Quality assurance manager jobs in Reston, VA - 982 jobs

Non-negotiable Requirement: Seeking Local candidates only in Washington, DC, Maryland & Virginia. Responsibilities: • Four-year degree in engineering, Quality Assurance, Business Management or related experience. • Minimum 8-10 years of quality management experience. • Perform as the Contractor's Quality Management Representative. • Responsible for the Quality Assurance (QA) OR Quality Control (QC) for the project. • Establish, implement, and maintain the Quality Management System. • Responsible for the preparation of acceptable documentation of all QC activities. • Experienced in establishing, implementing, and maintaining the Quality Management System, and performing compliance audits in the construction. • Responsible for ensuring that the Quality Management System is effective in ensuring that the Contract requirements are satisfied. • Ensuring that construction activities are performed according to plans and specifications. • Responsible for the oversight of onsite and offsite testing by the Contractor. • Quality inspection or auditing is a must have. Why this company? • Competitive pay rates. • Incredible opportunities for career growth. • Secure and diverse positions to showcase your talents. • Benefits package with medical, dental, vision, and 401K plan.

At BAE Systems, we're passionate about harnessing the power of technology to drive innovation and make a meaningful impact. Our team is dedicated to delivering cutting-edge solutions that support our government customer's mission-critical objectives. We're now seeking a highly skilled Quality Assurance Specialist to join our dynamic team and help us ensure the quality of our software applications. We're looking for a talented Quality Assurance Specialist to play a key role in ensuring the functionality and performance of our OSINT applications. As a Quality Assurance Specialist, you will be responsible for conducting rigorous and thorough testing across OSINT applications, covering UI and back-end functions, and identifying defects. Responsibilities: * Conduct rigorous and thorough testing across OSINT applications, covering UI and back-end functions, ensuring functionality and performance across environments * Perform unit, integration, and acceptance testing and document test outcomes, identify defects, and bug reports * Support leading and overseeing teams in the conduct of thorough testing of OSINT applications, ensuring functionality and performance across environments * Document test outcomes and identify defects Required Education, Experience, & Skills Bachelor's degree in an area related to the labor category from a college or university accredited by an agency recognized by the U.S. Department of Education Experienced with SW development and testing, UI/UX development, development and execution of test and evaluation (T&E) plans Experience in automating T&E plans 8 years of experience conducting analysis relevant to the specific labor category, with a portion of the experience within the last 2 years Preferred Education, Experience, & Skills * Master's degree in relevant major preferred. * Safe Agile expereince and certifications a plus. #EKS01 #LI-TO1 Pay Information Full-Time Salary Range: $81156 - $137964 Please note: This range is based on our market pay structures. However, individual salaries are determined by a variety of factors including, but not limited to: business considerations, local market conditions, and internal equity, as well as candidate qualifications, such as skills, education, and experience. Employee Benefits: At BAE Systems, we support our employees in all aspects of their life, including their health and financial well-being. Regular employees scheduled to work 20+ hours per week are offered: health, dental, and vision insurance; health savings accounts; a 401(k) savings plan; disability coverage; and life and accident insurance. We also have an employee assistance program, a legal plan, and other perks including discounts on things like home, auto, and pet insurance. Our leave programs include paid time off, paid holidays, as well as other types of leave, including paid parental, military, bereavement, and any applicable federal and state sick leave. Employees may participate in the company recognition program to receive monetary or non-monetary recognition awards. Other incentives may be available based on position level and/or job specifics. About BAE Systems Intelligence & Security BAE Systems, Inc. is the U.S. subsidiary of BAE Systems plc, an international defense, aerospace and security company which delivers a full range of products and services for air, land and naval forces, as well as advanced electronics, security, information technology solutions and customer support services. Improving the future and protecting lives is an ambitious mission, but it's what we do at BAE Systems. Working here means using your passion and ingenuity where it counts - defending national security with breakthrough technology, superior products, and intelligence solutions. As you develop the latest technology and defend national security, you will continually hone your skills on a team-making a big impact on a global scale. At BAE Systems, you'll find a rewarding career that truly makes a difference. Intelligence & Security (I&S), based in McLean, Virginia, designs and delivers advanced defense, intelligence, and security solutions that support the important missions of our customers. Our pride and dedication shows in everything we do-from intelligence analysis, cyber operations and IT expertise to systems development, systems integration, and operations and maintenance services. Knowing that our work enables the U.S. military and government to recognize, manage and defeat threats inspires us to push ourselves and our technologies to new levels. This position will be posted for at least 5 calendar days. The posting will remain active until the position is filled, or a qualified pool of candidates is identified.

A leading biopharmaceutical company is seeking a Senior Director of Quality Policy and Advocacy to lead global policy initiatives. This role requires extensive experience in Quality strategies, particularly within North American regulatory landscapes. You will be responsible for advocating Gilead's portfolio interests and engaging with stakeholders to resolve complex Quality issues. The ideal candidate will have a strong background in regulatory affairs, leadership skills, and the ability to communicate effectively with diverse audiences. This role offers a competitive salary and benefits. #J-18808-Ljbffr

