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Sterile Supervisor

Job in Milan, Lombardy, Italy
Listing for: Chiesi Group
Full Time position
Listed on 2026-10-12
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Regulatory Compliance Specialist, Validation Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 39000 EUR Yearly EUR 39000.00 YEAR
Job Description & How to Apply Below
Questa posizione è in Chiesi Group

Il processo di selezione sarà interamente gestito Chiesi Group.

-
- # Sterile Supervisor

** Date:
** 30 Jul 2026

** Department:
** Plant Operations Italy, Parma 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
** 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 coach operators in cleanroom…
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