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Evening Medical Device Design Jobs in Indiana (NOW HIRING)

Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With ...

Quality Engineer

Noblesville, IN · On-site

$67K - $87K/yr

Quality Assurance Department: QA, Noblesville Employment Type: Full-time Req ID: 9887 We are seeking a Quality Engineer with experience in medical device design quality and risk management to support ...

Weld Operator

Fort Wayne, IN · On-site

$800/wk

Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life enhancing medical devices. We do this ...

Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life enhancing medical devices. We do this ...

Worker is subject to noise, vibration, coolants, a #INDHP Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest ...

If you have hands-on experience in the research, design, manufacture or testing of active devices we'd love to hear from you. As a Technical Reviewer, you will work with medical device manufacturers ...

If you have hands-on experience in the research, design, manufacture or testing of active devices we'd love to hear from you. As a Technical Reviewer, you will work with medical device manufacturers ...

CNC Machinist

Fort Wayne, IN · On-site

$800/wk

Worker is subject to noise, vibration, coolants, a #INDHP Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest ...

Laser Etch Operator

Indianapolis, IN · On-site

$17 - $21.50/hr

Ability to read and interpret blueprints to determine set-up and operations Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to ...

Home Ownership Program Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life enhancing medical ...

Responsibilities: * Assist in the design, development, maintenance, and continuous improvement of the Prizm Medical Device Database * Own and implement the Medical Device Data Management System (MDMS ...

Showing results 21-40

Evening Medical Device Design information

What is an evening medical device design?

An Evening Medical Device Design job involves creating, developing, and testing medical devices during evening or non-traditional work hours. Professionals in this role typically work on the design and improvement of medical equipment, collaborating with engineers, clinicians, and regulatory experts to ensure devices are safe, effective, and compliant with industry standards. This schedule can be ideal for those seeking flexibility or companies operating on extended shifts. Responsibilities may include CAD modeling, prototyping, documentation, and product testing. Evening roles are common in organizations needing round-the-clock development or support for critical healthcare projects.

What is the difference between Evening Medical Device Design vs Night Medical Device Design?

AspectEvening Medical Device DesignNight Medical Device Design
Work HoursTypically evening shifts, often from 2 PM to 10 PMPrimarily night shifts, usually from 10 PM to 6 AM
Work EnvironmentDesign labs and offices with daytime supportDesign labs with overnight team collaboration
CertificationsRelevant engineering or design certifications, FDA knowledgeSame as Evening Medical Device Design, with additional night shift safety protocols

Both roles involve designing medical devices, but the main difference lies in shift timing. Evening Medical Device Design professionals work during late afternoons and evenings, while Night Medical Device Design roles focus on overnight hours. The core skills, certifications, and industry usage are similar, with shift hours being the primary distinction.

What are some common challenges faced when working evening shifts in medical device design teams?

Working evening shifts in medical device design can present unique challenges, such as coordinating effectively with cross-functional teams who may be on daytime schedules and ensuring timely communication regarding project updates or urgent issues. Additionally, there can be fewer on-site resources or support staff available during evening hours, requiring greater independence and proactive problem-solving. However, evening shifts can also offer a quieter environment for focused design work and may provide opportunities to handle urgent tasks that arise outside of regular hours, demonstrating reliability and adaptability to managers.

What key skills and qualifications are needed to thrive as an evening medical device design engineer?

To excel in Evening Medical Device Design, you need a solid background in biomedical engineering or a related field, with expertise in device design principles and compliance with medical regulations. Familiarity with CAD software, prototyping tools, and relevant quality management systems (such as ISO 13485) is typically required. Strong problem-solving skills, attention to detail, and effective communication are crucial for collaborating with cross-functional teams and addressing design challenges. These competencies ensure the creation of safe, effective devices that meet regulatory standards and improve patient outcomes.
What are the most commonly searched types of Medical Device Design jobs in Indiana? The most popular types of Medical Device Design jobs in Indiana are:
What cities in Indiana are hiring for Evening Medical Device Design jobs? Cities in Indiana with the most Evening Medical Device Design job openings:

Design Quality Engineer

Prophecy Technologies

Indianapolis, IN • On-site

Full-time

Posted 11 days ago


Job description

Design Quality Engineer
Technical/Functional
Skills • Strong understanding of Medical Device Product Development Process and Design Control requirements. • Knowledge of FDA 21 CFR Part 820, ISO 13485, ISO 14971, and applicable regulatory standards. • Strong knowledge of Design Controls and medical device product development. • Experience with Design History File (DHF) development, review, and remediation.
• Hands-on experience with Risk Management activities including: o dFMEA o uFMEA o Preliminary Hazard Analysis (PHA) o Hazard Analysis • Knowledge of FDA 21 CFR Part 820, ISO 13485, and ISO 14971. • Experience with Design Verification and Validation (V&V). • Understanding of User Needs, Design Inputs, Design Outputs, and Traceability requirements. • Experience preparing and reviewing: o Product Specification Documents (PSD) o Product Characterization documents o CTQ (Critical-to-Quality) documents • Experience with CAPA, Nonconformance, and root cause investigations. • Familiarity with PLM systems such as Windchill, or Teamcenter. • Experience with Cockpit Cognition DHF Build and DHF traceability management. • Strong documentation, technical writing, and audit support skills.
Roles & Responsibilities • Support quality activities throughout the product development lifecycle. • Review and maintain Design History File (DHF) documentation for compliance with regulatory and quality requirements. • Lead and support risk management activities including dFMEA, uFMEA, and PHA updates. • Ensure traceability between User Needs, Design Inputs, Risk Controls, Verification, Validation, and Design Outputs. • Support Design Verification and Validation planning, execution, and documentation reviews. • Review Product Characterization, Product Specification (PSD), and CTQ documents. • Participate in design reviews and ensure compliance with
Design Control processes. • Support Cockpit Cognition DHF Build activities, including documentation organization and traceability linkages. • Conduct DHF gap assessments and support remediation activities. • Collaborate with R&D, Manufacturing, Regulatory Affairs, and Supplier Quality teams. • Support CAPA investigations, root cause analysis, and implementation of corrective actions. • Ensure compliance with FDA, ISO 13485, ISO 14971, and internal quality procedures. • Support internal audits, customer audits, and regulatory inspections. • Drive continuous improvement initiatives related to design quality and risk management processes.