• Sr. Validation Engineer

    PCI Pharma Services (Rockford, IL)
    …the future of PCI. **Job Title: Senior Validation Engineer - Medical Device Assembly (CDMO)** **Location:** [Rockford] **Department:** Quality **Reports To:** ... device production. + Collaborate with cross-functional teams, including Manufacturing, Quality , Engineering , and Regulatory Affairs. + Review and approve… more
    PCI Pharma Services (12/18/25)
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  • Intern, R&D

    Terumo Neuro (Aliso Viejo, CA)
    …HR (Human Resources), HR Communications, Talent Development, Marketing, R&D, Manufacturing, Quality , Regulatory, Accounting, and more. R&D Intern The R&D Intern will ... assist in supporting development of medical device products through project work focused on verifying specifications, designs, fixtures, test processes, equipment… more
    Terumo Neuro (12/02/25)
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  • Project Engineer - Controls & Robotics

    ATS Automation (Warren, MI)
    …responsible for long-lead equipment, ensuring alignment to technical requirements, quality expectations, and project timelines. The Project Engineer also supports ... management in all change-management proceedings, helping evaluate, document, and implement engineering changes as the project evolves. Overall, this role is both… more
    ATS Automation (12/10/25)
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  • Sr. Engineer II, Process Development

    Terumo Medical Corporation (Elkton, MD)
    …teams including Project Management Office (PMO), Product Development, Operations Engineering , Quality , and Manufacturing. + Attend project meetings, ... Corporation (TMC) develops, manufactures, and markets a complete, solutions-based portfolio of high- quality medical devices used in a broad range of applications for… more
    Terumo Medical Corporation (12/17/25)
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  • Sr. Engineer I, Process Development

    Terumo Medical Corporation (Elkton, MD)
    …cross-functional teams including Project Management Office (PMO), Product Development, Operations Engineering , Quality , and Manufacturing. + Attend project team ... Corporation (TMC) develops, manufactures, and markets a complete, solutions-based portfolio of high- quality medical devices used in a broad range of applications for… more
    Terumo Medical Corporation (11/06/25)
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  • Program & Technical Advisor (Sr.…

    Guidehouse (Mclean, VA)
    …and controls); process development, process scale-up and process optimization; device development and manufacturing, reliability engineering , Software, Assay ... and controls); process development, process scale-up and process optimization; device development and manufacturing, reliability engineering , Software, Assay… more
    Guidehouse (11/09/25)
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  • Director, Manufacturing Engineer

    Otsuka America Pharmaceutical Inc. (Palo Alto, CA)
    …the company's long-term goals. + Manage budgets, resource allocation, and timelines for engineering projects. + ** Quality Assurance:** + Establish and maintain ... **Position Overview:** We are seeking a highly skilled and experienced Director of Engineering , Manufacturing to lead our engineering team. The ideal candidate… more
    Otsuka America Pharmaceutical Inc. (11/25/25)
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  • Sr Principal Engineer, Human Factors

    Edwards Lifesciences (Irvine, CA)
    …of our R&D Engineering team, you will work closely with our Quality and Manufacturing teams to develop the latest tools and technologies to address significant, ... a unique opportunity to foster and support human factors and usability engineering activities with new product development and commercial teams across projects and… more
    Edwards Lifesciences (11/15/25)
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  • Regulatory Affairs Program Manager, Digital Health

    Olympus Corporation of the Americas (Westborough, MA)
    …for digital health products and solutions, ensuring compliance with global medical device regulations. As part of a high-growth, innovative team, this position ... solutions, including Artificial Intelligence (AI) exempt from the medical device classification, and connected technologies. + Provide regulatory guidance,… more
    Olympus Corporation of the Americas (11/07/25)
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  • Regulatory Affairs Specialist

    Access Dubuque (Dubuque, IA)
    …Regulatory Affairs Specialist to join our team. This person will work directly with Engineering and Quality Assurance to maintain the knowledge base of existing ... Biology, Chemistry, or related field with 1-3 years of regulatory affairs, quality , or medical device experience. Lead Auditor experience preferred. Strong… more
    Access Dubuque (12/14/25)
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