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Associate Engineer - Engineering

Catalent Pharma Solutions

Madison, WIOnsitePosted 33 days ago
Full TimeEntry LevelManufacturing & CMCCDMO
Original posting ↗

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.

Job description

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

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

Benefits

  • Medical, Dental & Vision
  • Paid Time Off
  • Paid Holidays
  • Tuition Reimbursement
  • Career Development

Company overview

Catalent Pharma Solutions, now known as Catalent, Inc., is a leading global contract development and manufacturing organization (CDMO) headquartered in Tampa, Florida. Founded in 2007 as a spin-off from Cardinal Health's pharmaceutical technologies segment, the company has grown into a major player in the pharmaceutical services industry. Catalent provides comprehensive drug development and manufacturing solutions including drug delivery technologies, formulation development, analytical testing, clinical and commercial manufacturing, clinical packaging, and supply chain services. The company operates over 50 facilities across four continents and has supported more than half of all FDA-approved products over the past decade. With approximately 16,900 employees, Catalent produces over 70 billion doses annually for more than 8,000 products, serving major pharmaceutical companies like Pfizer, Moderna, Novo Nordisk, and Bristol-Myers Squibb. In 2024, the company was acquired by Novo Holdings A/S for $16.5 billion, further strengthening its position in the global pharmaceutical manufacturing landscape.

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