Revvity | 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 diverse 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.
Position Overview
This position supports the Quality team in the release of raw materials and finished products, general administration for the QMS, and aids in the release of Laboratory Operations service results.
Responsibilities
1. Quality Control of Raw Materials and Finished Products:
Conduct inspections and release items requiring Certificates of Analysis (CofA) and packaging checks.
Perform laboratory testing and release kit components using the T-SPOT® assay platform.
2. Quality Assurance Support:
Assist with QA reviews and control of QMS documentation.
Ensure the proper handling and storage of documentation, both physically and electronically via OI’s ERP system.
Support Non-Conformance Reports (NCR) and Corrective and Preventive Action (CAPA) investigations.
Manage equipment certification and documentation.
3. Manufacturing Support for Product Release:
Conduct in-process quality checks of manufacturing operations.
Review and approve kit and component labels, as well as manufacturing batch records.
Oversee documentation related to heat treatment and sterilization of critical consumables.
Investigate out-of-specification bioburden results.
Generate product CofAs.
4. General Laboratory Maintenance:
Maintain laboratory cleanliness and ensure cleaning records are up to date.
Prepare media aliquots and verify non-critical laboratory equipment.
5. QC of Patient Test Results:
Perform quality control of patient test results in line with ISO 17025:2017 and GCP requirements.
6. Compliance Monitoring and QMS Tracking:
Assist with tracking systems associated with ISO 13485:2016, ISO 17025:2017, and QSR.
Support the Director, Quality in ensuring the continued effectiveness of the QMS.
7. Miscellaneous Duties:
Update QMS documentation following the Document Control process using the eQMS.
Manage and dispose of quality stock as needed.
Ensure the department is always audit-ready.
Control and manage stock movement through OI’s ERP system.
Key Deliverables:
Monitor product conformity through incoming quality control.
Collaborate to ensure that areas of responsibility do not contribute to non-conformance during audits (GCP, GMP, MDSAP, ISO 13485:2016, ISO 17025:2017).
Contribute to maintaining product quality in alignment with company goals.
Uphold Revvity’s Company Values in all interactions and work activities.
Candidate 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.
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 a positive impact in the world around us
Apply today to join our team and help us make a difference!
#LI-EMEA
Similar Jobs
- Laboratory Operations Technician Abingdon, England, United Kingdom
- Laboratory Operations Compliance Specialist Abingdon, England, United Kingdom