• Principal Engineer, New Product Introduction

    Terumo Medical Corporation (Elkton, MD)
    …R&D, and manufacturing teams. f. Ensure all newly transferred products meet FDA regulations, ISO standards, GMP requirements specific to medical devices ... and equipment integration a strong plus. e. Strong knowledge of FDA regulations, ISO 13485, GMP , and risk management practices (eg, FMEA, pFMEA). f. Experience… more
    Terumo Medical Corporation (08/13/25)
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  • Sr Operator, Manufacturing - Staging

    ThermoFisher Scientific (Frederick, MD)
    …procedures (SOPs).​ + Quality and Compliance: Monitor and enforce compliance with ISO, GMP , and FDA standards. Perform visual inspections, manage batch records, ... lbs. without assistance, Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Cold Room/Freezers -22degreesF/-6degrees C, Fluctuating Temps… more
    ThermoFisher Scientific (08/13/25)
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  • Senior Industrial Eng I

    Terumo Medical Corporation (Elkton, MD)
    …leading project teams is required. **Qualifications/ Background Experiences** Knowledge of GMP / FDA regulations. Ability to create and work from engineering ... drawings. Excellent communication skills both verbal and written. This position requires the ability to improve and validate manufacturing processes, and /or solve complex engineering problems. Requires strong communications skills to understand and explain… more
    Terumo Medical Corporation (07/09/25)
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  • Director of Global Regulatory Affairs

    Danaher Corporation (Timonium, MD)
    …Thorough understanding of ISO 9001 and AS9100 / CAA Part 145/CAA Part 21 standards. GMP , FDA knowledge and other ISO standards an advantage. + Good understanding ... of applicable regulatory requirements covering Food Contact, Product Compliance (Ce Marking, ATEX, ASME etc.), Product Environmental Compliance (ROHS/REACH) and airworthiness (CAA/FAA) The salary range for this role is 155,000 - 180,000. This is the range that… more
    Danaher Corporation (07/09/25)
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  • Sr Operator, Manufacturing - Filling

    ThermoFisher Scientific (Frederick, MD)
    …+ **Quality Assurance and Compliance:** Monitor and enforce compliance with ISO, GMP , and FDA standards. Perform visual inspections, manage batch records, ... lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Some degree of PPE (Personal Protective Equipment) required… more
    ThermoFisher Scientific (08/10/25)
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  • Staff Engineer, Process Development

    Terumo Medical Corporation (Elkton, MD)
    …Industry 4.0 concepts, and equipment integration a strong plus. e. Strong knowledge of FDA regulations, ISO 13485, GMP , and risk management practices (eg, FMEA, ... management and preparing detailed technical reports for regulatory bodies like the FDA . c. Proven ability to lead cross-functional technical teams and mentor junior… more
    Terumo Medical Corporation (08/13/25)
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  • Principal Engineer, Automation & Controls

    Terumo Medical Corporation (Elkton, MD)
    …and production issues. d. Ensure all automation and control systems comply with FDA regulations, ISO standards, GMP requirements specific to medical devices and ... management and preparing detailed technical reports for regulatory bodies like the FDA . 3. Problem-Solving Skills: a. Strong troubleshooting skills for equipment and… more
    Terumo Medical Corporation (08/13/25)
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  • Sr. Engineer I - Validation

    Terumo Medical Corporation (Elkton, MD)
    …Requirements** **Knowledge, Skills and Abilities (KSA)** + Strong understanding of FDA regulations, ISO 13485, GMP , and other relevant quality ... and compliance standards + In-depth knowledge of process validation, equipment qualification (IQ/OQ/PQ), and software validation. + Strong familiarity with quality management systems (QMS), including change management, design controls, CAPA, risk management,… more
    Terumo Medical Corporation (08/02/25)
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  • QM Associate Scientist

    BD (Becton, Dickinson and Company) (Hunt Valley, MD)
    …and doffing clean room garments. + Knowledge of the following industry regulations FDA (Food and Drug Administration), GMP (Good Manufacturing Practice) / QSR ... Manufacturing Practice) and In-depth understanding of good documentation practices in a GMP environment. + Knowledge of PC spreadsheet, word processing, and database… more
    BD (Becton, Dickinson and Company) (08/23/25)
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  • Manager Trainee - Operations (Travel Program;…

    BioLife Plasma Services (Annapolis, MD)
    …tasks require prolonged glove wear **Preferred Qualifications** + Familiarity with SOPs, GDP, GMP , CLIA, and FDA regulations + Experience working in a regulated ... industry or high-compliance environment **We Offer Comprehensive Benefits from Day One** + Major medical, dental, and vision insurance and prescription coverage for eligible employees + A minimum of 15 vacation days and 10 company-paid holidays + Tuition… more
    BioLife Plasma Services (07/13/25)
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