Related skills
risk management gmp quality audits quality management system fda regulations📋 Description
- Oversee QA for Kao Group products in the designated region
- Monitor internal and external quality data for deviations
- Initiate root cause investigations and corrective actions
- Audit compliance with quality standards and regulatory requirements
- Lead product recalls and regional quality initiatives
- Report QA status to the Global Quality Management Committee
🎯 Requirements
- Bachelor’s degree in chemistry, pharmacy, or related field; advanced degrees preferred
- ISO 9001 Lead Auditor certification desirable
- Strong knowledge of quality mgmt systems and regulatory requirements (GMP, FDA)
- Proven leadership and ability to collaborate with cross-functional teams
- Exceptional quality risk management capabilities
- Ability to provide constructive feedback and challenge decisions
🎁 Benefits
- Healthcare and 401(k) with company match
- 41 total days off (vacation + holidays + sick)
- Flexible work environment and development opportunities
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