Qc Inspector

Anteris is a structural heart company delivering clinically superior solutions that help healthcare professionals create life-changing outcomes for patients. We are currently developing the first-in-class biomimetic TAVR valve as a growing and inclusive Medtech team with global office locations in Minneapolis, MN, US; Geneva, Switzerland; and Brisbane and Perth, Australia. Help us build a team that will shape the future of TAVR.

The **QC Inspector **is responsible for performing visual inspection on manufactured product to disposition it as pass or fail. This individual will perform inspection on final labelled product to ensure meets all labelling criteria. Additional duties include support for environmental monitoring and material release, test sample preparation & dispatch batch record review, archiving, and equipment cleaning.

The QC Inspector is a professional who is responsible for assisting with the monitoring and inspection of final products in order to meet established quality standards. The individual will use the tools and company guidelines to make sure products have been crafted correctly and are ready for the customer.

**Main Responsibilities**:
Participate in routine Quality Control duties:

- Perform visual inspection inside a controlled cleanroom area on manufactured product to disposition it as pass or fail.
- Perform AQL inspection of packaged finished product and final product visual inspection.
- Support Environmental monitoring duties such as performing the monitoring and plate reading to ensure clean room standards and cleaning effectiveness are being maintained.
- Liaise with approved third-party contract testing laboratories for external microbiological testing such as for growth promotion testing of environmental monitoring plates, identification of micro-organisms, in process and finished product testing.
- Support for environmental monitoring and material release, test sample preparation & dispatch batch record review, archiving, and equipment cleaning Ensure compliance with site SOPs and GMP. As required, raise deviations, and investigate accordingly.
- Participate in continuous improvement projects, or implementation of new processes or systems as required.
- Make recommendations for improvement.
- Participate in internal and external audits relating to Quality.
- Participate in cross-training of duties as required.
- Address and discuss issues and proposed solutions with superiors
- Other duties, as required.

**Skills, Knowledge, Experience & Qualifications**
- Knowledge of general laboratory practices.
- Prior experience working in small multi-disciplinary teams (desirable).
- Proficient in the use of Microsoft computer software (e.g., MS Office).
- Sound communication and interpersonal skills.
- Administrative competencies and attention to detail.
- Ability to work in laboratory and cleanroom settings where PPE and special gowning requirements are essential.

**What We Offer**:

- Opportunity to make a significant impact on the healthcare industry by advancing groundbreaking therapies.
- Collaborative and dynamic work environment with a culture of innovation and excellence.
- Competitive compensation package + 12% superannuation
- Career development opportunities and a chance to be part of a growing company that values its employees.

**Job Types**: Part-time, Permanent

Expected hours: 24 per week

Schedule:

- 8 hour shift

**Experience**:

- QC: 3 years (preferred)

Work Authorisation:

- Australia (required)

**Location**:

- Malaga, WA (required)

Work Location: In person