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Our system has scored these top jobs to be 87% compatible with you!Locum Tenens Anesthesia Physician MedStaff National Medical Staffing - Manassas, VA Jul 21, 2017 - Anesthesia physician employment in Virginia : Medstaff has a client located in northwestern Virginia looking for general Anesthesiology... more » Anesthesia physician employment in Virginia : Medstaff has a client located in northwestern Virginia looking for general Anesthesiology coverage for the month of August. Will be M-F, daytime hours. Expected cases include Endoscopies and main OR services excluding cardiac surgeries. Requires Board Certification, Virginia license, DEA and some general anesthesia experience. For more information please contact Lori Jannings at ljannings@MedstaffLT.com or call her at 800-476-3275. Positions for CDL-A Company Drivers and Owner Operators TopPayForDrivers.com - Reston, VA Jul 21, 2017 - In Just a Few Minutes, You Could be on Your Way to Choosing the Best Trucking Job Offer From the Best Carriers. We Work with 500+... more » In Just a Few Minutes, You Could be on Your Way to Choosing the Best Trucking Job Offer From the Best Carriers. We Work with 500+ Companies to Match You to Positions Matching Your Criteria. Typical Benefits Include: $0.42 - $0.65 CPM for Company Drivers $.95 - $2.10 CPM or Up to 86% of Haul for Owner Operators 401K / Retirement Matching Family Health Insurance Scheduled Home Time Pet & Rider Policies Stop Sifting Through Jobs You Don't Want, and Apply to Get Matched With the Perfect Driving Job for You! Registered Nurse RN - Home Infusion (part time) EOM - Woodbridge VA CVS Health - Chantilly, VA Jul 13, 2017 - Position Summary: As a Registered Nurse (RN), Home Infusion you will work outside the walls of a hospital setting in a growing... more » Position Summary: As a Registered Nurse (RN), Home Infusion you will work outside the walls of a hospital setting in a growing specialized area of the nursing field. If you are spending 12 hours on your feet or rushing from patient to patient with no time to provide quality patient care, this would be the perfect opportunity to change your work environment. Our nurses have the time and a balanced schedule to build strong one-on-one relationships with your patients and their families. As a Home Infusion RN you will… * Provide a broad range of infusion therapies in our patients’ homes * Make a difference by using your clinical IV experience and personal touch to assist our patients recover in the comfort of their own home. * Provide one-on-one home infusion nursing care visits and patient education in accordance with the physician’s plan of treatment. * Additional licensure may be required in multi state service areas * Use excellent written and verbal customer service skills in order to interact with the patient, physician, pharmacist and other partners. * Challenge your clinical nursing (RN) skills by receiving continuous training on leading edge technology and clinical requirements in specialty infusion. Certification and recertification expenses can be reimbursed for eligible RN’s such as Certified Registered Nurse of Infusion (CRNI)! In this part time position (includes company benefits), you will work a minimum of 30 hours weekly visiting patients in the greater Woodbridge, Dale City and surrounding areas which may require travel of 150 miles radius (travel time and mileage paid). On-call requirements are 5 nights per month to include 1 weekend per month or as determined by staffing and business needs. Registered Nurses (RN) with Coram CVS/specialty infusion services have a uniquely rewarding setting to use their exceptional nursing skills. As a national leader in the home infusion field and a Fortune 7 company, we seek those special RNs who not only possess strong clinical expertise with creative ideas but have the kind of deep compassion and sensitivity it takes to treat people in their homes. Infusion, Home Infusion, RN, Registered Nurse, IV Therapy, Home Health, Hospice, ER, Trauma, ICU, Pediatrics, PRN, Vascular Access, IV Team, Oncology, PICC, Central Line, Infusion clinic, Ambulatory infusion, Cath lab, Transplant, Part Time, Per Diem, Case Manager, CVSHEC13 Required Qualifications: * Registered Nurse with current license in the state of Virginia * Minimum three years nursing experience with a minimum of one year hi tech infusion/IV experience * Have and maintain current CPR certification * Possess a valid and current driver’s license and auto insurance * Experience with Microsoft Office, Excel, Outlook and Word to document and track patient care activity * Participate in on call rotation as indicated by staffing and business needs Preferred Qualifications: * Pediatric care experience highly preferred * Acute care and home health care experience are a plus * CRNI certification Education: RN Diploma, Associates or B.S. degree in nursing Business Overview: Coram CVS/specialty infusion services is a leading national provider of specialty home infusion and specialty pharmacy services. The integration of Coram into CVS Health enables the company to offer enhanced, comprehensive infusion services; expanded payer access; and a national network of more than 85 locations, including 65 ambulatory infusion suites. Providing infusion therapies and services to over 20,000 patients each month, Coram cares for patients through all phases of their healthcare continuum including