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Quality Inspection Manager Jobs in Virginia (NOW HIRING)

Pro-Type Industries

Quality Inspector

Sterling, VA · On-site

$22 - $30/hr

Ability to communicate quality concerns professionally and work collaboratively with Production, Engineering, and Management. * Ability to work independently, prioritize inspection requirements, and ...

Pro-Type Industries

Quality Inspector

Sterling, VA

$22 - $30/hr

Ability to communicate quality concerns professionally and work collaboratively with Production, Engineering, and Management. * Ability to work independently, prioritize inspection requirements, and ...

Prestige Brands

Quality Inspector

Lynchburg, VA · On-site

Dispositions materials based on inspection findings in the inventory management system. Performs quality checks of finished goods during production. Responsibilities also include completion of ...

The Building People

Quality Manager

Quantico, VA

Develop procedures for inspections and surveillance to include scheduling, measuring, and analyzing ... Manage all quality related documentation and records. * Engage in appropriate communication and ...

The Building People

Quality Manager

Quantico, VA · On-site

Develop procedures for inspections and surveillance to include scheduling, measuring, and analyzing ... Manage all quality related documentation and records. * Engage in appropriate communication and ...

Koerber

Quality Inspector

Richmond, VA · On-site

You will document all inspection results in compliance with internal procedures, input quality data ... Able to manage multiple priorities in a fast-paced environment * Proficient in SAP, Microsoft Excel ...

Körber Group

Quality Inspector

Richmond, VA · On-site

You will document all inspection results in compliance with internal procedures, input quality data ... Able to manage multiple priorities in a fast-paced environment * Proficient in SAP, Microsoft Excel ...

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Quality Inspection Manager information

What does a quality inspection manager do?

A Quality Inspection Manager oversees quality control processes to ensure that products meet established standards and customer requirements. They develop inspection procedures, manage a team of quality inspectors, and monitor compliance with industry regulations. Their responsibilities also include analyzing inspection data, identifying areas for improvement, and collaborating with other departments to resolve quality issues. Quality Inspection Managers play a crucial role in maintaining product consistency and preventing defects throughout the manufacturing process.

What are some common challenges faced by quality inspection managers, and how can they be addressed?

Quality Inspection Managers often encounter challenges such as maintaining consistency across inspection teams, adapting to changing regulatory standards, and balancing production schedules with thorough quality checks. Addressing these issues requires strong communication skills, ongoing training for staff, and the implementation of robust quality management systems. Collaborating closely with production, engineering, and compliance teams helps ensure that quality standards are upheld without compromising efficiency.

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

To thrive as a Quality Inspection Manager, you need strong analytical abilities, in-depth knowledge of quality control standards, and a background in engineering or manufacturing, often supported by a relevant degree. Familiarity with quality management systems (like ISO 9001), statistical process control tools, and inspection software is typically required. Excellent leadership, attention to detail, and strong communication skills help facilitate team performance and effective problem-solving. These skills ensure consistent product quality, regulatory compliance, and drive continuous improvement within manufacturing environments.

What is the difference between Quality Inspection Manager vs Quality Control Supervisor?

AspectQuality Inspection ManagerQuality Control Supervisor
CertificationsISO 9001, Six Sigma, ASQ certificationsISO 9001, Six Sigma, ASQ certifications
Work EnvironmentOversees inspection teams across manufacturing or production facilitiesSupervises quality control staff on the shop floor or production lines
Employer & Industry UsageUsed in manufacturing, aerospace, automotive, and electronics industriesCommon in manufacturing, food production, and industrial sectors

The Quality Inspection Manager typically has broader responsibilities, overseeing multiple inspection teams and ensuring compliance with quality standards across departments. The Quality Control Supervisor focuses more on supervising daily inspection activities on the production floor. Both roles require similar certifications and are vital in maintaining product quality, but the manager role involves higher-level planning and coordination.

