42 Quality Assurance And Engineering jobs in Washington.

Hiring now: Proj Engr @ Precision , Mgr Of Regulatory Affairs @ Tempus, Mgr Cqv Eng @ Precision , Intern @ Mcra, Sr Mgr Of Prod Stewardshi @ Albemarle, Proj Engr @ Project Fa, Mgr Qa Compliance @ Alertus Te, Divisional Clinical Eng M @ Agiliti, Computer Systems Validati @ Cai, Facility Mgr Ii @ Charles Ri.Explore more at jobswithgpt.com.

🔥 Skills

project management (7) Project Management (7) medical devices (7) GMP (7) Patient Focused (6) Quality Assurance (5) Regulatory Compliance (5) Training (5) problem-solving (4) Validation (4)

📍 Locations

Washington (13) Rockville (9) Bethesda (5) Gaithersburg (5) Baltimore (3) Columbia (3) Hunt Valley (2) Germantown (1) Hanover (1)

Precision For Medicine

Skills & Focus: cross-functional collaboration, engineering life cycle, system validation, GxP practices, technical documentation, problem-solving, project management, client-facing support, manufacturing processes, philanthropic opportunities
About the Company: Precision for Medicine, Manufacturing Solutions is the leading advanced therapy technical operations consulting company in the life science industry. We are co…
Experience: A minimum of 1 year of Project Engineer, Consulting, and/or relevant industry experience.
Salary: $60,000 — $75,000 USD
Type: Full-time
Benefits: Competitive salary, aggressive bonus structure, medical/dental/vision insurance, 401k plan with company match, paid tim…
Skills & Focus: Project Engineer, Quality compliance, Validation, Life science, Manufacturing processes, Technical documents, Project management, Problem-solving skills, Patient Focused, People First
About the Company: Precision for Medicine, Manufacturing Solutions, the leading advanced therapy technical operations consulting company in the life science industry, is committe…
Experience: A minimum of 1 year of Project Engineer, Consulting, and/or relevant industry experience.
Salary: $60,000 – $75,000 USD
Type: Full-time
Benefits: Competitive salary based on experience, Aggressive bonus structure, Medical, Dental, and Vision insurance, 401k Plan wi…
Skills & Focus: Project Management, Validation, Engineering, Quality Compliance, GxP best practices, Technical Documents, Problem Solving, Cross-functional Teams, Client Support, Patient Focused
About the Company: Precision for Medicine is the leading advanced therapy technical operations consulting company in the life science industry, providing project management, vali…
Experience: Bachelor’s degree in Life Science, Engineering, or related discipline
Salary: $58,000 — $63,000 USD
Type: Full-time
Benefits: Competitive salary based on experience, Aggressive bonus structure, Medical, Dental, and Vision insurance, 401k Plan wi…

Tempus

Skills & Focus: regulatory strategies, 510(k), PMA, De Novo authorizations, MDR CE marking, UKCA marking, quality compliance, medical devices, clinical decision support, premarket approval
About the Company: Tempus is a technology company that uses artificial intelligence and clinical data to improve personalized medicine and healthcare.
Experience: Minimum of 7+ years of experience in Regulatory Affairs related to medical devices
Salary: $110,000 - $180,000 USD
Type: Full-time
Benefits: Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and o…

Precision For Medicine, Manufacturing Solutions

Skills & Focus: CQV Engineering, life science, advanced therapy, project delivery, Manufacturing Solutions, subject matter expert, client satisfaction, technical solutions, philanthropic drive, patient focused
About the Company: Leading advanced therapy technical operations consulting company in the life science industry.
Experience: 4-6 years of advanced therapy, life science, pharmaceutical or biotech experience; 4-6+ years managing high-performing teams; 4+ years business development, lead generation or sales experience
Salary: $50,000 — $240,000 USD
Type: Full-time
Benefits: Competitive salary, aggressive bonus structure, medical/dental/vision insurance, 401k Plan with company match, paid tim…

Tempus

Skills & Focus: regulatory strategies, submissions, global regulatory authorities, medical devices, PMA applications, 510(k), Quality Assurance, technology assessment, clinical decision support, risk management
About the Company: Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical in…
Experience: Minimum of 10+ years of experience in Regulatory Affairs related to medical devices
Salary: $180,000 - $280,000 USD
Type: Full-time
Benefits: Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and o…

