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Product Specialist
Envista Holdings Corporation. Support day-to-day product management activities across assigned restorative and endodontic product portfolios .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in product management and labeling coordination, ensuring compliance with MDR and FDA regulations while effectively managing product lifecycles and documentation workflows. Proficient in utilizing tools like Microsoft Office and Adobe Illustrator to support product launches and labeling updates.
Highest-signal resume keywords
Labeling CoordinationRegulatory DocumentationProduct MarketingProject ManagementMedical Device Compliance
ATS Keywords
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Hard Skills
Labeling CoordinationRegulatory DocumentationProduct MarketingProject ManagementMDR ComplianceFDA ComplianceLabel Management SystemsECO DocumentationAdobe IllustratorMicrosoft Office
Soft Skills
Organizational SkillsCommunication Skills
Tools & Technologies
Label Management SystemsMicrosoft OfficeAdobe Illustrator
Industry Keywords
Medical DeviceEndodonticsRestorative ProductsHealthcare IndustryLabeling Requirements
About the role
Key responsibilities & impact- Support day-to-day product management activities across assigned restorative and endodontic product portfolios
- Maintain SKUs, product information, and product lifecycle coordination
- Assist with product launches, line extensions, rationalization efforts, and commercialization readiness
- Monitor product performance, customer feedback, competitive activity, and market trends
- Coordinate updates to product labels, IFUs, and packaging artwork
- Implement labeling changes including color coding, variable content updates, and layout improvements
- Maintain label master files and version control
- Ensure labeling changes comply with MDR and FDA regulations
- Support regulatory submissions and documentation, including 6012 forms and ECO approvals
- Track and archive label samples and artwork revisions for audit readiness
- Liaise with Merida and Pomona teams for label implementation and sample reviews
- Partner with Regulatory and Product Management teams on re-labeling projects and product launches
- Manage labeling updates for Endodontics and Rotary portfolios
- Identify opportunities to simplify and standardize labeling processes
- Support Kaizen initiatives and action plans related to labeling workflows
Requirements
What you’ll need- Bachelor’s degree in Business, Marketing, Regulatory Affairs, or related field
- 2–4 years of experience in labeling coordination, regulatory documentation, or product marketing
- Familiarity with medical device labeling requirements (MDR, FDA)
- Strong organizational and project management skills
- Proficiency in Microsoft Office, Adobe Illustrator, and label management systems
- Experience in dental or healthcare industry preferred
- Understanding of ECO and RA documentation workflows preferred
- Must reside within a commutable distance to both Brea, CA and Pomona, CA
- Must be available for onsite presence 4 days per week
Benefits
Comp & perks- Annual performance bonus may be included
- Medical, dental, and vision benefits may be included
- 401K match may be included
- Other applicable compensation plans may be included