Top 68 Quality improvement specialist Jobs in Frederick Md

QA Specialist II
Kite Pharma —Frederick, MD
- $92,820 - $120,120 a year
- Full-time
- Mid-level
- High school diploma or GED
- Analysis skills
- Health insurance
- Dental insurance
4d
ADMINISTRATIVE SPECIALIST II
State of Maryland - MDH Local Health - Frederick County —Frederick, MD
- $49,214 - $63,669 a year
- Online Application
- Mid-level
- Office
- Administrative experience
4d
Creative Services Specialist
AMSG —Frederick, MD
- Full-time
- Microsoft Excel
- Mid-level
- 3 years
- Health insurance
- Dental insurance
Quick Apply
5d
RCM Client Billing Specialist
GeneDx —Gaithersburg, MD
- $35 - $37 an hour
- Remote
- Mid-level
- Continuous improvement
- Business
4d
Creative Services Specialist
Advanced Management Strategies Group —Frederick, MD
- $100,000 - $115,000 a year
- Contract
- Microsoft Excel
- Mid-level
- 3 years
- Health insurance
- Dental insurance
Quick Apply
4d
E-commerce Marketing Specialist
Monument Metals —Frederick, MD
- $70,000 - $80,000 a year
- Overtime
- Merchandising
- Research
- Office
- Health insurance
- Dental insurance
Quick Apply
10d
Creative Services Specialist
ADVANCED MANAGEMENT STRATEGIES GROUP(AMSG) —Frederick, MD
- Full-time
- Microsoft Excel
- Mid-level
- 3 years
- Health insurance
- Dental insurance
5d
Workday HCM Specialist, Day Shift, HR Technology
Adventist HealthCare —Gaithersburg, MD
- $71,932.12 - $107,889.60 a year
- Full-time
- Customer service
- Pass drug screening
- Mid-level
- Free parking
- AD&D insurance
Quality Systems Technical Specialist
Specialty Granules —Hagerstown, MD
- $76,000 - $104,500 a year
- Extended hours
- Google Workspace
- Microsoft Access
- 5 years
- Paid holidays
- Health insurance
Program Specialist II, Grade 21
Montgomery County Government —Derwood, MD
- $72,567 - $104,286 a year
- Email
- CDL B
- CDL A
- Research
- Wellness program
- Paid parental leave
5d
Microbiology Specialist I
Katalyst Healthcares & Life Sciences —Walkersville, MD
- Hybrid work
- Mid-level
- Bachelor's degree
- 1 year
Quick Apply
Customer Engagement Specialist
GeneDx —Gaithersburg, MD
- $21 - $26 an hour
- Full-time
- Bilingual
- Microsoft Excel
- Writing skills
Healthcare Value Analysis Specialist - Full-time
Frederick Health —Frederick, MD
- $55,036 - $78,624 a year
- Overtime
- Mid-level
- In-person
- 1 year
- Disability insurance
- Health insurance
Quick Apply
Property Management Quality Assurance Specialist
Loudoun County Government —Leesburg, VA
- $53,592.20 - $91,106.75 a year
- Full-time
- Clean driving record
- Microsoft Excel
- Microsoft Outlook
11d
Community Integration Specialist/Navigator, Residential Transition
Sheppard Pratt —Sykesville, MD
- $20.95 an hour
- Day shift
- Clean driving record
- Mid-level
- Residential
- Health insurance
- Dental insurance
Quick Apply
3d
Clinical Lab Information Specialist
Precision Medicine Group —Frederick, MD
- $83,200 - $124,800 a year
- Online Application
- 5 years
- Master's degree
- Bachelor's degree
Billing Support Specialist I
GeneDx —Gaithersburg, MD
- $23.50 - $25.50 an hour
- Bilingual
- Writing skills
- Office
Accounts Payable Specialist
Ruppert Landscape - Corporate —Laytonsville, MD
- $26 - $29 an hour
- Overtime
- Computer literacy
- Mid-level
- Office
- Paid holidays
- Health insurance
Quick Apply
6d
Infection Prevention Specialist
Meritus Medical Center Inc —Hagerstown, MD
- $82,201.60 - $123,302.40 a year
- Nursing
- RN License
- Hospital
- Disability insurance
- Health insurance
Quick Apply
10d
Clinical Lab Information Specialist
Precision for Medicine —Frederick, MD
- $83,200 - $124,800 a year
- Online Application
- 5 years
- Master's degree
- Bachelor's degree
Quick Apply

