Engineer 2, Quality Assurance

Arete Associates Inc Longmont , CO 80504

Posted 1 week ago

Aret Associates, an employee-owned company, is a growing research and development firm recognized for contributing to national security objectives by supplying innovative solutions to challenging technical problems faced by the United States. We have an immediate need for a Quality Engineer for our software development and laser manufacturing facility. We are looking for a dedicated professional who thrives in challenging environments. Our QA department focuses on creating, building, testing, and inspecting software & hardware products. As the QA engineer, you will be responsible for site level Quality Assurance functions.

SUMMARY:

Develops, modifies, applies and maintains quality evaluation and control systems and protocols for processing materials into partially finished or finished materials product. Collaborates with engineering laboratory and production functions to ensure quality standards are in place. Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment. Designs and analyzes inspection and testing processes, mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess control and manage risks of product quality and determine the responsibility for products or materials that do not meet required standards and specifications. Audits quality systems for development acceptance criteria (parameters based on product result). May undertake root cause analysis of incidents requiring corrective action. Ensures that corrective measures and deviation meet acceptable reliability standards and that documentation is compliant with requirements. May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality. May be certified in lean and six-sigma quality methodologies and utilize quality tools to help drive continuous improvement.

Primary responsibilities:

  • Provide QA support for the development and production of laser products in our production facility. These products are hardware related with software elements integrated.

  • Review requirements, specifications and technical design documents to provide timely and meaningful feedback

  • Monitor, audit and provide performance reporting on the production of deliverable hardware products.

  • Investigate the causes of non-conforming software and train users to implement solutions

  • Track quality assurance metrics, for instance, non-conformances, bug reports, root causes and corrective action activities.

  • Witness and verify regression testing and product acceptance testing.

  • Monitor and review quarterly supplier data

  • Review and process incoming material in support of production builds

  • Provide quarterly inspection data and quality assurance reports to senior management

  • Participate in all QA meetings Provide program managers and engineers with necessary data

  • Create and document inspection plans for incoming material and in process assemblies

Required Qualifications & Experience:

Bachelor's Degree or equivalent in Business Administration, Quality Assurance Engineering or related field preferred

  • 3+ years' experience in quality assurance

  • 2+ years' experience in electronics manufacturing environment

  • 1+ years' experience in software industry (secondary skill - a plus)

  • Strong knowledge of QA methodologies, tools and processes

  • Proficiency with Microsoft Office applications, including Word, Excel, and PowerPoint

  • Excellent written and verbal communication skills

  • Excellent organizational skills

  • Capacity to work independently and in a team

  • Proven capability to comprehend and represent technical product specifications

  • U.S. Citizenship and ability to acquire a security clearance

  • Experience working in an Agile/Scrum development process (a plus)

  • Understanding of QA process for software development, debugging and release (a plus)

Aret Associates offers an excellent compensation and a full benefits package. U.S. citizenship, background screen and drug test are required to meet position eligibility. Please submit your resume on-line at: http://www.arete.com

Aret Associates is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

If you are a qualified individual with a disability or a disabled veteran, you have the right to request an accommodation if you are unable or limited in your ability to use or access our career center as a result of your disability. To request an accommodation, contact a Arete Associates Human Resources Representative.

Aret will consider for employment-qualified applicants with criminal histories in a manner consistent with the requirements of the Los Angeles Fair Chance Initiative for Hiring.


icon no score

See how you match
to the job

Find your dream job anywhere
with the LiveCareer app.
Mobile App Icon
Download the
LiveCareer app and find
your dream job anywhere
App Store Icon Google Play Icon
lc_ad

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Senior Manager Quality Lean Lab

