Pharma Production Jobs at Nectar Lifesciences Pvt Ltd, Apply on Rasayanika
Company name : Nectar Lifesciences Pvt Ltd
Job Title : Production Oral , Quality management systems (QMS) Officer
Location : Baddi , Solan (Himachal Pradesh)
Employment Type : Full Time, Permanent
Qualification : 2 to 4yr exp in pharmaceuticals, B.pharma , M.pharma, BSc , MSc Microbiology .
Experience : 2 to 4 yrs experience in pharma , BSc ,MSc background
Gender : No such preference
Salary : 3-4 Lacs P.A
Job Summary:
The QC Officer – QMS is responsible for implementing and maintaining Quality Management System (QMS) processes within the QC department at Nectar Lifesciences. This includes handling documentation, deviations, change controls, investigations, CAPA, and supporting compliance with cGMP, regulatory requirements, and internal quality standards. The role ensures that QC operations are aligned with global quality guidelines, supporting continuous improvement and readiness for regulatory inspections.
Roles and Responsibilities –
-
QMS Documentation & Control
• Prepare, review, and control SOPs, specifications, protocols, and QC-related documents.
• Ensure proper document version control, archival, and retrieval as per GDP (Good Documentation Practices).
• Maintain controlled copies for QC department and ensure compliance with approved procedures. -
Deviation, OOS, and CAPA Management
• Document and investigate QC-related deviations, Out-of-Specification (OOS), and Out-of-Trend (OOT) results.
• Coordinate with QA/Production to determine root cause and implement Corrective and Preventive Actions (CAPA). -
Change Control & Risk Assessment
• Initiate and review change control requests related to QC methods, specifications, or equipment.
• Conduct risk assessments and ensure that changes are implemented in a controlled manner. -
Audit & Regulatory Compliance
• Ensure QC department readiness for internal audits, regulatory inspections (USFDA, MHRA, WHO-GMP).
• Compile and present QC documents and data during audits.
• Address audit observations and implement agreed actions. -
Training & Awareness
• Conduct periodic training sessions for QC analysts on QMS, SOP adherence, and data integrity.
• Maintain training records and competency assessments for QC staff. -
Continuous Improvement
• Identify gaps in QC documentation, compliance, and process efficiency.
• Support implementation of electronic systems (LIMS, Document Management Systems) if applicable.
• Participate in quality risk management and continuous improvement initiatives. -
Reporting & Coordination
• Generate periodic QMS metrics (deviation closure rate, CAPA effectiveness, documentation review timelines).
• Coordinate with QA, Production, and R&D for cross-functional quality improvements.
Qualifications & Experience
• Education: B.Pharm / M.Pharm / M.Sc. (Pharmaceutical Sciences / Chemistry / Biotechnology).
• Experience: 2–4 years of experience in QA-QMS in a pharmaceutical manufacturing facility (API or formulations).
• Industry: Pharmaceutical / Biopharma (OSD, Injectables, API).
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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