Senior Specialist, Manufacturing Gmp Investigations

ImmunityBio, Inc.

El Segundo, CA, United States
Base: $44.55 to $49.00 ph; bonus/equity: discretio...
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Gmp manufacturing operations
Quality records
Deviation management
** ImmunityBio, Inc. is seeking a Senior Specialist for Manufacturing GMP Investigations in El Segundo, CA. The role involves managing GMP manufacturing quality records and ensuring compliance while contributing to the development of innovative cancer therapies. **

Job Summary

  • The Senior Specialist, Manufacturing GMP Investigations is responsible for writing and owning quality records for GMP Manufacturing Operation activities in support of the release of product.
  • This position provides a unique opportunity to make an immediate impact and lay the foundation for processes and procedures in a fast-paced dynamic environment.
  • ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines.

Matching Summary

Match Score: 75

** ImmunityBio, Inc. is seeking a Senior Specialist for Manufacturing GMP Investigations in El Segundo, CA. The role involves managing GMP manufacturing quality records and ensuring compliance while contributing to the development of innovative cancer therapies. **

Salary

Base: $44.55 to $49.00 per hour; Bonus/Equity: discretionary bonus and equity award; Benefits: Medical, Dental and Vision Plan Options, Health and Financial Wellness Programs, Employer Assistance Program (EAP), Company Paid and Voluntary Life/AD&D, Short-Term and Long-Term Disability, Healthcare and Dependent Care Flexible Spending Accounts, 401(k) Retirement Plan with Company Match, 529 Education Savings Program, Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks, Paid Time Off (PTO)

Skills & Requirements

Must-have

  • GMP manufacturing operations
  • quality records
  • deviation management
  • root cause analysis
  • corrective actions
  • cross-functional collaboration

Nice-to-have

  • facility and engineering knowledge
  • continuous improvement leadership
  • audit participation

Key Requirements

  • Bachelor's degree in biological science, chemistry, engineering, or related science field
  • 4+ years of experience in the pharmaceutical/biopharmaceutical industry
  • Experience with biologics cGMP manufacturing
  • Experience with cell therapy cGMP manufacturing

Work Rights

Not specified

Tailored Resume

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