Mcra

Intern Washington
Skills & Focus: Regulatory Affairs, Digital Health, task analysis, use-related risk analysis, usability study, IEC 62366, FDA 2016 guidance, use scenarios, medical devices, workflows
About the Company: MCRA, an IQVIA business, is a leading medical device advisory firm and clinical research organization (CRO). MCRA's value contribution rests within its industr…
Type: Intern
Skills & Focus: Regulatory Affairs, Orthopedics, Spine, Data Analysis, Mechanical Test Data, FDA, Market Analysis, Emerging Technologies, Client Evaluation, Project Presentation
About the Company: MCRA, an IQVIA business, is a leading medical device advisory firm and clinical research organization (CRO). MCRA's value contribution rests within its industr…

Precision For Medicine, Manufacturing Solutions

Skills & Focus: CQV Engineering, Project Management, Technical Documentation, Validation Life Cycle, Cross-functional collaboration, Mentoring, Business Development, Regulatory Compliance, Patient Focused, Team Leadership
About the Company: We are the leading advanced therapy technical operations consulting company in the life science industry, committed to advancing manufacturing to achieve opera…
Experience: Minimum of 3 years of Project Engineer, Consulting, and/or relevant industry experience.
Salary: $50,000 — $240,000 USD
Type: Full-time
Benefits: Competitive salary, aggressive bonus structure, medical/dental/vision insurance, 401k Plan with company match, paid tim…

Precision For Medicine

Skills & Focus: cross-functional, engineering life cycle, technical documents, validation protocols, GxP best practices, critical thinking, problem-solving, project management, manufacturing processes, patient focused
About the Company: Leading advanced therapy technical operations consulting company in the life science industry.
Experience: Bachelor’s degree in Life Science, Engineering, or related discipline and/or comparable military experience.
Salary: $58,000 - $63,000 USD
Type: Full-time
Benefits: Competitive salary based on experience, Aggressive bonus structure, Medical, Dental, and Vision insurance effective you…

Albemarle

Skills & Focus: product stewardship, regulatory compliance, hazard communication, toxicology, team leadership, new product development, chemical control regulations, risk assessment, safety assessment, collaboration
Experience: 10+ years of experience in relevant fields or equivalent degrees.
Type: Full Time

Mcra

Intern Washington
Skills & Focus: Regulatory Affairs, Biocompatibility, Toxicology, data collection, chemical characterization, medical devices, toxicologically relevant compounds, biocompatibility strategies, analysis, database
About the Company: MCRA, an IQVIA business, is a leading medical device advisory firm and clinical research organization (CRO). MCRA's value contribution rests within its industr…

Project Farma (Pf)

Skills & Focus: biomanufacturing, Project Management, Cell and Gene Therapy, Quality Compliance, Engineering, Validation, Technical Documents, Project Timelines, Patient Focused, Technical Aptitude
About the Company: Project Farma (PF) is the leading advanced therapy technical operations consulting company in the life science industry. We provide biomanufacturing strategy a…
Experience: 0-3 years of consulting and/or project engineer experience
Salary: Competitive salary based on experience
Type: Full-time
Benefits: Aggressive bonus structure, Medical, Dental, and Vision insurance effective your first day of employment, 401k Plan wit…

Alertus Technologies

Skills & Focus: quality assurance, compliance management, regulatory compliance, internal audits, product certifications, industry standards, continuous improvement, software development lifecycle, risk management, Federal regulations
About the Company: At Alertus, protecting people from harm is our mission and our passion. As the leader in mass notification, we are committed to providing customizable, scalabl…
Experience: 5+ years of experience in quality assurance, compliance management, or regulatory affairs, preferably in a technology or manufacturing industry.
Salary: $72,000 - $110,000 a year
Type: Full-Time
Benefits: Unlimited Paid Time Off, Paid Holidays, 401(k) Retirement Plan, Medical, Dental, and Vision Plans, Short-term Disabilit…

Agiliti

Skills & Focus: Technical Services Management, Clinical Engineering Services, Revenue Growth, Customer Relations, Quality Audits, Data Gathering, Biomedical Engineering, Healthcare Industry, Medical Equipment Management Plan, Training and Development
About the Company: Agiliti is a nationwide company of passionate medical equipment management experts who proudly serve hospitals and healthcare facilities to ensure quality medi…
Experience: Minimum of 7-10 years of professional experience in biomedical engineering, electronics or related field in the healthcare industry.
Type: Full-time
Benefits: Robust suite of benefits including health insurance options, Short- and Long-Term Disability plans, Flexible Spending A…

