Jobs in the United States

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Added 20 mins ago
Firmware Engineering Manager, Data Center BIOS
Advanced Micro Devices, Inc
Austin, TX
…and fostering a culture of ownership, rigor, and continuous improvement. Critical thinking, clear communication, and the ability to translate complex architectural tradeoffs into actionable…
Added 1 hour ago
Mechanical Engineer - Advanced Mechanical Products (5865)
Honeywell
Kansas City, MO
You Must Have
Added 1 hour ago
Automation Manufacturing Engineer
KOCH INDUSTRIES INC
PHILLIPS, WI
Added 1 hour ago
Manufacturing Engineer Co Op Jan June
WATTS REGULATOR CO
GERMANTOWN, WI
…operations. In this hands-on role, you will contribute to the improvement and sustainment of manufacturing processes and equipment for existing products, while also supporting continuous…
Added 1 hour ago
Automation Technician
KOCH INDUSTRIES INC
MENOMONIE, WI
Added 1 hour ago
Manufacturing Quality Engineer Intern
ABB, INC.
NEW BERLIN, WI
Candidates must reside within a 50-mile radius of the office location · Intern must have reliable transportation to and from the worksite
Added 1 hour ago
Sales Application Engineer Data Centers
REXNORD INDUSTRIES, LLC
MILWAUKEE, WI
…applicable requirements. ____________________ Position:Application Engineer, Data Centers Vertical Reports To:VP of Sales Location:100% Remote (preferably East Coast USA or Central USA)…
Added 1 hour ago
EG
AI Automation Analyst
Eliassen Group
Madison, WI
- $70 to $75 USD / hour
Our client seeks an AI-driven process automation leader to support a large expert network and drive operational excellence. The role will identify, design, and deliver intelligent…
Added 1 hour ago
O
Network Security and Firewall Engineer - City
OKC
OKLAHOMA CITY, OK · Oklahoma City, OK
- $44.42 to $67.92 USD / hour
…an immediate supervisor. The Network Security and Firewall Engineer is responsible for designing, implementing, configuring, managing, and maintaining firewall infrastructure to protect the…
Added 1 hour ago
XL Batteries
XL Batteries
Marlborough, MA
The Chemical Process Engineer II is a full-time, on-site role based in Marlborough, MA, responsible for developing, optimizing, and scaling chemical processes for XL Batteries’ Organic Flow…
Added 1 hour ago
FC
Chief Building Engineer
Fairfax County
Fairfax, VA
- $37.01 to $64.77 USD / hour
Chief Building Engineer – Lead Operations for a Multi-Building Organization
Added 1 hour ago
Sr Security Engineer - IAM (SailPoint)
Hays
Raleigh, NC
MUST HAVE IAM Solution and Architecture Experience- specifically SailPoint · Must have knowledge of cloud directories such as Entra ID, AWS Directory Service and Google Cloud Identity
Added 2 hours ago
Senior Director, Software and Quality Engineering
OneStream
United States
Build a culture of ownership, high trust, inclusion, and continuous improvement, and upskill the organization on modern practices, including AI tools.
Added 2 hours ago
Continuous Improvement Engineer/Leader - Manufacturing
IPG
Clinton, IA
Assure execution of continuous improvement projects, supporting project sponsors or process owners in their successful completion. Assist continuous improvements teams with method…
Added 2 hours ago
I
Junior CPU Verification Engineer
Intel
Hillsboro, OR
- $91,150 to $128,690 USD / year
You must possess the below minimum qualifications to be initially considered for this position
Added 2 hours ago
Manufacturing /Industrial Engineer
Celestica
Portland, OR
The Manufacturing Process Engineer is responsible for designing, developing, deploying and optimizing processes for manufacturing to achieve quality, cost and delivery goals for Celestica…
Added 2 hours ago
EG
AI Automation Analyst
Eliassen Group
Salem, OR
- $70 to $75 USD / hour
Our client seeks an AI-driven process automation leader to support a large expert network and drive operational excellence. The role will identify, design, and deliver intelligent…
Added 2 hours ago
ENGINEER NUCLEAR 4
Huntington Ingalls Industries
Newport News, VA
…learning management system (LMS), and implement continuous improvement initiatives for training operations. RTNE instructors must be strong in using MS Office suite, especially presentation…
Added 2 hours ago
Naval Architect Engineer 3 - 30097 1
Huntington Ingalls Industries
Virginia Beach, VA
Shape the Future – Bring ideas, curiosity, and continuous improvement.
Added 2 hours ago
Advanced Training Systems Acquisition Engineer (Engineering Technician 3) - 31115
Huntington Ingalls Industries
Virginia Beach, VA
What You Must Have · Candidate must have experience in Navy combat systems modernization aligned with the Navy Modernization Process (NMP) framework
Added 2 hours ago
Full Stack Engineer 4 (Go, AWS)
Capital One
McLean, VA
Proactively identify areas for improvement, implementing targeted refactoring and contributing to efforts that reduce technical debt and enhance system performance
Added 2 hours ago
Full-stack Engineer 4, Cyber Endpoint Security
Capital One
Richmond, VA
Proactively identify areas for improvement, implementing targeted refactoring and contributing to efforts that reduce technical debt and enhance system performance
Added 2 hours ago
Full-Stack Engineer 4 (Python, AWS) (Cloud Operations Resilience Engineering)
Capital One
McLean, VA · Richmond, VA
Proactively identify areas for improvement, implementing targeted refactoring and contributing to efforts that reduce technical debt and enhance system performance
Added 2 hours ago
Staff Eng, Process Control
Smurfit Westrock
West Point, VA
The Process Control Engineer position: provides technological and engineering expertise for the implementation of new process control technology and equipment; evaluates and resolves…
Added 2 hours ago
B
Senior Electrical Controls Systems Engineer
BWXT
Lynchburg, VA
- $136,000 USD / year
BWXT is seeking a Senior Electrical Controls Systems Engineer to join our team in Lynchburg, VA. In this role, you will design, program, test, and optimize advanced control systems that…

Closed listing

Jobgether

Quality Systems Manager

Remote, United States

This opening has closed.

The original listing is kept below for reference.

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About employer

Job details

Experience: 5–10 years of experience in a medical device, pharmaceutical, biomedical, or other regulated quality environment.
Posting language: English
Posted: Nov 6, 2026

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Original job description

Archived listing. The details below describe a past opening.

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Quality Systems Manager based in the United States.

The Quality Systems Manager will oversee and continuously improve the Quality Management System (QMS) supporting a regulated medical device environment. This role ensures that internal processes, product quality, and distribution activities meet applicable regulatory requirements and industry standards. You will work closely with cross-functional teams across Quality, Regulatory, Operations, Clinical, and external manufacturing partners to maintain compliance and strengthen quality performance. The position combines technical expertise, regulatory knowledge, and stakeholder leadership to identify risks and implement effective solutions. You will also lead audits, support regulatory inspections, and drive initiatives that improve organizational quality capabilities. This is an opportunity to make a meaningful contribution to the safety, reliability, and quality of medical technologies. Accountabilities

In this role, you will lead Quality Systems activities, support regulatory compliance, and promote continuous improvement across internal teams and external partners. Your responsibilities will include:

• Quality Management System Oversight: Manage Quality Systems activities in accordance with organizational policies and applicable medical device regulations and standards.

• Cross-Functional Collaboration: Serve as the primary Quality Systems contact for internal stakeholders, supporting coordination with corporate Quality, Regulatory, Operations, and Clinical teams.

• Physician Communications: Manage communications with physicians regarding returned product analysis test results.

• Product Quality and Distribution: Lead and support cross-functional teams to ensure product quality and distribution activities comply with regulatory requirements, industry standards, and internal procedures.

• Process Management and Improvement: Implement, maintain, and improve quality processes and procedures, including internal audits, change management, supplier quality, clinical research quality, complaint handling, and document control.

• External Partner Management: Manage external contract design and manufacturing organizations (CMDOs) in collaboration with the sourcing team.

