gujarat pharmaceutical quality control Jobs – 130 Open Jobs Today

Officer, Manufacturing Process Operations
Amneal Pharmaceuticals —Dahej, Gujarat
- Full-time
- B.Sc
- Bachelor's degree
7h
Senior Executive, Technical Procurement
Amneal Pharmaceuticals —Ahmedabad, Gujarat
- Full-time
- B.Sc
- Master's degree
- Bachelor's degree
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Officer, Manufacturing Process Operations

Amneal Pharmaceuticals -
Dahej, Gujarat

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Job details

Full-time
7 hours ago

Qualifications

B.Sc
Bachelor's degree
B.E.
FDA regulations

Full job description

Description:

This role is responsible for supporting injectable manufacturing operations by executing processing, equipment operation, and aseptic production activities within a regulated sterile pharmaceutical environment. The role operates manufacturing equipment such as autoclaves, washing machines, sterilizers, filtration systems, mixing vessels, and filling-related equipment to ensure timely batch execution. The incumbent handles raw materials, components, intermediates, and finished injectable products in accordance with approved procedures, aseptic practices, and quality standards. It ensures accurate batch documentation, equipment cleanliness, and compliance with cGMP and global regulatory requirements. The role contributes to safe and efficient production, supports equipment upkeep, and participates in continuous improvement initiatives to enhance productivity, quality, and schedule adherence in injectable manufacturing operations.

Essential Functions:

Operate manufacturing equipment such as autoclaves, sterilizers, filtration units, mixing vessels, washing machines, and filling support systems as per SOPs

Execute injectable manufacturing activities including solution preparation, filtration, sterilization, filling support, and component handling as per batch records

Handle raw materials, containers, closures, intermediates, and finished injectable products in compliance with aseptic and GMP standards

Maintain accurate batch manufacturing records, equipment logbooks, and production documentation in line with GDP requirements

Perform equipment cleaning, sanitization, line clearance, and basic maintenance as per approved procedures

Ensure compliance with cGMP, aseptic practices, safety guidelines, and regulatory requirements including FDA and EMA standards

Support environmental control practices and maintain cleanliness of general and classified manufacturing areas

Identify and report deviations, equipment malfunctions, or process abnormalities to supervisors promptly

Participate in in-process checks and sampling activities to support product quality and batch release requirements

Contribute to process improvement initiatives focused on productivity, quality enhancement, cost control, and schedule adherence

Additional Responsibilities:

Education:

Bachelors Degree (BA/BS) B.E. - Required

M. Pharm M. Pharm - Preferred

Experience:

2 years or more in 2 - 5 Years

Specialized Knowledge: Licenses:

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