Associate Director, Quality Assurance - Technical (Providence)

Department: 107100 Quality Location: San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the lives of people living with rare disease. At Travere Therapeutics, we recognize that our exceptional employees are vital to our success. We are a dedicated team focused on meeting the unique needs of rare patients. Our work is rewarding - both professionally and personally - because we are making a difference. We are passionate about what we do. We are seeking talented individuals who will thrive in our collaborative, diverse, fast‑paced environment and share in our mission - to identify, develop and deliver life‑changing therapies to people living with rare disease. We stick by our values centered on patients, courage, community, and collaboration to pursue our vision of becoming a leading biopharmaceutical company dedicated to the delivery of innovation and hope to patients in the global rare disease community. At Travere Therapeutics, we are in rare for life. We continue to courageously forge new paths as we move toward a common goal of elevating science and service for rare patients. Position Summary The Associate Director, Quality Assurance - Technical, is responsible for leading and providing GxP Analytical quality/compliance support and/or oversight as per requirements and applicable guidance. This role works closely with the cross‑functional Travere team and Travere’s contract vendors for testing of product for clinical and commercial use. Responsibilities Lead and support analytical qualification, validation, and transfer of analytical methods for small and large molecules. Review, approve and/or oversee various aspects of analytical validation activities, including but not limited to: Method Validation Protocol Raw Data Review Method Validation Report Test methods Serve as the primary point of contact for Travere cross‑functional groups and contract vendors for analytical questions, issues, and resolution of: Laboratory Deviations Out of Specification / Out of Trend Results Change Controls CAPA Provide subject matter expertise in aiding risk assessment activities to appropriately assess the impact on product quality while supporting mitigation recommendations for the above. Support product(s) stability program with review and approval of protocols, interim reports, raw data review, and final reports. Support the analytical review of data for regulatory submissions. Provide technical input to Travere Policies, SOPs, Work Instructions, etc., assuring internal needs are defined while complying with Regulatory requirements, Guidance and/or industry standards. Maintain up-to-date knowledge of analytical regulatory requirements, practices, and processes (ex. FDA, ICH, EMA, and USP requirements). Aid in the internal and external Quality audit function, as needed. Provide support and contribute to inspections, audits and due diligence activities as needed. Support QA and Travere Senior Management with various projects as needed. Education/Experience Requirements Bachelor's degree in life science or related field of study required. A relevant technical or scientific field, Chemistry, Biology, or Chemical Engineering is preferred. Equivalent combination of education and applicable job experience may be considered. 8 years of experience in an analytical function supporting drug/biologics development and commercialization in the biotechnology or pharmaceutical industry required. Direct experience in GMP Quality Assurance, Analytical Qualification/Validation and/or Quality Systems. Broad knowledge of cGMPs (CFR/ICH) and applicable international regulations and guidelines. Additional Skills/Experience The ideal candidate will embody Travere's core values: Courage, Community Spirit, Patient Focus and Teamwork. Demonstrated ability to critically assess/analyze information, draw the appropriate technical conclusions based upon system knowledge, influence approach, and work effectively across different internal and external functions to resolve complex technical quality issues. Strong interpersonal and organizational skills and excellent verbal and written communication skills are required. Adept problem‑solving skills, a strong sense of urgency, keen attention to detail, ability to work independently and be able to effectively manage multiple priorities in an environment under time and resource pressures. Ability to travel up to 10-20% domestic and international. All positions have an essential job function to be able to perform face to face work with colleagues and/or onsite in San Diego. No role is expected to be 100% remote. Total Rewards Offerings Travere provides comprehensive total rewards offerings that demonstrate our commitment as a diverse, equitable, people‑centric, and pay‑for‑performance organization. Benefits Our benefits include premium health, financial, work‑life and well‑being offerings for eligible employees and dependents, wellness and employee support programs, life insurance, disability, retirement plans with employer match and generous paid time off. Compensation Our competitive compensation package includes a combination of both cash compensation (base pay and short‑term incentive) and long‑term incentive compensation (company stock), designed to recognize, retain, and reward employees. Target Base Pay Range $150,000.00 - $195,000.00 *This information is current as of the date of this posting and may be modified in the future. Actual pay offered to a candidate will depend on a variety of factors including the candidate's experience, education, skills, and location. Travere Therapeutics, Inc. is an EEO/AA/Veteran/Disability Employer. J-18808-Ljbffr

