Pharma Analytical QA Jobs at Nectar Lifesciences Pvt Ltd, Apply on Rasayanika
Company name : Nectar Lifesciences Pvt Ltd
Job Title : Analytical Quality Assurance (AQA) 1-3 Years
Location : Baddi , Solan (Himachal Pradesh)
Employment Type : Full Time, Permanent
Qualification : 1 to 3yr exp in pharmaceuticals, B.pharma , M.pharma, B.Sc , M.Sc , biotech
Experience : 1 to 3 yrs experience in pharma , BSc ,MSc background
Gender : No such preference
Salary : Rs. 19K-25K/Month
Job Summary:
The Analytical Quality Assurance (AQA) Officer is responsible for ensuring data integrity, compliance, and adherence to cGMP in all analytical activities carried out in the QC laboratory. The role involves reviewing analytical documents, monitoring laboratory activities, and supporting investigations to ensure the accuracy, reliability, and regulatory compliance of test results.
Roles & Responsibilities
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Review & Verification of Analytical Data
• Review analytical raw data, chromatograms, calculation sheets, and analytical reports.
• Verify compliance of test results with specifications and SOPs.
• Ensure adherence to ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate, plus Complete, Consistent, Enduring, and Available). -
Compliance Monitoring
• Monitor daily QC laboratory activities for compliance with cGMP and regulatory requirements.
• Ensure all instruments are calibrated, qualified, and used within validated parameters. -
Documentation & SOP Management
• Prepare, review, and update SOPs, protocols, and specifications related to analytical procedures.
• Maintain controlled documents and support change control activities related to QC laboratory practices. -
Investigations & Deviations
• Participate in laboratory investigations for OOS, OOT (Out-of-Trend), and deviations.
• Support root cause analysis and implement corrective and preventive actions (CAPA). -
Training & Audit Support
• Train QC staff on data integrity, documentation practices, and cGMP compliance.
• Assist during internal and external audits (regulatory / client audits) by providing required documentation and explanations. -
Continuous Improvement
• Identify gaps in lab compliance and suggest process improvements.
• Support implementation of electronic data management systems (if applicable).
Qualifications & Experience:
Experience : 1 to 3 yrs experience in pharma , BSc ,MSc background
Education: B.Pharm / M.Pharm / M.Sc. (Chemistry / Pharmaceutical Analysis).
Experience: 1–3 years in QA (AQA) or QC in a pharmaceutical industry (formulations or API).
Industry: Pharmaceutical / Biopharmaceutical / CRO.
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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