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Senior Officer – Quality Control

Apotex
3-6 years
INR 6 LPA – 8 LPA
Bangalore, India
1 June 19, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

Senior Officer – Quality Control

Location: Bangalore, Karnataka, India
Company: Apotex Inc.
Employment Type: Full-Time

Role Summary

The Senior Officer – Quality Control is responsible for performing sampling, testing, analysis, and reporting of raw materials, packaging materials, and water samples in compliance with GMP, cGLP, and regulatory requirements. The role ensures that all quality control activities are conducted accurately, efficiently, and in accordance with approved analytical methods and quality standards.

This position requires strong expertise in pharmaceutical quality control, laboratory operations, analytical testing, documentation practices, and regulatory compliance to support product quality and patient safety.

Key Responsibilities

Quality Control Testing & Analysis

  • Perform analysis of:
    • Raw Materials
    • Packaging Materials
    • Water Samples
  • Execute testing activities according to:
    • Approved Methods of Analysis
    • Standard Operating Procedures (SOPs)
    • Regulatory Requirements
  • Ensure timely completion of analytical testing activities.
  • Review and verify test results for accuracy and compliance.

Sampling & Laboratory Operations

  • Conduct sampling of:
    • Water Systems
    • Raw Materials
    • Packaging Components
  • Perform testing as per approved procedures and specifications.
  • Ensure proper sample handling, storage, and documentation.
  • Maintain laboratory readiness and operational efficiency.

Documentation & Data Integrity

  • Record analytical results accurately and contemporaneously.
  • Prepare and maintain:
    • Laboratory Records
    • Test Reports
    • Analytical Worksheets
    • Sampling Logs
    • Equipment Usage Records
  • Ensure compliance with:
    • Current Good Documentation Practices (cGDP)
    • Current Good Laboratory Practices (cGLP)
  • Maintain complete and audit-ready documentation.

Regulatory Compliance & Quality Systems

  • Perform all activities in compliance with:
    • Good Manufacturing Practices (GMP)
    • Current Good Laboratory Practices (cGLP)
    • Current Good Documentation Practices (cGDP)
    • Internal Quality Systems
    • Regulatory Guidelines
  • Support laboratory inspections and audits.
  • Ensure adherence to quality standards and company procedures.
  • Escalate quality issues and deviations when required.

Laboratory Equipment & Instrument Handling

  • Operate analytical instruments and laboratory equipment as per approved procedures.
  • Ensure proper usage, cleaning, and routine maintenance of laboratory instruments.
  • Report equipment malfunctions and coordinate corrective actions.
  • Support calibration and qualification activities when required.

Cross-Functional Collaboration

  • Work collaboratively with:
    • Quality Assurance
    • Manufacturing
    • Warehouse
    • Engineering
    • Regulatory Affairs
  • Support quality investigations and issue resolution activities.
  • Contribute to achieving departmental and organizational objectives.

Safety & Compliance Responsibilities

  • Follow all safety procedures and environmental requirements.
  • Maintain compliance with:
    • Global Business Ethics and Compliance Program
    • Global Quality Policies
    • Safety & Environmental Policies
    • HR Policies and Procedures
  • Promote safe laboratory practices and a culture of quality.
  • Perform assigned duties in accordance with company values and compliance expectations.

Continuous Improvement

  • Support laboratory efficiency and process improvement initiatives.
  • Identify opportunities to enhance testing processes and documentation practices.
  • Contribute to quality excellence and operational effectiveness.
  • Participate in training and continuous learning activities.

Required Qualifications

Education

One of the following qualifications:

  • Master of Science (M.Sc.)
  • Bachelor of Pharmacy (B.Pharm.)
  • Equivalent Degree in:
    • Pharmaceutical Sciences
    • Chemistry
    • Life Sciences
    • Related Scientific Discipline

Experience

  • Minimum 3–6 years of experience in a GMP-regulated pharmaceutical industry.
  • Experience in:
    • Quality Control Laboratories
    • Raw Material Testing
    • Packaging Material Testing
    • Water Analysis
    • Pharmaceutical Laboratory Operations
  • Experience working in regulated quality environments.