Open-Rank Tenure-Track Faculty of Anesthesiology (Columbus)

Open‑Rank Tenure‑Track Faculty of Anesthesiology Department: Medicine | Anesthesiology Tenure Faculty (regardless of rank) persons with the titles of professor, associate professor, assistant professor and instructor who serve on appointments totaling 50 % or more service to the university and who are eligible for tenure or who have obtained tenure. Duties and responsibilities are assigned in accordance with the workload guidelines laid out in the pattern of administration of each faculty member’s tenure initiation unit (TIU) and, as appropriate, regional campus; obligations will include research, service and/or teaching or clinical practice. These faculty will have earned a doctorate or other terminal degree in the relevant field of study or possession of equivalent experience. Open Faculty Search for Tenure‑Track Faculty with a PhD or MD/DO (Assistant Professor, Associate Professor or Professor) in Perioperative Health Care Research in Anesthesiology, Neuroscience, Pain and Addiction The Department of Anesthesiology at Wexner Medical Center/The Ohio State University College of Medicine is initiating a search for one (or more) Tenure Track faculty position in Basic, Translational and/or Clinical Research. To accelerate our research growth, we have recently recruited 2 NIH funded tenure track faculty and we plan to recruit additional faculty in strategic areas of research to complement our existing strengths and grow our capabilities. We encourage applicants to apply for Assistant, Associate or a Full Professor position. Qualified candidates for the Tenure Track will be focused on research relevant to perioperative care and anesthesiology, in subspecialty areas generally focused on Neuroscience, Pain and Addiction. Applications in other research areas may be considered and should complement ongoing research areas outlined below. Specific target areas of investigation could include, but are not limited to, neuromodulation, neuroimmune regulation, neuroinflammation and reactive glia, in the context of perioperative neural dysfunction, neuroprotection, pain signaling and analgesia, recovery and wound healing, or addiction research. Candidates focused on Women’s Health in the specific target areas are encouraged to apply. We are interested in recruiting either PhD or Physician scientists. Successful applicants will join a growing and dynamic research environment dedicated to translating innovative laboratory discoveries in basic mechanisms to human studies and clinical trials with a long‑term goal to improve patients’ lives. We have an emerging program on ischemic spinal cord injury following TAAA surgery to repair an aneurysm (targeting open surgical repair versus TEVAR), postsurgical delirium, neuromodulation and neuroprotection and perioperative pain management. One of our Tenured Professors is part of a recently funded NIH Blueprint Medtech Award in 2025 in collaboration with CoolSpine LLC, sponsored by NINDS & National Institute of Biomedical Imaging and Bioengineering through a U54 grant mechanism. He will work with his collaborators on an innovative project titled Intrathecal Cooling Catheter to Provide Neuroprotection to Avoid Paraplegia Resulting from Open and Endovascular Thoracic Aneurysm Repair ( https://blueprintneurotech.org/awardees/ ). We recently hosted the first international NIH R13 sponsored conference on strategies to combat ‘paraplegia after ischemic spinal cord injury in patients undergoing TAAA surgery. We also hosted an international conference sponsored by NIH to develop consensus guidelines for preventing opioid induced respiratory depression (OIRD). Our established NIH R01 funded program in basic, translational and clinical research is focused on pathogenic mechanisms of postoperative ileus and POGD that costs billions in healthcare costs due to extended hospitalizations, complications and re‑admissions. New or ongoing NIH R01 funded studies are investigating ‘Enteric neuropathy’, surgical trauma and mechanical stress induced Postoperative ileus (POI), and ‘GPCRs in neuroinflammation and POI. We are interested in developing novel therapeutic targets in postsurgical ileus (i.e. for neuroinflammation associated with glia, neurons and immune cells, purinergic signaling, ‘reactive glia’, Ca²⁺ neuroimaging, patch clamp recordings, neuroplasticity, alterations in neural circuit behavior, programmed cell death and ferroptosis). Our efforts are complemented by further development of enhanced recovery after surgery (ERAS) protocols that is a College of Medicine priority. The Medical Director of ERAS protocols in the College of Medicine is a physician scientist in our department who implemented over 20 ERAS protocols to date. The Chair of the department is the President of ERAS USA. Tremendous opportunities exist for research and RCTs. A funded multi‑institutional Patient Center Outcomes