Jobs in the United States

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Tool Room Supervisor - Livonia Area
The Pivot Group Network
Livonia · Livonia, MI
Experience with preventive maintenance tracking systems.
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Tool Room Supervisor - Coldwater Area
The Pivot Group Network
Coldwater · Coldwater, MI
Experience with preventive maintenance tracking systems.
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Project Manager - Houghton Area
The Pivot Group Network
Houghton · Houghton, MI
Familiarity with ERP and manufacturing execution systems.
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Laser Weld Engineer - Flint Area
The Pivot Group Network
Flint · Flint, MI
Are you a dedicated professional with a passion for excelling as a laser weld engineer? The Pivot Group Network, a Michigan manufacturing-focused recruiting group, is committed to fostering…
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Six Sigma Black Belt - Iron River Area
The Pivot Group Network
Iron River · Iron River, MI
Support audits and corrective actions for quality systems.
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Applications Engineer - Gladwin Area
The Pivot Group Network
Gladwin · Gladwin, MI
Are you a forward-thinking professional with a passion for excelling as a applications engineer? The Pivot Group Network, a Michigan manufacturing-focused recruiting group, is committed to…
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PLC Programmer - Petoskey Area
The Pivot Group Network
Petoskey · Petoskey, MI
…Technician, Automation Technician, Controls Technician, Electrical Engineer, Systems Integrator, Maintenance Technician, Controls Engineer, Automation…
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Embedded Systems Engineer - Coldwater Area
The Pivot Group Network
Coldwater · Coldwater, MI
Are you a meticulous professional with a passion for excelling as a embedded systems engineer? The Pivot Group Network, a Michigan manufacturing-focused recruiting group, is dedicated to…
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Quality Engineer - Houghton Area
The Pivot Group Network
Houghton · Houghton, MI
Manufacturing Quality Engineer, Quality Assurance Engineer, Process Quality Engineer, Customer Quality Engineer, Quality Systems Engineer, Continuous Improvement Engineer, Quality Analyst,…
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Advanced Quality Engineer - Iron Mountain Area
The Pivot Group Network
Iron Mountain · Iron Mountain, MI
Quality Systems Engineer, Process Quality Engineer, Customer Quality Engineer, Reliability Engineer, Quality Specialist, Quality Engineer, Supplier Quality Engineer, Manufacturing Quality…
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Quality Supervisor - Wixom Area
The Pivot Group Network
Wixom · Wixom, MI
Experience with quality software and ERP systems.
Added 2 mins ago
Quality Engineer - Marquette Area
The Pivot Group Network
Marquette · Marquette, MI
Quality Systems Engineer, Continuous Improvement Engineer, Quality Analyst, Reliability Engineer, Supplier Quality Engineer, Manufacturing Quality Engineer, Quality Assurance Engineer,…
Added 2 mins ago
Automation Engineer - Iron River Area
The Pivot Group Network
Iron River · Iron River, MI
Controls Engineer, Automation Technician, Manufacturing Engineer, Electrical Controls Engineer, Robotics Engineer, Process Automation Engineer, PLC Programmer, Maintenance Engineer, Systems…
Added 2 mins ago
Advanced Quality Engineer - Niles Area
The Pivot Group Network
Niles · Niles, MI
Supplier Quality Engineer, Manufacturing Quality Engineer, Quality Assurance Engineer, Continuous Improvement Engineer, Quality Systems Engineer, Process Quality Engineer, Customer Quality…
Added 2 mins ago
Applications Engineer - Croswell Area
The Pivot Group Network
Croswell · Croswell, MI
Are you a meticulous professional with a passion for excelling as a applications engineer? The Pivot Group Network, a Michigan manufacturing-focused recruiting group, is dedicated to…
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Quality Engineer - Flint Area
The Pivot Group Network
Flint · Flint, MI
Quality Systems Engineer, Continuous Improvement Engineer, Quality Analyst, Reliability Engineer, Supplier Quality Engineer, Manufacturing Quality Engineer, Quality Assurance Engineer,…
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Continuous Improvement Manager - Alpena Area
The Pivot Group Network
Alpena · Alpena, MI
Experience with ERP or manufacturing execution systems.
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Validation Engineer - Bad Axe Area
The Pivot Group Network
Bad Axe · Bad Axe, MI
Are you a dedicated professional with a passion for excelling as a validation engineer? The Pivot Group Network, a Michigan manufacturing-focused recruiting group, is committed to fostering…
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Engineering Manager - Gladwin Area
The Pivot Group Network
Gladwin · Gladwin, MI
Working knowledge of safety and quality management systems.
Added 4 mins ago
Laser Weld Engineer - Mount Pleasant Area
The Pivot Group Network
Mount Pleasant · Mount Pleasant, MI
Are you a dynamic leader with a passion for excelling as a laser weld engineer? The Pivot Group Network, a Michigan manufacturing-focused recruiting group, is dedicated to building…
Added 4 mins ago
Engineering Manager - Wixom Area
The Pivot Group Network
Wixom · Wixom, MI
Working knowledge of safety and quality management systems.
Added 4 mins ago
Packaging Engineer - Alpena Area
The Pivot Group Network
Alpena · Alpena, MI
Packaging Design Engineer, Packaging Specialist, Packaging Technologist, Product Packaging Engineer, Materials and Packaging Engineer, Packaging Project Engineer, Packaging Systems…
Added 4 mins ago
Project Manager - Wixom Area
The Pivot Group Network
Wixom · Wixom, MI
Familiarity with ERP and manufacturing execution systems.
Added 4 mins ago
Engineering Manager - Grayling Area
The Pivot Group Network
Grayling · Grayling, MI
Working knowledge of safety and quality management systems.
Added 4 mins ago
Lean Manufacturing Engineer - Dearborn Area
The Pivot Group Network
Dearborn · Dearborn, MI
Are you a skilled professional with a passion for excelling as a lean manufacturing engineer? The Pivot Group Network, a Michigan manufacturing-focused recruiting group, is dedicated to…

