Vacancy

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Audit & Compliance Executive
No. of Positions: 2
Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm
Experience: 6-8 years
Budget: 5-7 LPA
Job Role:
  • Regulatory & GMP Compliance
  • Internal Audit Management
  • Regulatory Audit Preparation
  • Deviation, Change Control & CAPA Oversight
  • Vendor & External Audit
  • Documentation & Data Integrity Control
  • Risk Management
QMS Executive
No. of Positions: 2 Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm Experience: 6-8 years Budget: 5-7 LPA Job Role:
  • Deviation Management
  • CAPA Management
  • Regulatory Audit Preparation
  • Change Control Management
  • Customer Complaints & Market Complaints
  • Product Quality Review (PQR / APR)
  • Documentation Control
  • Audit & Inspection Support
Process Validation Executive
No. of Positions: 1 Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm Experience: 6-8 years Budget: 5-7 LPA Job Role:
  • Audit & Inspection Support
  • Execution of Process Validation (Injectable / LVP Specific)
  • Continued Process Verification (CPV)
  • Risk Assessment & QRM
  • Documentation & Reporting
  • Regulatory & Audit Compliance
Lab QA Executive
No. of Positions: 2 Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm Experience: 6-8 years Budget: 5-7 LPA Job Role:
  • Laboratory Compliance Oversight
  • Analytical Data Review
  • OOS / OOT / OOC Handling
  • Stability Study Oversight
  • Microbiology Compliance (Critical for LVP)
Micro Officer (Male candidates)
No. of Positions: 2 Qualification: B.Sc (Micro) / M.Sc (Micro) Experience: 1-4 years Budget: 1-4 LPA Job Role:
  • Perform environmental monitoring of sterile areas including viable and non-viable monitoring.
  • Conduct air sampling, settle plates, contact plates, and swab sampling as per schedule.
  • Perform microbiological testing of Purified Water, WFI, and Clean Steam.
  • Conduct bioburden and endotoxin testing of water systems.
  • Handle sterility test isolator / LAF operations as per SOP.
  • Preparation and sterilization of culture media.
  • Perform Growth Promotion Test (GPT) for media.
  • Conduct bioburden testing of bulk products, raw materials, and packaging materials.
  • Perform microbial limit tests as per pharmacopeial methods.
  • Perform Bacterial Endotoxin Test (BET) using LAL method.
  • Maintain microbial culture stock and culture handling as per SOP.
  • Conduct culture identification when required.
  • Ensure proper calibration and qualification of microbiology instruments.
  • Maintain records of incubators, autoclaves, colony counters, LAF, and isolators.
Packing Officer
No. of Positions: 5 Qualification: B.Sc / M.Sc Experience: 1-4 years Budget: 1-4 LPA Job Role:
  • Execute entire packing activities of LVP products.
  • Ensure correct batch coding, overprinting, and label reconciliation.
  • Perform line clearance before batch start and after batch completion.
  • Verify product name, batch number, Mfg./Exp. date, and artwork before packing.
  • Monitor in-process checks during packing operations.
  • Ensure proper handling of printed packing materials.
  • Maintain and complete Batch Packing Records (BPR) accurately.
  • Record hourly output and reconciliation details.
  • Ensure compliance with cGMP, GDP, and Data Integrity requirements.
  • Perform reconciliation of labels, cartons, inserts, shippers, and printed materials.
  • Ensure zero mix-up and cross-contamination.
  • Control and account for rejected and damaged materials.
  • Allocate manpower as per packing plan.
  • Train operators on SOPs, packing procedures, and safety practices.
  • Ensure proper cleaning and line clearance of packing equipment.
  • Participate in qualification/validation activities
Production Officer
No. of Positions: 5 Qualification: B.Sc / M.Sc Experience: 1-4 years Budget: 1-4 LPA Job Role:
  • Execute LVP manufacturing activities (Washing, Filling, Sealing, Sterilization, Visual Inspection, Packing).
  • Ensure batch manufacturing as per approved BMR/BPR.
  • Monitor critical process parameters during production.
  • Ensure line clearance before start and after completion of batch.
  • Coordinate with Engineering for equipment readiness and breakdown handling.
  • Ensure accurate and timely documentation in BMR, logbooks, and formats.
  • Report deviations, incidents, and non-conformities immediately.
  • Participate in deviation investigation and CAPA implementation.
  • Ensure adherence to cGMP, GDP, and Data Integrity principles.
  • Ensure cleaning and sanitization of equipment as per SOP.
  • Participate in qualification/validation activities
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