• Sr Quality Manufacturing Engineer

    Philips (Murrysville, PA)
    …fit if:** + Bachelor's degree required. 5+ years of experience in a medical device or regulated industry (preferred). + Direct inspection engineering sustaining ... **Sr. Quality Manufacturing Engineer** **In this role you** Responsible...+ Basic understanding of CAPA, as well as global medical device regulations, requirements and standards such… more
    Philips (09/25/25)
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  • Quality Control Inspector 2

    Hologic (Marlborough, MA)
    …technical school education preferred. Minimum of 3 to 5 years related Quality Inspection experience in Medical Manufacturing environment. Experience with Oracle, ... Quality Control Inspector 2 Marlborough, MA, United States...facility to create a manufacturing process working on life-saving medical devices with potential for future growth. This is… more
    Hologic (09/25/25)
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  • Quality Engineer

    Actalent (Austin, TX)
    …experience, preferred; preferably in a FDA regulatory industry (ie, pharmaceutical, biomedical, medical device field) with an in-depth knowledge of current Good ... Quality Engineer Job Description * Provide Quality...and acceptance sampling within a regulated industry such as medical device manufacturing or pharmaceutical. * Personal… more
    Actalent (12/06/25)
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  • Lead Quality Inspector

    Integra LifeSciences (Plainsboro, NJ)
    …of overall corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. **This ... / Regulatory Compliance environment with a working knowledge preferably in the medical device , diagnostics or pharmaceutical industries. Familiarity with FDA… more
    Integra LifeSciences (11/05/25)
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  • Associate Director, Engineering - MDCP Technical…

    Merck (Wilson, NC)
    …considering patient safety and product quality . + Lead technical investigations of medical device and combination product for commercial products + Work with ... Operations Team. This role will serve as the primary medical device and combination product (MDCP) point...and maintain proficiency in ISO 13485 and other relevant quality management systems + Demonstrate the necessary inclusion skills… more
    Merck (12/04/25)
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  • Supplier Quality Specialist

    Bausch + Lomb (Clearwater, FL)
    …years experience in Quality related function in a pharmaceutical and or medical device environment, responsible for developing and implementing quality ... inspections is also desirable. Working knowledge and experience in a regulated medical device or pharmaceutical industry and experience with managing external… more
    Bausch + Lomb (12/09/25)
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  • Process Quality Engineer (Onsite in Latham,…

    Philips (Latham, NY)
    …acquired 2+ years of related Quality Engineering experience in the medical device industry preferred, or other regulated industries required (aerospace, ... **Process Quality Engineer (Onsite- Latham, NY)** The Process ...Sheets (Data Collects), change control, deviations, nonconformances, PFMEAs/control plans, Device History Records (DHRs) and Corrective and Preventive Actions… more
    Philips (12/13/25)
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  • Quality Engineer

    3M (Monroe, NC)
    …degree or higher in a science or engineering discipline. + Prior Experience as a quality engineer in life safety device manufacturing or electronic device ... **Job Description:** **Job Title** Quality Engineer* **Collaborate with Innovative 3Mers Around the...may be eligible for a range of benefits (eg, Medical , Dental & Vision, Health Savings Accounts, Health Care… more
    3M (10/29/25)
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  • Quality Engineer -Sustaining Engineering…

    PCI Pharma Services (Rockford, IL)
    …years of experience in an FDA regulated industry with strong preference to medical device or combination products. + Demonstrated proficiency with personal ... shape the future of PCI. **Summary of Objective:** The Quality Engineer (QE) is a key, customer-facing role that...+ Performs other duties as assigned by Manager/Supervisor within device assembly and packaging operations. May assist in the… more
    PCI Pharma Services (12/04/25)
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  • Supplier Quality Engineer - Intermediate

    ManpowerGroup (St. Paul, MN)
    …and testing processes, and drives corrective and preventive actions to maintain high- quality standards in our medical device manufacturing environment. ... + **Experience:** 4 -8 years of related work experience in supplier quality , preferably in the medical device industry. + Knowledge of CAPA, root cause… more
    ManpowerGroup (11/14/25)
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