QC Reviewer

Designation: QC Reviewer
CTC: ₹3–4- 5 LPA
Location: Wadi, Nagpur

Job Summary:
Responsible for reviewing all QC lab documents (reports, chromatograms, test records) to ensure accuracy, compliance, and completeness as per cGMP, SOPs, and regulatory guidelines.

Key Responsibilities:

• Review raw data, reports, and logbooks for accuracy.
• Ensure compliance with STPs, SOPs, and specifications.
• Check HPLC/GC/UV data, assay results, and dissolution profiles.
• Identify and report OOS or deviations.
• Maintain proper documentation and records.
• Coordinate with QC, QA, and other departments.
• Support audits by providing required documents.
• Monitor timelines and support training if needed.

Qualifications:

• B. Pharm / M. Pharm / M.Sc. (Chemistry or related field)
• 3–6 years of QC experience in pharma industry
• Good knowledge of cGMP, GLP, ICH, and regulatory norms
• Hands-on experience with HPLC, GC, UV, FTIR

Skills Required:

• Strong attention to detail
• Good documentation and analytical skills
• Effective communication and coordination
• Basic computer skills (MS Office, LIMS preferred)

Job Type: Full-time

Pay: ₹30,000.00 - ₹40,000.00 per month

Schedule:

• Day shift

Work Location: In person