Jobs: maa


  • Austin, United States MAA Wells Branch Full time

    Becoming a part of MAA is exciting and rewarding for those who enjoy working with a dynamic ; Join us as we exceed our residents expectations of a place to call home. Assistant Property Manager Are you ready to take the next step towards being a leader on a team in the multifamily h...

  • Certified Medication Tech with MAA Certification Needed

    Found in: Lensa US P 2 C2 - 3 weeks ago


    Fort Morgan, United States Aura Staffing Partners Full time

    Benefits/PerksFlexible SchedulingCompetitive CompensationCareers Advancement Location: Brush, COJob SummaryWe are seeking a Certified Medication Tech with MAA certification to join our team. In this position, you will assist patients with their daily living needs, provide compassionate care, and generally increase their quality of life. Responsibilities may...

  • Aeronautical Engineer

    Found in: Talent US A C2 - 2 weeks ago


    Warner Robins, United States Abacus Technology Corporation Full time

    OverviewAbacus Technology is seeking an Aeronautical Engineer to provide technical support at Robins AFB. This is a full-time position.ResponsibilitiesSupport the directorate in the performance of disciplined engineering activities to assure OSS&E for all products.Support the mechanical systems integrity program, maintain and update the critical safety...

  • Global Regulatory CMC Manager

    Found in: beBee S US - 2 weeks ago


    Summit, United States Axelon Services Corporation Full time

    5-7 years in the pharmaceutical industry, preferably with 1-3 years CMC regulatory experience.Participate in the development of the CMC regulatory strategy for small molecules, biologics and cell therapy submissions.These submissions include health authority briefing packages, IND/CTA, BLA/NDA and MAA regulatory filings.Prepare and review CMC submission...

  • Global Regulatory CMC Manager

    Found in: beBee jobs US - 3 weeks ago


    Akron, Ohio, United States Axelon Services Corporation Full time

    5-7 years in the pharmaceutical industry, preferably with 1-3 years CMC regulatory experience.Participate in the development of the CMC regulatory strategy for small molecules, biologics and cell therapy submissions.These submissions include health authority briefing packages, IND/CTA, BLA/NDA and MAA regulatory filings.Prepare and review CMC submission...


  • Baltimore, United States AMERICAN CABLING COMPANY Full time

    Job DescriptionJob Description– Individual must be a licensed construction supervisor for the State of Maryland. Position requires proven knowledge and experience in phased construction and integration, specifically of complex technology systems in public transportation venues. The Project Construction Superintendent shall be responsible for acquiring all...


  • Baltimore, United States AMERICAN CABLING COMPANY Full time

    Job DescriptionJob DescriptionBenefits:401(k)401(k) matchingCompetitive salaryHealth insurancePaid time off Individual must be a licensed construction supervisor for the State of Maryland. Position requires proven knowledge and experience in phased construction and integration, specifically of complex technology systems in public transportation venues. The...


  • Princeton, United States CareerBuilder Full time

    Job Description We are currently seeking a Senior Manager of Regulatory Operations. Within the role you will: * Develop and execute novel drug regulatory strategy * Develop and manage day-to-day operations through the use of project management and planning tools, create and maintain detailed project timelines * Establish sound regulatory advice/position on...


  • Atlanta, United States Destiny's Child Inc. Full time

    Job DescriptionJob Description Job Description MEDICAL ADMINISTRATIVE ASSISTANT DATA ENTRY COORDINATOR MAA/DEC DUTIES AND RESPONSIBILITIES: MEDICAL ASSISTANT DATA ENTRY COORDINATOR (MAA/DEC) is responsible for working with Administrative Staff and DDP collecting and inputting data for Individuals. Responsible for assisting Administrative Staff and DDP in the...


  • Plano, United States Benchmark Mortgage Full time

    Position Overview : Benchmark’s core values include Excellence , which means doing things exceptionally well. Our Underwriters uphold this core value reviewing loan applications and supporting documentation to assess financial risk during the mortgage application process. This role is also responsible for ensuring a successful underwriting partnership with...


  • Bridgewater, United States CareerBuilder Full time

    Regulatory Affairs - Bridgewater, NJ - Full Time Summary This position reports to the VP, Global Regulatory Affairs. The incumbent responsible for supporting the development and implementation of regulatory strategies, work closely with the cross functional asset teams to prepare, review and submit regulatory filing documents, manage documentation systems...


  • Bridgewater, United States Gan & Lee Pharmaceuticals Full time

    Job DescriptionJob DescriptionSummaryThis position reports to the VP, Global Regulatory Affairs. The incumbent responsible for supporting the development and implementation of regulatory strategies, work closely with the cross functional asset teams to prepare, review and submit regulatory filing documents, manage documentation systems and maintain...


  • Somerville, United States Gan & Lee Pharmaceuticals Full time

    Job DescriptionJob DescriptionSummaryThis position reports to the VP, Global Regulatory Affairs. The incumbent responsible for supporting the development and implementation of regulatory strategies, work closely with the cross functional asset teams to prepare, review and submit regulatory filing documents, manage documentation systems and maintain...


  • Bridgewater, United States Gan & Lee Pharmaceuticals Ltd Full time

    Summary This position reports to the VP, Global Regulatory Affairs. The incumbent responsible for supporting the development and implementation of regulatory strategies, work closely with the cross functional asset teams to prepare, review and submit regulatory filing documents, manage documentation systems and maintain interactions with regulatory agencies...


  • Bridgewater, United States Gan & Lee Pharmaceuticals Full time

    Job DescriptionJob DescriptionSummaryThis position reports to the VP, Global Regulatory Affairs. The incumbent responsible for supporting the development and implementation of regulatory strategies, work closely with the cross functional asset teams to prepare, review and submit regulatory filing documents, manage documentation systems and maintain...


  • Somerville, United States Gan & Lee Pharmaceuticals Full time

    Job DescriptionJob DescriptionSummaryThis position reports to the VP, Global Regulatory Affairs. The incumbent responsible for supporting the development and implementation of regulatory strategies, work closely with the cross functional asset teams to prepare, review and submit regulatory filing documents, manage documentation systems and maintain...

  • Manager/Sr. Manager

    2 weeks ago


    Trenton, United States CareerBuilder Full time

    Summary This position reports to the Functional Area Head, Global Regulatory Affairs. The incumbent responsible for supporting the development and implementation of regulatory strategies, work closely with the cross functional asset teams to prepare, review and submit regulatory filing documents, manage documentation systems and maintain interactions with...


  • Lawrence Twp, United States CareerBuilder Full time

    BS/BA degree in Scientific Discipline with 3 years in the pharmaceutical industry, preferably with 1 year CMC regulatory experience Responsibilities will include, but are not limited to, the following: 1. Participate in the development of the CMC regulatory strategy for biologics submissions. These submissions include health authority briefing packages,...

  • Senior Manager Regulatory Affairs

    Found in: Appcast Linkedin GBL C2 - 3 weeks ago


    Bridgewater, United States Gan & Lee Pharmaceuticals Full time

    SummaryThis position reports to the Functional Area Head, Global Regulatory Affairs. The incumbent responsible for supporting the development and implementation of regulatory strategies, work closely with the cross functional asset teams to prepare, review and submit regulatory filing documents, manage documentation systems and maintain interactions with...


  • San Diego, United States Crinetics Pharmaceuticals, Inc. Full time

    Senior Medical Director, Pharmacovigilance Categories: Pharmacovigilance Crinetics is a pharmaceutical company based in San Diego, California that develops much-needed therapies for people with rare endocrine diseases. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead...