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Project Manager Quality Systems Jobs (NOW HIRING)

Getinge

Manager, Quality Systems

Merrimack, NH · On-site

$115K - $140K/yr

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 ...

watlow

Manager, Quality Systems

Saint Louis, MO · On-site

The Quality Manager-Systems role to be located Saint Louis, Mo is a challenging opportunity for an ... Member of the Quality Leadership Team, leading and supporting action/projects in support of ...

Stratasys Ltd

Manager, Quality Systems

Belton, TX · On-site

$100 - $125/hr

Manager, Quality Systems Location: Belton, TX, US Job ID: 55440 Category: Manufacturing & Operations Stratasys is a world leader in 3D printing! Stratasys is leading the global shift to additive ...

Stratasys

Manager, Quality Systems

Belton, TX

The Manager, Quality Systems at Stratasys Direct Manufacturing (SDM) leads and maintains the Quality Management System to ensure product conformity, regulatory compliance, and customer satisfaction.

Nihon Kohden

Quality Systems Manager

Irvine, CA · On-site

$100K - $145K/yr

This role requires strong leadership, project management, and working knowledge of medical device quality system regulations and standards. Essential Functions and Main Duties * Manage Nihon Kohden ...

Rheinmetall

Project Manager - Quality

Auburn Hills, MI · On-site

$125 - $150/hr

Our expertise spans electronic and mechanical systems, fabricated structures, armored products ... Job Summary: The Project Manager oversees the company's compliance management software ...

Iambic Therapeutics, Inc

$152K - $190K/yr

JOB SUMMARY This role will assist in leading activities within Quality Systems and Compliance, with responsibility for designing and implementing a Quality Management System (QMS) that supports ...

Delta Research

Quality Systems Manager

Livonia, MI · On-site

$100 - $125/hr

Quality Systems Manager POSITION SUMMARY Reporting directly to the VP of Quality with ... Lead cross-functional quality improvement projects. * Support risk assessment and mitigation ...

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Project Manager Quality Systems information

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$117K

How much do project manager quality systems jobs pay per year?

As of Sep 9, 2026, the average yearly pay for project manager quality systems in the United States is $116,384.00, according to ZipRecruiter salary data. Most workers in this role earn between $116,500.00 and $116,500.00 per year, depending on experience, location, and employer.

What is a project manager quality systems?

A Project Manager Quality Systems is a professional responsible for overseeing the planning, implementation, and maintenance of quality management systems within an organization. They ensure that processes and deliverables meet regulatory standards and internal quality benchmarks throughout a project's lifecycle. This role often involves coordinating cross-functional teams, developing quality assurance protocols, conducting audits, and driving continuous improvement initiatives. Project Manager Quality Systems play a critical role in industries such as healthcare, manufacturing, and pharmaceuticals, where adherence to quality standards is essential.

How does a project manager quality systems typically collaborate with cross-functional teams to achieve quality objectives?

A Project Manager Quality Systems works closely with cross-functional teams, including engineering, manufacturing, regulatory, and quality assurance, to ensure that quality standards are integrated into every stage of a project. This often involves leading meetings, facilitating communication between departments, and aligning project goals with compliance requirements. Effective collaboration is key to identifying potential quality risks early and implementing corrective actions promptly. By fostering a culture of quality and continuous improvement, the Project Manager helps teams stay focused on delivering consistent, high-quality results.

What are the key skills and qualifications needed to thrive as a project manager quality systems, and why are they important?

To thrive as a Project Manager Quality Systems, you need strong project management abilities, a solid understanding of quality assurance principles, and typically a relevant degree such as engineering or life sciences. Familiarity with quality management systems (QMS), regulatory compliance standards (like ISO 9001), and project management tools (such as MS Project or Jira) is essential. Outstanding communication, leadership, and problem-solving skills help you drive cross-functional collaboration and continuous improvement. These competencies are vital to ensure projects are delivered efficiently while meeting stringent quality and regulatory requirements.

What is the difference between Project Manager Quality Systems vs Quality Assurance Specialist?

AspectProject Manager Quality SystemsQuality Assurance Specialist
CertificationsISO 9001 Lead Auditor, PMPISO 9001 Lead Auditor, CQE
Work EnvironmentCross-departmental, project-focusedQuality department, compliance-focused
Employer & Industry UsageManufacturing, pharma, techManufacturing, healthcare, biotech

The Project Manager Quality Systems oversees quality projects, ensuring compliance and process improvements across departments. The Quality Assurance Specialist focuses on maintaining quality standards, conducting audits, and ensuring product compliance. While both roles require similar certifications and work within quality frameworks, the project manager emphasizes managing initiatives, whereas the QA specialist concentrates on compliance and testing.

What cities are hiring for Project Manager Quality Systems jobs?

Cities with the most Project Manager Quality Systems job openings:

What states have the most Project Manager Quality Systems jobs?

States with the most job openings for Project Manager Quality Systems jobs include:

What are popular job titles related to Project Manager Quality Systems jobs?

For Project Manager Quality Systems jobs, the most frequently searched job titles are:

Infographic showing various Project Manager Quality Systems job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $116,384 per year, or $56 per hour.

Manager, Quality Systems

Merrimack, NH • On-site

Getinge
Medical Equipment and Supplies Manufacturing • 10K+ employees
Learn more about Getingeexternal

$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

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Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Dr Wayne, NJ, US

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