At Cipla Ltd, we constantly work towards ensuring access to high quality and affordable medicines to support patients in need. Which is why, we have been trusted by health care professionals and patients across geographies for the last 8 decades.
We are hiring for following departments
Job Location: Goa, Bangalore, Indore
Departments: QC / Production / Microbiology / SCM / Engineering / Warehouse
Junior Team Member – QC Accountabilities
- Prepare documents like SOPs, specifications and non-routine documentation and ensure timely availability across the site to provide support during the analysis
II. Review the latest pharmacopeial updates, supplements and amendments by evaluating the updates required in the available document to ensure the compliance with the current pharmacopoeia through consent with regulatory body
III. Review the assigned documents by referring the concern backup and pre-defined quality procedure to ensure its compliance against the quality requirements
IV. Issue documents to applicable units, by maintaining the record of the same in the issuance record (bound book) so the current version of the common document is available at the unit
V. Execute harmonization and simplification process of documents to reduce complexities in processes and ensure standardized procedures are followed.
Manager – Microbiology (EM & QMS)
- Ensure proper organisation of the activities in the individual team of Enviornment Monitoring by routine monitoring of each team member in order to ensure that is performing to the best and in compliance to the cGMP requirements
- Handling QMS activities for Microbilogy department, participate in investigations of non compliance
II. Ensure the smooth functioning of the activities relevant to the cross functional departments and teams by conducting periodic interactions/ meetings in order to ensure smooth functioning of each team and to provide necessary support to the manufacturing task and schedules.
III. Ensure the availability and effective implementation of different quality systems and controls across the different teams in the non -routine section by confirming availability of required standard procedures and its trainings in order to ensure that all the operations in section are performed referring the valid standard approved procedures and in compliance to the cGMP requirements to finally support the quality agenda of the organisation.
IV. Ensure the continuous improvements at all the teams of non-routine section by implementing different good practices in the section in order to achieve good output and cost savings.
Junior Officer – Production
Monitor and execute the production activities in an area during the shift by maintaining cGMP and safety norms to achieve production targets
- Execute production activities in a shift by managing available resources to achieve production target
II. Maintain standard process parameters as per BMRs and other supporting documents for achieving production target and maintaining quality
III. Prepare manufacturing records and update online documentation to meet production and cGMP requirements
IV. Follow safe work processes and ensure safety appliances are utilised during production activities in shifts to create a safe working environment
V. Execute production activities in a shift by managing available resources to achieve production target
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