Cipla Ltd Walk-in Interview 2025.Cipla Limited Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue..
Vacancy details:
- Department: Junior Team Member – QA/QC/Junior Officer – Packing
- Experience: (0-3 years)
- Qualification: B. Sc. (Chemistry) or B. Pharm./Msc/Mpharm
Important Details :
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
Job Description: Greeting from Cipla Limited.!!!!!
Job Purpose
Review the compliance level of site for deficiency response, prepare master validation protocol and report as per company quality policy and applicable regulatory guidelines
Key Accountabilities (1/6)
Collate, review and provide required work plans on received deficiencies to HO in order to respond to regulatory authorities in a timely manner
Collect data from all SPOCs with respect to received work plan for review
Escalate any delays in receiving response from unit with respect to work plan
Review of collected data for work plan fulfilment
Send data to HO for compilation of deficiency response
Take follow up with HO to receive updated dossier for product updates
Review Master Validation protocol and report for timely execution of validation batches and timely submission of documents in order to response for deficiencies
Job Purpose
Monitor and execute the packing activities in a shift by maintaining cGMP and safety norms to achieve production targets
Key Accountabilities (1/6)
Execute shift packing activity by managing available resources and reduces micro stoppage of machine to achieve shift target
Utilise shift resources optimally to get desired production output
Regulate usage of consumables in the production process at optimum level to save cost
Job Purpose
Provide analytical support to API R&D, Regulatory Affairs, Manufacturing units and other analytical laboratories by method development of raw materials, intermediates and final API in order to ensure the drug development is carried out as per the project timelines and adheres to all regulatory requirements
Key Accountabilities (1/6)
Provide method development and routine analysis under GLP environment to finalise the specification for standardization of the molecule and for final DMF submission
Conduct extensive literature search
Analyse raw materials, intermediates, final API, forced degradation samples, stability samples, GTIâs on different analytical instruments under GLP environment
Conduct Fate and Purge studies/carryover studies
Perform method validation
Prepare specification based on carryover studies
Perform method transfer to manufacturing units for routine QC analysis
Shaik Sufiya
Can u please pin interview location details