Overview
Conceivable Life Sciences is pioneering the world's first AI-powered, automated IVF laboratory, revolutionizing reproductive healthcare through cutting-edge robotics and artificial intelligence. We are seeking a passionate and dedicated Regulatory Affairs Director to lead our comprehensive regulatory compliance strategy across multiple frameworks including ISO standards, and cybersecurity certifications.
Responsibilities
- Lead multi-framework regulatory strategy encompassing SOC2 type II compliance, ISO 9001 / 13485 quality management systems, HITRUST cybersecurity framework, and GAMP.
- Collaborate with cross-functional teams to ensure integrated compliance approach across products - hardware and software.
- Manage regulatory submission timelines, documentation requirements, stakeholder communications for complex medical device applications.
- Establish and maintain Design Controls and quality management systems supporting multiple regulatory frameworks.
- Support creation of comprehensive documentation cybersecurity frameworks. Interface with clinical partners and key opinion leaders to support regulatory strategy development.
Qualifications
BS in Biomedical Engineering, Computer Science or related engineering discipline.4-5 years of proven experience in medical device regulatory affairs and compliance knowledge of Design Controls (21 CFR 820), ISO 13485, and medical device quality management systems.Experience with Computer System Validation (CSV) and GAMP 5 principles.Strong understanding of risk management principles (ISO 14971) and hazard analysis methodologies.Excellent project management skills with ability to manage multiple concurrent regulatory streams.Outstanding written and verbal communication skills for regulatory submissions and stakeholder management.Fluent in both English and SpanishSeniority level
DirectorEmployment type
Full-timeJob function
LegalIndustries
Human Resources Services#J-18808-Ljbffr