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femtherapeutics

Senior Product Development Manager

Montreal, QC, Canada

Full-time

Apply About employer

Applications open in a new tab.

Job details

Job type: Full-time
Apply by: May 1, 2027
Posting language: English
Posted: Nov 2, 2026

Original job description

Company Description

femtherapeutics is transforming access to pelvic health by creating a better entry point for people experiencing pelvic conditions. The company’s flagship product is world's first home-use pessary for pelvic organ prolapse and postpartum recovery, designed for self-management without a prescription or clinic visit. This device is delivered alongside a digital platform that supports clinical screening, education, and care navigation. Through this combination of hardware and software, femtherapeutics provides direct access to screening and treatment across pelvic health needs from postpartum through postmenopause. femtherapeutics has raised over $7M+ from venture capital and institutional funds, been featured in Forbes and Fast Company, and has been named by CIX as one of the Top 20 Innovative Companies in Canada and by Mastercard in Canada's Small Business 100 list.

Role Description

The Senior Product Development Manager is a full-time, hybrid role based in Montreal, QC, with flexibility for partial work from home. We’re building the first OTC pessary for pelvic organ prolapse and postpartum recovery and are currently in V&V on the way to a 510(k). We’re looking for a Senior Product Development Manager who can take the device from verification through design transfer. This role owns the product’s development end to end: design controls and the traceability matrix, the ISO 14971 risk file, verification protocols and test method validation, and the bench testing sections of the 510(k). It also covers running our in-house lab, working with contract manufacturers on design outputs and DFM, and leading design transfer, including oversight of process validation (IQ/OQ/PQ). The ideal candidate has hands-on experience designing regulated medical devices in SolidWorks and taking them through verification, and wants to own the product’s plan, timeline, and budget while staying close to the work.

About the Level: Manager here means you own the product, not a team. You’ll run the pessary’s development from V&V through design transfer, including the plan, timeline, budget, and technical calls. There are no direct reports, and you’ll be hands-on every week. We’re open to senior engineers and to R&D managers who miss doing the work.

Qualifications

Bachelor's degree in Biomedical Engineering, Mechanical Engineering or a related field
5+ years in product design and development as a mechanical, biomechanical or R&D engineer, or as an R&D or product development manager
Hands-on experience with design controls and ISO 14971 risk management for regulated medical devices
Verification testing experience, including writing and executing protocols to FDA-recognized consensus standards (e.g., ASTM, ISO) and working with external test labs
Experience leading design transfer with contract manufacturers and suppliers, including process validation (IQ/OQ/PQ)
Contributed to a 510(k) or comparable submission (e.g., Health Canada, EU MDR), including writing performance testing sections
Proficiency in SolidWorks and FDM/SLA 3D printing

Job Responsibilities

Own the product development plan and strategy, manage project risks with clear mitigation plans, and deliver on time and on budget
Design, model and optimize the device in SolidWorks from prototype to final product, prototyping on our FDM and SLA 3D printers
Own design controls: refine design inputs so requirements stay testable, maintain the traceability matrix (user needs → requirements → risk controls → verification → validation), run design reviews, and maintain the Design History File
Keep the ISO 14971 risk file current as designs and test results change, including the hazard analysis, FMEAs, and links from risk controls to verification evidence
Develop and validate test methods, then write, execute and report on verification protocols (bench-top, functional and material), updating the verification plan as needed
Run the in-house lab, including equipment qualification, calibration, maintenance and jig design
Coordinate external testing, including accelerated aging (ASTM F1980), distribution and biocompatibility (ISO 10993)
Work with our contract manufacturers on design outputs (drawings, specs, inspection and test plans) and DFM, and lead design transfer, including review of process validation (IQ/OQ/PQ)
Support supplier qualification and Quality and Supplier Agreements, and define incoming inspection and acceptance criteria
Write the bench testing sections and predicate comparison data for the 510(k), per FDA performance testing guidance
Write and revise controlled documents under document control and change control SOPs, and document all experiments
Flag technical problems early and bring solutions, working closely with internal and external teams

At fem, we value our employees and offer a comprehensive benefits package:

Competitive salary + stock options so you can own a piece of what we're building.
Comprehensive group benefits including medical and dental coverage.
Hybrid work arrangements, with 3 days in the office and 2 days remote.
3 weeks of vacation (+ 2 Sick Days) + Paid holiday closure in December so you can fully enjoy the festive season.
Quarterly team activities and social events to foster a collaborative and fun work environment.
A beautiful office environment located on Sherbrooke/Crescent right in the heart of downtown Montreal.

How to Apply

Please submit your CV to Negin Ashouri, Co-Founder & CTO, by email at negin.ashouri@femtherapeutics.com. Please include "Senior Product Development Manager - Application" in the subject line. Apply by Monday November 9, 5pm ET.

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More about this job

Responsibilities

Own the pessary’s development from verification and validation through design transfer, including the product plan, schedule, budget, design controls, risk file, and verification activities. Manage in-house and external testing, supplier and contract manufacturer coordination, process validation oversight, and preparation of bench-testing content for the 510(k).

Requirements

Requires a bachelor’s degree in biomedical engineering, mechanical engineering, or a related field, plus at least five years of relevant product design and development experience. Candidates should have hands-on regulated medical device experience with design controls, ISO 14971, verification testing, design transfer and process validation, 510(k) or comparable submissions, SolidWorks, and FDM/SLA 3D printing.

Skills

Medical Device Product Development
SolidWorks
Design Controls
ISO 14971 Risk Management
Verification Testing
Test Method Validation
Design Transfer
Process Validation
510(k) Submissions
FDM And SLA 3D Printing
Design For Manufacturing
ISO 10993 Biocompatibility Testing
ASTM Standards
Design History File Management
Project Planning And Budgeting

Benefits

Stock Options
Medical Insurance
Dental Insurance
Hybrid Work Arrangements
Three Weeks Of Vacation
Two Sick Days
Paid December Holiday Closure
Quarterly Team Activities And Social Events

Visa sponsorship

Not detected in the job text

Hiring contact

Negin Ashouri

Hiring contact email

negin.ashouri@femtherapeutics.com

Keywords

Medical Devices
Pelvic Organ Prolapse
Pessary
Product Development
SolidWorks
FDM 3D Printing
SLA 3D Printing
Design Controls
Design History File
Traceability Matrix
ISO 14971
Risk Management
Hazard Analysis
FMEA
Verification And Validation
Test Method Validation
ASTM Standards
ISO Standards
Accelerated Aging
ASTM F1980
ISO 10993
Biocompatibility
510(k)
FDA Performance Testing Guidance
Design For Manufacturing
Contract Manufacturing
Design Transfer
IQ/OQ/PQ
Supplier Qualification
Document Control

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