? Ensure compliance with regulatory requirements and industry standards.
? Write, review, and approve QA documents, including SOPs, specifications, procedures, templates, and forms.
? Manage and lead quality events and deviations that occur during the product manufacturing stages.
? Performing risk assessments and evaluations
? Managing CAPAs, Change Control action items, training execution, and effectiveness checks
? Investigate customer complaints related to quality issues
? Support internal and external audits
Requirements: ? B.Sc. in Life Sciences, Chemistry, Chemical or Biotechnology Engineering mandatory
? 1-3 years of experience in a pharmaceutical or medical device company mandatory
? Excellent communication and teamwork skills (must be collaborative and a team player)
? Ability to learn quickly, with self-motivation and a strong can-do attitude
? Proficiency in English and Hebrew (both written and verbal)
? Experience in pharmaceutical QA Production or QA Compliance role an advantage
? CQE certification an advantage
This position is open to all candidates.