Qualifications:
Education: Bachelor's Degree - Engineering, Biology, Chemistry or Related Field; Preferred. Experience: Previous experience with with Validations/Process - Protocol & Written Reports; Required. Familiarity with ISO13485, microbials, endotoxins, bioburdens; Preferred. Strong communication & Project Management skills; Required.
Responsibilities:
If you want to discover your greatest potential, Client provides one-of-a-kind opportunities for innovative problem solvers. We're one of only two companies in the world that are consistently recognized as both a top Global Employer and a Top 100 Global Innovator, but Client's remarkable story and culture of innovation begins with a team of nearly 200,000creative, diverse, and passionate team members collaborating across the globe. We are committed to our mission to improve lives because, every day, we witness the enormous impact of our efforts on the world around us. The Quality Control Engineering Specialist will support our Filtrations Business with the introduction/transfer of 4 new product lines, involving the construction of a new Clean-Room Facility within Client Life Sciences' Portage, Wisconsin Manufacturing Site: Executing Validation protocols & writing final reports for test methods, manufacturing processes & facility validations. Leading process capability studies and compiling data using minitab. Leading quality control testing, involving particulate analysis, water, bioburden and bacterial testing. Leading investigations involving deviations to tests & protocols. Addressing customer complaints. Intended Contractor Duration: upwards of 6 Months +.