At Aurora Flight Sciences, we design, build, and fly advanced aircraft and enabling technologies from concept to reality. We are searching for a talented and self-motivated Quality Program Manager - Development & Prototype Programs to help us create the future of flight. Responsibilities will include but not be limited to the following: Responsibilities * Develop Quality Plan that is relevant and current to the program, conduct proactive periodic review of the Quality plan to ensure program compliance to Quality Plan. Initiate nonconformance and lead corrective actions if gaps identified. * Participate in all relevant Customer meetings associated with the program, lead any Quality specific meetings with the customer. Establish point of contact for Quality at customer end. Proactively establish communication with the customer and develop a communication plan and appropriate cadence. Have a good understanding of customer challenges and perception to lead Aurora to achieve world class customer experience. * Review proposal, Manufacturing work plan, FAI, Engineering Change, etc. to ensure compliance to Quality plan. Initiate and complete applicable updates if there are conflicts between the Quality Plan and other program specific documents. Communicate the changes effectively with key stakeholders. * Collaborate in new product development processes to ensure that quality standards are integrated from the design phase onward. * Report applicable Quality metrics and trend in program reviews. Establish targets for the metrics and communicate the targets to the program team. Provide additional details as needed including containment actions, recovery plan, corrective action and its effectiveness, and preventive action plan. Keep track of Risk, Issues, Opportunities and Help needed associated with Quality performance of the program. * Understand process execution for the program to identify key process/functions for successful execution of the program. Set clear program quality expectation on inputs/outputs, metrics, and improvement plan (as applicable) for key function that is aligned with program quality plan. Get buy in from key stakeholders within the program team for the expectation. Resolve conflicts as needed. Participates in various revies to ensure quality attributes are incorporated into product and process design. * Perform contract review and own the update of Quality plan as applicable and accountable other key program documents updates. * Work with the program manager to establish Program Quality Budget. Ensure, we have staffed appropriately, executing at 100% efficiency and resolve conflicts (with PMO) if there is legitimate work that needs to be performed and not budgeted. Identify single point of failure risk associated with resource and actively work towards establishing applicable countermeasures. * Ensure KPIs related to MRBs are achieved. Work with functional and program management to develop applicable countermeasures to achieve the established targets. * Develop and lead program preventative quality plan. Use Lean/Six Sigma/Quality tools to continuously improve process capability. * Develops quality criteria for supplier source selection. * Communicate and brief senior management on preparation for third party audits. * Assists in the development of new standard repairs as applicable for complex nonconforming materials, parts, and equipment. * Works under minimal direction. Minimum Requirements * Education/experience typically acquired through advanced education (e.g. Bachelor) and typically 6 or more years' related work experience or an equivalent combination of education and experience (e.g. Master+4 years' related work experience, 10 years' related work experience, etc.). * 5+ years of experience in Quality. * 3+ years of experience in driving quality improvement for new product development. * Must be a US Person. Preferred Requirements * AS9100 and AS9102 experience (3+ years). * 8-10+ years of Quality experience. * Bachelor degree in technical field. Physical Requirements * Ability to work in a manufacturing environment, wear proper PPE, and follow Boeing regulations for lifting. * Must be able to support occasional travel (up to 10%). * Work onsite in Manassas, VA. Salary Range (Annualized USD) * Minimum Range: $84,000.00 to $150,000.00 * Maximum Range: $104,000.00 to $185,000.00

**US Based Candidates Only** Granules Pharmaceuticals, Inc., located in Chantilly, VA was the 10th fastest growing generic pharma company in United States in 2024 based on sales growth! We manufacture dosage forms with specific release capabilities including pulsatile drug release in tablet and capsule dosage form, orally disintegrating modified release tablets (XR, MR, ER), modified release suspension and controlled substances capabilities in an abuse deterrent technology platform, all supported by our API business. Granules is one of the few pharmaceutical companies to be vertically integrated from API to packaging. As a Director, QA Compliance, you will be accountable for the leadership activities and to direct all facets of Quality Compliance including, but not limited to, managing Quality Systems (incidents resolution, CAPAs, change control, complaints resolution), host FDA inspections and respond to questions arising from the inspections, oversee remediation activities for site-wide compliance improvements, external and internal audits, training with effectiveness checks, Quality metrics, data trending and evaluation with recommendations for cGMP Compliance improvements. Additionaly, you will ensure sustainable cGMP compliance, participate with regulatory bodies to address questions, and act as the lead for drafting responses to FDA Form 483 observations. The Director, QA Compliance, will provide regular monthly updates to senior management regarding the progress and status of cGMP Compliance. This is an on-site position. Provide leadership and direction regarding cGMP Compliance at the Chantilly site to ensure adherence to applicable Regulations. Excellent knowledge of the 21CFR, ICH, and USP to interpret and apply Regulations with respect to any questions related to cGMP Operations at the Chantilly site. Represents the department during high level discussions and investigations with external customers, vendors, and FDA representatives. Lead as the site Quality representative during FDA inspections. Lead the site in inspections conducted by external regulators and business partners. Conduct Compliance GAP analysis with recommendations for gap closure, implementation and follow up of effectiveness checks. Implement and follow through with site-wide remediation and improvement plans based on assessment of Quality metrics. Maintain Quality metrics for the site with analysis of data to sustain Compliance at the site. Responsible for building effective systems, processes and cross-functional teams to manage Compliance at the site. Manage and develop direct reports by setting clear expectations and resolving conflicts. Responsible to ensure adherence to company protocols and close in a timely manner any deviations from procedures or cGMP requirements. Interface with different departments regarding quality issues, audits and special projects. Provide guidance to manufacturing regarding Quality cGMP issues to ensure compliance with applicable standards and regulations. Provide technical expertise for personnel training, deviations, CAPA, inventory management, cGMP compliance and data trending. Review and approve, as required, OOS, SOPs, protocols and investigations. Coordinate and supervise the collection of data reported in the product review. Prepare, as required, and review documentation required for regulatory submissions. Serve on the Quality Task Force and participate in the generation and review of company standard operating procedures. Ensure the site remains current with all changes to applicable compendia, regulations and guidance. Manage direct reports, Responsibility includes training and developing direct reports to keep abreast of current technology as it relates to cGMP Compliance. Requirements Reports to Global Quality Head Minimum Experience & Education BA/BS in Biochemistry, Chemistry or related field, MS/MA preferable 13 + years of experience in Quality within the biotech or pharmaceutical industry, specifically with OSD Manufacturing highly preferred 5+ years experience in leadership position within Quality Required Knowledge & Skills Knowledge of 21CFR, ICH, USP and other applicable regulatory requirements and standards. Manage and host Regulatory inspections. Ability to maintain integrity and honesty at all times. Ability to communicate and lead with transparency. Lead department for optimal performance and set course for future improvements. Accountable for performance and results of department. Management experience required The above information on this description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job.

