Qa Manager

Role OverviewJoin 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 ResponsibilitiesKEY DUTIES AND RESPONSIBILITIES:

Your duties as the Quality Assurance GMP R&D Manager will be varied; however, the key duties and responsibilities are as follows:


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 RequirementsROLE REQUIREMENTS:

To be successful in your application to this exciting role as the Quality Assurance GMP R&D Manager, we are looking to identify the following on your profile and past history:


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.

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