Facilities Calibration Technician II – Onsite

Catalent Pharma Solutions; Madison (WI); On-site; USD 52,000 - 72,000; Full time

Benefits offered by this job

Medical, dental, and vision benefits (

Tuition reimbursement

Paid time off + 8 holidays

Volunteer work / community engagement

Job summary

Catalent in Madison, WI, is seeking a Technician II - Facilities, Calibration to maintain equipment reliability in a state-of-the-art biologics facility. You will calibrate, service, and document activities to support cGMP compliance and production schedules.

This onsite role offers Monday–Friday 8am–5pm, with opportunities to lead equipment onboarding, work with cross‑functional teams, and contribute to continuous improvement within a regulated biomanufacturing environment.

Qualifications

• High school diploma or equivalent with 5+ years in maintenance, or technical/associate/bachelor’s with 2+ years in manufacturing facility maintenance.
• Proven mechanical and electrical aptitude.
• Experience with facility repair, maintenance and upkeep.
• Ability to read and apply basic math; proficient in Excel/Office.

Responsibilities

• Work independently and with minimal supervision while mentoring others.
• Coordinate with departments to align activities with production schedules.
• Create out-of-tolerance reports and assist in documentation review.
• Develop instructions for routine and new tasks.
• Lead onboarding of new equipment and retirement of obsolete equipment.
• Perform complex troubleshooting and contribute to calibration and maintenance procedures.

Skills

Mechanical aptitude

Electrical aptitude

Office productivity (Excel/Word)

Problem solving

Team coordination

Education

High school diploma or equivalent

Technical/Associate degree or Bachelor’s in related field

Tools

BlueMountain (BMRAM)

cGMP environment experience

Job description

Catalent in Madison, WI, is seeking a Technician II - Facilities, Calibration to maintain equipment reliability in a state-of-the-art biologics facility. You will calibrate, service, and document activities to support cGMP compliance and production schedules.

This onsite role offers Monday–Friday 8am–5pm, with opportunities to lead equipment onboarding, work with cross‑functional teams, and contribute to continuous improvement within a regulated biomanufacturing environment.