Reston Virginia Healthcare Exp 5-7 yrs Deg Bachelors Relo Bonus Occasional Travel Job Description Director of Hospital Quality • Works collaboratively with the Administrative Officers in developing a quality management strategy and annual goals. • Works with the Capital Division to facilitate corporate and division performance improvement initiatives such as Core Measure Compliance, Sepsis Improvement Project, Blood Utilization Initiative, SPAE and HAC reduction programs and reducing Hospital readmission rates. • Facilitates the development of the Quality Management strategy and goals throughout the hospital, utilizing the Hospital data farm and Performance Improvement projects • Leads the Quality Management department in the development and application of quality management and cost reduction strategies throughout the hospital. • Assumes responsibility for communication and education regarding quality management activities in the organization and the community and serves as a resource. • Responsible for and provides direction for Quality Improvement implementation, Core Measures compliance and Performance Improvement Outcomes Measurement. • Responsible for Leapfrog Survey (Quality Patient Safety Org), Q-HIP and pay for performance programs. • Utilize and maintain Crimson to monitor physician Quality performance issues and for Physician OPPE. • Liaison with Washington Regional Transplant Consortium. • Oversee Hospital Wide Policy and procedures on Policy Stat • Utilize QualityNet a Hospital Inpatient Quality Reporting Program • Interface with the VHQC (Commonwealth of Va. QIO) for reported quality of care issues. Qualifications Does this describe you? Does the candidate have recent Hospital Quality Experience? Does candidate have a minimum of a Bachelor's in Nursing Master's degree preferred CPHQ certification preferred Proven Leadership skills Excellent Customer Service Skills Experience in Core Measures compliance Performance Improvement Outcomes Measurement Additional Information All your information will be kept confidential according to EEO guidelines. Direct Staffing Inc

Full-time Description **US Based Candidates Only** Granules Pharmaceuticals, Inc., located in Chantilly, VA was the 10th fastest growing generic pharma company in United States in 2024 based on sales growth! We manufacture dosage forms with specific release capabilities including pulsatile drug release in tablet and capsule dosage form, orally disintegrating modified release tablets (XR, MR, ER), modified release suspension and controlled substances capabilities in an abuse deterrent technology platform, all supported by our API business. Granules is one of the few pharmaceutical companies to be vertically integrated from API to packaging. As a Director, QA Compliance, you will be accountable for the leadership activities and to direct all facets of Quality Compliance including, but not limited to, managing Quality Systems (incidents resolution, CAPAs, change control, complaints resolution), host FDA inspections and respond to questions arising from the inspections, oversee remediation activities for site-wide compliance improvements, external and internal audits, training with effectiveness checks, Quality metrics, data trending and evaluation with recommendations for cGMP Compliance improvements. Additionaly, you will ensure sustainable cGMP compliance, participate with regulatory bodies to address questions, and act as the lead for drafting responses to FDA Form 483 observations. The Director, QA Compliance, will provide regular monthly updates to senior management regarding the progress and status of cGMP Compliance. This is an on-site position. Provide leadership and direction regarding cGMP Compliance at the Chantilly site to ensure adherence to applicable Regulations. Excellent knowledge of the 21CFR, ICH, and USP to interpret and apply Regulations with respect to any questions related to cGMP Operations at the Chantilly site. Represents the department during high level discussions and investigations with external customers, vendors, and FDA representatives. Lead as the site Quality representative during FDA inspections. Lead the site in inspections conducted by external regulators and business partners. Conduct Compliance GAP analysis with recommendations for gap closure, implementation and follow up of effectiveness checks. Implement and follow through with site-wide remediation and improvement plans based on assessment of Quality metrics. Maintain Quality metrics for the site with analysis of data to sustain Compliance at the site. Responsible for building effective systems, processes and cross-functional teams to manage Compliance at the site. Manage and develop direct reports by setting clear expectations and resolving conflicts. Responsible to ensure adherence to company protocols and close in a timely manner any deviations from procedures or cGMP requirements. Interface with different departments regarding quality issues, audits and special projects. Provide guidance to manufacturing regarding Quality cGMP issues to ensure compliance with applicable standards and regulations. Provide technical expertise for personnel training, deviations, CAPA, inventory management, cGMP compliance and data trending. Review and approve, as required, OOS, SOPs, protocols and investigations. Coordinate and supervise the collection of data reported in the product review. Prepare, as required, and review documentation required for regulatory submissions. Serve on the Quality Task Force and participate in the generation and review of company standard operating procedures. Ensure the site remains current with all changes to applicable compendia, regulations and guidance. Manage direct reports, Responsibility includes training and developing direct reports to keep abreast of current technology as it relates to cGMP Compliance. Requirements Reports to Global Quality Head Minimum Experience & Education BA/BS in Biochemistry, Chemistry or related field, MS/MA preferable 13 + years of experience in Quality within the biotech or pharmaceutical industry, specifically with OSD Manufacturing highly preferred 5+ years experience in leadership position within Quality Required Knowledge & Skills Knowledge of 21CFR, ICH, USP and other applicable regulatory requirements and standards. Manage and host Regulatory inspections. Ability to maintain integrity and honesty at all times. Ability to communicate and lead with transparency. Lead department for optimal performance and set course for future improvements. Accountable for performance and results of department. Management experience required The above information on this description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job.

