Details
Posted: 28-Apr-22
Location: Madison , Wisconsin
Type: Full Time
Categories:
Pharmaceutical
Quality
Quality Engineering
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.
ABOUT US
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.
CULTURE & COMMUNITY
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.
YOUR CHALLENGE
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 passionate team of Scientific/Engineering professionals responsible for the Promega Quality Validation program. This multidiscipline team manages Equipment Qualification, Method Validation and more.
YOUR ROLE:
You are our go-to Quality representative for equipment qualification of equipment used to manufacture medical devices. You have a passion and demonstrated experience establishing procedures for validating equipment and processes, evaluating risk and serve as our expert on all things validation related.
YOUR EXPERIENCE:
You have an extensive background in IVD/Medical device validation, including molecular method and process validation. Ideally your experience would include filling, packaging and other manufacturing equipment. You are a complex thinker and have the ability to communicate across all levels of the organization. Strong cross functional teamwork experience is desired.
To apply, view a complete job description, and learn more about our company, please visit:
https://uscareers.promega.com/jobs/3116?lang=en-us
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.