Principal Scientist, Sterile Drug Product Aseptic (manufacturing, Science & Technology)

Bristol Myers Squibb UK

Cruiserath, Ireland
On-site
Sterility oversight for aseptic filling
Media fill program owner
Contamination control strategy
Bristol Myers Squibb is seeking a Principal Scientist for their Sterile Drug Product Aseptic team in Cruiserath, Ireland. The role focuses on ensuring sterility oversight and regulatory compliance for aseptically manufactured products, requiring extensive experience in sterile drug product manufacturing

Job Summary

  • The incumbent will provide sterility oversight to ensure of the aseptic filling process and Quality & Regulatory Compliance for the aseptically manufactured products, processes & systems occurs in accordance with Regulations and BMS requirements.
  • This position must comply with all Security guidelines, Environmental Health and Safety regulations and the current Good Manufacturing Practices required by the job function.
  • You’ll get a competitive salary and a great benefits package including an annual bonus, pension contribution, family medical allowance, 27 days of annual leave, life assurance and on-site gym.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Principal Scientist for their Sterile Drug Product Aseptic team in Cruiserath, Ireland. The role focuses on ensuring sterility oversight and regulatory compliance for aseptically manufactured products, requiring extensive experience in sterile drug product manufacturing.

Skills & Requirements

Must-have

  • Sterility oversight for aseptic filling
  • Media Fill program owner
  • Contamination Control Strategy
  • cGMP and regulatory compliance
  • Aseptic Process Simulations experience

Nice-to-have

  • Leading and coaching teams
  • Proactive stakeholder collaboration
  • Innovative approach to regulatory trends

Key Requirements

  • 10 years sterile drug product manufacturing experience
  • 5 years media fills/aseptic process simulations experience
  • BS in Life Sciences (Master's preferred)
  • Proficient in cGMPs and FDA/EMA regulations
  • Experience in Contamination Control Strategy and Quality Risk Management

Work Rights

Not specified

Tailored Resume

Cover Letter