Encapsulation Operator

Catalent, Inc.; Saint Petersburg (FL); Presencial; USD 40.000 - 56.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Paid time off

8 paid holidays

Healthcare benefits

Tuition reimbursement

Employee Resource Groups

Environmental initiatives

Career development

WellHub program

PerkSpot discounts

Descripción de la vacante

Catalent, Inc. in St. Petersburg, FL is seeking an Encapsulation Operator to manufacture pharmaceutical softgels. You will gain hands-on experience with multiple technologies and collaborate with product development to support new product innovations.

The role involves a rotating 12-hour shift, on-site work, and strict adherence to cGMP and batch documentation. The position requires the ability to lift and move materials and work in a high-noise manufacturing area.

Formación

• Experience with GMP environments and batch records.
• Strong safety mindset and adherence to protocols.
• Ability to read and follow batch instructions precisely.

Responsabilidades

• Operate and maintain encapsulation machines.
• Follow batch records and cGMP standards; document activities.
• Troubleshoot equipment issues to minimize downtime.
• Monitor material usage and ensure components are within expiry.
• Maintain clean work area and perform in-process quality checks.
• Handle hazardous and regulated materials per safety protocols.

Conocimientos

GMP experience

Batch record reading

Safety awareness

Educación

High school diploma or equivalent

Descripción del empleo

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 Summary

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 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. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

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 [e-mail]. 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.

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Massachusetts Lie Detector Test Notice

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.