Junior Team Member – QC

Req ID: 102416
Location: Baddi, Himachal Pradesh
Country: India
Posted On: 11 February 2026
Experience Required: 1 – 3 Years
Education: M.Sc. / B. Pharma

🏢 Job Overview

The Junior Team Member – Quality Control (QC) will be responsible for preparing, updating, and reviewing specifications, SOPs, policies, and operating documents to ensure compliance with predefined quality standards, pharmacopeia requirements, and cGMP norms. The role supports document control, pharmacopoeial updates, and regulatory compliance activities across the site.

🎯 Job Purpose

To ensure preparation, review, and timely implementation of SOPs, specifications, and analytical documentation in alignment with regulatory standards, pharmacopeia updates, and cGMP requirements while maintaining system integrity and documentation accuracy.

🔑 Key Responsibilities

The Junior Team Member – QC will prepare and revise SOPs, specifications, general analytical methods, and non-routine documents to support material analysis and ensure compliance across the site. The role includes reviewing pharmacopoeial updates, supplements, amendments, and new or revised monographs to ensure timely implementation before effective dates and prevent non-conformances. The candidate will review instrument calibration data, coordinate with QC/QA teams, and escalate deviations where necessary.

The position requires maintaining system integrity by documenting activities online using approved formats and updating deviations and records in systems such as CipDox. The candidate will issue documents and bound books to applicable units while maintaining accurate issuance logs and ensuring current document versions are available. The role also involves driving harmonization and simplification of processes by coordinating with cross-functional teams (CFTs), standardizing documentation across units, and suggesting process improvements to enhance efficiency.

📌 Major Challenges

• Delays in method verification due to non-availability of supporting data
• Limited time for documentation updates due to shifting priorities
• Delays in cross-functional review approvals
• Ensuring timely pharmacopoeial implementation

🤝 Key Interactions

• CDC / QC / QA / RA (Daily document approvals)
• ADL / R&D (Data for deficiency responses)
• IPD (Data for new projects)

📊 Role Dimensions

• Supports documentation updates for 4 units
• Average 10 documentation preparations/reviews per month
• Finalize at least 80% of documents within defined timelines
• Ensure 100% implementation of pharmacopoeial updates upon data availability

🎓 Required Qualifications

• M.Sc. or B. Pharma
• 1–3 years of experience in the QC department of a pharmaceutical organization
• Strong knowledge of regulatory standards, pharmacopeia, and compliance norms

🚀 Apply Now

https://careers.cipla.com/job/Baddi-Junior-Team-Member-QC-Hima/1357081366/

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