101 - 120 of 511 Jobs

Senior C++ QT Software Engineer - Med Device

Motion Recruitment Partners, LLC

Marlborough, Massachusetts, USA

Full-time

Our client, a leading innovator in the medical device industry, is seeking a Senior Software Engineer with strong expertise in C++, Qt, and image processing/computer vision. This role offers the opportunity to contribute to advanced diagnostic and imaging solutions that have a real impact on patient care. Key Responsibilities: Design, develop, and maintain software applications using C++ and the Qt frameworkImplement and optimize algorithms for image processing and computer visionCollaborate wit

Senior Staff, Software Quality Assurance Engineer

Stryker

Portage, Michigan, USA

Full-time

Work Flexibility: Hybrid Senior Staff, Software Quality Assurance Engineer Stryker is seeking a Senior Staff Software Quality Assurance Engineer to support our Digital Robotics and Enabling Technologies business by driving quality processes. In this role, you will partner with R&D software development teams to guide them through internal quality system processes and ensure compliance with regulatory standards, including FDA, HIPAA, ISO, and SOC 2. Work Flexibility: Hybrid: Candidates must resi

Sr. Principal Statistics

PARAKEET WORLD SOLUTIONS LLC

Remote

Contract

Job Title: Sr. Principal StatisticsLocation: Remote Duration: 6 MonthsEmployment Type: W2 ContractExperience Level: Mid-SeniorEducation Required: Ph.D. or MS in Statistics or BiostatisticsIndustry: Pharmaceuticals Job Summary:The Sr. Principal Statistician will lead statistical activities in clinical trials, from protocol development to final study reporting. The role will also contribute to regulatory filings, in-licensing evaluations, and marketing support. Key Responsibilities:Review protocol

Sr. Validation & Verification Engineer

ConsultNet, LLC

Salt Lake City, Utah, USA

Full-time

Sr. Verification & Validation Engineer (onsite) Salt Lake City, UT Contract to hire Pay: $50-$65/hr Job Description: We are looking for a Senior Verification and Validation (V&V) Engineer to lead the development and execution of our testing strategy across hardware, embedded software, and clinical software systems. In our fast-paced startup environment, this role will be critical in planning, executing, and documenting V&V activities to ensure the safety, effectiveness, and regulatory compliance

Engineer Disposables R&D, Sustaining

Stefanini

Plymouth, Minnesota, USA

Contract

Stefanini Group is hiring! Stefanini is looking for Engineer - Disposables R&D, Sustaining in Plymouth, MN (Hybrid) For quick Apply, please reach out to Vipul Bhardwaj - call: / email: Work Hours: M-F (40 hours) Work Location: Plymouth, MN (Hybrid) Shift: 1st Shift Create new 3rd party supplier documentation including design specifications, labeling, design drawings, etc. for peritoneal dialysis disposable sets.Create, modify, and maintain design history files.Perform change control assessments.

Principal Engineer Disposables R&D, Sustaining

Stefanini

Plymouth, Minnesota, USA

Contract

Stefanini Group is hiring! Stefanini is looking for Principal Engineer - Disposables R&D, Sustaining in Plymouth, MN (Hybrid) For quick Apply, please reach out to Tuhin Podder- call: /email: Work Hours: M-F (40 hours) Work Location: Plymouth, MN (Hybrid) Shift: 1st Shift Technical lead for DHF structure within sustaining engineering for disposable medical devices.Manage new 3rd party supplier documentation strategy for peritoneal dialysis disposable sets.Manage change controls from initiation th

Statistical Programmer needed for Remote Job only EST candidates needed!!!

Nam Info Inc

Remote or US

Full-time, Contract, Third Party

Dear, Hope you are doing well. Send resumes along with expected bill rates on W2( NO Benefits) or Independent contractors only apply and share to Note : NO 3rd party candidates, or H1's/EAD's/OPT's please. Role :Statistical Programmer II Location :Remote Duration : 6+ months contract EST ZONE CANDIDATES ONLY Statistical Programming II: Key responsibilities At least 5 years of experience in ADaM/TLF. Create, validate, and maintain SAS programs for data analysis, reporting, and submission de

Engineering Documentation Expert

Katalyst Healthcares and Lifesciences

Fort Worth, Texas, USA

Full-time

Responsibilities: Develop comprehensive technical documentation, including user manuals, installation guides, labeling materials, and regulatory documentation for ophthalmic devices. Work closely with engineering, regulatory, and quality teams to ensure all documentation meets industry standards and regulatory requirements. Interpret engineering drawings and specifications to create detailed build and qualification procedures for complex ophthalmic systems. Collaborate with R&D and manufacturing

Labelling Manager

Altezzasys

Irving, Texas, USA

Contract, Third Party

Job Title:- Labelling Manager Location:- Irving, Texas (Onsite) Contract Job Description:- Lead and Coordinate Labeling Design Change projects for US and Global Medical device products. Ensures all Design change activities are planned, approved, and executed. Coordinate various team member activities to ensure project plan targets are defined and met.Prepare and executes a Design Change Notice to describe the proposed change, the project plan for accomplishing the design changes, and Design tran

Sr. SAS Programmer

Katalyst Healthcares and Lifesciences

Durham, North Carolina, USA

Full-time

Responsibilities: The Sr. SAS Programmer will be responsible for statistical programming for the client's clinical studies. In this role, you will develop and validate SAS programs for data presentation, analyses, and provide programming support to project team members. Our Ideal candidate will have a strong work ethic capable of thriving in a high growth, fast paced and intellectual environment. Serves as lead programmer for assigned projects to provide statistical and programming support i

