Process Development Lab Technician

SOLVENTUM•Eagan, MN

1d•Onsite

About The Position

Thank you for your interest in joining Solventum. Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. At Solventum, people are at the heart of every innovation we pursue. Guided by empathy, insight, and clinical intelligence, we collaborate with the best minds in healthcare to address our customers’ toughest challenges. At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers’ toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue. We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. As an PDL Technician you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world.

Requirements

Bachelor’s Degree or higher from an accredited university AND (2) two years of combined experience in manufacturing or laboratory experience in a Medical Device Manufacturing Company in a private, public, government or military environment
OR High School Diploma/GED from an accredited institution and a minimum (6) six years of manufacturing or laboratory experience in a Medical Device Manufacturing Company in a private, public, government or military environment
Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status)

Nice To Haves

Working in a Good Manufacturing Practice (GMP) environment
Medical Device Manufacturing experience
Experience with ISO 13485 compliance
Operating within a Environmental Controlled Room (ECR)

Responsibilities

Working on-site, in person, while operating equipment in a GMP environment: Extrusion, coating, rotary converting, slitting, mixing, drying/curing, and filling
Contributing to a cross functional team of Medical Device product and process developers to establish baseline operations for scale up in manufacturing sites
Participating in facility and equipment maintenance, calibration, and cleaning to assist in maintaining ISO 13485 certification
Corporate policies, procedures and security standards are complied with while performing assigned duties