- CTG (Kennebunk, ME)
- …CTG for this exciting opportunity!** CTG's premier client has a contract assignment for a Quality Engineer II. **Type** : Contract **Job Title** : Quality ... * Strong problem-solving and analytical skills **Description** : The Quality Engineer II will be responsible for...be responsible for the development, maintenance, and management of Medical Device Files (MDFs) in compliance with… more
- Actalent (Foster City, CA)
- Design Control Quality Engineer with Medical Device or Combo Device Experience! Description * Act as a quality engineer for medical ... Risk management, quality management system, iso 13485, medical device , design control Disqualifiers: - no... only with no design experience - prefers mechanical engineer experience/ mindset. Knowledge & Skills: * Demonstrates understanding… more
- Gilead Sciences, Inc. (Foster City, CA)
- …possible, together. **Job Description** **Responsibilities:** + Serve as a quality engineer for medical device combination product development projects, ... and suppliers to resolve complex technical issues related to drug- device combination products, processes, and quality . +...in quality assurance for the development of medical devices and/or drug- device combination products. +… more
- Actalent (Kendall, FL)
- …lead the junior Quality Engineer . Responsibilities + Participate in the quality assurance of medical device products. + Collaborate with Doctors and ... . Essential Skills + 2-3 years of experience as a Quality Engineer in the medical device industry. + Experience with Quality Management Systems. +… more
- Actalent (Warsaw, IN)
- …compliance with FDA and other relevant regulatory standards for medical device manufacturing. + Develop and implement quality assurance procedures for ... Job Title: Quality Engineer (Indianapolis, IN) Job Description...ensure compliance with FDA and other regulatory standards for medical device manufacturing. The role involves developing… more
- Bausch + Lomb (Kirkwood, MO)
- …with demonstrated technical leadership of cross-functional teams. + Broad understanding of medical device design and development processes, workflows, and tools ... in the future. **Objective:** The R&D Lead Principal Systems Engineer acts as the lead R&D representative for large,...projects conforming to applicable process standards and regulations for Medical Device Design Controls (21 CFR Ch1,… more
- United Therapeutics (Eden Prairie, MN)
- …, Device Development is responsible for leading research and development of medical device products and components used in combination products by applying ... Excellent written and oral communication skills **Minimum Requirements for** **_Senior Engineer , Device Development_** + Bachelor's Degree in materials science,… more
- Motion Recruitment Partners (Lake Forest, CA)
- Human Factors Engineer - Medical Device , IEC-60601, HFC Lake Forest, CA **Hybrid** Contract $65/hr - $80/hr Our client is a worldwide medical device ... The are urgently hiring for **contract-to-hire Sr. Human Factors Engineer ** to work hybrid 3-4 days a week onsite...of the state-of-the-art methods as applied to life-sciences / medical device industry. + The contracted service… more
- Integra LifeSciences (Boston, MA)
- … Engineering/ Quality Compliance/ Quality Assurance experience in the Medical Device or similar FDA regulated industry. Integra LifeSciences is an equal ... outcomes and set new standards of care. The Staff Quality Engineer is a subject matter expert...of statistical sampling and analysis. + Working knowledge of medical device regulations (including FDA QSRs, ISO13485).… more
- ManpowerGroup (San Antonio, TX)
- …collaborate with a wide range of disciplines. **Job Title:** Medical Device Product Design Verification and Stability Engineer **Location:** San Antonio, TX ... Our client in the medical device industry is seeking a Product Design Verification and Stability Engineer to join their team. As a Product DVnS Engineer … more