Process Development Associate Director
3 giorni fa
At Dompé Farmaceutici, we are not just a pharmaceutical company, we are an innovation-driven organization with over 130 years of experience, committed to advancing science and improving human health.About the Role:The Process Development Associate Director leads technology transfer projects from development to clinical manufacturing, ensuring compliance with GMP and regulatory standards while driving operational excellence and timely delivery.Responsibilities:Lead technology transfer activities for drug product from laboratory to pilot/industrial scale for clinical production.Support late-phase development and transfer of new product/processes to commercial manufacturing sites.Ensure compliance with GMP, ICH guidelines, and global regulatory requirements throughout the transfer process.Support manager in develop and implement transfer strategies, including timelines, resource planning, and risk mitigation plans.Coordinate cross-functional teams (R&D, Manufacturing, Quality Assurance, Regulatory Affairs) to guarantee seamless execution.Identify and activate new CDMO for clinical batch production.Oversee scale-up and process validation (where required) ensuring robust and reproducible manufacturing processes.Manage technical documentation, including protocols, reports, and knowledge transfer packages.Act as primary liaison between internal stakeholders and external partners/CDMOs for project alignment and issue resolution.Support CMC team in preparing documentation for IND, BLA, or NDA submissions.Drive continuous improvement initiatives to optimize tech transfer processes and reduce operational risks.Support global supply chain objectives, ensuring timely delivery and cost efficiency.Qualifications:Advanced degree (Master's or Ph.D.) in Pharmaceutical Sciences, Chemical Engineering, Biotechnology, or related field.Required Skills:Languages: Italian & English (fluent);Knowledge of the main productivity and collaboration tools (Google Workspace, MS Office);Strong knowledge of GMP, ICH guidelines, and global regulatory requirements.Expertise in process development, scale-up, and validation for drug substance and drug product.Familiarity with aseptic processing, biologics manufacturing, and analytical methods.Proficiency in project management tools and risk assessment methodologies.
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Process Development Associate Director
3 giorni fa
L’Aquila, Italia Dompé A tempo pienoAt Dompé Farmaceutici, we are not just a pharmaceutical company, we are an innovation-driven organization with over 130 years of experience, committed to advancing science and improving human health.About the Role:The Process Development Associate Director leads technology transfer projects from development to clinical manufacturing, ensuring compliance...
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Process Development Associate Director
3 settimane fa
L’Aquila, Italia Dompé A tempo pienoAt Dompé Farmaceutici, we are not just a pharmaceutical company, we are an innovation-driven organization with over 130 years of experience, committed to advancing science and improving human health.About the Role:The Process Development Associate Director leads technology transfer projects from development to clinical manufacturing, ensuring compliance...
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Process Development Associate Director
3 settimane fa
L’Aquila, Italia Dompé A tempo pienoAt Dompé Farmaceutici, we are not just a pharmaceutical company, we are an innovation-driven organization with over 130 years of experience, committed to advancing science and improving human health.About the Role: The Process Development Associate Director leads technology transfer projects from development to clinical manufacturing, ensuring compliance...
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Performance, Learning
7 giorni fa
L’Aquila, Italia Altro A tempo pienoPerformance, Learning & Development SpecialistJoin to apply for the Performance, Learning & Development Specialist role at Toto Costruzioni Generali.TOTO S.p.A. Costruzioni Generali contributes to the growth and improvement of infrastructure in countries and communities for 60 years. We are a part of a leading industrial group in Italy, committed to...
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Performance, Learning
6 giorni fa
L’Aquila, Italia Toto Costruzioni Generali A tempo pienoPerformance, Learning & Development Specialist Join to apply for the Performance, Learning & Development Specialist role at Toto Costruzioni Generali. TOTO S.p.A. Costruzioni Generali contributes to the growth and improvement of infrastructure in countries and communities for 60 years. We are a part of a leading industrial group in Italy, committed to...
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Performance, Learning
7 giorni fa
L’Aquila, Italia Altro A tempo pienoPerformance, Learning & Development Specialist Join to apply for the Performance, Learning & Development Specialist role at Toto Costruzioni Generali.TOTO S.p.A. Costruzioni Generali contributes to the growth and improvement of infrastructure in countries and communities for 60 years. We are a part of a leading industrial group in Italy, committed to...
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Geospatial Technician
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L’Aquila, Italia XML International A tempo pienoGeospatial Information TechnicianLocation:Brindisi (Italy), Valencia (Spain), orRemote within EMEA Start Date:January 2026 Contract:6 months with possible extensions ⏳Applications open until:6 December 2025About the OpportunityDo you enjoy transforming complex data into meaningful maps?Do you want to work on projects where geospatial technology drives...
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L’Aquila, Italia Altro A tempo pienoThe Category Manager (CM) supports one or several procurement categories and works in close relation with the relevant Global Category Managers (GCM), the Categories Team Leader (CTL) and the Tactical Buyer (TB). All CM actions have to be aligned with the strategy defined by the GCM, and the CM will have a regular feedback loop with the GCM. The CM’s prime...
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Regulatory Affairs CMC
5 giorni fa
L’Aquila, Italia Dompé A tempo pienoDompé farmaceutici is an international biopharmaceutical company involved in all activities of the pharmaceutical value chain, from research to development, production and marketing.For our office in L'Aquila we are looking for a Regulatory Affairs CMC & Site Regulatory. The Regulatory Affairs CMC & Site Regulatory Specialist manages regulatory bodies,...
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Regulatory affairs cmc
3 giorni fa
L’Aquila, Italia Dompé A tempo pienoDompé farmaceutici is an international biopharmaceutical company involved in all activities of the pharmaceutical value chain, from research to development, production and marketing.For our office in L'Aquila we are looking for a Regulatory Affairs CMC & Site Regulatory. The Regulatory Affairs CMC & Site Regulatory Specialist manages regulatory bodies,...
