Quality Compliance Specialist
1 giorno fa
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
At Thermo Fisher Scientific, you’ll discover impactful work, innovative thinking and a culture dedicated to working the right way, for the right reasons - with the customer always on top of mind. The work we do matters, like helping customers find cures for cancer, protecting the environment, making sure our food is safe and delivering COVID-19 solutions. As the world leader in serving science, with the largest investment in R&D in the industry, our colleagues are empowered to realize their full potential as part of a fast-growing, global organization that values passion and outstanding contributions. Our dedication to our colleagues across the globe is to provide the resources and opportunities they need to make a difference in our world while building an exciting and fulfilling career with us.
**Location/division specific information**:
We - the Thermo Fisher Scientific, Ferentino Site - are one of the leaders in manufacturing sterile liquid and lyophilized products. At Ferentino, you will be part of a passionate Team which is dedicated to support a broad range of customers who are developing the treatments and pharmaceuticals of the future.
**Discover impactful work**:
As part of the Quality Assurance Team you will assure the quality of current and future products and satisfy the very high expectations of our customers in pharmaceutical manufacturing. You will achieve this by collaborating closely with other functions and departments to determine solutions for diverse challenges as well as independently striving for continual improvement of Quality Management System processes.
**A day in the life**:
- Continually improve required Supplier Qualifications and Risk Management activities
- Contribute to the Quality Supplier Management activities
- Review, update and contribute to the development of site procedures
- Ensure Quality Agreements with clients are established and maintained
- Contribute to the site’s improvement and new projects introduction
**Keys to success**:
**Education**
- B.Sc. or M.Sc. in Pharmacy, Chemistry, Industrial Pharmacy or a related field.
- Further Qualifications in Quality Management or Quality Assurance encouraged
**Experience**
- Knowledge of Quality Management Systems with at least 2 years of experience
- Experienced in working in project teams
- Knowledge of directives (EU-GMP, US FDA 21 CFR)
**Knowledge, skills, abilities**
- Structured and very diligent working style including ability to organize yourself independently
- Analytical skills with proven ability to troubleshoot complex problems
- Strong interpersonal skills to work as a member of a team and collaborate effectively with other Teams and Functions
- Able to communicate clearly with internal and external partners regarding supplier management
- Good critical and logical thinking skills.
- Effective written, interpersonal, and presentation skills.
- Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint).
- Strong statistics knowledge and experience with Trackwise
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