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Catalent, Inc. in St. Petersburg, FL is seeking an Encapsulation Operator to manufacture softgels and support the product development team with new ideas.
You will operate encapsulation equipment, follow batch records and cGMP standards, and ensure quality through in-process checks. This 12-hour rotating shift role requires the ability to lift up to 30 lbs and work in a high-noise manufacturing area. Catalent offers growth opportunities within a global life sciences network and a comprehensive
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.
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.
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.
St. Petersburg, FL 100% on-site
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.
High school diploma or equivalent required.
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.
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 merchants in various categories.
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.
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.