Research Institute (PCORI) grant is investigating new therapeutic strategies to reduce or prevent postoperative delirium, POCD and provide neuroprotection in elderly patients. An ongoing 5‑year FDA/P50 consortium grant between OSU Department of Anesthesiology and Nationwide Children’s Hospital seeks to accelerate implementation of pediatric devices into clinical practice. A multi‑center NIH (NHLBI) SBIR grant is focused on “Advanced Prediction of Emerging Respiratory Decline with the Linshom Continuous Predictive Respiratory Sensor (CPRS)”. Recently, we recruited the first NIH‑R01 funded woman scientist from the Magee Women’s Institute, with a track record of NIH funding as PI on women’s postsurgical recovery, immune cell dysregulation and wound healing in women with diabetes. We also recruited an NIH funded Tenured Professor of Anesthesiology, with a focus on neurotoxicity to anesthetics following neonatal exposure and mitochondrial dysfunction. Her research program is at the intersection of neuroscience, stem cell biology, and mitochondrial medicine. Dr. Bai’s research centers on elucidating mitochondrial, non‑coding RNA, and redox‑mediated mechanisms underlying anesthetic‑and alcohol‑induced neurotoxicity using human stem cell‑based systems and complementary animal models. A central contribution of her program has been the development and application of human induced pluripotent stem cell (hiPSC)‑derived models, particularly three‑dimensional cerebral organoids (mini brains) as translational platforms for studying neurodevelopmental injury. Ongoing and new funding through the Office of Naval Research is focused on basic science mechanisms of “Mitochondrial Directed Therapy in Oxygen Toxicity and Decompression Sickness”. Our Pain Center is investigating lower back pain mechanisms and neuromodulation therapies in collaboration with the Spine Institute. NIH funded studies are evaluating spine treatment strategies for chronic low back pain, by targeting innovative strategies, including ‘biomarkers’, identification of low back pain patient phenotypes to optimize treatment outcomes, combining physical therapy with mindfulness for treatment, and developing a wearable sensor for enabling functional assessment of chronic lower back pain. Other areas of investigation seeking extramural funding for pain research include ‘acute post‑cesarian pain’, and an R34 study on opioid use disorder after surgery (OID), industry funded clinical trials or investigator‑initiated studies on SCS‑Neuromodulation therapy, and development of computational methods/models to better assess pain. We pride ourselves in supporting our clinical trainees through FAER, MDSR and WSFA that includes medical students, residents, fellows and postdocs. The Department of Anesthesiology is innovating in both basic science and patient‑oriented research. On the clinical front, we have a robust clinical research infrastructure and are supporting more than 50 active trials, including multicenter industry funded clinical trials, investigator‑initiated studies and trials, including trials on postoperative ileus, postoperative nausea and vomiting, spinal cord stimulation, as well as NIH funded translational studies and studies to test clinical monitoring devices. We are looking to expand these efforts. We have implemented a new Perioperative Outcomes Research Collaborative in Anesthesiology (PORCA), focused on harnessing the power of “large database analysis” to complement our efforts on original research hub organized by senior Anesthesia faculty meets regularly and supports over 40 trainees and faculty in scholarly and research activities. We have close collaborations with the Biostatistics Core, Bioinformatics and the Clinical Trial Monitoring Organization (CTMO) in the College of Medicine to meet all our statistical needs, regulatory support, compliance on human subject research, and aid in our budgets and clinical staff recruitment efforts. Potential opportunities also exist for collaborations with the Neurological Institute, Behavioral Institute, Neuroscience Department, Psychiatry and Addiction Center, Neurosurgery, Sarah Ross Soter Women’s Health Research Program, Pathology, Gastroenterology and Bioengineering. Topics of discussion at our upcoming Department research retreat include our strategic research plan and vision for the future, research opportunities for trainees, infrastructure and resources to support our research. Team‑science involving PhD and MD investigators is highly valued and encouraged. The CATALYST program (Center for the Advancement of Team Science, Analytics and Systems Thinking in Health Services and Implementation Science Research) provides a peer group of scholars with a range of interests in health services research and implementation science, mentorship by senior investigators, and training through seminars, didactics, leadership development activities and mentored development of grant applications. Team science and collaborations a

General Manager (Waldorf)

