Manufacturing Process Tecnologist - Monza, Italia - Thermo Fisher Scientific

Thermo Fisher Scientific

Azienda verificata

Monza, Italia

2 settimane fa

Inviato da:

Piero Bianchi

Reclutatore di talenti per beBee

Descrizione

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of more than $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer.

Whether our customers are accelerating life sciences research, solving complex analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them.

Our distributed team delivers an outstanding combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.

PDS BU at Monza DPD Site is looking for a Clinical and Commercial Manufacturing Process Scientist

You will join a newly-built and state of the art Pharmaceutical Development unit, and as a part of our pilot scale manufacturing department, you will support our Clients in developing new manufacturing processes and technology transfer for small scale/clinical trial sterile production.

In this role you will lead client's projects from a technical standpoint, developing the optimal manufacturing process, defining the equipment needed, and configuring manufacturing equipment to meet production requirements.

A hands-on, determined approach will be key in exceeding client's expectations, and the ability to "think out of the box", coupled with a strong technical experience, will help you in troubleshooting and finding new solutions to problems.

Responsibilities

As the technical owner of the project, defines the materials to be used during the manufacturing of liquid and lyophilized products and decides the manufacturing process flow.
Act as the main point of contact with internal and external partners, leading the approval process.
Prepare the technical documentation required by internal SOP such as Protocol, Report and Master Batch Record
Participate to clinical/commercial batches manufacturing inside PDS sterile suite.
Update the clients about the state of the project, proactively anticipating issue and ensure a timely management of technical problems

Required Skills and Experience

Degree in Chemistry/ CTF/ Biological Sciences or similar fields
At least 2 years of experience in pharmaceutical R&D, in engineering, manufacturing or quality units with liquid and lyophilized sterile injectables
Experience with drugs formulation and aseptic manufacturing process
Experience in drafting GMP documentation such as MRBs (Master Batch Record)
Strong communication and teamworking skills
Ability to organize and lead multiple projects and activities in a highly dynamic environment
Fluent English and Italian

This role offers the opportunity to grow as a technical leader of R&D manufacturing processes with state-of-the-art equipment and, as a client facing role, the chance to directly interact with pharmaceutical companies from all over the world and improve your communication and project management skills.

Thermo Fisher Scientific is an Equal Opportunity Employer.

All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.

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