INDUS PHARMA PVT. LTD Hiring B.Sc / M.Sc. / B.Tech (Biotechnology)/B.Pharma / M.Pharma for IPQA-Officer/Sr. Officer

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)