$112,000 – $125,000
Listed on Beckman Coulter’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
This role leads complaint and defect tracking for medical device products in a regulated environment, working with cross-functional teams to resolve post-market quality issues and author investigation reports. It suits experienced microbiology professionals with a background in pharmaceutical or medical device quality assurance who want to take on broader leadership and strategic quality responsibilities.
Our summary, not Beckman Coulter’s wording. The full posting is on their site.
Skills this role names
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What they ask for
Required
- Bachelor's degree
- Minimum 5 years in regulated medical device or pharmaceutical environment
- At least 3 years coordinating post-market surveillance and quality assurance
- Demonstrated microbiology laboratory competence including microscopy and Gram staining
- Knowledge of cGMP and ISO 13485 quality systems
- Proficiency with Microsoft Excel, PowerPoint, Word and Teams
- Valid driver's license with acceptable driving record
- Ability to lift and carry equipment up to 50 pounds
- Ability to travel up to 10%
Nice to have
- Master's degree or ASQ certification
- 4-6 years post-market surveillance and CAPA experience
- Advanced statistical analysis tools like Minitab or quality engineering certifications
- Working knowledge of USP 61 & 62