Pharmavise Corporation
Biotechnology • Pharmaceuticals • Healthcare Insurance
Pharmavise Corporation is the first Continuous Compliance Organization (CCO) dedicated to maintaining the highest standards of quality and regulatory compliance in the life sciences industry. Our esteemed client base includes Fortune 500 companies in pharmaceuticals, medical devices, and biotechnology. We offer bespoke solutions tailored to meet the specific compliance needs of our clients, supporting them from development through commercialization and ensuring they exceed their compliance goals while enhancing patient health and safety.
Medical Device Quality Compliance Expert
Job not on LinkedIn
January 10
Pharmavise Corporation
Biotechnology • Pharmaceuticals • Healthcare Insurance
Pharmavise Corporation is the first Continuous Compliance Organization (CCO) dedicated to maintaining the highest standards of quality and regulatory compliance in the life sciences industry. Our esteemed client base includes Fortune 500 companies in pharmaceuticals, medical devices, and biotechnology. We offer bespoke solutions tailored to meet the specific compliance needs of our clients, supporting them from development through commercialization and ensuring they exceed their compliance goals while enhancing patient health and safety.
📋 Description
• Lead quality management system activities for medical devices. • Develop and implement compliance strategies. • Conduct risk assessments and provide guidance on regulatory submissions. • Collaborate with R&D, manufacturing, and regulatory affairs teams. • Stay updated on regulatory trends affecting the medical device industry.
🎯 Requirements
• 8 years of experience in quality assurance and regulatory compliance. • Advanced degree preferred. • Knowledge of ISO 13485, FDA QSR, and EU MDR. • Experience leading quality management systems. • Strong understanding of risk management principles. • Excellent communication and interpersonal skills. • Quality and regulatory certifications preferred.
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