clinical and compliance monitoring, and individual patient counseling. CVS Health, through our unmatched breadth of service offerings, is the nation’s largest pharmacy health care provider transforming the delivery of health care services in the U.S. Our energetic and service-oriented colleagues embrace fresh ideas, new perspectives, a diversity of experiences, and a dedication to service to meet the needs of the many people and businesses relying on us each day. CVS Health is an equal opportunity employer. We do not discriminate in hiring or employment against any individual on the basis of race, ethnicity, ancestry, color, religion, sex/gender (including pregnancy), national origin, sexual orientation, gender identity or expression, physical or mental disability, medical condition, age, veteran status, military status, marital status, genetic information, citizenship status, unemployment status, political affiliation, or on any other basis or characteristic prohibited by applicable federal, state or local law. CVS Health will consider qualified job candidates with criminal histories in a manner consistent with federal, state and local laws. CVS Health will not discharge or in any other manner discriminate against any Colleague or applicant for employment because such Colleague or applicant has inquired about, discussed, or disclosed the compensation of the Colleague or applicant or another Colleague or applicant. Furthermore, we comply with the laws and regulations set forth in the following EEO is the Law Poster: EEO IS THE LAW and EEO IS THE LAW SUPPLEMENT Position Summary: As a Registered Nurse (RN), Home Infusion you will work outside the walls of a hospital setting in a ...
Hair Stylist Salon Cielo - Ashburn, VA Jul 23, 2017 - Salon Cielo is now hiring Hair Stylists in the Virginia area! Nurture Your Passion With HC, you’ll never have limits on commissions.... more » Salon Cielo is now hiring Hair Stylists in the Virginia area! Nurture Your Passion With HC, you’ll never have limits on commissions. Our trend-forward learning opportunities means you’ll be empowered to build guest loyalty, boost earnings and so much more. Smart A smart career choice is joining a thriving organization dedicated to helping you grow personally, professionally and financially. Bold Be bold and challenge your creativity! Experience trend-forward education to grow your Guest’s loyalty even faster. Beautiful Enrich your life by sharing your passion for beauty. Work with purpose to delight Guests and positively impact your community. •Join a thriving organization that supports personal, professional and financial growth. •Advance your skills with REDKEN color & design training. •Enjoy product and service discounts. •Receive performance incentives and rewards celebrations. Taking care of your health and wellness is a big part of how we support you personally, and professionally. Whether its a flexible schedule you need or great insurance options, we offer it all because you deserve it all. Let your creativity flow knowing that HC offers programs to help you invest in the future and be strong today, and then some. •Health & Dental Insurance •FSA for Adults and Children •Life & Disability Insurance •Company-Matched 401K •Vacation & PTO Senior Regulatory Affairs Director AstraZeneca Pharmaceuticals LP - Gaithersburg, MD Jul 20, 2017 - Location:Gaithersburg, Maryland, United StatesJob reference: R-011153Posted date: Jul. 20, 2017 At AstraZeneca we work together across... more » Location:Gaithersburg, Maryland, United StatesJob reference: R-011153Posted date: Jul. 20, 2017 At AstraZeneca we work together across global boundaries to make an impact and find answers to challenges. We do this with the upmost integrity even in the most difficult situations because we are committed to doing the right thing. We continuously forge partnerships that help pursue world-class medicines in new ways, combining our people’s exceptional skills with those of people from all over the globe. As a Senior Regulatory Affairs Director in Gaithersburg, MD, you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives. GMD (Global Medicines Development) drives late-stage development of our innovative pipeline, transforming exciting science into valued new medicines and ensuring patients around the world can access them. Main Duties and ResponsibilitiesAs the Senior Regulatory Affairs Director you will be accountable for leading the development and implementation of the global regulatory strategy for a product/group of products of increasing complexity. You will ensure that the strategy is designed to deliver rapid approval with advantageous labeling in keeping with the properties of the product(s) and the needs identified by the business, markets and patients. You will show strategic leadership skills, and a deep understanding of global regulatory science and overall drug/biologic development processes and strategies for high profile, complex or novel development programs.You will lead the planning and construction of the global dossier and core prescribing information. You will conduct regulatory risk planning and mitigation. You will leads the Global Regulatory Sub-team (GRST) with key contributing members from a regional perspective, emerging markets, RA CMC as well as delivery & enablement. You will be accountable for the delivery of all regulatory milestones including assessment of the probability of regulatory success together with