Dipharma Francis S.r.l
QA Specialist
Job Location
Mereto di Tomba, Italy
Job Description
We are looking for a “ Quality Assurance Specialist ” who will report to the GMP Quality Assurance Manager and who will give his/her contribution to quality policies in support of Quality System. In particular the successful candidate will be responsible for: writing, reviewing and approving documents (SOPs, PQRs, validations etc.); revision of production and quality control batch records; managing GMP QA operations, change control, deviation and documentation systems; identifying and recommending future improvements; implementing action plans; developing quality strategies and priorities and translating them into short and long-term objectives; risk assessment; interacting with other members of the company and customers. The ideal candidate should have: Scientific master degre (ideally in CTF, Chemistry, Biology, etc.) Ideally previous experience in Quality Assurance; Comprehensive knowledge of GMP and other regulations with a good understanding of global quality standards relating to product development, submission and clinical experimentation; A high level of English language, both written and spoken; A high level of attention to detail and with the ability to prioritize working tasks; A strong flexibility in changing tasks and priorities; The ability to work independently as well as coordinate members of his/her team; Excellent interpersonal skills and ability to work in teams.
Location: Mereto di Tomba, Friuli-Venezia Giulia, IT
Posted Date: 7/9/2025
Location: Mereto di Tomba, Friuli-Venezia Giulia, IT
Posted Date: 7/9/2025
Contact Information
Contact | Human Resources Dipharma Francis S.r.l |
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