Biologics Validation Specialist

Catalent

Kansas City, Missouri, United States
Not specified; not specified; benefits: medical, d...
100% onsite
Bachelor's degree in life sciences or engineering
Minimum 2 years laboratory validation experience
Equipment qualification (fat, sat, oq, pq) execution
The role involves generating, executing, and summarizing validation documentation for process equipment qualification within a premier drug development facility

Job Summary

  • The role involves generating, executing, and summarizing validation documentation for process equipment qualification within a premier drug development facility.
  • Candidates will coordinate with Quality, technical scientists, and vendors to manage validation protocols, change controls, and data integrity reviews.
  • Catalent offers day-one benefits including medical, dental, vision, 401(k) match, and tuition reimbursement alongside a mission-driven workplace culture.

Matching Summary

The role involves generating, executing, and summarizing validation documentation for process equipment qualification within a premier drug development facility.

Salary

Not specified; Not specified; Benefits: Medical, dental, vision, 401(k) match, tuition reimbursement, wellness perks, 152 hours PTO plus 8 holidays

Skills & Requirements

Must-have

  • Bachelor's Degree in Life Sciences or Engineering
  • Minimum 2 years laboratory validation experience
  • Equipment Qualification (FAT, SAT, OQ, PQ) execution

Nice-to-have

  • Prior cGMP experience in pharmaceutical environment
  • Strong collaboration with Quality and technical scientists
  • Experience with continuous improvement initiatives

Key Requirements

  • Bachelor's Degree in Life Sciences, Physical Science, or Engineering
  • Minimum 2 years of relatable experience in laboratory or validation
  • cGMP experience highly preferred

Work Rights

Not specified

Tailored Resume

Cover Letter