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General Atomics Aeronautical Systems, Inc. (GA-ASI), an affiliate of General Atomics, is a world leader in proven, reliable remotely piloted aircraft and tactical reconnaissance radars, as well as advanced high-resolution surveillance systems. This position, working with our MENA (Middle East, North African) group, is responsible for managing and coordinating the operational aspects of one or more project(s) and serves as the liaison between project management and the project team, planning, and line management for sharing information and resolving basic problems. Continually reviews status of the project(s) and budgets to ensure project(s) are completed on time and within budget. Assesses project issues and develops solutions to meet production, quality, and customer-satisfaction goals and objectives. Develops mechanisms for monitoring project progress and for intervention and problem solving with project management, line management, and the customer. DUTIES AND RESPONSIBILITIES Assist with development of project plan(s) and manage resources to ensure project schedule, budget, quality and specification goals are attained. Manage and monitor project schedule, timelines, and milestones from initiation to delivery to meet delivery goals. Coordinate departmental and/or cross-functional teams to assign and prioritize tasks focused on delivering new or upgrading existing products and/or services. Assign and monitor work of project management staff, providing technical support and direction when necessary. Administer and execute policies, processes, and procedures that impact the assigned project. Develop and deliver progress reports, proposals, requirements documentation, and may present results to project management team and/or management. Collaborate across management and project team to expand services and potential business opportunities. Ensure compliance with environmental and other regulations. Identify and assess project issues and develop recommendations for solutions to meet productivity, quality and customer satisfaction goals and objectives. Act as a lead providing direction and guidance to employees working on assigned project. May participate in or lead segments of the request for proposal (RFP) process to generate new business. Maintain the strict confidentiality of sensitive information. Responsible for ensuring all laws, regulations and other applicable obligations are observed wherever and whenever business is conducted on behalf of the Company. Responsible for ensuring work is accomplished in a safe manner in accordance with established operating procedures and practices. Other duties as assigned or required. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. 51958 Job Qualifications: Typically requires a Bachelors in Business Administration or related discipline and nine or more years of progressively complex experience in the project administration field with at least three of those years in project management. May substitute equivalent experience in lieu of education. Must have a thorough understanding of project management processes and procedures, planning and scheduling methods, and budget management as well as the ability to organize, schedule, and coordinate workloads to meet established milestones and budgets. Experience working with and resolving production challenges with multiple functional groups, for example Quality, Subcontracts, Engineering. Expertise working and/or managing in a fast paced, multi technology (Cables, Machine/Fabrication shop, Circuit board assembly, integration, flight ops) manufacturing facility Prior experience utilizing a production MRP system, preferably SAP Understanding of production metrics and reporting approaches Must possess: The ability to initiate, plan and manage projects The ability to identify issues, analyze and interpret data and develop solutions to a wide range of complex issues Strong communication, computer, documentation, presentation, and interpersonal skills The ability to work independently and as part of a team. Must be able to work extended hours and travel as required. Ability to obtain and maintain DoD security clearance is required. Salary:$90,930 - $162,788Travel Percentage Required 0 - 25Relocation Assistance Provided Not Provided US Citizenship Required? YesClearance Required? Desired Clearance LevelSenior (8+ years) WorkstyleHybrid
The Company Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Dexcom began as a small company with a big dream: To forever change how diabetes is managed. To unlock information and insights that drive better health outcomes. Here we are 25 years later, having pioneered an industry. And we're just getting started. We are broadening our vision beyond diabetes to empower people to take control of health. That means personalized, actionable insights aimed at solving important health challenges. To continue what we've started: Improving human health. We are driven by thousands of ambitious, passionate people worldwide who are willing to fight like warriors to earn the trust of our customers by listening, serving with integrity, thinking big, and being dependable. We've already changed millions of lives and we're ready to change millions more. Our future ambition is to become a leading consumer health technology company while continuing to develop solutions for serious health conditions. We'll get there by constantly reinventing unique biosensing-technology experiences. Though we've come a long way from our small company days, our dreams are bigger than ever. The opportunity to improve health on a global scale stands before us. Meet the team: You will be part of the Global Engineering team within Operations, tasked with end-to-end technical oversight of our manufacturing technologies spanning our suppliers, contract manufactures and automation houses. Including providing technical support for