Top 112 Quality specialist Jobs in Germantown Md

Quality Specialist II
Thermo Fisher Scientific —Rockville, MD
- $66,000 - $99,000 a year
- Full-time
- Mid-level
- Office
- Bachelor's degree
- Commuter assistance
- Paid parental leave
5h
Quality Assurance Specialist 3
Merck KGaA —Rockville, MD
- $70,800 - $106,200 a year
- Data analysis skills
- Mid-level
- US work authorization
- Health insurance
- Paid time off
Quality Specialist 3 - Compliance and Audits
Merck KGaA —Rockville, MD
- $70,800 - $106,200 a year
- Laboratory experience
- Mid-level
- Analysis skills
- Health insurance
- Paid time off
QA Label Specialist
Smith & Nephew —Columbia, MD
- $22.83 - $34.25 an hour
- 8 hour shift
- Hybrid work
- Ability to sit for extended periods
- 1 year
- Associate's degree
- Health savings account
- Employee stock purchase plan
10d
AI Data Quality Specialist - AI Trainer
DataAnnotation —Falls Church, VA
- $50 - $100 an hour
- Part-time
- Remote
- Computer Science
- Writing skills
- English
- Flexible schedule
Quick Apply
AI Data Quality Specialist - AI Trainer
DataAnnotation —Maryland
- $50 - $100 an hour
- Part-time
- Remote
- Writing skills
- English
- Mid-level
- Flexible schedule
Quick Apply
HELP DESK MANAGER (MAC SPECIALIST / QUALITY ASSURANCE) - Top Secret clearance
General Dynamics Information Technology —Washington, DC
- $107,744 - $126,500 a year
- Bachelor of Science
- English
- Mid-level
- Paid holidays
- On-the-job training
Flow Cytometry Specialist
Axle —Bethesda, MD
- $70,000 - $80,000 a year
- Mid-level
- 3 years
- Analysis skills
- Paid holidays
- Health insurance
Quick Apply
Clinical Quality Management Specialist
Technical Resources International, Inc. —Bethesda, MD
- $65,000 - $85,000 a year
- Full-time
- Bachelor of Science
- Mid-level
- Quality control
4d
Specialist, School Quality and Accountability
DC Public Charter School Board —Washington, DC
- $77,924 - $90,911 a year
- Full-time
- Mid-level
- Office
- Continuous improvement
- Loan forgiveness
Quick Apply
Quality Assurance Specialist
Vision Solution LLC —Rockville, MD
- $90,000 - $100,000 a year
- Contract
- Hybrid work
- Software troubleshooting
- Mid-level
- SQL
Quick Apply
Quality Assurance Specialist (GCP/GLP)
Pharmaron —Germantown, MD
- Full-time
- Mid-level
- Bachelor's degree
- Communication skills
Quick Apply
Quality Control and Continuous Improvement Specialist I
ENVIGO RMS LLC —Frederick, MD
- Full-time
- Mid-level
- Analysis skills
- Mentoring
- Paid parental leave
- Disability insurance
Quick Apply
1d
Product Complaint Specialist I
Meso Scale Diagnostics, LLC. —Rockville, MD
- $59,100 - $87,900 a year
- Mid-level
- Office
- Continuous improvement
- Paid parental leave
- AD&D insurance
Quick Apply
Acquisition Quality Assurance Specialist
Hive Group LLC —McLean, VA
- $85,000 - $100,000 a year
- Email
- Hybrid work
- Google Workspace
- Finance
- Analysis skills
- Paid holidays
- Disability insurance
Quick Apply
QA QC Specialist
MCKISSACK & MCKISSACK —Washington, DC
- $140,000 - $183,000 a year
- Urgently hiring
- Construction site
- 5 years
- Continuous improvement
- Commuter assistance
- Health savings account
Quick Apply
Document Control and Quality Specialist
CICONIX, LLC —Fort Detrick, MD
- $55,000 - $58,000 a year
- Full-time
- Background check
- Microsoft Excel
- Microsoft Outlook
- 401(k)
- Paid time off
Quick Apply
5d
Retail Quality Assurance Specialist I
Ahold Delhaize USA —Columbia, MD
- $72,880 - $109,320 a year
- Monday to Friday
- Microsoft Word
- Computer literacy
- Merchandising
Data Operations Specialist – Head Start (Data Quality, Records & Governance)
JBS International —North Bethesda, MD
- Mid-level
- 3 years
- Ability to lift 50 pounds
Quick Apply
Quality Management Research Specialist
North Carolina State University —Laurel, MD
- $45,454 - $109,409 a year
- Full-time
- Mid-level
- Driver's License
- Bachelor's degree
- Paid holidays
- Disability insurance

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Quality Specialist II

Thermo Fisher Scientific -
Rockville, MD

Apply Now

Job Details

Full-time
$66,000 - $99,000 a year
5 hours ago

Benefits

Commuter assistance
Paid parental leave
Caregiver leave
Employee stock purchase plan
Paid holidays
Disability insurance
Health insurance
Dental insurance
401(k)
Tuition reimbursement
Paid time off
Parental leave
Employee assistance program
Vision insurance
Life insurance

Qualifications

Customer communication
Bachelor's degree

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

Discover Impactful Work

Join our Clinical Trials Division (CTD) Quality team in Rockville, Maryland, and help ensure the quality and compliance of services supporting clinical trial products for a diverse portfolio of pharmaceutical and biotechnology clients.

