HPLC QC Officer Jobs For Pharma & Chemistry at Nectar Lifesciences Pvt Ltd, Apply on Rasayanika
Company name : Nectar Lifesciences Pvt Ltd
Job Title : QC Officer-HPLC (1-3 years)
Location : Baddi , Solan (Himachal Pradesh)
Employment Type : Full Time, Permanent
Qualification : 1-3 years , in relevant field of pharma , B.pharma and MSc etc
Experience : 1 to 3 yrs experience in pharma , BSc ,MSc background
Gender : No such preference
Salary : Rs. 17K-22K/Month
Job Summary:
The Quality Officer – HPLC is responsible for performing routine and non-routine analysis of raw materials, in-process samples, finished products, and stability samples using High-Performance Liquid Chromatography (HPLC). The role ensures that all testing is conducted in compliance with cGMP, GLP, and regulatory requirements, with accurate documentation and timely reporting of results.
Roles & Responsibilities
-
Sample Analysis
• Perform qualitative and quantitative analysis of raw materials, intermediates, in-process, and finished products using HPLC as per approved methods and SOPs.
• Conduct dissolution testing, assay, related substances, content uniformity, and stability studies. -
Instrument Handling & Maintenance
• Operate HPLC systems (Empower / Chromeleon / OpenLab software-based systems).
• Perform routine maintenance, calibration, and troubleshooting of HPLC instruments.
• Ensure instrument readiness and maintain logbooks. -
Documentation & Compliance
• Record and review analytical data in compliance with ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, Enduring, and Available).
• Prepare and maintain test reports, raw data, and chromatograms for audit readiness. -
Method Validation & Transfer Support
• Participate in method validation, verification, and method transfer activities when required.
• Support analytical method development teams for new product testing. -
Deviation & OOS Investigation
• Report any Out-of-Specification (OOS) or Out-of-Trend (OOT) results immediately.
• Support QC lead in investigation, root cause analysis, and CAPA implementation. -
Regulatory & GMP Compliance
• Follow cGMP, GLP, ICH, and regulatory guidelines strictly during testing.
• Maintain readiness for internal, client, and regulatory audits by ensuring proper documentation and data integrity. -
Coordination & Training
• Coordinate with production, QA, and R&D for sample analysis priorities.
• Train junior analysts in HPLC techniques, instrument handling, and documentation practices.
Key Skills & Competencies
• Proficiency in HPLC operation and chromatography software (Empower/Chromeleon/OpenLab).
• Good understanding of analytical chemistry principles and troubleshooting.
• Knowledge of cGMP, GLP, ICH, WHO, and USFDA guidelines.
• Strong documentation and data integrity practices.
• Good communication and teamwork skills.
Qualifications & Experience:
Education: B.Pharm / M.Pharm / M.Sc. (Analytical Chemistry, Pharmaceutical Chemistry, or related discipline).
Experience: 1–3 years of experience in QC (HPLC analysis) in pharmaceutical / CRO / biopharma industry.
Industry: Pharmaceutical (Formulation / API), Biopharmaceutical, or Contract Research Organization.
Interview Process:
• Mode: Direct Interview/Virtual Mode
• Rounds: 3 Rounds
• First round can be virtual but all the interview after that will be on site / direct interview.
• First round will be with supervisor.
• Second round will be with HOD.
• Third round will be with the director of the company.
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