Quality Supervisor II
Cartago, Costa Rica · 2+ years experience · Onsite · Posted Oct 12, 2026
At a glance
- Experience
- 2+ years experience
- Workplace
- Onsite
- Location
- Cartago, Costa Rica
About the role
- The Quality Supervisor II leads the Quality Control (QC) inspection team to ensure inspection activities are properly prioritized, executed, documented, and compliant with applicable manufacturing requirements, quality procedures, regulations, and standards.
- The role supports efficient daily operations by aligning resources, resolving inspection-related issues, developing team capability, and partnering with Operations, Engineering, Planning, and other stakeholders.
Responsibilities
- Lead the Quality Control (QC) inspection team to ensure inspection activities are properly prioritized, executed, documented, and compliant with applicable manufacturing requirements, quality procedures, regulations, and standards
- Support efficient daily operations by aligning resources and resolving inspection-related issues
- Develop team capability
- Partner with Operations, Engineering, Planning, and other stakeholders to meet business needs without compromising product quality or compliance
Requirements
- Bachelor’s degree in engineering with 4+ years of experience in the fields of Quality, Biomedical, Life Sciences, Physical Sciences, Engineering, or equivalent combination of education and experience
- Strong oral, written and interpersonal communication skills required
- English Level: B2 (MCER) – Intermediate proficiency required
- Knowledge and understanding of FDA QSRs, ISO standards, and applicable medical device regulatory requirements
- Proficiency with Microsoft Office (Word, Excel, Access, PowerPoint)
- High degree of accuracy and attention to detail
- Solid problem analysis and decision-making ability and leadership skills
Preferred qualifications
- 2+ years of experience in a Lead/Rotational Supervisory role desired
- Knowledge of sterilization requirements for medical devices preferred
- Knowledge of controlled environments for medical devices preferred
- ASQ certifications for CQIA, CQA, or equivalent preferred
Skills
- Microsoft Office
- Word
- Excel
- Access
- PowerPoint
