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Qs Auditor Jobs (NOW HIRING)

Manager, Quality Systems

Merrimack, NH · On-site

$115K - $140K/yr

This role is responsible for managing the timelines for QS initiatives including audit programs ... Certified Quality Auditor (CQA), Six Sigma, or similar certification * Experience serving as an ...

Manager, Quality Systems

Merrimack, NH · On-site

$125 - $150/hr

This role is responsible for managing the timelines for QS initiatives including audit programs ... Certified Quality Auditor (CQA), Six Sigma, or similar certification * Experience serving as an ...

What You'll Do: * Assist with SEC filings, including 10-Qs and 10-Ks * Support monthly and year-end ... Partner with internal and external auditors * Support acquisitions, divestitures, and other complex ...

Working knowledge of IATF 16949 and ISO 14001; internal auditor certification preferred ... Our family of companies also includes QS Nurses, and Aerospace Solutions. Looking for your dream ...

... 10-Qs, 10-Ks, 8-Ks, earnings presentations, and the annual proxy statement. The Vice President ... Manage the external auditor relationship for the quarterly review and annual audit of the Company ...

... 10-Qs, 10-Ks, 8-Ks, earnings presentations, and the annual proxy statement. The Vice President ... Manage the external auditor relationship for the quarterly review and annual audit of the Company ...

Working knowledge of IATF 16949 and ISO 14001; internal auditor certification preferred ... Our family of companies also includes QS Nurses , and Aerospace Solutions . Looking for your dream ...

Knowledge of ISO/AS/QS standards and precepts. Preferred * Experience in welding, machining and ... ASQ Certifications (CQE, Certified Auditor) strongly preferred Travel Travel requirement is 15% or ...

... QS, Dietary Ingredients and Supplements, and GMP standards. * Engage closely with Process ... Participate in the site's Food Safety Team, GMP auditing team, and team meetings to support daily ...

Associate

Plano, TX · On-site

$60 - $80/hr

... 10-Qs, Form 10-Ks, Form 8-Ks and earnings releases * Develop and maintain relationships with ... Interface with internal and external auditors * Develop and maintain workpapers that are SOX ...

Auditing product related issues and facilitating the process for assisting suppliers with product ... Our family of companies also includes QS Nurses , and Aerospace Solutions . Looking for your dream ...

Senior Quality Engineer

Jackson, MN · On-site

$83K - $113K/yr

Experience in Infinity QS - SPC tool. * Experience in ERP system. * Experience in facilitating customer/regulatory audits * Certified Quality Engineer (CQE), Certified Quality Auditor (CQA) or Six ...

Sr. Quality Engineer

Richfield, WI

$88K - $119K/yr

QS / ISO System experience. * Previous auditing experience. * Experience with ISO class 8 cleanroom. * Experience in working with a team, ability to drive change and influence cultural change. To ...

IL · On-site

$97K - $132K/yr

Experience preparing and reviewing 10-Ks, 10-Qs, proxy statements, and related disclosures. * Experience working with external auditors and managing complex reporting timelines. * Strong technical ...

Showing results 21-40

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How much do qs auditor jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for qs auditor in the United States is $19.21, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $19.23 per hour, depending on experience, location, and employer.

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Infographic showing various Qs Auditor job openings in the United States as of August 2026, with employment types broken down into 86% Full Time, 10% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $39,947 per year, or $19.2 per hour.

