Regulatory Affairs Specialist

Instant Systems Inc

$80K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 3-5 years of regulatory affairs experience focusing on 510k submissions
  • Bachelor's degree in a relevant field preferred
  • In-depth knowledge of medical device regulations and standards
  • Experience navigating regulatory submissions and agency interactions
  • Strong problem-solving skills with a focus on company-centered solutions

Responsibilities

  • Gain successful 510k and NDA approvals with USFDA
  • Serve as a regulatory liaison across cross-functional teams
  • Research and implement strategies for medical device compliance
  • Prepare and submit regulatory applications and reports
  • Respond promptly to inquiries from regulatory bodies
  • Maintain updated knowledge of relevant regulations
  • Develop standard operating procedures for compliance

Benefits

  • 401K plan
  • Comprehensive health coverage including medical, dental, and vision
  • Wellness program
  • Life insurance
  • Corporate sponsored events
  • Opportunities for skill development
  • Short term disability coverage
  • Clear pathways for career advancement
  • Collaborate with proactive and innovative teammates
  • Engage in a mission-driven environment
Full Job Description
Division

Description

The Regulatory Affairs Specialist (RAS) works to gain successful 510k approval by leveraging their skills and expertise to anticipate regulatory requirements and integrate compliance into project plans. The RAS streamlines preparation and submissions, by ensuring documentation is accurate, complete, organized and accessible. The RAS will work effectively with other departments to compile information and ensure that compliance requirements are met throughout the product lifecycle.

Primary function: successfully gain 510k & NDA approval with USFDA

Other responsibilities:
  • Represents regulatory affairs and serves as a liaison between regulatory bodies when working with cross-functional teams by providing regulatory feedback and guidance throughout the product development cycle.
  • Research, develop and implement regulatory and compliance strategies for new and modified medical devices in accordance with applicable regulatory bodies.
  • Prepares and submits applications and reports to applicable regulatory agencies of medical devices.
  • Responds to all requests for information from regulatory bodies in a timely and organized manner.
  • Maintains a current and working knowledge of regulations applicable to the company.
  • Develop and maintain positive and professional relationships with device reviewers through oral and written communications.
  • Develop and maintain standard operating procedures, work instructions, and policies to maintain compliance with applicable regulations and standards.
  • Compiles and communicates regulatory impact assessments and submission approval status reports.
  • Supports various audits.
    • Other Responsibilities
    • As assigned


To be considered you'll need:
  • A minimum of 3-5 years of relevant work experience in regulatory affairs, specifically working to compile and submit 510k applications
  • Bachelors degree in a relevant field preferred
  • Strong knowledge of medical device regulations and standards
  • Experience with regulatory submissions and interactions with regulatory authorities
  • Solid company-centric ideology.
  • Creative problem-solving skills.
  • The ability to balance multiple priorities.
  • Core values of honesty and respect.
  • The desire to be challenged.


You will thrive if you:
  • Enjoy an autonomous work environment.
  • Have a LEAN mindset.
  • Are the first person to help.
  • Seek out opportunities to bring added value.


Company Benefits & Perks
  • 401K
  • Health Benefits: Medical, Dental, Vision
  • Wellness Program
  • Life Insurance
  • Corporate Sponsored Events
  • Skill growth opportunities
  • Short Term Disability
  • Ability to Advance
  • Working with energetic & creative problem solvers
  • A mission worthy of your energy and expertise


Full-Time/Part-Time
Full-Time

Salary Range

This position is currently accepting applications.

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