
Pharmaceutical Documentation Associate
2 days ago
*PLEASE READ BEFORE APPLYING* THIS IS NOT IT RELATED JOB*
We are seeking a detail-oriented Pharmaceutical Documents Associate to join our Company. The ideal candidate will meet all criteria mentioned below:
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 of pharmacopoeia applications
- 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.
Only Candidates who meet above criteria will be reviewed for interview.
Job Type: Full-time
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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