Responsibilities We are seeking a Quality Director to join our team of qualified, diverse individuals. The ideal candidates will be responsible for developing a quality management system that ensures processes and deliverables for mission-critical FAA systems meet defined quality standards. This position works closely with internal and external leadership stakeholders. This position offers an excellent opportunity to build a quality organization that supports high-visibility aviation programs. In this position, you will: * Provide leadership and direction for the quality management system (QMS) to ensure product and service excellence. * Serve as a member of the program's leadership team * Communicate and coordinate directly with internal and external stakeholders on all activities of the QMS * Lead a high-performing team of multi-disciplined quality practitioners Qualifications * 16+ years of relevant experience, to include leadership roles. * U.S. Citizenship Required. * Must have the ability to obtain / maintain a Public Trust clearance. * Strong knowledge of quality frameworks and best practices. * Experience implementing an ISO 9001:2015 QMS. * Experience leading multi-disciplined organizations through managers. * Demonstrated ability to make decisions guided by program strategy and priorities to ensure alignment. Preferred Qualifications: * Experience supporting FAA or aviation-related systems. * Experience supporting highly complex quality initiatives. * Experience leading integration teams with complex supplier relationships. * Experience using automation, tools, or innovative processes to increase efficiency and effectiveness of the quality management system. * Certifications such as Six Sigma Green belt / Black belt, PMP Peraton Overview Peraton is a next-generation national security company that drives missions of consequence spanning the globe and extending to the farthest reaches of the galaxy. As the world's leading mission capability integrator and transformative enterprise IT provider, we deliver trusted, highly differentiated solutions and technologies to protect our nation and allies. Peraton operates at the critical nexus between traditional and nontraditional threats across all domains: land, sea, space, air, and cyberspace. The company serves as a valued partner to essential government agencies and supports every branch of the U.S. armed forces. Each day, our employees do the can't be done by solving the most daunting challenges facing our customers. Visit peraton.com to learn how we're keeping people around the world safe and secure. Target Salary Range $135,000 - $216,000. This represents the typical salary range for this position. Salary is determined by various factors, including but not limited to, the scope and responsibilities of the position, the individual's experience, education, knowledge, skills, and competencies, as well as geographic location and business and contract considerations. Depending on the position, employees may be eligible for overtime, shift differential, and a discretionary bonus in addition to base pay. EEO EEO: Equal opportunity employer, including disability and protected veterans, or other characteristics protected by law.

Peterson Companies As one of the region's largest privately-owned real estate developers, Peterson Companies has been consistently delivering some of the area's most exciting destinations for more than 50 years. With a portfolio that includes National Harbor, Downtown Silver Spring, Fair Lakes, and Fairfax Corner, we continually strive to enhance the local community. We develop vibrant properties, and entire neighborhoods, that bring people together. Who You Are Seeking an energetic, personable, dependable individual to join a dynamic team responsible for the management and operations of a large Government campus in Chantilly, Virginia. The QA/QC Manager is an active team member responsible for maintaining high standards by ensuring that all operational activities and services meet or exceed customer expectations. Job duties include conducting routine inspections, managing contractors, developing and implementing improvement processes, communicating regularly with the team and customer, and assisting the team with project management duties. Must be comfortable working in a fast-paced environment. What You Bring Bachelor's or Associate's degree (preferred). Minimum 10 years' experience in facilities management, property management, construction or related field. Must be detailed oriented, organized, and possess strong communication skills. Proficient with Microsoft Office Suite and Adobe Acrobat. Must possess a Top-Secret security clearance. Key Responsibilities Establish and implement a quality assurance and quality control program to ensure all projects, management services and operational activities are completed at a high level of performance. Conduct comprehensive building and site inspections. Note deficiencies and any abnormalities. Work with the program management team to implement solutions. Become familiar with projects, contracted services and their scopes of work to verify quality of maintenance and construction by contractors. Contracted services include, but are not limited to janitorial, landscape, irrigation, trash removal, and snow removal. Assist with tracking and preparation of contract deliverables to ensure compliance. Manage or assist with management of contracts, services, and projects as assigned. Develop and maintain relationships with building staff, contractors, and customers. Handle customer complaints efficiently to maintain customer satisfaction. Assume other responsibilities and duties as required. Peterson Companies is an Equal Opportunity Employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, national origin, disability, protected veteran status, age, genetic information, marital status, or any other basis protected by law.

