Associate Engineer - Engineering

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

About Site

Associate Engineer - Engineering About Site Catalent’s Madison, Wisconsin site is a state‑of‑the‑art biologics development and manufacturing facility supporting customers from research through early‑and mid‑stage clinical production. Located at 726 Heartland Trail in Madison, the approximately 102,700‑square‑foot GMP facility specializes in mammalian cell line engineering, drug substance biomanufacturing, and biopharmaceutical development, utilizing flexible single‑use systems to enable rapid scale‑up and customization. The site is home to Catalent’s proprietary GPEx® and GPEx® Lightning technologies, which are used to generate high‑yielding mammalian cell lines for biologic therapies, and supports production scales ranging from 50 to 4,000 liters for clinical manufacturing. Following a $45 million expansion announced in 2025, the Madison site has significantly increased capacity, added new equipment, and created approximately 200 highly skilled biohealth jobs, further strengthening its role within Catalent’s global biologics network and Wisconsin’s growing life sciences ecosystem.

Position Summary

We have an opportunity for an Associate Engineer - Engineering to join our team. In this role, you will perform hands‑on activities to install, onboard, and retire equipment. You will draft and edit Standard Operating Procedures, manage asset induction and retirement requests, and coordinate calibration and installation activities. You will also support validation documentation, change control actions, and training development for new technologies, while troubleshooting equipment issues and driving process improvements.

Shift: Monday -Friday, 8:00 AM-4:30 PM or 8:30 AM-5:00 PM with a 30‑minute unpaid lunch

Location: Madison, WI 100% Onsite

The Role

• Perform hands‑on equipment lifecycle activities including installation, onboarding, calibration, maintenance, and retirement
• Prepare and maintain Standard Operating Procedures and validation documentation
• Manage asset induction and retirement requests
• Coordinate calibration and setup activities with internal and external stakeholders
• Support change control implementation and contribute to training development for new technologies
• Troubleshoot equipment failures as needed
• Edit and modify Standard Operating Procedures for equipment operations, maintenance, and calibration
• Identify improvements and efficiencies in equipment lifecycle and reliability engineering
• Create and maintain all aspects of equipment design files
• Complete change control tasks related to equipment, including writing or updating procedures, identifying spare parts, and supporting new technology introduction
• Partner with equipment technicians to ensure proper implementation of preventative and repair maintenance activities
• Support process improvement implementation
• Perform other duties as assigned

The Candidate Minimum Requirements

• Technical or Associate degree in technology, computer‑based, or related field with 1-2 years of related work experience, or Bachelor’s degree in Industrial, Electrical, Mechanical, Chemical, Computer Science, or Civil Engineering, or Equivalent combination of training, education, and experience
• Previous intern, co‑op experience, or related work experience
• Requires frequent sitting, standing, walking, reading documents, computer use, reaching, communication, and writing, with occasional bending, kneeling, crouching, carrying, and lifting up to 50 pounds

Preferred Skills & Background

• Ability to independently interpret data, analyze trends, and provide insight into potential issues and solutions
• Ability to cross‑train on techniques across multiple groups
• Ability to provide ideas, introduce new technology, and drive process improvements
• Work with other groups to develop, qualify, and transfer methods accordingly

Why You Should Join Catalent

• Defined career path and annual performance review and feedback process
• Diverse, inclusive culture
• Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
• Competitive paid time off plus 8 paid holidays
• Community engagement and green initiatives
• Medical, dental, and vision benefits effective day one of employment
• Tuition Reimbursement

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life‑saving and life‑enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to [e-mail].

This option is reserved for individuals who require accommodation due to a disability.

Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life‑cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life‑enhancing and life‑saving treatments for patients annually.