Cai

Skills & Focus: Computer Systems Validation, GxP, 21 CFR Part 11, GAMP, compliance, biotech, pharma, Data Integrity, Process Control Systems, S88/S95 batch control standard
About the Company: CAI is a 100% employee-owned company established in 1996 that has grown to more than 700 people worldwide. We provide commissioning, qualification, validation,…
Experience: 3+ years experience with Computer systems validation
Salary: competitive compensation
Type: Full-time
Benefits: up to 15% retirement contribution, 24 days PTO and 5 sick days per year, health insurance at extremely low cost to empl…

Precision For Medicine, Manufacturing Solutions

Skills & Focus: Project Management, Validation, Engineering, Quality/Compliance, Technical Documents, GxP Best Practices, Critical Thinking, Problem Solving, Client Relations, Patient Focused
About the Company: The leading advanced therapy technical operations consulting company in the life science industry, committed to advancing manufacturing to achieve operational …
Experience: A minimum of 1 year of Project Engineer, Consulting, and/or relevant industry experience.
Salary: $60,000 - $75,000 USD
Type: Full-time
Benefits: Competitive salary based on experience, Aggressive bonus structure, Medical, Dental, and Vision insurance effective you…

Charles River Laboratories, Inc.

Skills & Focus: Facility Management, Animal Care, Quality Assurance, Biomedical, GMP, GLP, Training, Supervisory Experience, Research, Environmental Monitoring
About the Company: Charles River is an early-stage contract research organization (CRO) focused on laboratory animal medicine and science to provide discovery and safety assessme…
Experience: Minimum of 6 years’ experience in a research vivarium facility, with at least 2 years’ experience in an ABSL3 environment, and 3 years of supervisory experience.
Salary: $45.00 to $50.00 USD per hour
Type: Full-time
Benefits: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, emplo…

Precision For Medicine, Manufacturing Solutions

Skills & Focus: project management, engineering life cycle, validation protocols, GxP best practices, technical documents, problem-solving, cross-functional alignment, client support, manufacturing processes, patient focused
About the Company: Leading advanced therapy technical operations consulting company in the life science industry. Committed to advancing manufacturing and achieving operational e…
Experience: A minimum of 1 year of Project Engineer, Consulting, and/or relevant industry experience.
Salary: $60,000 — $75,000 USD
Type: Full-time
Benefits: Competitive salary, Aggressive bonus structure, Medical, Dental, and Vision insurance, 401k Plan with company match, Pa…

Project Farma

Skills & Focus: biomanufacturing, Project Management, Cell and Gene Therapy, Validation Life Cycle, Quality Compliance, Technical Delivery, Engineering Automation, Capital Projects, Patient Focused, Cross-functional Coordination
About the Company: Project Farma (PF) is the leading advanced therapy technical operations consulting company in the life science industry, providing biomanufacturing strategy an…
Experience: 1-4 years of consulting and/or project engineer experience
Salary: Competitive salary based on experience
Benefits: Competitive salary, Aggressive bonus structure, Medical, Dental, and Vision insurance, 401k Plan with company match, Pa…
Skills & Focus: Automation Controls, Life Science, Project Management, Business Development, High Performing Teams, Client Satisfaction, Technical Solutions, Cost Reduction, Quality Compliance, Clinical Validation
About the Company: As a Patient Focused, People First delivery team, we are committed to advancing manufacturing to achieve operational excellence and accelerate speed to market …
Experience: A minimum of 8 years of advanced therapy, life science, pharmaceutical, or biotech experience. 6 years of managing high-performing teams. 4 years business development, lead generation, or sales experience.
Salary: $50,000 — $240,000 USD
Type: Full-time
Benefits: Competitive salary based on experience, Annual bonus (discretionary), Medical, Dental, and Vision insurance effective y…

Iqvia

Skills & Focus: regulatory submissions, regulatory strategy, cardiac Interventional devices, business development, FDA, clinical testing, technical writing, analytical skills, problem-solving, client relationships
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industri…
Experience: 7+ years of regulatory affairs experience, 4+ years of cardiovascular medical device experience.
Salary: $134,800.00 - $250,300.00
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Smith+Nephew

Skills & Focus: Compliance, Advanced Wound Management, Medical Device, Pharmaceutical, Risk Assessment, Regulatory, Monitoring, Training, Auditing, Project Management
About the Company: Life Unlimited. At Smith+Nephew, we design and manufacture technology that takes the limits off living.
Experience: 7+ years of experience related to implementing a compliance programme in USA.
Benefits: 401k Matching Program, 401k Plus Program, Discounted Stock Options, Tuition Reimbursement, Flexible Personal/Vacation T…
Skills & Focus: manufacturing, human tissue products, cGMP, documentation practices, aspetic technique, batch production records, compliance, cleanroom environment, team environment, housekeeping
About the Company: At Smith+Nephew we design and manufacture technology that takes the limits off living.
Experience: 0-5 years of experience in a manufacturing setting
Benefits: 401k Matching Program, 401k Plus Program, Discounted Stock Options, Tuition Reimbursement, Flexible Personal/Vacation T…

