Quality Assurance Engineer Jobs in Maryland

Job Title: Staff - Engineer - Quality Assur Company: B Braun Medical Inc Location: Baltimore, MD Description: Company: B.BraunRequisition #: 1653Job Title: Staff - Engineer - Quality AssuranceState: PennsylvaniaCity: AllentownJob Description: B. Braun is a leading manufacturer of infusion therapy and pain management products with anenvironmentally-friendly focus. Guided by the company's "Sharing Expertise?" philosophy,B. Braun addresses the critical issues of infection prevention, medication safety andenvironmental responsibility by promoting best practices that help clinicians reduce medicationerrors, prevent healthcare-acquired infections (HAIs) and achieve sustainability objectives.Consistently recognized by Frost & Sullivan and KLAS for its medical technology and supportservices, B. Braun employees share their knowledge with colleagues and customers to improveworking processes in hospitals and medical practices and to enhance the safety of patients andhealthcare professionals. For more information, visit B. Braun at www.bbraunusa.com.We are currently seeking a Quality Engineer to support our Speciality Products Business Unit. This position will provide Engineering support and project management skills toward the design, development, installation, startup, validation, and maintenance of products, processes, and equipment, and provide technical expertise within Quality Assurance.(1) Research, develop, and prepare specifications for improvements to existing and/or new products, processes, equipment, and technology.(2) Support projects by contributing to the development of project schedules, teams, tracking costs, preparing status reports, conducting team meetings, and communicating issues and progress to management.(3) Prepare Request Capital Investments including project description, schedule, and costs.(4) Supervise and direct contract personnel and outside vendors in the performance of contracted services.(5) Provide leadership and guidance to subordinates within the Engineering organization.(6) Provide direction and technical decision making for management involving capital asset purchases and expenses for projects and/or strategic initiatives involving up to $2MM (capital/expense/revenue potentials).(7) Prepare and present technical investigative reports to middle level management.(8) Preparation of specifications and protocols for the development, testing, and qualification of equipment, processes, and products.Required:- Bachelor's degree (B.S. Engineering) from four-year college or university and 6-7 years related experience and/or training; or equivalent combination of 14 years of education and experience.Domestic travel with the possibility of occasional International travel.B.Braun offers an excellent benefits package, which includes healthcare, a 401(k) plan, company sponsored pension, and tuition reimbursement. To learn more about B. Braun and our safety healthcare products or view a listing of our employment opportunities, please visit us on the internet at www.bbraunusa.com An EOEThrough its "Sharing Expertise?" initiative, B. Braun promotes best practices for continuous improvement of healthcare products and services.Job Type: Full Time - RegularShift: 1st

Job Title: QUALITY ENGINEER Company: Location: Frederick, MD Description: QUALITY ENGINEER Trans-Tech, Inc., a subsidiary of Skyworks Solutions, Inc. (NASDAQ: SWKS), is located 5 miles south of Frederick, MD and is a manufacturer of advanced technical ceramics. This position develops, evaluates, revises and applies quality assurance methods to inspection, manufacturing processes, equipment and product. Ensures activities and items are in compliance to internal and external standards such as ISO 9001. Performs analysis, identifies trends and recommends actions when necessary. Ensures that established inspection, sampling and statistical process controls are followed. Evaluates and analyzes the efforts in organizing, documenting and interpreting inspection support documents and records. Requirements include Bachelors or 2 years experience, Outlook, and MS office with strong Excel skills. Experienced in using statistical software to analyze data, trouble shoot and resolve issues (e.g., SPC, Encore, JMP, SQC, Data Power). Knowledge of Documentation System Software, QSI, and FEMA. Able to apply strong problem solving skills while maintaining continuous improvement (e.g., Six Sigma, 8D, DOE). Please apply as follows: http://www.skyworksinc.apply2jobs.com/index.cfm?fuseaction=mExternal.showJob&RID=2608&CurrentPage=1 or apply to: TRANS-TECH, INC., 5520 Adamstown Rd., Adamstown, MD 21710. e-mail Register to View -EOE-

