Qa Manager
Social network you want to login/join with: Role Overview Join a leading pharmaceutical company based close to Rome as a Quality Assurance GMP R&D Manager. In this pivotal on-site role, you will spearhead the quality assurance initiatives, ensuring the highest standards of GMP compliance within a dynamic and forward-thinking environment. Key Duties and Responsibilities Champion the development and maintenance of a robust company-wide quality system, aligning with current GMP regulations. Oversee the analysis and processing of technical documents, ensuring adherence to internal and regulatory standards. Lead the creation and revision of master batch records for experimental medicinal products, guaranteeing compliance with product specifications and quality benchmarks. Conduct meticulous batch record reviews and document evaluations, upholding the integrity of the Oral Solids R&D Pilot Plant operations. Role Requirements A degree within Pharmacy, Chemistry, Engineering, or a related field. Extensive experience in Quality Assurance within the GMP sphere, particularly with Oral Solids and APIs. A track record of managing people effectively and a pragmatic approach to problem-solving. Proficiency in English and Italian, with exceptional communication skills, coupled with strong organizational and negotiation abilities. J-18808-Ljbffr
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