Responsible for preparing, reviewing, and managing quality-related documents to ensure compliance with GMP and regulatory standards.
Key Responsibilities:
Prepare and maintain SOPs, MFRs, BMRs, and quality documents.
Ensure proper documentation control and version management.
Maintain records for validation, calibration, and training activities.
Assist in documenting deviations, change controls, and audit findings.
Support audits by providing accurate documentation.
Skills and Competencies:
Attention to detail and organizational skills.
Basic knowledge of GMP and quality systems.
Strong written and verbal communication skills.
Education and Experience:
Bachelor's/Master's degree in Science (BSc/MSc) in Chemistry, Microbiology, or related fields.
2-4 years of experience in QA or documentation roles.
Job Type: Full-time
Pay: ?150,000.00 - ?300,000.00 per year
Education:
Bachelor's (Required)
Experience:
QA/QC: 2 years (Required)
Location:
Palghar, Maharashtra (Required)
Work Location: In person
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