Quality Associate

hace 3 días


En remoto, España Thermo Fisher Scientific A tiempo completo

At Thermo Fisher Scientific team, you’ll discover impactful work, innovative thinking and a culture dedicated to working the right way, for the right reasons - with the customer always 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 unique contributions. Our commitment to our colleagues across the globe is to provide the resources and opportunities they need to make a difference in our world while building a fulfilling career with us.

**Summary of Key Responsibilities and Function**: This position will perform the day-to-day approval of
**IVDR products** within Thermo Fisher Diagnostics. Secondary responsibilities include continuous improvement in the products verification process, make recommendations to the reporting manager, and work with Thermo Fisher Diagnostics functions to effectively conduct these changes.

Location: UK and Europe wide, with fully remote working available.
**Key Responsibilities**:

- Responsible for receiving and storing product data in our inventory management system (SAP).
- Operation of our desk-verification process as well as having good with our warehouses to perform the warehouse-verification process.
- Responsible for the close coordination with Thermo Fisher Scientific manufacturers, 3rd party product suppliers, verify product data is received, stored and verified.
- Supports Quality Assessments/ audits against Quality Standards working towards inspection readiness.
- Work with relevant partners to ensure that the process is efficient and well-functioning.
- Ensure accurate issuance, tracking, reviewing and closure for all levels of document changes.
- Responsible for training of other members of the desk-verification team, the Quality Management Representatives (QMR’s), and other relevant resources.
- Assist the Supply Quality Lead in other Quality Assurance activities as required.
- Assist in accumulation of Key Performance Indicators on quality processes.
- Ability to operate in a cross functional, Global environment.
- Perform ad-hoc duties.

**Minimum Requirements**:

- Science related degree (preferred).
- Minimum of 2 years of experience in a corporate environment (preferably an organisation certified to ISO 13485 or other regulatory standards.)
- Proficient in MS Word and MS Excel.
- Well spoken and written English language skills and at least one additional European language (Spanish, Italian, German, and/or French, also written and spoken).

**Personal attributes**:

- Ability to take the initiative and make good judgments in work methods and interpreting Team goals.
- Ability to learn quickly.
- Excellent interpersonal skills
- Keen eye for detail.
- Strong analytical and problem solving skills required.
- Proven collaborative skills at a fast-paced environment.

**Preferred Requirements**:

- Experience working with SAP.
- Involved in Continuous Improvement activities.
- Knowledge of Supply Quality such as, approval of suppliers, SCARS, Non Conformance, CAPA’S.
- Use of Master Control (QMS software) a bonus.
- Formal qualifications in MS Office.

**Travel Requirement**:

- Minimal travel, although possibility to travel, within Europe to TFD sites when required.

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
**Accessibility/Disability Access**:



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