AHMEDABAD · FULLTIME
Associate, Manufacturing Injectables
Amneal Pharmaceuticals
Ahmedabad · onsite · Posted 41d ago
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Undisclosed2–5 yrsfulltimeAhmedabad
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Section · 01
About this role
Description:
Essential Functions:
Additional Responsibilities: Education:
This role is responsible for performing a variety of tasks related to the processing and assembly of ingredients and pharmaceutical products within a regulated sterile manufacturing environment, with a specific focus on injectable dosage form production. The position operates manufacturing equipment used in the production of injectable pharmaceutical products including filling machines, autoclaves, and filtration apparatus. It handles raw materials and intermediate or finished sterile products in accordance with established aseptic procedures and quality standards. The role supports the preparation and processing of injectable formulations including solutions, suspensions, and emulsions to meet product specifications. It performs general maintece as required on manufacturing equipment to ensure operational continuity in a sterile environment. Standard operating procedures are executed to meet current Good Manufacturing Practices and all associated documentation requirements are maintained accurately. The position ensures full compliance with regulatory requirements including FDA and EMA guidelines applicable to sterile pharmaceutical manufacturing. It actively participates in program or functional team projects aimed at developing process improvement methods and solutions to enhance quality, cost efficiency, and scheduling outcomes.
Essential Functions:
- Operate manufacturing equipment for injectable pharmaceutical production including filling machines, autoclaves, and filtration apparatus in compliance with established SOPs
- Handle raw materials and intermediate sterile pharmaceutical products with accuracy and strict adherence to aseptic technique and safety protocols
- Support preparation and processing of injectable formulations including solutions, suspensions, and emulsions to meet product specifications
- Perform general maintece on manufacturing equipment as required to ensure operational readiness in a sterile environment
- Execute standard operating procedures to meet current Good Manufacturing Practices (cGMP) requirements for sterile manufacturing
- Maintain accurate batch documentation records in compliance with regulatory and internal requirements
- Ensure all tasks are completed in full compliance with applicable regulatory requirements including FDA and EMA guidelines
- Participate in process improvement projects to enhance quality, cost efficiency, and production scheduling
- Conduct area cleaning and sanitization activities in accordance with cleanroom and aseptic GMP standards
Additional Responsibilities: Education:
- Undergraduate HSC - Required
- Diploma DBM - Preferred
- 2 years or more in 2 - 5 Years
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
Sourced from naukri
Section · 02
Skills
Production SchedulingCGMPProcess ImprovementSterilePharmaceutical ProductionSafety protocolsPharmaceutical ManufacturingGeneral MaintenanceManufacturingmaintenancecompliancePharmaceutical
Section · Company
About Amneal Pharmaceuticals

Amneal Pharmaceuticals
Pharma
5.5k+
employees
2002
24 years old
Bridgewater, New Jersey
United States (USA)
About
Amneal Pharmaceuticals operates in the pharmaceutical sector, focusing on developing accessible and affordable medicines to address critical healthcare challenges.
Industries
PharmaBiotechnologyClinical Research
Employee ratings
1,455 reviews
4.2/ 5
Culture
4.0
Career growth
3.5
Work-life
4.2
Employees rate it well for
Work Culture190Senior Management93Work Life Balance87Work Environment69HR Policies65
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