Pharmaceutical Documentation Associate
2 weeks ago
_**PLEASE READ BEFORE APPLYING* THIS IS NOT IT RELATED JOB**_
**Must have Sound Knowledge OR Experience**:
- Experience or Sound knowledge in Active Pharmaceutical Ingredients, Finish Product, Packaging Material Standards and Quality Management and Quality Control.
- Knowledge or experience about Quality control tests applicable to all different formulations and API like Assay, Dissolution, Disintegration, Uniformity of Weight/dosage, Impurity testing, Water content, etc and applicable methods like HPLC, GC, TLC, IR/UV, Disso, etc
- Knowledge about all documentation applicable in QA/QC
- Knowledge or experience preparing BMR, SPEC, STP, AMV/PDR Protocol, Report and various other documents.
**Duties**:
- Prepare documents related to QA/QC
- Prepare STP, AMV Reports, etc
- Prepare other documents for regulatory team as requested
- Maintain accurate and up-to-date documentation in accordance with Good Documentation Practices (GDP).
- Work closely with regulatory, production and quality teams to improve process efficiencies and compliance.
Pay: From ₹15,000.00 per month
**Benefits**:
- Flexible schedule
- Paid sick time
Ability to commute/relocate:
- Ahmedabad, Gujarat: Reliably commute or planning to relocate before starting work (required)
**Education**:
- Diploma (required)
**Experience**:
- Pharmaceutical: 1 year (preferred)
**Location**:
- Ahmedabad, Gujarat (required)
Shift availability:
- Day Shift (preferred)
- Night Shift (preferred)
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