Associate Engineer – Equipment Lifecycle & Validation

Catalent Pharma Solutions; United States; On-site; USD 65,000 - 85,000; Full time

Benefits offered by this job

Medical, dental, vision benefits

8 paid holidays

Tuition reimbursement

Diverse, inclusive culture

Job summary

Catalent Pharma Solutions in Madison, WI, is hiring for an Associate Engineer in Engineering. You will perform hands-on equipment lifecycle activities, draft and edit SOPs, and manage asset induction and retirement requests, with calibration coordination and training support.

The role emphasizes troubleshooting, process improvements, and collaboration with internal and external stakeholders to maintain reliability and compliance in a 102,700-square-foot GMP biologics facility.

Qualifications

• Demonstrated ability to install, onboard, and retire equipment.
• Experience drafting SOPs and maintaining validation documentation.
• Ability to coordinate calibration with internal and external parties.

Responsibilities

• Perform hands-on equipment lifecycle activities (installation, onboarding, calibration, maintenance, retirement).
• Prepare and maintain Standard Operating Procedures and validation documentation.
• Manage asset induction and retirement requests.
• Coordinate calibration and setup activities with stakeholders.
• Support change control implementation and training development for new technologies.
• Troubleshoot equipment failures and drive improvements.

Skills

Equipment lifecycle

Troubleshooting

Technical writing

Process improvement

Education

Bachelor's degree in Industrial/Mechanical/Chemical/Electrical/Computer Science or Civil Engineering

Technical or Associate degree in technology or related field

Job description

Catalent Pharma Solutions in Madison, WI, is hiring for an Associate Engineer in Engineering. You will perform hands-on equipment lifecycle activities, draft and edit SOPs, and manage asset induction and retirement requests, with calibration coordination and training support.

The role emphasizes troubleshooting, process improvements, and collaboration with internal and external stakeholders to maintain reliability and compliance in a 102,700-square-foot GMP biologics facility.