Job Title: GMP QUALITY ASSURANCE SPECIALIST
Department: QA
Philogen S.p.A. is looking for a GMP Quality Assurance Specialist who will report to the GMP Quality Assurance Manager and contribute to quality policies in support of Philogen’s Quality System.
In particular, the successful candidate will be responsible for:
* Writing, reviewing, and approving documents (SOPs, PQRs, IMPDs, validation protocols and reports, technical reports, etc.);
* Revision of production and quality control batch records;
* Managing GMP QA operations, change control, deviations, CAPA, 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;
* Writing and reviewing risk assessments;
* Interacting with other members of the company and clinical center staff.
The ideal candidate should have:
* A good scientific background (ideally in Biology, Biotechnology, etc.);
* Previous experience in Quality Assurance (at least three years);
* Comprehensive knowledge of GMP and other regulations with a good understanding of global quality standards relating to product development and manufacturing;
* Knowledge of regulations for submission and clinical trials of IMP is a plus;
* A high level of English language, both written and spoken;
* A high level of attention to detail and 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.
We offer:
A contract and salary proportional to the experience of the successful candidate.
Job location: Siena
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