Ourisman, Trusted Tradition Here\'s to those who think differently. The ones who think that a car dealership\'s first priority should be the guest. Such a candid idea could only come from Ourisman. Because we\'re forward thinking, just like the communities we serve. Individuals who won\'t be constrained by how things have always been done, but instead strive to do things how they could be done and how they should be done. It is a philosophy we have infused into every fabric of our dealerships, from the bottom up, in every department, and in every Ourisman team member. Changing the way we all think about car buying is just the beginning. Role Summary Ourisman Automotive Group is seeking an experienced and strategic General Manager to oversee all aspects of our dealership operations. The General Manager will be responsible for driving overall business performance, including sales, service, and administrative functions, while ensuring the highest levels of customer satisfaction and operational efficiency. More about the role Manage daily operations of the dealership, including sales, service, finance, and administrative functions, to ensure smooth and efficient business processes. Lead, mentor, and motivate department managers and staff to achieve business objectives and foster a collaborative and productive work environment. Develop and implement sales strategies to drive vehicle sales, meet revenue targets, and enhance customer acquisition and retention. Prepare and manage the dealership budget, analyze financial performance, and implement strategies to achieve profitability goals. Ensure exceptional customer service across all departments, addressing customer concerns and resolving issues to enhance satisfaction and loyalty. Stay informed about industry trends, market conditions, and competitor activities to adapt business strategies and maintain a competitive edge. Identify and pursue opportunities for growth, including new market segments, service offerings, and promotional activities. Ensure compliance with industry regulations, company policies, and safety standards, maintaining high operational and ethical standards. What we look for Proven experience as a General Manager or in a senior management role within the automotive industry, with a successful track record of achieving business objectives. Strong leadership and management skills, with the ability to inspire and lead a diverse team. In-depth knowledge of dealership operations, including sales, service, finance, and inventory management. Proficiency in budgeting, financial analysis, and profit and loss management. A commitment to delivering outstanding customer service and maintaining high levels of customer satisfaction. Excellent verbal and written communication skills, with the ability to effectively interact with customers, team members, and stakeholders. Strong analytical and problem-solving abilities, with a focus on driving operational improvements and business growth. Benefits Health, dental, and vision insurance Life insurance options Short-term and Long-term disability insurance 401(k) plan with company match Paid time off and holiday leave Opportunities for professional development and growth Ourisman Automotive Group is an equal opportunity employer. We believe in hiring a diverse workforce and sustaining an inclusive, people-first culture. We are committed to non-discrimination on any protected basis, such as disability and veteran status, or any other basis covered under applicable law. Should you require accommodation during the interview process, please advise the hiring manager when contacted for an interview. J-18808-Ljbffr

Direct and Workplace Banking Strategy - Vice President (Town of Islip)

Morgan Stanley (“MS”) is a global financial services firm that conducts its business through three principal business segments - Institutional Securities Group (“ISG”), Wealth Management (“WM”), and Asset Management. The US Banks - Morgan Stanley Private Bank, National Association (“MSPBNA”) and Morgan Stanley Bank, National Association (“MSBNA”) - provide cash management, deposit and lending products and services to serve the needs of WM & ISG clients.We are looking for an individual to join the Digital Direct and Workplace Banking Strategy team, which is responsible for growing Banking and Lending across E*TRADE and our Stockplan business. This role is a great opportunity to combine strategic execution, leadership influence, and banking and lending expertise to drive value for our end clients.The ideal candidate can create structure in ambiguity, apply critical thinking to abstract problems, and build strong relationships across product, sales, marketing, technology, risk, legal, and compliance.Position SummaryIdentify and evaluate growth opportunities across business segments, partnering internally to assess scale, feasibility, client impact, and strategic fitDevelop executive-level materials that clearly frame recommendations, tradeoffs, progress, and decisions for stakeholders at all levels.Translate prioritized opportunities into detailed implementation plans, including milestones, dependencies, risks, and drive stakeholder alignment.Partner across teams to deliver the system, process, and operating changes required to improve client experience.Experience5-10 years of professional experience in strategy & execution / product development / distribution roles in either management consulting or internal strategy teams – ideally within wealth management, retail banking or lending, and/or consumer financial servicesBachelor’s degree required.Skills/Abilities PreferredHigh