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QA Specialist II

Kite Pharma -
Frederick, MD

Apply Now

Job Details

Full-time
$92,820 - $120,120 a year
4 days ago

Benefits

Health insurance
Dental insurance
Paid time off
Vision insurance
Life insurance

Qualifications

Project management tools
Project team coordination
Performance dashboard reports
Project reporting
Performance monitoring
Dashboard development
Six Sigma Certification
Operational analysis
Performance improvement leadership
Content creation for technical audiences
Quality records maintenance
Production data analysis
Defect resolution root cause analysis
Data analysis reporting
Document control experience within pharmaceutical industry
Procedural guides
Preventive action implementation
Operations coordination planning
Technical writing experience within manufacturing
Dashboard creation support
Production deviation management
Compliance audits & assessments
Six Sigma methodology implementation
Value stream mapping
Corrective and preventive actions (CAPA)
GMP
Training material drafting
Metrics Reporting
Mid-level
Incident Escalation

Full Job Description

Job Description

We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet.

Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows.

Job Description

Position Summary: The QA Operations Specialist II - Continuous Improvement supports Quality Assurance Operations, operational excellence, and continuous improvement within a GMP-regulated environment. The role performs assigned support activities while applying structured problem-solving, data analysis, project coordination, and performance monitoring to improve compliance, quality, efficiency, and process reliability. The position partners with cross-functional stakeholders to identify, implement, and sustain improvements and may support additional QA Operations activities based on business needs.

Key Responsibilities:

Perform QA Operations activities to ensure compliance with GMP regulations, company procedures, site quality standards, and applicable regulatory requirements.
Review manufacturing, laboratory, environmental monitoring, and quality system documentation for accuracy, completeness, compliance, and adherence to approved procedures.
Support quality systems activities, including deviations, investigations, CAPAs, change controls, risk assessments, audits, inspection readiness, and effectiveness monitoring.
Develop, revise, and maintain controlled documents, including SOPs, work instructions, forms, training materials, and quality records.
Partner with cross-functional teams to identify compliance risks, resolve quality issues, and support timely escalation and resolution of concerns.
Support implementation of new products, processes, systems, and workflows by establishing quality requirements, controls, checkpoints, and performance metrics.
Drive and support continuous improvement initiatives utilizing Lean, Six Sigma, PDCA, A3, Value Stream Mapping, and root cause analysis methodologies.
Collect, analyze, trend, and communicate quality and operational data to identify improvement opportunities and measure effectiveness.
Develop and maintain dashboards, scorecards, project trackers, action logs, risk logs, and performance reporting tools.
Coordinate project activities including schedules, meetings, agendas, action items, risk management, and follow-up activities.
Assist with project planning and execution, including project charters, current-state assessments, future-state recommendations, implementation plans, and benefit tracking.
Support process improvement implementation and sustainment through standardization, effectiveness monitoring, and continuous evaluation.
Partner with Quality Assurance, Quality Control, Manufacturing, MSAT, Engineering, Materials Management, Site Planning, and R&D teams on quality and operational improvement initiatives.
Support inspection readiness and audit preparedness through documentation management, metric monitoring, visual management, and remediation efforts.
Prepare trend reports, quality reviews, management presentations, and training materials to support operational decision-making.
Maintain accurate, traceable, and inspection-ready records while exercising sound judgment and escalating issues when appropriate.

