Manager Validation

479

Wilson, NC, United States
Base: $90,816-$126,991; bonus/equity: 10% target b...
Cgmp facility experience
Validation master plan
Equipment malfunction troubleshooting
Oversees the development and improvement of chemical and biological manufacturing processes for drugs and biological materials, while addressing issues related to the production scale-up and ensuring compliance with formulation specifications

Job Summary

  • Oversees the development and improvement of chemical and biological manufacturing processes for drugs and biological materials, while addressing issues related to the production scale-up and ensuring compliance with formulation specifications.
  • Manages the preparation and approval of validation protocols for critical equipment and reviews final documentation packages for all major validated systems at the plant.
  • Offers a comprehensive benefits package including a 401(k) plan with company contributions, paid time off, employee assistance program, and health benefits.

Matching Summary

Oversees the development and improvement of chemical and biological manufacturing processes for drugs and biological materials, while addressing issues related to the production scale-up and ensuring compliance with formulation specifications.

Salary

Base: $90,816-$126,991; Bonus/Equity: 10% target bonus; Benefits: Comprehensive benefits package

Skills & Requirements

Must-have

  • cGMP facility experience
  • Validation Master Plan
  • Equipment malfunction troubleshooting
  • Process scale-up
  • Formulation specifications compliance

Nice-to-have

  • Leadership skills
  • Good communication skills
  • New technological equipment recommendations

Key Requirements

  • 4+ years related experience
  • 4-year degree in Science or Engineering
  • IQ, OQ, PQ protocol generation and execution
  • Knowledge of cGMPs and industry guidance

Work Rights

Not specified

Tailored Resume

Cover Letter