. You can tell the difference between what compliance genuinely demands and what habit has layered on top, and you build the lightest system that fully meets the requirement.
You have personally maintained records that someone later reviewed or audited. You have done the filing and chased the signatures, not only read the procedures.
You are rigorous and thorough in your documentation, and you are willing to be the one to say a record is incomplete.
You are organized enough to maintain a cadence when nobody is checking, and you say so plainly when something slips.
You can read a procedure and follow it precisely, and you ask when something is unclear rather than guessing.
You have the software skills to work in an electronic quality system, and enough technical curiosity to sit with engineers and scientists.
You communicate clearly in writing and in person, and you work across teams without needing authority to get cooperation.
You have a Bachelor’s degree in Engineering, Science, or a related field.
(Advantage) You have worked with a physical consumable, a reagent, or a laboratory supply chain.
If you don’t exactly match the description but still believe you are the right person to join the team, please reach out. We value mindset and character.
Why you’ll love working at Eli
You’ll work with a group of talented and mission-driven people eager to improve lifelong health at scale.
You’ll be part of the core team developing and commercializing the first product that monitors hormonal data daily and over a lifetime.
You’ll own our quality system outright, early in your career, at a point where the decisions you make about how it works will still be in place years from now.
You’ll be part of a small (
You’ll be in an environment where people drive their own work, think creatively about open-ended problems, and solve them proactively.
You’ll get health insurance (medical, dental, vision, and more) to ensure you and your family stay physically and mentally at your best.
You’ll have flexibility over your schedule and vacations. We seek to hire great people, then give them the autonomy and space they need to achieve their goals.
Although our office and R&D facilities are in Montreal, we have a distributed team. We prioritize asynchronous workflows and minimize meetings to focus on the work itself.
You and your +1 will have unlimited free access to the Bota Bota spa in Montreal to recharge.
#J-18808-Ljbffr
Developed over six years of R&D, over 2,000 product iterations, and backed by a dozen patent-pending innovations, Eli’s award-winning platform turns hormones into measurable signals you can track and improve. Just as the thermometer and glucometer have transformed health for millions, Eli’s platform is poised to be the next major evolution in tracking changes in stress, endurance, sleep, and more.
About the roleEli is looking for a QA/RA Manager to own our quality management system end-to-end. Eli's QMS is built to comply with FDA 21 CFR Part 820: running and updating core processes, keeping the system audit-ready, and making quality work at the pace of a company bringing a novel diagnostic to market. You will work closely with manufacturing and regulatory. Your primary responsibilities will be to:
Own and run the core QMS processes on a defined cadence: document control, change control, non-conformances, CAPA, training records, and equipment management.
Maintain and improve our electronic QMS while keeping it practical for the teams who use it daily.
Keep design and production documentation up to date as the product evolves, including the Design History File and Device Master Record.
Own supplier qualification and supplier quality — audits, agreements, and documentation.
Support internal audits and coordinate Eli through external audits.
Train new and existing employees on the QMS and applicable regulations, and follow through until records are complete.
Work with the CTO to define, communicate, and meet quality policies and objectives.
This description is not exhaustive. We are looking for someone who wants to own a quality system, not administer one corner of someone else’s.
About you
You have 3-5 years of QA/RA experience in medical devices, diagnostics, or another regulated industry where records are part of the work rather than paperwork after it.
You think about regulation from first principles. You go back to what a standard actually requires and why, rather than reproducing the system you used elsewhere. You can tell the difference between what compliance genuinely demands and what habit has layered on top, and you build the lightest system that fully meets the requirement.
You have personally maintained records that someone later reviewed or audited. You have done the filing and chased the signatures, not only read the procedures.
You are rigorous and thorough in your documentation, and you are willing to be the one to say a record is incomplete.
You are organized enough to maintain a cadence when nobody is checking, and you say so plainly when something slips.
You can read a procedure and follow it precisely, and you ask when something is unclear rather than guessing.
You have the software skills to work in an electronic quality system, and enough technical curiosity to sit with engineers and scientists.
You communicate clearly in writing and in person, and you work across teams without needing authority to get cooperation.
You have a Bachelor’s degree in Engineering, Science, or a related field.
(Advantage) You have worked with a physical consumable, a reagent, or a laboratory supply chain.
If you don’t exactly match the description but still believe you are the right person to join the team, please reach out. We value mindset and character.
Why you’ll love working at Eli
You’ll work with a group of talented and mission-driven people eager to improve lifelong health at scale.
You’ll be part of the core team developing and commercializing the first product that monitors hormonal data daily and over a lifetime.
You’ll own our quality system outright, early in your career, at a point where the decisions you make about how it works will still be in place years from now.
You’ll be part of a small (
You’ll be in an environment where people drive their own work, think creatively about open-ended problems, and solve them proactively.
