Jobs in the United States

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Added 41 mins ago
Manufacturing /Industrial Engineer
Celestica
Portland, OR
The Manufacturing Process Engineer is responsible for designing, developing, deploying and optimizing processes for manufacturing to achieve quality, cost and delivery goals for Celestica…
Added 1 hour ago
SUPERVISORY MECHANICAL ENGINEER
United States Fleet Forces Command
Naval Shipyard, VA
Added 1 hour ago
SOFTWARE DEVELOPMENT ENGINEER 1
Huntington Ingalls Industries
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…performance models and algorithms, threat models and command and control models. Simulates real-time operations and develops software that simulates behavior of systems. Develops integrates…
Added 1 hour ago
ENGINEER SYS MODELING SIMUL 2
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…performance models and algorithms, threat models and command and control models. Simulates real-time operations and develops software that simulates behavior of systems. Develops integrates…
Added 1 hour ago
Naval Architect Engineer 3 - 30097 1
Huntington Ingalls Industries
Virginia Beach, VA
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Added 1 hour ago
Advanced Training Systems Acquisition Engineer (Engineering Technician 3) - 31115
Huntington Ingalls Industries
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B
Senior Electrical Controls Systems Engineer
BWXT
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- $136,000 USD / year
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Added 1 hour ago
Production Control Engineer I, II, III
Prism Maritime
Chesapeake, VA
Must have a H.S
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Naval Architect Engineer 3 - 30097 1
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Added 1 hour ago
Advanced Training Systems Acquisition Engineer (Engineering Technician 3) - 31115
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Added 1 hour ago
Production Planner
Hill Phoenix, Inc.
Conyers, GA
Process customer and internal changes (quantity, date, configuration, cancellation) through a controlled change process.
Added 1 hour ago
Mid-Level Systems Engineer
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North Logan, UT
Join the Space Dynamics Laboratory (SDL) team and contribute to groundbreaking innovations in national security and advanced technology! We are seeking a mid-level Systems Engineer to join…
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Software Program Manager
Space Dynamics Laboratory
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Space Dynamics Laboratory (SDL) is seeking an experienced and detail-oriented advanced career Software Program Manager to lead the development and sustainment of complex software systems…
Added 1 hour ago
Student: Software Engineering Assistant
Space Dynamics Laboratory
North Logan, UT
The selected Student Software Engineer will work alongside experienced software, systems, and infrastructure engineers to evaluate, integrate, test, troubleshoot, and improve software and…
Added 1 hour ago
Systems Engineer
INNOVA SOLUTIONS INC
SALT LAKE CITY, UT
A client of Innova Solutions is immediately hiring for aSystems Specialist Engineer Position Type: Full-Time Contract, Contract to hire Duration: 12 months Location: Salt Lake City, UT…
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ICU MEDICAL INC
SALT LAKE CITY, UT
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Senior Information Systems Security Engineer - Security Control Assessor (SCA)
Peraton
Quantico, VA
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Senior Information Systems Security Engineer - Security Control Assessor (SCA)
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Washington, DC
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Software Engineer and Data Automation Specialist
U. S. Sentencing Commission
Washington, DC
For example, to qualify for the JS-13, one (1) year of specialized experience must have been at the GS-12 level or equivalent
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Senior Data & AI Engineer, Population Health Analytics
Alera Group
UNAVAILABLE
- $160,000 to $170,000 USD / year
Vital Incite, an Alera Group Company, is searching for a Senior Data & AI Engineer to join their team!
Added 2 hours ago
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Intern - Electrical Engineer
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Redwood City, CA
- $25 to $35 USD / hour
Advanced Energy (Nasdaq: AEIS) is a global leader in the design and manufacturing of highly engineered, precision power conversion, measurement and control solutions for mission-critical…
Added 2 hours ago
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CXR Senior Process & Integration Engineer
Stanford University
Stanford, CA
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…microelectronics. Within this ecosystem, CXR provides CMOS+X prototyping, process development, and integration services to enable the heterogeneous integration of commercial foundry CMOS…
Added 2 hours ago
Senior Electrical Engineer- Power Conversion
Insight Global
Irvine, CA
● Professional Engineer (PE) license or equivalent advanced credential.
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Senior Staff Software Engineer, Agent Registry
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Share Senior Staff Software Engineer, Agent Registry
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Lead Principal Engineer, Enterprise Agentic AI Platform
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Cresilon, Inc.

Senior Medical Device Research and Development Engineer

Brooklyn, NY, United States

$100,000 to $160,000 USD / year

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Job details

Pay: $100,000 to $160,000 USD / year
Experience: A minimum of 5+ years of product development experience is required.
Posting language: English
Posted: Sep 1, 2026

Original job description

Cresilon® is a Brooklyn-based biotechnology and medical device company that develops, manufactures, and markets hemostatic products, driven by a singular mission: to save lives. Powered by proprietary plant-based hydrogel technology, Cresilon's products are redefining the standard of care by stopping bleeding in seconds across diverse patients, procedures, and care settings. The company's current commercial portfolio includes TRAUMAGEL® for human trauma and VETIGEL® for veterinary applications, with planned expansion into human surgical applications and beyond. Learn more at www.cresilon.com

Description:

The Senior Medical Device R&D Engineer is responsible for leading the design and development activities of new products and improving existing products in compliance with all quality and regulatory requirements. They will be responsible for authoring technical documents for the development of medical devices and combination products according to relevant Design Control regulations and standards. The person in this position will also be responsible for providing project-specific support, including technical analysis and review of supplier documentation as required. The position has a scientific focus that includes formulation development, product performance characterization, and implementation, including prototype design and fabrication, and data generation through designed experiments. The Senior Medical Device Engineer is expected to aspire for excellence with a bias toward action, willing to roll up their sleeves, get hands-on, and do what’s necessary to move projects forward in a fast-paced environment. They are committed to designing and developing products that dominate the marketplace and improve healthcare by partnering with our customers to drive purposeful innovation, resulting in best-in-class products. The Medical Device Engineer will work with a multidisciplinary team of researchers. This is a multi-faceted job in a highly collaborative environment across multiple functions that will require flexibility as well as an ability to learn about and develop new technologies and explore new techniques in pursuit of product innovation and robustness. Role level is contingent on experience, but this is not an entry-level role. This is a full-time, on-site position, located in Brooklyn, New York.