Is quality inspection manager a good career?

A quality inspection manager oversees quality control processes within an organization, ensuring products meet standards and regulations. The role typically requires strong attention to detail, knowledge of industry standards, and often involves certifications such as Six Sigma or ISO. It can offer stable employment and opportunities for advancement in manufacturing, production, or engineering environments.

What cities in Virginia are hiring for Quality Inspection Manager jobs?

Cities in Virginia with the most Quality Inspection Manager job openings:

Quality Inspection Manager jobs near you
Infographic showing various Quality Inspection Manager job openings in Virginia 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 86% Physical, 2% Hybrid, and 12% Remote job distribution.

Director, Quality Inspection Management

Celldex Therapeutics, Inc.

Hampton, VA • On-site

$177 - $229/hr

Other

Medical, Retirement, PTO

Posted 12 days ago

Job description

Overview

This role will serve as the primary architect and leader of Celldex's inspection management program, ensuring continued state of readiness for regulatory authority inspections, partner audits, and commercial launch activities.

The Director will collaborate across Quality, Manufacturing, Supply Chain, Technical Operations, Regulatory Affairs, Clinical Development, and Commercial functions to establish and maintain a sustainable inspection readiness framework. The successful candidate will play a key role in supporting Celldex's transition from a clinical-stage organization to a commercial biotechnology company while ensuring compliance with FDA, EMA, MHRA, Health Canada, ICH, and other global regulatory requirements. This individual will provide leadership for GMP compliance initiatives, inspection preparation, audit response management, quality risk mitigation, and continuous improvement activities throughout the product lifecycle.

Responsibilities
  • Creation of an Inspection Management Program for Celldex and our Contract Development and Manufacturing Organizations (CDMO).
  • Creation of a living inspection readiness program to ensure Celldex, and its CDMOs remain inspection ready.
  • Work with the Quality CDMO Management team to ensure "Hot Topics" at our CDMOs are prepared for prior to Health Authority Inspections.
  • Establishment of a Health Authority Inspection Management Process for Celldex, and for our CDMOs.
  • Responsible for the response process for all Health Authority Inspection.
  • Responsible for ensuring CAPAs created by Health Authority Inspections are followed up on and are complete on time 100% of the time.
  • Development of metrics to track performance
Qualifications
  • Bachelor's degree in Life Sciences, Pharmacy, Engineering, Chemistry, Microbiology, or related discipline. Advanced degree is a plus.
  • Minimum 10+ years of experience in Quality Assurance, GMP Compliance, Regulatory Inspection Management, or Quality Systems within biotechnology, pharmaceuticals, or biologics manufacturing.
  • Demonstrated experience leading FDA and international regulatory inspections.
  • Direct experience working with CMOs and global supply networks.
  • Experience managing Health Authority responses and CAPA follow ups
  • Experience supporting biologics, monoclonal antibodies, sterile products, or advanced therapeutics preferred.
  • Experience within both clinical-stage and commercial-stage environments strongly preferred.
  • Experience with commercial launch readiness and post-approval quality operations highly desirable.
  • Patient Focused
  • Strategic Leadership
  • Cross-Functional Stake Holder Management
  • Balanced Judgement
  • Risk Based Decision Making
  • Results Driven
Compensation Statement

The expected base salary for this position is: $176659.00 to $229427.00. We are committed to compensating employees equitably based on several factors including experience, education, licensure/certifications, skill level, location of the position, and availability of similar talent in a competitive market. Subject to eligibility and applicable plan terms, compensation includes base salary, annual discretionary bonus, long term incentive, 401(K) plan with employer contribution, health care and other insurance benefits (for employee and family), paid holidays, vacation, and sick days. A summary of our benefits can be found on our careers page Celldex is proud to be an equal opportunity employer that strives to foster a culture of diversity, equity, and inclusion. We are committed to promoting a diverse environment through development, recruiting and community outreach.

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