ownership, accountability, and autonomy, with the judgment to take initiative and drive progress without clear direction.Experience delivering products or initiatives to retail clients, with disciplined project/program management skills.Advanced ability to influence stakeholders and partner with teams across marketing, technology, and product to prioritize workstreams.Quantitative and qualitative analytical capability, with a creative and flexible approach to solving ambiguous problems.Clear communication, influencing, and executive presentation skills across written and verbal formats.Technical skills and experience with analytics tools are a plus.WHAT YOU CAN EXPECT FROM MORGAN STANLEY:At Morgan Stanley, we raise, manage and allocate capital for our clients – helping them reach their goals. We do it in a way that’s differentiated – and we’ve done that for 90 years. Our values - putting clients first, doing the right thing, leading with exceptional ideas, committing to diversity and inclusion, and giving back - aren’t just beliefs, they guide the decisions we make every day to do what's best for our clients, communities and more than 80,000 employees in 1,200 offices across 42 countries. At Morgan Stanley, you’ll find an opportunity to work alongside the best and the brightest, in an environment where you are supported and empowered. Our teams are relentless collaborators and creative thinkers, fueled by their diverse backgrounds and experiences. We are proud to support our employees and their families at every point along their work-life journey, offering some of the most attractive and comprehensive employee benefits and perks in the industry. There’s also ample opportunity to move about the business for those who show passion and grit in their work.To learn more about our offices across the globe, please copy and paste https://www.morganstanley.com/about-us/global-offices into your browser.Expected base pay rates for the role will be between $110,000 and $190,000 per year at the commencement of employment. However, base pay if hired will be determined on an individualized basis and is only part of the total compensation package, which, depending on the position, may also include commission earnings, incentive compensation, discretionary bonuses, other short and long-term incentive packages, and other Morgan Stanley sponsored benefit programs.Morgan Stanley is an equal opportunity employer committed to building and maintaining a workforce that is diverse in experience and background. Our recruiting efforts reflect our strong commitment to a culture of inclusion, where individuals are hired, developed, and advanced based on their skills and talents.Our workforce reflects a broad cross-section of the global communities in which we operate, bringing a variety of backgrounds, talents, perspectives, and experiences.For more information, please visit : https://www.morganstanley.com/people-opportunities/eeo . J-18808-Ljbffr

Director, Product Management-Prenatal Genetics (Secaucus)

Job Description This position will be responsible for establishing profitable growth strategies for the prenatal genetics product segment. The position leads new solution development, life cycle management and improves profitability for the segment through a cross-functional team. Advocates and prioritizes business cases to the GM of the Clinical Segment and wins support to execute strategies through Marketing and the value-delivery organization. The product director also works to build the business case and secure resources for new initiatives. Some of the key partners day to day will be Finance, R&D, HR, IT, Operations, Medical, Marketing and Sales. Benefits Information We are proud to offer best-in-class benefits and programs to support employees and their families in living healthy, happy lives. Our pay and benefit plans have been designed to promote employee health in all respects - physical, financial, and developmental. Depending on whether it is a part-time or full-time position, some of the benefits offered may include: Day 1 Medical, supplemental health, dental & vision for FT employees who work 30 hours Best-in-class well-being programs Annual, no-cost health assessment program Blueprint for Wellness healthyMINDS mental health program Vacation and Health/Flex Time 6 Holidays plus 1 MyDay off FinFit financial coaching and services 401(k) pre-tax and/or Roth IRA with company match up to 5% after 12 months of service Employee stock purchase plan Life and disability insurance, plus buy-up option Flexible Spending Accounts Annual incentive plans Matching gifts program Education assistance through MyQuest for Education Career advancement opportunities and so much more! Responsibilities Drive profitable growth strategy (organic and acquired) for the segment as part of annual strategic planning process Develop Annual Operating Plan (AOP) Rigorously assess and improve profitability for the clinical segment by reducing both denials & cost of testing, and improving pricing Own P&L responsibility for segment Lead launch team, to ensure pricing, coding, reporting, training, advertising/promotion, channel strategies and tactics are launch ready Understand continuum of care requirements and gaps Assure the voice of customer is brought into the in-line and product/solution