ph3About us /h3pChiesi 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 Agevolazioni 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. /ph3Global Technical Operations Supply /h3pGlobal Technical Operations Supply (Global TechOpS) is Chiesi’s global manufacturing and supply area, responsible for ensuring consistent, outstanding quality, service and value across our end‑to‑end supply chain. Global TechOpS oversees the entire lifecycle of the drug: from process optimization and industrialization, to manufacturing, engineering, quality oversight, and supply chain management. Throughout this journey, Operational Excellence drives continuous improvement. This end‑to‑end model is powered by our four manufacturing sites - Parma (IT), Blois (FR), Santana de Parnaíba (BR), and Nerviano (IT) - together with our Virtual Plant network of external partners. /ph3This is what you will do /h3pWe are seeking a skilled Process Engineer to oversee and optimize pharmaceutical manufacturing processes. This role is responsible for ensuring process efficiency, robustness, and compliance with GMP and regulatory standards, while supporting production, technology transfer, and continuous improvement initiatives.



/ph3You will be responsible for /h3ulliManaging and optimizing pharmaceutical manufacturing processes (drug substance and/or drug product) /liliEnsuring compliance with GMP (Good Manufacturing Practices) and regulatory requirements (e.g., FDA, EMA, ICH) /liliSupporting process validation activities (IQ/OQ/PQ) and ongoing process verification (CPV) /liliSupporting technology transfer from development to manufacturing sites engineering point of view /liliMonitoring process performance using data analysis and implement improvements /liliInvestigating deviations, non-conformances, and implement CAPA (Corrective and Preventive Actions) /liliCollaborating with cross-functional teams including Manufacturing, Quality Assurance, Validation, and HSE /liliContributing to process risk assessments (e.g., FMEA) and control strategies /liliSupporting audits and regulatory inspections /liliDriving/Supporting continuous improvement initiatives /liliEnsuring proper documentation in line with GMP standards /li /ulh3You will need to have /h3ulliBachelor’s or master’s degree in chemical engineering, Pharmaceutical Engineering, or related field /liliAt least 6 months of experience in manufacturing or process engineering /liliStrong problem-solving and organizational skills /li /ulh3We would prefer for you to have /h3ulliExperience in pharmaceutical company and/or GMP environments /liliExperience with process validation and manufacturing support /liliGood understanding of data analysis and process monitoring tools /liliFamiliarity with Process Analytical Technology (PAT) and Quality by Design (QbD) /liliExperience with digital systems (e.g., MES, SAP, LIMS)



/liliExposure to technology transfer projects /li /ulh3Key Skills /h3ulliProcess optimization and troubleshooting /liliData analysis and statistical thinking /liliRegulatory compliance and documentation /liliCross-functional collaboration /liliTime and project management /liliCommunication and stakeholder management /li /ulh3Location /h3pParma /ph3Compensation Range /h3pThe minimum salary for this role is €39.760, aligned to our established salary framework. The final offer will reflect the candidate’s skills, experience, qualifications and internal equity considerations. /ppThe package outlined above is based on the rolebeing located inItaly. Where the role is offered in a different country, the applicable salary,bonusand benefits will be aligned to the relevant local market and internal frameworks. /ppIn addition, we offer a comprehensive benefits package includingpension, private medical insurance, wellbeing programme, flexible benefits programme... /ph3What we offer /h3pNo 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. /ppChiesi 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. /p /p #J-18808-Ljbffr

📌 Site Process Engineer - TEMPORARY (Parma, IT)
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