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Job Title: Head of Quality Control - Pharmaceutical Industry

QC manager

Key Responsibilities

• Lead and oversee the Quality Control department, including chemical and microbiological laboratories
• Ensure all analytical testing is conducted in compliance with GLP, EU GMP, and relevant regulatory requirements
• Supervise and perform analyses using HPLC, GC, LC-MS/MS, GC-MS, and ICP-MS
• Develop, validate, and implement pharmacopoeial methods (e.g. Ph. Eur., USP)
• Prepare and support EU GMP inspections, audits, and regulatory submissions
• Maintain, review, and approve QC documentation, including analytical methods, specifications, and SOPs
• Monitor laboratory performance and ensure accurate and timely release of materials and products
• Provide training, mentorship, and performance evaluations for QC personnel
• Oversee and support the microbiology laboratory in testing and environmental monitoring
• Collaborate closely with QA and Production, to ensure smooth cross-functional operations
• Drive continuous improvement initiatives within the QC function
• Ensure proper calibration, qualification, and maintenance of analytical instruments

Qualifications

• Degree in Pharmaceutical Sciences, Chemistry, Biochemistry, or a related field
• Minimum 5 years of experience in pharmaceutical QC within an EU-GMP environment
• Hands-on experience with HPLC, GC, LC-MS, GC-MS, and ICP-MS
• In-depth knowledge of European Pharmacopoeia (Ph. Eur.), USP, and method validation principles
• Experience with EU GMP inspections and audit readiness
• Strong leadership and organizational skills, with ability to manage multiple priorities
• Detail-oriented with excellent problem-solving and decision-making abilities
• Fluent in English

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