TRD Quality Process & Engineering ManagerJob ID: 394643BR
Date: Sep 09, 2024
Location: Italy
SummaryThe TRD Quality Process & Engineering Manager will collaborate with the RLT Engineering organization for RLT TRD to establish, maintain, and improve the engineering processes concerning buildings, equipment, utilities, and energy. This role includes oversight of operational and validation activities and continuous process improvements.
About the RoleKey Responsibilities: Support a discipline and/or provide a service individually or within a team of associates. May provide functional expertise to Line Unit and other QA Units in the area of responsibility.Write, review, decide on approval, and release GMP-relevant deliverables and/or related tools as per area of responsibility to ensure compliance with cGMP and project quality deliverables.Manage project-related activities (e.g., TRD product portfolio, development of new tools, processes, Quality initiatives, Quality Manual implementation, Quality Plans, Quality Risk Assessments, training activities, qualification and facility upgrade activities, IT validation projects) as per area of responsibility.Support Project management functions as a project team member.Provide support to TRD line functions in GMP-related topics as per area of responsibility.Comply with internal and external guidelines regarding quality and safety (Quality Manual, regulatory cGMP guidelines, Health Authority guidance, SOPs, etc.).Ensure manufacturing processes, facilities, equipment, and software are properly qualified and validated for GMP use.Generate and maintain VMP to ensure all facility, equipment, process, utilities, analytical methods, cleaning, and computerized systems are qualified in compliance with regulations, standards, and specifically with GMP.Oversee external parties responsible for maintenance and qualification/re-qualification of pilot plant areas and equipment.Review and approve URS, DQ, IQ, OQ, and PQ documentation.Drive continuous quality improvement program for aseptic manufacturing operations and partner with production, engineering, and supply chain teams to implement/optimize to improve efficiency (right the first time) and monitor/escalate as needed.Ensure review, decision, and approval of all GMP deliverables.Approval of the whole set of documents in the area of analytical instruments and production equipment qualification and operation.Approval of equipment periodic reviews.Approval of Change Controls (CCP).Review/Approval of Deviations, Actions, CAPAs, and Quality Events.Support for inspections preparation.Review of SOPs in ESOPS D2.Fluent in Italian and English.Communication skills to sufficiently address GMP and logistic-related questions with line unit experts. Scientific, technical, and regulatory knowledge in a specific area.Basic knowledge of drug development.Detailed knowledge of cGMP, working knowledge of safety and environmental regulations and guidelines. Good organizational skills.Why Novartis? Our purpose is to reimagine medicine to improve and extend people's lives, and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: Novartis People and Culture You will receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook: Benefits and Rewards Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: Novartis Network
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