Freshers & experience Walk-in 4th & 5th March 2025 for Executive / Sr Executive AT Sekhmet Pharmaventures Pvt. Ltd

Role & responsibilities

Maintain discipline and respect towards superiors in the work area.

Adhere to the companys Quality and EHS policies.

Ensure compliance with safety and environmental requirements in the manufacturing area.

Maintain cGMP norms in the manufacturing area.

Follow Standard Operating Procedures (SOPs) for operations.

Monitor and implement procedures per pre-approved instructions in the manufacturing area.

Ensure the shop floor is clean and tidy.

Follow and monitor processes as per pre-approved instructions in the BPR.

Manage indenting and receipt of BPRs and all production-related documents.

Verify the issuance and quantity of Raw Materials & Packing Materials as per requisition.

Submit samples to QC and report any abnormal results to superiors immediately.

Report deviations to the reporting authority and take corrective actions as per instructions.

Review executed Batch Production Records and hand them over to the QA department.

Ensure equipment calibration and preventive maintenance are carried out on schedule.

Maintain all necessary records and documentation related to the process.

Ensure proper storage and handling of materials as per defined procedures.

Follow the labeling procedure as per SOP.

Assign work and instructions to subordinates as needed.

Report to the next level authority in the absence of the reporting authority.

Ensure proper shift handover of tasks to the next shift.

Participate in preparation, review, and execution of process validation protocols.

Evaluate proposed changes in product, process, or equipment.

Coordinate with departments like safety, HR, maintenance, warehouse, QC, and QA.

Involve in dispatch activities in coordination with the warehouse and QA.

Prepare and execute the production planning schedule.

Continuously improve safety, product yield, and quality.

Provide training on new processes and BPRs.

Perform any other duties assigned by the reporting authority.

Role & responsibilities

Knowledge on handling on Change controls, Deviations and CAPA.

Knowledge of Vendor qualification.

Preparation and Review of product quality reviews.

Review of master batch production records and batch cleaning records.

Review of executed BPR’s and BCR’s.

Review of analytical raw data (Soft& Hard copies).

Knowledge of LIMS and SAP.