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Senior Scientist, Analytical Research & Development

Catalent Pharma Solutions
St. Petersburg, United Statesfull_timeVerifiedPosted 1 May 2026

About the role

Senior Scientist, Analytical Research & Development

Position Summary

  • Work Schedule: Standard Hours; Monday through Friday

  • 100% on-site

Join Catalent’s flagship softgel development and manufacturing facility in North America, located in St. Petersburg, FL, with a capacity of 18 billion capsules per year. This role offers competitive pay, day-one benefits, and career growth in a state-of-the-art, turn-key facility.

The Senior Scientist, Analytical Research & Development supports the development and validation of analytical test methods, raw material evaluation, and testing of non-commercial materials to advance product development, manufacturing, process validation, and new material qualifications in accordance with regulatory and quality standards. At Catalent, this role offers exceptional exposure to a diverse portfolio of molecules formulated into the softgel platform — spanning women’s health, oncology, prescription therapeutics, and more — providing hands-on experience from development through commercial validation. As part of a CDMO environment, the position delivers broad cross-functional collaboration and the opportunity to build advanced analytical skill sets.

The Role

  • Independently develop, validate, and routinely execute instrumental test methods in support of Drug Substances and Drug Products; analyze data, document results in accordance with cGMP and internal guidelines, and communicate findings through written and oral presentations.

  • Serve as lead scientist for designated projects, including direct client communications, participation in project team meetings and teleconferences, and support of new product development in collaboration with customers and suppliers.

  • Perform analysis of finished products, in-process materials, raw materials, fill moisture, cleaning verification/validation samples, and support the Material Evaluation Process for new materials according to assigned specifications, methods, and protocols.

  • Write, review, and support analytical methods, deviations, protocols, specifications, SOPs, and laboratory investigations using appropriate Root Cause Analysis tools; lead analytical method transfer activities as required.

  • Ensure right-first-time execution of departmental methods and SOPs; audit and verify analytical results for accuracy and data integrity; maintain proper records in notebooks, reports, and logbooks in compliance with FDA, EPA, OSHA, and company regulations.

  • Safely handle potent and teratogenic compounds; prepare reagents, standards, and media; manage hazardous waste disposal; support ordering and maintenance of laboratory materials and equipment.

  • Contribute to continuous improvement by training colleagues, leading and coordinating personnel training, participating in inter-departmental teams, interfacing with management, self-scheduling assignments, and working flexible hours as required to support production and validation schedules.

  • Other duties as assigned.

Qualifications

  • Doctorate in scientific field with 3-years’ experience in lab, 2 in GMP required OR

  • Master’s in scientific field with 5+yrs experience in lab, 3 in GMP required OR

  • Bachelor’s in scientific field with 10-yrs experience in lab, 8 in GMP required

  • Minimum of 5 years’ experience with identification or separation techniques such as HPLC, UPLC, GC, MS, NMR and experience with method development and or validation.

  • VISION: Ability to read written documents and computer monitors, differentiate color, and maintain 20/30 vision with or without corrective lenses; able to work extended or off-hours as required.

  • Individual may be required to sit, stand, walk regularly and occasionally lift to 15 pounds; no lifting greater than 44.09 pounds without assistance.

Why You Should Join Catalent

  • Tuition reimbursement to support educational goals

  • WellHub program to promote physical wellness & Access to Perkspot discounts from over 900 merchants

  • 152 hours of PTO plus 8 paid holidays

  • Medical, dental, and vision benefits effective day one

  • Defined career path with annual performance reviews & strong potential for career growth within a mission-driven organization

  • Inclusive culture with active Employee Resource Groups & Community engagement and green initiatives

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

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Company

Catalent Pharma Solutions

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