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Senior Process Engineer - Medical Device

Master Compliance Inc

Danvers, Massachusetts, USA

Contract

Job Title: Sr Process Engineer Medical Device Job Location: Danvers, Massachusetts (Fully onsite) Type: W2 contract Job Description: Candidates need to have knowledge of RJG Co-pilot system and setting up DC2 and DC3 processes or they will get rejected as this is required for the role. Must Have: RJG Master molder Scientific Molding Nice To Have: Conduct a mold flow analysis Micro molding SolidWorks Technical skills that are required for the role: Injection Molding Process Development Scienti

Medical Device Systems Design Engineer - Contract - Hybrid Schedule

Integrity Consulting

Dublin, California, USA

Contract

**UNFORTUNATELY UNABLE TO WORK WITH VISAS OR C2C** **NOT A SOFTWARE DEVELOPMENT ROLE** We are seeking a highly motivated Systems Design Engineer to join our dynamic medical device development team. In this role, you will be responsible for the end-to-end systems engineering process, including requirements gathering, architecture design, risk management, integration, and verification/validation activities. You will work cross-functionally with mechanical, electrical, software, quality, and regula

Product Manager - Medical Devices

Motion Recruitment Partners, LLC

Marlborough, Massachusetts, USA

Full-time

A medical device manufacturer and distributor in Marlborough is looking for talented Product Managers to join their team. They recently launched a novel FDA approved medical device that is being used to treat impulse control, addiction, and depression. This product has the potential to be revolutionary in the mental wellness space. They are looking for Product Managers who hav a strong background in medical device product management with a background either in biology or biomechanical engineeri

Packaging Engineer (R&D) -Medical Device

Yochana IT Solutions

Columbus, Nebraska, USA

Contract, Third Party

Title:Packaging Engineer (R&D) Onsite-Medical Device Location:Columbus, NE VISA: ANY VISA JD: Rich experience as a package development engineer or a strong understanding of the package development process and responsibilities Working knowledge of 21CFR Part 820 & EU MDR -745/2017 regulations, as well as the requirement of Medical Device packaging standards per ISO11607-1 & 2. Expertise in Package qualification by performing various design verification testings' such as Package integrity, Seal

Medical devices Product Security Engineer

Laiba Technologies LLC

Danvers, Massachusetts, USA

Contract, Third Party

Role: Product Security Engineer(Medical devices) Location: Danvers, MA-01923 [On-site] Security risk management techniques Regulatory standards and compliance frameworks (e.g., NIST Cybersecurity Framework,ISO27001, SOC2, HIPAA, GDPR) Pre-market product development activities Medical devices FDA 5+ years industry experience in Information Security. Working knowledge of regulatory standards and compliance frameworks (e.g., NIST Cybersecurity Framework,ISO27001, SOC2, HIPAA, GDPR). Experience wit

Medical Devices Project Manager - PMP

TekVivid

Danvers, Massachusetts, USA

Contract

Job Title: Medical Devices Project Manager Jama & Jira | PMP Certified Location: Danvers, MA - Onsite Job Type: Contract W2. Experience Level: Senior not less than 10 Yrs. Certifications: PMP Certification Mandatory. Job Summary: We are seeking a highly organized and results-driven Project Manager with hands-on experience using Jama and Jira, and a PMP certification. The ideal candidate will be responsible for planning, executing, and delivering complex projects on time and within budget while m

Medical Device Validation/Quality Engineer (ONSITE- No H1B/C2C)

NetSource, Inc.

Rochester, New York, USA

Contract

Please submit your resume only if you have a Bachelor Degree in Medical Device. The client may consider a degree in biology, chemistry, or a clinical field. Please don't send technical resumes; this is not a technical role. Technical resumes will be rejected. No H1B/C2C Please note that this is a 1-year position. Prefer candidates with a BS in Medical Technology. Candidates with this background are better suited for the senior-level position. Strong understanding of the lab environment and day

Integration Engineer (Embedded or Test Engineer)-Automotive/Medical device exprience

PROLIM Global Corporation

Ann Arbor, Michigan, USA

Contract, Third Party

PROLIM Global Corporation () is currently seeking Integration Engineer (Embedded or Test Engineer)-Automotive/Medical device exprience for location Ann Arbor, MI/ Plano, TX for one of our top client. Job Description: Integration Engineer (Embedded or Test Engineer)-Automotive/Medical device exprience We are seeking a highly motivated and experienced Integration Engineer to be responsible for building the bridge between physical ECUs and our virtual vehicle network for the next generation of aut

Clinical Development Scientist - Medical Devices - scientific publications.

