Regulatory Affairs Manager

Katalyst CRO; Austin (TX); On-site; USD 100,000 - 150,000; Full time

Job summary

Dentsply Sirona Essential Dental Solutions is seeking an experienced Regulatory Affairs leader to oversee day-to-day operations of the team and drive regulatory strategy for medical devices globally.

You will manage 510(k) submissions, liaise with FDA and EU bodies, mentor staff, and ensure compliance across US and international markets while supporting product development through lifecycle.

Strong leadership, regulatory writing, and project management skills are essential.

Qualifications

• 5+ years of experience in regulatory affairs, preferably in the medical device industry.
• Experience with leading regulatory submissions and managing regulatory projects.
• In-depth knowledge of FDA 510(k) and international regulations (e.g., EN ISO 13485, EU MDR).

Responsibilities

• Overseeing day-to-day functions of the Dentsply Sirona Essential Dental Solutions team.
• Develops regulatory strategies for existing, new, and modified medical devices and other (regulated) products.
• Manages and submits 510ks for the products and manages communications with FDA including pre-subs.
• Mentors and guides direct reports and cross-functional teams on US and EU regulatory requirements.
• Works with business partners for registrations to ensure global compliance and champions initiatives to improve systems and compliance.
• Develops and implements strategies to obtain and maintain regulatory approvals for medical devices globally.
• Leads regulatory submissions, including 510(k) submissions, and technical files for CE marking.
• Manages communications with FDA and EU notified bodies for pre-submissions, 510(k) submissions, and CE technical files.
• Provides regulatory guidance to cross-functional teams across the product lifecycle.
• Reviews and interprets regulatory requirements to ensure compliance.
• Coordinates regulatory activities with internal teams and external agencies.
• Reviews and approves product labeling and claims for US/EU markets.
• Keeps current with regulatory requirements and updates policies.
• Fosters professional interactions with stakeholders and mentors regulatory staff.
• Performs other duties as assigned or needed.

Skills

Regulatory leadership

FDA submissions

Regulatory strategy

Communication

Cross-functional collaboration

Education

Bachelor's degree

Tools

Microsoft Office

Regulatory software

Job description

• The primary job responsibility for this position is overseeing the day-to-day functions of the Dentsply Sirona Essential Dental Solutions team
• This role develops regulatory strategies for existing, new, and modified medical devices and other (regulated) products
• This role manages and submits 510ks for the products and manages communications with FDA including pre-subs
• The individual will also be responsible for mentoring and providing guidance to their direct reports and cross-functional product development teams on US and EU regulatory requirements
• This role works closely with business partners for registrations in their respective countries to ensure compliance globally and acts as an internal champion for initiatives aimed at improving business systems and compliance
• Develops and implements regulatory strategies to obtain and maintain regulatory approvals for medical devices and other regulated products globally
• Leads and manages regulatory submissions, including 510(k) submissions, and technical files for CE marking
• Manages communications with FDA and EU notified bodies on behalf of the company for FDA pre submissions, FDA 510(k) submissions, and EU technical files submissions
• Provides regulatory guidance and support to cross-functional teams throughout the product lifecycle
• Reviews and interprets regulatory requirements and guidance documents to ensure compliance
• Coordinates regulatory activities with internal teams and external regulatory agencies
• Reviews and approves product labelling and claims for the US and EU markets
• Stays current with regulatory requirements and updates affected policies and procedures
• Fosters professional interactions with internal and external stakeholders through various communication channels, enhancing business relationships
• Manages day to day activities for less senior Regulatory Affairs professionals, including but not limited to mentoring, coaching, performance reviews, developmental plans, succession planning
• Complies with company and departmental policies and administrative requirements
• Performs other duties as assigned or as needed
• Actively articulates and promotes Dentsply Sirona's vision and direction
• Advocates on behalf of the customer
• Values driven with an insistence on excellence
• Promotes high performance, innovation, and continual improvement
• Consistently meets Company standards, ethics, and compliance requirements
• Resolves conflicts and fosters a positive working environment
• Bachelor's degree in a relevant field, such as life sciences, regulatory affairs, or a related discipline
  

Responsibilities

• The primary job responsibility for this position is overseeing the day-to-day functions of the Dentsply Sirona Essential Dental Solutions team
• This role develops regulatory strategies for existing, new, and modified medical devices and other (regulated) products
• This role manages and submits 510ks for the products and manages communications with FDA including pre-subs
• The individual will also be responsible for mentoring and providing guidance to their direct reports and cross-functional product development teams on US and EU regulatory requirements
• This role works closely with business partners for registrations in their respective countries to ensure compliance globally and acts as an internal champion for initiatives aimed at improving business systems and compliance
• Develops and implements regulatory strategies to obtain and maintain regulatory approvals for medical devices and other regulated products globally
• Leads and manages regulatory submissions, including 510(k) submissions, and technical files for CE marking
• Manages communications with FDA and EU notified bodies on behalf of the company for FDA pre submissions, FDA 510(k) submissions, and EU technical files submissions
• Provides regulatory guidance and support to cross-functional teams throughout the product lifecycle
• Reviews and interprets regulatory requirements and guidance documents to ensure compliance
• Coordinates regulatory activities with internal teams and external regulatory agencies
• Reviews and approves product labelling and claims for the US and EU markets
• Stays current with regulatory requirements and updates affected policies and procedures
• Fosters professional interactions
• Manages day to day activities for less senior Regulatory Affairs professionals, including but not limited to mentoring, coaching, performance reviews, developmental plans, succession planning
• Complies with company and departmental policies and administrative requirements
• Performs other duties as assigned or as needed
• Actively articulates and promotes Dentsply Sirona's vision and direction
• Advocates on behalf of the customer
• Values driven with an insistence on excellence
• Promotes high performance, innovation, and continual improvement
• Consistently meets Company standards, ethics, and compliance requirements
• Resolves conflicts and fosters a positive working environment
• Bachelor's degree in a relevant field, such as life sciences, regulatory affairs, or a related discipline
  

Requirements

• 5(+) years of experience in regulatory affairs, preferably in the medical device industry
• Experience with leading regulatory submissions and managing regulatory projects
• In-depth knowledge of FDA 510(k) and international regulations (e.g., EN ISO 13485, EU MDR)
• Required Computer / Software Skills:
• Proficiency with Microsoft Office Suite
• Proficiency with Regulatory software
• Strong leadership, project management, and organizational skills including attention to detail
• Strong written and verbal communication skills
• Prior technical writing experience and proven track record with FDA and EU regulatory submissions
• Excellent interpersonal skills
• Ability to work effectively in a team environment and independently
• Knowledge of regulatory affairs principles and practices
• Ability to critically review detailed scientific information and assess whether technical arguments are presented clearly, and conclusions are adequately supported
• Willingness to learn and adapt to new processes and technologies
• Leadership experience within medical device organizations
• Strong results orientation and analytical skills
• Clear and effective communication with key stakeholders, which span across multiple levels, socio-geographic areas, and functional expertise