About the role
As Quality Specialist you will take all the skills, learning, knowledge from previous experience to the next level. You will gain a greater technical understanding of our QMS with regards to Material Management, Sample and Equipment Management. More importantly, you will be a key player in the approval of change controls, risk assessments, unplanned events and effectiveness checks for CAPAs.
You will have responsibility for performing real-time audits of live lab documentation and process audits and ensuring the internal audit schedule is met.
You will promote the company values and the Quality Departments mission to “get everyone doing the right thing even when no-one is watching” through your actions and by training-out key aspects of the QMS companywide with particular focus on meeting the requirements of ISO 9001: 2015.
We would like you to have the following qualifications:
- A graduate in a Life Science subject.
- Have good knowledge of ISO 9001: 2015.
- Be able to communicate complex issues in an open and supportive manner.
- Have experience in managing quality records within a LIMS or QMS system such as Q-Pulse.
- Proficiency in MS Office, Teams and other relevant software as appropriate, with an aptitude to learn how to use new software to record, track and communicate to the wider organisation in real time and/or when requested.
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