Internal Quality Audit Medical Device Jobs

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Quality Engineer - Medical Devices  

Growing Medical Devices Company - Milwaukee, WI

Candidate must have proven project management skills and demonstrated experience using statistical process control, design of experiments, failure mode and effects analysis and process validation. Strong preference for QA experience in a high speed, high... Internal Quality Audit Medical Device Work careers ...

from: - 2 days ago

Plant Quality Manager - Medical Devices  

Growing Medical Devices Company - Missoula, MT

Growing medical devices company seeks a Plant Quality Manager to oversee all quality activities at one of the company's manufacturing sites near Missoula, MT. The Plant Quality Manager will: Bachelor's degree, preferably in an engineering or scientific... Internal Quality Audit Medical Device careers...

from: - 2 days ago

Senior Quality Engineer-Medical Devices  

Kimberly Clark-Healthcare - Irvine, CA

Perform quality engineering duties associated with new product development: design requirements and validation, design controls, quality planning, risk management, human factors engineering and establishment of appropriate manufacturing process validations... $107K

from: - 4 days ago

Quality Engineer (Medical Device / FDA)  

SWAT Solutions - Minneapolis, MN

Experience in medical device process and product validation, sampling, sample size determination, DOE, process analysis/capability, hypothesis testing, analysis of variance, and repeatability and reproducibility. Recommend and implement quality improvements...

from: - 2 days ago

Quality Manager (Medical Device)  

Labtopia, Inc. - Houston, TX

The Quality System Manager (“QSM”) provides support to key business of the organization including client and account services, production, and business development. The QSM will gather information and generate documents such as flowcharts, procedures...

from: - 8 days ago

Quality Engineer : Medical Devices  

Growing Medical Devices Company - milwaukee, wisconsin

Supports new product development activities as directed through core team participation in the development of Master Validation Plans, PFMEA's, Control Plans, etc. Candidate must be familiar with and have working knowledge of FDA Quality Systems Regulations... Permanent...

from: - 8 days ago

Quality Engineer medical device-ISO 13485:23 CAPA  

taffstaff - Arcadia, CA

Provide Quality Engineering support to development and production activities (product and process) to ensure processes and products developed and implemented meet specified standards and specifications and comply with the quality system and applicable...

from: - 10 days ago

Regulatory Affairs Specialist - (Medical Device)  

Inventiv Health Clinical - Berkeley Heights, NJ

• Provides regulatory affairs support for clinical studies including pre-market, post-market and physician initiated studies • Supports regulatory compliance activities, including manufacturing site registration, GMP audit, post-market vigilance reporting...

from: - 5 days ago

Quality Engineer - Medical Devices  

QCI Technical Staffing - Detroit, MI 48201

Growing company north of Detroit, MI is looking to add a Quality Engineer to their staff who will be responsible for: Internal audits Regulatory affairs (Class II and III) PPAPS, PFMEA, capability studies, Gage R&R's, IMDS Validation; creation and execution... Any...

from: Beyond Network - 10 days ago

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Sr. Project Manager: Medical Device  

Recruitment Trends, Inc. - Jersey City, NJ (+1 location)

The PM will be responsible for organizing cross functional team activities which include project schedule creation, project meetings, publishing detailed minutes consisting of action items and deliverables, while monitoring progress against the schedule...

from: - 7 days ago

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