11/05 | IMMEDIATE OPPORTUNITY in Minneapolis MN for a Manufacturing Process Engineer to work with a Worldwide Manufacturer of Medical Equipment. This is a One Year Plus Contract Position. Responsibilities Production Support and Trouble Shooting Provides engineering support to manufacturing operation on routine basis Addresses product related issues arising on the production floor Defines and generates all | THINK ENERGY GRO... | | | map | | salary | action |
10/26 | CTG is currently assisting one of its premiere clients in staffing several Validation Engineers in Santa Clara, CA. Position: Validation Engineer Location: Santa Clara, CA Duration: 5 month contract with possible extensions. Position Description/Requirements: Our client is in need of individuals with at least 1-2 years of experience supporting validation programs. Individual should have a BS degre | CTG | | | map | | | action |
11/10 | MicroVention is a rapidly growing medical device company that is pioneering the development of catheter-based technologies for the endovascular treatment of peripheral and cerebral vascular diseases. Today, MicroVention is focused on proprietary technologies that provide therapeutic advantages for cerebral aneurysm treatment in a minimally invasive platform. The company is currently marketing two f | MicroVention | | | map | | | action |
10/27 | Bioness is searching for a Quality Engineer with demonstrated proficiency in quality and project management, problem solving, and statistical analysis. Must have excellent communication and leadership skills. POSITION SUMMARY: Responsible for designing, implementing and maintaining product assurance systems and activities in numerous areas such as documentation, inspection, process validation, pro | Bioness | | | map | | | action |
11/21 | Sr. Mechanical Engineer - Medical Device We are an established publicly traded international medical device company. We have an immediate need to hire a full time Sr. Mechanical Engineer. This position is located in Salt Lake City, UT and requires a minimum of 5+ years of experience as a Mechanical Engineer in the medical device industry. Relocation is provided for qualified candidates. Job Respon | Laguna Source | | | map | | salary | action |
11/20 | Senior R&D Engineer/Medical Device Our client is a progressive medical device company looking for a top notch R&D Manager to lead new project teams and drive innovation. If you are looking for an excellent opportunity combined with a great lifestyle, read on! The Sr. R&D Engineer fully participates in and successfully contributes to project teams. They have a proven ability to lead multi-disciplin | MRINetwork | | | map | | | action |
11/17 | World wide leader of medical products and services is seeking three FDA Process and Equipment Validation Engineers for 10+ month contract assignments in Duluth, GA. Responsibilities Candidate will focus on the master cleaning validation plan and protocol for the cleaning of equipment recently installed for a new manufacturing line Candidate will enforce commissioning and qualification standards fo | THINK ENERGY GRO... | | | map | | salary | action |
11/16 | Mechanical Engineer Neurostimulation Devices Austin, TX Our Client is developing a neurostimulation system for the treatment of chronic pain and several other neurological indications. Current pharmaceutical treatments are costly, have negative side effects, and are not effective for large percentages of the patient population. This company’s innovative device is smaller than a grain of rice and i | MRINetwork | | | map | | | action |
11/13 | Senior Manufacturing Engineer ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Leadership Lead projects and project teams Lead systems improvement projects Provide training to others beyond the production group Act as a leader within manufacturing engineering group and the company Resolve disputes on his/her own Act as mentor to non-senior level manufactur | MRINetwork | Multiple locatio... | | | | | action |
11/13 | Sr. Research & Development Engineer Purpose: This position will be responsible for working directly with surgeons and marketing to design and development medical devices, and must fully understand medical device design control requirements in order to effectively manage multiple project tasks and work effectively in a cross functional team. Key responsibilities include: Work directly with Surgeons | MRINetwork | Multiple locatio... | | | | | action |
11/09 | A company located in North Central North Carolina has an immediate need for a Biomechanical Engineer for a twelve month contract position. Client would prefer local candidates for this position. This position must be filled now! Responsibilities Apply working knowledge of design and mechanical engineering principals for solving technical problems Participate in cross-functional project groups to d | THINK ENERGY GRO... | | | map | | salary | action |
11/06 | Job Summary Responsible for the design, testing, and implementation of sterile and non-sterile packaging systems for all company product lines. Provides project management for support of new product introductions, line extensions and external development alliances. Interfaces with Corporate Director of Packaging in developing Corporate wide packaging and labeling practices. Principal Duties and Re | Talent Finders | | | map | | | action |
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10/27 | Engineer is responsible for all technical aspects of designing medical devices for manufacturing and market success. This individual is expected to design new products, improve redesign existing products, develop new manufacturing process, improve existing processes, identify and implement cost reduction projects, specify production equipment and provide support to Maintenance and Manufacturing in | Pinnacle Recruit... | | | map | | salary | action |
10/26 | MEDICAL DEVICE QUALITY ASSURANCE ENGINEER : Minimum of four years of quality or regulatory experience in an FDA regulated industry. Working knowledge of FDA Quality System Regulation, Medical Device Directive, CDMCAS requirements and ISO13485:2003 is required. Experience with quality system responsibilities of Receiving Inspection, Non-Conforming Material Processing and Process Validation is requi | Oxford Solutions | | | map | | salary | action |
10/02 | About the Job Join a rapidly growing and financially successful OEM medical device company in the Boston area. We offer excellent compensation, benefits, bonus opportunity and relocation package. Responsibilities: Provide support to project development teams regarding quality issues and measurement techniques. Review and interpret customer specifications and negotiate requirements. Create purchasi | Boston Berkeley ... | | | map | | salary | action |
11/20 | This is a direct-hire position and offers full benefits, growth potential, and extensive relocation assistance. Job Summary: Develops new or modified process formulations, defines processing or handling equipment requirements and specifications, and reviews processing techniques and methods applied in the manufacture, fabrication, and evaluation of products. Involvement may begin at any step from p | HireSource Solut... | | | map | | | action |
11/10 | MicroVention is a rapidly growing medical device company that is pioneering the development of catheter-based technologies for the endovascular treatment of peripheral and cerebral vascular diseases. Today, MicroVention is focused on proprietary technologies that provide therapeutic advantages for cerebral aneurysm treatment in a minimally invasive platform. The company is currently marketing two f | MicroVention | | | map | | | action |
11/10 | MicroVention is a rapidly growing medical device company that is pioneering the development of catheter-based technologies for the endovascular treatment of peripheral and cerebral vascular diseases. Today, MicroVention is focused on proprietary technologies that provide therapeutic advantages for cerebral aneurysm treatment in a minimally invasive platform. The company is currently marketing two f | MicroVention | | | map | | | action |
11/06 | We currently have a long-term contract in Andover, MA for a seasoned SQE/Project Manager with strong experience in the R&D Medical Device field ( 8-10+ years experience with Class II- III Medical devices in an R&D environment) MUST HAVE Please email your resume to for review. Responsible for managing the development & execution of Design Control deliverables, including the following: Review SW req | Adecco Engineeri... | | | map | | | action |
10/22 | · IMMEDIATE OPPORTUNITY in Southern Indiana for Senior Manufacturing Engineers to work with a Worldwide Manufacturer of Medical Device Equipment. These are permanent positions. Responsibilities MUST HAVE 7YRS MEDICAL DEVICE EXPERIENCE Develop and implement manufacturing business improvement projects and processes for disposable medical devices Support teams to make improvements to existing devices | Company Confiden... | | | map | | salary | action |
10/17 | Job Summary: This position will report into the R&D organization to provide hands-on engineering design support and validation testing for all phases of medical device product development; from concept to launch and ongoing product improvement. Additional responsibilities include creating engineering drawings, designing test protocols, maintaining design history files, evaluating results, and comp | Company Confiden... | | | map | | salary | action |
10/17 | Job Summary: This position is in PORTLAND, OR, just 3 short hours south of Seattle. Come relocate to Portland and enjoy everything you love about Seattle, just on a slightly smaller scale! This position will report into the R&D organization to provide hands-on engineering design support and validation testing for all phases of medical device product development; from concept to launch and ongoing p | Company Confiden... | | | map | | salary | action |
11/20 | With over 1,600 dedicated employees in 18 different countries, Angiotech is a global specialty pharmaceutical and medical device company. Our tagline “redefining success” describes how Angiotech is striving to create novel medical solutions that elevate the standard of care and improve people’s lives. Job ID: 369 Position Description: Basic Function The Validation Engineer will monitor and approve | Angiotech Pharma... | | | map | | | action |
11/12 | Description Of Duties: · interface with teams and provide team leadership - Generate test cases (test scripts) based on the system requirements (or usage scenarios) - Generate equipment and software IQ/OQ protocols following procedures and regulations - Generate templates for all equipment which require software validation activities - Review tests and test results. - Document and resolve issues. - | ENTEGEE Engineer... | | | map | | | action |
11/12 | The Company: Defibtech, LLC is a leading innovator in the field of Automated External Defibrillators (AEDs). The company designs and manufactures automated external defibrillators and related accessories. Products are sold exclusively through a network of distribution partners in the United States and around the world. Defibtech was recently named one of the fastest-growing technology companies in | Defibtech | | | map | | | action |