101 - 120 of 502 Jobs

Design Quality Engineer

Thunderhawk Technology Partners

North Haven, Connecticut, USA

Full-time, Contract

Job Description: * Evaluate product issues to ensure patient, user and security risk are assessed, and acting as the lead Design Quality Engineer for Post-Market Design Changes on Capital Hardware * Update DFMEA and DHF documents as needed as part of the post market design change management process * Provide comprehensive support to Post Market Development Teams with a focus on Design Quality and Risk Management * Collaborate with different departments across the organization to understand and

Senior SAP PP/PM Functional Consultant -( Healthcare MANUFACTURING & MAINTENANCE)

Wise Equation Solutions Inc.

Saint Paul, Minnesota, USA

Contract

SAP MAKE DOMAIN CONSULTANT - MANUFACTURING & MAINTENANCE Job Title: Senior SAP PP/PM Functional Consultant (Manufacturing & Maintenance) Location: Twin Cities, USA (Hybrid) Experience: 10+ years Required Skills & Experience: SAP Implementation Experience: 10+ years of comprehensive SAP PP/PM implementation experience with minimum 5 full lifecycle manufacturing projectsProven track record of leading complex manufacturing implementations in process and discrete industriesDeep technical expertise i

Senior Manufacturing Engineer - Beverage Experience Highly Preferred

Jobot

Lewisville, Texas, USA

Full-time

Hands-On Role, Path to Engineering Director This Jobot Job is hosted by: Tracy Hann Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $100,000 - $135,000 per year A bit about us: We are a privately held manufacturer in the health and wellness industry, producing a broad portfolio of nutritional supplements, ready-to-drink beverages, and personal care items. With decades of experience and operations across the southern U.S., we manage the full

Validation Engineer

Katalyst Healthcares and Lifesciences

Libertyville, Illinois, USA

Full-time

Responsibilities: Lead validation efforts for injection molding machines, auxiliary equipment (e.g., dryers, chillers, robots), and integrated automation systems. Develop and execute validation protocols (SAT, FAT, IQ, OQ, PQ) for molding and downstream equipment. Support the qualification of new production lines involving injection-molded components. Perform process characterization, capability studies, and stability testing for moulded parts. Collaborate with tooling, manufacturing, and q

Remote QA Manager with Healthcare Payer and Claims exp

Infinite Computer Solutions (ICS)

Remote

Full-time

Note : GCEAD, L2EAD, consultant can apply for this position who can work on W2. Job Summary: We are looking for an experienced QA Healthcare Manager to lead the quality assurance team in ensuring the reliability, security, and compliance of healthcare applications. The ideal candidate should have a strong background in healthcare software testing, regulatory compliance (HIPAA, CMS, FDA), test automation, and team leadership. Key Responsibilities: we need someone who understand healthacre paye

Sr. Embedded Software Engineer

Abbott Laboratories

Alameda, California, USA

Full-time

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'

Sr. Instrument Verification and Validation Engineer

Katalyst Healthcares and Lifesciences

Rochester, New York, USA

Full-time

Responsibilities: Designing and implementing software of embedded devices and systems. Designing, developing, coding, testing, and debugging system software. Develop Requirements based manual test procedures. Access requirements for testability and determine best test approach. Compile and analyze test results. Document and manage system software defects. Participate in regular scheduling and team meetings. Participate in regular off hour meetings with partner in China. Understand projec

Product Security Engineer

E-Solutions, Inc.

US

Third Party, Contract

Role: Product Security Engineer Location: Remote Deliver documentation for pre-market product development activities including security plans, architecturediagrams, data fl ow diagrams, threat models, security requirements, Design for Security, SBOM, and risk management documentation. Drive and monitor and post-market vulnerability management activities, with adherence to strict timelines. Support compliance certification activities, such as SOC2, FedRAMP, ISO 27001, etc. Job description + ye

Systems Analyst (Hybrid)

Beacon Systems, Inc

Austin, 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 Services. We have a vast portfolio of clients across the country. 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: Systems AnalystDuration: 12

AI Engineer, Medical Imaging

OSI Engineering, Inc.

Pleasanton, California, USA

Contract

AI Engineer, Medical Imaging We are seeking a Senior level AI Engineer to join our algorithm team as a contractor, focused on developing and optimizing AI models for medical imaging applications. The ideal candidate will have deep expertise in convolutional neural networks (CNNs), experience with embedded system integration, and strong software engineering fundamentals. This position plays a critical role in refining our AI pipeline for intravascular ultrasound (IVUS) imaging. You ll be working

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

Packaging Supervisor

Mice Groups

Livermore, California, USA

Full-time

Job Title: Packaging Supervisor Salary Range: $68,000 $80,000 Shift Preference: Swing shift preferred, but day shift is also an option Job Summary: The Packaging Supervisor oversees employees in a manufacturing and assembly setting. Responsibilities include planning work, enforcing safety and food standards, and improving production processes. Key Duties: Implement and manage production schedulesAssign and supervise line personnelCommunicate with staff about performance, scheduling, and qualityM

Medical Lab Scientist (MLS)

University Health

San Antonio, Texas, USA

Full-time

POSITION SUMMARY/RESPONSIBILITIES Performs procedures for testing or analysis on specimens submitted to the laboratory. Evaluates test results for accuracy and submits results for the purpose of aiding the physician in diagnostic and therapeutic treatment of patients. Performs analyses that may involve a complex network of steps, variable fine-line discriminations of several parameters, correction of a variety of errors, and the operation and maintenance of complicated instruments. Demonstrate

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

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

Technical Writer

Cube Hub, Inc.

Batesville, Indiana, USA

Contract

Job Title Technical Writer Location - Batesville, IN Duration - 12 months with a possibility of extension Shift Details First Shift, Hybrid (In-office Tuesday, Wednesday, Thursday) Pay Range - $33/hr - $35/hr Job Description: Key Responsibilities Under supervision, edit, format, and proofread operational and instructional documents for medical devices Ensure documentation adheres to departmental style guidelines and quality standards Collaborate with Sustaining Engineering to upd

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

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

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