Basic Qualifications:

Bachelor's degree with at least 4 years of relevant experience

OR

OR an associate degree and at least 5 years of relevant experience;

OR

OR a high school diploma/equivalent and at least 6 years of relevant experience.
Onsite Monday-Friday

Preferred Qualifications:

Experience supporting continuous improvement projects in a GMP-regulated pharmaceutical, biotechnology, or cell-therapy environment.
Experience with process mapping, Value Stream Mapping, PDCA, A3, root-cause analysis, or Lean/Six Sigma tools.
Experience creating and maintaining dashboards, metrics, visual-management systems, or project-tracking tools.
Experience supporting cross-functional projects from planning through implementation and sustainment.
Lean, Six Sigma, project management, or related training/certification.
Strong analytical, technical writing, presentation, and stakeholder-coordination skills.

The salary range for this position is: $92,820.00 - $120,120.00. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.

For additional benefits information, visit:

https://www.gilead.com/careers/compensation-benefits-and-wellbeing

Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.

Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA.

NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT

Kite Pharma will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law.

Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.

Kite Pharma provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.

For Current Kite Pharma Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.

Apply Now

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Job Description

Job Description

Key Responsibilities:

Perform QA Operations activities to ensure compliance with GMP regulations, company procedures, site quality standards, and applicable regulatory requirements.

Review manufacturing, laboratory, environmental monitoring, and quality system documentation for accuracy, completeness, compliance, and adherence to approved procedures.

Support quality systems activities, including deviations, investigations, CAPAs, change controls, risk assessments, audits, inspection readiness, and effectiveness monitoring.

Develop, revise, and maintain controlled documents, including SOPs, work instructions, forms, training materials, and quality records.

Partner with cross-functional teams to identify compliance risks, resolve quality issues, and support timely escalation and resolution of concerns.

Support implementation of new products, processes, systems, and workflows by establishing quality requirements, controls, checkpoints, and performance metrics.

Drive and support continuous improvement initiatives utilizing Lean, Six Sigma, PDCA, A3, Value Stream Mapping, and root cause analysis methodologies.

Collect, analyze, trend, and communicate quality and operational data to identify improvement opportunities and measure effectiveness.

Develop and maintain dashboards, scorecards, project trackers, action logs, risk logs, and performance reporting tools.

Coordinate project activities including schedules, meetings, agendas, action items, risk management, and follow-up activities.

Assist with project planning and execution, including project charters, current-state assessments, future-state recommendations, implementation plans, and benefit tracking.

Support process improvement implementation and sustainment through standardization, effectiveness monitoring, and continuous evaluation.

Partner with Quality Assurance, Quality Control, Manufacturing, MSAT, Engineering, Materials Management, Site Planning, and R&D teams on quality and operational improvement initiatives.

Support inspection readiness and audit preparedness through documentation management, metric monitoring, visual management, and remediation efforts.

Prepare trend reports, quality reviews, management presentations, and training materials to support operational decision-making.

Maintain accurate, traceable, and inspection-ready records while exercising sound judgment and escalating issues when appropriate.

Basic Qualifications:

Bachelor's degree with at least 4 years of relevant experience

OR

OR an associate degree and at least 5 years of relevant experience;

OR

OR a high school diploma/equivalent and at least 6 years of relevant experience.

Onsite Monday-Friday

Preferred Qualifications:

Experience supporting continuous improvement projects in a GMP-regulated pharmaceutical, biotechnology, or cell-therapy environment.

Experience with process mapping, Value Stream Mapping, PDCA, A3, root-cause analysis, or Lean/Six Sigma tools.

Experience creating and maintaining dashboards, metrics, visual-management systems, or project-tracking tools.

Experience supporting cross-functional projects from planning through implementation and sustainment.

Lean, Six Sigma, project management, or related training/certification.

Strong analytical, technical writing, presentation, and stakeholder-coordination skills.

For Current Kite Pharma Employees and Contractors: