Chemist / Officer - QA
2 Nos.
138007
Full Time
2.0 Year(s) To 7.0 Year(s)
2.00 LPA TO 5.00 LPA
Pharma / Biotech / Healthcare / Medical / R&D
Pharma/Biotech/Clinical Research
B.Sc - Chemistry; M.Sc / MS Science - Chemistry
Job Description:
- Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).
- Perform line clearance and in-process checks.
- Ensure compliance with cGMP, GDP, and SOP requirements.
- Handle deviations, change control, CAPA, OOS, and OOT investigations.
- Prepare, review, and update SOPs and QA documents.
- Conduct GMP audits and shop floor inspections.
- Monitor documentation and maintain data integrity.
- Coordinate with Production, QC, Warehouse, and Engineering teams.
- Support internal, customer, and regulatory audits.
- Participate in process validation and cleaning validation activities.
- Review batch documents and support batch release.
- Conduct GMP training and maintain training records.
Company Profile
--- --- ---. Ltd. is a prominent manufacturer of specialty ---icals and active pharmaceutical ingredients, maintaining a significant market presence all over the world.
We are recognized as the largest manufacturer of Piroctone Olamine.
Our company is led by an experienced board of management with decades of expertise in ---ical distribution and manufacturing. The core management team is dedicated to profitable growth and safety, boasting strong track records and project management skills.
Walk-in Interview Available
- Walk-in interview are scheduled for this job opening.
- Interested candidates are requested to apply and choose available interview date for interview.
- Please sign In and confirm Walk-in interview schedule.