Felix Generics Private Limited Walk-In Interview for Production, QC, Engineering, and QA Roles in Pithampur – July 6, 2025

Felix Generics Private Limited, a fast-growing pharmaceutical company located in the Special Economic Zone, Phase II, Pithampur, Madhya Pradesh, is hosting a walk-in interview for its USFDA and EU-GMP approved manufacturing facility. Specializing in Oral Solid Dosage (OSD) and injectable formulations, Felix Generics invites skilled professionals to join our team to support high-quality pharmaceutical production.

Rated 3.7/5 on AmbitionBox for job security, we offer a dynamic environment for career growth in a regulatory-compliant setting.

Walk-In Interview Details

• Date: Sunday, July 6, 2025
• Time: 9:30 AM to 3:30 PM
• Venue: Hotel Ramada Ahmedabad, SG Highway, Corporate Road, Near Prahlad Nagar, Ahmedabad, Gujarat – 380015
• Work Location: Felix Generics Private Limited, Special Economic Zone, Phase II, Pithampur, Distt. Dhar, Madhya Pradesh – 454775
• Contact:
  • Email resumes to jobs@felixvet.com
  • Call +91 9109996408 for inquiries

Required Documents:

• Updated resume (2 copies)
• Original and photocopies of educational certificates (M.Sc/M.Pharm/B.Pharm/D.Pharm/Diploma/ITI)
• Last 3 months’ payslips and latest increment letter
• Relieving and service certificates from previous organizations
• Aadhar card and PAN card
• Passport-size photographs (2)

Note:

• Candidates must have experience in USFDA/EU-GMP approved plants.
• Candidates interviewed at Felix Generics in the last 6 months are ineligible.
• Good communication skills are mandatory.
• Immediate joiners preferred.

Open Positions

Production (OSD)

Role: Officer to Executive (Granulation/Compression/Packing)

• Qualification: M.Pharm / B.Pharm
• Experience: 2–5 years
• Responsibilities: Manage granulation, compression, and packing operations; handle material handling, electronic batch record (EBR) filling/review, SAP PP PI T-codes, QMS, deviations, change control, SOPs, daily reports, and manpower management; ensure USFDA/EU-GMP audit compliance.
• Key Skills: Expertise in OSD processes, SAP, cGMP, and regulatory audits.

Role: Technician (Granulation/Liquid & Paste Manufacturing/Liquid Filling/Bottle Primary Packing)

• Qualification: D.Pharm / Diploma / ITI
• Experience: 2–6 years
• Responsibilities: Independently operate granulation equipment, top spraying, roll compaction, liquid/paste manufacturing, primary bottle packing (CVC line), and liquid filling; perform cleaning, changeovers, and alarm handling; ensure cGMP compliance.
• Key Skills: Equipment operation, computer proficiency, cGMP, and regulatory audit exposure.

Quality Control (OSD)

Role: Validation Analyst (Senior Officer to Senior Executive)

• Qualification: M.Sc / M.Pharm / B.Pharm
• Experience: 4–9 years
• Responsibilities: Conduct analytical method validation, method transfer, and cleaning validation; operate HPLC, GC, DR, and other instruments; review analytical data; prepare validation protocols and reports.
• Key Skills: Expertise in validation, HPLC/GC operation, and regulatory compliance (USFDA/EU-GMP).

Role: Senior Officer / Executive

• Qualification: M.Sc / M.Pharm / B.Pharm
• Experience: 4–8 years
• Responsibilities: Analyze stability, in-process, finished product (FP), and raw material (RM) samples; operate HPLC, GC, FTIR, UV, DR, SSA; review analytical data for regulatory compliance.
• Key Skills: Proficiency in QC instruments, cGMP, and audit readiness.

Engineering (OSD/Injectable)

Role: Officer / Senior Officer (Plant Maintenance)

• Qualification: B.E (Electrical)
• Experience: 8–10 years
• Responsibilities: Perform preventive and breakdown maintenance of OSD/injectable process equipment and instruments; maintain schedules, training records, protocols, and quality documentation per cGMP.
• Key Skills: Expertise in electrical maintenance, cGMP, and regulatory audits.

Role: Technician / Senior Technician (Plant Maintenance)

• Qualification: Diploma (Electrical) / ITI
• Experience: 6–8 years
• Responsibilities: Conduct preventive and breakdown maintenance of OSD/injectable process equipment and instruments; maintain documentation per cGMP.
• Key Skills: Equipment maintenance, cGMP, and regulatory compliance.

Role: Technician / Senior Technician (Water System/HVAC)

• Qualification: Diploma (Electrical) / ITI
• Experience: 6–8 years
• Responsibilities: Maintain and troubleshoot HVAC and water systems for OSD/injectable plants; ensure cGMP compliance and documentation.
• Key Skills: HVAC/water system expertise, cGMP, and audit readiness.

