- Full Time
- Pithampur Plant

Website Felix Generics Private Limited
Table of Contents
ToggleAbout Felix Generics Private Limited
We are a leading pharmaceutical generics business with an HPRA-approved facility (April 2021) for veterinary generic medicines. Our parent entity is based in Ireland, with our Indian corporate office located in Gurgaon, an R&D center in Greater Noida, and a state-of-the-art manufacturing facility at SEZ Pithampur, Indore.
Walk-In-Interview Details
Date: 02nd February 2025 (Sunday)
Time: 10:00 AM to 03:30 PM
Venue: Hotel NOVOTEL Ahmedabad
Iscon Cross Roads, Sarkhej – Gandhinagar Hwy,
Next to Wide Angle Cinema, Ahmedabad, Gujarat – 380015
Job Openings
Quality Control (OSD)
1. Stability Section In-Charge
- Experience: 10–11 years
- Qualification: M.Sc./M. Pharma/B. Pharma
- Responsibilities:
- Team management, work allocation, and preparation/review of Stability Study Protocols, schedules, and summaries.
- Stability data management, including regulatory compliance (ANDA filings, new product applications), Field Alert Reports, and data tracking.
- Chamber management: sample pullout planning, batch charging, storage, reconciliation, and smooth operation of stability chambers.
- Expertise in regulatory audits and stability studies.
2. QC Validation Officer to Executive
- Experience: 3–8 years
- Qualification: M.Sc./M. Pharma/B. Pharma
- Responsibilities:
- Analytical method validation, verification, and transfer.
- Cleaning method validation and instrument handling (HPLC, GC, DR).
- Preparation and review of validation protocols and reports.
3. QC Sr. Officer to Executive
- Experience: 4–8 years
- Qualification: M.Sc./M. Pharma/B. Pharma
- Responsibilities:
- QC analysis of Stability, In-process, FP, RM samples.
- Instrument handling (HPLC, GC, FTIR, UV, DR, SSA) and SAP documentation.
- Preparation and review of analytical documentation.
Production (OSD)
1. Granulation/Compression/Packing Officer
- Experience: 2–4 years
- Qualification: M. Pharma/B. Pharma
- Responsibilities:
- Handling granulation, compression, and packing activities.
2. Granulation/Compression Executive to Assistant Manager
- Experience: 4–10 years
- Qualification: M. Pharma/B. Pharma
- Responsibilities:
- Material handling, electronic batch record review, SAP system expertise.
- Managing QMS, deviations, SOPs, reports, and manpower in a USFDA-approved facility.
3. Technician
- Experience: 2–5 years
- Qualification: D. Pharma/Diploma/ITI
- Responsibilities:
- Operating granulation, compression, and primary/secondary bottle packing (CVC line).
- Machine operations, cleaning, changeovers, alarm handling, and computer operations.
Job Location
Pithampur Plant
Eligibility
Candidates with experience working in USFDA-approved facilities and possessing excellent communication skills are encouraged to apply.
How to Apply
Walk-in directly to the venue or contact us for further details. Bring along your updated CV, educational certificates, and experience documents.
Don’t miss this opportunity to join a reputed pharmaceutical generics company!
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