QA QC Manager

Position Overview

The QC/QA Manager will be responsible for overseeing the complete Quality Control and Quality Assurance functions across the factory. This includes managing QC laboratory operations, ensuring adherence to quality standards, supervising QA activities, and driving SOP development and documentation for all departments. The ideal candidate must have extensive experience in chemical manufacturing or related industries, along with strong leadership, technical, and compliance management skills.

Key Responsibilities

Quality Control (QC) Responsibilities

• Lead and supervise the QC team to ensure accurate testing, analysis, and reporting of raw materials, intermediates, and finished goods.
• Oversee calibration, validation, and maintenance of analytical instruments (HPLC, GC, UV, KF, etc.).
• Ensure compliance with internal quality standards, regulatory guidelines, and customer specifications.
• Review and approve COAs, test results, and QC reports.
• Investigate quality deviations, OOS/OOT results, and ensure timely CAPA implementation.
  

Quality Assurance (QA) Responsibilities

• Oversee the development, revision, and implementation of SOPs for all departments across the factory.
• Ensure robust documentation practices in accordance with ISO, GMP, and regulatory requirements.
• Conduct internal audits, quality compliance checks, and ensure closure of audit observations.
• Manage document control, change control, deviation handling, and CAPA systems.
• Ensure batch manufacturing and packing records are properly reviewed and approved.
• Coordinate with production, QC, R&D, and other cross-functional teams on quality matters.
  

Team Management & Leadership

• Lead a team of QC/QA professionals with strong focus on mentoring, performance monitoring, and skill development.
• Ensure smooth day-to-day functioning of QC lab and QA department.
• Foster a culture of continuous improvement and compliance.
  

Required Qualifications & Experience

• Bachelors or Master’s degree in Chemistry, Analytical Chemistry, Industrial Chemistry, or related fields.
• 20+ years of experience in QC/QA functions within chemical, pharmaceutical, or life sciences manufacturing industry.
• Minimum 5 years of experience in a Managerial position with proven team-handling skills.
• Strong knowledge of regulatory requirements such as ISO, GMP, GLP, and quality management systems.
• Expertise in documentation, SOP preparation, audit handling, and compliance activities.
• Hands-on experience with analytical instruments and QC lab operations.
• Excellent communication, leadership, and problem-solving skills.