You’ll get health insurance (medical, dental, vision, and more) to ensure you and your family stay physically and mentally at your best.
You’ll have flexibility over your schedule and vacations. We seek to hire great people, then give them the autonomy and space they need to achieve their goals.
Although our office and R&D facilities are in Montreal, we have a distributed team. We prioritize asynchronous workflows and minimize meetings to focus on the work itself.
You and your +1 will have unlimited free access to the Bota Bota spa in Montreal to recharge.
#J-18808-Ljbffr
Vacancy posted 50 minutes ago
Similar jobs that could be interesting for youBased on the Quality Assurance And Regulatory Affairs Manager in Winnipeg, MB vacancy
- ...Manager, Quality AssuranceApply: Remote, ON: Full time: Posted Yesterday: R2616835Our... ...Job Details The Manager, Quality Assurance (Consulting) is a hands-on people leadership... ...lead internal, client, third-party and regulatory audits or inspections, including...SuggestedFull timeRemote work
$95k - $105k per year
...Quality Assurance Manager Winnipeg, MB | Full-Time | Permanent | $95,000 – $105,000 per year About the Opportunity Staffmax is excited... ...and process controls Serving as the go-to contact for regulatory information, staying current on changing requirements and...SuggestedPermanent employmentFull timeCasual workWork at officeNight shift- ...Reporting to the Sr. Director, Quality, the Director, Quality Assurance leads QA Operations, Quality Systems... ...continuous improvement, quality risk management, and escalation of significant quality... ..., GMP requirements, and applicable regulatory expectations, while remaining...SuggestedFlexible hours
- ...SUMMARY: Ensure the New Flyer Quality system is fully understood, executed... ...Winnipeg facility. The Quality Manager provides leadership to the Quality Assurance Department and the plant overall,... ...are adhering to all safety, regulatory and legal requirements defined by...SuggestedFull timeInternshipImmediate startFlexible hoursShift work
- ...protecting and saving lives. Job Summary The Quality Assurance Deviations and CAPA Specialist provides support by managing deviations and corrective/preventative actions... ...Winnipeg facility that are in compliance with regulatory requirements. This position is primarily...SuggestedFlexible hours
- ...integrated, single-source solutions provider delivering consistent, high-quality aluminum permanent mold castings to our customers. We are currently seeking a reliable and hardworking Quality Assurance Manager to join our team in a fast-paced manufacturing environment. Why...Permanent employmentFull timeFlexible hoursShift work
- ...perform to your expectations. We are proud of our long-standing partnerships with family-owned Canadian chicken farmers to produce high quality products. Role: Responsible for monitoring employee GMP compliance and product quality specification compliance of the raw...Full timeAfternoon shift
- Education: College, CEGEP or other non-university certificate or diploma from a program of 1 year to 2 years. Security and safety: Criminal record check. Screening questions: Do you have experience working in this field?. Employment terms options: Evening. Experience: 1 year...Hourly payLong term contractPermanent employmentImmediate startDay shiftAfternoon shift
$109k - $159k per year
...Vancouver office is looking for a Senior Manager to join the Assurance team and own the following... ...clients, prepare working papers per regulatory standards. Build positive working... ...positive, professional, and delivering high quality work You identify, recommend, and...Work at officeLocal areaFlexible hours- ...perform to your expectations. We are proud of our long-standing partnerships with family-owned Canadian chicken farmers to produce high quality products. Role: Responsible for monitoring employee GMP compliance and product quality specification compliance of the raw...Contract work
- ...SUMMARY: The Director of Quality – Transit leads the Quality organization... ...Quality, ensures the Quality Management System is effective, develops... ...product, reliability, regulatory, and potential product-safety... ...problem solving, and quality assurance into everyday work. Drive...Permanent employmentFull timeImmediate start
- ...Summary The Specialist I, Quality Compliance is responsible for... ...representing Emergent during regulatory inspections, customer audits,... ...audit and inspection activities, managing preparation and logistics,... ..., acting as the Quality Assurance representative and providing...Flexible hours
- ...ensure flight and product efficiency. As a Quality Inspector , you will ensure that all aircraft... ...repaired, or overhauled in full compliance with regulatory standards, OEM specifications, and the company’s quality management system (QMS). You will act as a key control...Long term contractTemporary workTraineeshipInternshipImmediate startFlexible hoursShift workWeekend work
- Senior Quality Assurance/Regulatory Affairs SpecialistFull-Time Hybrid Position - Based in Toronto (3 days per week in office) ABOUT MIMOSA DIAGNOSTICSMIMOSA provides a proactive approach to skin health and wound care, empowering clinicians to implement earlier interventions...Work at officeRemote work3 days per week
- ...and a commitment to people. Our dependable quality, reliable delivery, and knowledgeable... ...Café offers free Tea and Coffee. Quality Assurance Technician (Full Time - Permanent) The... ...Technician will report directly to the Plant Manager and will help meet our mission and target...Permanent employmentFull timeWork at office
- Lead Quality Assurance and Regulatory Affairs at Piramal Pharma Solutions’ Aurora site, directing QMS priorities, compliance oversight, and quality decision-making.This Senior Manager provides leadership across QA, Quality Management Systems, and Regulatory Affairs. The position...
