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New · posted Nov 3

Integer · Medical Devices

Regulatory Affairs Specialist

  • Plymouth, MN
  • On-site
  • Full-time
  • Associate & Specialist
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Pay$73K–$108K
EmploymentFull-time
LocationPlymouth, MN
LevelAssociate & Specialist
FunctionRegulatory Operations
DeadlineOpen until filled

The role

By living according to a common set of values, we create a culture that unifies, embraces the uniqueness we all bring to the company, and positions Integer for long-term success.

At Integer, our values are embedded in everything we do.

Customer

We focus on our customers’ success

Innovation

We create better solutions

Collaboration

We create success together

Inclusion

We always interact with others respectfully

Candor

We are open and honest with one another

Integrity

We do the right things and do things right

Who are we?

Integer is a global organization providing innovative, high-quality technologies and manufacturing to Medical Device OEM’s (original equipment manufacturers) to enhance the lives of patients worldwide and a provider of high-end niche batteries for specialized applications in the energy, military, and environmental markets. We are guided by our six Values, including focus on Customers, Innovation, Collaboration, Inclusion, Candor, and Integrity. Working at Integer means you are part of a team passionately pursuing excellence in all that we do and always reaching for the next great achievement.

Regulatory Submissions/Approvals

  •  You will be responsible to prepare national and international regulatory submissions for Integer owned devices. You will provide team support for product submissions and consult with multiple sources for information to prepare submissions.
  • You will review Change Requests that require regulatory review and approval to ensure compliance with national and international government regulations.
  • You will prepare and maintain no-file decisions, external regulatory databases (ex. FDA FURLS, GUDID, EUDAMED, etc.), and product files consistent with Integer quality system requirements and department procedures.

Customer Support

  • You will coordinate the review of and responses to customer requests/queries for information related to process and products and maintain respective tracking logs.
  • You will participate in customer notification of changes and assist in maintaining respective tracking log.
  • You will obtain external regulatory documents in support of customer requests (ex. CFG’s, CFS’s) and facilitate the legalization/authentication/apostilling of such documents, as required.

External and Internal Audits

  • You may perform and support internal quality system audits in accordance with Integer quality management system procedures and according to the external requirements as indicated in the Integer Quality Manual.
  • You will participate in regulatory and Notified Body audits as a regulatory team member in either back room or front room activities and may compile, organize and track responses to findings.

Manufacturing Excellence Imperatives

  • Provide support of Integer’s Manufacturing Excellence and Market Focused Innovation Strategies
  • Participation or Leadership in Site Hoshin Planning, Quality Planning, Validation master plans and associated quality improvement imperatives
  • Provide data as required for QA RA weekly and monthly metrics, supporting the walk to differentiated quality.
  • Support Leadership of Sustained Change ensuring customer change notifications are initiated and completed, as necessary, and supporting continuous improvement activities as required.
  • Support the standardisation of workplace organization & visual controls (5S), Manufacturing Standard Work, and robust training & certification programs where applicable.
  • Associate Engagement promoted through the adoption of standardized problem solving. methodologies, behaviour-based safety programs, and improvement idea and suggestion systems.
  • Systems & Process Optimization through adoption of principles of built in quality.

What you need

Skills named in this posting

What you'll do

What you’ll do in this role

The primary purpose of this job is to provide team support to Regulatory Affairs managers and department management in being responsible for capturing, archiving, and publishing of regulatory documents.  Develop strategies and prepare submissions for national and international product registrations.  Prepares and maintains regulatory files, regulatory reports, and databases.

  • You adhere to Integer’s Values and all safety, environmental, security and quality requirements including, but not limited to: Quality Management Systems (QMS), Safety, Environmental and Security Management Systems, U.S. Food and Drug Administration (FDA) regulations, company policies and operating procedures, and other regulatory requirements.

Quality System Responsibilities

  • You will perform work on projects where you will follow Integer’s standard quality management system methodologies to investigate opportunities for process improvements.
  • You are expected to collaborate with others in the exchange of information, ask questions and regularly check for understanding in support of your development as a regulatory professional.
  • You embed Quality within the Regulatory discipline – “I own Quality.”  You are a standard bearer for Quality in everything we do at Integer, by assuring adherence to our Quality Management System (QMS), facilitating and/or contributing to corrective and preventive actions, and contributing to the successful attainment of our quality KPI’s and journey to differentiated quality.
  • You may perform other duties as needed and as directed by your line of supervision.

How you will be measured

  • Safety is our highest priority; you will be an active supporter of the Integer Environmental, Health & Safety programs.
  • You will have defined Goals and Objectives specifying key projects and expected milestones to achieve.
  • Achievement of site quality KPI’s
  • Innovation and ideation are critical aspects of your role, and you will be expected to generate continuous improvement suggestions and support the implementation of them.

