Home
Jobs

Regulatory Affairs Specialist

2 years

0 Lacs

Posted:2 days ago| Platform: Linkedin logo

Apply

Work Mode

On-site

Job Type

Full Time

Job Description

JOB SUMMARY:

The

Regulatory Affairs (RA) Specialist

is responsible for supporting the Regulatory Affairs department in global submissions, registrations, approvals, and audits; especially as it relates to footprints projects and sustaining activities. This is a great learning opportunity for someone interested in a Regulatory Affairs career in medical devices. Will train an enthusiastic, eager learner with a team attitude and passion for medical devices and helping patients thrive.

Primary Duties & Responsibilities

  • Supports footprints projects with the ability to multi-task
  • Assembles and submits documents for global registrations with direct oversight from the RA team
  • Ensures all deadlines are met, paying particular attention to any government deadlines
  • Collaborates with other departments to gather documentation needed for global submissions
  • Responds effectively and timely to internal and external partners
  • Tracks submissions and maintains applicable dashboards
  • Prepares weekly reports on status of current items/issues to manager
  • Organizes and maintains files, folders and databases to support the integrity of regulatory documentation
  • Orders documents, subscriptions, articles, standards and other items; including Free Sale Certificates and Certificates to Foreign Government
  • Coordinates audits as needed
  • Coordinates notarization and authentication (legalization) of documents
  • Coordinates shipment of documents (UPS, etc.) and may also be responsible in coordinating samples
  • Prepares data for audits, as needed
  • Reviews publications to keep abreast of regulatory landscape for medical devices
  • Performs special projects at the direction of the Regulatory Affairs Management
  • May assist in the regulatory review of product claims and literature

Job Requirements

REQUIREMENTS:

  • Bachelor’s degree in a related field plus 2 years of relevant work experience required, preferably in the Medical Device or Pharmaceutical industry or technical field.

Operating Company

Kerr
Envista and its family of companies (Envista) will not accept unsolicited resumes from any source other than directly from a candidate. Envista will consider unsolicited referrals and/or resumes submitted by vendors such as search firms, staffing agencies, professional recruiters, fee-based referral services and recruiting agencies (Agency) to have been referred by the Agency free of charge and Envista will not pay a fee for any placement resulting from the receipt such unsolicited resumes. An Agency must obtain advance written approval from Envista's internal Talent Acquisition or Human Resources team to submit resumes, and then only in conjunction with a valid fully-executed contract approved by the Global Talent Acquisition leader and in response to a specific job opening. Envista will not pay a fee to any Agency that does not have such agreement and written approval in place.

Mock Interview

Practice Video Interview with JobPe AI

Start Audits Interview Now
cta

Start Your Job Search Today

Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.

Job Application AI Bot

Job Application AI Bot

Apply to 20+ Portals in one click

Download Now

Download the Mobile App

Instantly access job listings, apply easily, and track applications.

coding practice

Enhance Your Skills

Practice coding challenges to boost your skills

Start Practicing Now

RecommendedJobs for You