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:
Performing the QC of raw materials used in the Manufacturing process, including:
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.
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
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.
Competence Level
Foundation Level
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