At a Glance
- Tasks: Lead usability assessments and manage risk for innovative medical devices in women's health.
- Company: Join Flo, the world’s #1 health & fitness app with a mission to improve female health.
- Benefits: Competitive salary, performance incentives, paid leave, and professional growth opportunities.
- Other info: Dynamic, mission-driven team with a focus on collaboration and innovation.
- Why this job: Make a real impact on women's health while working with cutting-edge technology.
- Qualifications: Degree in Human Factors Engineering and experience with software-based medical devices required.
The predicted salary is between 50000 - 60000 £ per year.
Flo is the world’s #1 health & fitness app on a mission to build a better future for female health. The job involves leading usability assessments and managing risk for medical devices, engaging with cross‑functional teams, and contributing to regulatory submissions. This role is an excellent opportunity for an experienced Human Factors Engineer looking to take the lead on and work independently on software as a medical device in women’s health.
Your Experience Must have:
- Degree or higher in Human Factors Engineering, or relevant related subject
- Fluency and confidence understanding IEC 62366‑1, ISO 14971, and FDA regulations
- Significant experience conducting human factors research with software based medical devices that is compliant with IEC 62366‑1, ISO 14971, and FDA regulations
- Experience in creating and maintaining usability documentation to ensure compliance with IEC 62366‑1, ISO 14971, and FDA regulations
- Applied understanding of the product development process
- Applied understanding of medical device industry
- Relevant industrial experience commensurate with requirements of an experienced and independent contractor
- Exceptional attention to detail and precise data handling and analytical skills
- Technical report writing skills
- Exceptional time management skills and an ability to work well under pressure
Nice to have:
- Experience with software as a medical device in the women’s health space
- Experience conducting training on IEC 62366‑1 and FDA Human Factors guidance, and practical implementation in a medical device environment
What you’ll be doing
- Establishing Usability Engineering at Flo Health
- Assessing current development, design control, quality, and risk management processes to identify where usability engineering activities and artefacts should be embedded
- Defining a lean end‑to‑end usability engineering process, including activities, inputs/outputs, decision points, roles, responsibilities, and interfaces to risk management and design controls
- Defining the required usability engineering documentation and templates that comply with IEC 62366‑1, ISO 14971, and FDA regulations
- Conducting/Leading Formative and Summative Evaluations
- Maintaining and updating the Usability Engineering File
- Conducting the necessary formative evaluations to identify and mitigate use‑related issues prior to summative testing
- Refining the critical task analysis, use‑related risk analysis, and hazard‑related use scenarios to ensure appropriate summative coverage
- Defining the summative evaluation scope, including device/product configuration(s), user groups, use environments, and critical tasks
- Creating the Summative Evaluation Protocol including acceptance criteria, sample size rationale, recruitment criteria, test scenarios, and success metrics
- Preparing all required summative testing materials, including moderator guide, participant materials, observation forms, and any other study documentation needed for execution
- Conducting the summative evaluation and documenting the results in a Summative Evaluation Report
- Assessing residual use‑related risks and documenting conclusions and traceability within the usability engineering file
- Upskilling the UXR Team
- Coaching on how to conduct and document formative and summative evaluations and use‑related risk activities
- Supporting the team in building reusable templates, checklists, and playbooks
Please note that this is a contractor role. As such, employee benefits do not apply.
How we work
We’re a mission‑led, product‑driven team. We move fast, stay focused and take ownership – from brief to build to impact. Debate is encouraged. Decisions are shared. We care about craft, ship with purpose, and always raise the bar. You’ll be working with people who take their work seriously, not themselves. It takes commitment, resilience, and the drive to keep going when things get tough. Because better health outcomes are worth it.
What you’ll get
- Competitive salary and annual reviews
- Opportunity to participate in Flo’s performance incentive scheme
- Paid holiday, sick leave, and female health leave
- Enhanced parental leave and pay for maternity, paternity, same‑sex and adoptive parents
- Accelerated professional growth through world‑changing work and learning support
- In‑person collaboration and work in a hybrid model, with 3 days per week spent in the office
- 5‑week fully paid sabbatical at 5‑year Floversary
- Flo Premium for friends & family, plus more health, pension and wellbeing perks
Diversity, equity and inclusion
Our strength is in our differences. At Flo, hiring is based on merit, skill and what you bring to the role – nothing else. We’re proud to be an equal opportunity employer, and we welcome applicants from all backgrounds, communities and identities.
Human Factors Engineer (Contract) employer: Femtech Insider Ltd.
Flo is an exceptional employer, offering a dynamic and mission-driven work environment where innovation in women's health is at the forefront. Employees benefit from competitive salaries, generous leave policies, and opportunities for professional growth, all while collaborating with a passionate team dedicated to making a meaningful impact. With a strong commitment to diversity and inclusion, Flo fosters a culture that values every individual's contribution, making it an ideal place for those looking to thrive in their careers.
StudySmarter Expert Advice🤫
We think this is how you could land Human Factors Engineer (Contract)
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect with potential colleagues on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its products. Understand Flo's mission and values, and think about how your skills in human factors engineering can contribute to their goals. Tailor your responses to show you're a perfect fit!
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or mentors to refine your answers and get comfortable discussing your experience. Focus on showcasing your expertise in usability assessments and regulatory compliance.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining the Flo team and contributing to the future of female health.
We think you need these skills to ace Human Factors Engineer (Contract)
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Human Factors Engineer role. Highlight your experience with IEC 62366‑1, ISO 14971, and FDA regulations, as well as any relevant projects you've worked on in the medical device space.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about women's health and how your skills align with our mission at Flo. Be sure to mention specific experiences that demonstrate your expertise in usability assessments.
Showcase Your Attention to Detail:In this role, attention to detail is key. When you submit your application, double-check for any typos or formatting issues. A polished application reflects your commitment to quality and precision, which is crucial in human factors engineering.
Apply Through Our Website:We encourage you to apply directly through our website. This ensures your application gets to the right people quickly and shows us you're serious about joining our team. Plus, it's super easy!
How to prepare for a job interview at Femtech Insider Ltd.
✨Know Your Regulations
Make sure you brush up on IEC 62366‑1, ISO 14971, and FDA regulations before the interview. Being able to discuss these standards confidently will show that you understand the compliance landscape for medical devices, which is crucial for the role.
✨Showcase Your Experience
Prepare specific examples from your past work where you've conducted human factors research or usability assessments. Highlight how your contributions led to successful outcomes, especially in software-based medical devices, as this will resonate well with the interviewers.
✨Engage with Cross-Functional Teams
Since the role involves working with various teams, be ready to discuss how you've collaborated with different departments in previous roles. Share stories that demonstrate your ability to communicate effectively and lead projects across functions.
✨Prepare for Technical Questions
Expect technical questions related to usability engineering processes and risk management. Brush up on your knowledge of creating usability documentation and be prepared to explain your approach to conducting formative and summative evaluations.