Senior Executive, Manufacturing Injectables

Amneal Pharmaceuticals; India; On-site; INR 1,200,000 - 1,600,000; Full time

Job summary

Amneal Pharmaceuticals in India is seeking a senior executive for sterile injectable manufacturing. You will operate and monitor equipment, handle raw materials, and oversee filling and compounding per batch records to ensure product quality and sterility.

The role requires a B. Pharm and 5+ years experience in aseptic manufacturing, with preference for a Master’s degree. Regulatory compliance and documentation are essential in daily tasks.

Qualifications

• B. Pharm is required; Master degree preferred.
• 5+ years of experience in sterile injectable manufacturing (5–8 years).
• Experience with cGMP, FDA/EMA guidance, and batch records.

Responsibilities

• Operate and monitor sterile injectable manufacturing equipment per approved procedures.
• Handle raw materials, intermediates, and finished products to maintain sterility.
• Oversee compounding, filling and related processes per batch records.
• Maintain equipment and perform general maintenance to ensure uptime.
• Adhere to SOPs and maintain compliant batch documentation.
• Support process improvements to enhance quality and efficiency.
• Assist in area cleaning, sanitization, and mentor junior team members.

Skills

Aseptic Manufacturing

Contamination Control

Data Integrity

GDP (Good Documentation Practices)

Documentation & Record Control

Manufacturing Process Monitoring

Material Handling & Storage

Regulatory Label Compliance

Safety & Hygiene

Education

B. Pharm

M. Sc. (MS/MA) - Preferred

Job description

India

Job Description

Description: This role is responsible for performing a variety of tasks related to the manufacturing of injectable pharmaceutical products within a regulated sterile manufacturing environment at a senior executive level. The position operates and monitors injectable manufacturing equipment and related apparatus to support parenteral product production objectives with greater independence and accountability. It involves the careful handling of raw materials as well as intermediate and finished injectable pharmaceutical products to maintain product integrity, sterility, and quality. The role contributes to the execution and oversight of injectable manufacturing operations including compounding, filling, and related processes in accordance with established formulations and batch manufacturing records. General maintenance activities on injectable manufacturing equipment and related machinery are performed as required to ensure operational continuity. All activities are executed in strict adherence to Standard Operating Procedures and current Good Manufacturing Practices to meet regulatory requirements. Accurate and timely completion of batch records and manufacturing documentation is maintained as a core accountability. The position participates in and may lead process improvement initiatives aimed at enhancing quality, reducing costs, and optimizing production scheduling within the injectable manufacturing function.

Essential Functions

• Operate and monitor injectable manufacturing equipment and related apparatus with greater independence in accordance with validated procedures and GMP standards.
• Handle raw materials, intermediate products, and finished injectable goods with care to maintain product quality, sterility, and prevent contamination.
• Perform and oversee injectable manufacturing operations including compounding, filling, and related processes per approved batch manufacturing records.
• Mix and compound ingredients for injectable formulations, suspensions, and sterile products per approved procedures.
• Conduct general maintenance on injectable manufacturing equipment and related apparatus to ensure operational readiness.
• Execute Standard Operating Procedures and maintain accurate batch documentation records in compliance with cGMP requirements.
• Ensure all tasks are completed in full compliance with applicable regulatory requirements including FDA and EMA guidelines.
• Lead or participate in functional team projects focused on developing process improvement methods to enhance quality, cost efficiency, and scheduling.
• Support area cleaning and sanitization activities and mentor junior team members to maintain a compliant and sterile injectable manufacturing environment.

Additional Responsibilities:

Qualifications

Education:

• B. Pharm B. Pharm - Required
• Master Degree (MS/MA) M. Sc. - Preferred

Experience:

• 5 years or more in 5 - 8 Years

Specialized Knowledge: Licenses:

Required Skills

• Aseptic Manufacturing & Contamination Control
• Data Integrity & Documentation Security
• Documentation & Record Control
• Good Documentation Practices (GDP)
• Manufacturing Process Monitoring
• Material Handling and Storage
• Regulatory Label Compliance Review
• Safety & Hygiene Practices
• Sterility Assurance

Job Info

• Job Identification 8830
• Job Category Manufacturing Process Operations
• Posting Date 08/25/2026, 11:25 AM
• Locations Survey number 253,255,256,257, GJ, IN