Jobs at MSVL Group

Qualifications, Skills and Experience 

• Minimum Master's degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related scientific field. hat is
• Minimum 10 years of experience in QA/QC management, including at least 5 years in a senior management role.
• Proven experience in quality management within the pharmaceutical manufacturing industry.
• Strong knowledge of WHO GMP, EU GMP, cGMP, regulatory compliance, and pharmaceutical quality management systems.
• Experience in regulatory inspections, audits, CAPA, validation, quality risk management, and product release processes.
• Strong leadership, strategic planning, analytical, problem-solving, and stakeholder management skills.
• Excellent communication, organizational, and team management abilities.
• Proficiency in Microsoft Office and quality reporting systems.

Key Responsibilities

• Develop and implement quality policies, strategies, SOPs, and quality management systems in compliance with WHO GMP, EU GMP, and regulatory requirements.
• Oversee QA/QC operations, product quality, batch documentation, and final product release or rejection.
• Lead internal audits, self-inspections, supplier audits, and regulatory inspections, ensuring timely closure of findings and CAPA implementation.
• Manage validation, qualification, quality risk assessments, investigations, deviations, complaints, and product recalls.
• Ensure compliance with cGMP, GDocP, data integrity principles (ALCOA), and applicable statutory requirements.
• Monitor quality performance, compliance trends, departmental KPIs, budgets, and continuous improvement initiatives.
• Lead, train, and develop quality teams while ensuring effective resource planning and departmental performance.
• Coordinate with senior management, regulatory authorities, external auditors, and internal departments on quality and compliance matters. 

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Qualifications, Skills and Experience

• Bachelor's degree in Chemistry, Pharmacy, Pharmaceutical Sciences, Microbiology, Laboratory Technology, or a related scientific field.
• Minimum 7 years of QA/QC experience in pharmaceutical manufacturing, including at least 5 years in a managerial role.
• Strong experience in pharmaceutical QC testing, analytical methods, laboratory operations, and quality management systems.
• In-depth knowledge of cGMP, GLP, regulatory compliance, SOPS, and pharmaceutical quality standards.
• Experience in method validation, stability studies, equipment qualification, audits, and quality investigations.
• Strong understanding of QC laboratory instruments, analytical equipment, and quality documentation systems.
• Proven leadership, analytical, problem-solving, organizational, and communication skills.
• Proficiency in Microsoft Office and laboratory reporting systems.

Key Responsibilities

• Oversee QC laboratory operations, ensuring timely testing of raw materials, packaging materials, intermediates, and finished products.
• Develop and maintain QC standards, specifications, SOPs, testing procedures, and quality documentation.
• Ensure compliance with cGMP, GLP, regulatory requirements, and data integrity standards.
• Manage analytical method validation, stability testing, equipment calibration, qualification, and laboratory maintenance.
• Review batch records, analytical results, and approve or reject materials and products based on QC findings.
• Lead investigations into deviations, out-of-specification results, customer complaints, and corrective actions.
• Coordinate internal and external audits, regulatory inspections, quality risk management, and continuous improvement initiatives. 
• Manage departmental budgets, laboratory resources, performance targets, and QC team training and development.