Gmp Documentation Intern
When you're part of the team at Thermo Fisher Scientific, you'll do important work.
You'll have the opportunity to grow and learn in a culture that empowers your development.
We have created an inclusive, global environment that values the power of diverse talent, backgrounds, and experiences to drive speed, productivity, innovation, and growth.
Our internship program will give you a chance to get real world business experience and build your network before graduation.
We are seeking an energetic, responsible intern to join our growing organization.
In this position, you will be expected to learn the ins-and-outs of our daily routines and procedures.
You will focus on learning how our organization runs, and can be expected to gain valuable insight that can further your interest in your chosen career field.
You will join the Pharmaceutical Manufacturing Plant in Monza to support the Quality Teams.
Leveraging your academic background, you will gain a hands-on experience in a highly dynamic and international manufacturing environment.
During the six-month paid internship, you will focus on the following activities:
- collaborate with colleagues in reviewing SOPs and unsure that are managed in compliance with the qualitative requirements of the procedures in force, protocols and cGMP;
- support colleagues in drafting and approval of the internal documentation (i. e.
loogbok, URS ) through, if needed, the specific company computer system in compliance with corporate and regulations quality standard
**How you will get there**:
- MSc in Pharmacy, CTF, Chemistry or similar scientific fields;
- Fluent English (written and spoken)
- Computer skills: advanced MS Office (Word, Excel);
- Good communication skills, attention to details and procedures
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