Inavitas
Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries ? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas .
Following a new opportunity, we are currently looking for a QA Consultant based in Florence.
You will be responsible for
- Quality Assurance projects (e.g. PQR, Auditing, Change Control, Complaints, Deviations, CAPAs, OOS, Batch Record review, Documentation management, Training, Supplier Management)
- Support complex projects related to Health Authority Inspection Readiness Programs, from preparation to post-inspection phase (e.g.FDA, EMA, HEALTH CANADA)
- Support Quality Management Systems implementation and/or improvement projects
- Support projects in the field of Technology Transfer / Validation (i.e. Analytical, Cleaning, Process, Sterility)
- Participation in Risk Assessments projects (e.g. Process, Cross-Contamination)
About you
- 1 years or more experience in pharmaceutical industries related to Quality Assurance activities
- General knowledge of Pharmaceutical processes and deep knowledge of Sterile Drug Product manufacturing practices
- Bachelor's degree in Physical and Mathematic science (preferred Chemistry, Biotechnology, Microbiology, Biology, Pharmaceutical Technologies);
- Fluent english
- Availability to travel up to 60%
Location: Florence
As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation . PQE Group gives you the opportunity to work on international projects , improve your skills and interact with colleagues from all corners of the world.
If you are looking for a rewarding and exciting career , PQE Group is the perfect place for you.
Apply now and take the first step towards an amazing future with us.
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