Pds Ctm Intern

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 support client's projects from a readiness standpoint, ensuring the one time delivery of our services, being responsible for the project manufacturing documentation management and archive
A hands-on, goal-driven 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**
- Ensure the correct management meaning uploading and approval of process documentation on main electronic system (i.e MBR, BOM for clinical and engineering batches)
- Management of codes creation to support the readiness of PDS projects
- Ensure the proper project documentation archive
**Required Skills and Experience**
- Strong communication and team-working skills
- GMP, Pharma background, manufacturing of sterile products (preferred)
- Well-organized, detail oriented
This role offers the opportunity to grow as a PDS Manufacturing Documentation Specialist.
You be responsible for the management of process documentation associated to PDS projects and to support the Scientist team in satisfy our Clients request.