Job Title: Quality Engineer 3 (L) Company: Honeywell Location: Columbia, MD Description: This is an part time, temporary and on-callposition with no benefits associated with it.This position requires performance of duties supporting Aerospace quality initiatives, ranging from subject matter expert activity to auditing and training. The successful candidate may be called upon to perform auditing and insight/oversight of quality operations and products at aerospace or DOD suppliers and subcontractor locations.Review processes that show how activities are performed in operations, engineering, documentation, maintenance, industrial safety, training, and other disciplines for their technical content and adequacy. Perform administrative tasks such as preparing and submitting technical reports. Participate individually or as a member of an audit team and work with customer and contractor personnel on specific issues. Conduct professional audits and assessments in accordance with ISO 9000 and AS9100 guidelines. Provide a comprehensive and detail analysis of quality management systems, manufacturing processes, product inspection techniques, procedures, engineering drawings, and testing processes. Provide clear, concise, and detail analytical reports on reviews made during process audits, quality system assessments, mishap investigations, independent engineering technical reviews, and product inspections. Proficient in understanding engineering drawings and the interpretation and proper application of technical standards and specifications. Senior external and internal customer and program management interfaces are required. Participate in management review meetings as required. Develops, modifies, applies, and maintains quality standards for receiving, in-process, and final inspection in accordance with contractual requirements. Conducts tests, inspections, audits and validations to ensure process compliance withcontract requirements and specifications.

Job Title: Sr Quality Engineer - Production Company: AREVA Location: Baltimore, MD Description: Title: Sr Quality Engineer - ProductionLocation: Pennsylvania-CharleroiLooking for an exciting opportunity to work as a SR Quality Engineer? Areva T&D has just the opportunity for you!AREVA T&D is currently seeking a Sr Quality Engineer - Production. The Senior Design Quality Engineer will serve as the primary Quality Assurance representative for new product development projects. This person will provide feedback regarding the integrity and acceptance of design proposals as well as make recommendations concerning possible improvements or enhancements. The Senior Design Quality Engineer will also lead and participate in multi-departmental working groups to modify / generate new procedures as well as coordinate their implementation. He or she will lead efforts to investigate and resolve related quality issues and properly document these incidents. This person shall also assist, as necessary, in the implementation and maintenance of the company's quality management system as well as the general continuous improvement of the company's systems, processes, and products. The primary role will include:ESSENTIAL DUTIES AND RESPONSIBILITIES include the following.* Serves as primary Quality Assurance representative in R&D development project working groups* Participates in and provides feedback / recommendation in R&D development project Gate Reviews* Works with Production Industrial Engineers, QA Production Quality Engineers and R&D Project Managers to generate applicable quality procedures and processes* Evaluates R&D design proposals from multiple perspectives to determine integrity and validity* Works with Production Industrial Engineers and QA Production Quality Engineers to modify / develop, coordinate the implementation, and verify the effectiveness of Production procedures and processes* Leads multi-departmental working groups to investigate and resolve outstanding design quality issues and processes* Works with R&D, Inventory Control, Production, and Purchasing to define and document part handling and storage requirements* Generates and documents reports to record quality issues* Suggests and debates alternative methods and procedures in order to problem solve and to assist the organization in meeting changing technical and market requirements* Identifies areas for improvement and proposes, implements, and reviews effectiveness of subsequent corrective action(s)* Supports the Quality Assurance Manager in the maintenance of the Company's Quality Management System; Develops new procedures and work instructions, where appropriate* Uses the Company's electronic databases for the documentation of quality related data; Employs statistical methods to measure and analyze quality data as required* Participates and provides input, as required, relative to