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Our system has scored these top jobs to be 88% compatible with you!Warehouse Workers - Become a Lyft Driver Lyft - Poolesville, MD Jul 25, 2017 - Make up to $1500/week driving for Lyft. What is Lyft? Lyft matches drivers with passengers who request rides through our smartphone... more » Make up to $1500/week driving for Lyft. What is Lyft? Lyft matches drivers with passengers who request rides through our smartphone app, and passengers pay automatically through the app. Signing up to be a Lyft driver is the perfect opportunity for you to earn extra cash – whether you’re trying to offset costs of your car, cover this month’s bills, or fund your dreams. Why Lyft? Keep Your Tips - Earn Tips from your passengers and keep the whole amount - they're yours Make More Money - With increased Prime Time pricing during peak hours, you make more with Lyft Best Community - The Lyft community is full of awesome, friendly people. How Lyft Driving Works Open the app and turn on driver mode Accept a ride request Pick up your passenger Once the ride ends, the app processes pay from the passenger's saved credit card Lyft provides additional insurance policies, at no cost to the driver. We worked with leading insurance carriers to get our drivers: commercial auto liability insurance up to $1M per occurrence, contingent collision insurance for drivers who carry collision coverage on their personal auto policy, and coverage for bodily injury caused by uninsured/underinsured motorists. If you already carry commercial insurance or personal coverage providing specific coverage for ridesharing, Lyft’s policy will continue to be excess to your insurance coverage. Please note, the above coverage may be modified to comply with local regulations or state laws. Lyft’s policy is not available in New York State at this time. Passenger Ratings Drivers rate passengers after each ride, so you’ve always got a say. We also require passengers to provide valid credit card information for identity verification purposes. Lyft is Everywhere Lyft is available in over 60 cities in the US and launching in new cities every week! What are Lyft’s requirements? You must be at least 21 and own an iPhone or Android phone. As part of our approval process, you’ll undergo a DMV check, plus a national and county background check. This will require a Social Security number, in addition to an in-state driver’s license that is at least a year old. Learn more about our background check standards on our Safety page, and our comprehensive driver requirements in the Help Center. Your car needs to have four external door handles and at least five total seat belts. You must be a covered party on your car’s in-state insurance, and have in-state license plates. We’ll confirm all of this during your 19-point vehicle inspection. Cars have Lyft age requirements too, which can vary by state. See your state-specific requirements. Uber Driver Partner - Summer Part Time Uber - Ashburn, VA Jul 25, 2017 - WHO WE ARE:Drive with Uber and get paid weekly in fares by helping our community of riders get around town. Driving with Uber is a great... more » WHO WE ARE:Drive with Uber and get paid weekly in fares by helping our community of riders get around town. Driving with Uber is a great way to earn cash on your schedule. The more you drive, the more you can earn. It's simple and perfect for those looking for seasonal, work from home, entry level, temporary, or any type of job opportunities.What you need to know: Earn Great Money: The more you drive, the more you earn.Flexible Schedule: Make your own schedule as a contractor _ any time day or night.Getting Started is Easy: Signing up is quick & easy.Get Paid Weekly: Get checks deposited into your bank account weekly.Requirements: You're at least 21 years oldYou have a 4-door vehicleYou have a driverÍs license and insuranceYou're friendly and excited to earn money on your schedule!Additional Information:If you have previous employment experience in transportation (such as a delivery driver, driver, professional driver, driving job, truck driver, heavy and tractor-trailer driver, cdl truck driver, class a or class b driver, local truck driver, company truck driver, taxi driver, taxi chauffeur, cab driver, cab chauffeur, taxi cab driver, transit bus driver, bus driver, coach bus driver, bus operator, shuttle driver, bus chauffeur) you might also consider partnering with Uber and earn great money. We also welcome drivers who have worked with other peer-to-peer ridesharing or driving networks like Lyft, Sidecar, Deliv, Postmates, Roadie. Our driver partners come from all backgrounds and industries ranging from traditional driving and transportation industries to other industries. Seafood Production Part Time Wegmans Food Markets - Sterling, VA Jul 22, 2017 - Want a job you’ll LOVE?Our Seafood department offers a variety of fresh, unique fish and prepared seafood items to our customers. In this... more » Want a job you’ll LOVE?Our Seafood department offers a variety of fresh, unique fish and prepared seafood items to our customers. In this role, you’ll provide incredible service by educating customers on the different varieties we offer and suggesting meal solutions for any occasion. If