Scientist - Qa Parenteral

Liljamesofficial

Raleigh-Durham, North Carolina, United States
Base: $65,250 - $169,400; bonus/equity: compyny bo...
Cgmp compliance expertise
Quality assurance in parenteral manufacturing
Verification and validation oversight
Lilly is a global healthcare leader dedicated to discovering and delivering life-changing medicines while fostering a strong quality culture and teamwork

Job Summary

  • Lilly is a global healthcare leader dedicated to discovering and delivering life-changing medicines while fostering a strong quality culture and teamwork.
  • The Quality Assurance Representative will lead GMP compliance and quality oversight for the design, verification, and startup of a new parenteral facility in Raleigh-Durham, North Carolina.
  • Employees are offered comprehensive benefits including bonuses, 401(k), pension, medical coverage, and participation in employee resource groups supporting diversity and inclusion.

Matching Summary

Lilly is a global healthcare leader dedicated to discovering and delivering life-changing medicines while fostering a strong quality culture and teamwork.

Salary

Base: $65,250 - $169,400; Bonus/Equity: Company bonus eligibility; Benefits: Comprehensive medical, dental, vision, 401(k), pension, vacation, and well-being programs

Skills & Requirements

Must-have

  • cGMP compliance expertise
  • Quality Assurance in parenteral manufacturing
  • Verification and validation oversight
  • Project delivery and startup support
  • Regulatory approval facilitation
  • Cross-functional team collaboration
  • Quality document review and approval

Nice-to-have

  • Mentoring and training capabilities
  • Strong oral and written communication skills
  • Experience with barrier or isolator technologies
  • Knowledge of Manufacturing Execution Systems
  • Experience with global parenteral platforms
  • Technical aptitude and independent work
  • Proficiency with electronic validation software

Key Requirements

  • At least 5 years quality experience in parenteral manufacturing
  • Experience with C&Q / Verification and Validation oversight
  • Ability to work Monday through Friday 8-hour days
  • Availability for overtime and off-shift operational support
  • Willingness to travel up to 10%

Work Rights

Not specified

Tailored Resume

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