contract, project, and design reviews; Confers with Engineers in order to assure quality of new products and/or designs* Develops, directs, and implements quality assurance training for personnel as necessary* Performs other duties as necessary or assigned.AREVA T&D- The AREVA T&D division is an active player around the globe. It designs, manufactures and supplies a complete range of equipment, systems and services for all stages in the transfer of electricity, from the generator to the large end-user.AREVA- With manufacturing facilities in 41 countries and a sales network in more than 100, AREVA offers customers reliable technological solutions for CO2-free power generation and electricity transmission and distribution. We are the world leader in nuclear power and the only company to cover all industrial activities in this field. Our 65,000 employees are committed to continuous improvement on a daily basis, making sustainable development the focal point of the group's industrial strategy. AREVA's businesses help meet the 21stcentury's greatest challenges: making energy available to all, protecting the planet, and acting responsibly towards future generations.We offer competitive salaries, an excellent benefits package, and flexible work options, as well as a uniquely diverse and unified team of professionals. Our culture supports an environment where employees can continuously learn and gain professional growth through education, exciting projects and career mobility. AREVA recognizes your achievements and excellent performance through various performance incentive, recognition and reward programs. Our commitment is to you, the employee.Come work in an environment that is driven by integrity, innovation and visionary thinking. Join AREVA today, revolutionize the energy industry and energize your future!All candidates must meet the following minimum requirements in order to be considered for this opportunity. Candidates who exceed minimum qualifications may be considered for a higher level position.EDUCATION and/or EXPERIENCE* Bachelor's degree (B.S.) from a four-year college or university in a technical field and* 5 years experience in quality assurance related to a manufacturing environment (or* Equivalent combination of education and experience.

Job Title: QA Engineer Company: GE Location: Baltimore, MD Description: Job Number 1145237Business GE Technology InfrastructureBusiness Segment Technology Infrastructure - HealthcareAbout Us Thomas Medical Products is located in Malvern, PA. is a subsidiary of Vital Signs, Inc. is a wholly owned GE Healthcare company specializing in single-use patient interface devices. With a global workforce of 1500 employees and $400MM in annual sales, Vital Signs develops, manufactures and distributes a broad range of products to prevent and reduce hospital-acquired infections. These products include anesthesia breathing circuits, blood pressure cuffs, laryngoscopes, facemasks and body temperature control devices. As an affiliate business, Vital Signs participates in an independent benefits plan.GE Healthcare offers a broad range of products and services that are improving productivity in health and enhancing patient care by enabling healthcare providers to better diagnose and treat cancer, heart disease, neurological diseases, and other conditions. Headquartered in the United Kingdom, GE Healthcare is a $15 billion unit of General Electric Company (NYSE: GE). Worldwide, GE Healthcare employs more than 43,000 people committed to serving healthcare professionals and their patients in more than 100 countries.Posted Position Title QA EngineerCareer Level ExperiencedFunction QualityFunction Segment Quality AssuranceLocation United StatesU.S. State or China Province PennsylvaniaCity MalvernPostal Code 19355-1302Relocation Expenses NoneRole Summary/Purpose The Quality Assurance Engineer is responsible for providing manufacturing and/or engineering process support in accordance with documented procedures and practices. The Quality Assurance Engineer is responsible for the development, implementation, improvement and continuous reinforcement of established Quality Assurance fundamental practices that are utilized in the local business.Essential Responsibilities .Responsible for ensuring 100 percent quality and regulatory compliance in accordance with documented procedures for all aspects of functional responsibility..Responsible for the development, implementation, and continuous improvement of process effectiveness and efficiency at the site..Develops process improvement plans using a variety of Quality and Continuous Process Improvement tools, including but not limited to Six Sigma, Lean Manufacturing, 5S, SPC, engineering studies, DOE, Gauge R&R, etc..Ensures process efficiency and