QC Head Pharmaceutical Industry

Company Description Atco Pharma is a well-established pharmaceutical company serving both human and veterinary health care markets, and is ranked among the leading manufacturers in Egypt. The company produces a broad range of therapeutic products in facilities that operate according to Good Manufacturing Practice (GMP) standards. Atco Pharma also follows ISO guidelines, underscoring its systematic approach to quality, safety, and consistency. In 2015, the company received the International Quality Crown Award in recognition of its commitment to excellence. Atco Pharma is dedicated to improving health and well-being by delivering reliable, effective, and high-quality pharmaceutical solutions.Role Description The QC Head – Pharma Industry is a full-time, on-site role based in Markaz Qowesna, responsible for leading and managing all Quality Control activities within the manufacturing site. This role oversees daily operations of the QC laboratory, including planning and supervising testing of raw materials, in-process samples, finished products, and stability studies in compliance with GMP and relevant regulatory requirements. The QC Head ensures timely release of materials and products, reviews and approves analytical results, investigates out-of-specification and out-of-trend results, and implements corrective and preventive actions. The position collaborates closely with Production, Quality Assurance, and Regulatory Affairs to maintain robust quality systems, support audits and inspections, and drive continuous improvement. The QC Head also leads, mentors, and develops the QC team, ensuring adherence to standard operating procedures, data integrity, and safety standards.Qualifications Strong Quality Control and Quality Management skills, with experience leading QC operations in a pharmaceutical manufacturing environment.Proficient Analytical Skills and Laboratory Skills, including familiarity with common analytical techniques and instruments (e.g., HPLC, GC, UV, dissolution).Experience in Quality Assurance practices, including GMP, ISO standards, documentation control, and handling audits and regulatory inspections.Demonstrated ability to manage, train, and motivate cross-functional QC teams, with effective people management and leadership capabilities.Excellent problem-solving, root cause analysis, and decision-making skills, with a focus on data integrity and continuous improvement.Strong written and verbal communication skills, with the ability to prepare and review technical reports, SOPs, and validation documentation.Bachelor’s or higher degree in Pharmacy, Chemistry, Pharmaceutical Sciences, or a related field; advanced qualifications or professional certifications in quality are an advantage.Proven experience in an on-site pharmaceutical QC leadership role, preferably within solid dosage, sterile, or veterinary product manufacturing.