A pharmaceutical generics business company. HPRA Approved (April 2021) facility for veterinary generic medicines. Parent entity based in Ireland. Indian corporate office located at Gurgaon and R&D Center is at Greater Noida. Manufacturing facility based at SEZ Pithampur, Indore.
Walk In Interview at Ahmedabad for Pithampur Plant
Production (Injectable)
Designation : Technician
Qualification : ITI / Diploma
Experience : 2–6 Years
Key Responsibilities : Aseptic Filling / Filtration Operator / Vial Washing / Autoclave / Microsphere Manufacturing / Controlled Area.
Designation : Senior Officer
Qualification : M.Pharma / B.Pharma
Experience : 4–5 Years
Key Responsibilities : Packing area, labelling area and visual inspection.
Designation : Executive
Qualification : M. Pharma / B. Pharma
Experience : 5–8 Years
Key Responsibilities : Aseptic area (Filling / Filtration / Capping).
Quality Control Micro (Injectable)
Designation : Officer / Senior Executive
Qualification : M.Sc. (Microbiology / Biotechnology)
Experience : 2–7 Years
Key Responsibilities : Microbiological testing (e.g., Sterility, BET, MLT, GPT, etc.) and method validations, QMS investigations, compliance documentation, audit readiness, data integrity, and GMP-regulated laboratory operations.
Quality Control (Injectable)
Designation : Officer to Executive
Qualification : M.Sc. (Chemistry) / M. Pharm. / B. Pharm.
Experience : 2–8 Years
Key Responsibilities : Experience in handling and calibration of instruments like HPLC, GC, FTIR, UV, auto-titrator, KF, etc., and exposure to analysis of raw materials, water, FP, stability, and MV samples.
Quality Assurance (Injectable)
Designation : Officer to Senior Executive
Qualification : M. Pharma / B. Pharma
Experience : 2–8 Years
Key Responsibilities : IPQA: Line clearance, sampling, in-process checks, AQL, media fills, aseptic supervision, batch record review, audit trail review and batch release. Documentation: Management of documentation, including issuance, retrieval and archival of documents. Preparation and review of SOPs. Candidates should have a strong understanding of good manufacturing practices.
Technology Transfer (OSD)
Designation : Assistant / Deputy Manager
Qualification : M. Pharma / B. Pharma
Experience : 10–14 Years
Key Responsibilities : Experience in technology transfer, process optimization and validation, along with knowledge of cGMP, regulatory guidelines, and preparation, review and approval of GMP documents (SOPs, BMR/BPR, protocols, reports). Strong exposure to handling change controls, risk assessments (QRM), deviations and investigations.
Validation (OSD)
Designation : Officer to Deputy Manager
Qualification : M. Pharma / B. Pharma
Experience : 4–15 Years
Key Responsibilities : Greenfield project — Equipment Qualification and Computer System Validation, HVAC, Water System, Compressed Air, Nitrogen System Qualification and Temperature Mapping.
Quality Control (OSD) — Routine and Non-Routine Testing
Designation : Officer to Senior Executive
Qualification : M.Sc. / M. Pharma / B. Pharma
Experience : 4–7 Years
Key Responsibilities : Perform routine and non-routine quality control activities on raw materials, in-process samples and finished products using appropriate analytical techniques and instruments (e.g., HPLC, GC, UV, KF, potentiometer, IR, dissolution, Malvern Mastersizer). Ensure compliance with SOPs (Standard Operating Procedures), GLP (Good Laboratory Practices) and regulatory standards.
Quality Control (OSD) — Method Validation / Verification
Designation : Officer to Senior Executive
Qualification : M.Sc. / M. Pharma / B. Pharma
Experience : 4–7 Years
Key Responsibilities : Perform method validation / verification and transfer activities as per ICH Q2(R1)/Q2(R2) guidelines using appropriate analytical techniques and instruments (e.g., HPLC, GC, UV, KF, potentiometer, IR, dissolution, Malvern Mastersizer). Preparation and review of analytical method validation / verification and transfer protocols.
Production (OSD) — Executive
Designation : Executive (Granulation / Compression / Packing)
Qualification : M. Pharma / B. Pharma
Experience : 4–7 Years
Key Responsibilities : Audit exposure in a USFDA / EUGMP-approved company. Exposure to Material Handling / Electronic Batch Record filling and review. Good knowledge of SAP System and T-codes for PP, machine alarm handling, QMS, deviation / change control, SOPs, daily reports preparation and manpower handling.
Production (OSD) — Officer
Designation : Officer (Granulation / Compression / Coating / Liquid & Paste Manufacturing / Packing)
Qualification : M. Pharma / B. Pharma
Experience : 2–4 Years
Key Responsibilities : Audit exposure in a USFDA / EUGMP-approved company.
Production (OSD) — Technician
Designation : Technician (Granulation / Compression / Coating / Liquid & Paste Manufacturing / Liquid Filling / Bottle Primary Packing)
Qualification : D. Pharma / Diploma / ITI
Experience : 2–6 Years
Key Responsibilities : Independently handle granulation-area equipment. Expertise in top spraying and roll compaction processes. Handle liquid and paste manufacturing equipment and their processes, coating processes, and work in primary bottle packing (CVC line) / liquid filling. Good computer knowledge, machine operation, cleaning, changeover and alarm handling.
Walk in Interview
Date : 25th October 2026 (Sunday)
Timing : 9:30 AM – 3:30 PM
Venue : Pride Plaza Hotel Judges Bungalow Road, S.G. Road, Bodakdev, Ahmedabad, Gujarat – 380054, India.
Important Note
• Candidates should have exposure to a USFDA-approved company and possess good communication skills.
• Candidates who cannot attend the interview can share their resumes by email.
Email : jobs@felixvet.com
See All B.Pharm Alerts M.Pharm Alerts M.Sc Alerts Ph.D Alerts
See All Other Jobs in our Database
Subscribe to Pharmatutor Job Alerts by Email