compliance effectiveness through the development and implementation of process verification and validation plans, including Master Validation Plans (Site Level), Validation Master Plans (Product or Process specific plans), and the development of simple yet detailed process flow diagrams that describe critical process interdependencies with respect to process inputs, outputs, risks and impacts..Supports continuous product and process improvement through detailed failure analysis for non-conformances, and investigates, develops and implements effective and compliant solutions for product or process corrections, retrospective and remediation action plans, and for corrective and preventive actions (CAPA Program)..Develops risk management tools and aids for use by the organization in accordance with documented procedures, including but not limited to PFMEA, DFMEA, Fault Tree Analysis, Failure Mode Analysis, etc. Supports design mitigation efforts. Develops process mitigation plans and strategies that are designed to mitigate the risks identified through the Risk Management process..Ensures process compliance through the development of simple yet comprehensive procedures, work instructions, flowcharts, forms, templates, checklists, worksheets, and other product and process related documentation..Performs a broad variety of tasks in support of product and process design as assigned by the departmental manager.Qualifications/Requirements 1.Bachelor's degree (or high school diploma/GED plus 4 years working experience in Quality Engineering or Quality Assurance Management.2.Demonstrated understanding or aptitude to understand Medical Device QMS requirements and regulatory requirements including but not limited to FDA CFR 21 820 and ISO 13485.3.Demonstrated understanding of product development lifecycles, design change and document change control, process verification and validation methodologies, manufacturing / production process control methodologies, and servicing in a medical device environment.4.Minimum 3 years Quality Assurance/Quality Engineering experience in the medical device or pharmaceutical industry5.Demonstrated experience using word processing, spreadsheet, and presentation software.6.Demonstrated understanding of continuous quality / process improvement tools:(As defined by the local site, e.g. DMIAC, SPC, Lean SS, 5S,)7.Ability to communicate using English (or local language)Additional Eligibility Qualifications GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.Desired Characteristics 1.Demonstrated knowledge of Quality Management System tools, continuous improvement methodologies & in-depth understanding of site level products & related processes2.Demonstrated expertise to effectively communicate within all levels of the organization around concepts of design controls, design verification and validation activities; production &process controls; Corrective & Preventive Action (CAPA), complaints & risk management; & product quality improvement using tools such as six sigma, DFR, etc.3.Demonstrated collaboration, negotiation & conflict resolution skills4.Excellent oral communication & report, business correspondence & procedure-writing skills5.Demonstrated ability to lead, acknowledge, develop, communicate & implement a strategy under crisis situations to ensure compliance6.Change agent with energy, passion & enthusiasm to drive change7.Exceptional analytical, problem solving & root-cause analysis skills8.Ability to multi-task & handle tasks with competing priorities effectively9.Integrity: Accepting & adhering to high ethical, moral & personal values in decisions, communications, actions & when dealing with others10.External Focus: Understanding customer needs, marketplace dynamics, industry trends, & the competitive landscape in the industry/function & considering the external impact of business activities & decisions on the external environment11.Inclusiveness: Energizing others by building a connection with the team through personal involvement & trust & providing feedback & coaching to help develop others12.Clear thinker: Simplifying strategy into specific actions with clear accountability, making decisions with speed & accuracy based on best available information & communicating priorities clearly & concisely 13. GEHC experience

