Regulatory Affairs Specialist - Shockwave

Remote: 
Full Remote
Contract: 
Work from: 

Offer summary

Qualifications:

Bachelor's degree and a minimum of 2 years of related experience, or an advanced degree without experience, or equivalent work experience., Working knowledge of applicable domestic and international regulatory guidelines, policies, and regulations., Ability to work collaboratively in a fast-paced environment while managing multiple priorities., Strong communication skills for effective interaction with internal stakeholders..

Key responsibilities:

  • Assist with compiling, preparing, reviewing, and submitting regulatory submissions to authorities outside the US and EU.
  • Maintain regulatory shipping authorization documentation and assist with product registration documents.
  • Work with various departments to ensure compliance with applicable standards and interpret regulatory requirements.
  • Write and edit technical documents while supporting functional groups in developing data for regulatory submissions.

Johnson & Johnson Innovative Medicine logo
Johnson & Johnson Innovative Medicine https://innovativemedicine.jnj.com/
10001 Employees
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Job description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function:

Regulatory Affairs Group

Job Sub Function:

Regulatory Affairs

Job Category:

Professional

All Job Posting Locations:

Santa Clara, California, United States of America

Job Description:

Johnson & Johnson is hiring for a Regulatory Affairs Specialist – Shockwave to join our team located in Santa Clara, CA.

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease. Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.

Position Overview

The Regulatory Affairs Specialist is an individual contributor that works closely and partners with internal departments to efficiently and effectively meet assigned regulatory requirements. Under the direction of the Regulatory Affairs Team, the function of a Regulatory Affairs Specialist is to provide support for the regulatory department, including submission support and maintenance of existing product files, and ensures that deadlines are met.

Essential Job Functions

· Assist with compiling, preparing, reviewing and submitting regulatory submissions to authorities outside the US and EU (e.g., Latin America, Middle East, etc.)

· Assist with the preparation of OUS product registration(s) documents by working with distributors, and/or Local Responsible Person (LRP)

· Provide other country specific regulatory support

· Maintain Regulatory shipping authorization documentation for assigned geographies

· Assist with review of R&D, quality, preclinical and clinical documentation for submission filing

· Prepare and maintain annual licenses, registrations/listings, and registration renewal documentation

· Work with Regulatory management, product development, quality and operations functions to assist with interpretation and compliance of applicable standards (e.g., ISO and IEC standards, ROHS, applicable sections of 21 CFR, regulatory agency guidance documents)

· Effectively communicates, prepares, and negotiates with internal stakeholders. Properly interprets and applies regulatory requirements.

· Evaluate import/export requirements

· Ensure personal compliance with applicable company policies and procedures

· Write and edit technical documents

· Ability to perform multiple tasks concurrently with accuracy

· Knowledge of business functions and cross group dependencies/relationships

· Support functional groups in the development of relevant data to complete a regulatory submission

· Other duties as assigned

Requirements

· Bachelor's degree and a minimum of 2 years of related experience; or an advanced degree without experience; or equivalent work experience.

· Ability to work collaboratively in a fast-paced environment while managing multiple priorities

· Working knowledge of applicable domestic and international regulatory guidelines, policies and regulations

Additional Information:

The anticipated salary range for this position is:

Bay Area: $86,000-$138,000

Outside of Bay Area: $74,000-$119,600

The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation’s performance over a calendar/performance year. Bonuses are awarded at the Company’s discretion on an individual basis.

  • Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
  • Employees may be eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).
  • This position is eligible to participate in the Company’s long-term incentive program.
  • Employees are eligible for the following time off benefits:
    • Vacation – up to 120 hours per calendar year
    • Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington – up to 56 hours per calendar year
    • Holiday pay, including Floating Holidays – up to 13 days per calendar year
    • Work, Personal and Family Time - up to 40 hours per calendar year
  • Additional information can be found through the link below.  https://www.careers.jnj.com/employee-benefits

The compensation and benefits information set forth in this posting applies to candidates hired in the United States.

·      Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. 

Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center  (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource

The anticipated base pay range for this position is :

Bay Area: $86,000-$138,000 / Outside of Bay Area: $74,000-$119,600

Additional Description for Pay Transparency:

Required profile

Experience

Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Collaboration
  • Time Management
  • Communication

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