on-market production at our manufacturing sites. You will bring your expertise and passion for the qualification, validation and change management of complex manufacturing automation equipment, working closely in cross-functional teams to integrate cutting-edge technology into our manufacturing processes. You will ensure high efficiency, precision, and quality in our operations. You will play a pivotal role in ensuring robust new product introduction, capacity expansions, and sustained on-market performance. This crucial role supports Dexcom's thrilling growth trajectory in delivering essential, life- changing products to our valued customers. As part of this dynamic and highly effective team, you will collaborate closely across multiple functions, gaining broad exposure to our entire product life cycle. Where you come in: • You will lead validation strategy, execution, and compliance for manufacturing processes, equipment, and technologies across Dexcom’s global manufacturing sites, including New Generation Sensor programs. • You will develop validation master plans and protocols (IQ/OQ/PQ) and oversee execution to ensure compliance with applicable standards. • You will support equipment optimization, modernization projects, and continuous improvement initiatives across global sites to enhance performance, reliability, and scalability. • You will analyze validation results and drive continuous improvement and risk mitigation. • You will collaborate with R&D, Quality, Regulatory, and Manufacturing to integrate validation into the product lifecycle and manufacturing readiness. • You will partner with global engineering, operations, and suppliers to harmonize validation methodologies and share best practices worldwide. • You will provide subject matter expertise (SME) in validation and share best practices with peers and cross-functional teams. What makes you successful: • You have deep expertise in validation methodologies (IQ/OQ/PQ, process validation, CSV, CSA) with a strong track record of leading compliant validation activities. • You bring proficiency in statistical methods, data analysis, and risk management tools (DOE, SPC, FMEA, PFMEA). • You have experience leading validation programs across multi-site/global operations in a regulated industry. You are highly detail-oriented, data-driven, and skilled in problem-solving, with the ability to thrive in complex and fast-paced environments. • You have excellent communication, collaboration, and stakeholder management skills, and can influence across functions. • You are adaptable and able to manage ambiguity while maintaining focus on results. • Your proficiency in CAD (SolidWorks), validation systems (ValGenesis), or certifications such as PMP or Six Sigma is a nice to have. Key Competencies: • Expertise in regulatory requirements and standards such as FDA 21 CFR Part 11, and ISO standards. This includes the ability to develop and execute validation protocols (IQ/OQ/PQ) to ensure compliance. • Bachelor’s degree in mechanical, Biomedical or related engineering discipline with a strong focus on medical device manufacturing, automated systems and process technologies. • Possesses hands-on experience with high volume automation assembly machines from development to qualification through to on-market continuous improvement and change management. • Experience in statistical process control (SPC) and use of software tools such as Minitab or JMP for data analysis, process troubleshooting and optimization. • Demonstrated success in driving continuous improvement initiatives using LEAN, KAIZEN, and Six Sigma methodologies to significantly enhance equipment efficiency, reduce operational costs, and elevate product quality standards. What you’ll get: • A front row seat to life changing CGM technology. Learn about our brave #dexcomwarriors community. • A full and comprehensive benefits program. • Growth opportunities on a global scale. • Access to career development through in-house learning programs and/or qualified tuition reimbursement. Education and Experience: Typically requires a Bachelor’s degree in a technical discipline, and a minimum of 8-12 years related experience or Master’s degree and 5-7 years equivalent industry experience or a PhD and 2-4 years of experience Please note: The information contained herein is not intended to be an all-inclusive list of the duties and responsibilities of the job, nor are they intended to be an all-inclusive list of the skills and abilities required to do the job. Management may, at its discretion, assign or reassign duties and responsibilities to this job at any time. The duties and responsibilities in this job description may be subject to change at any time due to reasonable accommodation or other reasons. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Dexcom’s AAP may be viewed upon request by contacting Talent Acquisition at talentacquisition@dexcom.com. If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please contact Dexcom Talent Acquisition at talentacquisition@dexcom.com. Meritain, an Aetna Company, creates and publishes the Machine-Readable Files on behalf of Dexcom. To link to the Machine-Readable Files, please click on the URL provided: https://health1.meritain.com/app/public/#/one/insurerCode=MERITAIN_I&brandCode=MERITAINOVER/machine-readable-transparency-in-coverage?reportingEntityType=TPA_19874&lock=true To all Staffing and Recruiting Agencies: Our Careers Site is only for individuals seeking a job at Dexcom. Only authorized staffing and recruiting agencies may use this site or to submit profiles, applications or resumes on specific requisitions. Dexcom does not accept unsolicited resumes or applications from agencies. Please do not forward resumes to the Talent Acquisition team, Dexcom employees or any other company location. Dexcom is not responsible for any fees related to unsolicited resumes/applications. Salary: $111,100.00 - $185,100.00