Site Process Engineer

05 ago - Parma
Chiesi Group_Disabled

Questa posizione è in Chiesi Group disabled Il processo di selezione sarà interamente gestito Chiesi Group disabled.
-- 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 Agevolazioni 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.
Chiesi Global Manufacturing Division 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 ****, 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 ****, 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 The person will be responsible for the definition, optimization and control of production processes, constantly seeking greater efficiency and effectiveness of industrial plants to ensure the continuous improvement and business continuity of each department involved.




You will be responsible for Evaluating existing manufacturing processes and identifying areas for improvement and how to improve Developing and implementing systems and strategies to improve efficiency and reduce costs Designing, running, testing and upgrading systems and processes Creating process simulations and conducting risk assessments and related remediation, if any Performing process analysis and making recommendations for improvement Providing technical support and training to staff and junior engineers Ensuring that all processes and procedures comply with safety and environmental regulations Working closely with other specialists, including engineers and scientists, to develop processes Documenting all created processes and updating and maintaining these documents as changes occur Collect data and monitor the progress of processes Adapt the plants to current regulations, in terms of risk prevention and safety, reduction of environmental impact, use of energy sources Manage the construction, installation and operation of the installationsDevelop best practices, routines, and innovative solutions to improve production rates and quality of output Provide process documentation and operating instructions Provide process and equipment design, process optimization, and troubleshooting Manage cost and time constraints You will need to have Previous experience in roles within the pharmaceutical industry At least 5 years of working experience in pharmaceutical industry (manufacturing environment) Bachelor's degree or higher in Engineering/Science preferred in process engineering, chemical engineering, mechanical engineering, automation technology or a similar discipline.
Good command of English language Proficiency with Microsoft Office package, CAD and SAP Leadership and social influence Planning and organizational skills Innovative

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