Actalent

Quality Manager

Lawndale, CA, United States

$130,000 to $150,000 USD / year

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Job details

Pay: $130,000 to $150,000 USD / year
Experience: 5+ years of experience in quality management within the medical device industry.
Posting language: English
Posted: Nov 4, 2026

Original job description

Quality ManagerJob DescriptionThe Quality Manager leads and continuously improves the companys quality management system (QMS) to ensure full compliance with FDA regulations, ISO standards, and other applicable regulatory requirements within the medical device industry. This role oversees quality engineering, quality assurance, and quality control activities, drives effective corrective and preventive actions, and partners closely with cross-functional teams to embed quality into every stage of the product lifecycle. The Quality Manager serves as a key liaison during internal and external audits and provides clear, data-driven quality insights to senior leadership.Responsibilities

Lead, maintain, and continually improve the companys quality management system (QMS) in compliance with FDA regulations, ISO standards, and other applicable regulatory requirements.
Plan, manage, and host internal and external audits, including FDA inspections and ISO certification audits, ensuring audit readiness at all times.
Oversee corrective and preventive action (CAPA) processes, nonconformance investigations, and complaint handling to ensure timely, effective, and compliant resolutions.
Collaborate with cross-functional teams, including Research and Development, Manufacturing, and Regulatory, to ensure quality is built into every stage of the product lifecycle.
Develop, track, and analyze quality metrics and key performance indicators (KPIs), and present findings, trends, and recommendations to senior leadership.
Lead and coordinate training programs on quality standards, procedures, and best practices to ensure organization-wide understanding and adherence.
Manage document control and change control processes to maintain accurate, current, and compliant quality documentation and records.
Oversee risk management processes, ensuring that product and process risks are identified, evaluated, and mitigated in accordance with applicable standards.
Supervise quality assurance and quality control staff, providing coaching, guidance, and performance feedback to build a high-performing quality team.
Support and lead root cause analysis activities to identify underlying issues and implement sustainable corrective and preventive actions.
Participate in and lead special projects and other duties as assigned to support broader organizational goals related to quality and compliance.

Essential Skills

Bachelors degree in Engineering, Life Sciences, or a related field.
5+ years of experience in quality management within the medical device industry.
Strong knowledge of FDA Quality System Regulation (QSR) and relevant ISO-based quality management system requirements.
Demonstrated experience managing and maintaining a quality management system (QMS) in a regulated environment.
Hands-on experience with CAPA processes, including initiation, investigation, implementation, and effectiveness verification.
Proficiency in root cause analysis methodologies and tools to resolve quality issues and prevent recurrence.
Experience preparing for and managing internal and external audits, including regulatory inspections and ISO certification audits.
Solid background in quality engineering and quality assurance practices within medical device manufacturing.
Strong understanding of risk management principles and their application in product and process development.
Excellent leadership skills with experience supervising or leading quality assurance and quality control staff.
Effective written and verbal communication skills, with the ability to present quality metrics and findings to senior leadership.
Strong problem-solving and analytical skills, with the ability to interpret data and drive evidence-based decisions.

Additional Skills & Qualifications

Masters degree in Engineering, Life Sciences, or a related field is preferred.
Familiarity with aerospace quality standards such as AS9100 is beneficial, especially for organizations serving multiple regulated markets.
Experience developing and delivering training programs on quality standards, procedures, and best practices.
background in medical device quality systems, including complaint handling, nonconformance management, and audit readiness.
ASQ certifications, such as Certified Quality Engineer (CQE) or Certified Quality Auditor (CQA), are a plus.
Demonstrated ability to collaborate effectively with cross-functional teams, including R&D, Manufacturing, and Regulatory.
Proven capability to develop, monitor, and report on quality metrics and key performance indicators (KPIs).

Work EnvironmentThe Quality Manager works in a regulated medical device environment that emphasizes compliance, documentation integrity, and continuous improvement. The role involves close collaboration with cross-functional teams such as Research and Development, Manufacturing, Regulatory, and quality assurance and quality control staff. Work typically takes place in an office and manufacturing or laboratory setting where access to quality documentation systems, QMS tools, and audit preparation materials is essential. The position requires regular participation in internal meetings, audit activities, and training sessions, as well as periodic interaction with external auditors and regulatory representatives. The environment is structured, detail-oriented, and process-driven, with a strong focus on maintaining high product quality and meeting regulatory expectations. Job Type & LocationThis is a Permanent position based out of Lawndale, CA. Pay and BenefitsThe pay range for this position is $130000.00 - $150000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.health, dental, vision, pto, sick pay, retirement plan, and more Job Type & LocationThis is a Permanent position based out of Lawndale, CA. Application DeadlineThis position is anticipated to close on Nov 18, 2026. Workplace TypeThis is a fully onsite position in Lawndale,CA.About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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