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New · posted Nov 3

Cook Medical · Medical Devices

Regulatory Affairs Specialist II

  • Vandergrift, PA
  • On-site
  • Full-time
  • Associate & Specialist
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EmploymentFull-time
DeadlineCloses Nov 2, 2027

The role

The Regulatory Affairs Specialist II is responsible for the planning and preparation of submissions to obtain regulatory approvals for new and modified medical devices in specific markets. The Regulatory Affairs Specialist II develops regulatory strategies, obtains and maintains approvals, and serves as a communication liaison between the Cook manufacturer and the Cook International Local Office / Cook Distributor.

What you need

• Proficient in reading, writing and speaking English language.• Bachelor’s degree in relevant technical or scientific discipline.• Knowledge of medical device quality standards and regulatory requirements.• 3 years of experience in the medical device industry.• Computer experience required with working knowledge of Microsoft

Physical Requirements

• General office environment • Sits for extended periods• Requires close visual acuity when working with computers, etc.• Requires occasional early morning or late evening teleconferences• International and domestic travel as required

What you'll do

• Maintain an excellent understanding of global medical device regulations regarding the following: ISO 13485, MDR 2017/745, FDA 21 CFR Part 820 and others as required. • Serve as a liaison on regulatory issues between the Cook manufacturer and Cook Local Office and/or Cook Distributor and Notified Body.• Prepare regulatory submissions for new products, product changes, and re-registrations as required for the specific regions.• Create, organize, and maintain technical documentation.• Maintain registration information (license numbers, expiration dates, etc.) and obtain re-registration approvals in advance of license expirations to ensure no disruption in product availability.• Provide support to currently marketed products as necessary including input on/ creation of change requests, etc.• Support post market regulatory activities such as Post Market Surveillance Plans, Post Market Clinical Follow Up (PMCF) Plans and Reports, and Periodic Safety Update Reports (PSURs).

• Maintain and organize appropriate regulatory records to demonstrate compliance with applicable regulations.• Ability to multi-task and work within defined deadlines.• Ability to interpret regulations and apply them to real-world scenarios.• Must work and interact effectively and professionally with and for others throughout various levels of the global organization.• Detail-oriented with strong organizational and project management skills.• Maintain regular and punctual attendance.• Must maintain company quality and quantity standards.• Must have effective oral and written communication skills.• Excellent problem solving skills and ability to work in collaborative and independent work situations and environments with minimal supervision.• Ability to remain calm and receptive in fast paced situations.

Where you'll work

Vandergrift, PAOn-siteOpen in Maps (opens in a new tab)

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Job intelligence

The context around this role

Live data · November 3, 2026

Salary intelligence

How the pay compares

Associate & Specialist roles in the US31 roles publishing pay

Middle half $84,000 to $95,250, median $92,000
Annual base pay
Annual base payLowMedianHigh
All US$84,000$92,000$95,250

Comparisons: the base pay employers published on open Regulatory Affairs roles at the same level on Regulatory Jobs, November 3, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Regulatory Affairs

The general path across 302 open Regulatory Affairs roles on Regulatory Jobs, with the titles they carry most. Not Cook Medical's own promotion track.

  1. This role

    Associate & Specialist

    Often: Regulatory Affairs Specialist · Summer 2027 Internship

    $92K median42 open
  2. Next step

    Senior & Principal

    Often: Senior Regulatory Affairs Specialist · Principal Regulatory Affairs Specialist

    $141K median70 open
  3. Later

    Manager

    Often: Regulatory Affairs Manager · Manager, Regulatory Affairs

    $164K median65 open
  4. Later

    Director

    Often: Director, Regulatory Affairs · Senior Director, Regulatory Affairs

    $233K median105 open
  5. Later

    VP & Executive

    Often: Global Head of Injectable Aesthetics Regulatory Strategy · Global Head of Regulatory Affairs, Roche Diagnostics

    $333K median20 open

Skills DNA

What this role leans on

How many of the posting's 5 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 2 linesDocumentation and SOPs: 3 linesRegulatory submissions: 2 linesQuality systems and risk: 1 lineData and digital systems: 2 linesCollaboration and leadership: 2 linesGMPDocumentationSubmissionsQuality systemsData systemsTeamwork
  • Documentation and SOPs3
  • GMP and compliance2
  • Regulatory submissions2
  • Data and digital systems2
  • Collaboration and leadership2
  • Quality systems and risk1

Company hiring pulse

Cook Medical on Regulatory Jobs

9
Open roles
8
Distinct roles
5
Locations

By discipline

  • Quality6 67%
  • Regulatory2 22%
  • Clinical1 11%

By level

  • Senior & Principal5 56%
  • Associate & Specialist4 44%
See all 9 Cook Medical roles

More roles at Cook Medical

All 9 Cook Medical roles

Similar Regulatory Affairs roles elsewhere

Regulatory Affairs Specialist II at Cook Medical

Applications close November 2.

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