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Engineer, Manufacturing Engineering

Judge Group, Inc.

Salt Lake City, Utah, USA

Full-time

Location: Salt Lake City, UT Salary: $45.00 USD Hourly - $64.00 USD Hourly Description: Our client is currently seeking a Engineer, Manufacturing Engineering for a 2 year contract. Medical device experience is preferred. Provides engineering support to a manufacturing process, project or function. Evaluates manufacturing outcomes and implements continuous improvements and cost efficiencies. Supports NPI and new equipment/process introductions. This is an individual contributor role that r

Staff Software Engineer / .NET / Google Cloud Platform

Motion Recruitment Partners, LLC

Atlanta, Georgia, USA

Full-time

Our client, a leader in the medical device industry, is on the hunt for a Staff Software Developer to assist in building out internally and externally used web applications. The ideal candidate brings a solid background in C#, .NET, SQL Server. Experience with Google Cloud Platform is also a must. This role is preferred fully onsite (5 days/week) north/northwest of Atlanta. However, they might be open to a hybrid schedule. *Please note that we are unable to consider C2C candidates and those requ

Marketing Associate

Horizontal Talent

Alameda, California, USA

Contract

We are seeking a dynamic Marketing Associate to join our team and contribute to exciting marketing projects. This role offers the opportunity to work on innovative initiatives that support product launches and promotional activities. Responsibilities Execute marketing projects related to promotional materials and programs for both international and U.S. markets. Collaborate with cross-functional teams to develop and implement marketing plans that align with business objectives. Manage the submis

Engineer, Manufacturing Engineering

Judge Group, Inc.

Crystal Lake, Illinois, USA

Full-time

Location: Crystal Lake, IL Salary: $50.00 USD Hourly - $74.00 USD Hourly Description: Our client is currently seeking a Engineer, Manufacturing Engineering for a 12 month + contract. Medical device experience is preferred. Provides engineering support to a manufacturing process, project or function. Evaluates manufacturing outcomes and implements continuous improvements and cost efficiencies. Supports NPI and new equipment/process introductions. This is an individual contributor role that

Associate Engineer, Manufacturing Engineering

Judge Group, Inc.

Mahwah, New Jersey, USA

Full-time

Location: Mahwah, NJ Salary: $35.00 USD Hourly - $44.00 USD Hourly Description: Our client is currently seeking a Associate Engineer, Manufacturing Engineering for a 12 month + contract. Medical device or other highly regulated industry experience is preferred. Provides engineering support to a manufacturing process, project or function. Evaluates manufacturing outcomes and implements continuous improvements and cost efficiencies. Supports NPI and new equipment/process introductions. This

Controls/Automation Engineer

Katalyst Healthcares and Lifesciences

New Jersey, USA

Full-time

Roles and Responsibilities: 4+ years' experience in a medical device manufacturing environment. Strong preference for assembly automation systems experience. Validation experience: IQ, OQ, PQ and TMVs utomation control systems background - PLCs, HMIs, Vision systems, Servos & Robots. Familiarity with standard MS Office tools. Good verbal and written communication skills. Support design reviews, debug, acceptance and validation activities for equipment being developed by external suppliers.

Validation Engineer

Katalyst Healthcares and Lifesciences

Burlington, Massachusetts, USA

Full-time

Roles & Responsibilities: Bachelor's degree in engineering or a related technical discipline required. Minimum 5years of experience in procurement, sourcing, and supplier management. Proven success in sourcing within electromechanical components or complex assemblies. Medical device, pharmaceutical, or biotechnology industry experience strongly preferred. Strong negotiation skills with a track record of achieving cost and delivery targets. Familiarity with procurement software (e.g., SAP C

Equipment Engineer

Katalyst Healthcares and Lifesciences

Boston, Massachusetts, USA

Full-time

Responsibilities: Authoring and reviewing of SOP's (both new and existing). Authoring and reviewing Equipment Requirements Specifications. Document calibration and maintenance requirements, generate procedures. Supporting Equipment Management Program. Schedule and work with suppliers to perform service, installation, calibration, maintenance activities for facility, utilities, and equipment. Troubleshoot manufacturing issues to identify root cause and implement corrective actions. Initiate and e

Equipment Validation Engineer II

Katalyst Healthcares and Lifesciences

Boston, Massachusetts, USA

Full-time

Responsibilities: Authoring and/or reviewing of SOP's (both new and existing). Authoring and/or reviewing Equipment Requirements Specifications. Document calibration and maintenance requirements, generate procedures. Supporting Equipment Management Program. Schedule and work with suppliers to perform service, installation, calibration, maintenance activities for facility, utilities, and equipment. Troubleshoot manufacturing issues to identify root causes and implement corrective actions.

