Responsible for researching, identifying and assisting Grant Writer(s) with every aspect of grant applications/proposals to meet the needs of the Salvation Army HIPAC Division. In addition, the Grant Administrator is responsible for working with Corps Officers to capture metrics, manage grant spend down and gather required information for grant reporting related to grant

Coordinate internal and external resources to ensure the successful OTC certification. Implement weekly/monthly status meetings with the stakeholders and, when necessary, revise the schedule or budget to ensure that project requirements can be met Establish and maintain relationships with relevant client stakeholders, providing day to day contact on project status and cha

Senior Regulatory Affairs Associate Experience Biologic CMC 5+ years of experience Supported the CMC activities related to Vaccine/Biologic manufacturing and control including authoring of submission dossiers related to new application, post approval variations Understanding of EU/CA/WHO/US regulations & guidance allowing appropriate review and compilation of data to appr

Ability to perform tasks under deadlines. Ability to follow written and verbal instructions. Ability to prioritize work and complete multiple tasks under deadlines. Excellent reasoning and problem solving skills. Ability to interact with employees from other departments or groups. Must perform activities with a very high degree for attention to detail. Must have excellent

to relieve suffering for people with great needs, but few options. We are dedicated to discovering and developing life changing treatments for patients with under addressed neurological, endocrine and psychiatric disorders. The company's diverse portfolio includes FDA approved treatments for tardive dyskinesia, Parkinson's disease, endometriosis and uterine fibroids , as

OverviewIn alignment with our Microsoft values, we are committed to cultivating an inclusive work environment for all employees to positively impact our culture every day and we need you as a Regional Environmental Compliance Program Manager for the Americas. In this role, you will be managing the full spectrum of regulatory environmental requirements, including Federal, S

Intel Analyst, Quantico, VA

If you are passionate about innovative therapies, love leading complex regulatory filings, and live for quality, on time, and within budget project deliverables, Parexel is E X P A N D I N G and we currently have openings for Senior Regulatory Affairs Consultants / Regulatory Affairs Leads. These are incredible opportunities to join a tight knit team of amazingly nice and

Job Number R0194703 Strategic and Operational Planner, Senior The Opportunity As an expert in defense missions, your unique background inspires you to think bigger, push further, and askquestions others don't. We need your extensive industry knowledge and advisory skills to solve some of ourclient's most complex problems and find solutions that keep our nation safe.As a S

Doctrine Analyst, Quantico, VA

Access Your Future Service program for students interested in a career in the equipment industry as a Service Technician. This program provides a career path for a qualified student and a financial incentive upon successful completion of an approved diesel program. The Access Your Future Service Intern path offers students part time employment at a sponsoring store during

Job Announcement Fairfax County boasts a top notch school system, safe neighborhoods, thousands of acres of parkland, and bustling town centers. County government sits at the heart of this dynamic community of almost 1.2 million residents and seeks employees eager to bring their energy, enthusiasm and skills to serve Fairfax residents and to shape the county's future. Lan

JMSEL/JNEM Planner position in Suffolk, VA

Parexel's Strategic CGMP Compliance team is known for our unparalleled breadth and depth of expertise globally. Parexel CGMP Compliance offers services which create and maximize product value for clients throughout the product lifecycle, leveraging our unique fusion of scientific, regulatory, and business expertise. We are the pre eminent regulatory and GxP (Good Clinical

The Interoperability Regulations and Standards, Director will work with key external stakeholders to summarize lab related industry standards and regulations and translate any business impact to internal stakeholders. When impactful, this role will be responsible to coordinate internal stakeholders to further assess any impact and help establish solutions. The role will c