Amneal Pharmaceuticals, Inc. (NYSE: AMRX), a global pharmaceutical company with over 7,500 colleagues, develops, manufactures, and distributes a diverse portfolio of 270+ high-quality medicines. We are hosting a walk-in drive for Injectable Manufacturing positions at our USFDA-compliant facilities in Ahmedabad (SEZ Matoda, Pipan, Palli) on April 26 & 27, 2025. Join our team to make healthy possible through innovation and excellence in sterile manufacturing!
Event Details
- Dates: Saturday & Sunday, April 26 & 27, 2025
- Time: 9:00 AM to 5:00 PM
- Interview Location: Legend Sarovar Portico, Malpur, Tehsil Baddi, District Solan, Industrial Town of Baddi, Himachal Pradesh – 173205
- Work Location: Ahmedabad (SEZ Matoda, Pipan, Palli), Gujarat
Open Positions
We are seeking skilled professionals with 1-7 years of experience in injectable regulated manufacturing plants for roles in Manufacturing and Packing. Candidates with hands-on expertise in sterile/parenteral processes and equipment are highly preferred.
Manufacturing Operators Responsibilities and Requirements
- Qualification: ITI/Diploma
- Experience: 1-7 Years
Responsibilities:
- Operate equipment for aseptic processing, filling, sealing, filtration, and terminal sterilization in injectable manufacturing lines (Ophthalmic, Vial, PFS, LYO, Cartridges, Bag).
- Perform batch manufacturing and autoclave operations in compliance with cGMP standards.
- Execute cleaning, setup, and changeover of equipment like Groninger/Optima filling machines, Bosch filling machines, or Steriline systems.
- Maintain accurate batch records and adhere to Quality Management Systems (QMS) protocols.
- Support packing and labeling operations for sterile products.
Requirements:
- Hands-on experience with filling machines (Groninger/Optima, Bosch, Dyno Truking), steam sterilizers (Fedegari), or packing/labeling machines (Plumat, Pharmalab).
- Knowledge of cGMP, aseptic techniques, and batch documentation.
- Ability to work in shift operations and maintain high standards of safety and hygiene.
- Experience in sterile/parenteral manufacturing is mandatory.
Manufacturing Officers Responsibilities and Requirements
- Qualification: B.Sc/B.Pharm/M.Sc
- Experience: 1-7 Years
Responsibilities:
- Supervise aseptic manufacturing processes, including filling, sealing, and terminal sterilization for injectable lines (Ophthalmic, Vial, PFS, LYO, Cartridges, Bag).
- Monitor batch manufacturing and autoclave operations, ensuring compliance with cGMP and QMS standards.
- Troubleshoot equipment issues on filling machines (Groninger/Optima, Bosch) or sterilizers (Fedegari, Steriline).
- Review batch records and support packing/labeling activities for compliance and accuracy.
- Train operators on SOPs and maintain a sterile manufacturing environment.
Requirements:
- Practical experience with sterile manufacturing equipment (Groninger/Optima, Bosch, Dyno Truking, Steriline, Plumat, Pharmalab).
- Strong understanding of cGMP, QMS, and regulatory requirements for injectables.
- Effective communication and supervisory skills for team coordination.
- Familiarity with aseptic processes and terminal sterilization techniques.
Manufacturing Executives Responsibilities and Requirements
- Qualification: B.Pharm/M.Pharm/B.E
- Experience: 1-7 Years
Responsibilities:
- Lead manufacturing operations for injectable lines (Ophthalmic, Vial, PFS, LYO, Cartridges, Bag), ensuring cGMP compliance.
- Oversee aseptic processing, filling, sealing, filtration, and terminal sterilization using advanced equipment like Groninger/Optima, Bosch, or Steriline.
- Manage batch manufacturing, autoclave operations, and packing/labeling processes, ensuring adherence to QMS protocols.
- Coordinate equipment qualification, validation, and troubleshooting for filling machines and sterilizers.
- Prepare and review documentation for regulatory audits (e.g., USFDA) and support technology transfer activities.
Requirements:
- Extensive experience with injectable manufacturing equipment (Groninger/Optima, Bosch, Dyno Truking, Steriline, Fedegari, Plumat, Pharmalab).
- In-depth knowledge of cGMP, QMS, and USFDA regulatory standards.
- Proven leadership skills to manage teams and drive operational excellence.
- Expertise in aseptic manufacturing, terminal sterilization, and batch record management.
What to Bring to the Interview
- Updated resume
- Original academic certificates with one photocopy set
- Previous organization relieving letters
- Current organization offer and increment letters
- Last 3 months’ payslips
- Aadhar and PAN card photocopies
- Passport-sized photographs
How to Apply
Interested candidates should:
- Attend the walk-in interview with the required documents (resume, academic certificates, relieving letters, offer/increment letters, payslips, Aadhar/PAN card, photographs).
- Send their CV to indiacareers@amneal.com with the subject line “Application for INJ Manufacturing” if unable to attend.
- Apply online by scanning the QR code at the venue or visiting https://careers.amnealindia.com/.
- Visit https://www.amneal.com/ for more information about our company and career opportunities.
Additional Information
- Note: Candidates must have hands-on experience in sterile/parenteral manufacturing and familiarity with USFDA-regulated environments. Amneal Pharmaceuticals is committed to a fraud-free recruitment process. We do not use free email services (e.g., Gmail, Yahoo) for job offers or charge fees/security deposits. Verify offers at indiacareers@amneal.com and report suspicious activity.
- Benefits: Competitive salary, comprehensive training, and career growth opportunities in a global pharmaceutical company with USFDA-compliant facilities.
Contact Us
For inquiries, reach out via email at indiacareers@amneal.com or visit https://www.amneal.com/.
Join Amneal Pharmaceuticals and contribute to making healthy possible through innovative injectable manufacturing!