Job Title: Quality Account Manager (ITSM) Duration: Full -time. Salary: $130k to $140k Role Responsibilities: The Quality Account Manager will provide oversight and management of the federal contract in three key areas: Continual Service Improvement, Quality Control, and Data Analysis. Responsible for assuring consistent quality of services, products and solutions provided by the client. Contribute information and analysis to strategic plans and reviews. Prepare and complete action plans; implementing production, productivity, quality, and customer -service standards. Identify and resolve problems; completing audits; determining system improvements including SLA review and analysis as well as recommendations/implementation of improvement actions. Help implement change to move federal agency closer to best -in -federal -service. Continuously strive to improve understanding of project requirements, processes and deliverables required to contribute to successful project delivery. Investigate and analyze issues to root cause and propose the fix, verify and validate the final solution. Onsite work at client site in Washington D.C. Required Qualifications: Bachelor's Degree in Information Systems, Computer Science, Engineering, Business, or related field required 5+ years of proven experience as a Quality Assurance Manager or related role 3+ years of successful professional experience working in continual service improvement, quality control and design, or data analysis Extensive experience of ServiceNow reporting including workforce management modules Extensive experience with Service Desk operations Experience building and managing service desk teams Excellent writing and verbal communication skills, and ability to create substantial relevant project documentation based on client requirements Thorough knowledge of methodologies of quality assurance and standards Excellent numerical skills and understanding of data analysis/statistical method Required: ITIL v4 Foundation Certification Required: A Quality Assurance certification such as American Society for Quality, Six Sigma Black Belt, Lean Six Sigma Black Belt, etc., and proven documented experience. Candidates must be a US Citizen or a Legal Permanent Resident (Green Card status) for 3 years and be Federal Tax compliant. Optional/preferred Qualifications for QAM: PMP Certification Current MBI clearance with a federal agency Ability to build Forms and workflows using Microsoft PowerApps

Job Description Human Touch Home Health Care we are seeking a meticulous and dedicated Director of Clinical Compliance & Quality Assurance to join our team. As a QA Quality Assurance Specialist, you will play a crucial role in ensuring the quality and reliability of our home healthcare services. You will be responsible for designing and implementing tests, identifying defects, and collaborating with teams to resolve issues to deliver seamless experiences to our clients. About us: We are a home healthcare provider in the area. We provide comprehensive, skilled, and non-skilled services, to our home bound clients, with an excellent track record of client-focused care. We strive to help clients to improve their lives while in the comfort of their homes. To meet our standard of care, we offer a variety of affordable and high-quality home health care solutions that will meet the needs of the seniors, disabled, and ill members of the community. Benefits: Competitive salary commensurate with experience. Opportunities for professional development and career advancement. Comprehensive benefits package including: Health insurance Vision Dental Paid Time Off Sick Leave Retirement plans Responsibilities: Provide training to clinical staff on CMS and State specific guidance regarding outcome measures, compliance with regulatory requirements and education. Establish and implement home healthcare focused quality and performance improvement efforts in accordance with systems used (EVV, EMR, etc.) Train and supervise team members to ensure documentation of timely, fiscally sound, medically necessary care our clients and organization. Partner with administrator and DON to support continuous accreditation readiness (e.g. Mock surveys, Inter-Cycle Monitoring, Audits, etc.) Monitor and assist in preparing individualized clinical reports to help clinical management team improve patient care and outcomes. Support Peer Review efforts for Nurses and Caregivers on quality data, accreditation and regulatory standards. Supports activities/tasks resulting from client safety incidents/findings. Review past incidences, claims and liability reports to identify the risks the office is facing. Gather national and statewide data to provide comparison and guidance to determine where company is and develop new policies and procedures for improvement Provide recommendations and solutions to immediate quality assurance problems Create a risk management plan and conduct risk management training to clinical staff to help avert future problems. Develop new policies and procedures. Requirements: Must possess a current, unencumbered, active license to practice as an RN in this state (Compact License preferred). 5yrs (preferred) 3 yrs (required) Home Healthcare experience Current CPR and first aid certification 2 Yrs of Quality Assurance experience Experience in OASIS Strong knowledge of clinical operations, CMS and state regulations Management experience in the healthcare industry Experience interacting with multiple disciplinary teams Proficient in Microsoft Office Suite Excellent communication, relationship building and interpersonal skills Excellent Time management, organizational, and priority setting skills Excellent analytical and problem-solving skills Strong communication and collaboration skills Preferred Qualifications: Certified Professional in Healthcare Quality Certification (CPHQ) Work Schedule and Location: Full-time - Onsite Job Posted by ApplicantPro

Hi Consultant required for the below mentioned requirement QA Manager Duration : Long Term Prefer GC/citizen Skills • 4-5 Banking Industry Experience • MOBILE, MOBILE • Strong IT background - Developer background coupled with QA would be ideal • Experience managing teams - QA leads will be reporting into this person (THiS IS NOT A QA LEAD) • Responsible for reviewing all deliverables of Quality Engineers • Test strategy/risk management • Being able to speak to the product owners • Ensuring the right tools are in place for testing • Reviewing test scripts/automation scipts • Infrastrutuere in place • Technologies: SOAP, Cucumber, Ruby, Gethub (or other source management tool) • WORKED IN TRUE AGILE ENVIRONMENT IS KEY -- Thanks/Regards Ruchie Agarwal Desk: ************ Extn. 299 Cell : ************ Skype : ruchi.droisys Address: 4800 Patrick Henry Dr., Santa Clara, CA 95054 ********************** | *************** | Join Droisys Group “Don't wait for the perfect moment. Take the moment and make it perfect” Additional Information All your information will be kept confidential according to EEO guidelines.

