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Cadila Pharmaceuticals Limited
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Technical Supervisor

Technical Supervisor

Cadila Pharmaceuticals Limited

0 years

0 Lacs

Jammu Jammu & Kashmir India

Posted:2 days ago| Platform:

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Skills Required

manufacturing planning checks maintenance engineering tracking documentation report controls management audits training qc resolve reports sap api calculation reconciliation

Work Mode

On-site

Job Type

Full Time

Job Description

Major Purpose Of The Job:-

To ensure that cGMP practices shall be followed from the premises to their section.
To follow the all respective SOPs & BMR procedure in the department during operation.
Over seeing Manufacturing, Compression, Coating & Capsule filling related tasks including planning, control and trouble shooting.
Setting up production targets and achieve the same within time in Tablet Coating & Capsule Filling.
To review Daily Production plan for the Tablet Coating & Capsule filling activities.
To check and ensure dispensed batches for the day in advance.
To keep the area all time ready in line with c-GMP requirement.
To follow the process of product as per the respective batch manufacturing record and do the in-process checks at specified time interval.
To follow up with maintenance for solving engineering related issues and keep follow up with the maintenance for on time rectification of break down.

Principal Tasks:-

To maintain quality and productivity.
To ensure that Zero accident& Zero tolerance in the area.
To follow all respective SOP,s BMR Procedure & Discipline in the department & Operation .

Responsibilities:-

To follow proper Gowning / De-gowning procedure as per SOP.
To do the work allocation properly to workmen based on their competency to meet the daily Production Plan. Check and ensure that they are properly gowned and protected for the assigned work.
To keep the daily basis tracking for productivity of Manpower and Machines.
To check and ensure that all equipment’s used in the dept. are validated and their instruments are calibrated including the balances, ensure their cleanliness for use in good condition.
To check and ensure the area and Equipment Cleanliness of Coating & Capsule cubicle, Coating Machine & its related equipment’s, Capsule filling machine & its related equipment’s, SS vessels & Environmental Condition suitability and in process checks to be carried out properly before startup and during batch Coating & Capsule filling.
To do the online entry and documentation in batch manufacturing record and other production records.
To prepare the investigation report, fill online deviations if any, and other quality document like change Controls, CAPA wherever necessary for the strengthening of quality systems.
To monitor the yield of every products stage wise on daily basis.
Participate in resolving the issues in the CFT being a team member, and a functional representative of the CFT.
To ensure processes needed for integrated management system for establishing, implementing and maintaining properly for your own department.
To participate in periodic IMS system audits and maintains the records.
To participate in training for internal auditors for IMS System to participate in various Awareness trainings on Environment, Health and Safety.
To interact with the cross functional team (QA/QC/RM/ENGG) for all technical and non-technical issue and resolve the same timely without affecting the product quality and delivery.
Co-ordinate with Maintenance regarding breakdown and preventive of equipment’s or facility.
Give necessary instructions to the operators for Production activities effectively.
Inform to superiors of any breakdowns, Deviations, HR issues, productivity issues.
Prepare and submit daily reports as required.
Check and ensure that all SAP related entries completed on-line
To do the API Calculation & Reconciliation in the Batch records.

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