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 1 hour 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- 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...SuggestedWork at officeRemote work3 days per week
- 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...Suggested
- ...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...Full 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...Flexible 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
- ...Director of Quality Assurance Winnipeg, MB Full-Time, Onsite POSITION SUMMARY: The Director of Quality Assurance - Transit provides... ...strengthens operational excellence through a robust Quality Management System, develops high-performing teams, and partners across...Full timeInternshipImmediate start
- 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...
- ...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
- ...for people with serious diseases. We are seeking a Senior Manager, Regulatory Affairs to join our Regulatory Affairs team, supporting our Canadian... ...application and post-approval submissions. Develop high-quality, globally aligned regulatory strategies throughout relevant...InternshipLocal areaWorldwide
$85k - $95k per year
...candidates will be considered. Own the Quality Program. Inspire Your Team. Drive... ...satisfaction. We're seeking a Quality Assurance Manager who combines technical knowledge... ...internal audits, coordinate customer and regulatory audits, and facilitate the annual Quality...InternshipLocal area$98.72k - $123.4k per year
...neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to... ...are seeking an experienced Manager, Quality Assurance to provide leadership and oversight... ...provide technical expertise, support regulatory compliance, and partner closely with cross...InternshipWork at officeWorldwide$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- ...serving North American clients to create and manage built environments that play a vital role... ..., and improve procedures within the Quality Department nationally within RHS operations... ...that completed repairs meet company and regulatory requirements.Keep track and report quality...Full timePart timeInternshipWork at officeLocal areaRemote workFlexible hoursWeekend workAfternoon shift
- Shape governance and regulatory alignment for an Etobicoke Credit Union, combining policy oversight, corporate records, and adaptable project management skills.The Manager, Governance & Corporate Affairs reports to the CEO and supports effective governance execution. As the...
- ...College’s Planning, Institutional Research and Quality (PIRQ) department requires a full-time Manager, Quality Assurance. The Manager, Quality Assurance is responsible... ...academic programs and services meet or exceed regulatory, accreditation, and institutional standards. This...Full time
- ...country and beyond, we’re committed to quality, innovation, and sustainability as we shape... ...The RoleWe are seeking a Quality Assurance Manager to join our P&H Milling team. Reporting... ...ensures compliance with quality standards, regulatory requirements, and customer...Full timeLocal areaWork from home
- Lead pharmaceutical regulatory submissions at Apotex, applying project strategy, risk mitigation... ...to new product development.As Project Manager, New Product Development, you will lead submission... ...activities within Global Regulatory Affairs. Your work covers due diligence,...
- Drive regulatory strategies for Canadian projects at Regeneron as a Senior Manager in Regulatory Affairs. This hybrid role fosters meaningful collaboration and innovation while impacting... ...submissions and the development of high-quality regulatory strategies. This role involves...Local area
$128k - $144k per year
Job DescriptionSenior Project Manager, Regulatory Affairs provides management and leadership to plan, prepare, and execute high quality projects. S/he interfaces with internal departments and company leadership, and externally with sponsors and vendors. The Senior Project Manager...Local areaRemote workWorldwideFlexible hours$130k - $140k per year
...CANRemoteManagerFull-TimeRequisition #: QUALI007269Description SMS Equipment is seeking a detail-focused and collaborative Quality Assurance Manager to lead quality assurance for our enterprise resource planning (ERP) solutions and associated applications. This role...Work at officeRemote workMonday to friday- Quality Assurance ManagerCompany: Corporate StaysDepartment: OperationsJob Type: Full-Time FreelancerWork Arrangement: RemoteWorking Hours: Monday... ...for every guest.Position Overview The Quality Assurance Manager will be responsible for monitoring, evaluating, and...Full timeTemporary workFor contractorsLocal areaRemote work
$130k - $150k per year
...obtaining and maintaining the regulatory authorizations that will permit... ...three regimes that must be managed together: European pharmaceutical... ...departments involved e.G., Quality, Operations, Supply Chain, Research... ...the Head of Global Regulatory Affairs. Monitor and keep abreast...Work at officeRemote workFlexible hours- ...pelvic organ prolapse and postpartum recovery, designed for self-management without a prescription or clinic visit. This device is delivered... ...Top 20 Innovative Companies in Canada. Role DescriptionThe Quality Systems Manager is afull-time, hybrid role based inMontreal, QC,...Contract workWork at officeWork from home
$115.4k - $125k per year
Quality Assurance Manager# Johnson Electric Careers## Quality Assurance Manager申请: Canada, Stratford: Full time: 今天发布: R00031379# **Join Our Team as a Quality Assurance Manager at Johnson Electric!****Location:** Mississauga, ON (onsite) **Salary Range:** $115,400...Full timeInternshipWorldwide$100k - $160k per year
Quality Assurance Manager – ConstructionLocation: Toronto, ON | On-site Salary: $100,000–$160,000 + Benefits Relocation package included Skyline Recruitment is partnering with an established construction contractor to recruit a Quality Assurance & Control Manager...For contractorsFor subcontractorRelocation package$110k - $130k per year
The QA/QC Manager serves as the primary contact for all quality related items and issues associated with the project and plans, performs directs and supervises... ...project status reportsMonitor contractor quality assurance and quality control programsCoordinate resolution of...For contractorsFor subcontractorWork at office
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