Job Title: Microsoft .Net Sr. QA Engineer - To $90K Company: Betatech Location: Rockville, MD Description: Sr. Test/QA Manager.NET/C#Medical Research ApplicationsJoin an advanced Microsoft .NET applications development and testing team. This high-profile Sr. Test/QA Engineer opportunity in Rockville, MD offers stable employment, leading-edge technologies, and one of the best compensation and benefits packages in the industry. OverviewFor this position you will be a senior contributor and mentor on a team of 5 QA Engineers. You will be responsible for writing and executing test cases and scripts for Web and Windows based high-profile applications for the National Institutes of Health (NIH) in Rockville, Maryland. Using the .NET platform, C# and SQL Server on numerous systems, you will interact with developers through the entire life cycle to assemble data, and test applications critical to the scientific research of the NIH. This requires:* 3 years experience as the senior or lead on QA teams testing .Net applications* 7+ years hands-on experience writing and executing test cases/script for Web and Windows applications * BS in Computer Science or related field * Experience in writing and running SQL queries* Formal, structured testing; black box, white box, and regression * Problem solving, investigative, research and writing skills * Ability to work cooperatively as part of a small development team * Automation Tool experience a plus * Excellent ability to work cooperatively as part of a small, agile development team* Progressive, stable history in full life cycle formal testing * Financial/accounting background a plus This is a small, innovative consulting firm offering comprehensive services to corporations, government agencies and research organizations worldwide. Competitive salary and an excellent benefits package including medical, dental, vision, and 401(k).BetaTech, Inc.Attn: Peter Kenned Register to View Email: Register to View

Job Title: Production Manufacturing/Quality Engineer Company: NetCentric Technology, Inc. Location: Aberdeen, MD Description: Minimum Position Qualifications: Bachelor's degree in Electronics, Computer Science, Industrial Engineering, or Mechanical Engineering or the equivalent experience is required. Military test standards with a minimum of 3 years of experience. In addition, a minimum of 5 years of related experience is required demonstrating a sound understanding of materials, fabrication, finishing, and assembly processes. Knowledge and understanding of bidding and estimating techniques and the ability to review and advise the customer on production proposals (to include change orders). Excellent communication skills (verbal and written) as well as the ability to establish good working relationships with internal and external customers. The ability to analyze and resolve process issues varying from elementary to very complex. Preferred Additional Skills: Knowledge of Commercial/International Standards - ISO 9001:2000,CMMI, ISO 14001,ASME, ANSI, EIA, etc Working knowledge of processes and procedures to ensure compliance to specifications, procedures and industry standards. Ability to research and interpret unfamiliar standards & specifications. Basic understanding of contract quality requirements and flow down to suppliers/sub-contractors. Motivated, team player with the ability to work on cross functional teams. Strong people skills, customer service oriented, timely follow-up. Skill in Using PC applications (Microsoft Word, Excel). Skill in Use of basic inspection/measurement tools. Knowledge and understanding of documentation, processing and production paperwork Ability to read and understand drawings and product specifications Must have experience in progressive Quality methodologies, tools and systems such as Lean Manufacturing, Six Sigma principles, continuous improvement and AS 9100/ISO 9001 quality systems. Candidate must be: A US citizen Possess a U.S. Secret security clearance or be capable of obtaining one. Be able to travel 20% of the time.

Job Title: Senior Software Test Engineer - QA Test Engineer - Agile Test Engineer - TS/SCI w. FSP Company: CyberCoders Location: Columbia, MD Description: Senior Software Test Engineer - QA Test Engineer - Agile Test Engineer - TS/SCI w. FSP .body .body h4 .body .section tr.oddRow a, a:link, a:visited Senior Software Test Engineer - QA Test Engineer - Agile Test Engineer - TS/SCI w. FSP near Fort Meade, MD This job is open as of 3/4/2010. Apply Now! Not a fit for this job? Search other Test Engineer TS/SCI jobs! Are you an employer? Visit us for more info! Email this job to a friend - $1000 Location Fort Meade, MD; Columbia, MD Salary $95,000 - $120,000 Education Bachelor of Science Category Information Technology Experience Required At least 2 Years Short Description Senior Software Test Engineer - QA Test Engineer - Agile Test Engineer - TS/SCI w. FSP Required Skills Software Test Engineer, agile testing, automated testing, fitnesse, cucumber, selenium, HTML, javascripts, HTTP, HTTPS, GETS/POST request, Quality Assurance Engineer, SDET, Software Engineer in Test, Automated testing, COTs software, GOTs hardware, Mercury, Rational Recruiter Daniel Nadruz Date Updated 3/4/2010 Skills