Development Scientist Ii

Catalent

Greenville, North Carolina, United States
Gmp compliance in formulation
Clinical trial batch manufacturing
Oral solid dosage forms expertise
The Development Scientist II serves as a primary point of contact with clients regarding pharmaceutical development and clinical manufacturing activities

Job Summary

  • The Development Scientist II serves as a primary point of contact with clients regarding pharmaceutical development and clinical manufacturing activities.
  • This position requires full responsibility for GMP compliance in formulation and process development while supporting budget planning.
  • Catalent offers 152 hours of PTO plus 8 paid holidays and opportunities to advance life-saving medicines from early development to market.

Matching Summary

The Development Scientist II serves as a primary point of contact with clients regarding pharmaceutical development and clinical manufacturing activities.

Skills & Requirements

Must-have

  • GMP compliance in formulation
  • clinical trial batch manufacturing
  • oral solid dosage forms expertise
  • batch record and SOP writing
  • IQ/OQ/PQ document preparation

Nice-to-have

  • project management skills
  • customer contact experience
  • problem-solving abilities
  • independent work capability
  • dynamic fast-paced environment

Key Requirements

  • Bachelor's degree with 8+ years experience
  • Master's degree with 6+ years experience
  • Ph.D. with 4+ years experience
  • Experience in solids formulation
  • Ability to lift over 50 pounds
  • Respirator fit test clearance

Work Rights

Not specified

Tailored Resume

Cover Letter