Freshers Jobs at Cipla | BSc Chemistry Candidates Apply Now
Freshers Jobs at Cipla. A leading pharmaceutical organization in Rangpo, Sikkim, is hiring a Junior Team Member – QC to support sampling, analysis, documentation, and stability studies across raw materials, packing materials, and finished products. This role offers an excellent opportunity for fresh graduates and early-career professionals to gain hands-on experience in quality control operations aligned with strict GMP, GLP, and regulatory standards. BSc Chemistry Jobs.
At Cipla, we are committed to producing life-saving medicines for patients across the globe. As a leader in the pharmaceutical industry, we aim to innovate and develop solutions that improve healthcare and enhance lives. Join our team to make a meaningful impact in the pharmaceutical industry. Interested candidates apply for the Freshers Jobs at Cipla.
- Job Title: Junior Team Member – QC
- Country: India
- State: Sikkim
- Location: Rangpo
- Req Id: 95141
Job Purpose
Perform sampling, execute and document the analysis of raw materials, packing materials, 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
- Analyse the assigned samples and chromatographic tests using a suitable, valid procedure and calibrated instruments to ensure compliance with the specified standards.
- Perform analysis for the release of RM, PM, FP & water, and process/cleaning validation as per the commitment dates.
- Perform analysis for stability samples without any errors as per the schedule.
- Check the test results and evaluate them against the specifications.
- Review the TDS printed through LIMS for its completion before release.
Key Accountabilities
- Perform all activities as per current standard procedures by referring to all approved procedures/specifications to ensure compliance with GLP and safety norms.
- Gather all the samples for analysis by checking the consignment for sampling.
- Gather the essentials like standards, glassware, and solvents to perform the analysis as per the specification.
- Operate the instruments and perform routine/stability as per SOP and safety norms.
Key Accountabilities
- Document all activities performed as per valid procedure online by using standard/approved formats or templates to ensure that all entries are correct, accurate, and authentic.
- Maintain system integrity by updating documentation and deviations on CipDox while performing operations.
- Maintain all the online documentation and timely entries, and supporting documents.
- Prepare new documents and update existing records in accordance with GMP requirements.
- Maintain and keep the laboratory working area clean by disposing of all analysed solutions and samples after review, in accordance with valid disposal procedures, to ensure compliance with GLP.
- Maintain equipment, facility, and block premises as per SOP.
- Perform validation, qualification, and calibration as per the schedule and update the output of all activities in the systems.
Key Accountabilities
- Provide suggestions and ideas by exploring new possibilities to achieve cost savings and work simplification.
- Conduct operational studies to find improvement areas and implement new development projects.
- Strive for continuous automation of processes through the implementation of new processes.
Key Accountabilities
- Major Challenges: Delays in analysis or replanning due to frequent changes in production plans. Overcome by conducting performance dialogues and handshake meetings, identifying priorities.
- Delay in performing laboratory activity due to instrument breakdown. Overcome by ensuring the timely availability of parts and engineers.
- Delay in releasing the batches due to the non-availability of standards, glassware, and chemicals. Overcome by coordinating with CFTs and escalations.
Key Interactions
- Unit Planning for daily release of RM, PM, and FP (Daily).
- Site QC (Non-Routine) for essentials of analysis (Daily).
- CDC for specification changes implementation (Need Basis).
- Unit QA for non-conformances (Need Basis).
- Inventory stores (Daily).
Key Interactions
- Service Engineer to resolve instrument-related issues and breakdowns (Need Basis).
Dimensions
- Number of FP batches released: 3-4.
- Number of RM analyses conducted: 3-4.
- Number of studies conducted for Stability samples: 10.
- Non-conformance OOS/OOT to be closed within seven working days.
- Non-conformance rate should be below 1.5%.
Key Decisions
- Suggestions for improvement of QC productivity to the Team Leader (Routine/Stability).
- Procurement of required instruments and glassware standards to the Team Leader (Routine/Stability).
Education Qualification: B. Sc. (Chemistry) or B.Pharm.
Relevant Work Experience: 0-3 years of experience in the quality control function of a pharmaceutical organisation.
