Junior Team Member QC Job At Cipla
A leading pharmaceutical organization is hiring a Junior Team Member – QC in Baddi, Himachal Pradesh. This QC Job role focuses on SOP preparation, pharmacopoeia updates, GMP documentation, and regulatory compliance to ensure high-quality standards in pharmaceutical quality control operations. Graduates seeking B Pharma jobs or Pharma Jobs can apply now.
- Job Title: Junior Team Member – QC
- Location: Baddi, Himachal Pradesh, India
About the Company
The organization operates in the pharmaceutical sector with a strong focus on regulatory compliance, quality control excellence, and adherence to global pharmacopoeia standards. The QC department works closely with CDC, QA, RA, R&D, IPD, and cross-functional teams to ensure document integrity, harmonization, and compliance across multiple units.
Key Responsibilities
- Prepare, update, and review SOPs, specifications, policies, and operating documents.
- Prepare and revise corporate documents, including general analytical methods.
- Review applicable pharmacopoeia and guidelines and implement QC job-related updates.
- Review instrument calibration data with respect to operating documents.
- Review new/revised monographs as per the current pharmacopoeia.
- Monitor pharmacopoeia updates and ensure timely implementation in quality control functions.
- Escalate non-conformances to avoid operational delays.
- Maintain system integrity by updating documentation and deviations on CipDox for the QC Job team.
- Maintain accurate online documentation and supporting records.
- Issue documents and bound books while maintaining issuance logs.
- Execute harmonization and simplification of documents across units.
- Coordinate with cross-functional teams (CFTs) for process standardization, which is a core QC Job activity.
- Ensure 100% implementation of pharmacopoeia updates after receiving supporting data.
- Achieve finalization of at least 80% of documents within defined timelines.
Educational Requirements
-
B. Pharma
Skills Required
- 1–3 years of experience in the QC department of a pharmaceutical organization is essential for this QC Job.
- Knowledge of the latest regulatory standards and compliance norms.
- Strong understanding of pharmacopoeia requirements and updates.
- Familiarity with cGMP requirements, which are key for anyone holding a QC Job title.
- Experience in SOP preparation and documentation control systems.
- Good coordination and communication skills with cross-functional teams.
- Ability to manage timelines and handle documentation under pressure is vital in any QC job.
Why This Job Role?
This QC Job role provides hands-on exposure to pharmacopoeia compliance, GMP documentation systems, and regulatory quality standards. It is ideal for QC professionals looking to strengthen their expertise in documentation control, compliance management, and cross-functional coordination within a regulated pharmaceutical environment. Graduates seeking B Pharma jobs or Pharma Jobs can apply now.
