Medical devices Jobs

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SAP RAR (Revenue Accounting and Reporting) Consultant

Sage IT Inc

Franklin Township, New Jersey, USA

Third Party, Contract

Job Summary: We are seeking a highly skilled SAP RAR (Revenue Accounting and Reporting) Consultant with extensive experience in designing, configuring, and implementing SAP RAR solutions in compliance with IFRS 15 and ASC 606. This role requires deep expertise in RAR integrations with FI, and SD, modules, and a solid understanding of order-to-cash and revenue recognition processes in S/4 HANA environment. Key Responsibilities: Lead and support the implementation of SAP RAR including solut

Mechanical Engineer

Katalyst Healthcares and Lifesciences

Batesville, Indiana, USA

Full-time

Job Description: As part of the sustaining engineering team, you will be responsible for design changes for medical device products such as hospital beds and equipment. The engineering design changes may be related to design improvements, new compliance requirements, or supply chain support. Responsibilities: As a mechanical engineer on the team, you will be responsible for performing design analysis and engineering releases for small to medium projects or participate in portions of larger comp

Senior Post Market Engineer

Katalyst Healthcares and Lifesciences

Gainesville, Florida, USA

Full-time

Roles & Responsibilities: Bachelor's Degree in an Engineering discipline from an accredited institution required. Complaint product analysis and testing per procedures and requirements. Root cause analysis and supports conclusions with objective evidence and sound rationale. Complaint risk analysis and complaint history reviews. Knows and applies Quality System requirements and any appropriate FDA and international standards. Must have an understanding of root cause and risk analysis as wel

Quality Specialist II

Sunrise Systems, Inc.

Lititz, Pennsylvania, USA

Contract

Job Title: Quality Specialist II Job ID: 25-08786 Location: Lititz, PA 17543 Duration: 16 Months On W2 Contract Description: The Quality Specialist II will be accountable to support Product Review reports and to support investigations pertaining to observations or trends discovered during data collection. The Quality Specialist II will also be accountable for supporting Laboratory Information Management System (LIMS) Master Data changes needed by the Quality Control Laboratory. Key Responsibilit

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

Engineer II, Quality & Organizational Excellence

Thermo Fisher Scientific

Los Angeles, California, USA

Full-time

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description The Engineer II, Quality is responsible for creating a 1st class quality culture by enabling peer ownership of CAPAs, Quality Plans, Training, and PPI events. This position will drive these items with process owners to ensure timely and effective completion of required activities. Additionally, this role with assist in driving quality excellence through execution of Quality Evolution initiatives, own meaningful q

Technical Writer - Pittsburgh, PA - $70k per annum - fulltime

MetaSense, Inc.

Pittsburgh, Pennsylvania, USA

Full-time

PRINCIPAL RESPONSIBILITIES: 2+ years of experience as a Technical Writer (for SOP, QMS etc.) in the medical device industryPractical knowledge of standards and regulations pertaining to the medical device industry.Experience with CAD and VisioYou will be trained on client products and SOPs / templatesMaintain a backlog of all change requests to client's QMS design controls procedures/WIs/forms, in response to CAPAs or for efficiency improvements.Plan and execute the defining the specific procedu

Warehouse Associate II - International Fulfillment

Arthrex

Fort Myers, Florida, USA

Full-time

Arthrex, Inc. is a global medical device company and a leader in new product development and medical education. We are a privately held company that strives to accomplish our corporate mission of Helping Surgeons Treat Their Patients Better . We are committed to delivering uncompromising quality to the health care professionals who use our products, and ultimately, the millions of patients whose lives we impact. Arthrex Benefits Medical, Dental and Vision Insurance Company-Provided Life Insura

Quality Technician

Advantage Technical

Arden Hills, Minnesota, USA

Full-time

Join the Team as a Quality Technician! Step into an impactful role where your attention to detail and technical skills can make a difference. Advantage Technical is hiring a Quality Technician in the Roseville, MN, area to support post-market complaint investigations for medical devices. If you are ready to be hands-on, work collaboratively, and ensure the highest standards of quality, this opportunity is for you! Pay & Schedule: Pay Rate: $27.00 per hour Hours: Monday - Friday, 8:00 AM - 4:30

