AddressYour new company
This company is a growing business based in Brisbane working with innovative technology to support patients around the world.
Your new role
The role will review risk assessments, user requirements, protocols and reports for validation activities associated with computerised systems, facilities, utilities, equipment, methods, process and cleaning validation. The role will also support visually communicating completion vs expected timelines.
What you'll need to succeed
- Experience with Medical Device validation and ISO13485.
- PIC/S Code of GMP including Annex 11 Computerised Systems and Annex 15 Qualification and Validation; ideally also Annex 13 – Investigational Medicinal Products
- Validation lifecycle documents
- Experience/knowledge of 21CFR Part 11 Electronic Records; Electronic Signatures
- Quality Management Systems.
- Good documentation practices and Data Integrity requirements
What you'll get in return
The company offers a competitive salary and bonus structure as well as an employee share option plan. The company offers a 9-day fortnight to offer greater flexibility. You will be working in a brand-new facility with state-of-the art technology.
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.
#2845740