- Lead Quality Assurance and Regulatory Affairs at Piramal Pharma Solutions in Aurora, guiding QMS compliance and risk-based quality decisions.As Senior Manager, you will direct QA, Quality Management Systems, and Regulatory Affairs at the Aurora site. You will work with the Director...
- ...The Quality Control Inspector will provide Quality Process Audit support to the Assembly Line. This position will assist in reducing process variation through the use of statistical data analysis, process audits, and department metrics. The position emphasizes improving internal...Full timeTemporary work
- ...about SKF at. Position Overview We are seeking a skilled Quality Electrical Engineer to support customer and manufacturing quality... ...return investigations, Failure analysis, Internal non-conformance management, Material Review Board (MRB) activities, First-pass-yield...Permanent employment
- ...We are seeking a highly experienced and hands-on Supplier Quality Engineer (SQE) with strong expertise in casting and machining processes... ...and new product development. Key Responsibilities Lead and manage supplier quality activities for casting and machined components...
- ...class service, innovation and a commitment to people. Our dependable quality, reliable delivery, and knowledgeable follow-up service have made... ...translated into practical actions and measurable results. • Manage assigned improvement projects from data analysis and problem...
- Ensure compliance and product excellence with MIMOSA Diagnostics as a Senior Quality Assurance and Regulatory Affairs Specialist. Work hybrid from Toronto to drive improvements in quality standards. MIMOSA is committed to compassionate care through innovative solutions and...
- ...growth. THE POSITION The Quality Engineer leads the... ...conducting root cause analysis, managing corrective actions, and collaborating... ...that meets both customer and regulatory requirements. HOW YOU WILL... ...Collaborate with suppliers to manage and enhance supplier quality,...Full timeRemote work
- ...Lead enterprise governance and assurance at Interac, applying delivery standards, controls, and executive reporting in a flexible hybrid... ...Canada Apply enterprise governance, delivery assurance, risk management, and executive reporting expertise to Interac’s Canadian...Full timeInternshipFlexible hours
- ...portfolio continues to grow, we are seeking a Quality Coordinator (Site) to lead project... ...applicable codes, and Victor Energy's Quality Management System. This role is site-based and will... ...Responsible for execution of quality assurance and quality control activities on the project...Full timeContract work
- Lead SaMD quality and regulatory affairs remotely from Winnipeg, Manitoba, with expertise in FDA submissions and ISO 13485 systems.As the healthcare... ..., and operations.Key Responsibilities: Own the quality management system and regulatory submissionsLead FDA pre-submissions...Remote work
- ...professionals understand health earlier, manage it more proactively, and intervene when... ...Overview:Myant is looking for an experienced Regulatory Affairs Manager to support the commercialization... ...with Product, Engineering, Clinical, Quality, Manufacturing and other cross-...Immediate start
- ...Grounded in safety, quality, and ethics, our experts lead their fields... ...Assessments (to support regulatory applications), as well as, Environmental... ...projects, as required. Managing, shipping, and tracking... ...coordinating with laboratories Manage, compile, interpret, and analyze...Work at officeWorldwideShift work
- ...for people with serious diseases. We are seeking a Senior Manager, Regulatory Affairs to join our Regulatory Affairs team, supporting our Canadian... ...marketing application and post-approval submissions.Develop high-quality, globally aligned regulatory strategies throughout relevant...InternshipLocal areaWorldwide
$87k - $117k per year
...position reports to the Canada Regional Quality Manager. The Prescott, ON, Canada facility produces... ..., and other support leaders to assure the effective implementation of quality... ...safety regulations. Interfaces customer and regulatory agency inspection representatives during...Long term contractTemporary workInternshipWork at officeLocal areaImmediate startFlexible hoursWeekday work
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Quality Assurance And Regulatory Affairs Manager. Be the first to apply!
Related searches
- quality assurance manager Winnipeg, MB
- food safety & quality assurance manager Winnipeg, MB
- quality assurance coordinator Winnipeg, MB
- qa manager Winnipeg, MB
- regulatory manager Winnipeg, MB
- customs compliance manager Winnipeg, MB
- safety compliance manager Winnipeg, MB
- compliance manager Winnipeg, MB
- directeur juridique Winnipeg, MB
- quality compliance manager Winnipeg, MB

