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Regulatory Affairs Specialist 4

ICONMA, LLC

Sunnyvale, CA

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JOB DETAILS
SALARY
$53.65–$58.65 Per Hour
SKILLS
Biomedical Engineering, Biotech and Pharmaceutical, Communication Skills, Cross-Functional, Document Management, Documentation, Electrical Engineering, Health Canada, Health Plan, Interpersonal Skills, Manufacturing/Industrial Processes, Mechanical Engineering, Medical Equipment, Multitasking, Negotiation Skills, Pharmacy, Presentation/Verbal Skills, Product Control, Product Design, Product Lifecycle Management, Product Reviews, Product Testing, Regulations, Regulatory Submissions, Risk, Risk Management, Team Player, Technical Writing, Validation Testing, Writing Skills
LOCATION
Sunnyvale, CA
POSTED
12 days ago
Our Client, an American Biotechnology company, is looking for a Regulatory Affairs Specialist 4 for their Sunnyvale, CA/Hybrid location.
 
Responsibilities:
  • Provide regulatory guidance to product teams, develop regulatory plans, and review and approve product design control documentation.
  • Determine regulatory pathways and formulate regulatory strategies for the U.S. and Canadian markets.
  • Assess regulatory impact on design, materials, labeling, packaging, manufacturing processes, and facility changes. Influence and lead global regulatory strategies.
  • Coordinate with technical experts to provide additional data/information requested by regulatory agencies and prepare responses to facilitate regulatory approvals.
  • Provide risk-based guidance and regulatory input to projects and issues, ensuring cross- functional alignment and resolution.
  • Collaborate with international counterparts to support global regulatory submissions, approvals, and implementation rollouts.
 
Requirements:
  • Minimum 8 years of regulatory affairs experience working in a medical device company (can be in combination with a regulatory affairs master degree; e.g., Masters in Regulatory Science)
  • In-depth understanding of US Medical Device regulations, Health Canada guidance and EU MDR.
  • Regulatory working knowledge of product lifecycle management, design controls, risk management, verification and validation, and product labeling requirement
  • Ability to work in a fast-paced environment and handle multiple projects simultaneously
  • Strong verbal and written communication skills, proven ability to translate technical documentation into effective internal documentation, and regulatory submissions
  • Team player who seeks to help and learn from colleagues seeing the department success as their own
  • Strong interpersonal and negotiation/influencing skills while maintaining a high level of professionalism
  • Proactively seeks to develop and become well-versed within the regulatory landscape.
  • Required Education and Training
  • Minimum B.S. or higher in Biomedical Engineering, Electrical Engineering, Mechanical
  • Engineering, or Pharmacy preferred. Non-technical degrees with equivalent complex medical device experience are acceptable.
  • Preferred Skills and Experience
  • RAPS Regulatory Affairs Certification (RAC) is a plus.
 
Why Should You Apply?

About the Company

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ICONMA, LLC