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.
