• Project Engineer II

    PCI Pharma Services (Rockford, IL)
    …career path. At PCI, Project Engineers are given opportunities to grow into senior technical or people leadership roles. Several team members have been promoted into ... Engineering Manager roles from this track. **Key Responsibilities** Project Execution...processes. - Ensure strict adherence to all cGMP and FDA regulations and internal quality systems. **Required Qualifications** -… more
    PCI Pharma Services (12/18/25)
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  • Clinical Research Associate I

    Abbott (Alameda, CA)
    …(https://www.abbott.com/corpnewsroom/strategy-and-strength/tackling-student-debt-for-our-employees.html) student debt program and FreeU ... sites. + Perform study device accountability and reconciliation. + Assist senior staff in development of study-specific forms and trial-specific monitoring plans.… more
    Abbott (11/18/25)
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  • Business Development Representative

    Symetria Recovery (Joliet, IL)
    …delivery model. Key services delivered through our Opioid Treatment Program (OTP) licensure include MAT, medically monitored psychiatric care, individual ... Buprenorphine products, but they can also receive Methadone, and any other FDA -approved medication for addiction. What You Will Do: + Responsible for developing… more
    Symetria Recovery (12/19/25)
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  • Strategic Sourcing Director-IT

    Medtronic (Minneapolis, MN)
    …+ Lead contract negotiations + Engage and influence multiple stakeholders (primarily senior leadership) to adopt and implement strategies developed by the IT ... working in a large multi-divisional corporation + Knowledge of working in FDA -regulated industries + Excellent written and verbal communication + Excellent judgment,… more
    Medtronic (01/06/26)
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  • Quality Engineer III (Mitsubishi Chemical Advanced…

    Mitsubishi Chemical Group (Libertyville, IL)
    …the next level? As a **Quality Engineer III** , you'll be a senior leader driving strategic quality initiatives, advancing our Quality Management System (QMS), and ... future of quality excellence. You'll act as a **deputy to the Quality Manager ** , lead critical audits, and champion continuous improvement efforts that directly… more
    Mitsubishi Chemical Group (12/22/25)
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  • Data & AI Architect

    Medtronic (Duluth, GA)
    …patterns, and security models. + Ensure compliance with regulatory requirements (GDPR, HIPAA, FDA , SOX, etc.). + Apply security frameworks and safe AI patterns to ... uplift architectural maturity across teams. + Communicate complex architecture to senior leaders and non-technical stakeholders. + Champion adoption of AI-first… more
    Medtronic (12/24/25)
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  • Category Sourcing Director - Private Label

    Patterson Companies, Inc. (St. Paul, MN)
    …distribution industry. This individual is also the sourcing lead and category manager on certain categories to ensure delivery of sourcing goals. **Essential ... pricing strategies, and competitive sourcing. + Familiarity with regulatory requirements ( FDA , GMP, ISO, etc.) for healthcare products + Strong negotiation and… more
    Patterson Companies, Inc. (11/22/25)
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  • Director, Project Leadership

    Abbott (Alameda, CA)
    …Our location in Alameda, CA, currently has an opportunity for a Program Director. This person will manage our Customer Service Enablement project portfolio ... are consistent with the overall commercial and Divisional objectives of the program . **WHAT YOU'LL DO** + Portfolio leadership from intake through prioritization and… more
    Abbott (12/20/25)
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  • Quality Assurance Programmer/Analyst - Medical

    Techtronic Industries North America, Inc. (Anderson, SC)
    …(PowerPoint, SharePoint, Word, Excel, Outlook, Teams, OneNote) required. + Experience interacting with Senior Management. + FDA 21 CFR 820 and ISO 13485 ... and Manufacturing by way of dimensional feedback for parts. + Ability to program , operate and translate data from CMM, Vision System, and other measurement… more
    Techtronic Industries North America, Inc. (12/05/25)
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  • QC Scientist I Raw Materials

    Astellas Pharma (Westborough, MA)
    …**Organizational Context:** The QC Scientist I Raw Materials will typically report to the Senior Manager , Quality Control Raw Materials. This role is expected to ... relevant areas of 21CFR, ICH, USP, Ph. Eur. and FDA guidance documents as well as cGXPs in support...commercial manufacturing + Proven knowledge in cGMP raw material program (RM sampling plans and testing requirements) + Ensures… more
    Astellas Pharma (11/07/25)
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