QC Junior Team Member at Cipla | Freshers B Pharma Candidates 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: 95647
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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, and products assigned for testing, and complete all the stability studies to ensure their compliance with 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 a suitable valid procedure and calibrated instruments to ensure compliance with the set specifications/standards as a 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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Analyze stability samples without any errors as per the 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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To ensure compliance with GLP and safety norms, perform all activities according to current standard procedures, referring to all approved procedures/specifications.
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Gather all the samples for analysis by checking the consignment for sampling.
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Gather the essentials, such as standards, glassware, and solvents, as soon as possible to perform the analysis according to specification.
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Operate the instruments and perform routine/stability checks as per SOP and safety norms.
Key Accountabilities (3/6)
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Document all activities performed as per valid procedure online using standard/approved formats or templates to ensure that all entries are correct, accurate, and authentic.
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Maintain system integrity by updating documentation and deviations on CipDox while performing operations.
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Maintain all the online documentation, timely entries, and supporting documents as QC.
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Prepare new documents and update existing documents as per GMP requirements.
Key Accountabilities (4/6)
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Maintain and upkeep the laboratory working area by disposing of all analysed solutions and samples after review per valid disposal procedures to ensure compliance with 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 the 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 savings and work simplification.
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Conduct operational studies to find improvement areas and implement new development projects as a fresher.
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Strive for continuous automation of processes through the 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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There was a delay in performing the laboratory activity due to an instrument breakdown. Overcome by ensuring the timely availability of parts and engineers as QC
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There is a delay in releasing the batches due to the unavailability of standards, glassware, and 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 analyses 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 seven 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 the Team Leader (Routine/Stability)
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Procurement of required instruments and glassware standards to the Team Leader (Routine/Stability)
Relevant Work Experience
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0-3 years of experience in the quality control function of a pharmaceutical organisation
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