Ability to work designated schedule with regular and reliable attendance.
Ability to complete tasks onsite.
Ability to lift up to 50 pounds for approximately 5% of a typical working day.
Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 90% of a typical working day.
Ability to comply with any applicable personal protective equipment requirements.
Ability to use laboratory equipment and moving machinery.
Ability and means to travel between Madison locations.
Ability to travel 5% of working time away from work location, may include overnight/weekend travel.
Bachelor's degree in biology, Chemistry, or a related life science field. Equivalent experience may be considered in lieu of education.
3+ years of experience with daily operations, SOP documentation, instrument use in a heavily regulated environment such as biotech manufacturing in an FDA GMP or ISO 13485 environment for IVD or Research Use Only.
2+ years of experience with Agile or other electronic Quality Management Systems (eQMS) for creating documentation or reports, or process implementation through the change control process.
Proficient in Microsoft Office Suite.
Demonstrated ability to perform the Essential Duties of the position with or without accommodation.
Authorization to work in the United States without sponsorship.