risk mitigation measures. You will be accountable for product maintenance, supply and compliance activities associated with marketed brands.You will lead the objective assessment of emerging data against aspirations and update senior management on project risks/mitigation activities. You will partner with marketing company and regional regulatory affairs staff to influence developing views/guidance. You will lead the regulatory staff working, provide leadership and participate in skill-development, coaching, and performance feedback. Essential RequirementsAdvanced degree in a science related field and/or other appropriate knowledge/experience.Must have previous experience in leading Major Health Authority interactions.10 + years of experience or equivalent of regulatory drug development including product approval/launch.Expert knowledge of regulatory affairs within one or more therapeutic areas.Broad background of experience working in pharmaceutical business and prior experience in several areas within regulatory affairs.Experience in relevant therapy area (small molecules & biologics) is preferred.Proven leadership and program management experience.Ability to think strategically and critically evaluate risks to regulatory activities.Ability to work strategically within a complex, business critical and high profile development program.Successful contribution to a major regulatory approval at a global level.A scientific and clinical understanding of the regulatory sciences.Must demonstrate competencies of: strategic thinking, strategic influencing, innovation, initiative, leadership and excellent oral and written communication skills. Next Steps – Apply today!To be considered for this exciting opportunity, please complete the full application on our website at your earliest convenience – it is the only way that our Recruiter and Hiring Manager can know that you feel well qualified for this opportunity. If you know someone who would be a great fit, please share this posting with them. AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised. External Expert Engagement Specialist MedImmune, LLC - Gaithersburg, MD Jul 18, 2017 - Location:Cambridge, England, United KingdomGaithersburg, Maryland,... more » Location:Cambridge, England, United KingdomGaithersburg, Maryland, United StatesJob reference: R-004166Posted date: Jul. 18, 2017 Title: External Expert Engagement Specialist Location: Cambridge, UK & Gaithersburg, USA Salary: Competitive At MedImmune, relentless pursuit is matched with exceptional capabilities to break new ground in science. We have one of the most robust pipelines in the industry, and it’s because of our people. We’re entrepreneurial and deeply collaborative – a winning combination that’s delivering life-changing medicines to patients. If you’re inspired by the possibilities of science to change lives thrive when making brave decisions – join us. The External Expert Engagement specialist provides subject matter expertise and support across the global AstraZeneca Science Units, MedImmune and GPPS/GMA for activities involving scientific and medically qualified External Experts. The role interfaces with Business Engagement Owners, Project Managers, Budget Holders, Global Conferencing and Events, Global Transparency, Compliance, external Medical Communications Agencies, and other relevant parties involved with engagements of External Experts. Types of engagements are consultancy, virtual and F2F advisory board meetings, symposia, speaker engagements and steering committee meetings, delivered across global locations both internally and externally to AstraZeneca/MedImmune. The External Expert Engagement specialist is a highly motivated, customer-focused pivotal role that delivers a single point of contact for the business and External Expert to ensure contracting compliance through the contract to pay process. The External Expert Engagement specialist engages with the Business Engagement Owners to deliver their contracting needs and requirements in alignment with business objectives, and in adherence to Legal, Compliance and contracting conditions. The role requires a full understanding of the scope of the activity in relation to engaging with External Experts, contracting and payment requirements, impact on the business in terms of Compliance and Transparency reporting. Essential requirements: Bachelor’s degree or equivalent experience Proactive and consultative customer service, having the ability to identify customer needs and respond creatively, listening to information, asking probing questions, applying knowledge and determining solutions Able to manage multiple priorities and adjust workload as business needs require. Strong organizational and interpersonal skills Problem solving skills and capacity to problem solve, anticipating, initiating and resolving internal and external stakeholder issues Able to influence without authority Experience working with cross-functional teams and demonstrated ability to partner effectively with others. Desirable Requirements: Pharma/biotechnology or related industry experience preferred Knowledge and understanding of global transparency reporting requirements. Strong technical / systems experience and skills Project management experience Opening date: 18th July 2017 Closing date: 21st August 2017 AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised. *LI-MEDI Supplier Quality Specialist Sanaria Inc. - Rockville, MD Jul 17, 2017 - Sanaria Inc., a Rockville, MD based biotechnology company, is seeking a Supplier Quality Specialist for a challenging opportunity on a... more » Sanaria Inc., a Rockville, MD based biotechnology company, is seeking a Supplier Quality Specialist for a challenging opportunity on a world-class team working on the development and commercial manufacturing of a live sporozoite-based malaria vaccine that provides effective long-term immunity and lays the groundwork for eradication of malaria in areas where it is endemic. Sanaria’s vaccine production is based on the life cycle of the parasite. Sanaria is producing material intended for Phase 3 trials and launch. Sanaria’s manufacturing is a team-based environment. The Supplier Quality Specialist is responsible for ensuring quality standards of the components used in manufacturing and testing of final products compliant to FDA and EMEA CGMP regulations. The Specialist works closely with the procurement, warehouse receiving and distribution team to ensure consistent and robust quality standards maintained throughout supply chain. The position requires proficieny in CGMP FDA, EMEA regulations. The Supplier Quality Specialist must also be proficient in USP and EP compendiums for excipients. Job Responsibilities 1. Develop programs and SOPs for supplier quality. 2. Establish and maintain approved supplier list. 3. Establish and maintain quality agreement with supplier. 4. Responsible for overseeing critical material change management and work with Sanaria quality team to investigate final product impact assessment. 5. Establish audit schedule based on risk assessment of supplier. 6. Audit suppliers and CMOs 7. Manage and oversee Sanaria material specification program 8. Oversee routine disposition of incoming components for GMP use. 9. Development Sanaria retention program 10. Oversee and manage retention program Job Requirements Applicant must have a BS degree in microbiology, biochemistry, chemistry or related field with 3 years’ experience in pharmaceutical quality assurance. Experience in vaccine manufacturing quality a plus. At least one year experience in auditing GMP suppliers. Willing to travel 30% of the time. Work independently and achieve outstanding results. Strong verbal and written skills. For more information about Sanaria, visit our website, www.sanaria.com. To apply, please submit a cover letter and resume referencing Supplier Quality Specialist. Visa sponsorship is not available for this position. Sanaria is an equal opportunity employer. National Cancer Institute (NCI) Postdoc: Cancer Prevention Fellowship Program National Institutes of Health - Bethesda, MD Jul 16, 2017 - The National Cancer Institute (NCI) Cancer Prevention Fellowship Program (CPFP) is now accepting applications for Cancer Prevention... more » The National Cancer Institute (NCI) Cancer Prevention Fellowship Program (CPFP) is now accepting applications for Cancer Prevention Fellows. This is a unique postdoctoral training opportunity for scientists and clinicians in the fields of cancer prevention and control. The CPFP is multidisciplinary by nature, as we select fellows from a variety of disciplines and backgrounds to include basic science, epidemiology, health services research, medicine, behavioral science, nursing, social science, nutrition, health education/health promotion, law, dentistry, statistics, geography, exercise science, and engineering. Unlike some postdoctoral programs, our fellows have the opportunity to select their own preceptors, and develop and lead research activities based on their own interests. The Program provides: - Up to 4 years of financial support - Master of Public Health (MPH) or an equivalent degree at any one-year accredited university program, if needed depending on prior training - Mentored research opportunities at the National Cancer Institute (NCI) and Food and Drug Administration (FDA) - Dedicated training to build scientific and leadership skills - Competitive stipends, relocation expenses, travel allowances, and more Duration: The typical duration in the CPFP is 4 years (year 1: master's degree; years 2-4: NCI Summer Curriculum in Cancer Prevention and mentored research). To be considered for the CPFP, you must meet the following eligibility requirements: Doctoral degree: You must have an MD, PhD, JD or other doctoral degree in a related discipline (e.g., basic science, epidemiology, health services research, medicine, behavioral science, nursing, social science, nutrition, health education/health promotion, law, dentistry, statistics, geography, exercise science, or engineering). Applicants currently enrolled in accredited doctoral degree programs that have not yet fulfilled all degree requirements are welcome to apply with the understanding that all requirements will be completed before the start of the CPFP. Assurance to this effect must be supplied in writing by the chair of the dissertation committee (e.g., Ph.D. candidates) or the dean of the school (e.g., M.D. candidates). Foreign education must be comparable to that received in the United States. Prior postdoctoral experience: You must have less than five years of relevant postdoctoral research experience at the time of appointment. Citizenship: You must be a citizen or permanent resident of the United States at the time of application OR You must be applying through the Ireland-Northern Ireland-NCI Cancer Consortium. The application deadline is August 25, 2017.