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.
**The Scientist Support Intern has the task of supporting the figure of the Scientist in the management of activities necessary for the execution of projects intended for the production of sterile pharmaceutical products. In particular, the SSI will have the task of supporting the Scientist in the daily activities of selecting and handling materials for production, the forms necessary for the project, the loading/approval of manufacturing documentation (e.g. MBR) into the system and the writing of documents.**
**2. SPECIFIC TASKS/PRIMARY ACTIVITIES**:
- **Generation of forms in accordance with SOP for the creation of registry codes and management of materials**:
- **System loading and authorization of MBRs**:
- **Carry out the relevant activities, check their progress, all through the correct planning of daily activities, in compliance with the priorities defined by your superior and the company quality standards.**:
- **Ensure the correct management of the relevant documentation, also ensure the archiving and traceability of the data, whether of internal or external origin, according to current procedures, company quality standards and in compliance with the relevant protocols.**:
- **Participate in internal and external meetings (if necessary).**:
- **Participate in the design and development of the processes by supporting the formulation development activities and the freeze-drying process in support of the Scientist (if necessary).**:
- **Report the progress of the activities under your responsibility to the PDS Manufacturing Sciences Supervisor**
**3. REPORTS**:
- **Operations/Production**:
- **Analytical Development**:
- **Formulation Development**:
- **Quality Assurance**:
- **Project Manager**:
- **Logistics**:
- **Customers (if necessary)**:
- **Suppliers (if necessary)**
**4. REQUIREMENTS AND QUALIFICATIONS**:
**Studies/Diplomas/Training courses**:
- **Graduating in CTF, Chemistry, Chemical Engineering, Biotechnology or other similar experience**
**Technical and IT knowledge**:
- **Knowledge of cGMP and production of sterile products**:
- **Knowledge of the main software (Office package, statistical analysis programs)**
**Professional experiences**:
- **Experience in the development and manufacturing process of sterile liquid and freeze-dried products (nice to have)**
**Languages**:
- ** English**:
- ** Italian**
**Personality Traits**:
- ** Autonomy in managing your own work/Accountability**:
- ** Responsibility**:
- ** Flexibility**
Join us!