Quality Control Analyst Ii, Compliance

Takeda

Social Circle, GA, USA
Base: $71,800.00 - $112,860.00; bonus/equity: shor...
Onsite
Bachelor's degree in science or engineering
2-5 years pharmaceutical industry experience
Gmp laboratory operations knowledge
Takeda is seeking a Quality Control Analyst II for its QC Compliance team in Social Circle, GA. The role involves managing Quality Record activities, leading investigations, and ensuring compliance with regulatory standards in a biopharmaceutical environment

Job Summary

  • The role involves authoring and revising GMP documents while leading CAPA investigations and root-cause analysis sessions to ensure product quality.
  • Candidates must possess strong problem-solving skills to manage complex investigations using DMAIC tools and collaborate across cross-functional teams.
  • Takeda offers a comprehensive benefits package including medical, dental, vision insurance, 401(k) matching, and up to 80 hours of sick time annually.

Matching Summary

Match Score: 85

Takeda is seeking a Quality Control Analyst II for its QC Compliance team in Social Circle, GA. The role involves managing Quality Record activities, leading investigations, and ensuring compliance with regulatory standards in a biopharmaceutical environment.

Salary

Base: $71,800.00 - $112,860.00; Bonus/Equity: Short-term and/or long-term incentives eligible; Benefits: Medical, dental, vision, 401(k), paid vacation, sick time

Skills & Requirements

Must-have

  • Bachelor's degree in science or engineering
  • 2-5 years pharmaceutical industry experience
  • GMP laboratory operations knowledge
  • Laboratory investigation and root cause analysis
  • DMAIC tools and CAPA implementation
  • MS Office proficiency (Word, Excel, PowerPoint)

Nice-to-have

  • Advanced cGMP standards knowledge
  • Experience with medical device manufacturing labs
  • Self-driven individual requiring minimal supervision
  • Excellent interpersonal communication skills
  • Continuous improvement mindset

Key Requirements

  • Bachelor's degree in science, engineering, or related field
  • 2-5 years of experience in regulated pharmaceutical industry
  • Proficiency in managing multiple tasks and responsibilities

Work Rights

Not specified

Tailored Resume

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