GCP Director ensuring compliance in clinical trials for Evolution Research Group. Overseeing quality assurance and operations at the Clinical Pharmacology of Miami site.
About the role
- Quality Assurance Specialist ensuring compliance with quality standards in MedTech company. Collaborating with cross-functional teams and maintaining quality improvement processes.
Responsibilities
- Ensure the quality system is maintained and continuously improved
- Work closely with product teams to ensure compliance
- Educate employees on quality assurance practices
- Participate in internal and external audits
- Ensure the performance of the company's processes
Requirements
- Minimum 2 years of experience as a QARA Specialist
- Engineering degree or Master's in Biomedical Engineering or Biotechnology
- Adaptability and a willingness to learn
- Experience in a scale-up / start-up environment
- Effective communication with internal and external stakeholders
- Excellent organizational and analytical skills
- Fluent in English and French (minimum C1 level in both languages)
- Prior successful experience or specialization in Medical Device Quality Assurance (preferred)
Benefits
- Swile meal card
- Alan health insurance
- Equity plan (free shares)
- Hybrid work arrangement possible
- Active Works Council (CSE) benefits (sports & wellness pass, multi-activity, club-employes.com)
- Internal company events
- Employee referral bonus
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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