Pay and benefits

$73,425 – $107,690 a year

Employer provided
How this compares

What sets you apart

  • Preferably, you have earned, as a minimum, a bachelor’s degree and have at least 1 year of relevant experience.  Candidates who do not meet the education requirement may be considered if they have a minimum of 3 years’ relevant medical device or other regulated industry experience.
  • While you will have occasional support and guidance from more experienced regulatory professionals, supervisors or managers, you will demonstrate the ability to work independently as well as collaboratively with other associates and cross functional teams.
  • You demonstrate an understanding of the European Medical Device Regulation, US FDA regulations and other applicable regulations as identified in the Quality Manual.
  • You demonstrate a solid technical aptitude with the ability to be an effective contributor to a team or produce results of a technical nature as an individual.
  • You demonstrate competencies in both written and oral communications.
  • You are highly organized and able to work and track multiple projects simultaneously.
  • You possess intermediate to advanced skills using Microsoft Office (PowerPoint, Visio, Project, etc.)
  • You possess a positive, can-do attitude with an underlying belief that failure is not an option.

Salary Range $73,425 - $107,690

Our total rewards program is designed to attract, retain, and motivate associates to contribute to Integer’s success. Our compensation program includes base salary and a cash-based incentive program supporting our pay-for-performance philosophy. We provide a comprehensive benefits package with immediate eligibility including medical, dental, vision, disability, life insurance, and adoption benefits. Parental leave is available after one year. Optional employee-paid programs include supplemental life insurance, critical illness, hospital indemnity and accident insurance. Employees are immediately eligible to participate in the 401(k) plan with company matching contributions. We provide 80 hours (10 days) of company designated holidays per year plus an annual allotment of paid time off.

  • Medical, dental and vision insurance

  • Disability and life insurance

  • 401(k) with company match

  • Paid time off

  • 10 paid company holidays

  • Parental leave after one year

Where you'll work

Plymouth, MNOn-siteOpen in Maps (opens in a new tab)

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Equal opportunity, accessibility and legal noticesInteger's statements, word for word

The specific measures listed below may be subject to change and are not intended to be an all-inclusive list.

U.S. Applicants: Equal Opportunity Employer. In addition, veterans and individuals with disabilities are encouraged to apply.

Job intelligence

The context around this role

Live data · November 3, 2026

Salary intelligence

How the pay compares

This role's midpoint is 7% above the US median for Regulatory Operations roles at this level.

This roleEmployer provided

$73,425 to $107,690 a year

Associate & Specialist roles in the US7 roles publishing pay

Middle half $73,500 to $91,250, median $85,000
Annual base pay
Annual base payLowMedianHigh
This role$73,425—$107,690
All US$73,500$85,000$91,250

This role: Integer's own published range. Comparisons: the base pay employers published on open Regulatory Operations roles at the same level on Regulatory Jobs, November 3, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Regulatory Operations

The general path across 41 open Regulatory Operations roles on Regulatory Jobs, with the titles they carry most. Not Integer's own promotion track.

  1. This role

    Associate & Specialist

    Often: 2027 Summer Intern Regulatory Affairs & Operations · Product Support Regulatory Affairs Specialist

    $85K median8 open

  2. Next step

    Senior & Principal

    Often: Senior Associate, Regulatory Affairs Submission Management · Reporting and Solutions

    6 open

  3. Later

    Manager

    Often: Manager, Regulatory Operations · Senior Manager, Business Capability Analyst, Global Regulatory Information Data & Systems

    $176K median13 open

  4. Later

    Director

    Often: Associate Director, Global Regulatory Project Management and Strategic Planning · Associate Director, Regulatory Business Systems & Capability Strategy

    $199K median13 open

  5. Later

    VP & Executive

    Often: Vice President, Head of Global Regulatory Operations

    1 open

Career resources on Regulatory Operations

Skills DNA

What this role leans on

How many of the posting's 34 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 4 linesLab testing and methods: 2 linesDocumentation and SOPs: 5 linesInvestigations and CAPA: 1 lineValidation and qualification: 1 lineRegulatory submissions: 2 linesQuality systems and risk: 7 linesCollaboration and leadership: 8 linesGMPLab testingDocumentationInvestigationsValidationSubmissionsQuality systemsTeamwork
  • Collaboration and leadership8
  • Quality systems and risk7
  • Documentation and SOPs5
  • GMP and compliance4
  • Lab testing and methods2
  • Regulatory submissions2
  • Investigations and CAPA1
  • Validation and qualification1

Company hiring pulse

Integer on Regulatory Jobs

19
Open roles
17
Distinct roles
10
Locations

By discipline

  • Quality16 84%
  • Regulatory3 16%

By level

  • Associate & Specialist9 47%
  • Senior & Principal7 37%
  • Manager3 16%
See all 19 Integer roles

More roles at Integer

All 19 Integer roles

Similar Regulatory Operations roles elsewhere

Regulatory Affairs Specialist at Integer

Open until filled. $73K–$108K a year, employer provided.

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