Overview
To provide support and assistance to the overall Priontex Group on QA aspects. Assist and maintain regulatory compliance against ISO 13485 and Medical Device Directives, MDD 93/42/EEC.
Ensure compliance and Quality Control of manufactured products for Health Care. To ensure quality, safety and efficacy of all items manufactured in the facility, as well as adherence to good laboratory practice, good manufacturing practices and company guidelines. The earlier the detection of possible execution shortcomings, the more efficient and effective it will be to initiate corrective actions and preventative actions.
Key Performance Areas
- Sampling of product
- Quality Control
- Environmental Monitoring
- Inspection of samples
Minimum Requirements
- <2 years relevant experience in the laboratory/medical device industry (Advantageous)
- 1 – 2 years as a Quality Controller in a production environment – Medical Devices
- Good Document Practice Knowledge
- Tertiary education: Diploma in Basic Microbiology, Chemistry or any other relevant qualification
Job Type: Full-time
Education:
Experience:
- QA in a production environment: 1 year (Required)
Work Location: In person
