58 Quality Engineering jobs in Raleigh.

Skills & Focus: Medical Devices, Therapies, Manufacturing, Engineering, R&D, Quality Assurance, Sales, Information Technology, Clinical Support, Pharmaceuticals

About the Company: Baxter is dedicated to saving and sustaining lives by innovating medical devices and therapies, with a workforce that enriches by a diverse population of indiv…

Type: Full-time

Benefits: Comprehensive benefits options reflect the value we place in our employees.

Skills & Focus: Regulatory Engineering, Product Safety, EMC, Testing, Compliance, Cross-functional collaboration, Problem-solving, Document management, Product Safety Standards, Interdisciplinary team

About the Company: OnLogic is growing, and we want to give you the same opportunity to grow in your career! We design and manufacture specialized computers and hardware solutions…

Experience: Minimum of 10 years of regulatory engineering experience.

Salary: $110,000 to $140,000

Type: Full-time

Benefits: Comprehensive benefits package including 401k Plan with 3% Employer Contribution, Annual Profit Share Bonus, Paid Mater…

Skills & Focus: Shift Manager, Solid Dose Forms, Leadership, Manufacturing, Production Plans, Quality Objectives, Coaching, Team Development, Process Improvement, FDA Regulations

About the Company: For more than 100 years, Novo Nordisk has been tackling the unmet medical needs of people living with serious chronic diseases, such as diabetes & obesity. Bei…

Experience: Minimum of five (5) years of proven Leadership experience; Minimum of two (2) years of Bulk Processing experience preferred; Minimum of five (5) years of experience in a manufacturing industry, FDA regulated preferred.

Benefits: Leading pay and annual performance bonus for all positions; generous paid time off including 14 paid holidays; Health, …

Skills & Focus: QA Auditor, audits, quality assurance, GXP regulations, compliance, scheduling, planning, reporting, customer audits, risk management

About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…

Experience: 3 years of experience in pharmaceutical, technical, or related areas including GXP and/or Quality Assurance experience.

Salary: $67,500.00 - $112,500.00

Type: Full-time

Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Skills & Focus: product development, R&D management, medication management, pharmacy automation, hardware and software technologies, technical leadership, customer-centric culture, multi-functional development teams, engineering, medical device development

About the Company: BD is one of the largest global medical technology companies in the world.

Experience: Minimum of 10 years relevant experience with at least 5 years of applicable managerial experience in R&D management.

Salary: Competitive

Type: Full-Time

Benefits: Healthcare, Healthcare FSA, Employer Matching, Tuition Reimbursement, Professional Development, Maternity and Paternity…

Skills & Focus: MES implementation, manufacturing execution system, biotechnology, pharmaceutical industry, GxP environment, system validation, barcode scanners, Zebra printers, requirements gathering, technical operations

About the Company: Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines, including a suit…

Experience: 10+ years

Type: Full-time

Skills & Focus: manufacturing, FDA regulated, work cell, production processes, safety requirements, quality control, training competency, team leadership, scheduling, cGMP documentation

About the Company: For more than 100 years, Novo Nordisk has been tackling the unmet medical needs of people living with serious chronic diseases, such as diabetes & obesity. Bei…

Experience: Five (5) years of experience in a manufacturing industry required; Five (5) years of FDA regulated industry or solid dose manufacturing experience required.

Benefits: Leading pay and annual performance bonus for all positions, generous paid time off including 14 paid holidays, Health I…

Skills & Focus: Quality Management, Electromechanical Instrumentation, Quality Assurance/Control, FDA QSRs, Lean Manufacturing, Risk Management, ISO 13485, Statistical Analysis, Supplier Management, Project Management

About the Company: BD is one of the largest global medical technology companies in the world, focused on advancing the world of health.

Experience: Minimum of ten (10) years’ experience in Electromechanical Instrumentation, Quality Assurance/Control, Statistical analysis, FDA QSR’s and related areas.

Salary: Competitive

Type: Full-Time

Benefits: A competitive package of compensation and benefits programs.

Skills & Focus: Electrical Engineering, Pharmacy Automation, Product Development, Robotic Systems, Systems Architecture, Design Verification, Regulatory Certification, Embedded Control Systems, Collaboration, Problem Solving

About the Company: BD is one of the largest global medical technology companies in the world, advancing the world of health™.

