Manufacturing Associate III/IV - LSM Cell Culture (Day Shift)
Job Description
ABOUT THIS ROLE
Our Cell Culture team is looking for a self-starter who takes accountability, is willing to learn quickly in a dynamic environment, and prioritizes accurate and ethical data recordkeeping. In cell culture, we work in biosafety cabinets with mammalian cell culture and harvest in shake flasks and wave bags, stainless steel bioreactors, and centrifuges. We prioritize the possession of a few soft skills in addition to technical experience, with the opportunity for continued career development and on the job training. Key soft skills to look for are teamwork, interpersonal skills for conflict resolution, teachability, patience, and willingness to follow procedures. Preferred technical skills include prior cell culture, GMP experience, bioworks or biomanufacturing training, and degrees in microbiology, fermentation engineering, biotechnology, or biology.
Qualifications
WHAT YOU’LL DO
WHO YOU ARE
If you are a highly detailed, focused individual that enjoys problem solving and team work, you are a great fit for our manufacturing team! This position will provide you the opportunity to collaborate and innovate with a group of individuals who are all passionate about transforming patient lives.
Qualifications
REQUIRED EDUCATION / EXPERIENCE
Manufacturing Associate III:
High school diploma (or equivalent) in addition to 1.5 years of direct experience/3 years of related experience OR
BioWork Certificate or Associate’s Degree in addition to 1 year of direct experience/2.5 years of related experience OR
Bachelor’s degree with 6 months of direct experience/2 years of related experience
Manufacturing Associate IV:
High school diploma (or equivalent) in addition to 3 years of direct experience OR
BioWork Certificate or Associate’s Degree in addition to 2.5 years of direct experience OR
Bachelor’s degree with 2 years of direct experience
Additional Information
The Manufacturing Associate III performs and documents daily manufacturing operations in a cGMP environment that involves operation of process equipment, execution of validation protocols, creating/ revising cGMP documents and other assignments.