• Transmission Planning Unit Supervisor

    California Energy Commission (Sacramento, CA)
    …###@energy.ca.gov California Relay Service: ### (TTY), ### (Voice) TTY is a Telecommunications Device for the Deaf, and is reachable only from phones equipped with a ... TTY Device . Equal Opportunity Employer The State of California is...objective of the State of California to achieve a drug -free work place. Any applicant for state employment will… more
    California Energy Commission (04/28/25)
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  • Assistant Division Chief (Branch Manager)

    California Energy Commission (Sacramento, CA)
    …###@energy.ca.gov California Relay Service: ### (TTY), ### (Voice) TTY is a Telecommunications Device for the Deaf, and is reachable only from phones equipped with a ... TTY Device . Equal Opportunity Employer The State of California is...objective of the State of California to achieve a drug -free work place. Any applicant for state employment will… more
    California Energy Commission (04/28/25)
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  • Deputy Chief for Enforcement

    California Energy Commission (Sacramento, CA)
    …###@energy.ca.gov California Relay Service: ### (TTY), ### (Voice) TTY is a Telecommunications Device for the Deaf, and is reachable only from phones equipped with a ... TTY Device . Equal Opportunity Employer The State of California is...objective of the State of California to achieve a drug -free work place. Any applicant for state employment will… more
    California Energy Commission (04/28/25)
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  • Business Development Mgr, ESD (East Coast)

    Fujifilm (Sacramento, CA)
    …within the United States. + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 ... of experience with a Master's degree. + Minimum 8 years of medical device industry experience in a clinical capacity (clinical demonstration and education) with a… more
    Fujifilm (04/25/25)
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  • Supervisor, Security

    NTT America, Inc. (Sacramento, CA)
    …to outdoor weather conditions. + Must be able to pass a background check and drug test. + Must be willing to work outside normal business hours, including weekends, ... facility and may require use of a personal mobile device . A monthly stipend will be provided to cover...provided to cover expenses incurred for using a personal device , if applicable. NTT Global Data Centers Americas, Inc.… more
    NTT America, Inc. (04/25/25)
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  • Principal RF Electrical Engineer (Medical Devices)

    Abbott (Pleasanton, CA)
    …their heart failure + Lead the antenna designs on both the implantable device and external wearables + Drive the continued transformation of capabilities, equipment, ... FDA and ISO regulations + Comply with US Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures,… more
    Abbott (04/22/25)
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  • Staff Regulatory Affairs Specialist - Hybrid

    BD (Becton, Dickinson and Company) (Milpitas, CA)
    …Product Development with a focus on compliance to regulations from the US Food Drug & Administration (FDA) and the EU In Vitro Diagnostic Regulation (IVDR). This ... Requires a minimum of 5 years' experience in regulatory affairs in the device /diagnostic industry. + Demonstrated experience in authoring a PMA, De Novo, 510(k),… more
    BD (Becton, Dickinson and Company) (04/17/25)
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  • Manager, Regulatory Affairs (IVD)

    Hologic (San Diego, CA)
    …and professional work environment. + Complies with US Food and Drug Administration (FDA) and international regulations, other regulatory requirements, Company ... 8-10 years direct experience in Regulatory Affairs within the IVD or medical device industries. + Master's Degree in biomedical engineering and/or RAC preferred with… more
    Hologic (04/09/25)
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  • Quality Manager, Manufacturing

    Edwards Lifesciences (Irvine, CA)
    …regulated industry **What else we look for (Preferred Qualifications):** + Medical device , pharma, or biotech industry experience preferred + Project Management & ... operations + Understanding of the Product lifecycle in medical device , design & development, product commercial scale up &...Code of Federal Regulations (CFR) Part 820 Food and Drug Administration (FDA) Quality Systems Regulation (QSR) + Proven… more
    Edwards Lifesciences (04/09/25)
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  • QARA Project Manager

    Abbott (Alameda, CA)
    …cost, and proactive improvements. * Complies with US Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating ... and standard operating procedures a must * Understanding of medical device regulations (incl: device classifications and risk categorization) **Preferred… more
    Abbott (03/26/25)
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