Novavax

Skills & Focus: Quality Operations, cGMP, pharmaceutical, biologics, vaccine manufacturing, strategic, regulatory, development, batch release, team leadership
About the Company: Novavax is a global biotechnology company with a proven vaccine technology. We are focused on developing our R&D assets and establishing partnerships to levera…
Experience: Minimum of 15 years Quality Assurance experience in pharmaceutical, biologics and/or vaccine manufacturing
Salary: $226,200.00 - $305,350.00
Type: Full-time
Benefits: Novavax offers a base salary, annual bonus, equity grants, professional career development/growth opportunities, and a …

Astrazeneca

Skills & Focus: Process Engineering, Cell Therapy, Manufacturing, Scale-up, Optimization, Team Leadership, Regulatory Compliance, Continuous Improvement, GMP, Biologics
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies, dedicated to delivering life-changing medicines.
Experience: 15+ years in life sciences or pharmaceutical industry; 5+ years leadership experience.
Salary: $269,000 - $328,900
Type: Full-time
Skills & Focus: Quality Engineering, Combination Products, Medical Devices, Design Control, Risk Management, GMP, CAPAs, Design History File, Regulatory Compliance, Risk-based Sampling
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies.
Experience: Five (5) years or more of experience supporting Quality Engineering of Combination Products and/or Medical Devices
Salary: $106,501.60 to $159,752.40
Type: Full-time
Benefits: benefits included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health be…
Skills & Focus: cell therapy, supplier relationship, manufacturing operations, biopharmaceutical, compliance, supply chain, contract management, project management, risk management, budget management
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies, dedicated to helping patients globally by delivering life-ch…
Experience: Minimum 8+ years of experience in biopharmaceutical manufacturing, supply chain, or pharmaceutical development, with at least 2 years in cell and gene therapy manufacturing operations.
Salary: $115,000 - $173,000
Type: Full-time
Benefits: Short-term incentive bonus opportunity; eligibility for equity-based long-term incentive program; retirement program; p…

Leonardo Drs, Inc.

Skills & Focus: quality system development, product quality improvements, technical training, internal audits, non-conforming material, customer quality issues, continuous improvement initiatives, ISO Standards, statistical reports, engineering documentation
About the Company: DRS RADA Technologies, a subsidiary of Leonardo DRS, is focused on proprietary radar solutions and legacy avionics systems supporting the defense industry glob…
Experience: minimum of 2 years of experience
Salary: $81,356/year - $116,338/year
Type: Full-time
Benefits: Medical, dental, and vision coverage, health savings account, telemedicine, life and disability insurance, legal insura…

L3harris Technologies

Skills & Focus: quality control, process, testing, engineering, documentation, quality assurance, analytical skills, regulatory compliance, leadership, audits
About the Company: L3Harris is dedicated to recruiting and developing high-performing talent who are passionate about what they do. They provide an inclusive, engaging environmen…
Experience: 9 years with Bachelor's Degree, or 7 years with Graduate Degree, or 13 years without a degree
Salary: $114,000 - $212,000
Type: Full-time
Benefits: health and disability insurance, 401(k) match, flexible spending accounts, EAP, education assistance, parental leave, p…

Bd

Skills & Focus: manufacturing, maintenance, troubleshooting, quality control, GMP, leadership, coaching, process improvement, documentation, root-cause analysis
About the Company: BD is one of the largest global medical technology companies in the world, focused on advancing the world of health.
Experience: 3 years manufacturing experience required. Experience in a regulated environment required.
Salary: $27.10 - $42.00 USD Hourly
Type: Full-time
Benefits: Compensation and benefits programs for well-being and development.
Skills & Focus: Quality Engineering, ISO 13485, FDA, root cause analysis, statistical techniques, Continuous improvement, supplier quality, project management, compliance, healthcare
About the Company: BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the …
Experience: 3+ years’ experience in Quality Engineering or other related field.
Salary: $90,000.00 - $148,400.00 USD Annual
Type: Full-Time
Benefits: Healthcare, Healthcare FSA, Employer Matching, Tuition Reimbursement, Professional Development, Maternity and Paternity…

Charles River Laboratories, Inc.