We Are: Are you ready to step into the heart of digital transformation in one of the world's most critical - and most dynamic - industries? The Chemicals Industry is evolving at lightspeed: demand for sustainability-driven products is on the rise. At the same time, digital platforms, real-time analytics, AI, and SAP-enabled processes are no longer "nice to have" - they are foundational. As part of Accenture's SAP Chemical's Practice, you'll be delivering major SAP engagements (for example, Business Transformation Strategy & Roadmaps, migrations to SAP S/4HANA, process standardization, cloud-enablement) that help clients win in this new environment and guide major Chemical clients through the journey of business-model reinvention, process excellence and enterprise technology enablement You Are: Do you have a passion for storytelling and for originating, selling and delivering SAP-based Supply Chain Transformation projects that make a positive impact in your clients' business? Are you inspired by working with the best companies in their industries? Want a role that provides you with a sense of purpose and satisfaction? Then join Accenture and build a rewarding career improving the way the world works and lives, as you help clients innovate with leading-edge SAP and Accenture Supply Chain solutions and technologies on some of the most innovative projects in the world You will thrive in our highly collaborative, digitally-driven and innovation-led environment while nurturing your talent for thoughtful and game changing solutions in our inclusive culture that values diversity of ideas, experiences and backgrounds. Ultimately, you are a confident manager who spots and stays ahead of the SAP platform, industry and Supply Chain trends and knows how to translate client goals into clear and actionable outcomes that everyone can get behind. You know how to fully utilize the capabilities of various SAP platforms to drive business value, transform end-to-end functions and drive leading practices for your clients in markets all over the globe. The more complex their challenges, the more excited you are about leading the charge to solve them. The Work: Team with clients on their SAP functional transformation programs through your combined SAP application and functional process expertise which includes your ability to: * Engage with client executives on the business challenges/trends and the potential value of SAP solutions (current & future) * Lead customers in defining their SAP journey through the development of business cases & roadmaps including during sales origination, proposal development and client presentations * Architect E2E solutions that leverage SAP technologies, custom apps, & add on partner solutions * Advise, design and deliver solutions based on the latest industry and technology best practices leveraging a SAP solutions and embedded innovation. * Lead small teams - helping them achieve transformational roadmaps - onsite with clients or within Accenture * Become a trusted expert and advisor to your clients, team, and Accenture Leadership by staying current on regulations, trends, and innovations across your area of expertise * Be a thought leader, build assets and best practices and develop the next level of transformation experts Travel may be required for this role. The amount of travel will vary from 0 to 100% depending on business need and client requirements Qualification Here's what you need: * Minimum of 5 years of SAP functional and technical experience/expertise in Quality Management and/or Manufacturing. * Minimum 3 years of experience in SAP projects supporting Chemicals clients. (SAP support / managed services experience will not be considered for this requirement) * Minimum 2 end-to-end SAP S/4 implementations, including project planning, estimation and solution architecture for Chemicals clients * Experience managing SAP delivery teams, in a Global Delivery Model, including but not limited to the following responsibilities: driving complex workshops and leading design decisions, as well as leading the design and execution of system build, configuration, testing, cutover, and go-live in the SAP Transportation Management or Quality Management area * Prior experience in a Consulting and/or Advisory role * Bachelor's degree or equivalent (minimum 12 years' work experience). If Associate's Degree, must have equivalent minimum 6-year work experience Compensation at Accenture varies depending on a wide array of factors, which may include but are not limited to the specific office location, role, skill set, and level of experience. As required by local law, Accenture provides a reasonable range of compensation for roles that may be hired as set forth below. We anticipate this job posting will be posted on 01/24/2026 and open for at least 3 days. Accenture offers a market competitive suite of benefits including medical, dental, vision, life, and long-term disability coverage, a 401(k) plan, bonus opportunities, paid holidays, and paid time off. See more information on our benefits here: U.S. Employee Benefits | Accenture Role Location Annual Salary Range California $94,400 to $293,800 Cleveland $87,400 to $235,000 Colorado $94,400 to $253,800 District of Columbia $100,500 to $270,300 Illinois $87,400 to $253,800 Maryland $94,400 to $253,800 Massachusetts $94,400 to $270,300 Minnesota $94,400 to $253,800 New York $87,400 to $293,800 New Jersey $100,500 to $293,800 Washington $100,500 to $270,300 Locations

Department: CM FACILITIES Alpha Corporation established in 1979, is a full-service woman-owned firm, providing civil, and structural engineering, program and construction management, project controls, and technology services for various building types, transportation, and heavy infrastructure projects. We provide services to a broad spectrum of clients, including all levels of government agencies, public and private enterprises/partnerships. Alpha has been performing civil engineering design services since the firms inception. Our vision is to be recognized by our clients for responsive, innovative, and quality services in the building, transportation, and infrastructure sectors, and to be the employer of choice. Alpha was awarded the ENR Mid-Atlantic 2022 Design Firm of the Year and Top 100 PM/CM firm. If youre up for the challenge to stretch, grow and excel in your career as a Quality Control Manager consider joining our award-winning team at Alpha Corporation to support our growing team in our Dulles, VA office. Position Summary We are seeking a detail-oriented Quality Control Manager to provide quality control program oversite for clients in on site in data center environments. This individual will integrate with the general contractor team and play a pivotal role in ensuring construction quality aligns with standards, contract documents, and regulatory compliance throughout the lifecycle of the project. Responsibilities include: * Developing comprehensive QA/QC plans and assisting in developing work plans. * Reviewing contract drawings, specifications, and ensuring field compliance. * Verifying materials and equipment installations against approved submittals. submissions are approved and aligned with contract submittals. * Conducting frequent inspections to ensure quality and identify workmanship issues and improper installations. * Ensuring all testing and inspections are conducted as required and documented accordingly. * Tracking and documenting deficiencies; overseeing corrective actions; and conducting follow-up inspections. * Coordinating to prevent concealment of non-conforming work. * Leading QC coordination meetings to review open observations; schedules, including inspections, tests, and critical activities; logs; redlines, BIM, and as-builts; punch list items; and closeout documentation. * Ensure all preliminary work is complete and compliant before installation. Qualifications * 5 years of facility construction experience, BS preferred. * Proven experience in facilities quality control, data center experience preferred. * Strong knowledge of QA/QC documentation practices and coordination of subcontractors and special inspectors. * Proficient with construction drawings, specifications, and BIM coordination. * Proficient in Microsoft Office Suite and project management software. Procore experience preferred. Physical Demands The incumbent in this position can typically expect to sit and use his/her hands to handle and feel for more than 1/3 of the day. He/she can expect to stand or walk for more than 2/3 of the day. Talking and listening are also expected for more than 2/3 of the day. The ability to climb or balance, stoop, kneel, crouch or crawl, or reach with arms will be needed for less than 2/3 of the day. This position requires that the incumbent be able to lift items up to 10 pounds on an infrequent basis. The incumbent in this position should have clear vision at 20 inches or less. He/she should be able to view various reports and forms as well as information displayed on a computer monitor and have the ability to distinguish between different colors. Depth perception, peripheral vision, the ability to focus, and the ability to see from a distance are also necessary. EEO Statement Alpha Corporation is an equal-opportunity employer. We will not discriminate against employees or applicants for employment because of race, color, religion, sex, sexual orientation, gender identity, national origin, age, marital status, genetic information, disability or military status, or any other protected class. This policy shall apply to all employment actions, including but not limited to recruitment, hiring, upgrading, promotions, transfer, demotion, layoff, recall, termination, rates of pay, or other forms of compensation and selection for training, including apprenticeship, at all levels of employment.

