MPharm Job at Cipla | Apply Now for the Junior Team Member Role
A leading pharmaceutical organization is hiring a Junior Team Member – Quality Control (QC) for its manufacturing site in Rangpo, Sikkim. This MPharm Job involves document preparation, revision of SOPs, pharmacopoeial updates, and ensuring compliance with cGMP and regulatory standards. Candidates with experience in QC documentation, pharma guidelines, and analytical processes are ideal for this role.
- Job Title: Junior Team Member – QC
- Location: Rangpo
- Req Id: 99182
About the Company
Cipla, a global pharmaceutical company dedicated to ensuring affordable access to medicines for all. We are committed to providing innovative and reliable healthcare solutions with a focus on quality and compliance. Join us to be a part of our mission to make a difference in the health of people globally.
Quality Control Job Purpose
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 with respective standards / pharmacopeia and cGMP requirements.
Key Accountabilities of the Quality Control Job
1. Document Preparation & Review
- Prepare SOPs, specifications, and non-routine QC documents.
- Update corporate documents by coordinating with QC/QA teams.
- Review relevant pharmacopoeia and implement required changes.
- Review calibration data related to analytical instruments.
2. Pharmacopoeial Compliance
- Review updated pharmacopoeial monographs and supplements.
- Monitor implementation of pharmacopeial changes across units.
- Notify stakeholders to initiate updates before effective dates.
- Escalate delays or non-conformances to avoid operational gaps.
3. Documentation & Data Integrity
- Maintain online documentation through CipDox as per GMP guidelines.
- Ensure accurate, authentic, and contemporaneous entries.
- Prepare and update documents using approved formats/templates.
- Support deviation documentation and ensure system integrity.
4. Document Issuance & Control
- Issue required documents and maintain issuance logs in bound books.
- Track document versions and ensure only current formats are in use.
- Maintain complete records of all issued documents across units.
5. Harmonization & Simplification
- Standardize and harmonize documents across multiple units.
- Coordinate with cross-functional teams to simplify existing processes.
- Provide improvement ideas to enhance work efficiency.
6. Key Challenges
- Delays in method verification due to unavailable data—resolved through coordination.
- Tight timelines for updates—addressed with proper planning and communication.
- Delay in reviews from CFTs—managed through follow-ups and escalations.
Major Challenges:
- Delay in verification of methods for pharmacopeial updates due to non-availability of data. Overcome by coordinating with QC and.
- Inadequate time allotted for updating the documents due to late intimations and change in priorities. Overcome by understanding the requirements and proper planning and coordination with CFTs.
- Delay in meeting final timelines of the activities due to delay in getting review comments for cross-functional departments. Overcome by regular follow-ups and escalations.
Education Qualification: M.Sc. / B. Pharma.
Relevant Work Experience: 1-3 years of experience in QC department of a pharmaceutical organization with knowledge of latest regulatory standards and compliance norms.
