Job Information
Adecco US, Inc. Regulatory Affairs Specialist in San Diego, California
Regulatory Affairs Specialist
Full Time
San Diego, CA, US
Salary Range: $90,000.00 To 110,000.00 Annually
Monday - Friday, 8:30 am - 5:00 pm
Who we Are:
A global leader in dental manufacturing with headquarters in San Diego, CA, subsidiaries in Canada, Germany, UK, and China, and sales in 105 countries worldwide. We are 500 team members strong. Founded more than 50 years ago as a precious metals company in South Africa, We have grown to become the largest dental zirconia manufacturer in North America, largest dental alloy provider worldwide, and leader in digital dentistry solutions with a product offering that spans fixed, removable, ortho, implants, and equipment.
About the Opportunity:
The Regulatory Affairs Specialist is responsible for ensuring foreign and domestic compliance for regulated dental products adhering to Quality and Regulatory compliance. This role works in conjunction with the Quality and Regulatory team to create, maintain and approve regulatory technical documentation, licensing, registrations and inspections in compliance with local, state, national and international regulatory requirements.
In this role, the successful candidate will:
• Maintains Regulatory Affairs certifications for domestic and international customers and distributors.
• Ensures company uses relevant information and judgement to determine whether events or processes comply with laws, regulations, or standards.
• Reviews document changes, product labeling and in-house procedures to ensure regulatory requirements are met.
• Prepares for and facilitates internal, external, and third-party audits as necessary.
• Provides input for selecting the most effective regulatory course of action.
• Supports International Operations with foreign product registration through distributors according to each country's regulatory requirements.
• Researches and responds to internal and external customer requests for regulatory information.
• Interprets regulatory rules or rule changes and ensures that they are communicated through corporate policies and procedures.
• Interfaces with the FDA concerning issuing Certificates to Foreign Government for The company Corporation and its subsidiaries as needed.
• Maintains Quality Assurance and Quality Management Certificates (ISO and CE) for The company and its subsidiaries interfacing with Notified Bodies.
• Maintains Declaration of Conformities for all company products and its subsidiaries.
• Reviews product promotional materials, labeling, batch records, specification sheets, or test methods for compliance with applicable regulations and policies.
• Accurately maintains the regulatory database to reflect all current and obsolete products.
• Communicates with the Secretary of State office, Department of State and Foreign Embassies or Consulates regarding authentication of documents to support the registration process.
• Supports product registration for company's International Branches to meet foreign requirements for China, Canada, Taiwan, Korea, and others.
• Develops and generates customer-specific certificates of quality analysis and conformities to satisfy distributor and customer-specific needs.
• Completes supplier and subcontractor evaluations and approval forms for customers.
• Provides and submits regulatory documentation to notified bodies and Authorized Representative to support MDD/MDR requirements.
• Represents Regulatory Affairs and Quality team in yearly audits for quality and regulatory documentation including Technical Documentation.
• Contributes to Regulatory projects and deliverables to ensure company remains compliant to MDR and ISO requirements.
Qualifications:
• Bachelor's degree and 5+ years of progressive experience in quality assurance and regulatory experience, or equivalent combination of education and experience.
• Experience in the medical device industry preferred.
• Ability to comprehend and follow technical work instructions and standard operating procedures.
• Working knowledge of cGMP regulations ISO 13485, 21CFR Part 820, CMDR SOR/98-282, 93/42/EEC, RDC 16 2013, MHLW MO 169 and TG(MD)R Sch3 preferred
• Strong problem solving, administrative, and data management skills.
• Demonstrated attention to detail.
• Team player with ability to work independently.
• Ability to multi-task, work under pressure and meet deadlines.
• Strong written and verbal communication skills.
• Maintain certification for California Notary Public.
Our Awesome Benefits!
Working for a growing innovative company like ours means exciting opportunities for training and learning, career development and advancement from only the best in the dental industry. With all that hard work, the company is committed to ensuring the welfare of its employees and provides an amazing benefit package that includes:
• Health Plans
• Dental Plans
• Vision Plan
• 401k with Employer Match
• Paid Time Off and Paid Holidays
• Employee Events
• Wellness Programs
• Discounts for home, travel, entertainment, relaxation that includes Mobile phone service, Technology, Airline and Hotel, Theater/Theme Park tickets, Restaurants and so much more!
Pay Details: $90,000.00 to $110,000.00 per year
Equal Opportunity Employer/Veterans/Disabled
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to https://www.adeccousa.com/candidate-privacy
The Company will consider qualified applicants with arrest and conviction records subject to federal contractor requirements and/or security clearance requirements.