Quality Assurance Senior Specialist - Pharmaceutical sector

• Responsibility for GMP manufacturing area, conducts GMP internal and external audits, monitors and records inconsistencies with quality procedures and norms
• Provides information, support and guidance to team within the scope of the functional unit
• Initiates and coordinates CAPA issuance and resolution
• Contributes to ISO 9001, ISO 13485 audits and assist with ISO 9001, ISO 13485 program documentation and implementation
• Acts independently for product disposition, release or reject. Responsible for ensuring that each individual batch has been manufactured and tested in accordance with defined release procedures. Interacts with various departments in communicating QA standards

• A modern workplace built on trust and valued partnerships within a stable company
• Competitive remuneration based on performance, including an annual bonus and recognition awards
• Above-standard benefits such as a comprehensive employee assistance program, learning platforms, private healthcare, and more.
• Opportunities for professional development through various training programs in business, technical skills, and soft skills
• Join a multinational corporation that offers an exciting and diverse working environment for engineers, technicians, chemists, and professionals alike
• If you’re ready to make an impact in the world of supply chain management, we want to hear from you

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