Quality Control Manager Talent Pipeline | Ongoing Talent Pipeline | Always Hiring! Location: GlobalWhere: Onsite OpportunitiesClearance: Preferred (varies by role) Employment Type: Full-time Who We Are Working across the globe, V2X builds smart solutions designed to integrate physical and digital infrastructure from base to battlefield. We bring 120 years of successful mission support to improve security, streamline logistics, and enhance readiness. Aligned around a shared purpose, our $3.9B company and 16,000 people work alongside our clients, here and abroad, to tackle their most complex quality management challenges with integrity, respect, responsibility, and professionalism. If you are a quality-driven leader who thrives on implementing standards, driving process improvements, and ensuring compliance, we encourage you to join our Quality Control Manager Talent Pipeline today! This position description is subject to change at any time as needed to meet the requirements of the program or company. Responsibilities Roles We're Hiring For: We are always hiring across all levels for quality control management positions, including but not limited to: Mid-Level (3-7 Years Experience) + Quality Control Supervisor + Compliance & Process Analyst + QA/QC Engineer + Quality Systems Coordinator Senior-Level (7+ Years Experience) + Quality Control Manager + Senior Quality Assurance Manager + Director of Quality Management + Compliance & Risk Manager Qualifications Why Join V2X's Quality Control Manager Talent Pipeline? Career Growth: Access professional development, advanced training, and leadership opportunities.Competitive Benefits: Market-leading salaries, full benefits, and global career mobility.Mission-Driven Work: Lead quality assurance initiatives that enhance operational efficiency, compliance, and mission readiness worldwide. Who Should Apply? We are looking for quality assurance professionals with expertise in:✔ Quality control and process improvement✔ Regulatory compliance and ISO standards✔ Lean Six Sigma and continuous improvement✔ Risk assessment and mitigation✔ Supplier and subcontractor quality management✔ Defense, government, and mission-critical operations Certifications such as ISO 9001, Six Sigma (Green/Black Belt), ASQ Certified Quality Manager (CQM), and DoD-specific quality management qualifications are highly valued. Join V2X - Ongoing Talent Pipeline | Always Hiring Quality Control Managers! At V2X, we are deeply committed to both equal employment opportunity, including protection for Veterans and individuals with disabilities, and fostering an inclusive and diverse workplace. We ensure all individuals are treated with fairness, respect, and dignity, recognizing the strength that comes from a workforce rich in diverse experiences, perspectives, and skills. This commitment, aligned with our core Vision and Values of Integrity, Respect, and Responsibility, allows us to leverage differences, encourage innovation, and expand our success in the global marketplace, ultimately enabling us to best serve our clients.

Key Responsibilities: Provide daily on-site supervision of all construction activities. Coordinate subcontractors, vendors, deliveries, and materials. Ensure compliance with contract specifications, drawings, and schedules. Monitor progress, maintain production schedules, and provide daily reports. Conduct daily planning meetings with foremen and subcontractors. Serve as the primary point of contact for the field representatives. Safety (SSHO) Duties: Develop, implement, and manage the site-specific Accident Prevention Plan (APP). Ensure all site activities comply with EM 385-1-1 and OSHA standards. Conduct daily safety meetings, inspections, and audits. Maintain all safety documentation and logs. Report and investigate incidents, accidents, and near-misses. Promote a proactive safety culture across the project team. Quality Control (QC) Duties: Develop and implement the project-specific Quality Control Plan. Prepare and submit submittals and coordinate with design and procurement teams. Conduct 3-phase inspections (Preparatory, Initial, Follow-Up) for all definable features of work. Maintain the QC Daily Report, Deficiency Log, and ensure all work meets contract specifications. Coordinate to resolve any deficiencies. Required Qualifications: Minimum 5 years of experience in construction supervision, safety, and/or quality control. Must have completed the following training/certifications: EM 385-1-1 40-Hour Certification (current) OSHA 30-Hour Construction Safety CPR/First Aid Certification Construction Quality Management (CQM) for Contractors Strong knowledge of federal construction practices, submittal processes, and USACE procedures. Excellent organizational, communication, and leadership skills. Proficient in Microsoft Office Suite and construction management software. Preferred Qualifications: Bachelor's degree in Construction Management, Engineering, Safety, or related field. Previous experience in a combined Superintendent/SSHO/QC role. Experience with RMS 3.0 (Resident Management System). Active security clearance or the ability to obtain one (depending on project requirements). Work Environment: Must be willing to work in outdoor, construction site environments in various weather conditions. Ability to walk, climb, and stand for extended periods. Occasional travel may be required. Compensation: Competitive salary based on experience. Aleut offers the following benefits to eligible employees: Health insurance Dental/Vision insurance Paid Time Off Short- and Long-Term Disability Life insurance 401 (k) and match Aleut Federal, LLC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, sexual orientation, gender identity, or genetics. In addition to federal law requirements, AF complies with applicable state and local laws governing nondiscrimination in employment in every location where the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. AF prohibits workplace harassment based on race, color, sex, religion, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. #aac #zr

