Manufacturing Quality Specialist (2nd Shift)

Added
12 days ago
Type
Full time
Salary
Salary not provided

Related skills

iso 9001 root cause analysis qms iso 13485 capa

๐Ÿ“‹ Description

  • Quality and compliance across oligonucleotide manufacturing
  • Implement process control systems and audits
  • Support process improvements in production
  • Work with cross-functional teams on standards
  • Address nonconformities and regulatory needs
  • Collaborate on CAPA and QMS tasks

๐ŸŽฏ Requirements

  • Bachelorโ€™s in engineering, Life Sciences, Chemistry or related field
  • 3+ years QA/manufacturing QC in regulated industry
  • Knowledge of 21 CFR 820, ISO 9001, ISO 13485
  • Experience with audits, nonconformance, root cause analysis
  • Strong problem-solving and cross-functional collaboration
  • Detail-oriented in fast-paced environment

๐ŸŽ Benefits

  • Mon-Fri, 3 PM to 12 AM schedule
  • Medical, dental, vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
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