Company Introduction
Avantika Medex is a pharmaceutical manufacturing organization engaged in formulation development and regulated medicine production.
Core Responsibilities
- Review batch manufacturing records against approved formats using document checklists and controlled registers.
- Verify in process check sheets at compression and packing lines using line clearance forms.
- Inspect equipment qualification files including installation qualification and operational qualification reports.
- Track change control records through approved change request forms and closure logs.
- Check deviation records against investigation notes and corrective action preventive action documents.
- Support internal and regulatory audits by presenting quality manuals and audit response files.
Skills and Technical Exposure
- Batch manufacturing records and batch packing records.
- Standard operating procedures and quality manuals.
- Change control formats and corrective action preventive action documents.
- Equipment qualification protocols and validation reports.
- Good manufacturing practice guidelines and audit checklists.
Experience Context
- Work performed inside oral solid dosage manufacturing plants with controlled production lines.
- Exposure to multiple commercial batches reviewed before market release.
- Without this role documentation gaps lead to audit observations and product release delays.
How to Apply
Email hr@avantikamedex.com
