Offer summary
Qualifications:
University degree in a scientific discipline, Minimum of 3 years quality engineering experience, Proficient in qualifications/validations processes, Experience in pharma/medical device industry, Excellent English communication skills.
Key responsabilities:
- Manage quality aspects of validation programs
- Ensure compliance with FDA and ISO requirements
- Create and oversee test plans and sample management
- Conduct internal audits and promote continuous improvement
- Act as contact for subcontractor laboratories