Secondary Packaging pMDI Supervisor

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Department:
Plant Operations Italy, Nerviano Site
Business Area:
Industrial Operations & HSE
Job Type: Direct Employee
Contract Type:
Permanent

Location:

Milano, IT

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   Global Technical Operations & Supply (Global Tech Op&S) 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 Tech Op&S 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.
This is what you will do   We are seeking an experienced and highly motivated Secondary packaging Production Supervisor to join a unique greenfield project focused on biologics manufacturing.

This role offers the opportunity to contribute not only to daily manufacturing operations, but also to the design, implementation, and start‑up of a cutting‑edge secondary packaging 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 GMPcompliance.
Support layout review, equipment URS definition, and operational input during design and procurement phases.
Participate in FAT/SAT, commissioning, and qualification activities for packaging 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.
Operational Phase
Supervise day-to-day manufacturing operations related to secondary packaging
Ensure compliance with internal EHS and quality requirements
Lead and coach operators in GMP behaviour and ALCOA+ principles.
Monitor production performance, deviations, and investigations; drive timely resolution and continuous improvement.
Support inspection readiness activities.
Promote a strongquality and safety culture within the department.
You will need to have    Degree in Biotechnology, Pharmacy, Biology, Chemical Engineering, or related scientific disciplines
Minimum3–5 years of experience in secondary packaging manufacturing.
Knowledge of GMP, GDP and regulatory requirements applicable to pharmaceutical packaging.
Familiarity withprocess validation and equipment qualification
Strong documentation and deviation management capabilities
We would prefer for you to have    Experience…