Quality Specialist Jobs in Maryland
Quality Specialist jobs in Maryland concentrate in life sciences, defense manufacturing, and federal contracting, with demand running from entry-level inspection roles to senior systems quality managers. The strongest hiring activity is in the Baltimore metro, the Washington D.C. suburbs of Montgomery and Prince George's counties, and the Annapolis area, where employers like Northrop Grumman, Leidos, and Johns Hopkins Health System maintain large quality assurance teams. The most in-demand specialties are ISO compliance, FDA-regulated manufacturing quality, and software quality assurance tied to government systems work. Scan the live roles below and apply to whichever ones fit.
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Showing 5 of 30+ Quality Specialist jobs
As part of Laboratory Management and Stability (LMS) team, the role supports shared core responsibilities such as stability program coordination, sample flow oversight, inventory management, and the management of OOT/OOS, deviations, CAPAs, and continuous improvement initiatives.
Key Responsibilities:
- Digital Systems Integration: Lead onboarding and configuration of laboratory digital tools across QC processes, ensuring workflows, templates, roles, and access align with operational needs and controlled documentation.
- Stakeholder Collaboration: Act as liaison among laboratory staff, IT, QA, and project leadership to gather requirements, address concerns, align scope, and communicate status and decisions.
- Training & Documentation: Develop and deliver user-focused training, SOPs, quick reference guides, and controlled templates; conduct readiness assessments and provide postgolive support.
- Issue Resolution & Enhancements: Troubleshoot system onboarding and usage challenges; coordinate incident triage and enhancement delivery with technical teams; maintain issue/change logs and user feedback loops.
- Data Integrity & Compliance: Ensure GxP aligned configuration and use across systems; uphold 21 CFR Part 11/Annex 11 controls, audit trails, role-based access, validated states, and traceability to URS/FRS/test scripts.
- LMS Core Operations Support: Support sample flow oversight across QC CGT labs; assist with investigations for OOT, OOS, deviations, and CAPAs; contribute to stability program; and maintain inventory management processes including Kanban room controls, min/max levels, and timely replenishment to sustain compliant operation.
- Audit & Inspection Support: Prepare evidence packages (training records, configuration summaries, validation status, change histories) and participate in internal/external audits and inspections.
Minimum Qualifications:
- Associate’s degree with 3 years of relevant experience OR bachelor’s degree in Life Sciences, Chemistry, Engineering, Biotechnology, or a related field with at least 2 years of relevant experience
- Experience in GMP laboratory operations, pharmaceutical quality systems, manufacturing support, laboratory digital systems, equipment, materials, sample management, stability, or another regulated technical environment
- Working knowledge of GMP/GxP, data integrity, ALCOA+, and controlled documentation requirements
- Ability to learn and work across multiple LMS processes and laboratory systems, including GQCLIMS, 1Lab, MODA, Businessmap, SAP, or comparable systems
- Demonstrated ability to maintain accurate records, manage concurrent assignments, follow issues through closure, and escalate risks appropriately
- Effective written and verbal communication, stakeholder engagement, and cross-functional coordination skills
The annual base pay (or hourly rate of compensation) for this position ranges from $83,504.80 - 125,257.20. Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
12-Nov-2026Closing Date
18-Nov-2026Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
As part of Laboratory Management and Stability (LMS) team, the role supports shared core responsibilities such as stability program coordination, sample flow oversight, inventory management, and the management of OOT/OOS, deviations, CAPAs, and continuous improvement initiatives.
Key Responsibilities:
- Digital Systems Integration: Lead onboarding and configuration of laboratory digital tools across QC processes, ensuring workflows, templates, roles, and access align with operational needs and controlled documentation.
- Stakeholder Collaboration: Act as liaison among laboratory staff, IT, QA, and project leadership to gather requirements, address concerns, align scope, and communicate status and decisions.
- Training & Documentation: Develop and deliver user-focused training, SOPs, quick reference guides, and controlled templates; conduct readiness assessments and provide postgolive support.
- Issue Resolution & Enhancements: Troubleshoot system onboarding and usage challenges; coordinate incident triage and enhancement delivery with technical teams; maintain issue/change logs and user feedback loops.
- Data Integrity & Compliance: Ensure GxP aligned configuration and use across systems; uphold 21 CFR Part 11/Annex 11 controls, audit trails, role-based access, validated states, and traceability to URS/FRS/test scripts.
- LMS Core Operations Support: Support sample flow oversight across QC CGT labs; assist with investigations for OOT, OOS, deviations, and CAPAs; contribute to stability program; and maintain inventory management processes including Kanban room controls, min/max levels, and timely replenishment to sustain compliant operation.
- Audit & Inspection Support: Prepare evidence packages (training records, configuration summaries, validation status, change histories) and participate in internal/external audits and inspections.