Experience: 20 years of applicable experience required

Salary: Competitive

Type: Full-Time

Skills & Focus: IT lead, MES implementation, manufacturing support, GxP environment, system validation, project manager, technical lead, business processes, SaaS solutions, pharmaceutical industry

About the Company: Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. Its suite of gen…

Experience: 10+ years

Type: Full-time

Skills & Focus: Global Regulatory Affairs, Safety, IVD product registrations, MHRA, Notified Bodies, promotional material, on-market product support, UKRP audits, regulatory requirements, cross-functional stakeholders

About the Company: GRAIL is a healthcare company, pioneering new technologies to advance early cancer detection. We are using the power of next-generation sequencing (NGS), popul…

Skills & Focus: medical diagnostics, software development, image acquisition, image analysis, prototyping, algorithm development, cross-functional collaboration, design control, quality assurance, product development

About the Company: BioMérieux is a global leader in in vitro diagnostics and biotechnology, focusing on developing innovative products for the medical diagnostic market.

Experience: Ph.D. + 6 years, M.S. + 8 years, B.S. + 10 years

Skills & Focus: Quality Systems, Customer Quality, Electromechanical Instrumentation, FDA regulations, Continuous Improvement, Six Sigma, Lean, Project Management, Regulatory Inspections, Complaint Handling

About the Company: BD is one of the largest global medical technology companies in the world, focused on advancing the world of health.

Experience: Minimum 7 years relevant experience preferred

Salary: Competitive

Type: Full-Time

Benefits: Valuable, competitive package of compensation and benefits programs

Skills & Focus: Packaging Development, Design controls, Combination products, cGMP requirements, Regulatory submission, Medical devices, Lean Six Sigma, Cross-disciplinary teams, Packaging solutions, Sustainability objectives

About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies.

Experience: Minimum 7 years experience

Skills & Focus: validation, qualification, pharmaceutical, GMP, manufacturing, Six Sigma, cross-functional, compliance, cybersecurity, Lead

About the Company: AstraZeneca is one of the world's most forward-thinking and connected BioPharmaceutical companies, dedicated to delivering life-changing medicines.

Experience: 8+ years of relevant experience in the pharmaceutical industry

Skills & Focus: Quality Engineering, Combination Products, Medical Devices, Design Control, Risk Management, Compliance, Technical Specifications, Quality Systems, New Product Introduction, FMEA

About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies, committed to delivering life-changing medicines as a collabo…

Experience: Five (5) years or more of experience supporting Quality Engineering of Combination Products and/or Medical Devices

Type: Full-time

Skills & Focus: Medical Devices, Therapies, Manufacturing, Engineering, R&D, Quality Assurance, Sales, Information Technology, Clinical Support, Pharmaceuticals

About the Company: Baxter is dedicated to saving and sustaining lives by innovating medical devices and therapies, with a workforce that enriches by a diverse population of indiv…

Type: Full-time

Benefits: Comprehensive benefits options reflect the value we place in our employees.

Skills & Focus: Manufacturing, Quality, facility, innovators, collaborative environment, patients, impact, state-of-the-art, team, RTP

About the Company: Beam is preparing to open a state-of-the-art Manufacturing facility located on Davis Drive in RTP, NC, focused on helping patients and fostering a collaborativ…

Type: Full-time

Skills & Focus: facilities management, maintenance, biotechnology, GxP practices, budget management, cGMP, collaboration, team management, risk management, preventative maintenance

About the Company: Beam Therapeutics is committed to establishing the leading, fully integrated platform for precision genetic medicines. Beam has assembled a platform that inclu…

Experience: 10+ years’ experience leading maintenance personnel within a biotechnology / pharmaceutical / medical device manufacturing environment

Type: Full-time

Skills & Focus: Quality Management System (QMS), GxP compliance, Change Management, cGMP regulations, Continuous Improvement, Quality Event KPIs, SOPs, technical writing, regulatory inspections, Supplier Qualification

About the Company: Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this …

Experience: 10+ years’ experience in the pharmaceutical/biotech industry with 2+ years’ experience working with Quality Management Systems

Type: Full-time

Skills & Focus: manufacturing, equipment, production goals, cGMP, SOP, quality issues, FDA, safety, training, documentation

About the Company: For more than 100 years, Novo Nordisk has been tackling the unmet medical needs of people living with serious chronic diseases, such as diabetes & obesity. Our…

Experience: Minimum of one (1) year of experience in a manufacturing industry preferred

Type: Full-time

Benefits: Leading pay and annual performance bonus for all positions. Generous paid time off including 14 paid holidays. Health, …

Skills & Focus: manufacturing, cGMPs, SOPs, equipment, production, cleaning, sanitization, labelling, quality issues, safety

About the Company: Novo Nordisk has been tackling the unmet medical needs of people living with serious chronic diseases, such as diabetes & obesity.

