Diasorin is a global leader in diagnostic solutions. The Senior QA Technician is responsible for reviewing and verifying Device History Records (DHRs) to ensure compliance with internal procedures, FDA regulations, and ISO standards. The role supports the release of intermediate materials and finished medical devices and ensures product quality and regulatory compliance.
Requirements
- H.S. Diploma or equivalent required
- Associate's Degree in a life science or engineering or equivalent related experience preferred
- 3+ Years Experience in FDA regulated manufacturing environment, previous Quality experience preferred
- Good verbal and written communication skills in the English language
- Ability to interpret a variety of instructions in written oral form
- Computer skills (Microsoft Windows and Office programs), familiarity with Oracle preferred
- Working knowledge of GMP, GDP, and regulatory requirements (FDA, ISO 13485)
- Ability to apply sampling techniques
- Ability to manage and present data as it relates to product release
- Highly organized with proven time management and prioritization skills
- Ability to maintain attention to detail in a fast-paced environment
Benefits
- Impactful Work: When you join Diasorin, you become part of a team that's dedicated to improving lives.
- Global Reach & Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry.
- Diverse and Inclusive Culture: We believe in the strength of diversity, and our inclusive culture reflects this commitment.