Principal Custom Test Systems Engineer- ME (ONSITE)

Stryker

Portage, Michigan, USA

Full-time

Work Flexibility: Onsite As a Principal Test Systems Engineer you will act as a primary point of contact for the design, development, fabrication, and implementation of electro-mechanical test systems to aid in the development and verification testing of new medical devices. You will be responsible for establishing system level strategies for the development of new custom test equipment, coordinating closely across functional areas to ensure alignment, helping to set direction and engineering s

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

Omaha, Nebraska, USA

Full-time

Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming support for publication efforts and regulatory submissions. Manage the timely creation, review, completion, and delivery of statistical programming activities and deliverables for study projects. Perform acquisition and curation of data, including full Clinical Data Interchange Standards Consortium (CDISC) standardization and Pseudo-CDISC Standardization. Document and implement p

Sterility Engineer

Philips North America

Plymouth, Minnesota, USA

Full-time

Job Title Sterility Engineer Job Description The Sterility Engineer is responsible for supporting the ethylene oxide sterilization program, critical to current NPI/Sustaining initiatives for Philips' Image Guided Therapy Devices (IGTD) business. Your role: Assists with managing the ethylene oxide sterilization program that includes new validations, supporting ongoing production sterilization activities and annual requalification's.Conducts in-depth reviews of technical documentation, includin

Program Manager of Quality

Abbott Laboratories

Green Oaks, Illinois, 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. Yo

Imaging Service Engineer 2

Sodexo

Highland Park, Illinois, USA

Full-time

Role Overview Precise. Reliable. Powerful. Join a team as innovative as the technology we manage. Sodexo's Healthcare Technology Management (HTM) Division is looking for a highly skilled and confident individual to fulfill an Imaging Service Engineer II role located in Highland Park, IL. This person will inspect, repair, maintain, and calibrate basic diagnostic imaging equipment, devices, systems, and instruments. Interact on a routine basis with other clinical health providers in the identifi

Engineer II

Katalyst Healthcares and Lifesciences

West Point, Pennsylvania, USA

Full-time

Responsibilities: The basic function of this position is to author technical change assessment related to medical devices and to provide support to customer complaints - including ensuring the root cause appropriately. Consider the device and device constituents, author technical and risk assessments related to the device design change, and document the device risk analysis from complaints. Team supports multiple Medical Device and Combination Products (MDCP), such as vaccine prefilled syringes

Engineering Technician

Katalyst Healthcares and Lifesciences

Sumter, South Carolina, USA

Full-time

Job Description: Performs any combination of tasks involved in the fabrication, manufacture, assembly, testing and packaging of medical devices as well as setting up, operating, performing maintenance on and troubleshooting equipment. May conduct quality inspections on processing line in accordance with quality specifications. Works within clearly defined SOPs and / or scientific methods and adheres to quality guidelines. Requirements: High school diploma or equivalent. More than two years of

Product Quality Assurance Analyst III

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. Product Quality Analyst Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your tru

Quality Assurance Manager

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. Quality Assurance Manager (Bogdanoff) Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be

Principal Systems Engineer

Abbott Laboratories

Pleasanton, 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 your family, be your true self, and live a full li

Solution Engineer 4/Sr. R&D Sustaining Engineer

Katalyst Healthcares and Lifesciences

Austin, Texas, USA

Full-time

Roles & Responsibilities: Mechanical Engineering, Biomedical Engineering, Manufacturing Engineering. What are the 5 must-have skills for this position? Experience in design changes and maintenance releases in medical device products. Hands-on mechanical design experience, including building and prototype testing. bility to create drawings and assemblies within SolidWorks or other drafting applications. Supporting the maintenance and changes to design history files. Experience with root cause ana