Scientist Support Intern
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 managing 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 if necessary.
2. SPECIFIC TASKS/PRIMARY ACTIVITIES:
- Generation of forms in accordance with SOP for the creation of material 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
- LM+: Receive 1 Project assigned to complete the Research Thesis within 1 year
3. REPORTS:
Interior
- Operations/Production
- Analytical Development
- Formulation Development
- Quality Assurance
- Project Manager
- Logistics
External
- Customers (if necessary)
- Suppliers (if necessary)
4. REQUIREMENTS AND QUALIFICATIONS:
Studies/Diplomas/Training courses:
- Undergraduate in CTF, Chemistry, Biology, Biotechnology and others
Technical and IT knowledge:
- Knowledge of cGMP
- 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
Languages:
- English/Italian
Personality Traits:
- Autonomy in managing your own work
- Responsibility
- Availability
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