We are seeking a full-time Quality Assurance Associate with strong analytical skills for an immediate start.
The successful candidate will be self-motivated and capable of thriving in a fast-paced collaborative environment. They will bring sound theoretical and practical knowledge to support a dedicated team of professionals.
Reporting to the Quality Manager this role is responsible for supporting and maintaining the Quality Management System ensuring documentation and quality-related activities are coordinated efficiently and accurately.
Key Responsibilities
- Support and implement the Quality Management System in line with relevant standards.
- Promote staff awareness and understanding of quality requirements and processes.
- Recommend improvements and compile quality KPIs for laboratory management.
- Train staff on quality procedures and system use.
- Ensure company policies and procedures meet current quality standards.
- Raise and follow up on non-conformances to ensure timely resolution.
- Manage documentation: review publish distribute and archive.
- Coordinate and maintain quality system records.
- Organise and participate in internal and external audits.
- Conduct quality training relevant to staff roles.
- Adhere to the Eurofins Code of Ethics and all applicable policies.
Qualifications :
- Tertiary qualification in Science (preferably Microbiology or Biochemistry) preferred.
- Previous experience in a similar role within the pharmaceutical industry is preferred.
Skills & Attributes
- Experience in quality roles within a GMP/ ISO 17025 laboratory.
- Strong knowledge of quality systems CAPA change control and risk management.
- Proficiency in Microsoft Office especially Excel.
- Excellent attention to detail organisation and time management.
- Strong written and verbal communication skills.
- Ability to work both independently and collaboratively across teams.
- Problem-solving mindset with a proactive approach.
- Experience in audits documentation and equipment/software validation is an advantage.
- Commitment to continuous learning and improvement.
Additional Information :
This is an excellent opportunity for a self-motivated person with a passion in Quality Assurance to join a dynamic company that can offer a rewarding career path.
All candidate CVs and cover letters will be reviewed however please note that we are not always able to respond to every expression of interest submitted.
This opportunity is only open to candidates who are eligible to work in Australia/New Zealand and already have work rights or an appropriate working visa.
Please note: Current Eurofins employees should first speak with their Business Unit Manager before submitting an application for this position.
Remote Work :
No
Employment Type :
Full-time
We are seeking a full-time Quality Assurance Associate with strong analytical skills for an immediate start.The successful candidate will be self-motivated and capable of thriving in a fast-paced collaborative environment. They will bring sound theoretical and practical knowledge to support a dedica...
We are seeking a full-time Quality Assurance Associate with strong analytical skills for an immediate start.
The successful candidate will be self-motivated and capable of thriving in a fast-paced collaborative environment. They will bring sound theoretical and practical knowledge to support a dedicated team of professionals.
Reporting to the Quality Manager this role is responsible for supporting and maintaining the Quality Management System ensuring documentation and quality-related activities are coordinated efficiently and accurately.
Key Responsibilities
- Support and implement the Quality Management System in line with relevant standards.
- Promote staff awareness and understanding of quality requirements and processes.
- Recommend improvements and compile quality KPIs for laboratory management.
- Train staff on quality procedures and system use.
- Ensure company policies and procedures meet current quality standards.
- Raise and follow up on non-conformances to ensure timely resolution.
- Manage documentation: review publish distribute and archive.
- Coordinate and maintain quality system records.
- Organise and participate in internal and external audits.
- Conduct quality training relevant to staff roles.
- Adhere to the Eurofins Code of Ethics and all applicable policies.
Qualifications :
- Tertiary qualification in Science (preferably Microbiology or Biochemistry) preferred.
- Previous experience in a similar role within the pharmaceutical industry is preferred.
Skills & Attributes
- Experience in quality roles within a GMP/ ISO 17025 laboratory.
- Strong knowledge of quality systems CAPA change control and risk management.
- Proficiency in Microsoft Office especially Excel.
- Excellent attention to detail organisation and time management.
- Strong written and verbal communication skills.
- Ability to work both independently and collaboratively across teams.
- Problem-solving mindset with a proactive approach.
- Experience in audits documentation and equipment/software validation is an advantage.
- Commitment to continuous learning and improvement.
Additional Information :
This is an excellent opportunity for a self-motivated person with a passion in Quality Assurance to join a dynamic company that can offer a rewarding career path.
All candidate CVs and cover letters will be reviewed however please note that we are not always able to respond to every expression of interest submitted.
This opportunity is only open to candidates who are eligible to work in Australia/New Zealand and already have work rights or an appropriate working visa.
Please note: Current Eurofins employees should first speak with their Business Unit Manager before submitting an application for this position.
Remote Work :
No
Employment Type :
Full-time
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