creation process Understand the competitive landscape to ensure we have winning solutions in development and in the marketplace Execute effective life-cycle management across the segment through robust cross-functional team management Rigorously assess new products/solutions to enable prioritization within R&D, IT and Operations Work with R&D, BX/IT and Operations to bring new solutions to market Generate customer insights to define customer/market segment requirements to set product/portfolio solution, priority setting, risk management Define and manage product/service metrics (including TAT and other potential requirements such as billing programs, prior authorization, etc.) Support development of clinical KOLs and patient advocacy group relationships Qualifications Bachelor's degree in life sciences, business, marketing and/or product management required Advanced degree in Genetics preferred Excellent communication & presentation skills Storytelling skills Business insight and strategic mindset Dealing with ambiguity and complexity Quest Diagnostics honors our service members and encourages veterans to apply. While we appreciate and value our staffing partners, we do not accept unsolicited resumes from agencies. Quest will not be responsible for paying agency fees for any individual as to whom an agency has sent an unsolicited resume. Equal Opportunity Employer: Race/Color/Sex/Sexual Orientation/Gender Identity/Religion/National Origin/Disability/Vets or any other legally protected status. J-18808-Ljbffr

Test Pilot (Mobile)

Test PilotApplylocations: Mobile Area, ALtime type: Full timeposted on: Posted 30 Days Agotime left to apply: End Date: June 29, 2026 (30 days left to apply)job requisition id: JR10390593Airbus is committed to providing reasonable accommodations as an Equal Opportunity Employer to applicants with disabilities. If you require assistance or an accommodation to complete your application, please contact us at [email protected]* Notice: Know Your Rights: Workplace Discrimination is Illegal* Notice: Pay Transparency Nondiscrimination (English)* Aviso: Transparencia en el Pago No Discriminación (Spanish)Job Description:Airbus Commercial Aircraft is looking for a Test Pilot to join our Engineering department based in Mobile, AL.The Test Pilot is responsible for ensuring the proper execution of ground and flight tests on A220 and A320 production aircraft.Meet the team:Our Engineers at the Airbus U.S. Manufacturing facility take our aircraft from concept to customer delivery – working with production teams on every aspect of assembly from managing technical information, quality control, maintenance tasks and health & safety – along flowlines and flight lines. Join our team and watch our aircraft come to life.Your working environment:Nearby on ‘Airbus Way’ you will find the Airbus U.S. Manufacturing Facility for commercial aircraft. Opened at the Mobile Aeroplex at Brookley in 2015, the facility produces A320 Family aircraft and added a second product line for the A220 in 2019. The facility, which strengthens the U.S. aerospace industry, is part of Airbus’ strategy to enhance its global competitiveness by meeting the growing needs of its customers in the United States and beyond.How we care for you: Financial Rewards: Competitive base salary, incentive compensation which may include profit sharing schemes, retirement savings plan and the ability to participate in an Employee Stock Ownership Plan (“ESOP”)* Work/Life Balance: Paid time off including personal time, holidays and a generous paid parental leave program.* Health & Welfare: Comprehensive insurance coverage including medical (traditional and high-deductible health plans), prescription, dental, vision, life, disability, Employee Assistance Plan (“EAP”) and other supplemental benefit coverages.* Individual Development: Upskilling and development opportunities through our global Leadership University, including unlimited access to 10,000 e-learning courses focusing on ways to develop your employability, certifications, career path as well as the opportunity to participate in accelerated development programmes and both national and international mobility.At Airbus, we support you to work, connect and collaborate more easily and accessibly. Wherever possible, we support flexible working arrangements to stimulate innovative thinking.Your challenges: Responsibility for the entire flight, including signing the flight order prepared and co-signed by the L-FTE.* Captain, under DOA privilege and by delegation of the HO Flight Test, approves flight conditions according to Airbus procedure.* Strictly adhere to the authorized flight test plan. Based on real-time flight analysis, instrumentation issues, changing weather, or aircraft serviceability, the L-FTE may modify the flight test plan in-flight with the Captain's concurrence, provided it complies with the authorized flight envelope and aircraft limitations. The Captain always retains the right to delete unsuitable items from the existing Flight Order.* Attending post-flight technical debriefs and liaising with Engineering staff to expedite the resolution of faults or observations found during approved test flights.* The Captain is responsible for ensuring all ground and in-flight arrangements are made for safe and efficient flight conduct, including all briefings in coordination with the I-FTE and dispatch.* Continuous engagement with customers during the delivery process and dedicated customer-focused activities to effectively communicate Airbus's approved positions on major industry issues and flight test matters.* May be required to perform other tasks within the broader Flight Test perimeter, such as assisting Training Departments, conducting external flights (e.g., lease-recovery, developmental flights, commercial events), short-term assistance to other Flight Test centers (e.g., Toulouse, Hamburg, Tianjin, Mirabel), and attending/presenting at conferences.Your boarding pass: Graduate of an EASA recognized flight test school (ETPS, EPNER, USNTPS, USAFTPS, NTPS and ITPS)* 3000 total flight hours.* Flight test pilot experience of greater than 1000 flight hours.* Current multi-pilot instrument rating* ICAO ATPL that is eligible for conversion to an EASA ATPL* ICAO English Level 5* Recent Fly-By-Wire (FBW) experience* Demonstrates a refined approach to communication that resolves problems, facilitates consensus, and focuses on objectives* Capable of working in a dynamic, fast-paced environment both independently and collectively.* Dependable, self-motivated and accessible.* Ability to travel unaccompanied to international destinations (approx. 3 months);* Ability to work flexible and extended hours as required (nights, weekends and holidays) within the scope of the Airbus Flight Operations Manual.* Authorized to Work in the USPhysical Requirements: * Onsite or remote: Onsite 100%* Vision: able to see and read computer screens and other electronic equipment with screens, able to read documents, reports and engineering drawings.* Hearing: able to participate in conversations in person and via teleconference or phone and to hear sounds on the production floor including safety warnings or alarms.* Speaking: able to speak in conversations and meetings, deliver information and participate in communications.* Equipment Operation (personal computer, telephone, copies, fax machine, and related office equipment and using electronic identification card to enter building floors and internal doors): able to operate most office and personal electronic equipment and some tools including production tools such as hydraulic lifts.* Carrying: able to carry documents, tools, drawings, electronic equipment up to 30lbs/14kgs.* Lifting: able to lift documents, tools, drawings, electronic equipment up to 30lbs/14kgs.* Pushing / Pulling: able to push and pull small office furniture and some equipment and tools.* Sitting: able to sit for long periods of time in meetings, working on the computer.* Squatting / Kneeling: able to squat or kneel to retrieve or replace items stored on low shelving.* Standing: able to stand for discussions in offices or on the production floor.* Travel: able to travel independently and at short notice.* Walking (include routine walking such as to a shared printer to retrieve documents): able to walk through office and production areas including uneven surfaces.* Personal Protective Equipment required: Required PPE includes, but is not limited to, Safety Shoes, Safety Glasses, Hearing Protection, Respirators/Masks, and/or Protective Gloves as required by site and/or customer site.Take your career to a new level and apply online nowThis job requires an awareness of any potential compliance risks and a commitment to act with integrity, as the foundation for the Company’s success, reputation and sustainable growth.Company:Airbus Americas, Inc.Employment Type:US - Direct HireExperience Level:ProfessionalRemote Type:On-siteJob Family:Testing Job Posting End Date: 06.29.2026Airbus provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, genetics, pregnancy, marital status, veteran status or other legally protected status. In addition to federal law requirements, Airbus complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, demotion, termination, layoff, recall, transfer, leaves of absence, compensation, benefits and training. Airbus expressly prohibits any form of workplace harassment based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, genetics, pregnancy, marital status, veteran status or other legally protected status. As a matter of policy, Airbus does not sponsor visas for US positions unless specified. Only applicants with current work authorization will be considered. Airbus does not offer tenured or guaranteed employment. Employment with Airbus is at will, meaning either the company or the employee can terminate the employment relationship at any time, with or without cause, with or without notice. Airbus reserves the right to revise or change job duties and responsibilities as the need arises. This position description does not constitute a written or implied contract of employment.By submitting your CV or application you are consenting to Airbus using and storing information about you for monitoring purposes relating to your application or future employment. This information will only be used by Airbus. Airbus is committed to achieving workforce diversity and creating an inclusive working environment. We welcome all applications irrespective of social and cultural background, age, gender, disability, sexual orientation or religious belief. J-18808-Ljbffr