Cedent Consulting Inc.
Regulatory Affairs Specialist III (Plano, TX)
Cedent Consulting Inc., Plano, Texas, us, 75086
Regulatory Affairs Specialist III (Plano, TX)
The Regulatory Affairs Level III (Senior Specialist) position is responsible for global product registrations and ensuring regulatory compliance in the design, manufacturing, and sales of medical devices (including Class I and II devices, software as a medical device, and de novo devices). The role includes obtaining and maintaining regulatory approvals, supporting quality management system (QMS) objectives, and ensuring adherence to applicable regulatory standards.
Responsibilities (Specific tasks, duties, essential functions of the job)
Regulatory Submissions and Compliance:
Develop regulatory strategies to achieve market clearance in an effective and efficient manner
Prepare, submit, and maintain product registrations, certifications, and approvals to meet US, EU and other regulatory requirements as applicable
510(k) and/or De Novo submissions for FDA
Technical documentation for EU MDR compliance
International product registration activities to meet business objectives
Provide regulatory input to support product labeling
Monitor new and changing regulatory requirements and ensure the business understands relevant impacts
Lead corrective and preventive action (CAPA) efforts as assigned
Product Development Support:
Provide regulatory input throughout the product lifecycle, including design controls, to support regulatory submissions
Change Control Management:
Assess and document regulatory impacts of design changes, manufacturing changes, et al, including related updates to product registrations
Audits and Inspections:
Support and participate in internal and external audits and regulatory agency inspections
QMS Support:
Complete QMS training activities and provide regulatory expertise to continuous improvement activities
Supporting Lean and Kaizen initiatives
Comply with all company policies and procedures
Assist with any other duties as assigned
Qualifications (Experience and Education)
Education:
Bachelor of Science degree
Experience:
5-7 years of regulatory affairs experience in medical device industry, preferably with respiratory devices. Current experience leading multiple successful 510(k) clearances and CE marking is required, and experience with additional global regulatory pathways is preferred
Technical Skills:
Strong understanding of medical device product life cycle and regulatory requirements. In-depth knowledge of ISO 13485, FDA regulations (including 21 CFR Part 820), and EU MDR. Knowledge of ISO 14971 risk management for medical devices. Proficiency in database systems and advanced Microsoft Excel skills for reporting and analysis. Understanding of continuous improvement principles.
Personal Attributes:
Strong verbal and written communication skills, with the ability to articulate complex technical issues clearly and effectively to cross‑functional teams and regulatory bodies. Strong analytical and critical thinking skills, with the ability to resolve complex complaints and implement long‑term solutions. High level of attention to detail and accuracy, particularly when preparing regulatory submissions.
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Responsibilities (Specific tasks, duties, essential functions of the job)
Regulatory Submissions and Compliance:
Develop regulatory strategies to achieve market clearance in an effective and efficient manner
Prepare, submit, and maintain product registrations, certifications, and approvals to meet US, EU and other regulatory requirements as applicable
510(k) and/or De Novo submissions for FDA
Technical documentation for EU MDR compliance
International product registration activities to meet business objectives
Provide regulatory input to support product labeling
Monitor new and changing regulatory requirements and ensure the business understands relevant impacts
Lead corrective and preventive action (CAPA) efforts as assigned
Product Development Support:
Provide regulatory input throughout the product lifecycle, including design controls, to support regulatory submissions
Change Control Management:
Assess and document regulatory impacts of design changes, manufacturing changes, et al, including related updates to product registrations
Audits and Inspections:
Support and participate in internal and external audits and regulatory agency inspections
QMS Support:
Complete QMS training activities and provide regulatory expertise to continuous improvement activities
Supporting Lean and Kaizen initiatives
Comply with all company policies and procedures
Assist with any other duties as assigned
Qualifications (Experience and Education)
Education:
Bachelor of Science degree
Experience:
5-7 years of regulatory affairs experience in medical device industry, preferably with respiratory devices. Current experience leading multiple successful 510(k) clearances and CE marking is required, and experience with additional global regulatory pathways is preferred
Technical Skills:
Strong understanding of medical device product life cycle and regulatory requirements. In-depth knowledge of ISO 13485, FDA regulations (including 21 CFR Part 820), and EU MDR. Knowledge of ISO 14971 risk management for medical devices. Proficiency in database systems and advanced Microsoft Excel skills for reporting and analysis. Understanding of continuous improvement principles.
Personal Attributes:
Strong verbal and written communication skills, with the ability to articulate complex technical issues clearly and effectively to cross‑functional teams and regulatory bodies. Strong analytical and critical thinking skills, with the ability to resolve complex complaints and implement long‑term solutions. High level of attention to detail and accuracy, particularly when preparing regulatory submissions.
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