The Rockville site is not a manufacturing facility. The operation supports clinical trial product storage and repository activities, including temperature-controlled storage, shipping and receiving, with additional pharmacy and laboratory functions on site.

As a Quality Specialist II, you will play a highly visible, client-facing role within the Quality organization. A significant part of your work will involve preparing for, hosting, and following through on external client audits. With client audits occurring regularly, this role is well suited to someone who can confidently represent Quality, communicate with different audiences, navigate detailed questions, and keep multiple activities moving in a fast-paced environment.

When you are not supporting audits, you will perform day-to-day Quality activities including batch record review, validation protocol review, shipment label review, and quality system documentation.

A Day in the Life

Prepare for and host external client audits, serving as a primary Quality representative throughout the audit.
Partner with site operations and coordinate with subject matter experts across functions to address client questions and retrieve supporting information during audits.
Manage post-audit observations and findings through the quality system, including opening and maintaining records in TrackWise and coordinating responses through closure.
Drive timely follow-up with cross-functional partners responsible for audit observations or findings, reviewing responses for completeness, accuracy, and appropriate client-facing language.
Maintain clear communication with clients and internal stakeholders throughout audit preparation, execution, and follow-up.
Review master batch records and post-execution documentation in accordance with applicable procedures.
Review protocols associated with qualification and validation of temperature-controlled storage equipment, including freezers.
Review labels associated with clinical trial product shipments entering and leaving the repository.
Support Quality oversight activities within repository and storage areas, including periodic data-integrity and surveillance activities.
Apply established procedures and quality requirements while helping internal partners understand and appropriately execute their responsibilities.
Balance scheduled audit responsibilities with routine Quality work while maintaining accuracy, organization, and responsiveness.

Keys to Success

This role requires someone who is comfortable being highly visible with clients and taking ownership when priorities are moving quickly. You will be successful if you can remain composed during detailed or challenging client interactions, communicate clearly, and confidently guide an audit while knowing when to engage the appropriate subject matter expert.

You should also be comfortable driving work across functions. Audit findings may involve departments outside Quality, so success requires persistence, sound judgment, strong follow-through, and the ability to keep stakeholders accountable to deadlines while maintaining productive working relationships.

Education

Bachelor’s degree in a scientific, technical, quality, or related field.

Experience

Minimum of 2 years of relevant professional experience.
Experience participating in, supporting, or hosting client, customer, or internal audits within a regulated or quality-focused environment.
Experience in pharmaceutical, biotechnology, clinical trials, life sciences, or a comparable regulated industry is preferred but is not required.

Knowledge, Skills and Abilities

Demonstrated ability to interact professionally and confidently with clients, auditors, and cross-functional stakeholders.
Working knowledge of quality systems and controlled documentation in a regulated environment.
Ability to interpret procedures, identify the appropriate subject matter expert, and coordinate accurate responses to audit questions and findings.
Strong written communication and documentation skills, including the ability to review responses for clarity and appropriateness before client submission.
Strong organizational skills with the ability to manage audit preparation, follow-up activities, and routine Quality responsibilities simultaneously.
Ability to remain composed, professional, and customer-focused during challenging or demanding interactions.
Strong follow-through and the ability to drive actions to completion across multiple departments and competing priorities.
Experience with TrackWise or a comparable electronic quality management system is preferred.
Experience reviewing batch records, validation or qualification protocols, labels, or similar controlled quality documentation is preferred.
Proficiency with Microsoft Office and standard business systems.
Ability to work effectively both independently and as part of a collaborative Quality team.

Work Environment

This is a fully on-site position in Rockville, Maryland, working Monday through Friday, approximately 8:00 a.m. to 5:00 p.m. The role supports a clinical trial product storage and repository operation rather than a manufacturing environment.

The position includes regular interaction with external clients and movement through repository and operational areas containing ambient, refrigerated, frozen, walk-in, and liquid nitrogen storage. The role does not require routine cleanroom manufacturing work or rotating manufacturing shifts.

What Makes This Opportunity Unique

You will gain significant exposure to a broad range of pharmaceutical and biotechnology clients while developing deep experience in client audit hosting, quality systems, and cross-functional quality oversight. Because Quality is an important partner across the Rockville operation, this role provides the opportunity to build relationships across functions, broaden your quality expertise, and continue developing within the organization.

Compensation and Benefits

The salary range estimated for this position based in Maryland is $66,000.00–$99,000.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

A choice of national medical and dental plans, and a national vision plan, including health incentive programs
Employee assistance and family support programs, including commuter benefits and tuition reimbursement
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

Apply Now

Refine Your Search

quality specialist jobs in germantown md

Quality Specialist II

Quality Assurance Specialist 3

Quality Specialist 3 - Compliance and Audits

QA Label Specialist

AI Data Quality Specialist - AI Trainer

AI Data Quality Specialist - AI Trainer

HELP DESK MANAGER (MAC SPECIALIST / QUALITY ASSURANCE) - Top Secret clearance

Flow Cytometry Specialist

Clinical Quality Management Specialist

Specialist, School Quality and Accountability

Quality Assurance Specialist

Quality Assurance Specialist (GCP/GLP)

Quality Control and Continuous Improvement Specialist I

Product Complaint Specialist I

Acquisition Quality Assurance Specialist

QA QC Specialist

Document Control and Quality Specialist

Retail Quality Assurance Specialist I

Data Operations Specialist – Head Start (Data Quality, Records & Governance)

Quality Management Research Specialist

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