for the Quality Control Department. The candidate should have strong hands-on experience in pharmaceutical QC operations, handling sophisticated analytical instruments, and preparation of quality-related documentation to ensure smooth QC operations.
Key Responsibilities:
Perform analysis of raw materials, in-process samples, finished products, and stability samples.
Operate and maintain sophisticated analytical instruments such as
HPLC, UV Spectrophotometer, Dissolution Apparatus, and Karl Fischer
.
Ensure compliance with
GLP (Good Laboratory Practices)
.
Prepare, review, and maintain QC documentation including
AMV, Stability studies, OOS, OOT, and Laboratory Incident reports
.
Conduct method validation, verification, and stability studies as per regulatory requirements.
Ensure timely completion of QC activities to avoid work delays.
Follow SOPs, cGMP, and regulatory guidelines.
Support audits and inspections (internal/external).
Maintain proper documentation and data integrity in the QC laboratory.
Required Skills & Competencies:
Strong analytical and problem-solving skills.
Sound knowledge of pharmaceutical QC procedures and compliance.
Experience in handling investigations related to OOS, OOT, and lab incidents.
Ability to work independently with minimal supervision.
Good communication and documentation skills.
Reporting To:
QC Manager / Head - Quality
Job Type: Full-time
Pay: ₹25,838.83 - ₹50,410.09 per month
Benefits:
Paid time off
Provident Fund
Work Location: In person
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