Our client, a truly global law firm is looking to hire a junior to midlevel Associate in its market-leading Medical Devices team in Denver.
You will be assisting this fantastic team on medical device post-market compliance and enforcement matters; work on pre-market matters is also likely. The ideal candidate will have experience with FDA device enforcement matters, post-market compliance issues, quality systems requirements, recalls, adverse event reporting, distribution agreements, regulation and commercialization of software as a medical device, and state licensing. Prior work experience with the FDA or in the medical device (including in vitro diagnostics), pharmaceutical or biotechnology industries would be a plus but is not required.
Candidates with a scientific, health, biotech, software, or engineering background are preferred, but please reach out even if you do not have this.
The firm has gone from strength to strength in recent years, becoming a truly global, full-service firm with the best and biggest clients on its roster. The corporate and finance teams in particular have had exceptional growth, even in this tougher market.
There is also the ability to work from an overseas office for 6 months for those who are performing well. The firm is very well known for being one step ahead on its tech, meaning that working from home is a breeze. The firm offers very flexible working policies and
Though there is a 2000 hours billable target, you can include up to 150 pro bono hours as well as 50 hours of DE&I initiatives in this. The firm is very hot on diversity initiatives and is a great place to work for everyone. The culture is great and is the reason people stay so long.
