Pharmaceutical Project Manager

Catalent

St. Petersburg, Florida, US
Competitive pyy; not specified; day-one benefits i...
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Bachelor's degree in scientific field
5 years pharmaceutical industry experience
Fda-regulated cdmo company experience
** Catalent is seeking a Pharmaceutical Project Manager for their St. Petersburg, Florida facility. The role involves managing end-to-end client projects in a CDMO setting, ensuring customer satisfaction and compliance with regulatory standards while fostering career growth in a dynamic work environment. **

Job Summary

  • The Project Manager serves as the primary customer-facing leader responsible for managing end-to-end CDMO client projects across the full product lifecycle.
  • This role offers competitive pay, day-one benefits, and career growth in a state-of-the-art, turn-key facility located in St. Petersburg, FL.
  • Catalent produces more than 70 billion doses per year and offers 152 hours of PTO plus 8 paid holidays.

Matching Summary

Match Score: 75

** Catalent is seeking a Pharmaceutical Project Manager for their St. Petersburg, Florida facility. The role involves managing end-to-end client projects in a CDMO setting, ensuring customer satisfaction and compliance with regulatory standards while fostering career growth in a dynamic work environment. **

Salary

Competitive pay; Not specified; Day-one benefits included

Skills & Requirements

Must-have

  • Bachelor's degree in scientific field
  • 5 years pharmaceutical industry experience
  • FDA-regulated CDMO company experience
  • Working knowledge of project management principles
  • 2 years project management or team leadership experience
  • Proficiency in Microsoft Project Outlook Excel Word PowerPoint

Nice-to-have

  • PMP certification preferred
  • Experience with WorkFront software packages
  • Proactive risk management and escalation skills
  • Ability to host site visits and governance meetings

Key Requirements

  • Bachelor's degree required preferably in Chemistry Biology Pharmacy Engineering
  • At least 5 years of industry experience preferably in pharmaceutical industry
  • Most preferably with an FDA-regulated CDMO company
  • At least 2 years of project management experience or team leadership acumen
  • PMP certification is preferred
  • Training on Microsoft Project Outlook Excel Word PowerPoint WorkFront required

Work Rights

Not specified

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