14 Quality Engineering jobs in Dallas.

Hiring now: Smt Process Engr @ Sanmina, Quality Spec Biomedical T @ Iqvia, Dir Regulatory Affairs Pa @ Mckesson, Sr Spec Quality Assurance @ Cardinal H, Sr Solutions Architect Si @ Korn Ferry, Operator I @ Steris, Sr Regulatory Affairs Pro @ Johnson Jo, Food Safety Quality Mgr @ Hanagroup, Quality Systems Spec Iii @ Inogen, Quality And Regulatory Sp @ Sgs.Explore more at jobswithgpt.com.

šŸ”„ Skills

Regulatory Compliance (6) Risk Management (4) Quality Assurance (3) FDA (3) Project Management (3) Documentation (3) manufacturing (2) ISO 13485 (2) documentation (2) Regulatory Affairs (2)

šŸ“ Locations

Irving (4) Dallas (3) Plano (2) Richardson (2) Carrollton (1) Fort Worth (1) Grand Prairie (1)

Sanmina Corporation

Skills & Focus: SMT, medical device production, manufacturing, process optimization, ISO 13485, IPC-A-610, Lean Six Sigma, problem solver, process documentation, customer interface
About the Company: Sanmina Corporation (Nasdaq: SANM) is a leading integrated manufacturing solutions provider serving the fastest-growing segments of the global Electronics Manu…
Experience: Minimum 5 years experience supporting manufacturing

Iqvia

Skills & Focus: Biomedical Technician, Quality Inspector, travel, documentation, system auditing, software validation, data validation, client management, Microsoft Office Suite, Salesforce CRM
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: 5+ years of Biomedical Technician or Quality/Regulatory experience
Salary: $30 - $40/hour
Type: Part time
Benefits: Paid travel time, Holiday Pay based on recognized holidays, supplemental hours for less than 40 hours worked.

Mckesson

Skills & Focus: Regulatory Affairs, Patient Safety, Healthcare, Pharmaceuticals, Compliance, Quality Management, Pharmacovigilance, Leadership, Risk Reduction, Continuous Improvement
About the Company: McKesson is an impact-driven, Fortune 10 company that touches virtually every aspect of healthcare. We are known for delivering insights, products, and service…
Experience: A minimum of 10 years of experience in healthcare, pharmaceuticals, or regulated environment
Salary: $103,400 - $172,400
Type: remote
Benefits: Competitive compensation package including base pay, annual bonus or long-term incentive opportunities.

Cardinal Health

Skills & Focus: Quality Assurance, cGMP, documentation, manufacturing, pharmaceutical, medical device, training, product release, regulatory standards, ISO
About the Company: Cardinal Health is a global, healthcare services and products company that develops and implements quality policies, procedures, and processes to ensure produc…
Experience: 2+ years of experience in related science field preferred; 1-2 years of experience in Quality Assurance and/or cGMP regulated environment preferred.
Salary: $67,500-$96,400
Type: Full time
Benefits: Medical, dental and vision coverage; Paid time off plan; Health savings account (HSA); 401k savings plan; Access to wag…

Korn Ferry

Skills & Focus: Siemens, Polarion, Teamcenter, Ops Center, middleware, eQube, integration, medical devices, configurability, best practices
About the Company: Korn Ferry is a consulting firm that helps organizations improve performance through talent management solutions.
Experience: Proven expertise in the medical devices industry with demonstrated experience as an IT Solutions Architect.
Type: Contract

Steris Corporation

Operator I Grand Prairie
Skills & Focus: Manufacturing, Operations, Sterilization, FDA, ISO, GMP, Quality Control, Team Player, Safety, Customer Service
About the Company: STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention.
Experience: Minimum of 2 years warehouse experience in a FDA, ISO, GMP environment preferred.
Salary: $21.61/hour
Type: Full-time
Benefits: Competitive base salary plus bonus, comprehensive benefits package including medical, dental, vision, paid PTO and holi…

Johnson & Johnson

Skills & Focus: Regulatory Affairs, Product Development, Global Regulatory Strategies, Medical Devices, Licenses and Authorizations, Compliance, Data Gathering, Project Management, Cross-functional Teams, Regulatory Submission
About the Company: Johnson & Johnson is a medical devices, pharmaceutical and consumer packaged goods manufacturer that is committed to improving health for humanity through inno…
Experience: At least 6+ years (4+ with Advanced Degree) of regulatory affairs or related experience.
Type: Hybrid Work
Skills & Focus: Supplier Quality, Quality Assurance, Supplier Management, Quality Engineering, Risk Management, Process Improvement, Project Management, Stakeholder Collaboration, Analytical Skills, Regulatory Compliance
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Type: Full-time

Hanagroup

Skills & Focus: Food Safety, Quality Control, Regulatory Compliance, FDA, USDA, Supplier Quality, Audits, GMPs, HACCP, FSMA 204

Johnson & Johnson

Skills & Focus: Project Management, Quality Standards, Medical Device, Regulatory Compliance, Leadership, Risk Management, Budget Planning, Communication, Team Management, FDA Guidelines
About the Company: Johnson & Johnson is a leading global healthcare company that focuses on delivering innovative healthcare solutions across various medical fields.
Experience: Minimum of 8 years in the medical device or pharmaceutical industries
Salary: 120,000 to 207,000
Type: Hybrid

Inogen

Skills & Focus: Quality Management System, Regulatory Compliance, ISO 13485, FDA, QMS Management, CAPA, Audits, Continuous Improvement, Cross-Functional Collaboration, Documentation
Experience: Minimum of 5 years of experience in Quality Assurance, with at least 3 years specifically in QMS management within the medical device industry.
Salary: USD 75969.5550 - 106357.3820 Annually
Skills & Focus: quality management system, new product development, manufacturing processes, supplier quality, post-market activities, complaint investigations, medical device regulations, root cause investigations, corrective and preventive actions, training of QMS elements
Experience: Minimum of three years of experience as a Quality Engineer in the medical device industry.

Sgs

Skills & Focus: Quality Assurance, Regulatory Compliance, Good Clinical Practices, Good Laboratory Practices, ISO 17025, Standard Operating Procedures, Internal Audits, Risk Management, Training, Documentation
Skills & Focus: Quality Standards, Regulatory Compliance, Good Clinical Practices, Good Laboratory Practices, ISO 17025:2017, Standard Operating Procedures, Documentation, Risk Management, Internal Audits, Training