Freshers Chemistry Jobs at Cipla | Apply for Junior Team Member – QC Role
Freshers Chemistry Jobs at Cipla. The Junior Team Member – QC role offers an excellent entry-level opportunity for graduates in Chemistry and Pharmacy to begin their careers in pharmaceutical quality control. Based in Baddi, Himachal Pradesh, this position focuses on sampling, analysis, documentation, and stability studies to ensure products meet predefined quality standards and regulatory compliance. Interested candidates apply for the exciting opportunity at Cipla Careers. BSc Chemistry Jobs.
About Cipla
Cipla is a global pharmaceutical company committed to responsible processes and innovative products. Our mission is to provide affordable medication without compromising on quality, making a difference in the lives of millions of people. We believe in a culture of excellence, collaboration, and integrity.
- Job Title: Junior Team Member – QC
- Posting Date: 9 Dec 2025
- Country: India
- State: Himachal Pradesh
- Location: Baddi
- Req Id: 96017
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.
Part I:
- 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.
- 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.
Part II:
- 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.
Part III:
- 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 online documentation and timely entries, and supporting documents.
- Prepare new documents and update existing documents as per GMP requirements.
Part IV:
- Maintain and upkeep the laboratory working area 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.
Part V:
- 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.
Part VI:
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
- 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).
- Service Engineer to resolve instrument-related issues, breakdown (Need Basis).
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.
