A medical device company in the Hashron area is looking for a Quality Assurance Specialist to join our growing team. In this role, you will be responsible for implementing and supporting document control processes and general quality management system (QMS) activities. This position is crucial to maintaining Magentas high quality and regulatory compliance standards.
Reports to: QA Manager
Responsibilities
Operate and maintain the Electronic Quality Management system (eQMS).
Oversee and support all Document Control activities, ensuring timely and accurate processing.
Manage Document Change Orders (DCOs) and Engineering Change Orders (ECOs).
Maintain and update the Device History Files (DHF) and Device Master Records (DMR).
Collaborate with cross-functional teams to ensure compliance with internal procedures and regulatory requirements
Requirements: Bachelors degree in a relevant field (e.g., Life Sciences, Engineering, Quality Assurance ).
Minimum of 3 years of experience in a similar or relevant quality role within the medical device or life sciences industry.
Strong written and verbal communication skills.
Highly detail-oriented with excellent organizational abilities.
Effective time management skills and the ability to prioritize tasks independently.
Proficient in Microsoft Office Suite (Word, Excel, PowerPoint).
Comfortable working both independently and within cross-functional teams.
Fluency in English, both written and spoken.
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