Skills & Focus: Quality Assurance, CAPA, GMP, Deviation Management, Internal Audits, Change Control, Quality Metrics, Regulatory Compliance, Training, Pharmaceutical
About the Company: Charles River is an early-stage contract research organization (CRO) focused on laboratory animal medicine and science, providing a diverse portfolio of discov…
Experience: 5+ years in a GMP environment
Salary: $87,733 - $116,978
Type: Full-time
Benefits: bonus/incentives based on performance, 401K, paid time off, stock purchase program, health and wellness coverage, emplo…
Skills & Focus: Quality Assurance, GMP, Deviation, CAPA, Change Control, Audit, Quality Systems, Regulatory Compliance, Biological products, Training
About the Company: Charles River is an early-stage contract research organization (CRO) providing a diverse portfolio of discovery and safety assessment services, both Good Labor…
Experience: 5+ years of experience in a GMP environment
Salary: $87,733 - $116,978
Type: Full-time
Benefits: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, emplo…
Skills & Focus: Quality Assurance, GMP, CAPA, Deviation Management, Audit, Compliance, Change Control, Quality System, Training, Regulatory Requirements
About the Company: Charles River is an early-stage contract research organization (CRO) that supports clients from target identification through preclinical development, providin…
Experience: 5+ years of experience in a GMP environment
Salary: $87,733 - $116,978
Type: Full-time
Benefits: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, emplo…

Gmed North America

Skills & Focus: project management, medical devices, certification services, ISO 13485, MDSAP, CE marking, regulatory affairs, quality assurance, business development, team collaboration
About the Company: GMED North America is the US subsidiary of GMED, a leading Certification Organization, a distinguished Notified Body (CE0459) authorized to act under European …
Experience: 2+ years of medical devices industry experience; 4+ years preferred in regulatory affairs
Type: Full-Time
Benefits: Competitive benefits package including health insurance, flexible spending accounts, company-paid life insurance, 401K …

Arcellx

Skills & Focus: cell therapy, immunotherapies, quality system, Veeva, SOP's, document control, training, metrics, operational excellence, clinical-stage biotechnology
About the Company: a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable …
Type: Full-time

Gmed North America

Skills & Focus: Medical Devices, QA Auditing, ISO 13485, MDSAP, CE Marking, Quality Management Systems, Regulatory Requirements, Client Management, Engineering, Healthcare
About the Company: GMED North America is the US subsidiary of GMED, a leading Certification Organization, a distinguished Notified Body (CE0459) authorized to act under European …
Experience: A minimum of four years of full-time hands-on work experience in the field of medical devices or related sectors.
Type: Full-Time
Benefits: GMED North America offers a full and competitive benefits package including health, dental, and vision coverage, flexib…

Charles River Laboratories

Skills & Focus: biomanufacturing, cGMP, GLP, Quality, SOPs, cell therapy, fermentation, chromatography, quality documents, documentation
About the Company: Charles River is an early-stage contract research organization (CRO) that provides a diverse portfolio of discovery and safety assessment services, supporting …
Experience: 3 years of related experience with HS Diploma or equivalent; or 2.5 years with A.S.; or 1.5 years with B.S. in biology/life sciences, bioengineering, or related discipline.
Salary: $26.00 - $30.00 per hour
Type: Full-time
Benefits: Bonus/incentives based on performance, 401K, paid time off, stock purchase program, health and wellness coverage, and w…

Gmed North America

Skills & Focus: CE marking, medical devices, evaluations, product review, regulatory compliance, design dossiers, technical documentation, quality review, standards, healthcare products
About the Company: GMED North America is the US subsidiary of GMED, a leading Certification Organization, a distinguished Notified Body (CE0459) Authorized to act under European …
Experience: 4 years of professional experience in the field of healthcare products or related activities, including 2 years in the design, manufacture, testing, or use of the device or technology.
Type: Full-Time
Benefits: Group-sponsored health, dental, and vision coverage, flexible spending accounts, short-term and long-term disability, c…
Skills & Focus: clinical evaluation, medical devices, regulatory requirements, quality management, project management, risk assessments, clinical trials, customer service, medical device testing, data analysis
About the Company: GMED North America is the US subsidiary of GMED, a leading Certification Organization, a distinguished Notified Body (CE0459) Authorized to act under European …
Experience: Minimum of four years in health care services or related sectors, including minimum of two years in usage, development or testing/evaluation of medical devices.
Type: Full Time
Benefits: Full and competitive benefits package including health, dental, and vision coverage, flexible spending accounts, short-…