Responsibilities

Create and lead experimentation for exploratory and/or product development research focusing on polymeric materials devices and their use.
Define new product functional requirements (design inputs/user needs) and evaluate the design's overall effectiveness, cost, reliability, and safety.
Lead cross-functional teams to develop new products, address design issues, and maintain existing designs.
Apply strong problem-solving skills to find solutions to complex problems.
Work independently to plan and schedule own activities necessary to meet project timelines.
Work cooperatively with, quality, manufacturing, regulatory, clinical, and marketing to ensure project success.
Lead the creation of design history file documentation through the new product development process.
Develop new implant and instrument designs utilizing Solidworks and modeling/detail design specifications.
Generate technical protocols/reports to support device safety and efficacy.
Invent/create concepts and designs and submit invention disclosures.
Ensure that all design activities adhere to FDA Quality System Regulations and ISO 13485 design control and risk management requirements. Lead material/design/process changes through a design control process, with well-documented research/analyses.
Author protocols and reports including development studies and design verification/validation activities.
Develop and execute test methods to aid in exploratory research, product development, and quality control; conduct chemical and mechanical property evaluation tests to assess the desirability of process or formulation changes.
Exercise technical judgment in the design, execution, and interpretation of experiments within the scope of project responsibilities and ensure the use of professional concepts to solve complex problems in creative and effective ways, in conformance with scientific methods and procedures.
Prepare samples as required for testing, or other evaluations and data analysis, including in voice-of-customer (VOC) labs.
Interface with customers, suppliers, and internal cross-functional team members to develop specifications and coordinate prototype fabrication.
Maintain a laboratory notebook and other technical documentation to required GLP/GMP guidelines.
Maintain active dialogue with Regulatory Affairs as subject matter expert on all product design elements/documentation pertaining to research towards FDA/regulated authority submissions,
Provide support to marketing and sales team, support the introduction of new technologies with the development of presentations, sales tools, formulations, and applications data
Communicate results to the scientific community via published papers. Present research at academic/industry symposia as an external representative of the company.
Manage part-time staff as a research leader and mentor for ongoing research projects.
Work with company leadership to evaluate existing research practices and contribute to a culture of ethical, high-quality research operations within the organization.
Provide other project or product support as needed in order to support Cresilon’s business objective.
Responsibilities may include other duties as assigned and as required.

Required Qualifications

BS in Chemical Engineering, Polymer Engineering, Material Science, Biomedical Engineering, Mechanical Engineering, or related scientific discipline.
A minimum of 5+ years of product development experience is required.
A minimum of 4 years of hands-on experience in new product research and development in a cGMP-regulated industry is required (work experience in the Medical Device field is strongly preferred)
Adept experimentalist with hands-on experience in product development of medical devices and their safety/efficacy characterization in an R&D environment.
Experience gathering user needs, translating them to technical inputs, and developing viable V&V (Design Verification and Validation) plans.
Experience leading complex product development initiatives from concept through product launch/release.
Good working knowledge of anatomy and surgical procedures is required.
Demonstrated ability to solve difficult technical problems and deliver practical solutions that meet the application requirements is required. This includes strong analytical, problem-solving, and decision-making skills with the ability to be observant and to think creatively.
Demonstrated ability to design experiments and analyze data with appropriate quality and statistical methodologies.
Demonstrated ability to work independently as well as effectively be a strong team contributor and work cross-functionally to expedite the completion of critical project tasks
Ability to handle multiple project assignments of medium scope and complexity and able to prioritize and complete work with a sense of urgency in a timely manner.
Ability to lead directly and by influence, including strong problem-solving, conflict resolution, and analytical skills.
Requires strong leadership skills, excellent written and verbal communication and presentation skills.
Working knowledge of FDA requirements as per 21 CFR 820, ISO 9001, ISO 13485:2003, and ISO 14971:2007.
Working knowledge of Good Documentation Practices (GDP), and Good Manufacturing Practices (cGMP)
Good understanding of statistical tools and validation/verification techniques.
Proficiency in the use of Microsoft Excel, Microsoft Word, and Microsoft PowerPoint is required.
Legal authorization to work in the United States is required.

Preferred Qualifications

An advanced degree (MS or Ph.D.) is strongly preferred.
Hands-on experience in product development with Class II and Class III medical devices.
Experience developing test methods and protocols/reports for safety and efficacy testing of implant and instrument designs.
Experience with IDE and PMA submissions.
Six-Sigma green belt or black belt certification

Cresilon is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship. Cresilon makes hiring decisions based solely on qualifications, merit, and business needs at the time. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process and need an alternative method for applying, please contact our Human Resources Department at (347) 497-7984 or email Kduffy@cresilon.com.

Competitive annual base salary range of $100,000 - $160,000, depending upon job level and qualifications
Paid Vacation, Sick, & Holidays
Medical, Dental, and Vision Insurance, FSA: Dependent & Healthcare, Commuter & Parking Benefits, Long Term Disability Coverage
Company Paid Life and Short-Term Disability Coverage
Work/Life Employee Assistance Program
401(k) & Roth Retirement Savings Plan with company match up to 5%
Monthly MetroCard Reimbursement

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Jobs in the United States