In this exciting role, you will be part of a dynamic and inclusive team. You will act as lead investigator for complaints, critical deviations and the associated escalation process. You will provide quality oversight for our commercial production and the complaints at the Hillsboro site.
Requirements
- BS/MS Master's degree in Life Sciences or Engineering
- Significant relevant bio/pharmaceutical experience in a Good Manufacturing Practices environment
- 4+ years (level II) and 8+ years (level III) of industry experience in a biologics manufacturing environment
- Sound knowledge of cGMP, ISO standards and international regulations for pharmaceuticals
- Excellent communication skills
Benefits
- Relocation benefits
- Discretionary annual bonus
- Benefits detailed at the link provided