Junior Team Member at Cipla – for freshers, Apply Now!
Cipla is hiring a Junior Team Member – QC in Rangpo, Sikkim. This full-time role focuses on sampling, testing, and documenting raw materials, packing materials, and finished products to ensure they meet strict quality standards. Join Cipla’s quality control team and contribute to maintaining excellence in pharmaceutical manufacturing.
- Junior Team Member – QC at Cipla
- State: Sikkim
- Location: Rangpo
- Req Id: 95413
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Education Qualification: B.Sc. (Chemistry) or B. Pharm.
Job Purpose
Perform sampling, execute and document the analysis of raw materials, packing materials, products assigned for testing and complete all the stability studies in order to ensure its compliance to the laid down quality parameters and predefined specifications / standards and meet SRB targets
Key Accountabilities (1/6)
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Analyse the assigned samples and chromatographic tests for analysis by using the suitable valid procedure and calibrated instruments to ensure the compliance to the set specification / standards as fresher
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Perform analysis for release of RM, PM, FP & water analysis and process/cleaning validation as per commitment dates
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Perform analysis for stability samples without any errors as per schedule
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Check the results of the tests performed, evaluate them against the specifications as QC
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Review the TDS printed through LIMS for its completion before release
Key Accountabilities (2/6)
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Perform all activities as per current standard procedures by referring to all approved procedures/specifications to ensure compliance to GLP and safety norms
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Gather all the samples for analysis by checking the consignment for sampling
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Gather the essentials like standards, glassware, solvents to perform the analysis as per specification as fresher
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Operate the instruments and perform routine/stability as per SOP and safety norms
Key Accountabilities (3/6)
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Document all activities performed as per valid procedure online by using standard/approved formats or templates to ensure that all entries done are correct, accurate and authentic
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Maintain system integrity by updating documentations and deviations on CipDox while performing operations
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Maintain all the online documentation and timely entries and supporting documents as QC
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Prepare new documents and update existing documents as per GMP requirement
Key Accountabilities (4/6)
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Maintain and upkeep the laboratory working area by disposing off all analysed solutions and samples after review as per valid disposal procedures to ensure compliance to GLP
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Maintain equipment, facility and block premises as per SOP as QC
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Perform validation, qualification and calibration as per schedule and update output of all activities in the systems
Key Accountabilities (5/6)
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Provide suggestions and ideas by exploring new possibilities to achieve cost saving and work simplification
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Conduct operational studies to find improvement areas and implement new development projects as fresher
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Strive for continuous automation of processes through implementation of new processes
Key Accountabilities (6/6)
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Major Challenges
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Delay in performing analysis or re-planning due to frequent changes in production plans. Overcome by conducting performance dialogues and handshakes meetings identifying priorities
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Delay in performing laboratory activity due to instrument breakdown. Overcome by ensuring timely availability of parts and engineers as QC
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Delay in releasing the batches due to non-availability of standards, glassware, chemicals. Overcome by coordinating with CFTs and escalations
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Key Interactions (1/2)
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Unit Planning for daily release of RM, PM and FP (Daily)
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Site QC (Non-Routine) for essentials of analysis (Daily) as QC
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CDC for specification changes implementation (Need Basis)
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Unit QA for non-conformances (Need Basis)
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Stores for inventory (Daily)
Key Interactions
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Service Engineer to resolve instrument related issues, breakdown (Need Basis)
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Number of FP batches released: 3-4
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Number of RM analysis conducted: 3-4
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Number of studies conducted for stability samples: 10
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Non-conformance OOS/OOT to be closed within 7 working days
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Non-conformance rate should be below 1.5%
Key Decisions
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Suggestions for improvement of QC productivity to Team Leader (Routine/Stability)
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Procurement of required instruments and glassware standards to Team Leader (Routine/Stability)
Relevant Work Experience
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0-3 years of experience in quality control function of a pharmaceutical organisation
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