Quality Control, Specialist

Novartis

Durham, NC, US
Base: $85,400.00 - $158,600.00 annually; bonus/equ...
Onsite
Cgmp release and characterization testing
Bioanalytical method transfers and verifications
Quality control sops and documentation maintenance
The Specialist, Quality Control, assists and supports the organization with compliance and ongoing preparation, testing and monitoring conformance to established quality processes and standards for manufacturing and production

Job Summary

  • The Specialist, Quality Control, assists and supports the organization with compliance and ongoing preparation, testing and monitoring conformance to established quality processes and standards for manufacturing and production.
  • Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.
  • US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits.

Matching Summary

The Specialist, Quality Control, assists and supports the organization with compliance and ongoing preparation, testing and monitoring conformance to established quality processes and standards for manufacturing and production.

Salary

Base: $85,400.00 - $158,600.00 annually; Bonus/Equity: Performance-based cash incentive and eligibility for annual equity awards; Benefits: Comprehensive health, life, disability, 401(k) with company match, and generous time off package

Skills & Requirements

Must-have

  • cGMP release and characterization testing
  • Bioanalytical method transfers and verifications
  • Quality control SOPs and documentation maintenance
  • Nonconformance investigation and resolution
  • Analytical method qualification and trend analysis

Nice-to-have

  • Cross-functional collaboration
  • Technical writing skills
  • Problem solving and troubleshooting
  • Training departmental personnel
  • Risk assessment and audit participation

Key Requirements

  • Bachelor's degree in Biochemistry, Biology or related field
  • 5 years of experience in GMP environment
  • Strong verbal and written communication skills
  • Previous investigation experience
  • Ability to work effectively in a team environment

Work Rights

Must be able to work onsite in Durham, NC without relocation support

Tailored Resume

Cover Letter