Production Operator – Menomonie, WI* (Fixed Shift)

Scorpion Therapeutics; Wisconsin; On-site; USD 31,000 - 39,000; Full time

Job summary

Scorpion Therapeutics in Menomonie, WI seeks a Production Operator to support manufacturing, ensuring safe, efficient operations and product quality. You will operate equipment via computer controls and follow safety protocols to deliver quality products on schedule.

Role includes flexible fixed day or night shifts, potential overtime, and a climate-controlled GMP environment with opportunities for professional growth. Join a team focused on safety, policy compliance, and continuous improvement.

Qualifications

• High School Diploma or GED required.
• Ability to work 8-12 hour shifts, including overtime.
• Reliable transportation or willingness to relocate.
• Completion of a job readiness assessment.

Responsibilities

• Operate equipment via computer controls.
• Follow safety protocols and operating procedures.
• Produce quality products on schedule.
• Foster an inclusive work environment.

Skills

Basic computer skills

Education

High School Diploma or GED

Job description

Role

Production Operator supporting manufacturing in Menomonie, WI, ensuring safe, efficient operations and product quality.

Responsibilities

• Operate equipment via computer controls.
• Follow safety protocols and operating procedures.
• Produce quality products on schedule.
• Foster an inclusive work environment.

Requirements

• High School Diploma or GED.
• Ability to work 8-12 hour shifts, including overtime.
• Reliable transportation or willingness to relocate.
• Completion of a job readiness assessment.

Preferred

• Manufacturing experience.
• Basic computer skills.
• Post-secondary training.
• Self-motivated and dependable work ethic.

High-Value

• Roles involve GMP-compliant manufacturing in a climate-controlled environment.
• Potential up to 5% domestic travel.
• Pay ranges from $22.78 to $28.41/hour with shift differentials and pay increases.

Work setup

• Fixed day or night shifts; various schedules available.

The role emphasizes safety, compliance with policies, and contribution to continuous improvement in a regulated biopharma manufacturing setting.