• Performance Monitoring: Track departmental goals, metrics, and performance indicators to ensure quality objectives are achieved.

• Resource Planning: Support resource planning and provide input into departmental and organizational budgets and staffing requirements.

• Quality and Compliance Awareness: Promote understanding of regulatory, quality, and customer requirements throughout the organization.

• Risk Management: Identify and communicate potential quality and compliance risks, recommending appropriate corrective actions.

• Regulatory Compliance: Support the maintenance and improvement of compliance with FDA 21 CFR Part 820 Quality Management System Regulation (QMSR), ISO 13485, and other applicable requirements across internal and external sites.

• Audits and Inspections: Lead internal and external audits and support inspections conducted by regulatory agencies and notified bodies.

• Continuous Improvement: Drive initiatives to strengthen Quality Systems processes, compliance activities, and overall operational effectiveness.

Requirements

The ideal candidate will combine a solid technical background with practical experience in quality management within a regulated medical device, pharmaceutical, or biomedical environment. Strong analytical, communication, and influencing skills are essential, along with the ability to manage competing priorities. The qualifications include:

• Bachelor's degree in Engineering, Computer Science, Physics, Life Sciences, or a related technical field. An advanced degree is preferred.

• 5–10 years of experience in a medical device, pharmaceutical, biomedical, or other regulated quality environment.

• Experience supporting quality engineering activities within a regulated product environment.

• Strong understanding of risk management, supplier quality, complaint management, and Quality Management System requirements.

• Ability to communicate technical and regulatory requirements effectively across different organizational levels.

• Familiarity with configuration and change management practices.

• Demonstrated ability to influence cross-functional stakeholders and manage competing priorities.

• Strong analytical, organizational, and problem-solving skills.

• Excellent written and verbal communication skills.

• Working knowledge of FDA regulations, including 21 CFR Parts 11, 801, 803, 806, 807, 812, 820, 822, and 830.

• Working knowledge of ISO 13485 and medical device Quality Management Systems.

• Understanding of Good Manufacturing Practice (GMP) requirements.

• Knowledge of quality processes throughout the product lifecycle.

• Understanding of statistical methods and quality improvement tools.

• Strong engineering and technical aptitude across hardware, software, and systems development environments.

• Experience supporting regulatory submissions, audits, and inspections is preferred.

Nice to have:

• Experience participating in regulatory inspections and third-party audits.

• Relevant professional certification, such as ASQ Certified Quality Manager (CQM), Certified Quality Engineer (CQE), or equivalent.

• ISO 13485 Lead Auditor or ASQ Certified Quality Auditor (CQA) qualification.

Additional role details:

• No direct reports; the role leads cross-functional contributors through expertise and influence.

• Full-time position, Monday through Friday, with working hours potentially varying according to the time zones supported.

• Occasional evening or weekend work may be required depending on business needs.

• Limited, occasional travel for specific projects, meetings, or events.

• Primarily based in a professional office or remote office environment, with occasional participation in supplier-related activities and events.

• Requires regular mobility, frequent use of computers and mobile devices, and the ability to communicate and collaborate effectively over extended periods. Reasonable accommodations may be made for individuals with disabilities.

Benefits

• Work Arrangement: Remote position based out of Lake Oswego, Oregon.

• Employment Type: Full-time, permanent position.

• Working Schedule: Standard Monday-to-Friday schedule, with hours adapted to the time zones supported.

• Travel: Limited and occasional travel for assigned projects, meetings, or events.

• Equal Opportunity: All qualified applicants receive consideration without discrimination based on legally protected characteristics.

How Jobgether works:

We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.

We appreciate your interest and wish you the best!

Why Apply Through Jobgether?

Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.

About employer

More about this job

Skills

Quality control systems
Quality assurance procedures
Regulatory compliance
Leadership
Inspection
Process improvement
Manage footwear quality systems
Medical device regulations
Internal auditing
Change management
Clinical research
Risk management
Communication skills
Computer science
Problem solving
Good manufacturing practices

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Work requirements

Jobs in the United States