Vacancy for BPharm as Production Executive at Zydus Group Ltd, Ankleshwar, Gujarat

Website Zydus Group Ltd

Post Name: Production

Eligibility: BPharm

Job Description of Trainee Officer – Production

• To follow the entry and exit procedure of the manufacturing blocks including chemical and pharma areas.

• To perform all process operations as per BMR.

• To clean all equipment’s as per cleaning SOP, Procedure and PCR.

• Handling necessary and applicable software required to perform production operations.

• To follow all cGMP requirements in the Plant.

• To operate all operations as per Safety requirements.

• Review/verify the status of all the equipment and other activity logbooks.

• To Verify and ensure the housekeeping and sanitization of the areas.

• Verification of raw materials, packing materials, intermediates that are issued by Warehouse.

• To Ensure Segregation of the raw materials, packing materials, intermediates in the manufacturing storage areas.

• Ensure/ Update the equipment /area status board updation after operational activities.

• Performing the visual cleanliness verification of the operational equipment before starting the operation as per procedure.

• To Operate the equipment’s but not limited to, like reactor, filtration equipment, dryers, powder processing equipment.

• To ensure Charging and discharging of materials as per the approved batch manufacturing records.

• Packing and labelling of intermediates, drug intermediates and API.

• To perform the activities related to equipment Preventive maintenance/calibration as per schedule.

• Preparation of the general /breakdown maintenance and permit system as per the requirement.

• To ensure that the solid and liquid wastes are disposed off, along with its documentation.

• Involve in performance qualification /verification of the equipment as per the requirement.

• Preparation of the material requisition slip for the issuance of raw materials, packing materials as per the requirement.

• Online filling of the batch records during the execution of the activities.

• To submit the completed batch records & logbooks back to QA for review and archival.

• To verify the equipment and areas before line/area clearance activities and witness the clearance.

• To participate in internal, customer and regulatory audits.

Developed By Connect Globes