Required Software Test Engineer, agile testing, automated testing, fitnesse, cucumber, selenium, HTML, javascripts, HTTP, HTTPS, GETS/POST request, Quality Assurance Engineer, SDET, Software Engineer in Test, Automated testing, COTs software, GOTs hardware, Mercury, Rational Job Description Senior Software Test Engineer - QA Test Engineer - Agile Test Engineer - TS/SCI w. FSPWe are looking for Agile Testers who have a strong background doing automated testing and have an active Full Scope Poly! If you fit the bill.... please apply now!If you have worked with one of the following companies it is a plus! Caci, Saic, IBM, BAE, SRA International, Booz Allen Hamilton, Northrop Grumman, Praxis Engineering, Raytheon, General Dynamics, SGIS, CSC, Boeing, Halliburton, or Bechtel Group, please apply now!What you need:- You must have an active TS/SCI and FS Poly- Experience in software testing required. Good communication, collaboration, and writing skills required.- Understanding of web technology (HTML, Javascript, HTTP, HTTPS, GET/POST requests) required.- Experience with automated acceptance testing tools such as Fitnesse, Cucumber, Selenium, etc. desired- Experience working in an integrated environment made of COTs and GOTs software and hardware.- Developing Test Cases and Procedures- Experience working with Windows, Linux, and Unix based applicationsPurpose Of This Position:- Agile testers emphasize product testing from the perspective of customers who will utilize the system. - You will not emphasize rigidly defined testing procedures but focus on testing iteratively against newly developed code until quality is achieved from an end customer's perspective. - Developing Test Cases and Procedures- Agile testers provide information about the quality of the product under development and guide the development team in building quality in, not inspecting for problems after the fact. -Since working increments of the software are released often, there is also a need to test often.-The two goals are commonly achieved by a combination of automated acceptance testing and exploratory testing.What's in it for you:- Competitive salary- 20 days paid vacation- 10 days paid holidays- Bonus- 401k matching and 100% vested - Tuition ReimbursementSo, if you are a Senior Test Engineer or QA Engineer with Top Secret/SCI and Full Scope Poly, please apply today!Must be authorized to work in the United States on a full-time basis for any employer. Are you a fit for this position? Please Click Here to Apply! (your information will be kept strictly confidential!) Not a fit for this position? Click Here to Search Other CyberCoders Jobs! Looking forward to receiving your resume through our website and going over the position with you. Clicking apply is the best way to apply, or you may also: Email your resume in Word to: Register to View **Please do NOT change the email subject line in any way. You must keep the JobID: CC HotJobAp : DN-SW-Test-ENG-MD -- in the email subject line for your application to be considered.*** Daniel Nadruz - Executive Recruiter - CyberCoders Other Jobs

Job Title: PharmBio Product Quality Engineer Company: WL Gore Location: Elkton, MD Description: Gore is a technology-driven global company built on entrepreneurial innovation, integrity, and teamwork. Through our product leadership, we've been changing lives and changing industries including medical devices, fabrics, electronics, and manufacturing for more than 50 years.   We are seeking a Quality Engineer to join the Bioprocess Solutions Business Unit in our Industrial Products Division. In an organization dedicated to manufacturing products that are the highest quality, Quality Engineering at Gore is the place to be!   If you are searching for a company where you can make a difference, we're looking for you. Within this role you will have the opportunity to impact the quality of existing products during manufacturing as well as next-generation products during new product design and development.   The ideal candidate will Be passionate about manufacturing products that are the highest quality in their classBe energized by working in a hands-on, world-class manufacturing facility collaborating with Quality Assurance associates, process engineers, and new product development teamsRecognize the importance of building and maintaining strong interpersonal relationships   In the role of Quality Engineer, you will be responsible for Performing root cause analyses on product non-conformances, including product issues resulting from customer complaints, and driving resolution through engineering studies and corrective actionsSupporting elements of new product development by helping to drive the process development and documentation through validationDeveloping and implementing