Director of Quality Control

The QC Director will be responsible for overseeing all aspects of the Quality Control department, ensuring compliance with GMP regulations and maintaining the highest standards of quality across all processes and products.

This role involves managing large teams, providing strategic direction, and guiding employees to achieve organizational goals.

Key Responsibilities:

· Lead and manage the Quality Control department (including

Biology, Chromatography, Chemistry, Microbiology laboratories

and Logistics&Data Management QC Team).

· Develop and implement QC policies, procedures, and standards

in compliance with GMP regulations and industry best practices.

· Oversee all QC activities, including raw material testing, in-

process testing, finished product testing, and stability testing.

· Collaborate with other departments, such as Production, Quality

Assurance & R&D

· Guide and mentor managers, providing technical expertise and

fostering a culture of quality and compliance.

· Stay current with industry trends, regulatory changes, and

advancements in QC methodologies.

Qualifications:

· Msc/PhD degree in Chemistry, Biochemistry, Pharmaceutical

Sciences, or a related field.

· Proven experience in the pharmaceutical industry, with a strong

understanding of GMP regulations and quality control processes.

· Demonstrated ability to manage large departments and guide

managers effectively.

· Strong leadership skills with the ability to inspire and motivate

others.

· Excellent analytical, problem-solving, and decision-making

abilities.