Shift Incharge

1 day ago

Hyderabad Telangana, India Neuland Laboratories Ltd Full time

**Role Title**

Shift Incharge - Pharma

**Department**

Manufacturing

**Sub Department**

Production

**PURPOSE OF THE ROLE**

Responsible to achieve the desired production yield of pharmaceutical APIs by carrying out all the production activities, material management and manpower supervision in the shift in compliance with relevant standard operating procedures, quality and safety norms.

**JOB DESCRIPTION** (What the person needs to deliver at workplace)
- Proper takeover of shift operations as per defined procedure as a reliever
- Batch Process
- Follow Gowning Procedure before entering pharma area at cross over bench.
- Ensure raw materials from stores are received and update balance in Material Reconciliation Record.
- Collect Intermediate material from Intermediate area.
- Ensure availability of Utilities before charging the batch.
- While charging batches ensure raw material quantities, Intermediate material, execute production process and record process parameters progressively in Batch Manufacturing Sheet.
- 100% adherence to cGMP practices in line with 21 CFR.
- 100% adherence to EHS requirements as applicable to production shop floor.
- Carry on Filtration Activities (Leaf Filter, Pressure Filters and Micron Filters).
- Ensure Housekeeping and Hygiene in shop floor area in line with specified procedure.
- Ensure Pest Control in shop floor area.
- Dispense required samples to QC in line with specified procedure.
- Ensure packing activity and dispense finished material to stores for dispatch in line with specified procedure.
- Able to face Audits.
- Supervision on shift chemists and casual labour in the shift.
- Timely reporting of abnormalities/ deviations to the immediate supervisor/ appropriate authority.
- Documentation activity
- Receive batch manufacturing sheets / formats / records from QA department.
- Live recording of each activity in Batch Manufacturing Sheet and other records such as cleaning record, material reconciliation record, reactor logbook, etc.
- Handover completed documents to QA after proper review / ongoing documents to reliever.
- Maintenance activity
- Co-ordinate with plant maintenance in the shift for compliance with preventive maintenance and shutdown maintenance.
- Coordinate with plant maintenance team for ensuring temperature and pressure and humidity and to resolve breakdowns during the shift.
- Training

**QUALIFICATIONS/ EXPERIENCE REQUIREMENTS**

**Parameter**

**Minimum**

**Preferred**

Education

B.Sc. (Chemistry)

M.Sc. (Chemistry)

Experience (in Years)

6

8

Nature of Experience

Knowledge of production and quality systems, regulatory and cGMP guidelines, EHS requirements in Pharmaceutical API companies.

**COMPETENCY REQUIREMENTS**

**#**

**FUNCTIONAL**

Ability to understand systems and processes

Execution

Optimum Utilization of Resources

**BEHAVIOURAL**

Attention to detail

Teamwork

Problem Solving

Supervision

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