Senior Quality Associate

CSL Behring

Base: $94,000 - $111,000; bonus/equity: incentive ...
Manage deviations and investigations
Manage capas and change controls
Ensure gmp/gsp/gxp compliance
The Sr. Quality Associate is responsible for managing deviations, investigations, CAPAs, product technical complaints and change controls associated with development activities and manufacture of Investigational Medicinal Product

Job Summary

  • The Sr. Quality Associate is responsible for managing deviations, investigations, CAPAs, product technical complaints and change controls associated with development activities and manufacture of Investigational Medicinal Product.
  • This role reports to the Regional Product Development Quality Lead (APAC/EU) and has no direct reports.
  • The expected base salary range for this position at hiring is $94,000 - $111,000.

Matching Summary

The Sr. Quality Associate is responsible for managing deviations, investigations, CAPAs, product technical complaints and change controls associated with development activities and manufacture of Investigational Medicinal Product.

Salary

Base: $94,000 - $111,000; Bonus/Equity: Incentive compensation and equity may be included; Benefits: Not specified

Skills & Requirements

Must-have

  • Manage deviations and investigations
  • Manage CAPAs and change controls
  • Ensure GMP/GSP/GxP compliance
  • Provide quality guidance and support
  • Conduct self-inspections and follow-ups
  • Manage product technical complaints

Nice-to-have

  • Strong customer focus
  • Team oriented
  • Ability to self-motivate
  • Good interpersonal skills

Key Requirements

  • At least 3 years experience in manufacturing under GMP, Regulatory Affairs, Quality Assurance or relevant Process Development
  • Degree in a relevant biological science
  • In-depth understanding of GMP requirements
  • Previous Production, Quality or R&D experience within the Pharmaceutical industry

Work Rights

Not specified

Tailored Resume

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