INDUS PHARMA PVT. LTD Walk-in Interview .INDUS PHARMA PVT. LTD Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue.
Vacancy details:
- Department: IPQA
- Designation: Officer/Sr. Officer
- Experience: 03 Yrs – 08 Yrs
- Qualifications: B.Sc / M.Sc. / B.Tech (Biotechnology)/B.Pharma / M.Pharma
Important Details :
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face To Face Interview
- Interview Rounds of Interview: HR
Job Description: Greetings from INDUS PHARMA PVT. LTD .!!
INDUS PHARMA PVT. LTD.Vacancy for Our Manufacturing Plant located at Riico Industrial Area, Ghiloth, Neemrana, Rajasthan
Job Responsibilities:-
1. Line Clearance: Ensure proper line clearance before the start of manufacturing and packaging operations.
Verify cleanliness and absence of previous product traces in sterile areas.
2. In-Process Checks:Monitor critical process steps in real-time (e.g., formulation, filtration, filling, sealing).
Perform in-process checks like weight/volume, pH, temperature, and appearance.
3. Environmental Monitoring Oversight:Ensure that environmental monitoring (EM) in aseptic areas is performed as per schedule.
Verify adherence to cleanroom gowning and behavior protocols.
4. Batch Manufacturing Record (BMR) Review:Ensure real-time documentation and accuracy of entries in BMR/BPR (Batch Packaging Record).
Identify and report deviations or discrepancies immediately.
5. Monitoring Aseptic Practices:Observe operators during aseptic processing and intervene if any non-compliance is observed.
Ensure adherence to validated aseptic techniques and cleanroom discipline.
6. Sampling Activities:Supervise or perform in-process sampling (e.g., bioburden, particulate matter, endotoxins).
Ensure that samples are collected and handled as per SOPs and protocols.
7. Equipment and Area Verification:Ensure that equipment and manufacturing areas are cleaned, sanitized, and in validated state.
Verify calibration and qualification status of instruments used during production.
8. Documentation and Reporting:Record in-process observations and escalate deviations or out-of-specification (OOS) results.
Prepare and review IPQA-related documentation, logs, and checklists.
9. Control of Materials:
Ensure correct materials are used, properly labeled, and handled per GMP requirements.
Verify expiry dates, status labels (approved/rejected), and material traceability.
Please share your CV on : hr@induspharmaindia.com
+91-9990334200 (Only WA)
ABAC
/B.Pharma / M.Pharma for IPQA-Officer/Sr. Officer){kind=link}