Your role:
Helps to execute diverse complex tasks based on individual understanding and technical knowledge to address abnormalities within operational manufacturing processes.
Assists in remedying complex malfunctions, helps to execute product quality inspection activities within the project scope.
Works with limited supervision, escalating issues to superiors as needed and develops a substantial understanding of relevant regulations, requirements, and standards.
Aids to implement quality control procedures and protocols, ensuring adherence to good laboratory practices (GLP) and good manufacturing practices (GMP).
Helps in the documentation of regulatory requirements for good manufacturing controls for medical devices as outlined in quality control plans, assisting in implementing the laboratory chemical hygiene program.
Provides support towards the execution of validation protocols and testing methods for new products and processes to ensure they meet quality standards.
Engages in continuous learning and on-the-job training to enhance skills and knowledge and ensures quality of own work by conducting checks and taking responsibility for the accuracy of work.
Adheres to all safety protocols and guidelines, including the proper handling and disposal of hazardous materials, to maintain a safe working environment for oneself and others.
Escalates issues to superiors and participates in planning and priority settings within their area of responsibility.
You're the right fit if:
Bachelor’s degree in engineering (or equivalent).
ISO 9001/13485 related experience and knowledge.
Experience in Quality Control in a manufacturing environment.
A team player.
Field roles
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
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