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Quality Systems Manager Jobs in Frederick, MD (NOW HIRING)

VB Spine

Quality Systems Specialist

Leesburg, VA · On-site

$80 - $100/hr

Participate in Management Review, Quality Planning, and other key QMS forums * Identify improvement opportunities and drive initiatives to increase the effectiveness and efficiency of the QMS

VB Spine, LLC

Quality Systems Specialist

Leesburg, VA · On-site

$80 - $100/hr

Participate in Management Review, Quality Planning, and other key QMS forums * Identify improvement opportunities and drive initiatives to increase the effectiveness and efficiency of the QMS

GeneDx, Inc

Director Quality Systems

Gaithersburg, MD · On-site

GeneDx is seeking a Director, Quality Systems (FT, 40 hours) to work at our Gaithersburg, MD ... Four years clinical laboratory or quality compliance experience. * 1 year of management and ...

GeneDx, Inc

Director Quality Systems

Gaithersburg, MD · On-site

GeneDx is seeking a Director, Quality Systems (FT, 40 hours) to work at our Gaithersburg, MD ... Four years clinical laboratory or quality compliance experience. * 1 year of management and ...

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All JobsQuality Systems JobsQuality Systems Manager JobsQuality Systems Manager Jobs in Frederick, MD

Quality Systems Manager information

See Frederick, MD salary details

$53.7K

$98K

$153.1K

How much do quality systems manager jobs pay per year?

As of Sep 8, 2026, the average yearly pay for quality systems manager in Frederick, MD is $98,048.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,100.00 and $121,800.00 per year, depending on experience, location, and employer.

What does a quality systems manager do?

As a quality systems manager, your primary responsibilities are monitoring the production processes and ensuring factory machinery/goods are within company and industry requirements. Your duties include weighing, sampling, or testing products for quality and functionality. You may also report the results of quality control tests. You monitor the equipment and people involved, and help with the development and implementation of improved management systems. You are also in charge of creating a standard operating procedure for the specific plant where you work. You check that everything is running at full efficiency and the quality of merchandise is standardized.

What are the key skills and qualifications needed to thrive as a quality systems manager?

To thrive as a Quality Systems Manager, you need strong expertise in quality management principles, regulatory compliance, and process improvement, typically supported by a degree in engineering or a related field. Familiarity with ISO standards (like ISO 9001), quality management software, and certifications such as Six Sigma or ASQ Certified Manager of Quality/Organizational Excellence are commonly required. Leadership, analytical thinking, and effective communication are crucial soft skills for coordinating teams and driving continuous improvement. These skills and qualifications are essential to ensure consistent product quality, regulatory adherence, and overall organizational efficiency.

How does a quality systems manager typically collaborate with cross-functional teams to drive continuous improvement?

A Quality Systems Manager works closely with departments such as manufacturing, engineering, regulatory, and supply chain to ensure that quality standards are consistently met and improved. They often lead or participate in cross-functional meetings to identify process gaps, analyze data, and develop corrective and preventive action plans. Effective communication and project management skills are essential, as the role involves aligning diverse teams toward common quality objectives and facilitating training or audits to support compliance and improvement initiatives.

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

AspectQuality Systems ManagerQuality Assurance Manager
Primary FocusDeveloping and maintaining quality management systems and processesOverseeing product testing and ensuring quality standards are met during production
CertificationsISO 9001 Lead Auditor, CQEASQ certifications, QA certifications
Work EnvironmentQuality management departments, compliance teamsProduction lines, testing labs
Industry UsageManufacturing, healthcare, aerospaceManufacturing, software, healthcare

While both roles focus on quality, the Quality Systems Manager primarily manages the overall quality management system and compliance, whereas the Quality Assurance Manager concentrates on product testing and ensuring quality during production. Understanding these differences helps in selecting the right career path or hiring the appropriate professional.

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Quality Systems Manager jobs near you
Infographic showing various Quality Systems Manager job openings in Frederick, MD as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 20% Part Time, 3% Contract, and 1% Nights. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $98,048 per year, or $47.1 per hour.

Quality Systems Specialist

Leesburg, VA • On-site

VB Spine
See more jobs at VB Spineexternal

$80 - $100/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 7 days ago

Job description

Quality Systems Specialist

VB Spine – Leesburg, Virginia, United States

About this position

Looking for a career where your work truly matters? At VB Spine, you’ll be part of a mission-focused team that supports surgeons during life-changing spinal procedures. We’re the largest privately held spine company and among the largest family-owned medical technology companies in the world, dedicated to innovation, surgeon partnerships, and improving patient outcomes in spine care. As a Quality Systems Specialist in our Quality Systems function within the Spine division, you’ll play a key role in developing, maintaining, and continuously improving the Quality Management System (QMS) to ensure compliance with global regulatory requirements and support high‑quality, safe medical devices.

What You’ll Do
  • Support the development, implementation, and maintenance of the Quality Management System in alignment with US and international medical device regulations (FDA, ISO, MDD/MDR, etc.)
  • Contribute to the evolution of the QMS to meet current and future business needs while ensuring compliance and efficiency
  • Participate in Management Review, Quality Planning, and other key QMS forums
  • Identify improvement opportunities and drive initiatives to increase the effectiveness and efficiency of the QMS
  • Support GMP and GDP practices within the Quality organization
  • Develop and deliver QMS-related training and ensure effective communication of quality system requirements
  • Contribute to the creation and maintenance of policies, procedures, and work instructions
  • Support internal and external audits, including preparation, response, and follow‑up activities
  • Participate in QMS-related IS discussions and support change control assessments for quality systems
  • Serve as a Divisional Process Owner (if applicable), coordinating input, representing divisional needs, and ensuring effective implementation of global initiatives
  • Collaborate cross‑functionally with Quality, Regulatory, IT, and other teams to maintain a compliant and effective QMS
What You Bring
  • Bachelor’s degree in a science, engineering, business, or related discipline
  • Thorough knowledge and understanding of US and International Medical Device Regulations
  • Basic knowledge of Quality Systems elements (CAPA, Audits, Management Review, Quality Planning, etc.)
  • Strong interpersonal, written, and oral communication skills with the ability to influence and negotiate
  • Solid analytical, problem‑solving, and project management skills
  • Demonstrated ability to work effectively in cross‑functional team environments
  • Computer literacy and proficiency with standard business applications
  • Ability to travel 10‑15% as needed
Why VB Spine?

We believe in growing talent from within. At VB Spine, join a high‑performing team where you’ll play an important role in strengthening our Quality Management System and ensuring the highest standards of quality and compliance for innovative spinal products that improve patient lives.

Compensation

Pay for this role is competitive and based on experience, qualifications, and performance. The typical pay range for this position is $75,000.00 – $85,000.00 annually, with potential for bonuses and incentives plus benefits. Final compensation is determined on a case‑by‑case basis and considers a variety of factors including experience level, skillset, and market conditions.

Benefits include
  • Comprehensive health, dental, and vision insurance
  • 401(k) with company match
  • Paid time off (PTO) and holidays
  • Ongoing training and professional development opportunities
  • Opportunity to grow within a fast‑paced, dynamic company
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