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Lead Associate - Quality Assurance (Manufacturing)

Job

Dr. Reddy's Laboratories

Middleburgh, NY (In Person)

Full-Time

Posted 7 weeks ago (Updated 6 weeks ago) • Actively hiring

Expires 5/27/2026

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Job Description

Responsible for supporting management of the Quality System with a focus on continuous improvement and responsibility for ensuring compliance with c
GMP, FDA
requirements, and internal SOPs. Manage Reserve sample programs while adhering to internal procedures. Manage process for review of artwork and specification changes for labelling. Overview Industry
  • PHARMACEUTICAL / MEDICAL DEVICES / CRO
    Functional Area
  • IT Software Programming / Analysis / Quality / Testing / Training Job Role
  • Software Quality Assurance Analyst Employment type
  • Full Time Work Mode
  • In Office Qualifications Any Graduate
  • Any Specialization Any Post Graduate
  • Any Specialization Any Doctorate
  • Any Specialization Job Related Keywords Regulatory Compliance Cell Therapy Standard Operating Procedure (SOP)

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