Pharmaceutical Documentation Associate

*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)