Junior Team Member QC Job in Cipla Solan
A leading pharmaceutical organization is hiring a Junior Team Member – QC in Solan, Himachal Pradesh. The QC Job role involves preparing, reviewing, and updating essential QC documents to ensure compliance with pharmacopeia, regulatory guidelines, and cGMP standards. Graduates seeking for B pharma jobs and want to start their career with Cipla careers can apply now.
Job Details
- Position: Junior Team Member – QC
- Location: Solan, Himachal Pradesh
About the Company
The hiring organization is a reputed pharmaceutical manufacturer known for robust quality systems, regulatory compliance, and advanced QC practices. With multiple units and cross-functional teams, the company focuses on delivering safe, effective, and compliant pharmaceutical products globally. This QC Job role plays a significant role in the company.
Educational Requirements
-
B.Pharm
-
Strong understanding of QC systems, pharmacopeial standards, regulatory norms, and cGMP requirements
Key Responsibilities for QC Job Role
1. Documentation Preparation & Review
- Prepare SOPs, specifications, and non-routine documentation
- Revise corporate documents by coordinating with QC/QA
- Review applicable pharmacopeia updates and calibration data
2. Pharmacopeial Updates & Compliance
- Review new/revised monographs
- Monitor implementation of updates
- Alert stakeholders and escalate non-conformances
3. Online Documentation & System Integrity is essential for this QC Job role
- Maintain entries on CipDox
- Update documents and deviations
- Ensure all online documentation is accurate and authentic
4. Document Issuance & Record Maintenance
- Issue documents and bound books to units
- Maintain issuance logs and updated version controls
5. Harmonization & Simplification of Documents
- Standardize documents across units
- Coordinate with CFTs
- Suggest improvements for simplification
6. Managing Challenges
- Address delays in method verification
- Handle limited timelines
- Ensure timely review by cross-functional teams
Skills Required for QC Job Role
- Strong knowledge of analytical methods and pharmacopoeial guidelines
- Experience working with QC documentation systems like CipDox
- Understanding of regulatory standards: cGMP, FDA, MHRA, WHO
- Excellent coordination and communication skills
- Ability to work with cross-functional teams (QC, QA, RA, R&D)
- Detail-oriented with strong documentation accuracy
- Capability to manage timelines and multiple documentation assignments
- Graduates seeking for B pharma jobs and want to start their career with Cipla careers can apply now.
