Senior Officer Manufacturing Process Operations

Amneal Pharmaceuticals LLC; India; On-site; INR 420,000 - 540,000; Full time

Job summary

Amneal Pharmaceuticals LLC in India is seeking a manufacturing operator to monitor and operate equipment for API production, ensuring GMP-compliant batch records and precise documentation.

You will coordinate with engineering and QA, maintain process parameters, and participate in training and safety practices to support efficient, quality-driven production.

Qualifications

• B.E Chemical is required.
• M. Sc. preferred.
• 2+ years experience (2–5 years) in pharmaceutical manufacturing is expected.

Responsibilities

• Operate general manufacturing equipment including autoclaves, ovens, stills, and filtration apparatus.
• Handle raw materials, intermediate products, and finished pharmaceutical goods with proper care and documentation.
• Execute standard operating procedures to ensure GMP compliance at all times.
• Maintain accurate batch documentation records and production logs as required by regulatory and quality standards.
• Perform general maintenance tasks on pumps, homogenizers, filter presses, tablet compression machines, and other production equipment.
• Conduct area cleaning and sanitization activities to maintain manufacturing area standards.
• Ensure all production activities comply with applicable regulatory requirements including FDA, EMA, and internal guidelines.
• Provide guidance to junior team members on GMP compliance and manufacturing procedures.

Education

B.E Chemical - Required

M. Sc. Preferred

Job description

Job Description:

Description:

Operate and monitor manufacturing equipment and Instrument used in various stages of API production, such as reactors, Centrifuge, Dryer, Miller, sifter etc.
Maintaining accurate records and documentation of production activities, including batch Manufacturing Record (BMR), Batch Cleaning Record (BCR), Batch Packing Record (BPR) records, Equipment’s usage logs and Deviation reports if, any.
To co-ordinate with engineering department for the shift break down jobs.
To monitor the utility operation in the plant and report any abnormality to engineering department.
Collaborate with other shop floor personnel, shift in-charges, and cross-functional teams to ensure efficient and coordinated production.
Before charging of batch, cleanliness of Equipment’s to be verified by visual verification procedure.
To maintain good housekeeping in respective manufacturing area during process.
Receive, store, and handle raw materials, intermediates, and finished products. Maintain accurate reconciliation records and follow proper material handling procedures.
Follow established procedures to maintain product quality and consistency. This may involve sampling and testing intermediates, raw materials, and finished products.
To monitor the process online and record/fill the entire document legible.
Continuously monitor & maintain process parameters as per the desired product specifications and quality.
To record and maintain all the documents online as per CGMP.
Execute batch processing tasks according to standard operating procedures (SOPs), Batch Manufacturing Record (BMR), Batch Cleaning Record (BCR), Batch packing Record (BPR), and maintain the details of records in equipment usage logs Ensure that all steps are carried out accurately and in a timely manner.
To monitor and record temperature, Humidity and differential pressure in clean area (Level-I, Level-II & III).
To check and record daily weighing balance calibration and verification.
To take training online in AIMS software.
Participate in training programs to enhance knowledge and skills related to API/Intermediate’s manufacturing and safety point of view.
Adhere to and promote safety practices, including the use of personal protective equipment (PPE) and following safety procedures to prevent accidents or incidents.
Be prepared to respond to emergencies, such as spills, leaks, or safety incidents, by following established emergency procedures.
Participate in equipment cleaning and maintenance activities to ensure equipment is in good working condition.
Identify and address issues or deviations in the manufacturing process, such as equipment malfunctions or variations in product quality.
Comply with environmental regulations, including proper waste disposal and following procedures for managing hazardous materials.
Identify opportunities for process optimization, efficiency improvements, and waste reduction and communicate suggestions to higher-level personnel.
To co-ordinate with QA department for documents issuance/submission and warehouse for RM, Intermediate, API issuance/submission as per requirement.
To be maintained plant/process related consumable items Inventory as per requirement.
To review the manufacturing department executed documents like, Batch Manufacturing Record (BMR), Batch Cleaning Record (BCR), Batch packing Record (BPR) etc..
ERP/SAP related all activity carried out (Like BOM, Routing, Stock of Raw material, Intermediates, Finished product every batch)
To prepare/revised and review all documents for peptide / API product related products documents as per process given by R&D with related to respective production block/plant.
Responsible for preparation/review all required documents for manufacturing department.
Responsible for implement the E-log and SAP in Manufacturing department.

Essential Functions:

• Operate general manufacturing equipment including autoclaves, ovens, stills, and filtration apparatus in accordance with approved procedures with a higher level of proficiency.
• Handle raw materials, intermediate products, and finished pharmaceutical goods with appropriate care and documentation.
• Execute standard operating procedures to ensure compliance with current Good Manufacturing Practices at all times.
• Maintain accurate batch documentation records and production logs as required by regulatory and quality standards.
• Perform general maintenance tasks on pumps, homogenizers, filter presses, tablet compression machines, and other production equipment.
• Conduct area cleaning and sanitization activities to maintain manufacturing area standards.
• Ensure all production activities comply with applicable regulatory requirements including FDA, EMA, and internal quality guidelines.
• Participate in functional team projects focused on developing process improvement methods, solutions, and procedures to enhance quality and scheduling.
• Provide guidance and support to junior team members on GMP compliance and manufacturing procedures.

Qualifications

Education:

• B.E Chemical - Required
• M. Sc. Preferred

Experience:

• 2 years or more in 2 - 5 Years