Validation Engineer

Katalyst Healthcares and Lifesciences

Hartford, Connecticut, USA

Full-time

Responsibilities: Functional requirement specification, function risk assessment, installation qualification, operational. Qualification, performance qualification, traceability matrix, project release notes, system certification summary). Execute validation activities in computerized system and ensure 21 CFR part 11 compliance. Knowledge in GAMP. Preparing risk assessment for functional requirements and providing testing strategy, implementing technical & procedural controls as part of mitigat

Senior Validation Engineer

Katalyst Healthcares and Lifesciences

Pomona, California, USA

Full-time

Roles & Responsibilities: 6 to 8 years of Non-Product Software Validation engineer with Manufacturing background (Medical devices or Diagnostics). Non-Product software validation for Manufacturing Equipment's as per Regulatory standards (FDA, ISO requirements). Prepare, review functional requirements, design and testing documents. Prepare, review of SLC deliverables (Validation plan, change requests, User requirements specification, Functional requirement specification, function risk assessment,

IT Customer Support Engineer - Beverly, MA - $105,000

Michael Page International

Beverly, Massachusetts, USA

Full-time

Work for a global medical device manufacturerJoin a company making a real difference with excellent benefits About Our Client The company is a leading medical device manufacturer with multiple locations across the world, and an office HQ in Beverly, MA. They make a real difference in their field, and they're currently rapidly growing their IT division. They have fantastic benefits and offer candidates an excellent long-term career opportunity! Job Description The IT Customer Support Engineer

Senior Validation Engineer

Katalyst Healthcares and Lifesciences

Pomona, California, USA

Full-time

Responsibilities and requirements: 6 to 8 years of Non-Product Software Validation engineer with Manufacturing background (Medical devices or Diagnostics). Non-Product software validation for Manufacturing Equipment's as per Regulatory standards (FDA, ISO requirements). Prepare, review functional requirements, design and testing documents. Prepare, review of SLC deliverables (Validation plan, change requests, User requirements specification, Functional requirement specification, function risk a

Validation Engineer

Katalyst Healthcares and Lifesciences

Huntington, Texas, USA

Full-time

Roles & Responsibilities: M.S. in Engineering or Biomedical Engineering 1+ year of professional experience in a Medical Device Manufacturing Environment Lead, execute, document & manage the validation activities (IQ/OQ/PQ) necessary to support the introduction or revision of automated and semi-automated production equipment and processes for Ophtalmic medical devices Design, develop, validate and implement manufacturing processes to build opthalmic medical devices for cataract and vitroreti

Validation Engineer

Katalyst Healthcares and Lifesciences

Framingham, Massachusetts, USA

Full-time

Responsibilities: Execute validation activities in computerized system and ensure 21 CFR part 11 compliance. Knowledge in GAMP. Preparing trace matrix to ensure requirements are tested to meet the software intended use. Preparing risk assessment for functional requirements and providing testing. strategy, implementing technical & procedural controls as part of mitigation. Preparing SOP/Work instruction for equipment and software-based systems. Requirements: 6 to 8 years of Non-Product Software

Device Engineer

Katalyst Healthcares and Lifesciences

Thousand Oaks, California, USA

Full-time

Responsibilities: Conduct experimental testing to support failure investigations and root cause analysis. Develop and execute test procedures to evaluate device performance and functionality. Analyze test data and apply statistical tools to derive actionable insights. Lead testing efforts for design changes and validate proposed modifications. Support scale-up, global launch, and continuous improvement of drug delivery devices. Collaborate with contract manufacturers and suppliers to ensur

Pharmaceutical Equipment Commissioning & Qualification Engineer

Zachary Piper Solutions, LLC

Hopewell Township, New Jersey, USA

Full-time

Piper Companies is currently seeking a Pharmaceutical Equipment Commissioning & Qualification Engineer for an opportunity in Titusville, New Jersey or Raritan, New Jersey , to join a global pharmaceutical company. Responsibilities: Maintain, calibrate, qualify and validate equipment used in the production, testing and packaging of pharmaceutical products Develop, execute, and document equipment qualification protocols and test plans in accordance with cGMP regulations and industry standards C

Technical Lead

Learn Beyond Consulting LLC

Arlington, Tennessee, USA

Full-time

Technical Lead Location - Arlington, TN Key Responsibilities: Lead technical planning and execution of NPI projects from concept through commercialization.Collaborate with R&D, Quality, Regulatory, Manufacturing, and Supply Chain teams to ensure smooth product transition.Own the technical documentation including design history files (DHF), product specifications, and risk assessments.Apply Design for Manufacturability (DFM), Design for Assembly (DFA), and process validation (IQ/OQ/PQ) principle

Product Engineer I

Sunrise Systems, Inc.

Houston, Texas, USA

Contract

Job Title: Product Engineer I Job ID: 25-08312 Location: Houston, TX Duration: 24 Months On W2 ContractWork with Cataract and Vitreoretinal R&D groups on development projects resulting in achieving R&D's project goals. Tasks include supplier evaluation/qualification, component qualification, managing prototype builds, assuring assembly process is developed and documented, assure BOM's are entered and maintained correctly, assure product costs are accurate and rolled, conduct Production Readiness

Senior R&D Engineer

Stryker

Fremont, California, USA

Full-time

Work Flexibility: Onsite Stryker is one of the world's leading medical technology companies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. More information is available at ;br> Stryker's Neurovascular division is focused on advancing the practice of less invasive stroke therapies through its Complete Str