to join our analytical team. The QC Analyst will be responsible for testing raw materials, in-process samples, and finished products in compliance with cGMP and regulatory requirements.
Key Responsibilities:
Perform routine and non-routine analysis using HPLC, UV-Vis, IR, and other instrumentation.
Prepare and standardize reagents, solutions, and mobile phases.
Interpret and document analytical results accurately in laboratory notebooks, LIMS, or other systems.
Conduct method validation and transfer activities under supervision.
Ensure compliance with all relevant SOPs, cGMP guidelines, and safety standards.
Troubleshoot instruments and report equipment malfunctions.
Participate in laboratory investigations (OOS, OOT, deviations).
Support continuous improvement of lab practices and documentation.
Qualifications:
B.S.C or M.S.C in Chemistry, Pharmaceutical Sciences, or a related field.
1-3 years of hands-on HPLC experience in a regulated QC lab (pharmaceutical, biotech, or similar).
Working knowledge of USP/EP/ICH guidelines and cGMP.
Familiarity with analytical software (e.g., Empower, Chromeleon) is a plus.
Strong attention to detail, documentation, and organizational skills.
Ability to work independently and as part of a team.
Interested Candidates Share me your Cv on WhatsApp 7876456719
Job Type: Full-time
Pay: ?20,000.00 - ?30,000.00 per month
Benefits:
Flexible schedule
Food provided
Health insurance
Internet reimbursement
Leave encashment
Life insurance
Paid sick time
Paid time off
Provident Fund
Work Location: In person
Application Deadline: 25/07/2025
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