Cette offre est lié au département Quality
About Dreem
The company
Every night around the world, hundreds of millions of people suffer from poor sleep(e)We’re in the middle of a global sleep crisis, with serious ramifications for society(e)At Dreem, a team of 50 experts (that’s us) is on a mission to solve sleep disorders(e)In the 7 years since our creation, we’ve collected 2.5M nights of sleep data and helped tens of thousands of people improve their sleep(e)We also accumulated 45 patents, completed 3 full hardware iterations and 100s of software iterations(e)We raised $60M from leading investors including Laurent Alexandre, Xavier Niel, MAIF, BPI and Johnson & Johnson(e)Along the way, we also created a research network of 350 leading laboratories and hospitals, and a scientific board of 4 of the most renowned neuroscientists and sleep experts in the world.
Today, we are developing a digital sleep clinic — Dreem Health — providing comprehensive patient care(e)With screening, diagnosis, and treatment methods for insomnia and sleep apnea, the clinic combines the best sleep experts with the best technologies(e)A unique alliance facilitating access to remote care, increasing patient satisfaction, improving clinical outcomes, and providing payers with lower costs(e)The best of sleep care, made simple(e)But the services we provide go beyond the reach of care(e)Today, our services are also used by more than 350 research labs in the context of clinical trials — including the Harvard Medical School, MIT, Stanford University, European Space Agency, and 10 of the largest pharmaceutical companies(e)That’s how we provide our patients with the best care — by pushing the boundaries of sleep science.
The team
Dreem is a fast-paced and dynamic work environment(e)The team’s fields of expertise encompass sleep research, neuroscience, behavioral therapies, mechanical engineering, machine learning, electronic design, embedded systems, testing, ergonomics, development of proprietary applications and software, product design, marketing and much more(e)Joining the team is challenging but hugely rewarding — it means pushing the boundaries of science and being able to bring real positive change to people around the world(e)
Above all, Dreem is a close knit team(e)Here is what we stand for: — We are committed to caring: everything we do starts out with people(e)We put people first(e)Be it our patients, our partners, or even our colleagues. — We are not afraid of challenging the status quo : we use our ambition and passion to push limits(e)The limits of what we know(e)The limits of what we create(e)The limits of what we set to achieve. — We never compromise on integrity: we hold ourselves accountable for our actions(e)Healthcare is a responsibility(e)Trust is a must, not a perk.
About the role
Importance of the role (a.k.a(e)this is why we need you)
Today our missions with top pharmaceutical companies and prestigious research centers are growing rapidly and we are looking for a Quality Assurance Intern to join and contribute to this scale up.
Job description
We are seeking a highly motivated Quality Assurance Intern who will work to keep Dreem Quality Management System compliant with all the applicable regulations and standards(e)You will report to the Quality Manager and work in collaboration with all departments (Clinical, Hardware, Software, Analytics, etc.) and in close collaboration with the Regulatory Affairs department.
Key Missions
Under the management of our Quality Manager and in collaboration with our Quality Assurance Pharmacist, you will participate in the following missions (non-exhaustive list) :
· Maintenance of a robust and fully compliant Quality Management System in accordance with ISO 13485 and 21 CFR 820;
· Management of CAPA, NC, complaints, CC, regulatory watch;
· Preparation of quality documentation including procedures, records, templates;
· Support in Data analysis and Management review activities;
· Support in audit activities;
· Support in software validation activities;
· Management of quality training to employees.
Depending on the ongoing activities, you could be part in Regulatory Affairs missions as well (design & development projects).
About You
- You are a life sciences, pharmacy or biomedical engineer student (Bac +4 / 5 / 6);
- Strong interest in the medical device field;
- You have effective project management skills and are able to work in English;
- Highly organized, proactive and willing to learn;
- Easy-going: positive attitude, resourceful and team-spirit.
Bonus Skills
- Experience in digital medical devices;
- Knowledge of ISO 13485 and 21 CFR 820;
- Knowledge in risk management (ISO 14971, ISO 24971).
Additional Information
- 🏡 Great office in the center of Paris (75003)
- 🍽 Swile (Tickets Restaurants)
- 🏃♂️ Gymlib
- 🚈 50% pass Navigo or bike indemnities