Lead Associate - Quality Assurance (Manufacturing)
Job
Dr. Reddy's Laboratories
Middleburgh, NY (In Person)
Full-Time
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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 IndustryPHARMACEUTICAL / 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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