Technology Transfer (OSD/Injectable)

Role: Senior Officer to Senior Executive

• Qualification: B.Pharm / M.Pharm
• Experience: 5–10 years
• Responsibilities: Prepare BMRs, BPRs, protocols, and reports for trial, scale-up, exhibit, and process validation batches; execute scale-up and validation batches; review departmental SOPs.
• Key Skills: Expertise in technology transfer, cGMP, and regulatory documentation.

Validation (OSD/Injectable)

Role: Officer / Senior Officer / Executive / Senior Executive

• Qualification: B.Pharm / M.Pharm
• Experience: 4–8 years
• Responsibilities: Conduct equipment, HVAC, utility, cleaning validation, computer system validation, and SAP validation for liquid/dry powder injectables and tablet/liquid oral/semisolid formulations; prepare and execute protocols.
• Key Skills: Validation expertise, cGMP, and regulatory audit exposure.

Quality Control (Injectable)

Role: Officer to Senior Executive

• Qualification: M.Sc (Chemistry) / M.Pharm / B.Pharm
• Experience: 2–8 years
• Responsibilities: Perform analysis and calibration of HPLC, GC, FTIR, UV, auto-titrator, and KF for RM, water, FP, stability, and method validation samples; ensure cGMP compliance.
• Key Skills: Proficiency in QC instruments, cGMP, and regulatory audits.

Quality Control (Microbiology – Injectable)

Role: Officer to Senior Executive

• Qualification: M.Sc (Microbiology/Biotechnology)
• Experience: 2–5 years
• Responsibilities: Conduct microbiological testing (sterility, BET, MLT, GPT) and method validations; ensure compliance with cGMP and regulatory standards.
• Key Skills: Expertise in microbiological testing, cGMP, and audit readiness.

Quality Assurance (Injectable)

Role: Officer to Senior Executive

• Qualification: M.Sc / M.Pharm
• Experience: 2–8 years (QMS Incharge: 10+ years in sterile formulations)
• Responsibilities: Manage QMS activities (deviations, CAPA, change control); oversee IPQA for sterile formulations; ensure compliance with cGMP and regulatory audits.
• Key Skills: Expertise in QMS, IPQA, cGMP, and USFDA/EU-GMP audits.

Production (Injectable)

Role: Officer to Executive

• Qualification: M.Sc / B.Pharm
• Experience: 4–6 years
• Responsibilities: Supervise visual inspection, packing, and aseptic process activities; prepare SOPs; troubleshoot NVPC failures, aseptic behavior during power failures, and EM failure remediation; ensure GDP and cGMP compliance.
• Key Skills: Expertise in parenteral packing, aseptic processes, and regulatory audits.

Role: Technician

• Qualification: ITI / Diploma
• Experience: 4–6 years
• Responsibilities: Perform aseptic dispensing, compounding, visual inspection, and packing/labeling operations; ensure cGMP compliance.
• Key Skills: Hands-on experience in injectable processes, cGMP, and GDP.

Why Join Felix Generics?

• Regulatory Excellence: Work in a USFDA and EU-GMP approved facility, ensuring high-quality OSD and injectable production.
• Career Growth: Join a growing company with opportunities for skill development, though employee feedback notes moderate appraisals (3.5/5 on AmbitionBox).
• Innovative Environment: Contribute to a facility specializing in complex formulations, supported by advanced R&D and manufacturing capabilities.
• Strategic Location: Pithampur SEZ offers a modern industrial hub with robust infrastructure.

How to Apply

• Walk-In: Attend the interview on July 6, 2025, at Hotel Ramada Ahmedabad with all required documents.
• For Those Unable to Attend: Email your updated CV to jobs@felixvet.com, mentioning the specific role and department (e.g., “QC Validation Analyst” or “Production Technician – OSD”) in the subject line. Include total experience, current CTC, expected CTC, and notice period.

Note: Candidates with USFDA/EU-GMP approved plant experience are preferred.

About Felix Generics

Felix Generics Private Limited, located in Pithampur SEZ, Madhya Pradesh, is a dynamic pharmaceutical manufacturer specializing in OSD and injectable formulations. With a focus on regulatory compliance (USFDA, EU-GMP), Felix supports global markets with high-quality generics and contract manufacturing services.

The Pithampur plant is equipped for advanced OSD and sterile production, backed by a dedicated team and robust quality systems. Learn more at www.felixvet.com.

Important Disclaimer

Felix Generics Private Limited does not charge any fees for recruitment or authorize agencies to collect payments. Report suspicious job offers to jobs@felixvet.com.

Join Felix Generics and contribute to quality healthcare in a globally compliant pharmaceutical environment!