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Director, Engineering and Facilities

Job in Saint Petersburg, Pinellas County, Florida, 33739, USA
Listing for: Catalent
Full Time position
Listed on 2026-09-13
Job specializations:
  • Engineering
    Operations Management, Manufacturing Engineer
  • Manufacturing / Production
    Operations Management, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 150000 - 210000 USD Yearly USD 150000.00 210000.00 YEAR
Job Description & How to Apply Below

Director of Engineering and Facilities

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.

St. Petersburg is our primary softgel development and manufacturing facility in North America with a capacity of 18 billion capsules per year. The featured RP Scherer softgel technology is a proven oral drug delivery solution to enhance bioavailability of poorly soluble Rx and OTC drug candidates. Non-gelatin based Opti Shell® and Vegicaps® capsules expand the range of molecules into softgel, ideal for challenging fill formulation.

Within the Catalent network, we offer a broad range of integrated formulation and analytical services to solve your most difficult development and manufacturing challenges.

Catalent Pharma Solutions in St. Petersburg, FL is hiring a Director who is responsible for overseeing engineering and maintenance operations, ensuring equipment reliability, facility integrity, and compliance with regulatory standards. This role manages capital projects, supports automation initiatives, and leads a team of engineers and technicians to drive continuous improvement and operational excellence.

Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee.

The Role
  • Oversee maintenance, safety, and operational integrity of facility, utilities, and grounds.
  • Lead capital planning and execution for facility upgrades and expansions.
  • Ensure compliance with OSHA, cGMP, and environmental regulations.
  • Maintain facility documentation, drawings, and records.
  • Direct vendor relationships for facility services and maintenance.
  • Lead maintenance strategy for all production and support equipment, ensuring uptime and reliability.
  • Oversee calibration programs and preventative maintenance schedules.
  • Support reliability engineering using management systems.
  • Supervise machine shop for equipment design, fabrication, and repair.
  • Drive continuous improvement in mixing, packaging, and encapsulation equipment.
  • Lead cross-functional engineering projects to enhance throughput, quality, and efficiency.
  • Collaborate with IT and automation teams to implement smart manufacturing technologies.
  • Evaluate and implement new technologies for product innovation and scalability.
  • Lead and develop a diverse team of engineers, technicians, and support staff.
  • Oversee buyers supporting equipment spare parts and QC operations.
  • Other duties as assigned.
The Candidate
  • Bachelor’s Degree in Mechanical, Electrical, or Industrial Engineering (Master’s preferred);
  • Ten (10)+ years of engineering management experience in a regulated manufacturing environment;
  • Capable of learning and understanding all functions of the manufacturing process;
  • Ability to work effectively under pressure with constantly changing priorities and deadlines.
  • Experience in pharmaceutical manufacturing and understanding of GMP requirements required;
  • Certified Lean Six Sigma Green Belt or Black Belt preferred;
  • Demonstrable…
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