Junior Team Member – Quality Control Job | Chemistry Job at Cipla Careers

Junior Team Member – Quality Control Job | Chemistry Job at Cipla Careers

Are you looking for a Quality Control Job or a Chemistry Job in the pharmaceutical industry? Join as a Junior Team Member – QC in Rangpo, Sikkim, and gain hands-on experience in documentation, SOPs, and compliance with cGMP and pharmacopeia standards. This opportunity is part of Cipla Careers, ideal for professionals seeking a Fresher Job, a QC Job, or a career in Pharmaceutical Jobs.

Job Details

• Job Title: Junior Team Member – QC
• Location: Rangpo, Sikkim, India
• Job ID: 96520
• Type: Full-time
• Education Qualification: M.Sc. / B. Pharma

Job Purpose:

Prepare, update, and review specifications, SOPs, policy, and operating documents for material analysis to ensure alignment with predefined quality parameters and compliance with cGMP requirements and pharmacopeia standards. This Quality Control Job also provides hands-on experience for professionals interested in Chemistry Jobs.

Key Responsibilities:

1. Document Preparation & Review:

   • Prepare SOPs, specifications, and non-routine documents for QC analysis.

   • Coordinate with QC/QA teams to update corporate documents.

   • Review applicable pharmacopoeia and guidelines for necessary updates.

2. Pharmacopeial Compliance:

   • Review new/revised monographs and supplements.

   • Ensure timely implementation of updates to avoid non-conformances.

   • Notify stakeholders to complete activities before the effective dates.

3. Documentation Accuracy:

   • Maintain accurate entries using approved formats or CIPDox.

   • Update existing documents as per GMP requirements.

4. Issuance & Record Maintenance:

   • Issue documents and bound books to units and maintain issuance records.

   • Ensure current versions are available for operations.

5. Process Simplification & Harmonization:

   • Standardize and simplify documents across all units.

   • Coordinate with cross-functional teams (CFTs) for process improvement.

6. Challenges & Coordination:

   • Handle delays in verification and review by proactive coordination.

   • Escalate issues and follow up with cross-functional departments.

Key Interactions:

• CDC / QC / QA / RA for document approvals
• ADL / R&D for data updates
• IPD for new project documentation

Performance Metrics:

• Support 4 units with documentation updates
• Prepare/review an average of 10 documents per month
• Finalize ≥80% documents within defined timelines
• Ensure 100% implementation of pharmacopeial updates

Relevant Work Experience:

• 1–3 years in QC within a pharmaceutical organization
• Knowledge of the latest regulatory standards and compliance norms

APPLY ONLINE HERE