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QA Associate

1 month ago

East Grinstead, United Kingdom Thermo Fisher Scientific Full time

When you’re part of Thermo Fisher Scientific, you’ll do challenging work, and join a team that values performance, quality and innovation. As part of a successful, growing global organization you will be encouraged to perform at your best. With revenues of more than $40 billion and the largest investment in R&D in the industry, we give our people the resources and chances to create significant contributions to the world.

**Position Summary**:
Our MBD East Grinstead facility is at the forefront of our quest to keep Antibiotics effective and relevant for today’s results-oriented environments. The East Grinstead site is the only manufacturer of the Sensititre range of AST products, critical in the fight against primary infections and Covid 19 secondary infections. These vital products enable healthcare professionals to make an accurate diagnosis and to prescribe the right amount of the required antibiotic.

Working with our East Grinstead Sensititre products, our customers save lives every day, and we help them to make the world healthier, cleaner and safer. What we do makes a difference

Our Sensititre AST/ID products are used globally to determine which antibiotics a particular bacterium is sensitive or resistant to and help to ensure patients are given the most appropriate treatment. Sensititre products can be used in Clinical, Pharmaceutical and Veterinary settings.

Playing a key role in our Site Mission is the Quality Assurance team, who ensure that all medical devices manufactured on site are compliant to the Quality Management System as per ISO 13485:2016. This team is both dynamic and diverse, with plenty of scope for development and progression within the structure.

This is a huge opportunity to learn from the best, develop as a quality profession al and fulfill your true potential. You will be part of a team who are a key interface across the various areas on site. Working within this team you will ensure product release and documentation for the QMS is maintained as part of document control and control of records. The position requires a proficient communication and IT skills to support the site on the day to day administration of key quality tasks such as batch release and new product approvals.

**Responsibilities**:

- Ensure that general day to day activities such as approval of manufacturing documentation including technical reports, review/approval of non-conformances, deviations, reviewer/approver for SOP’s, briefs, software, specifications and forms
- Ensure compliance and assist in the audits (pre audit and post audit follow up to external (regulatory) requirements, including Quality Management Systems (ISO 13485:2016, FDA, CMDCAS) and the In Vitro Diagnostics Directive/Regulation. Ensure corrective actions are implemented for issues arising from the audits.
- Responsible for reviewing and approving SOPs in line with change process.
- Co-ordinate investigation of customer complaints and general quality advice to the business.
- Undertake QA responsibilities regarding supplier control, review and performance.
- To act as coordinator and/or QA Representative on Corrective Action investigations.
- Perform internal audits to ensure compliance to external regulatory requirements.
- Assist in metric data for the Quality department.
- Assist in training for Quality functions and relevant documentation in up-to-date
- Any other duties/projects as are reasonable and within the skills and ability of the post-holder.

**Minimum Requirements/Qualifications**:

- Degree in microbiology/degree in a related field
- Confirmed experience in a QMS role preferably within MDD/IVD
- High attention to detail
- Ability to communicate openly
- Work flexibly to ensure targets are met
- Competent in the use of the MS Office suite

**Knowledge, Skills, Abilities**:

- Ability to work independently and in a group setting with little direction or direct supervision.
- Experience in audit involvement.
- Work flexibly to ensure deadlines are met
- Experience with writing concise/accurate and maintain reports/records

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.

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