Director of Quality and Regulatory Affairs

  • Guilford, CT, USA
  • Full-time

Company Description

At 4Catalyzer we are transforming 21st century medicine by solving today’s most challenging problems in the biomedical sciences. We aspire to create significant societal impact and are motivated by the idea that our products will change the lives of people we love. We seek the talent of truly gifted, self-starting and driven individuals to help advance this mission. We provide a stimulating environment, surrounded by brilliant, highly committed individuals who are given both the autonomy and project ownership to solve difficult problems and be the first to publish.

 

Job Description

Quality and Regulatory Affairs Lead coordinates all activities involving development, implementation and maintenance of quality management systems and compliance across the company. This position is ultimately responsible for establishing and maintaining the quality management system and ensuring quality standards are upheld across the organization, as well as establishing and maintaining key processes, procedures and documentation to support regulatory requirements and filings.  Ensures internal and external compliance with stated practices and procedures and support regulatory and agency inspections and/or audits as necessary.

Qualifications

·        Minimum 7 years in a QA leadership role within the medical device industry with knowledge in GMP and GCP experience

·        Bachelor of Science or higher degree in a technical discipline

·        Experience in medical imaging strongly preferred     

·        Demonstrated experience in QA oversight and management of products through the lifecycle of medical device product development;

·        Experienced QA leadership background with a track record of establishing and maintaining quality systems, practices and policies in device development environment;

·      Deep experience with establishing and maintaining ISO, CFR, GxP, and other relevant compliant quality management systems across the device spectrum;

·         Experience applying GxP Quality knowledge through standard operating procedures (SOPs) to facilitate business operations and when needed develop procedural solutions to resolve quality and compliance challenges;

·        Experience applying Quality Systems (e.g., change control, deviations, CAPA, complaint management, and documentation management among others)

·        Thorough knowledge of FDA assessments of QSR processes;

·        Lead, support, and participate in auditing activities and regulatory inspections; evaluate responses to audit findings for adequacy and assurance of risk management

·        Track record of successfully working with and managing third-party vendors;

·        Knowledge of 510(k), PMA, international regulatory filings, and ongoing submission maintenance requirements a plus;

 ​​​​​

 

Additional Information

4Catalyzer is an equal opportunity employer regardless of race, color, ancestry, religion, gender, national origin, sexual orientation, age, citizenship, marital status, disability, or Veteran status.