Experience: Minimum of one (1) year of experience in a manufacturing industry preferred.

Benefits: Health Insurance, Dental Insurance, Vision Insurance, 401K contribution, parental leave, tuition assistance, life & dis…

Skills & Focus: Facilities Coordination, Biopharmaceutical, Manufacturing, Maintenance, Engineering, cGMP, Documentation, Project Management, Data Analysis, Communication

About the Company: Amgen is a biotechnology company that focuses on developing innovative medicines to help patients living with serious illnesses since 1980.

Experience: High school/GED + 2 years or Associate’s + 6 months or Bachelor’s

Salary: 77,155.00 USD - 103,568.00 USD

Type: Full-time

Skills & Focus: Manufacturing, Information Systems, Automation, Engineering, Biotechnology, Pharmaceutical, Cloud, Software Development, GMP regulations, Industry 4.0

About the Company: Amgen is a biotechnology company that pioneers the development of innovative medicines for serious illnesses, focusing on four therapeutic areas: Oncology, Inf…

Experience: Doctorate degree, OR Master’s degree and 2 years of Information Systems, Engineering and/or Information technology experience, OR Bachelor’s degree and 4 years of Information Systems, Engineering and/or Information technology experience, OR Associate’s degree and 8 years of Information Systems, Engineering and/or Information technology experience, OR High school diploma/GED and 10 years of Information Systems, Engineering and/or Information technology experience

Salary: 142,955.00 USD - 162,947.00 USD

Type: Full time

Skills & Focus: manufacturing, cGMP, safety, compliance, operations, biotechnology, pharmaceutical, process, documentation, cleaning

About the Company: Amgen is one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide.

Experience: High School/GED + 2 years manufacturing and/or other regulated environment experience

Salary: 73,359.00 USD - 85,625.00 USD

Type: Full-time

Benefits: Comprehensive employee benefits package, including a Retirement and Savings Plan, group medical, dental and vision cove…

Skills & Focus: ISO 13485, Quality Management System, CAPA, Internal Audits, Medical Device Directive, MDD, IEC Standards, Problem Solving, Quality Systems, Regulatory Compliance

About the Company: As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. We offer a diverse portfol…

Experience: At least 5 years of experience in Quality Systems or Quality Engineering with a minimum of 3 years in the medical device industry.

Skills & Focus: ISO 13485, Quality Management System, Regulatory Compliance, Auditing, CAPA, Change Management, Training, Internal Audits, Quality Data Analysis, Problem Solving

About the Company: As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. We offer a diverse portfol…

Experience: At least 5 years of experience in Quality Systems or Quality Engineering with a minimum of 3 years in the medical device industry.

Type: Contract

Skills & Focus: R&D, Process Engineer, Injection Molding, Medical Device, Tooling Development, Quality Improvement, Manufacturing, Process Validation, Technical Expertise, Project Management

About the Company: A global provider of medical technologies focused on improving health and quality of people's lives through innovative solutions in various medical fields.

Experience: At least 5 years minimum preferably within a medical device company

Skills & Focus: Commissioning, Qualification, Validation, pharmaceutical facilities, protocol writing, regulatory industry, utilities, project management, troubleshooting, document development

About the Company: CAI is a 100% employee-owned company established in 1996 that has grown to more than 800 people worldwide. We provide commissioning, qualification, validation,…

Experience: 2-4 years' experience in commissioning and qualification in a regulated industry

Salary: Not specified in job posting

Type: Full-time

Benefits: Competitive compensation and benefits which include: up to 15% retirement contribution, 24 days PTO and 5 sick days per…

Skills & Focus: technical documents, SOPs, requirements specifications, testing protocols, GxP best practices, system validation, engineering life cycle, project deliverables, problem-solving, cross-functional team alignment

About the Company: The leading advanced therapy technical operations consulting company in the life science industry, committed to advancing manufacturing to achieve operational …

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, Aggressive bonus structure, Medical, Dental, and Vision insurance, 401k Plan with company match, Pa…

Skills & Focus: Software Systems Engineering, Software Development, Medical Devices, Agile Methodologies, Innovation, Cross-Functional Teams, Risk Management, Regulatory Compliance, Team Leadership, Embedded Systems

About the Company: Baxter’s Research and Development teams work cross functionally to innovate, develop and introduce creative solutions for patient needs globally.

