• Specialist, Quality Documentation

    Integra LifeSciences (Princeton, NJ)
    …in Integra's corporate document control and training systems to transact changes to quality system documents. + Support quality system training and management of ... (archiving for offsite, electronic signature) + Execute change orders in alignment with quality system priorities and the global priorities as defined in the CMP and… more
    Integra LifeSciences (12/20/25)
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  • Supplier Quality Engineer Internship

    Danaher Corporation (Indianapolis, IN)
    …with quality systems related to supplied parts in a device manufacturing environment. Interns will work closely with cross-functional teams including ... Supplier Quality Engineer Accelerating answers Are you ready to...manufacturing, quality and...are you: . Currently pursuing a bachelor's degree in Engineering , or related discipline. . 0-2 years of experience… more
    Danaher Corporation (11/14/25)
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  • Quality Engineer I

    Zimmer Biomet (Warsaw, IN)
    …with certification as a quality engineer (eg CQE). + Certified Quality Engineer (CQE) and Medical device , particularly Orthopedic industry, experience ... feels included, respected, empowered and recognised. **What You Can Expect** The Quality Engineer I is an entry level position responsible for assuring products… more
    Zimmer Biomet (10/28/25)
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  • Quality Control Technician

    Actalent (Vernon Hills, IL)
    Job Title: Quality Control Technician Job Description The Quality Control Technician is entrusted with the authority to approve or reject all raw materials, ... one year experience in a cGMP environment, preferably in the Medical Device , Pharmaceutical, and/or Health Care Industry Work Environment The role involves spending… more
    Actalent (12/20/25)
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  • Quality Assurance Specialist

    Mentor Technical Group (Juncos, PR)
    …solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure ... compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, Puerto Rico, and Boston, United States, we… more
    Mentor Technical Group (12/15/25)
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  • Associate Director, Program/ Portfolio Manager

    BD (Becton, Dickinson and Company) (Salt Lake City, UT)
    …of global medical device regulatory requirements (FDA, Anvisa, NMPA, MDR) and quality standards (ISO, GB, JISC) + Complete understanding of medical device ... imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions...to other conflicting/dependent programs. + Responsible for the execution, quality , and results of the projects and the success… more
    BD (Becton, Dickinson and Company) (12/17/25)
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  • Manufacturing Engineer II or III - NPI

    Cretex (Bloomington, MN)
    Overview About QTS QTS offers critical end-of-line services for medical device OEMs including finished device assembly, packaging and sterilization management. ... and timeline development for defined projects. + Interface with Quality to integrate new products or processes into the...the company. + Analyze and solve problems from basic engineering principles, theories, and concepts. + Identify the root… more
    Cretex (12/05/25)
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  • Quality Inspector I

    Neotech (Longmont, CO)
    …to all ESD requirements and Board Handling. + Use of Moisture Sensitive Device (MSD) handling requirements based on component moisture sensitive levels (MSL). + ... inspection results by completing reports and logs as applicable. + Resolve quality -related issues in a timely matter. + Approves finished material and/or product… more
    Neotech (12/18/25)
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  • Quality Compliance Manager, ECMP Site…

    Integra LifeSciences (Princeton, NJ)
    …to advance patient outcomes and set new standards of care. The ** Quality Compliance Manager, ECMP Site Facilitator** , provides tactical support and oversight ... defined timeline and plan. Site Facilitators will work closely with existing site Quality and Operations leaders and may have responsibility for more than one site.… more
    Integra LifeSciences (11/22/25)
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  • Quality Engineer II

    Zimmer Biomet (Warsaw, IN)
    …(eg CQE). + Minimum 1 year of relevant work experience. + Certified Quality Engineer (CQE) and Medical Device , particularly Orthopedic Industry experience ... suppliers, and experts outside Zimmer Biomet to implement Zimmer Biomet quality goals. **How You'll Create Impact** + Formulates procedures, specifications, and… more
    Zimmer Biomet (10/23/25)
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