Senior Regulatory Affairs Specialist - Remote @ Avanos Medical | Jobright.ai
JOBSarrow
RecommendedLiked
0
Applied
0
External
0
Senior Regulatory Affairs Specialist - Remote jobs in United States
Be an early applicantLess than 25 applicants
company-logo

Avanos Medical · 1 day ago

Senior Regulatory Affairs Specialist - Remote

ftfMaximize your interview chances
Health CareHospital

Insider Connection @Avanos Medical

Discover valuable connections within the company who might provide insights and potential referrals.
Get 3x more responses when you reach out via email instead of LinkedIn.

Responsibilities

Regulatory Submissions and Documentation
Compliance and Post-Market Activities
Cross-Functional Collaboration
Regulatory Strategy and Guidance
Audits and Inspections

Qualification

Find out how your skills align with this job's requirements. If anything seems off, you can easily click on the tags to select or unselect skills to reflect your actual expertise.

Regulatory ExpertiseEU MDR 2017/745Regulatory Affairs CertificationPost-Market ComplianceRisk ManagementCE Marking SubmissionsVigilance ReportingGlobal Medical Device RegulationsProject ManagementTechnical DocumentationDigital Health TechnologiesSoftware as a Medical DeviceISO 13485ISO 14971MDSAPChina NMPAJapan PMDACanada RegulationsAustralia Regulations

Required

Bachelor’s degree in a scientific, engineering, or medical field (e.g., Biology, Biomedical Engineering, Regulatory Science).
In-depth knowledge of MDR requirements, technical documentation, and post-market compliance activities.
Strong organizational and time-management skills to manage multiple priorities and deliverables.
Excellent written and verbal communication skills to convey regulatory requirements clearly to diverse stakeholders.
Analytical and critical thinking skills to assess regulatory risks and develop practical solutions.
Ability to work effectively with cross-functional teams and external partners to meet regulatory and business objectives.
High level of accuracy and thoroughness in regulatory submissions and documentation.
Ability to navigate complex and evolving regulatory landscapes effectively.
4 years of experience in regulatory affairs within the medical device industry or 2 years of experience with an advanced degree.
Extensive knowledge of EU MDR 2017/745, including technical documentation, clinical evaluations, post-market surveillance, and risk management requirements.
Proven experience in preparing and managing CE marking submissions and working with Notified Bodies.
Familiarity with global medical device regulations (e.g., FDA, ISO 13485, ISO 14971, MDSAP).
Experience in post-market regulatory activities, including vigilance reporting and field safety corrective actions.

Preferred

Advanced degree (Master’s or Ph.D.) is a plus.
Regulatory Affairs Certification (RAC) or equivalent certification is preferred.
Experience with digital health technologies, software as a medical device (SaMD), or combination products is an advantage.
Familiarity with additional global regulatory frameworks (e.g., China NMPA, Japan PMDA, Canada, Australia) is a plus.

Benefits

401(k) employer match of 100% of each pretax dollar you contribute on the first 4% and 50% of the next 2% of pay contributed with immediate vesting.
Benefits on day 1

Company

Avanos Medical

twittertwittertwitter
company-logo
Avanos Medical is a medical technology company that delivers clinical products and solutions for healthcare industries.

Funding

Current Stage
Public Company
Total Funding
unknown
2018-07-02IPO

Leadership Team

leader-logo
Joe Woody
Chief Executive Officer
linkedin
Company data provided by crunchbase
logo

Orion

Your AI Copilot