Reporting to the Technical Manager, your role is integral in ensuring you are working together with manufacturing teams to conduct non-conformance investigation and reporting-CAPA, updating Standard Operating Procedure's (SOPs) where required to meet the highest level of quality standards and overall manage compliance to documentation. You will be admired for your amazing organisational skills and ability to whip up a detailed yet concise report in no time!
What will you be doing?
- Working closely with cross-functional teams to conduct a thorough root cause analysis on non-conformances to drive sustainable corrective and preventative actions.
- Manage and co-ordinate change controls, implement improvements to the production line.
- Update and maintain SOP's and ensure they are accurate and user friendly.
- Calibration of equipment.
- Work in a GMP environment.
What skills and experience do you bring?
- You will have a tertiary qualification in Science or related.
- Minimum 2 years experience in a Quality Assurance, Quality Control or similar role in a medical device, pharmaceutical, infant formula or similar industry.
- You will come with a demonstrated history of managing documentation and have an eye for detail.
- Ability to be proactive, flexible, multitask and manage your time effectively.
- Passionate about quality, documentation, standards and integrity.
Benefits
- Join a growing business with a commitment to continue building on the company's great values and culture.
- Excellent job security on offer, you will be truly valued for the work you do.
- Opportunity to make your mark and contribute in a wider way
- Flexible hours AND work from home options!
- Competitive salary to match your experience.
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