Avexis

Posted 2 days ago

VIEW JOBS 4/19/2019 12:00:00 AM 2019-07-18T00:00 Overview Ready to join a team committed to moving gene therapies into the clinical and commercial settings for patients and families devastated by rare neurological genetic diseases? AveXis is advancing cutting-edge science to treat rare and life-threatening genetic diseases starting with our clinical-stage, proprietary gene therapy candidate, AVXS-101 (ZOLGENSMA®). We are in the midst of an incredible journey and are looking for passionate individuals to join us on this important mission. AveXis, Inc., a Novartis Company, is a clinical-stage gene therapy company, dedicated to developing and commercializing novel treatments for patients suffering from rare and life-threatening neurological genetic diseases. Our initial product candidate, AVXS-101, is our proprietary gene therapy product candidate currently in development for the treatment of spinal muscular atrophy, or SMA, Type 1, the leading genetic cause of infant mortality, and for the treatment of SMA Type 2. The U.S. Food and Drug Administration, or FDA, has granted AVXS-101 Orphan Drug Designation for the treatment of all types of SMA and Breakthrough Therapy Designation, as well as Fast Track Designation for the treatment of SMA Type 1. In addition to developing AVXS-101 to treat SMA Type 1 and Type 2, we also plan to develop other novel treatments for rare neurological diseases, including Rett syndrome (RTT) and a genetic form of amyotrophic lateral sclerosis (ALS) caused by mutations in the superoxide dismutase 1 (SOD1) gene. The Senior Manager will play a critical role in helping QC nurture a culture of continuous improvement by implementing Lean Laboratory management systems and approaches. This person will help Identify and implement continuous improvement activities within the QC laboratories. The Senior Manager will coordinate activities relating to continuous improvement and enhance knowledge of the tools and techniques of continuous improvement / Lean methodologies. The successful candidate will work in a cGMP environment and must have the ability to manage multiple ongoing projects concurrently, have strong meeting facilitation and conflict resolution skills, a strong technical writing capability, be action oriented and compliant minded. The Senior Manager must have the ability to problem solve in an environment that is focused heavily on Chemical and Biological issues. The successful candidate will understand the concepts incorporated in Quality Assurance in a GMP environment. Responsibilities * Identifies and implements continuous improvement activities in the QC laboratories. Improvement projects include, but are not limited to cycle time improvement, consumable use reduction, cost reduction, variation reduction, constraint improvement, non-conformance reduction. * Provides coordination of activities relating to continuous improvement and enhancing knowledge of the tools and techniques of continuous improvement / Lean methods. * Identifies, plans and assists with the execution of various continuous improvement projects targeted towards improving the business performance related to quality, productivity, safety, compliance and cost. * Assist with manufacturing projects, from the initial scoping and chartering stage through project close-out with benefits realization. * Train laboratory staff on various operational excellence tools. * Encourages a Lean culture by influencing and empowering employees to identify opportunities to apply techniques and tools in everyday work activities. * Facilitate sharing of best practices and project successes across the organization. * Works on projects both individually and cross functionally. * Management of multiple projects and timelines concurrently. * Conflict resolution, problem solving in a cross functional setting, and ability to meet timelines. * Support strategic proposals, progress updates and presentations to all levels of the site organization. * Support implementation of Lean Laboratory principles throughout the AveXis network. Qualifications * Bachelor of Arts/Science or equivalent combination of education with strong and broad relevant experience. * Minimum of 6 years of practical experience with Lean methods / continuous improvement in a GMP environment. * Proficient facilitator of workshops and process improvement initiatives using continuous improvement methodologies. * Ability to quickly understand details, determine interdependencies and develop operationally practical and efficient solutions. * Experience/Knowledge in the OE/CI best practice methodologies, e.g. principles of Six Sigma, Lean Manufacturing, KPI development, RCA. * Must have one of the following: Six Sigma Black Belt, Green Belt, Yellow Belt or formal Six Sigma training. * Strong working knowledge of QC laboratory processes and instruments in a GMP environment. * Must have the ability to work in a fast paced, high workload environment, and be able to manage multiple projects and objectives for on-time event closure. * Must work well on a team and be able to trouble shoot and problem solve in a cross functional team setting. * Must be proactive, action oriented, and adaptable to change. * Must be able to identify and flag risks in a timely manner to keep deliverables on track. * Must have strong communication skills both verbally and written. * Must have proven logic and decision-making abilities, critical thinking skills. * Must be able to accommodate manufacturing schedule as required. * Must have strong Microsoft Office Suite (Word, Excel, and PowerPoint) skills. The level of this position will be based on the final candidate's qualifications. Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice. AveXis is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, national origin, genetics, disability, age, sexual orientation or veteran status. #LI-RM1 Avexis Longmont CO

Engineer 2, Quality Assurance

Arete Associates Inc