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Technician I at Sun Pharmaceutical Industries Ltd

Halol, gujarat, India -

Full Time

Start Date

Immediate

Expiry Date

11 Sep, 26

Salary

0.0

Posted On

13 Jun, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Batch Manufacturing Record, Risk Assessment, Change Control, Corrective and Preventive Action, SOP Preparation, Environmental Monitoring System, GMP Compliance, Process Validation, Failure Mode Effect Analysis, In-process Control

Industry

Pharmaceutical Manufacturing

Description

Qualification: B. Pharma Experience: 7 to 10 Years Job Responsibilities: Authorized to sign as a doer and verifier in: Batch Manufacturing Record, BMR Requisition, BMR Issuance Logbook. Protocols, Risk Assessment. Authorized to sign as a checker/verifier in following document, Finished product logbook etc. To prepare new BMR, revise BMRs within time. To assist in preparation of Change Control, Corrective Action Plan & New Equipment’s preparation. Handling of corrective and preventive action. To ensure the compliance of various in-process control instructions provided in BMR, MBMR. Preparation and updation of SOPs, BMRs, Log books, protocols and compliance thereof with training of people on the same. Handling and monitoring of Environmental monitoring system (EMS) system. To maintain daily production report, machine utilization on day to day basis. To learn EMS, review the report on daily basis. (Action, alert limit, breakdown maintenance). Training to all technician & supervisor for new BMRs and revised BMRs to comply with the GMP. To prepare process performance qualification/process validation protocols, study protocols. To prepare failure mode effect analysis, risk assessment for product/process. To undergo functional training, cGMP training or any other training identified as per schedule. Any other responsibility assigned by department head after ensuring the relevant training status.

Responsibilities

Responsible for preparing and revising Batch Manufacturing Records (BMR) and ensuring compliance with GMP and in-process control instructions. Manages environmental monitoring systems, production reports, and conducts training for technicians and supervisors.