Sr. Associate Ii, Quality Assurance

Biogen

Research Triangle Park, US
Base: $93,000.00-$121,000.00; bonus/equity: cash b...
Quality management systems
Cgmp compliance
Data integrity governance
The Sr. Associate II is responsible for the oversight of key strategic, tactical, and operational aspects within Quality Assurance at the Biogen Research Triangle Park (RTP) facility

Job Summary

  • The Sr. Associate II is responsible for the oversight of key strategic, tactical, and operational aspects within Quality Assurance at the Biogen Research Triangle Park (RTP) facility.
  • This individual has advanced understanding of the Quality Management Systems and applies that knowledge by coaching peers and ensuring continuous improvement cross-functionally.
  • 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

The Sr. Associate II is responsible for the oversight of key strategic, tactical, and operational aspects within Quality Assurance at the Biogen Research Triangle Park (RTP) facility.

Salary

Base: $93,000.00-$121,000.00; Bonus/Equity: Cash bonus and equity incentive opportunities; Benefits: Medical, Dental, Vision, & Life insurances, Fitness & Wellness programs, Disability insurance, Paid time off, Company paid holidays, Paid Maternity and Parental Leave, 401(k) program, Employee stock purchase plan, Tuition reimbursement

Skills & Requirements

Must-have

  • Quality Management Systems
  • cGMP compliance
  • data integrity governance
  • regulatory compliance guidance
  • batch record review

Nice-to-have

  • continuous improvement
  • root cause analysis
  • cross-functional collaboration
  • pioneering spirit
  • culture of inclusion and belonging

Key Requirements

  • Bachelor’s Degree or Associate's Degree plus 7+ years of experience
  • Minimum 5 years of relevant quality assurance experience
  • Experience reviewing and approving batch records, master records, SOPs and technical documents
  • Advanced understanding of global quality systems
  • Experience working on the floor within manufacturing environment

Work Rights

Not specified

Tailored Resume

Cover Letter