Cipla Career: QC Job in Sikkim | BSc Chemistry Graduates Apply Now
Are you searching for a QC Job in the pharmaceutical industry? This exciting Cipla Career opportunity for Team Member – Quality Operations in Sikkim is ideal for candidates looking for a BSc Chemistry Job or a Freshers Job in pharma quality control. The role offers practical exposure to analytical testing, stability studies, and GMP documentation, making it a strong starting point for long-term Chemistry careers.
About Cipla
Cipla is a leading global pharmaceutical company headquartered in India, known for its commitment to quality, innovation, and affordable healthcare solutions. With a strong presence across regulated and emerging markets, Cipla operates advanced manufacturing facilities that follow strict GMP and global compliance standards. A Cipla Career offers excellent opportunities in manufacturing, research, and quality functions. For candidates seeking a QC Job, BSc Chemistry Job, or Freshers Job, Cipla provides structured training, hands-on laboratory exposure, and clear growth opportunities into senior quality, regulatory, and leadership roles within the pharmaceutical industry.
- Job Title: Team Member – Quality Operations
- State: Sikkim
- Location: Rangpo
- Req Id: 100134
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 their compliance with the laid down quality parameters and predefined specifications/standards, and meet SRB targets.Key Accountabilities (1/6)
- Analyse the assigned samples and chromatographic tests for analysis by using a suitable, valid procedure and calibrated instruments to ensure compliance with the set specification/standards
- Perform analysis for release of RM, PM, FP & water analysis and process/cleaning validation as per commitment dates
- Perform analysis for stability samples without any errors as per the schedule
- Check the results of the tests performed, and evaluate them against the specifications
- Review the TDS printed through LIMS for its completion before release
Key Accountabilities (2/6)
- 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 (3/6)
- 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 documents as per GMP requirements
Key Accountabilities (4/6)
- Maintain and upkeep the laboratory working area by disposing of all analysed solutions and samples after review as per 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 (5/6)
- 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 (6/6)
Major Challenges
- Delay in performing analysis or re-planning 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 (1/2)
- 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)
- Stores for inventory (Daily)
Key Interactions (2/2)
Service Engineer to resolve instrument-related issues, breakdown (Need Basis)
Dimensions (1/2)
- 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 7 working days
- Non-conformance rate should be below 1.5%
Dimensions (2/2)
Key Decisions (1/2)
- 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)
Key Decisions (2/2)
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.
