Job Summary:
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