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Regulatory Affairs Lead

We challenge you to change the world. To have more fun. To bring your full self to work. To take on a career that means more. At Promega, you will.
Promega offers welcoming careers where you can stay, contribute and grow. Here, you’ll have a role in solving more of the world’s most pressing problems, experience more camaraderie, gain more satisfaction and get more reward.
We are Promega: an international bio-tech company made up of scientists and non-scientists, with over 4000 high quality products that have been sparking inspiration and discovery in science for over 40 years. We support scientists researching life and disease, pharma companies developing new treatments, forensic labs matching DNA from crime scenes and clinical labs running and confirming health tests – and that’s just the beginning. Just this past year, we provided our technologies to support COVID-19 testing and research.
We challenge ourselves to improve the communities we operate in a little bit every day. To create an open, inviting and inclusive culture. To foster a work environment where collaborative givers, continuous learners and ambitious go-getters thrive.
Want to improve yourself, your team, your community and your world? We challenge you to find a better place to do it.

To explore what #LifeatPromega is like, search that hashtag on LinkedIn and Instagram, check out our campus through this map, and learn more about our people and sustainable practices
OUR TEAM: We are a small team of very motivated and energetic individuals. We are always seeking to drive speed to market by the least burdensome, but compliant path. We work very closely together on new product development and realization projects and ensure that we support each other in our day-to-day roles and in our department.

YOUR ROLE:  You will function as the Regulatory Affairs Lead and will be an important part of our in vitro diagnostic (IVD) new product development and realization teams from start to finish making sure all regulatory compliance is met. You will provide regulatory support to different areas of the company to ensure that Promega products comply with relevant domestic and international medical device and electrical equipment regulations.  Demonstrated regulatory affairs experience with IVD/Medical Devices is crucial for this position. You will have at least 5 years regulatory experience with a graduate degree, or 8+ years regulatory work experience with a bachelor’s degree.
To apply, view a complete job description, and learn more about our company, please visit:
Diversity is important at Promega. We are proud to be an Equal Opportunity Employer, and make employment decisions without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, disability, or any other protected class.