Varex Imaging Regulatory Affairs Analyst participates in ensuring compliance of medical and industrial X-ray products. The Regulatory Affairs Analysts is a key player in a cross-functional team that includes Engineering, Manufacturing, Sales, Marketing, Quality and Customers. In addition, the regulatory affairs analyst is expected to perform the following:
Job Description
- Keeps abreast of medical device regulatory procedures, medical device safety standards and changes in global regulations.
- Strong working knowledge of FDA regulations, UK, EU, ISO13485, Brazil, Australia, China, Japan, Canada, and Rest of World
- Compiles all materials required in submissions, license renewal and annual registrations to FDA, Health Canada, China NMPA, and other international authorities.
- Supports global product registrations, including the compilation and maintenance of regulatory dossiers, technical documentation, and country-specific submission materials.
- Performs device classification assessments in accordance with regulatory frameworks in the U.S., Canada, EU, China, and other global markets
- Maintains strong understanding of country-specific documentation and regulatory expectations for product submissions, compliance, and import/export.
- Prepares and provides Certificates of Compliance, Declarations of Conformity, and other supporting compliance documents for internal and external stakeholders.
- Participates in post-market surveillance, GMP compliance, 3rd party audits, inspections, reviews and approves advertising and promotions materials.
- Recommends changes for labeling, manufacturing, marketing, and usability protocols for medical device regulatory compliance.
- Participate as team member to plan, develop, and implement regulatory strategy throughout the medical device product lifecycle.
- Reviews and approves design outputs.
- Uses regulatory information and knowledge to integrate regulatory perspectives into the organization, its policies, and procedures.
- Reviews, approves, and recommends changes for labeling, manufacturing, marketing, and test protocols for regulatory compliance and/or approval.
Required Skills and Experiences
- Bachelor's Degree in life sciences, engineering, regulatory compliance,
- 2+ years of experience in regulatory compliance in the medical device industry and medical device safety standards.
- 2+ years of experience driving related medical device safety standards into design requirements.
- 2+ years of experience completing multiple submissions across health authorities.
- Experience with Class I, II, and/or III medical devices and industrial products (including experience determining device classifications globally).
- Proven track record of preparing and managing regulatory submissions (e.g., FDA 510(k), Health Canada License Applications, EU Technical Files, NMPA dossiers, etc.).
- Experience supporting product registrations and certifications across multiple international markets.
- Microsoft Office/ERP/QMS Software competency
What we offer
- A unique opportunity to become part of growing organization in India being part of a global market leader in Xray imaging components.
- Excellent development potential
- An international work environment with global teams collaborating on various projects across several countries.
- Competitive compensation package including participation in Varex incentive plans
- Corporate Health Benefits
- Additional benefits will be added as we grow
