Engineer - Engineering

Catalent

Madison, Wisconsin

JOB DETAILS
SKILLS
Alzheimer's, Automation Engineering, Biotech and Pharmaceutical, Blood Disorders, Business Growth, Calibration, Cancer, Capacity Utilization, Capital Expenditure (CAPEX), Change Control, Change Management, Civil Engineering, Clinical Trial, Commissioning, Communication Skills, Computer Science, Computerized Maintenance Management System (CMMS), Continuous Improvement, Current Good Manufacturing Practice (cGMP), Diabetes, Drug Development, Electricity, Engineering, Entrepreneurship, FDA Requirements, GMP (Good Manufacturing Practices), HIV/AIDS (Acquired Immune Deficiency Syndrome), HVAC, Identify Issues, Leadership, Maintain Compliance, Manufacturing, Manufacturing Equipment, Medical Products, Onboarding, Patient Care, Performance Reviews, Preventative Maintenance, Process Improvement, Product Design, Property Maintenance, Pulmonary Disease, Quality Management, Safety/Work Safety, Standard Operating Procedures (SOP), Standards Development, Technical Recruiting, Tuition Reimbursement, Writing Skills
LOCATION
Madison, Wisconsin
POSTED
5 days ago

Engineer

Position Summary:

  • Work Schedule: M-F 8am-5pm
  • 100% on-site

Working for Catalent Biologics is an opportunity to join an entrepreneurial team. Catalent Biologics is making significant investments in people and capabilities. This is a unique opening to join a small, fast-growing business, backed by a global public company. People joining our team will have the opportunity for career development as our business continues to grow and expand. Catalent-Madison employees are helping to improve future patient outcomes by working on products that are designed to treat COVID-19, cancer, various autoimmune, fibrotic and blood disorders, HIV, diabetes, heart and lung diseases as well as Alzheimer’s.

Catalent Pharma Solutions in Madison, WI is hiring an Engineer. The Equipment Engineering group has oversight of equipment lifecycle management inclusive of equipment design (URS through qualification support and release), equipment updates (design modifications via change management), and general equipment support through troubleshooting, training, and continuous improvement. This function also maintains ownership of the capital expenditure (CapEx) process.

The Role:

  • Support the utility systems facility, including HVAC systems, process utilities, and bio-containment systems
  • Support selection and installation of manufacturing equipment
  • Equipment Lifecycle management - onboarding new technologies, Preventive Maintenance schedules, CMMS tracking, spare parts, retirement and decommissioning
  • Assess current and future state of site utility system capacity and utilization for improvement and maturity projects
  • Proactively and effectively partner with the facility commissioning/validation team, including operational protocol development, to implement compliance with FDA GMP requirements
  • Draft SOPs for building operation, maintenance, and calibration
  • Provide engineering guidance and execution on facilities and equipment projects
  • Perform hands-on activities as needed to help troubleshoot facility problems and support facility staff
  • Drive continuity and development of standards in FAC/EQP Engineering to ensure smooth and effective communication flow between internal resources and customers, operational efficiency, and equipment and personnel safety
  • Create and maintain all aspects of equipment and facility design files
  • Maintain facility compliance in accordance with the site quality management system
  • Guide the specification and selection of manufacturing/utility equipment to support site facility/ process needs
  • Author deviation investigation and change control process
  • Other duties as assigned

The Candidate:

  • Minimum B.S. degree in Industrial, Electrical, Mechanical, Chemical, Computer Science, Civil Engineering, or related scientific/engineering field with 3+ years' facilities operation/automation engineering experience in a cGMP environment (preferably biopharmaceutical) OR
  • M.S. degree in Industrial, Electrical, Mechanical, Chemical, Computer Science, Civil Engineering, or related scientific/engineering field with 1+ years' facilities operation/automation engineering experience in a cGMP environment (preferably biopharmaceutical)
  • Previous experience leading cross-department facility and/or site improvement projects, a plus

Why you should join Catalent:

  • Defined career path and annual performance review and feedback process 
  • Diverse, inclusive culture 
  • Positive working environment focusing on continually improving processes to remain innovative
  • Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives 
  • 152 hours of PTO + 8 paid holidays
  • Generous 401K match 
  • Medical, dental and vision benefits effective day one of employment 
  • Tuition Reimbursement - Let us help you finish your degree or start a new degree

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

DisabilityAccommodations@catalent.com

. 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.

    

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.

About the Company

C

Catalent