Pharmaceutical Documentation Associate

2 weeks ago


Ahmedabad Gujarat, India Swiftmed International Private Limited Full time

_**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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