you’re passionate about food and are looking for the opportunity to learn and develop your skills, this could be the position for you!Looking for Career Growth? Watch our video!http://youtu.be/Bw7gG0U6DqMHow do I make a difference?Providing Incredible, Knowledge Based Customer ServiceProactively approach customers at the counter and on the sales floor, answer questions about products, fillet, weigh, skin, cut, and package seafood as customers requestSeek to learn about products and practices and share your knowledge to better assist customersEnsuring High Quality Products & IngredientsClean and cut a variety of fish into portions for presentation in seafood cases while following correct practices to reduce the amount of wasteSet up fresh cases, refill product, ensure proper signage and are well-merchandised following company standards to showcase quality and freshness and drive sales Unload and breakdown deliveries, stock refrigerator and freezer, clean cases, scales and counters and rotate for freshness Properly handle products, use equipment, keep accurate logs and follow sanitation practices in accordance with food and human safety guidelines and Simplification 5S proceduresLiving Who We AreSupport, encourage, and respect co-workersWork with supervisor to set and achieve goals for professional development Comply with Wegmans Policies and Work Rules, as well as, federal and state lawsMaintain open lines of communication with supervisors and coworkers to ensure the most efficient operations in the departmentSeeking Candidates Who… Live our values: caring, respect, empowerment, making a difference, high standards Possess teamwork & diversity awareness Seek continuous learning opportunities Provide incredible customer service Ensure food & human safety Possess organizational skills Provide knowledge based service Educate self and others about product knowledge Use and explain Wegmans cooking techniques Preferred Skills and Experience Customer service experience, preferably in a food service, grocery or retail setting Knowledge of, passion for and experience working with, seafood Experience utilizing a variety of cooking techniques Experience cutting fish Work Environment Work involves continuous interaction with customers and co-workers in a fast-paced environment Typical motions include repetitive hand and arm movements, bending and reaching Responsible for moving and lifting an average of 5-10 pounds with a maximum lifted of 50 pounds rarely Must be able to use hand/power jack equipment, knives, and other kitchen equipment May be exposed to various allergens and work environments, including cold temperatures near hot equipment Will spend the majority of time on his or her feet and stand or walk without a break for up to 4 hour * Employment at Wegmans may be contingent upon your completion and our evaluation of a drug screen and/or criminal background check. All Applicants will be screened; only those closely matching the job posting will be interviewed
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. REGISTERED NURSE: Operating Room Tower Surgical Partners - Rockville, MD Jul 11, 2017 - REGISTERED NURSE: Operating Room $5,000 Sign on Bonus! Innovations Surgery Center (innovationsasc.com) is a state-of-the-art, single... more » REGISTERED NURSE: Operating Room $5,000 Sign on Bonus! Innovations Surgery Center (innovationsasc.com) is a state-of-the-art, single specialty, GYN surgery center. The ISC’s focus is on “new procedural technology” developed by its advanced GYN surgical specialists. The center maintains the highest levels of clinical and patient outcomes. An analysis of the GYN procedures performed at the ISC shows the lowest complication rates and costs of any surgical GYN procedures currently available. The potential for expanding marketing share and growth is exceptional. Patient care and attention is a primary focus of the on-site clinical staff. Our patients receive a personalized approach to care that is unmatched in other surgical environments. Patient satisfaction is directly correlated to the advanced procedures offered, clinical outcomes and caring yet efficient staff interactions. The Registered OR Nurse provides nursing care to patients in compliance with, but not limited to, Standards of Practice as defined by ANA, AORN, ASPAN and State Practice Act Standards, and organization protocols, policies, procedures, and guidelines. Develops, implements, evaluates, and revises plan of care based on physical, psychosocial, spiritual, and educational needs of the patient/caregiver. Maintains clinical knowledge and skills competencies to facilitate patient care in accordance with current standards of practice and monitors the environment to provide safe patient care. Supervises and directs patient care in a single operating room. ____________________________________________________________________________ REPORTS TO : Clinical Coordinator / Administrator LOCATION : ROCKVILLE, MD ____________________________________________________________________________ The Registered Nurse: OR Responsibilities & Experience Participates as a team member in support of the total perioperative process Organizes time, equipment, supplies, and personnel to provide effective and efficient case management