APN Software Services, Inc

Bothell, Washington, USA

Contract

Please contact Abdul on "" OR email me at "" Notes from the manager: I need a PHD or MD candidate who has a scientist background - This is a requirement. I need someone who has worked in the medical device space who has designed studies for regulatory environments. Reporting protocols experience within this industry also required. US Regulations experience is required and China NPA would be highly desired. I am not looking for a candidate who is a medical writer. Ultrasound, Senior Clinical Dev

Medical Device Manufacturing Engineer

Experis

San Antonio, Texas, USA

Full-time

Our client, a leader in healthcare innovation, is seeking a Manufacturing Engineer to join their team. As a Manufacturing Engineer, you will be part of the Operations Integration team supporting the development of advanced medical devices. The ideal candidate will have strong analytical skills, excellent communication abilities, and a collaborative mindset which will align successfully in the organization. Job Title: Manufacturing Engineer Location: San Antonio, TX (in the office one day a week

Medical Device Quality Inspector

Equiliem

Madison, Wisconsin, USA

Contract

Medical Device Quality Inspector Desired: Experience with optical measurement machines or a CMM Familiar with ISO13485 or ISO 9001 The Medical Device Quality Inspection group is responsible for assuring that materials, activities, processes, and specified conditions related to the daily device manufacturing, processing and packaging meet current GMP standards and comply with applicable procedures and standards such as to ensure the quality integrity of the product. The medical device quality ins

Medical Device Assembler

Equiliem

Madison, Wisconsin, USA

Contract

Summary Assemble and test medical device assemblies, final products, and accessories per the manufacturing documentation provided. Perform assembly diagnosis, repair with limited supervision. Ensure work is completed in compliance with company quality system and medical device regulations. Essential Functions Assemble and test finished and semi-finished medical devices per established work instructions Document and record assembly and testing result activities in electronic record system (SAP) a

Manufacturing Technician Medical Device - Onsite

VIVA USA INC

Waukesha, Wisconsin, USA

Contract

Title: Manufacturing Technician Medical Device - Onsite Mandatory skills: Manufacturing, manufacturing environment, production, production flow, product manufacturing, production equipment, digital records, CT detector, PCCT, hazards, safety, detector engineering, process development, process improvement, equipment readiness, 5S protocol, technical information, design, collaboration, quality, documentation, troubleshoot, problem solving Description: Summary: As Photon Counting CT (PCCT) Pre-pr

Medical Device Technician

Equiliem

Madison, Wisconsin, USA

Contract

Medical Device Technician Scope of Work: Assemble and test medical device assemblies, final products, and accessories per the manufacturing documentation provided. Perform assembly diagnosis, repair, and test equipment maintenance with supervision. Ensure work is completed in compliance with company quality system and medical device regulations. Essential Functions Assemble, test, and repair work per established work instructions, policies and procedures. Performs assembly diagnosis and repair.

Medical Device Quality Engineer-Junior

Master Compliance Inc

Lafayette, Colorado, USA

Contract

Job Title: Quality Engineer-Medical Device Job Location: Lafayette, Colorado (On-site) Type: W2 Contract Duration: Position is 6 months from the start date of the candidate Job Description: Responsibilities may include the following and other duties may be assigned: Drawing and specification reviews Manufacturing process control plan reviews Measurement System Analysis (MSA), Test Method Validation (TMV) reviews Manufacturing process validation reviews Manufacturing process capability assessment

Medical Device Assembler

Equiliem

Madison, Wisconsin, USA

Contract

Summary Assemble and test medical device assemblies, final products, and accessories per the manufacturing documentation provided. Perform assembly diagnosis, repair with limited supervision. Ensure work is completed in compliance with company quality system and medical device regulations. Essential Functions Assemble and test finished and semi-finished medical devices per established work instructions Document and record assembly and testing result activities in electronic record system (SAP) a

Product Security Engineer (Medical Devices & Embedded Systems)

Rishabh Software Pvt. Ltd

US

Full-time, Contract

Job Title: Product Security Engineer (Medical Devices & Embedded Systems) Location: Remote Duration: 02/24/2025 to 12/31/2025 The Challenge: The Product Security Engineer will drive the implementation of enterprise Product Security strategy within the orthopedics portfolio. This role involves enhancing security processes, collaborating across teams, developing security metrics, and promoting security awareness. Key responsibilities include: Supporting new product development by reviewing secu

Medical Device Quality Complaints Analyst

Akkodis

Skaneateles, New York, USA

Full-time

Akkodis is recruiting for 5 Medical Device Quality Complaints Analysts in Skaneateles, NY. In this role, you will primarily be responsible for investigation, review, and completion of all Quality Engineering complaint issue analysis tasks utilizing various quality system inputs. Review individual complaints and associated service data to determine risk level and complete investigation into the as determined problem code and cause codes for each complaint. The hourly rate for this Quality Engin

C++ Staff Software Engineer - Medical Device - Norwood - $185k

Michael Page International

Norwood, Massachusetts, USA

Full-time

Work for a global medical equipment manufacturer on revolutionary devicesHelp shape the future of the organizations software engineering division About Our Client This organization is an industry leading medical device company that are a global provider of scientific and analytical solutions. They have locations in both the US and the UK! Job Description Some of the responsibilities for the successful Embedded C++ Software Engineer will include: Contributing as an Embedded Software Engineer

Medical Device Manufacturing Engineer

PrimaSoft Inc

Plymouth, Minnesota, USA

Full-time, Part-time, Contract, Third Party

Position: Medical Device Manufacturing Engineer Location: Plymouth, MN Key Responsibilities: Lead the design, development, and optimization of manufacturing processes for medical devices. Collaborate with R&D teams to transition new products from design to manufacturing. Ensure compliance with FDA regulations (21 CFR 820) and ISO 13485 standards. Develop and implement process validation and qualification plans. Perform root cause analysis for process issues and implement corrective action