Manager, Quality Systems

Getinge

Merrimack, NH • On-site

$115K - $140K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 6 days ago


Getinge rating

9.3

Company rating: 9.3 out of 10

Based on 14 frontline employees who took The Breakroom Quiz

13th of 499 rated machine equipment manufacturers


Job description

With a passion for life
Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers - and to save more lives, we need team players, forward thinkers, and game changers.
Are you looking for an inspiring career? You just found it.
Job Overview
This role is responsible for leading quality-related initiatives, i.e. MQRB and Regulatory Audits, including identifying quality deliverables as outlined in the Quality Processes. The position plays an important role in enabling regulatory readiness and serves as the Backroom Manager during audits and inspections. You are responsible for leading and directing the workload of Quality System (QS) projects as required with key quality deliverables as specified. This role is responsible for managing the timelines for QS initiatives including audit programs, responses, QMS compliance efforts, and system-level improvements to ensure adherence to FDA and global regulatory standards. This role is to manage the QMS elements, while supporting the implementation and deployment of Quality Process enhancements. In this role, you will use your experience or expertise to develop and deliver on quality requirements, solve problems, influence a quality minded culture, develop and execute objectives for self and others, and be able to effect short-term and long-term /business goals. Contribute to continuous improvement initiatives to enhance quality project delivery and operational effectiveness.
Job Responsibilities and Essential Duties
  • Work with the Quality System (QS) team to develop and maintain timelines and milestones for assigned Quality initiatives by leading and managing the following Quality elements:
    • Management System Plans (MSPs) - Issuance, review, monitoring of actions and tracking status to closure.
    • External Audit Program and the coordination of responses.
  • Work with QS team to define scope, deliverables, timelines, and milestones for QMS elements to completion.
  • Develop and maintain QMS updates and progress to completion
  • Work with Program Management to align resources impacting quality projects.
  • Ensure alignment of projects within the QMS requirements and regulatory agency expectations
  • Drive continuous improvement of Quality Systems processes and tools
  • Partner with site Quality, Regulatory, Program Management, Engineering, Manufacturing, and Operations teams, as well as appropriate Global functions.

Audit Management
  • Serve as Backroom Manager for External audits (FDA, Notified Bodies, Customers, etc.)
  • Coordinate audit logistics, training, documentation readiness, and subject matter expert (SME) support
  • Lead post-audit activities including observations and commitments tracking

Governance & Reporting
  • Generate status updates.
  • Work with PMO regarding overall Quality System updates for project reviews.
  • Ensure effective escalation and resolution of quality project risks and delays

Project Risk Management & Compliance
  • Identify and proactively manage risks related to compliance and quality system performance
  • Ensure QS elements meet regulatory requirements (FDA, ISO 13485, GMP, etc.)
  • Maintain alignment with Global processes and initiatives

Minimum Requirements
  • Minimum of a bachelor's degree in engineering or science, or equivalent experience
  • Minimum of seven years of experience in medical device, pharmaceutical, or regulated industry.
  • Good ability to drive continuous improvement, correct deficiencies and to prevent recurrence
  • Strong knowledge of Quality Management Systems (QMS), FDA regulations (21 CFR Part 820 / 21 CFR Part 11), and ISO 13485 and applicable global standards

Required Knowledge, Skills and Abilities
  • Demonstrated experience managing Quality Systems elements (audits, regulatory inspections, and compliance initiatives)
  • Strong understanding of audit processes and regulatory inspections
  • Proven ability to drive complex projects and continuous improvement, correct deficiencies and to prevent recurrence to closure
  • Excellent attention to detail, communication, problem-solving, analytical, and organizational skills.
  • Ability to manage multiple priorities in a fast-paced environment
  • Proficient computer skills required; expert knowledge of Microsoft Office (including Word, PowerPoint and Excel) required, experience with Enterprise Resource Planning (ERP) system (such as SAP) required.

Preferred Qualifications
  • Certified Quality Auditor (CQA), Six Sigma, or similar certification
  • Experience serving as an audit backroom lead

Supervision/Management Of Others:
  • Responsible for the development and management of a small team of engineering/quality professionals.

Internal and External Contacts/Relationships
All levels internally and externally.
Annual salary of $115K to140K depending on experience plus 15% STIP
#LI-YA2
About us
With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.
Benefits at Getinge:
At Getinge, we offer a comprehensive benefits package, which includes:
  • Health, Dental, and Vision insurance benefits
  • 401k plan with company match
  • Paid Time Off
  • Wellness initiative & Health Assistance Resources
  • Life Insurance
  • Short and Long Term Disability Benefits
  • Health and Dependent Care Flexible Spending Accounts
  • Commuter Benefits
  • Parental and Caregiver Leave
  • Tuition Reimbursement

Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law. Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.

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About Getinge

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Dr Wayne, NJ, US