Research Scientist

4 weeks ago


Greenville, North Carolina, United States Disability Solutions Full time

About the Role

The Pharmaceutical Development Specialist plays a key part in Catalent's Greenville facility, which specializes in end-to-end turn-key solutions for oral solid dosage forms. This state-of-the-art facility features fit-for-scale capacity with potent handling capabilities.

In this role, you will serve as the primary point of contact with clients regarding pharmaceutical development and clinical manufacturing project activities. Your responsibilities will include supporting these activities in supervision, process development, clinical trial batch manufacturing, packing, and documentation.

Key Responsibilities

  • Organize multiple tasks to ensure timely execution and prioritize accordingly.
  • Assist in designing, coordinating, and executing development and CTM activities, including formulation, data interpretation, equipment selection, generation of batch records, and problem-solving exercises.
  • Maintain ongoing communication with internal support groups, resources, vendors, staff, and occasionally clients.
  • Support departmental and corporate objectives.

Requirements

  • Associate degree in Life Sciences with at least two years of pharmaceutical experience or Bachelor's degree in a relevant field (e.g., Chemistry, Engineering, Pharmaceutical Sciences).
  • Some exposure to hazardous chemicals and other active chemical ingredients.
  • Able to handle objects using hands and arms and occasionally lift items over 50 pounds.

Why Work at Catalent?

  • Spearhead innovative projects in a dynamic environment.
  • High visibility within the organization.
  • 152 hours of PTO + 8 paid holidays.

Catalent offers rewarding opportunities for career growth.

Estimated salary: $65,000 - $80,000 per year.



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