Sun Pharma Ltd Walk In Interview 2023.Sun Pharma Ltd Notification full details below.Interested and eligible candidates can attend interview on scheduled time and venue.Sun Pharma Ltd. is one of the leading contract manufacturing pharmaceutical company, manufacturing more than 12% of India’s domestically consumed medicines.
Selection Process: The selection will be on the basis of Interview.
To perform line clearance in NOSD (Parenteral) manufacturing facility
To perform In-process checks during manufacturing, filling operation and sampling for any study as applicable
To perform In-process (Bulk) & Finish product sampling, rinse water sampling any other sampling and management of samples through LIMS and release in SAP HANA as applicable.
To actively participate in the media fill simulation, review / Preparation of the media fill protocol and summary report.
To perform assessment of breakdown of manufacturing machines / system as per requirement.
To review of process records, review of SOPs qualification documents and other relevant documents
Operation and review of NVPC Instruments and relevant documents
Handling of activities in SAP HANA as applicable
Preparation and Execution of process validation Protocol and report
Compilation of Annual product Quality review (APQR)
To perform and participate in investigation as per requirement.
To ensure GMP compliance of NOSD manufacturing facility
Initiate / Prepare, review and approval of SOPs Change control6, Deviation as applicable in EDMS/Track wise.
Ensure completion of all applicable / assigned trainings in LMS / applicable methods
To check the audit trails of manufacturing systems as applicable.
To Execute, Monitor review and approval of Quality management systems i.e. Change control, Deviation and CAPA management as per requirements.
To Review and approve standard Operating Procedure
To ensure the Compliance of documentation at Various stages of the process i.e. (Manufacturing, Filtration, filling and other packing operations)
To review and approve the master and executed BMR, BPR, Validation, Qualification and other GMP documents.
To evaluate and monitor the Aseptic process simulation (Media fill) activities with respect to the APS planner
To review, update, response to GQS / Regulatory audit observation within the Stipulated time frame.
To participate in the review and approval of investigation in case of Non-conformance events i.e. Process Deviation, OOS, OOT & Product Quality Complaints.
To ensure release, approval or rejection of RM, PM, Intermediate, FP as per approved specification.
To ensure completion and implementation of CAPA as per established procedures and follow up to verify the effectiveness of CAPA
To ensure the compliance of electronic system such as manufacturing equipment/Instruments etc
To ensure equipment / instrument, Qualification / Calibration and PM are performed as per approved planner
To ensure that processing and storage areas are qualified as per the approved procedure and GMP requirements
To ensure and perform work as per established approved procedures regulatory norms and its compliance as per the current regulatory requirements.
To be part of Internal / external quality audits pertaining to NOSD.
To ensure handling of product recalls as per the approved procedures as applicable
Perform any other responsibility assigned by the quality Head / Management
Interested candidates can send their resume directly to [email protected]
