FAQs
What is the work schedule for the PDS QA Project Intern position?
The work schedule is standard from Monday to Friday.
What environmental conditions should I be aware of?
Adherence to all Good Manufacturing Practices (GMP) and Safety Standards is required, in addition to working in an office environment.
What type of team will I be joining as a PDS QA Project Intern?
You will join the Quality operation team dedicated to supporting the Pharmaceutical Development Service Unit.
What responsibilities will I have in this role?
You will be responsible for ownership of project meetings, managing QA-related topics, organizing meetings with clients, reviewing deviations, contributing to quality objectives, responding to client inquiries, and generating documentation for batch release.
What skills are required for this internship?
A degree in Chemistry, CTF, Biological Sciences, or similar fields is required, along with good problem-solving abilities, excellent communication and teamwork skills, and the ability to prioritize under time constraints.
What languages do I need to speak for this position?
Proficiency in both Italian and English is required.
Will I have interactions with clients and regulatory authorities?
Yes, you will participate in customer visits and audits by customers and/or regulatory authorities.
How does this internship contribute to my career growth?
You will build a strong GMP background and effective interpersonal skills while working in a dynamic environment and being involved in meaningful projects that have a positive global impact.
Is this position suitable for recent graduates?
Yes, this position is suitable for recent graduates with a relevant degree and a passion for quality assurance in a pharmaceutical setting.
Will I receive training as part of this internship?
Yes, you will gain hands-on experience and training in quality operations and GMP practices while working alongside experienced colleagues.