Deputy Manager, Manufacturing Injectables

Amneal Pharmaceuticals LLC; Ahmedabad District; On-site; INR 2,800,000 - 4,400,000; Full time

Job summary

Amneal Pharmaceuticals LLC in Ahmedabad seeks a Deputy Manager for Manufacturing Injectables to lead aseptic production on the assigned shift. Strong focus on cGMP/GDP compliance, line validation, and batch documentation ensures quality output.

The role demands extensive experience in aseptic processing, CAPA, SOP implementation, and active training of the team, with collaboration across QA/QC, Engineering, and Warehouse. Location is Ahmedabad city, Gujarat, India.

Qualifications

• Education: B. Pharm required; M. Pharm preferred.
• 12+ years in sterile injectable manufacturing or closely related areas.
• Experience with cGMP and GDP in general, control, and aseptic areas.

Responsibilities

• Supervise injectable production activities on the assigned shift.
• Ensure equipment and lines are validated and calibrated before use.
• Perform line clearance before batch commencement.
• Manage Change Control, Deviations, Investigations, and CAPA processes.
• Review and implement SOPs for sterile manufacturing.
• Monitor production plan vs. actual output daily and monthly.
• Ensure aseptic techniques and contamination control practices.

Skills

Aseptic Manufacturing

Contamination Control

BMR Completion

Deviation Control

Equipment Validation

Process Monitoring

Regulatory & Audit Readiness

SOP Development

CAPA Management

Training & Coaching

Education

B. Pharm

M. Pharm

Job description

Deputy Manager, Manufacturing Injectables

Ahmedabad City, Gujarat, India

Job Description

Essential Functions

• Ensure compliance with cGMP (Current Good Manufacturing Practices) and GDP (Good Documentation Practices) across General, Control, and Aseptic areas
• Supervise overall injectable production activities during the assigned shift
• Ensure all equipment and manufacturing lines are validated and calibrated before use
• Perform and verify line clearance activities prior to batch commencement
• Handle Change Control, Deviations, Investigations, and CAPA (Corrective and Preventive Action) processes
• Review, approve, revise, and implement SOPs (Standard Operating Procedures) for sterile manufacturing
• Monitor execution of production plan vs actual output on daily and monthly basis
• Ensure strict adherence to aseptic techniques and contamination control practices
• Oversee cleaning, sanitization, and environmental monitoring activities
• Coordinate with QA, QC, Engineering, and Warehouse for seamless operations
• Review and maintain online production and batch documentation
• Responsible for preparation & review of the all-master documents of production
• Responsible to update on self-hygiene
• Responsible to attend the training as per training schedule and to ensure training of the team as per TNI
• Support audit readiness and regulatory inspections as required

Additional Responsibilities

• Activities other than defined in the job responsibility are to be done, as per the requirement of HOD, by following HODs instruction and guidance.
• Responsible to give training to all the subordinates, technicians, and operators of the department. Responsible to update on self-hygiene.
• Responsible to attend the training as per training schedule and to ensure training as per TNI.

Qualifications

Education:

• B. Pharm B. Pharm - Required

• M. Pharm M. Pharm - Preferred

Experience:

• 12 years or more in 12 - 15 Years

Specialized Knowledge: Licenses:

Required Skills

• Aseptic Manufacturing & Contamination Control
• Batch Manufacturing Record (BMR) Completion
• Deviation Control & Compliance
• Equipment and Process Validation
• Process Monitoring & Control
• Quality Risk Analysis & Control
• Regulatory & Audit Preparedness
• Regulatory Compliance
• Sterile & Aseptic Processing
• Sterility Assurance

Job Info

• Job Identification 9105
• Job Category Manufacturing Process Operations
• Posting Date 09/26/2026, 08:27 AM
• Locations Survey number 253,255,256,257, GJ, IN