Quality Control Jobs in Cipla | Build a Rewarding Pharmaceutical Career| Apply Now
Looking to begin your journey in Quality Control Jobs within the pharmaceutical industry? Here’s your chance! The Junior Team Member – QC role in Baddi, Himachal Pradesh, offers a fantastic opportunity to work in a leading pharmaceutical organization dedicated to innovation and excellence. Among quality control jobs, this position stands out as a way to join a team where your skills in compliance, documentation, and analytical processes can flourish — and take a meaningful step forward in your Pharmaceutical Career.
- Job Title: Junior Team Member – QC
- Posting Date: 26 Oct 2025
- Country: India
- Location: Himachal Pradesh, Baddi, India.
- Req Id: 98188
- Division: Department
- Sub Department: 1
About the Company:
This opportunity is with a leading pharmaceutical company recognized for its commitment to innovation, research, and excellence in healthcare. The organization fosters professional growth while ensuring global compliance with cGMP and regulatory standards, making it a trusted name for those pursuing long-term Pharmaceutical Careers. Excelling in quality control roles is part of this growth.
Job Description:
Prepare, update and review the specifications, SOPs, policy and operating documents for analysis of materials in order to ensure alignment to predefined quality parameters and compliance to respective standards / pharmacopeia and cGMP requirements. Achieving excellence in quality control jobs’ standards is crucial.
Qualifications:
- Education: M.Sc. / B. Pharm
- Experience: 1–3 years in a QC department within a pharmaceutical organization, with strong knowledge of regulatory standards, documentation, and compliance practices essential for quality control job excellence.
Key Responsibilities:
- Prepare and update SOPs, specifications, and non-routine documentation to support analysis and ensure timely availability across the site.
- Revise corporate documents such as analytical methods and coordinate with site QC/QA teams.
- Review pharmacopeial updates, monographs, and amendments to maintain compliance with current standards.
- Maintain accurate documentation using validated formats and ensure data integrity through systems like CipDox. Securing quality control jobs requires such attention to detail.
- Issue and control bound books and relevant documents to ensure correct versions are available across all departments.
- Implement harmonization and standardization of documentation across units to simplify processes.
- Coordinate with cross-functional teams (CFTs) to achieve documentation goals and ensure compliance with GMP standards.
- Support the pharmacopeial update process, ensuring timely implementation post data verification.
Major Challenges – Overcoming Barriers in Quality Control Jobs
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Managing limited timelines for document updates and verification.
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Coordinating with multiple departments for review and feedback.
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Ensuring timely completion of documentation under regulatory timeline
Key Interactions – Cross-Functional Collaboration in Pharmaceutical Careers
- Collaborate daily with QC, QA, CDC, and RA teams for document approvals.
- Coordinate with ADL and R&D for data updates, and IPD for new project documentation.
Dimensions – Performance Metrics in Quality Control Jobs
- Support for 4 pharma units in document updates.
- Manage approximately 10 document reviews per month.
- Ensure 80% of documentation finalized on time and 100% compliance with pharmacopeial standards.
Key Decisions
- Implement process simplifications and harmonization across CDC and other sites.
- Resolve user documentation queries in collaboration with the Section Head – CDC.