Considers cost containment by using supplies economically and in effective turnover time Performs comprehensive assessment of patient’s clinical condition and psychosocial needs inclusive of caregiver needs during the Perioperative period. Ensure patient readiness for surgery including, but not limited to, NPO status, medication administration, surgical site verification and marking and chart completeness. Implement plan of care safely and effectively and provides safe environment, including, but not limited to:1) positioning patient safely, padding bony prominences and ensuring respiratory and circulatory protection 2) Ensuring correct prepping and draping procedures 3) Conducting “time out” process prior to incision to ensure correct patient, correct procedures and correct surgical site. 4) Ensure asepsis during all procedures. Opens and presents sterile items to sterile field aseptically; ensures supplies are not expired. 5) Accounting for all sponges, needles, sharps, during and after the procedures and documenting appropriately. Provides comfort and reassurance to patient Maintains patients’ privacy and dignity Explains intra-operative phase of routine procedures and care to the patient Performs the circulating nurse’s role and functions following approved operating room procedures to meet the requirements of scheduled procedures Prepares and cleanse operating room before, between and after cases according to requirements of patient/procedure to be performed Anticipates needs of surgical team and assists anesthesia personnel by supporting patient during administration of anesthesia Assists with the proper and safe positioning of the patient and prepares operative site as directed by established procedures Monitors compliance with principles of aseptic technique according to accepted standards Accurately records, labels, and handles specimens. Provides continuity of patient care by communicating with other perioperative care personnel and documenting records accordingly Responds in a timely manner to meet the needs of the patient and physician Accurately comprehends and interprets verbal orders/directions Accurately advises others responsible for care of the patient about patient’s status Collaborates with other members of the surgical team to ensure efficient turn-around time between procedures. Required: High school graduate or GED certificate recipient Graduate of accredited school of nursing RN with active license in appropriate state BLS certified Leadership qualities Strong ethical and moral character references Language skills adequate for high-level written, interpersonal, and telephone communication in American English Must be able to provide proof of identity and their right to work in the United States. Preferred: Experience in Hospital Main OR Laparoscopic troubleshooting skills GYN and General experience ASC experience Computer literacy This is an exciting position that allows the OR nurse to work with an unparalleled team at an exceptional facility. The position is available immediately. REGISTERED NURSE: Operating Room$5,000 Sign on Bonus!Innovations Surgery Center (innovati... Pilot Production Technician I MedImmune, LLC - Gaithersburg, MD Jul 18, 2017 - Location:Gaithersburg, Maryland, United StatesJob reference:... more » Location:Gaithersburg, Maryland, United StatesJob reference: R-010989Posted date: Jul. 18, 2017 If you’re inspired by the possibilities of science to change lives and you thrive when making brave decisions – join us. MedImmune is the worldwide biologics research and development arm of AstraZeneca. Here, you’ll have the opportunity to make a difference in people’s lives every day. As one of the world’s premier biotechnology companies, our mission is centered on delivering life-changing products that advance world health, and help fight and cure disease. As a Pilot Production Technician I in Gaithersburg MD, you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives. We’re constantly pushing the boundaries of science to deliver life-changing medicines to patients, with a passion for discovery and a pipeline to show for it. We’re pioneering innovative research and exploring novel pathways across key therapeutic areas including oncology, respiratory, inflammation and autoimmunity, cardiovascular and metabolic disease, and infection and vaccines. And we’re industry-leading in immunology, protein engineering and translational science. We offer a unique and strong collaborative network as part of the AstraZeneca family, as together we explore synergies between small and large molecules. MedImmune has a dynamic environment that fosters collaboration and innovation. We attract top minds, and we nurture and build top talent. Summary The technician is responsible for the operation of equipment according to established Standard Operating Procedures and Master Production Records for the manufacture of therapeutic proteins and vaccines in accordance with Current Good Manufacturing Practices (cGMP’s). Principal Duties Operates production equipment such as bioreactors, centrifuges, filtration devices, chromatography equipment, washers and autoclaves. Weighs and checks raw materials, assembles and cleans process equipment, monitors processes. Completes production records and