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.
This position will assist the Quality team in maintaining the Revvity measurement, analysis & improvement systems in conjunction with Quality Management System (QMS) and the relevant standards including ISO 13485:2016, MDSAP, IEC 62304:2006A1 & ISO 17025:2017
Role Description:
Reviewing and managing non-conformance records within the company’s electronic QMS (eQMS) and ensuring non-conformance associated tasks are completed within the required timescales by relevant staff.
Review and management of corrective and preventative actions (CAPA) within the company’s eQMS and ensuring CAPA completion within the required timescales by relevant staff.
Assisting during internal and external audits as required.
Assisting and acting as Document Controller/Administrator of the eQMS and ensuring that documents are mastered and periodically reviewed within the required timescales.
Responsibility for creating Training requirements and events within the eQMS and ensuring training records are up to date and relevant.
Assisting in the Quality activities within the Supply chain and ensuring all supplier and distributor reviews are conducted and records are maintained in compliance to appropriate standards and requirements.
Ensuring adherence to all internal company processes, as well as updating and improving those processes as required.
Performing miscellaneous duties as necessary for the effective completion of the requirements of this position.
Following Quality System requirements as necessary.
Always working to Revvity Company Values and always following Health and Safety requirements
Specific deliverables for the role are:
Monitoring of QMS conformity through NCR/CAPA.
Collaborating and assisting with the team 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 level or equivalent in a relevant subject or with relevant technical/practical experience required for this position.
General use of computers with Microsoft Office programs, such as Outlook, Teams, Word, Excel, PowerPoint, Power BI.
Experienced in working to GLP and Quality Management principles such as ISO 13485 would be an advantage.
Excellent attention to detail and knowledge of GDP
Emotional skills and abilities
Proven capability in working efficiently in order to meet required deadlines.
Proactive in identifying and investigating issues and presenting potential solutions.
Able to work independently and as part of a wider team.
Able to prioritize and to handle multiple tasks effectively at the same time.
Confidence to communicate with members of staff across different departments and seniority levels.
Foundation Competence 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
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