Pharma Manufacturing Jobs at Amneal Careers: Deputy Manager, Injectables Role | Apply Now
Pharma Manufacturing Jobs at Amneal Careers present an excellent opportunity for experienced sterile manufacturing professionals seeking career growth in injectable operations. This Deputy Manager Manufacturing Injectables role in Ahmedabad focuses on greenfield project execution, routine sterile manufacturing operations, and strict compliance with global regulatory standards, making it a valuable opportunity within Amneal Careers.
Job Details
- Position: Deputy Manager, Manufacturing Injectables
- Location: Ahmedabad City, Gujarat, India
- Job ID: 7187
About the Company
Amneal Careers offers diverse Pharma Manufacturing Jobs in an inclusive and professional work environment. Amneal is an equal opportunity employer and does not discriminate based on caste, religion, gender, disability, or any other legally protected status. The company is committed to fostering diversity, inclusion, and professional excellence across all Pharma Manufacturing Jobs.
Job Description
This Deputy Manager, Manufacturing Injectables position under Pharma Manufacturing Jobs at Amneal Careers involves supporting greenfield project execution and managing routine sterile injectable operations. The role requires active participation in equipment installation, commissioning, validation, and daily production activities while maintaining full compliance with cGMP, Annex 1, and USFDA guidelines.
Key Responsibilities
Greenfield Project Execution
- Assist in installation, commissioning, and qualification (IQ/OQ/PQ) of Optima PFS filling line, isolators, and associated equipment.
- Participate in CSPE (Comprehensive Scientific Process Engineering) activities to ensure smooth and timely production startup.
- Support validation and engineering teams during FAT/SAT and process simulations.
Routine Operations
- Operate Optima PFS filling systems for ready-to-use (RTU) syringes in nested tubs, ensuring sterile and accurate filling.
- Perform de-bagging, Tyvek® film removal, filling, closing, and secondary processing steps such as labeling and safety device assembly.
- Monitor in-process controls (IPC), including fill volume, stopper height, and container integrity, using systems like SIRM (Syringe Inspection and Reject Machine).
- Ensure isolator integrity and aseptic conditions throughout the production cycle.
Compliance & Documentation
- Maintain accurate batch records, logbooks, and equipment usage documentation.
- Adhere strictly to cGMP, Annex 1, and USFDA guidelines for sterile manufacturing.
- Support internal audits and regulatory inspections with proper documentation and operational readiness.
Qualifications
Educational Qualification & Experience
- B.Pharm with 3–8 years of experience in sterile injectable operations.
- Prior experience with PFS filling lines in isolator-based setups.
- Familiarity with aseptic techniques, cleanroom protocols, and IPC systems.
Preferred Skills
- Experience in greenfield project execution or facility startup.
- Knowledge of IPAS (Intelligent Production Assistance Services) for digital monitoring and troubleshooting.
- Ability to work in a high-speed, high-precision environment with minimal supervision.
- Strong documentation and communication skills.