maintains clean room environment to comply with regulatory requirements. Edits Master Production Records and Standard Operating Procedures as required to accurately reflect process steps and capture process changes. Adheres to Good Manufacturing Practices and standard operating procedures. Works on routine manufacturing assignments per written procedures, where ability to recognize deviation from accepted practice is required. Provides training and operational guidance to junior staff and also serves to mentor junior staff in clinical manufacturing techniques. May work on assignments that are moderate to complex in nature, where judgment is required to resolve operational issues without negatively impacting clinical manufacturing efforts. Examples include Standard Operating Procedure (SOP) or Master Production Record (MPR) revision or generalized trouble shooting of equipment problems. Normally receives minimal to no instructions on routine work and general instructions on new assignments. Has good interpersonal skills, is attentive and approachable. Discusses problems with colleagues and senior personnel. Maintains a professional and productive relationship with supervisor and co-workers. Works under moderate to periodic supervision from supervisor or senior technician. Qualifications Bachelor’s degree in the sciences preferred and 0 to 2+ years relevant experience. Associates degree and High School Diploma acceptable with relevant experience. 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. *LI-MEDI ~BSP Please See Description Practice Administrator III Johns Hopkins Community Physicians - Bethesda, MD Jul 11, 2017 - Practice Administrator III Johns Hopkins Community Physicians Bethesda, MD Full Time, Day Shift Setting the standard of excellence in... more » Practice Administrator III Johns Hopkins Community Physicians Bethesda, MD Full Time, Day Shift Setting the standard of excellence in patient care, research and education. At Johns Hopkins Community Physicians, we work to set the standard of excellence for medical care in the world and in the nation. Our faculty and staff members work together to provide the best care possible to patients, train tomorrow’s physicians and nurses, and continue our history of being on the front lines of biomedical science and research. It’s their skills, talent, and dedication that make it possible for us to lead the national and global medical fields in quality and innovation, and help our patients get well and stay well. Take advantage of this opportunity to join our team as a Practice Administrator at our Heart Care Practice located in Bethesda, Maryland. The Practice Administrator reports to the Administrator, and will be responsible for the daily operations of a large health center/practice typically staffed with 12 or more FTE providers in a free-standing location. Daily operations include budget management and the hiring, supervision, staffing, evaluation and discipline of staff. The successful candidate will work effectively with providers and other staff to develop and implement common priorities and goals related to providing optimal customer service, maximizing operational efficiency, assuring financial viability and rendering high quality health care services. The Practice Administrator is expected to demonstrate leadership through example, visible organizational support and a positive attitude to create a positive work environment and enhance provider and staff morale. Also responsible for fostering a positive relationship with the local community served by the health center. Requirements: Bachelor's degree required, Master's degree preferred. Six years' experience in a healthcare, managed care setting 6-8 years management experience. Must demonstrate a record of increasing job responsibility linked to accomplishments in healthcare management. If a Practice Administrator also has clinical nurse responsibilities, the following education, training, licensing and certification requirements apply: R.N. training and a degree from an approved school of nursing. Current Maryland State Licensure. Current CPR certification or ability to successfully complete CPR certification. Ability to demonstrate knowledge and skills necessary to provide care appropriate to the ages of the patients served in the department. To apply and learn more, please click here or visit https://jobs.hopkinsmedicine.org/community-physicians and reference requisition # 151705. It’s because we value the people who work here that we offer an unparalleled benefits package that includes medical, vision and dental coverage, up to 100% tuition reimbursement for employees, 403B Retirement Plan and even college grant tuition for your dependents. Johns Hopkins Health System and its affiliates are Equal Opportunity / Affirmative Action employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity and expression, age, national origin, mental or physical disability, genetic information, veteran status, or any other status protected by federal, state, or local law. Johns Hopkins Health System and its affiliates are drug-free workplace employers. Practice Administrator III Johns Hopkins Community Physicians Bethesda, MD Full Time, Day Shift ... 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.