Quality Technician I

Euroimmun; Oxford; On-site; GBP 25,000 - 35,000; Full time

Job summary

A global health solutions provider is seeking a Quality Technician I in Oxford to support quality assurance in product release and laboratory operations. The role involves conducting inspections, performing lab tests, and assisting with documentation control in compliance with industry standards. Candidates should have a degree in a relevant scientific field and strong attention to detail. This position offers a dynamic working culture and the chance to be part of a committed team.

Benefits

Purposeful work environment

Dynamic culture

Access to cutting-edge expertise

Qualifications

• Educated to degree level in a relevant scientific subject or with relevant technical experience.
• General use of computers with MS programs and the Internet.

Responsibilities

• Conduct inspection and release of items requiring CofA checks.
• Perform laboratory testing and release of kit components.
• Support QA review and control of QMS documentation.
• Perform QC of patient test results under specified standards.

Skills

Attention to detail

Team collaboration

Numeracy and literacy

Education

Degree in a relevant scientific subject

Tools

MS Office

Job description

Job Title

Quality Technician I

Location(s)

Oxford, UK - Oxford Immunotec

About Us

Revvity is a developer and provider of end-to-end solutions designed to help scientists, researchers, and clinicians solve the world’s greatest health challenges. We pair the enthusiasm of an industry disruptor with the experience of a longtime leader. Our team of 11,000+ colleagues from around the globe are vital to our success and the reason we’re able to push boundaries in pursuit of better human health.

Find your future at Revvity

This position supports the Quality team in the release of raw materials and finished product, general administration for the QMS and aids the release of Laboratory Operations service results.

Role Description

Overall responsibilities:

• Inspection and release of items requiring CofA/packaging checks.
• Laboratory testing and release of kit components using the T-SPOT® assay platform.

Assisting with QA review and control of QMS documentation, including:

• Appropriate handling and storage of documentation, physically and electronically using OI’s ERP system.
• Assisting with NCR and CAPA investigations, as required.
• Equipment certificate handling.

Performing critical activities to support Manufacturing in product release, including:

• In-process Quality checks of Manufacturing operations.
• Review and approval of kit and kit component labels.
• Review and approval of Manufacturing batch records for labelling and assembly operations.
• Review of documentation for the heat treatment and sterilisation of consumables critical for the manufacturing process.
• Review of bioburden certificates, including investigation of out of specification results.
• Creation of product CofAs.

Performing General Laboratory Maintenance, Such As

• Cleaning of laboratory equipment and maintenance of cleaning records.
• Preparation of media aliquots.
• Verification of non-critical laboratory equipment e.g., internal pipette verification.

QC of patient test results from the Laboratory Operations testing service under ISO 17025:2017/GCP requirements.

Assisting with the monitoring of compliance with the QMS and with tracking systems associated with ISO 13485:2016 and ISO 17025:2017 and the QSR.

• Assist the Director, Quality to ensure the continuing effectiveness of the QMS.

Perform Miscellaneous Duties As Necessary, Such As

• Updates of QMS documentation following the Document Control process using the eQMS.
• Maintaining and disposing of Quality stock.
• Ensuring the department is audit ready at all times.
• Control and movement of stock, both physically and electronically using OI’s ERP system.

Specific Deliverables For The Role Are

• 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.
• Contributing towards the maintenance of the quality of products in fulfillment of Company goals.
• Working to Revvity’s Company Values at all times.

Role Requirements

Technical skills and abilities

• Educated to degree 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.
• Works carefully to get things right the first time and identifies non-compliance.

Competences

• Compliance & Integrity.
• Customer Focus.
• Personal Learning.
• Accountability.
• Building Effective Teams.
• Working to a common goal.
• Communication & Relationships.
• Perseverance.
• Creativity & Innovation.

What We Offer

• Purposeful 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.