Senior SAS Programmer

Katalyst Healthcares and Lifesciences

Seattle, Washington, USA

Full-time

Responsibilities: The Senior SAS Programmer will be responsible for statistical programming for the client's clinical studies. In this role, you will develop and validate SAS programs for data presentation, analyses, and provide programming support to project team members. Our Ideal candidate will have a strong work ethic capable of thriving in a high growth, fast paced and intellectual environment. Serves as lead programmer for assigned projects to provide statistical and programming suppor

Labeling Design SME

Involgix

Irving, Texas, USA

Third Party, Contract

Please find below updated job details ,kindly share and Upload candidate profiles. Lead and Coordinate Labeling Design Change projects for US and Global Medical device products. Ensures all Design change activities are planned, approved, and executed. Coordinate various team member activities to ensure project plan targets are defined and met.Prepare and executes a Design Change Notice to describe the proposed change, the project plan for accomplishing the design changes, and Design transfers. P

Hiring- Software Engineer / R & D Software Engineer

Recruitment.ai

Tennessee City, Tennessee, USA

Contract

Job Title: Software Engineer / R&D Software Engineer Location: East Tennessee - Hybrid Position Summary Software Engineers and R&D Software Engineers to join a growing development team. These roles will involve designing and developing advanced medical imaging software solutions used in orthopedic diagnostics and computer-assisted surgery. As a member of our team, they will work in a collaborative, fast-paced environment where innovation and excellence are highly valued. You will play a key role

Validation Engineer III

Katalyst Healthcares and Lifesciences

Mounds View, Minnesota, USA

Full-time

Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Perform, oversee, and guide supplier process validations (IQ/OQ/PQ) for sterile barrier packaging material manufacturing processes. Ensure supplier process validation requirements (CTQs, drawings, specifications, risk levels, and protocols) are communicated, understood, and executed. Collaborate with suppliers to review and approve validation documentation, including prot

Quality Management Systems (QMS) Specialist (W2)

Sovereign Technologies

Irvine, California, USA

Contract

Title: Document Control Coordinator - QMS Location: Irvine, CA Onsite Document Control Specialist QMS Job Description We are seeking a dedicated Quality Management Systems (QMS) Specialist who will play a crucial role in ensuring compliance with internal and external regulatory requirements. This role involves engaging in the development of future state QMS for business needs, executing modifications, and contributing to the quality planning process. Responsibilities Ensure QMS compliance with a

Batch Processing Engineer

Beacon Systems, Inc

Dallas, Texas, USA

Contract

About Beacon Systems, Inc Beacon Systems, Inc, delivers Program Management, Science, Engineering, and Technology Solutions to Federal, Commercial, State, and Local Agencies. We are a subsidiary of Radiant Digital Solutions. Our Technology support to many DoD Agencies, NASA, Voice of America, FDA, and State Agencies such as State of FL, RI, MS, ND, VA, and WV extends our delivery of solutions worldwide. Position: Batch Processing Systems Engineer Location: Hybrid - Dallas, TX Duration: 12 Months

Healthcare Data Scientist FHIR & HL7 Expertise

E-Solutions, Inc.

Philadelphia, Pennsylvania, USA

Third Party

Job title: - Healthcare Data Scientist FHIR & HL7 Expertise Location: Philadelphia PA Job Summary: We are seeking a curious and motivated Machine Learning Engineer to join the Foundational Data Analytics (FDA) Program - a strategic initiative aimed at building a modern, intelligent data ecosystem. In this role, you will support the development and deployment of machine learning models that power enterprise analytics, deliver predictive insights, and drive transformation across the healthcare

AME Automation Engineer

GE Healthcare

Waukesha, Wisconsin, USA

Full-time

Job Description Summary We are seeking a detail-oriented and innovative Automation Engineer to join our Advanced Manufacturing Engineering (AME) team within a regulated medical device manufacturing environment. This role is responsible for designing, developing, and implementing automation solutions that enhance manufacturing efficiency, ensure product quality, and maintain compliance with FDA and ISO standards. The ideal candidate will have experience in highly regulated industries and a passio

Commissioning and Qualification Engineer

Katalyst Healthcares and Lifesciences

Raleigh, North Carolina, USA

Full-time

Responsibilities: Lead or support C&Q activities for pharmaceutical utilities and process equipment, ensuring compliance with industry standards and regulatory requirements. Execute FAT (Factory Acceptance Testing) to validate equipment functionality and performance. Support the qualification of Black and Clean utilities, such as water systems, clean steam, HVAC, and gas utilities. Perform process equipment qualification to meet GMP and production readiness standards. Develop and execute C&Q pro

Microbiology Team Lead

ITS Technologies, Inc.

Bowling Green, Ohio, USA

Full-time

Integrated Talent Strategies (ITS) is seeking a Microbiology Team Lead to work in the Perrysburg, OH area. This is a direct hire position that offers a variety of great benefits, including health insurance, 401(k), and paid time off.DescriptionResponsible for USP microbiological quality control testing on various products, including FDA-regulated OTC drugs, cosmetics, and EPA-registered disinfectants. Establishes microbial monitoring limits and oversees environmental monitoring to ensure facili