- NextEra Energy (Sloughhouse, CA)
- …must demonstrate a strong aptitude in mechanical work, understand relevant regulatory requirements, is experienced in reading and implementing GCCS plans, equipment ... and increase efficiency in a timely and cost-effective manner to ensure regulatory compliance of their gas collection systems. + Possess proficiency with MS… more
- Kelly Services (Pleasanton, CA)
- …Practice (GLP), Good Clinical Laboratory Practice (GCLP), and other applicable regulatory standards for our bioanalytical GLP lab. This role reports directly ... the CEO. **Schedule:** M-F, onsite **Responsibilities:** + Host client and regulatory inspections, including preparing and submitting responses to findings. + Audit… more
- APTIM (San Diego, CA)
- …10+ years of proven expertise in environmental compliance, air permitting, and regulatory strategy. This key role supports both internal teams and external clients ... Title V, New Source Review, and Permits by Rule--as well as compiling regulatory compliance reports such as annual emissions inventories and Title V, NSPS, and… more
- Gilead Sciences, Inc. (Foster City, CA)
- …including study protocol preparation, other study or investigator documentation, medical monitoring, data analysis plans, study reporting, and clinical development ... input into regulatory documentation, publications, and scientific presentations. Scope may include...and response to health authority inquiries + Serve as medical monitor for clinical trials or oversee medical… more
- AbbVie (Irvine, CA)
- … medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations and emerging issues. ... medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's… more
- AbbVie (Irvine, CA)
- …medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's ... Specific areas of work may include clinical trials, patient safety, and global medical affairs. The Associate Director works in partnership with experts in multiple… more
- Medtronic (Los Angeles, CA)
- …technology transforms lives Ensure complete and accurate maintenance and reporting of Medical Device Reports (MDRs), Adverse Drug Experience (ADE) data or adverse ... reaction data as required by regulatory agencies Review and analyze clinical databases for the...to meet goals and objectives. Understand current and upcoming Medical Device Reporting (MDRs) and EU Vigilance Reporting requirements… more
- AbbVie (South San Francisco, CA)
- …medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's ... Specific areas of work may include clinical trials, patient safety, and global medical affairs (GMA). The Associate Director works in partnership with experts in… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …trial and submission support, lead the R&D audit program, engage with regulatory authorities, and maintain clinical data integrity. The leader will be responsible ... and follow-up of internal and external audits to ensure compliance with regulatory requirements. + ** Regulatory Authority Engagement:** Act as the primary… more
- LA Care Health Plan (Los Angeles, CA)
- …and presentation skills, able to monitor and be compliant with strict regulatory deadlines. Knowledge of Medical terminology. Preferred: In depth knowledge ... (DHCS), Department of Managed Health Care (DMHC), Managed Risk Medical Insurance Board (MRMIB) and National Committee for Quality...Care offers a wide range of benefits including + Medical , Dental and Vision + Wellness Program + Paid… more