PpSelect how often (in days) to receive an alert: /ph3bRD Manufacturing Technology Transfer Manager /b /h3pDate: Jan 20, 2026 /ppDepartment: GTD Global Technical Development /ppJob Type: Direct Employee /ppBusiness Area: RD, Pharmacovigilance Regulatory Affairs /ppContract Type: Permanent /ppLocation: Parma, IT /ppbAbout us /b /ppChiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular purpose: promoting a healthier world for our people, patients, and the planet. This is what drives us as we research, develop, and market innovative drugs across our main therapeutic areas. Discover more here. /ppAt Chiesi we are thinking generations ahead, driving sustainable innovation with purpose. This fosters a culture of reliability, transparency, and ethical behaviour at every level. As a Benefit Corporation and a certified B Corp, we have embedded sustainability in our bylaws and continuously measure our impact. /ppDiversity and inclusion are at the heart of who we are. We believe our differences make us stronger. We are a vibrant ecosystem of passionate, talented individuals united by strong values, each bringing unique perspectives that help us to continuously challenge the status quo for the better. /ppbChiesi Research Development /b /ppOur RD team represents a fundamental asset for the business. It is divided into integrated functional areas focusing on pipeline projects including discovery and preclinical research, global technical development, drug delivery technology, clinical development, regulatory affairs, pharmacovigilance, intellectual property, quality assurance, RD project and portfolio management. Headquartered in the new purpose-built and fully integrated Research and Development Centre in Parma (Italy), the team also has important operations in Paris (France), Chippenham (UK), Cary (US), Stockholm (Sweden), Toronto (Canada) and Shanghai (China). /ph3bWho we are looking for /b /h3h3bThis is what you will do /b /h3pIn this role, you will lead and coordinate technical teams, laboratories, and equipment to support formulation and manufacturing process development activities, from laboratory to industrial scale, for MDIs and liquid dosage forms, including technology transfer. You will play a key role in advancing innovative technologies to support pipeline projects, while ensuring the highest standards of compliance with GMP/cGMP and HSE requirements across facilities, documentation, and personnel. /ph3bYou’ll be responsible for: /b /h3ulliLead and develop technical personnel, ensuring adequate project support in formulation and manufacturing process development, while promoting continuous technical, scientific, and soft-skills growth in compliance with GMP/cGMP, quality, and safety regulations (including D. Lgs 81/08). /liliOversee laboratories, rooms, and equipment, ensuring efficient use and full compliance with company, quality, safety, and regulatory requirements. /liliSupport planning, manufacturing, and evaluation of development batches, contributing to process development, scale-up, and technology transfer in collaboration with scientific teams. /liliPromote the application of QbD, QRM, PAT, and Lean/6σ approaches to enhance process understanding and robustness. /liliSupervise the development and implementation of new technologies to support innovation and pipeline projects. /liliEnsure compliance with regulatory and quality requirements by reviewing technical documentation, supporting change control, and contributing to quality investigations (deviations, OOS, complaints), while managing laboratories in accordance with Health Authority authorizations. /liliContribute to budget planning for laboratory equipment and investments. /li /ulh3bYou will need to have /b /h3ulliScientific degree (preferably Biotechnology, Chemical Engineering, chemistry, CTF or pharmacy). /liliSignificant experience (≥ 6 years) in technical development of pharmaceutical products. /liliExperience in sterile liquids manufacturing. /li /ulh3bTechnical Skills /b /h3ulliStrong knowledge of key manufacturing methods and of the main techniques for technological characterization and process control of different pharmaceutical dosage forms, with particular focus on biological products. /liliSolid knowledge of technology transfer processes and the industrialization of new products. /liliGood capability to lead new technological implementation projects and the introduction of new systems. /liliProficiency in statistics and its application to drug manufacturing processes. /liliGood understanding of QbD (Quality by Design) approach and PAT (Process Analytical Technology) methodologies. /liliKnowledge of GMP/cGMP, safety, ISO standards, and key European and U.S. pharmaceutical regulations. /liliGood command of English (both written and spoken). /li /ulh3bPower Skills /b /h3ulliLeadership and influence; /liliSound decision-making and results orientation; /liliEffective planning and execution; /liliCollaboration and team building; /liliResilience and learning agility. /li /ulh3bLocation /b /h3pParma /ppbWhat we offer /b /ppNo matter where your path starts at Chiesi, it leads to inspiring possibilities. Your future is our focus, and we are committed to nurturing your development in our dynamic, friendly environment with access to resources and training every step of the way. /ppWe provide top-class benefits, including comprehensive healthcare programs, work-life balance initiatives, and robust relocation support. Our salary package is competitive, comprising a basic salary, performance bonuses, and benefits benchmarked against the external market. Additionally, we offer flexible working arrangements, remote work options, and tax assistance services for foreign colleagues, all designed to help you thrive. /ppbChiesi is an equal opportunity employer committed to hiring a diverse workforce at all levels of our business. All qualified applicants receive consideration for employment based on attitude and merit, without regard to race, national origin, age, sex, religion, disability, sexual orientation, marital status, military status, gender identity or expression, or any other basis protected by applicable laws. This policy applies to all aspects of employment, including hiring, transfer, promotion, compensation, eligibility for benefits, and termination. /b /ph3Discover all our opportunities /h3h3Screen readers cannot read the following searchable map. /h3 /p #J-18808-Ljbffr