Associate Iii, Quality Assurance (on The Floor, Swing Shift)

Bilbao HR

Research Triangle Park, NC, United States
Base: $69,000.00-$90,000.00; bonus/equity: cash bo...
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Cgmp compliance
Gxp regulations
Quality management systems
** Biogen is seeking a Quality Assurance Associate III for an on-site role in Research Triangle Park, NC, working a swing shift from noon to midnight. The position requires a strong understanding of quality assurance in a GMP environment, along with collaboration and communication skills to ensure compliance and support manufacturing operations. **

Job Summary

  • Ensure disposition documentation and other documents supporting batch and cell bank disposition are compliant and determine acceptability for use in cGMP production activities and/or release of product for further processing and/or distribution.
  • Supports resolution of both technical and compliance issues/gaps of low complexity and CAPAs can be assigned and closed based on their understanding of the CAPA intent and review/approval of the associated document.
  • Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being.

Matching Summary

Match Score: 75

** Biogen is seeking a Quality Assurance Associate III for an on-site role in Research Triangle Park, NC, working a swing shift from noon to midnight. The position requires a strong understanding of quality assurance in a GMP environment, along with collaboration and communication skills to ensure compliance and support manufacturing operations. **

Salary

Base: $69,000.00-$90,000.00; Bonus/Equity: cash bonus and equity incentive opportunities; Benefits: Medical, Dental, Vision, & Life insurances, Fitness & Wellness programs, Disability insurance, paid vacation, holidays, paid time off, sick time, Paid Maternity and Parental Leave, 401(k) program, Employee stock purchase plan, Tuition reimbursement

Skills & Requirements

Must-have

  • cGMP compliance
  • GxP regulations
  • Quality Management Systems
  • batch disposition documentation review
  • manufacturing floor observations

Nice-to-have

  • downstream process manufacturing familiarity
  • column packing experience
  • independent and team framework
  • collaboration with colleagues

Key Requirements

  • Bachelor’s Degree in life sciences
  • Minimum of 2 years of experience
  • GMP pharma or biotech manufacturing environment

Work Rights

Not specified

Tailored Resume

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