Bio Manufacturing Operator – Day/Night

Your Role

An operator is responsible for performing and documenting all tasks and activities associated with biologics manufacturing at the Elwood, Kansas monoclonal antibody (mAb) manufacturing facility.

Upstream Processing

Prepare, sterilize, inoculate, and monitor single-use bioreactors and seed-train vessels; execute sterile media/feed preparation and aseptic sampling for cell count and viability.

Downstream Processing

Set up, operate, and sanitize automated chromatography skids, depth filtration, viral filtration/inactivation, and Tangential Flow Filtration (TFF/UFDF) systems for mAb isolation and purification.

Core Operations

• Execute and monitor core mAb manufacturing processes (media/buffer prep, upstream/downstream processing, formulation, fill/finish, secondary packaging).
• Maintain cGMP compliance in a regulated environment (USDA/FDA/EMA).
• Follow SOPs and batch records precisely for equipment operation, processing, and daily tasks with strict Good Documentation Practices (GDP).
• Perform aseptic manipulations and maintain a sterile, classified cleanroom environment.
• Support equipment preparation, maintenance, and process improvements, while interfacing with QC for sampling and environmental monitoring.

What You Need to Succeed (Minimum Qualifications)

• High School Diploma / GED.
• Proficient in basic computer skills (Windows/Microsoft Office) and communication (written & verbal).
• Demonstrates teamwork, initiative, strong work ethics, and a positive attitude.
• Must be able to wear appropriate gowning and personal protective equipment (PPE) in production and manufacturing support areas.

What will give you a competitive edge (preferred qualifications)

• Associate or Bachelor's degree in a biomanufacturing related discipline (eg. biology, chemistry, engineering, etc.).
• Experience in a regulated, commercial GMP biomanufacturing environment (relevant experience may include media and buffer preparation, cell culture, fermentation, aseptic processing, chromatography, TFF, final formulation, and fill/finish).
• Understanding of USDA, FDA, and EU GMP regulatory standards for veterinary biologics.
• Good mechanical aptitude.