Global Senior Regulatory Affairs Specialist
2 months ago
Driven by the passion to improve quality of people’s lives, WS Audiology continues to grow as market leader in the hearing aid industry. With our commitment to increase penetration in an underserved hearing care market, we want to accelerate our business transformation in order to reach more people, more effectively.
The role
Are you ready to take on a pivotal role in a company at the forefront of the medical device industry? At WSAudiology, we’re navigating a rapidly evolving regulatory landscape, and we’re looking for a Global Senior Regulatory Affairs Specialist to join our team.
In this HQ-based position, you will be integral to ensuring that WSAudiology products meet the highest standards of compliance. Your role will be central to our day-to-day regulatory problem-solving and will involve active collaboration with our global Regulatory Affairs team and other key stakeholders across the organization.
Your mission will be to provide expert guidance and support, ensuring that our regulatory strategies are robust, and our compliance standards are upheld. You'll manage interactions with both HQ and global stakeholders while building confidence in the advice and support you offer.
Reporting directly to the Senior Director of Global Regulatory Affairs, you’ll play a crucial role in steering our regulatory affairs practices through this exciting transformation. If you're passionate about making a significant impact in the medical device sector and thrive in a dynamic environment, this role is for you.
In this role, you will specifically be expected to:
Serve as a primary knowledge resource for EU MDR, US FDA 21 CFR 820, and ISO 13485, with deep expertise in areas such as Technical Documentation requirements Lead Regulatory Affairs problem-solving initiatives and manage regulatory projects from concept to completionProvide expert guidance to the global organization on Classification, Intended Use, labeling requirements, and the Declaration of Conformity for hearing instruments, medical apps, and related accessoriesAct as the Subject Matter Expert (SME) on Regulatory Affairs during audits and inspections, ensuring compliance and addressing any regulatory concerns.Manage CAPA processes related to Regulatory Affairs, ensuring timely and effective resolution of issuesContribute to the development and execution of the Global Regulatory Affairs strategy, driving continuous improvement and regulatory excellenceCandidate profile
The ideal candidate has a proven track record as a Global Senior Regulatory Affairs Specialist and Project Lead in a complex organization, with demonstrated success in embedding a strong compliance culture throughout the entire organization. Additionally, you are likely to possess:
Experience
Personal competencies
A results-driven mindset with a deep commitment to delivering on promises and meticulous attention to detail The ability to interpret and enforce regulatory requirements pragmatically and effectively A dedication to compliance, consistently seeking opportunities to enhance and promote regulatory adherence Excellent interpersonal and intercultural communication skills, enabling effective collaboration with global colleagues and stakeholders Professional-level proficiency in English, both written and spokenSounds Wonderful? Join us
If the above sounds exciting, don't hesitate to send your CV, as we continuously review applicants.
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