Quality Assurance Associate
Excellent Contract Opportunity for a Quality Assurance Associate to join a global pharmaceutical for document review, change control & validation work
- Global Pharmaceutical Manufacturer
- Excellent Contract Opportunity - START ASAP
- Melbourne Metro Area
About the Company
Operating as a global pharmaceutical manufacturer, our client is well known for its growth and innovation offering a range of healthcare and pharmaceutical products to local & global markets.
Due to increase in project requirements, an opportunity has now arisen for a Quality Assurance Associate to support manufacturing operations with document review, change control & validation work.
About the Opportunity
Reporting to the Quality Manager, key duties include the following:
The successful candidate will have the following skills & experience:
This is an Excellent Contract Opportunity for a Quality Assurance Associate to join a leading global pharmaceutical organisation to support manufacturing operations, drive change controls & deviations for a major project.
How To Apply
To Apply for this role, please click the APPLY NOW button.
For a confidential discussion, please contact Sue Campbell on 0417 994 917 for further information.
NB - Only Shortlisted candidates will be contacted
Operating as a global pharmaceutical manufacturer, our client is well known for its growth and innovation offering a range of healthcare and pharmaceutical products to local & global markets.
Due to increase in project requirements, an opportunity has now arisen for a Quality Assurance Associate to support manufacturing operations with document review, change control & validation work.
About the Opportunity
Reporting to the Quality Manager, key duties include the following:
- Support manufacturing operations for document review, change controls & validation.
- Ensure all manufacturing is completed to GMP standards.
- Support review of deviations, quality review, CAPA's & change controls ensuring documents meet GMP quality standards.
- Review validation protocols and engage with stakeholders for quality review of reports and documents.
- Work with teams to ensure improve compliance for CAPA's.
- Effectively liaise with internal & external key stakeholders of the projects.
The successful candidate will have the following skills & experience:
- Tertiary qualifications in Science or Engineering.
- Sound knowledge of QA, CAPA's, deviations, change controls & deviations within pharmaceutical manufacturing.
- Sound experience in Pharmaceutical/Medical Device Manufacturing or highly regulated environment.
- Strong GMP knowledge.
- Excellent Attention to detail & strong organisational skills.
- Ability to work with wide range of stakeholders.
This is an Excellent Contract Opportunity for a Quality Assurance Associate to join a leading global pharmaceutical organisation to support manufacturing operations, drive change controls & deviations for a major project.
How To Apply
To Apply for this role, please click the APPLY NOW button.
For a confidential discussion, please contact Sue Campbell on 0417 994 917 for further information.
NB - Only Shortlisted candidates will be contacted
Science & Biotechnology > Quality Assurance / Testing > Science & Biotechnology