specifications for raw materials, components, and productsDeveloping and validating test methods for product safety, efficacy, and fitness for useRisk management   More specifically, you will Perform and write validations of products, processes, and equipment in accordance with Food and Drug Administration (FDA) and International Standards Organization (ISO) guidelinesDesign, execute, and analyze experiments based on statistical techniquesWrite procedures, train other associates, and assist other technical associatesEvaluate proposed improvements to processes and products based on analyses of regulatory requirements, product quality needs, ergonomics, safety, environmental, and economicsDesign and test prototypesDocument work via reports, technology notebooks, and design file entries  Required:   A Bachelors' degree in Science or Engineering; ChE, ME, Materials or Polymer Science, preferred7 + years engineering experience; previous hands on experience in process, quality or complex new product development preferredStrong project management skills, including demonstrated ability to prioritize, initiate, and drive projects to completionSolid knowledge of engineering fundamentals, including statistics, and the ability to apply this knowledge to manufacturing and product designAn ability to use experimental design, fundamentals of probability, and statistical process control tools to assure reliability, process maintainability, and product safetyStrong problem-solving skillsAn ability to lead teams by networking and interfacing effectively with a broad range of associates spanning varied disciplines and responsibilitiesDemonstrated excellent communication skills, both written and oral, including presentation skillsA working understanding of, or the willingness to learn, Quality System Regulations (QSRs) for appropriate Current Good Manufacturing Practices (cGMP) [21CFR 820, 21CFR 211, 21CFR 600 (including design control and risk management)] ISO 13485, and ISO 9000 requirementsDemonstrated ability to document thoroughlyAbility to work effectively in the Quality SystemWillingness to travel up to 15% Desirable Background in biochemistryPrevious hands-on experience with medical component manufacturing and/or product manufacturing EEO/AA Employer (applies to all positions located in the U.S.)Additional Information:Travel Percentage: 15%

Job Title: Quality Engineer 3 (L) Company: Honeywell Location: Baltimore, MD Description: Title: Quality Engineer 3 (L)Location: MD-GreenbeltThis is a part time, temporary, on call position with no benefits associated with itWORK WILL BE PERFORMED AT NASA Goddard Space Flight Center, Greenbelt, Maryland25% Travel Required.Quality Engineer on the Mission Assurance Services Contract providing insight and oversight activities for spacecraft manufacturing processes.Develop, implement, and maintain quality inspection programs for incoming, process, and final approval material and product inspections. Analyze compiled data from test and inspection reports to identify problems. Summarize, evaluate, and present data to management (both HTSI and NASA) for review and action. Coordinate Manufacturing/Quality Assurance/Safety reporting and interactions regarding flight hardware quality/safety. Assist other discipline engineering personnel with root cause and corrective actions associated with manufacturing issues. Participate in Material Review Board meetings and monitor corrective actions to closure. Assist in the development of test controls, process controls, and acceptance standards for new and existing products. Plan, conduct, and report audits on supplier and/or subcontractor processes. Ensure quality control programs and procedures are used to develop product and material.Other duties as assignedBasic Qualifications:Bachelor Degree plus five years of related experience. 13 years of directly related experience in lieu of formal education. Contract specific requiements will prevail.Experience with NASA, Flight hardware systems and components, EEE Parts, ISO9000, AS9100, and other related industry standards is required.Must be a U.S. CitizenKey Attributes:Excellent customer communication/interaction and presentation skills to various technical and non-technical audiences is required. Written skills must demonstrate the ability to accurately describe technical processes/requirements in a logical and grammatically correct manner is required.Ability to be self-directed with minimal management oversight is required.Workmanship Certification to NASA Workmanship Standards is required.Ability to produce work products using MS Office Word/PowerPoint/Excel is required.Knowledge of quality control programs and procedures.As an Equal Opportunity Employer, we are committed to a diverse workforce.