Experience: 8+ years of related experience

Salary: $128,000.00 to $176,000.00 annually

Type: Full-time

Benefits: Comprehensive compensation and benefits packages including medical coverage, 401(k) matching, flexible spending account…

Skills & Focus: Quality Assurance, Compliance, GMP, FDA, Drug substance, Leadership, Continuous Improvement, Quality systems, Digital integration, Regulatory requirements

About the Company: Johnson & Johnson is the world's largest and most broadly-based healthcare company, committed to using its reach and size for good, improving access and afford…

Type: Hybrid Work

Skills & Focus: Regulatory Affairs, Senior Manager, Medical Device, Software, SaMD, SiMD, Healthcare, Compliance, Quality, Innovation

About the Company: Baxter International is a leading medical device company that develops life-saving therapies and medical products, driven by a diverse population of individual…

Type: Full time

Benefits: Comprehensive benefits options reflecting the value placed on employees.

Skills & Focus: Quality Assurance, clinical teams, SOPs, compliance, audits, CAPA, process improvement, regulatory inspections, training materials, corrective actions

Skills & Focus: Computer Software Validation, clinical trial software, requirements gathering, test scripts, risk-based approach, validation testing, change control documentation, technical expertise, GCP Guidance, software development cycle

About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…

Experience: 1+ year of experience in a CSV for clinical trial software (CTMS, CDMS, eTMF, etc.)

Salary: $60,000 - $100,000

Type: Full-time

Benefits: Medical, dental, vision, and basic life insurance; Flexible PTO and company paid holidays; Retirement programs; 1% char…

Skills & Focus: automation controls, life science, technical expertise, business development, project delivery, team building, client satisfaction, high performing teams, consulting mindset, biomanufacturing

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: Minimum of 8 years of advanced therapy, life science, pharmaceutical, or biotech experience. 6 years managing high-performing teams, 4 years in business development or sales.

Salary: $50,000 — $240,000 USD

Type: Full-time

Benefits: Competitive salary based on experience, annual discretionary bonus, medical, dental, and vision insurance effective you…

Skills & Focus: Configuration Consultant, RTSM, cloud-based solutions, life sciences, project configuration, study requirements, attention to detail, team collaboration, customer needs, flexible work environment

About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster.

Type: Full-time

Skills & Focus: Quality Engineer, Quality Systems, cGMP, Continuous Improvement, Root Cause Analysis, Statistical Analysis, Supplier Quality, CAPA, Risk Analysis, Six Sigma

Experience: 1-5 years’ experience in QA or a pharmaceutical manufacturing environment

Skills & Focus: Quality Analyst, Product Release, Quality Metrics, GMP, Audits, Customer Inquiries, Batch Record Review, Label Preparation, CAPA, Change Control

Experience: 1-3 years pharmaceutical manufacturing experience preferred

Skills & Focus: cross-functional, Validation, Manufacturing, Quality, Supply Chain, Engineering, technical documents, GxP best practices, project management, problem-solving

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…

Skills & Focus: biomanufacturing, project management, cell and gene therapy, capital projects, facility builds, tech transfers, validation life cycle, commissioning and qualification, quality, regulatory compliance

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

Benefits: Competitive salary based on experience, Aggressive bonus structure, Medical, Dental, and Vision insurance effective you…

Skills & Focus: Project Management, Validation, Engineering, Quality/Compliance, Technical Documents, System Validation, GxP Best Practices, Cross-functional Collaboration, Problem Solving, Philanthropy

About the Company: Leading advanced therapy technical operations consulting company in the life science industry, dedicated to advancing manufacturing to achieve operational exce…

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, aggressive bonus structure, medical, dental, and vision insurance, 401k plan with company match, pa…

Skills & Focus: Clinical Data Management System, EDC, data cleaning, reporting, database design, data collection, customer-facing, implementation, regulatory compliance, software specifications

