Biologics Manufacturing Operator — mAb Production

Elanco Tiergesundheit AG; Elwood (KS); On-site; USD 42,000 - 64,000; Full time

Benefits offered by this job

8‑week parental leave

Employee Resource Groups

Annual bonuses up to 6%

401(k) matching

Sign‑on bonus up to $2,500 (eligible)

Comprehensive benefits package

Job summary

Elanco is hiring an Operator to support biologics manufacturing at its Elwood, KS monoclonal antibody (mAb) facility. The role involves executing core manufacturing steps, maintaining aseptic conditions, and ensuring compliance with cGMP standards; you will document activities and collaborate with QC for sampling.

The shift is 12 hours (5:00 PM – 5:00 AM) with premium pay on weekends and overtime outside shift hours.

Qualifications

• High School Diploma or equivalent.
• Proficient in basic computer skills (Windows/Microsoft Office) and communication.
• Demonstrates teamwork, initiative, a strong work ethic, and a positive attitude.
• Able to wear appropriate gowning and PPE in production areas.

Responsibilities

• Perform and document all tasks and activities associated with biologics manufacturing.
• Execute and monitor core mAb manufacturing processes (media/buffer preparation, upstream/downstream processing, formulation, fill/finish, secondary packaging).
• Maintain cGMP compliance in a regulated environment (USDA/FDA/EMA).
• Follow SOPs and batch records for equipment operation, processing and daily tasks.
• Perform aseptic manipulations and maintain a sterile environment.
• Support equipment preparation, maintenance, and process improvements, interfacing with QC for sampling and environmental monitoring.

Skills

Teamwork

Initiative

Strong work ethic

Positive attitude

Communication

Basic computer skills

Education

Associate or Bachelor’s degree in Biomanufacturing related discipline

Tools

Windows

Microsoft Office

Job description

Elanco is hiring an Operator to support biologics manufacturing at its Elwood, KS monoclonal antibody (mAb) facility. The role involves executing core manufacturing steps, maintaining aseptic conditions, and ensuring compliance with cGMP standards; you will document activities and collaborate with QC for sampling.

The shift is 12 hours (5:00 PM – 5:00 AM) with premium pay on weekends and overtime outside shift hours.