Coventry, West Midlands, England, UKCoventryWest MidlandsUKCV6 5SF
Job Ref:
J2165836
Sector:
Engineering
Sub-sector:
Medical Devices
Date Added:
18 July 2022
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SRG are currently recruiting for a QMS Administrator to join a medical device company in Coventry who are looking for someone to join them on a temporary basis of 9-12 months. Salary is competitive.
Overall Purpose
The key purpose of the role will be to work closely within the Quality department to develop and deliver a range of proactive and responsive QMS initiatives including the management of the systems for:
Documents control
Equipment monitoring and calibration
Manufacturing batch history records review
Key tasks and responsibilities
Review and manage the manufacturing/production batch history records to ensure Good Documentation Practices
Co-ordinate equipment calibration
Manage, co-ordinate document control within the business via use of the electronic document control system, contributing to the drafting of documentation, managing the review and approval of documents including procedures, SOPs, WIs, and forms within the SFM QMS
Support internal audits as an internal auditor, along with management of corrective actions
Support the delivery of the non-conformance and CAPA management system in the business
Champion compliance to all applicable standards, regulations and internal procedures by proactively interpreting quality and regulatory requirements and implementing solutions
Work within the Quality department to promote continuous improvement and ensure compliance with quality policies across the business
Demonstrate the values of the team and be a Quality Champion in the business
Any other duties as assigned by the line manager or the business
Key Requirements
Scientific degree or equivalent
Experience working to or in an ISO 9001 and ISO 13485 environment
Experience of document control management in a relevant environment
Able to work with minimum supervision and as part of a team
Strong communication skills, both verbal and written
Capable to working under pressure to tight and constantly changing deadlines