About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…

Experience: 5+ years

Salary: $80,000 - $200,000

Type: Full-time

Benefits: Medical, dental, vision, and basic life insurance; Flexible PTO; Retirement programs; 1% charitable giving program

Skills & Focus: manufacturing, safety, operations, packaging, documentation, equipment, chemicals, reactors, logistics, compliance

Experience: Previous PSM manufacturing experience preferred

Skills & Focus: computer software validation, clinical trial software, RTSM software, technical writing, validation process, project management, customer implementation, product excellence, lifesciences industry, remote work

About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…

Experience: Strong technical writing capabilities and expertise in clinical trial software validation

Type: Full-time

Benefits: Flexible work environment, remote work options (Work Anywhere policy)

Skills & Focus: quality assurance, training, compliance, cGMP, SOPs, documentation, investigation, root-cause analysis, auditing, employee training

About the Company: Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plas…

Experience: Typically requires no previous related experience.

Type: Regular Full-Time

Skills & Focus: biomanufacturing, project management, quality/compliance, engineering, client management, team collaboration, technical documentation, capital project management, validation life cycle, business development

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: A minimum of 3 years of Project Engineer, Consulting, and/or relevant industry experience.

Salary: Competitive salary based on experience

Benefits: Competitive salary based on experience, Aggressive bonus structure, Medical, Dental, and Vision insurance effective you…

Skills & Focus: pharmacovigilance, risk management, compliance, drug safety, leadership, audit, FDA, vendor oversight, safety reporting, REMS

Experience: Minimum of 5-7 years of experience in a drug safety/pharmacovigilance setting.

Skills & Focus: Quality Audits, Quality Assurance, Risk Management, Audit Universe, Vendor Oversight, Regulatory Compliance, Internal Audits, CAPA, Project Management, Training and Development

About the Company: PrimeVigilance is a global leader in pharmacovigilance, offering comprehensive drug safety services to pharmaceutical and biotechnology companies.

Experience: Significant experience in Quality Assurance and Audit roles, particularly in the pharmaceutical industry.

Type: Full-time

Skills & Focus: Project Engineer, Manufacturing, Life Science, Quality, Supply Chain, Engineering, GxP, Validation, Technical Documents, Problem-Solving

About the Company: Precision for Medicine, Manufacturing Solutions is the leading advanced therapy technical operations consulting company in the life science industry, dedicated…

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: Quality Assurance, clinical trials, compliance, SOPs, audits, inspections, process improvement, corrective actions, training, data review

Skills & Focus: Quality Control, Microbiology, GxP, Biopharmaceutical, Compliance, Laboratory, Technical Leadership, Contamination, Investigation, Environmental Monitoring

About the Company: Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in …

Experience: At least 5 years of experience in Quality Control Microbiology laboratory providing technical and compliance leadership within GxP Biopharmaceutical Manufacturing operations.

Skills & Focus: Quality Assurance, Quality Control, cGMP, Validation, Investigation, Process Improvement, Regulatory Compliance, Analytical Testing, Documentation, Quality Review

Experience: 2+ years of experience with a BA/BS degree; or other education and experience combination.

Salary: $80,300.00 to $133,900.00

Type: Full time

Benefits: 401(k) plan with Pfizer Matching Contributions, paid vacation, holiday and personal days, medical, prescription drug, d…

Skills & Focus: LIMS, compliance, system administration, technical support, GxP, quality operations, SDLC, ITIL, project management, troubleshooting

About the Company: Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in …

Experience: At least 3 years of hands-on IT support experience, including troubleshooting complex issues, system management, and working directly with end-users and business partners.

Type: Full-time

Skills & Focus: automation engineer, biopharma, SCADA, PLC, GMP, Data Integrity, manufacturing systems, process systems, technical skills, collaborative environment

About the Company: Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines.

Experience: Minimum 5 years of experience as an automation engineer in the pharmaceutical, biopharma, and/or life sciences industries.

Type: Full-time

Skills & Focus: Quality Control, Analytical, GxP, Biopharmaceutical, Laboratory, Compliance, Analytical Methods, Technical Leadership, Risk Management, Quality Management

About the Company: Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in …

Experience: At least 5 years of experience in Quality Control Analytical Laboratory providing technical and compliance leadership within GxP Biopharmaceutical Manufacturing operations.