Job Description
St. Petersburg in the primary softgel development and manufacturing facility in North America. The site has the capability to develop lipid formulations in a dedicated pilot plant which supports rapid transition from laboratory scale to clinical supply. Liquid in bottle, as well as Liquid fill Hard shell capabilities at the facility provide diversification and offerings that increase the speed to clinic. Within the Catalent network, we offer a broad range of integrated formulation and analytical services to solve your most difficult development and manufacturing challenges. Our analytical laboratory provides a full service offering from development of analytical methods to routine QC testing, supporting commercial and development stability studies. With capacity to generate over 18 billion softgels per year and servicing over 100 markets globally, the St. Petersburg site can handle any Over the Counter (OTC), Prescription (Rx), Medical Device, Controlled Substance, or Dietary Supplement manufacturing needs.
Position Summar y
As an Encapsulation Operator, you will contribute to the manufacturing of pharmaceutical softgels, gaining hands-on experience with multiple technologies and equipment. You’ll also collaborate with the on-site Product Development team to support new product innovations.
Work Schedule : Rotating 12-hour shift from 7 AM to 7 PM EST, operating on a two-week cycle. Week 1 includes Monday, Tuesday, Friday, Saturday, and Sunday; Week 2 includes Wednesday and Thursday.
Location: St. Petersburg, FL
100% on-site
The Role
Operates and maintains up to two encapsulation machines, covering up to four during breaks.
Manufactures softgels by following batch record instructions and cGMP standards, completing all required documentation.
Troubleshoot equipment issues to maintain consistent product quality and minimize downtime. Coordinate with crib mechanics during machine changeovers; performs teardown and setup when utilities are unavailable.
Monitors material and gel usage, ensuring components are used within expiration limits and replenishing solvents/lubricants as needed.
Maintains a clean work area, performs in-process quality checks, and ensures timely transport of empty receivers.
Assembles, handles, and stages tray stacks with manufactured softgels; ensures department supplies are stocked.
Handles non-hazardous, hazardous, and DEA-regulated materials and waste in compliance with safety protocols.
Other duties as assigned.
Minimum Qualifications
High school diploma or equivalent required.
Preferred Qualifications
Previous manufacturing experience in a GMP-regulated industry preferred.
Ability to sit, stand, walk, and lift up to 30 lbs regularly during a 12-hour shift; must be able to access the manufacturing floor.
No lifting over 44.09 lbs without assistance; must be able to push/pull up to 500 kg (approximately 1,100 lbs).
Must pass Ishihara Color Vision Screening and achieve 20/30 visual acuity (near and far), with or without corrective lenses.
Primary workstation is in a high-noise manufacturing area with exposure to industrial chemicals, detergents, flammable materials, and potent drug compounds; annual physical required for handling potent compounds.
Work schedule may include nights, weekends, and overtime as needed.
Why You Should Join Catalent
Positive and fast-paced working environment focusing on continual improvement and innovation.
Competitive Paid Time Off plus 8 paid holidays.
Medical, dental, and vision benefits effective day one of employment.
Tuition reimbursement to help you finish your degree or earn a new one.
Employee Resource Groups focusing on diversity and inclusion.
Environmentally friendly initiatives, including regular participation in beach clean-up activities.
Defined career path with annual performance reviews and potential for growth within an expanding team.
WellHub program promoting physical and mental wellness.
Perkspot offering exclusive discounts from over 900…