GMP Biomanufacturing Operator I (Mon-Fri 3:00pm - 11:30pm)

Danaher•Fargo, ND

6d•Onsite

About The Position

Aldevron, one of Danaher's operating companies, is seeking a GMP Biomanufacturing Operator I for their GMP Manufacturing department in Fargo, ND. This on-site role is responsible for executing production events in a GMP manufacturing environment. Aldevron is a CDMO that accelerates the development of groundbreaking therapies, with a mission to be the engine of innovation for genomic medicine pioneers. The company emphasizes a culture of belonging, continuous improvement, and a commitment to innovation for tangible impact, with work that saves lives. The GMP Biomanufacturing Operator I will contribute to bringing life-changing innovations to life by combining deep scientific expertise, unwavering commitment to quality, and a collaborative spirit.

Requirements

H.S. diploma or GED
Ability to read, write, understand English, and apply basic math.
Good communication skills as needed for reporting, documentation, and scheduling.
Ability to use hands, stand and/or sit for extended periods of time, bend, and lift up to 50 lbs.
Ability to lift and carry up to 50 pounds.
Ability to stand, sit, stoop, bend, walk, reach, squat, kneel, push and pull for long periods of time.
Able to climb a ladder and flex the upper and lower body.

Nice To Haves

Previous experience in a manufacturing or GMP biomanufacturing setting
Following standard operating procedures
Schedule flexibility such as weekend work or extended/altered schedules may be required at times depending on production need.

Responsibilities

Execute manufacturing processes such as transformations, cell banking, fermentation, lysis, chromatography, diafiltration, and final fill to support pDNA, mRNA, and protein product types.
Ensure a safety-first and audit-ready mindset and manage environment within manufacturing areas.
Maintain a quality-first mindset and adhere to good manufacturing practices by following appropriate gowning protocols, standard operating procedures, good documentation practices, and regulatory expectations.