Quality Control

Roles and Responsibilities:

• Sampling & Analysis: Sampling of raw materials, in-process materials, finished products and packaging materials as per approved SOPs; performing chemical, physical and instrumental testing as per Pharmacopoeia standards and in-house specifications; conducting analysis of water samples; ensuring proper labelling, handling and traceability of all samples and test materials.
• Instrument Operation & Maintenance: Operating analytical instruments; performing calibrations; maintaining instrument logbooks and ensuring all instruments are in a validated state before use.
• Documentation & Reporting: Recording all observations and analytical data accurately in analytical worksheets and logbooks as per GDP; preparing and reviewing Certificates of Analysis (CoA) for approval and release; maintaining and updating STPs, SOPs and specification records; ensuring timely reporting of test results and communicating any abnormal findings to superiors.
• Stability Studies: Conducting stability testing of products as per ICH guidelines; ensuring proper placement, withdrawal and testing of stability samples; recording, compiling and reporting stability data.
• Reagent & Solution Management: Preparing and standardising volumetric solutions, reagents, mobile phases and buffers as per SOP; labelling all prepared reagents with preparation and expiry dates; ensuring proper storage and disposal of chemicals and waste as per EHS guidelines.
• Compliance & Quality Systems: Adhering strictly to GLP and GMP at all times; following approved SOPs, test methods and safety protocols; assisting in investigation of OOS, OOT and deviation reports; maintaining cleanliness and environmental control of laboratory areas.
• Coordination & Communication: Coordinating with Production, QA and Warehouse teams for sampling and release activities; reporting non-conformities and analytical abnormalities immediately to the QC Manager.

Key Competencies:

• Raw Material, In-Process & Finished Product Testing
• Pharmacopoeia Methods - IP / BP / USP / EP
• HPLC Method Execution & System Suitability
• Certificate of Analysis (CoA) Preparation & Review
• Stability Testing as per ICH Guidelines
• OOS / OOT Investigation & CAPA Support
• Reagent Preparation, Standardisation & Inventory
• GLP / GMP / GDP Compliance in QC Operations

Qualification:

• M. Pharm (Pharmaceutics / Quality Assurance /Pharmacognosy) - Preferred
• M.Sc. (Pharmaceutical / Industrial / Applied Chemistry) with 0-2 years of relevant experience
• B. Pharm with 1-2 years of relevant experience in QC in an OSD pharmaceutical environment
• Work Experience: 0-2 years in QC/ Analytical laboratory in Pharma / Nutraceutical manufacturing.

Interested candidates can apply through E-mail: [email protected] or whatsapp to: 6360250430

Pay: ₹276,000.00 - ₹300,000.00 per year

Benefits:

• Food provided
• Health insurance
• Provident Fund

Work Location: In person