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.