Assistant, Compression

Amneal India; Gujarat; On-site; INR 400,000 - 600,000; Full time

Job summary

Amneal India in Gujarat seeks a manufacturing professional to support processing and assembly of pharmaceutical ingredients and finished products in a regulated facility.

The role involves operating autoclaves, ovens, stills, and filtration equipment, handling materials, and adhering to batch records and SOPs to ensure GMP compliance and quality.

Responsibilities

• Perform processing and assembly tasks of pharmaceutical ingredients and finished products in GMP-compliant manner
• Operate autoclaves, ovens, stills, and filtration equipment per SOPs
• Handle raw materials, intermediates, and finished goods with precision and safety
• Mix compound ingredients for liquids, suspensions, ointments, tablets, and capsules per batch records
• Perform routine maintenance on pumps, homogenizers, filter presses, and tablet presses
• Follow SOPs to meet GMP and regulatory requirements
• Ensure compliance with FDA and EMA guidelines in all tasks
• Contribute to process improvements, quality, and production scheduling
• Participate in team projects to enhance program quality and cost efficiency

Job description

Description

This role is responsible for performing a variety of tasks related to the processing and assembly of ingredients and pharmaceutical products within a regulated manufacturing environment. The incumbent operates general manufacturing equipment including autoclaves, ovens, stills, and filtration apparatus to support production activities. Raw materials, intermediate products, and finished goods are handled in accordance with established procedures and safety standards. Compound ingredients are mixed for liquid products, suspensions, ointments, tablet granulations, and capsule powders to meet formulation specifications. General maintenance activities are performed on equipment such as pumps, homogenizers, filter presses, and tablet compression machines as required. Standard operating procedures are followed to meet current Good Manufacturing Practices and all applicable regulatory requirements. Accurate and complete manufacturing records are maintained in compliance with documentation standards. The role contributes to process improvement initiatives aimed at enhancing quality, reducing costs, and optimizing production scheduling within the pharmaceutical manufacturing function.

Essential Functions

• Perform processing and assembly tasks related to pharmaceutical ingredients and finished products in compliance with GMP standards
• Operate general manufacturing equipment including autoclaves, ovens, stills, and filtration apparatus as per standard operating procedures
• Handle raw materials, intermediate products, and finished goods with accuracy and adherence to safety and quality protocols
• Mix compound ingredients for liquid products, suspensions, ointments, tablet granulations, and capsule powders per batch records
• Perform general maintenance on pumps, homogenizers, filter presses, and tablet compression machines as required
• Execute standard operating procedures to meet current Good Manufacturing Practices and maintain all required manufacturing records
• Ensure all tasks are completed in compliance with regulatory requirements including FDA and EMA guidelines
• Participate in program or functional team projects to develop process improvement methods, solutions, and procedures
• Support enhancement of program quality, cost efficiency, and production scheduling through active team participation