Minimum Qualifications:
- Associate’s degree with 3 years of relevant experience OR bachelor’s degree in Life Sciences, Chemistry, Engineering, Biotechnology, or a related field with at least 2 years of relevant experience
- Experience in GMP laboratory operations, pharmaceutical quality systems, manufacturing support, laboratory digital systems, equipment, materials, sample management, stability, or another regulated technical environment
- Working knowledge of GMP/GxP, data integrity, ALCOA+, and controlled documentation requirements
- Ability to learn and work across multiple LMS processes and laboratory systems, including GQCLIMS, 1Lab, MODA, Businessmap, SAP, or comparable systems
- Demonstrated ability to maintain accurate records, manage concurrent assignments, follow issues through closure, and escalate risks appropriately
- Effective written and verbal communication, stakeholder engagement, and cross-functional coordination skills
The annual base pay (or hourly rate of compensation) for this position ranges from $83,504.80 - 125,257.20. Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
12-Nov-2026Closing Date
18-Nov-2026Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
See All 30 Quality Specialist Jobs in Maryland
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Find Quality Specialist JobsQuality Specialist Jobs by City in Maryland
Where Maryland roles are concentrated, by current openings.
Quality Specialist Job Market in Maryland
A snapshot from current Maryland openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Aerospace & Defense
What Maryland Employers Look For
The qualifications that appear most often in quality specialist jobs across Maryland.
- Bachelor's degree in engineering, life sciences, or a related technical field required
- Experience with ISO 9001 or AS9100 quality management systems strongly preferred
- Familiarity with FDA 21 CFR Part 820 or GMP regulations for regulated industry roles
- ASQ Certified Quality Auditor or Certified Quality Engineer credential valued by employers
- Proficiency with quality tools such as CAPA, FMEA, root cause analysis, and SPC
- Strong written communication skills for preparing audit reports and compliance documentation
Quality Specialist Jobs in Maryland: Frequently Asked Questions
How do you become a quality specialist in Maryland?
Most Maryland quality specialist positions require a bachelor's degree in engineering, a natural science, or a related technical discipline, though some manufacturing roles accept an associate degree paired with hands-on experience. Maryland does not issue a state license specific to quality specialists, so employers lean heavily on industry credentials: the ASQ Certified Quality Auditor and Certified Quality Engineer designations are widely recognized across the state's defense, biotech, and healthcare manufacturing sectors. Candidates targeting FDA-regulated employers should also be familiar with GMP and 21 CFR requirements before applying.
Which companies hire quality specialists in Maryland?
Maryland quality specialist roles are posted by University of Maryland Medical System, AstraZeneca, and Clark Construction and others right now, based on current listings on Migrate Mate as of November 2026. Maryland's concentration of defense contractors, FDA-regulated medical device firms, and large hospital systems means quality openings appear consistently across both the private sector and government-adjacent organizations throughout the state.
Which Maryland cities have the most quality specialist jobs?
Baltimore, Rockville, and Frederick lead Maryland in quality specialist openings. Baltimore anchors demand through its pharmaceutical, medical device, and hospital system employers, while the Washington D.C. suburbs of Rockville, Bethesda, and Gaithersburg generate significant openings tied to federal health agencies and the biotech corridor along I-270, making those suburban markets consistently active even though they are smaller cities.
Are there remote quality specialist jobs in Maryland?
Yes, but they are rare. Many quality specialist duties, including physical inspection, line audits, and lab-based compliance work, require an on-site presence. About 43% of quality specialist openings tied to Maryland are remote or hybrid as of November 2026, which reflects the hands-on nature of most roles in the field. The sub-areas most likely to offer remote or hybrid flexibility are quality documentation, supplier audit coordination, and quality management system administration.
How can I get hired as a quality specialist in Maryland with little or no experience?
The most realistic entry path is a quality inspector or quality technician role, which Maryland's defense manufacturers and medical device companies regularly fill with candidates who have a technical associate degree or a bachelor's in progress. Northrop Grumman, Leidos, and mid-size FDA-regulated manufacturers in the Baltimore-Washington corridor run internship and co-op programs that feed into full-time quality roles. Moving laterally from manufacturing operations, laboratory technician, or supply chain positions is also common. Earning an ASQ Certified Quality Process Analyst credential before applying gives candidates a measurable edge over other entry-level applicants.
Where can I find and apply to quality specialist jobs in Maryland?
You can find and apply to quality specialist jobs in Maryland on Migrate Mate, which lists current Maryland openings from employers across the state. Search the listings for roles that match your experience level and specialization, then apply directly to the ones that fit.
See All 30 Quality Specialist Jobs in Maryland
Find roles in Maryland that match your experience and apply in just a few clicks.
Find Quality Specialist Jobs