Quality Administrator (No prior experience required)

Job Overview: Quality Administrator (no prior experience required!)

Company: Oxford Immunotec
Location: Abingdon, UK
Position Type: Full-time, perm position
Work Arrangement: On-site

Company Overview:

Oxford Immunotec, a Revvity company is a leading global diagnostics company dedicated to bringing energy and innovation to the field of diagnostic testing. We offer regulated ELISPOT assays for T cell measurement, providing diagnostic solutions approved around the world. Prior experience in quality, documentation and data analysis is not required. We will train for this position. If you have a knack for data analytics, detailed oriented and have an interest in biotechnology, consider applying to this role!

Position Overview:
The Quality Administrator plays a crucial role in ensuring the quality and integrity of testing service results and raw materials. This position involves the release of Open Development Labs (ODL) testing service results, quality checks of Certimmune results, and assisting the Quality team with the approval of raw materials. Additionally, the Quality Administrator supports the administration of documentation for the Quality Management System (QMS). This role requires a keen eye for detail, strong organizational skills, and an understanding of quality control and assurance processes.

Overall responsibilities:

- To have main responsibility for the quality check (QC) of results from the ODL testing service

- To have main responsibility QC’ing results for Certimmune studies

- Review and approval of equipment servicing and maintenance records against Quality specifications

- To aid the Quality Control team in tasks such as:

• QC of incoming raw materials requiring CofA/packaging checks

• Labelling and assembly manufacturing checks

• Review and approval of manufacturing batch records

• Assist QC staff on general laboratory maintenance, including lab cleaning, stock control.

- Assisting with the control of Quality Management system documentation

• Scanning and filing of Quality documents

- Assist the Quality Team to ensure the continuing effectiveness of the QMS

- Assist during internal and external audits as required

- Perform miscellaneous duties as necessary

Specific deliverables for the role are:

• Successfully reviewing request forms, laboratory notebooks and results.

• Contributing towards the maintenance of the quality of products in fulfillment of Company goals.

• Assist with monitoring of product conformity through incoming QC

• Collaborate and assist to ensure that areas of responsibility do not contribute to any major non-conformance during external audits for GCP, GMP, MDSAP, ISO 13485:2016 and ISO 17025:2017.

• Working to Revvity’s Company Values at all times.

Role Requirements:

Technical skills and abilities

• Educated to A-Level or equivalent in a relevant scientific subject or with relevant technical/practical experience

• General use of computers with MS programs and the Internet

Emotional skills and abilities

• Pleasant disposition with a co-operative attitude

• Attention to detail and Quality ‘mindset’

• High standard of numeracy and literacy

• Conscientious

• Able to work under pressure

• Work well alone and as part of a team

Competence Level

Foundation Level

• Compliance & Integrity

• Customer Focus

• Personal Learning

• Accountability

• Building Effective Teams

• Working to a common goal

• Communication & Relationships

• Perseverance

• Creativity & Innovation

What we Offer:

• Purposeful & inclusive work environment

• Dynamic culture in which customers are at the forefront 

• Being part of a highly qualified team that is committed to excellence  

• Access to cutting-edge expertise through which you can make positive impact in the world around us­­