Head of Quality Control - Pharmaceutical Industry

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Job Title: Head of Quality Control - Pharmaceutical Industry

Job Summary:

The Head of Quality Control in the pharmaceutical industry is a leadership role responsible for overseeing and managing all aspects of the quality control function. This includes developing and implementing quality control strategies, ensuring compliance with regulatory standards, and driving continuous improvement initiatives. The role involves leading a team of quality professionals to maintain the highest standards in pharmaceutical product testing and analysis.

Key Responsibilities:

  1. Strategic Leadership:
    • Provide strategic direction for the quality control function, aligning with organizational goals and regulatory requirements.
    • Develop and implement a vision for the continuous improvement of quality control processes.
  2. Team Management:
    • Lead, mentor, and manage a team of quality control professionals.
    • Foster a culture of excellence, teamwork, and continuous learning within the quality control department.
  3. Analytical Testing Oversight:
    • Oversee and coordinate all activities related to analytical testing of raw materials, intermediates, and finished products.
    • Ensure that testing procedures are in compliance with regulatory requirements and industry standards.
  4. Method Validation and Development:
    • Lead efforts in the development and validation of analytical methods.
    • Stay abreast of emerging technologies and methodologies in analytical testing and incorporate them as appropriate.
  5. Instrumentation and Equipment Management:
    • Ensure the proper functioning, calibration, and maintenance of analytical instruments and equipment.
    • Stay informed about advancements in analytical technology and recommend updates or new acquisitions.
  6. Quality Documentation:
    • Establish and maintain accurate and detailed records of all quality control activities.
    • Review and approve documentation related to analytical testing and method validation.
  7. Regulatory Compliance:
    • Stay current with applicable regulatory requirements (e.g., FDA, EMA) and industry guidelines.
    • Ensure that quality control processes align with regulatory expectations and are inspection-ready.
  8. Continuous Improvement:
    • Identify opportunities for process improvement within the quality control laboratory.
    • Implement initiatives to enhance efficiency, accuracy, and overall effectiveness.
  9. Collaboration with Cross-Functional Teams:
    • Collaborate with manufacturing, quality assurance, regulatory affairs, and other relevant departments.
    • Provide support during regulatory inspections and audits.

Qualifications and Experience:

  • Bachelor's or advanced degree in Pharmaceutical Sciences with specialization in quality control.
  • Extensive experience in pharmaceutical quality control, including leadership roles.
  • Strong knowledge of analytical techniques and instrumentation.
  • Experience with method validation and development.
  • Familiarity with cGMP (Current Good Manufacturing Practice) regulations.
  • Excellent organizational, communication, and problem-solving skills.
  • Leadership experience with the ability to inspire and develop a high-performing team.


Additional information: Candidates who meet the above conditions can send their CVs to email:  [најави се за да го видиш е-маилот]

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