Felix Generics Urgent Requirement for Production Injectable Role
Felix Generics Private Limited, a renowned name in pharmaceutical manufacturing, has announced an urgent hiring drive for Technician positions in Production Injectable at its USFDA-approved facility in Pithampur, Madhya Pradesh. This is an excellent opportunity for candidates with hands-on experience in injectable manufacturing and sterile area operations to grow their careers with a company committed to quality and global standards.
Job Details at a Glance
👉 Never Miss a Pharma Job Again
💼 Join our LIVE WhatsApp Group & Get Instant Updates. 📢 Click below to join:
📱 Join Click HereCompany Name: Felix Generics Pvt. Ltd.
Location: Special Economic Zone, Phase II, Pithampur, Dist. Dhar, Madhya Pradesh – 454775
Department: Production (Injectables)
Designation: Technician
Qualification: ITI / Diploma
Experience Required: 2 to 4 Years
Industry Type: Pharmaceutical (Injectable Manufacturing – USFDA Approved Unit)
Contact Email: [email protected]
Contact Numbers: 9109996408, 9754808066
Key Responsibilities
As a Production Injectable Technician at Felix Generics, your core responsibilities will include:
- Operating Sterile Area Equipment: Experience with Autoclave, Manufacturing & Holding Vessels, Vial Washing & Depyrogenation Units, Filling Machines, and Spray Dryers for microsphere production.
- Validation & Qualification: Support in IQ/OQ/PQ protocols for aseptic filling lines, autoclaves, and cleanroom equipment.
- Sterile Manufacturing Operations: Involvement in aseptic compounding, vial filling, and capping under strict GMP guidelines.
- GMP Documentation: Maintaining accurate and regulatory-compliant documentation, batch records, and equipment logs.
- Troubleshooting: Hands-on troubleshooting of process equipment and sterile area machinery to ensure uninterrupted production.
What We’re Looking For
The ideal candidate should bring:
- Prior Experience in Injectables: Proven work history in an injectable production facility, preferably one approved by USFDA or other international regulators.
- Strong Technical Skills: Familiarity with cleanroom operations and equipment handling.
- Regulatory Mindset: Understanding of current GMP (cGMP) and documentation practices.
- Team Collaboration: Ability to work in cross-functional teams and communicate effectively within a regulated production environment.
Application Process
Interested and eligible candidates can send their updated resume to:
Email: [email protected]
Phone: 9109996408 / 9754808066