Senior Officer Packaging

Amneal Pharmaceuticals LLC; Ahmedabad District; On-site; INR 600,000 - 900,000; Full time

Job summary

Amneal Pharmaceuticals LLC seeks a manufacturing and packaging supervisor to lead operations across CVC, blister, bottle filling, labeling, and track & trace systems in a regulated pharmaceutical environment.

You will manage batch documentation, MBMR/MBPR and qualification activities, coordinate with QA/QC, and drive continuous improvement while ensuring cGMP compliance, training, and on-time delivery.

Qualifications

• B. Pharm degree is required.
• Master's degree (MS/MA or M.Sc.) preferred.
• 2–5 years of experience in pharma manufacturing/packaging.

Responsibilities

• Supervise and execute manufacturing and packaging activities on CVC lines, blister lines, bottle filling, labeling, and track & trace systems.
• Guide and lead production officers and operators to achieve production, quality, and delivery targets.
• Prepare, review, and implement MBMR and MBPR; review URS and qualification protocols.
• Execute and review commercial, process validation, stability, and qualification batches as per protocols.
• Prepare, review, and implement qualification records and equipment qualification activities.
• Ensure accurate batch documentation, ERP work orders, shipment confirmation, and production reporting.
• Manage deviations, change controls, investigations, and CAPA related to manufacturing and packaging operations.
• Coordinate with QA, QC, Stores, Purchase, HR, Engineering, Maintenance, and external vendors for timely batch execution.
• Conduct training on SOPs, GDP, OJT modules, and update training records in AIMS.
• Maintain cGMP compliance, housekeeping, calibration schedules, track & trace CSV updates, and continuous improvement.

Skills

Supervisory leadership

cGMP compliance

Documentation & record keeping

ERP transactions

Production planning

CAPA & deviations

Training delivery

OEE data entry

Vendor coordination

Continuous improvement

Education

B. Pharm

M.S./M.Sc.

Tools

AIMS system

ERP system

Job description

Job Description

This role is responsible for executing manufacturing and packaging operations within a regulated pharmaceutical environment, ensuring products are packed accurately, efficiently, and in compliance with cGMP and global regulatory requirements. The role oversees packaging lines including CVC lines, blister lines, bottle filling, labeling, and track & trace systems while ensuring operational readiness, productivity, and data integrity. The incumbent leads production officers and operators, manages batch documentation, master records, validations, equipment qualifications, ERP transactions, and training programs. It coordinates with internal functions and external vendors to ensure timely execution of commercial, validation, and stability batches. The role drives continuous improvement, compliance, deviation management, and overall departmental performance aligned with quality, safety, and delivery goals.

Essential Functions

• Supervise and execute manufacturing and packaging activities on CVC lines, blister lines, bottle filling, labeling, and track & trace systems
• Guide, coordinate, allocate work, and lead production officers and operators to achieve production, quality, and delivery targets
• Prepare, review, and implement SOPs, formats, Master Batch Manufacturing Records (MBMR), and Master Batch Packaging Records (MBPR)
• Execute and review commercial, process validation, stability, and qualification batches as per approved protocols
• Prepare, review, and implement URS, qualification protocols, performance qualification records, and equipment qualification activities
• Ensure accurate batch documentation, final BPR review, ERP work order completion, shipment confirmation, OEE data entry, and production reporting
• Manage deviations, change controls, investigations, and CAPA related to manufacturing and packaging operations
• Coordinate with QA, QC, Stores, Purchase, HR, Engineering, Maintenance, and external vendors for timely batch execution and issue resolution
• Conduct training on SOPs, GDP, OJT modules, and update training records in systems such as AIMS
• Maintain department compliance with cGMP norms, housekeeping, calibration schedules, track & trace CSV updates, and continuous improvement initiatives

Education

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

Experience

• 2 years or more in 2 - 5 Years