We are seeking a dedicated Quality Control Manager to oversee the construction of a $40 million insulated warehouse at Fort Meade. This project is currently a year in progress and has two more years to completion. The role involves managing the construction's steel structure, concrete, MEP installations, and the overall build. Responsibilities * Implement the entire Quality Control (QC) program. * Attend all post-award conferences, CQC plan meetings, and coordination and mutual understanding meetings. * Conduct CQC meetings. * Perform the three phases of the quality control process. * Review and approve submittals. * Ensure all required testing is performed. Essential Skills * Experience in quality control and OSHA compliance. * Experience with federal construction projects and USACE regulations. * Must possess an active QC certification. * Experience managing projects valued at $25 million or more. * Excellent verbal and written communication skills. * Ability to obtain an AOC Badge. * Certified Quality Control Manager. Additional Skills & Qualifications * Experience with MEP (Mechanical, Electrical, and Plumbing) systems. Work Environment The position is located on the construction site at Fort Meade. The work will be conducted during daytime hours, and the environment will involve working with cutting-edge technology. The company culture encourages learning from experienced project managers and executives, fostering a mindset of ownership as part of an ESOP company. Job Type & Location This is a Contract to Hire position based out of Sterling, VA. Pay and Benefits The pay range for this position is $90000.00 - $140000.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Sterling,VA. Application Deadline This position is anticipated to close on Jan 31, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

As the Quality Control Manager, you will be responsible for overall management and implementation of internal quality and serve as the central point of contact for quality matters. EDUATION & EXPERIENCE: Associates degree in Quality Management is preferred The QCM shall have a minimum of five (5) years' experience as a QCM, to include a minimum of two (2) years QCM experience in facility operations, maintenance and repair. KNOWLEDGE & SKILLS: The QCM shall have hands-on knowledge and experience in, as a minimum, the following areas: Progress Control, Quality Data Analysis, and Statistical Sampling. SECURITY CLEARANCE: Top Secret SCI w/ Polygraph Intrepid Acquisition Holdings, LLC ****************** Intrepid Acquisition Holdings, LLC. (IAH), is a leading provider of global-scale logistics, facilities management, and advanced professional and technical services. IAH provides a broad spectrum of services and solutions to U.S. and international government agencies, and organizations. As a world-class leader in providing seasoned program management, IAH leverages and integrates its capabilities to provide safe, innovative, and reliable solutions to meet customers' diverse and complex challenges. Intrepid Acquisition Holdings, LLC. (“IAH” and/or “Company”) and its affiliates, including but not limited to IAP World Services, Inc., Readiness Management Support L.C., JPATS Logistics Services, LLC., and subsidiaries is an EOE, including disability/vets. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Job DescriptionDescription: Manage and oversee inventory control and quality assurance operations for Pacific-region CIF facilities supporting NECC. Ensure accurate accountability, storage, and disposition of Infantry Combat Equipment (ICE) and related assets. Develop and maintain warehouse layout plans, storage configurations, and material flow to optimize space utilization and operational efficiency. Plan, coordinate, and execute cyclical, wall-to-wall, and spot inventories to maintain audit readiness and data integrity. Conduct quality control inspections on received, issued, returned, and reconstituted gear to ensure serviceability standards are met. Identify discrepancies, trends, and systemic issues; implement corrective actions in coordination with site leadership and the Project Manager. Oversee packing and preparation of material for shipment, transfer, or disposition through DLA Disposition Services. Ensure all inventory activities comply with PWS requirements, security protocols, and government property accountability standards. Support warehouse leadership in training staff on inventory procedures, documentation, and quality standards. Serve as a subject-matter expert for inventory accuracy, audit preparation, and process improvement. Requirements: Minimum of 3-4 years of experience in warehouse operations, inventory management, or quality control in a logistics environment. Prior experience in DoD, federal, or defense-related warehousing strongly preferred. Demonstrated experience managing inventory in high-accountability environments. Experience supporting audit readiness, physical inventories, and reconciliation processes. Skills & Competencies Strong understanding of inventory control principles and warehouse operations. Exceptional attention to detail and organizational discipline. Ability to analyze inventory data and identify process gaps. Effective written and verbal communication skills. Ability to lead by influence and collaborate with site leadership and warehouse staff. Proficiency with warehouse management systems (WMS) and inventory tracking tools. Commitment to accuracy, compliance, and operational integrity. Certifications / Education Associate's or bachelor's degree in Logistics, Supply Chain, Business, or related field preferred (or equivalent experience). Certifications in inventory management, quality assurance, or logistics are a plus. Security Requirement Public Trust is required. Candidates must be eligible to maintain clearance throughout employment.