Clinical Trial Manufacturing - 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

The Quality Difference at

Thermo Fisher Scientific:

What makes our quality teams unique is a shared passion for getting it done right the first time and working for the right reasons with our customers always in mind.

Our team of Quality professionals understand our customers rely on the accuracy, safety, and effectiveness of our products and services that are improving lives around the world.

When you join our team of quality professionals, you'll collaborate on projects on a global scale while being encouraged to grow your skills and discover new career paths with us.

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, increasing productivity 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 unrivaled 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 CTM Intern.

You will join a newly-built and pioneering 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 support 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 attitude 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

To support the Scientist group in the uploading and approval of Documentation for the execution of Manufacturing batches (Protocols and MBRs)
To ensure documentation and materials are available prior to the execution of the batches
To improve the process knowledge and support the Scientist team in the preparation of Documents for the batches manufacturing (Protocols and MBRs)

Required Skills and Experience

Degree in Chemistry, CTF, Pharmacy, Biotechnology, Biology is a nice to have
Experience with drugs formulation, lab batch manufacturing and Good Laboratory Practices (GLP)
Good Language Skills (English required) writing and speaking
Strong communication and teamworking skills
Experience with GMP documentation (Protocols, MBRs and Reports) (It is a PLUS)

This role offers the opportunity to grow as a Formulation and Preparation Expert.

It gives the opportunity to develop new skills in laboratory batches execution, being able to support the Scientist team in developing new processes for our Clients.

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.

Join U