Sterile Supervisor, Nerviano Site

Questa posizione è in Chiesi Groupdisabled

Il processo di selezione sarà interamente gestito Chiesi Group disabled.

Questa opportunità è disponibile in Nerviano - Italy, Milano - Italy.

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About us Chiesi 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.)( At 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. Diversity 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. Global Technical Operations & Supply Chiesi Group has three production plants: Parma (Italy), the strategic hub for the production and distribution of our products, serving as an international supply center with exports to over 80 countries. Here, solid medicines such as tablets and dry powders for inhalers, solutions and suspensions for inhalations and sterile suspension vials for endotracheal administration are produced. In 2024, a new Biotech Centre of Excellence has launched in Parma. The new facility is dedicated to developing and producing monoclonal antibodies, enzymes, and other proteins. Blois-La Chaussée Saint Victor plant (France), a center of excellence specializing in the production of Dry Powder Inhalers and Metered Dose Inhalers (MDIs). The site manages direct distribution to customers in the French market and exports to other markets, effectively meeting both local and international needs. Santana de Parnaiba (Brazil), specialized in the production of pressurized solutions and suspensions for inhalation therapy (pMDIs). Additionally, it has an area dedicated to nasal sprays for the European market. Santana produces pressurised solutions and suspensions for inhalation therapy (MDI). In 2025, a new investment in Nerviano (Italy) has been announced with the construction of a new facility which will be primarily dedicated to manufacturing carbon minimal inhalers (reinforcing the company’s commitment to both patients’ health and sustainable healthcare solutions), dry powder inhalers and sterile biological products. Who we are looking for

This is what you will do

We are seeking an experienced and highly motivated Sterile Production Supervisor to join a unique greenfield project focused on biologics manufacturing . This role offers the opportunity to contribute not only to daily sterile operations, but also to the design, implementation, and start-up of a next-generation sterile production department . The successful candidate will play a key role in shaping processes, supporting equipment and facility design decisions, and establishing operational standards for a biologics manufacturing environment. This is a rare opportunity to be part of a site built from the ground up , contributing to technical excellence, compliance, and long-term operational success.

You will be responsible for

Project & Start-up Phase

• Contribute to process and facility design discussions , ensuring manufacturability and GMP compliance.
• Support layout review, equipment URS definition, and operational input during design and procurement phases.
• Participate in FAT/SAT, commissioning, and qualification activities for sterile biologics manufacturing lines.
• Collaborate with MS&T, Engineering, QA, and Validation teams to define robust operational workflows.
• Contribute to the development of SOPs, batch records, training programs, and aseptic practices .

Operational Phase

• Supervise day-to-day sterile biologics manufacturing operations (e.g., aseptic processing, filtration, filling, formulation).
• Ensure compliance with GMP, Annex 1, and aseptic processing standards .
• Lead and coac