Air Quality Engineer Salary in California, USA

Quality Engineer IIIJob LocationsUS-CA-Redwood CityReq No.2020-6485CategoryITTypeRegular Full-TimeSummary of Major ResponsibilitiesAs a member of the Quality Engineering (QE) team in the IT Software Engineering department, the QE will play a key role in contributing to the successful delivery of products from conception to go-live with emphasis on software quality for an exceptional customer experience. This role will be involved in all phases of system development, including requirements, analysis, design, development, testing, and support.  The ideal candidate must demonstrate the ability to understand system architecture, design, implementation and possess the ability to succinctly develop the strategy to deliver high-quality results in a time-sensitive environment. Essential Duties and ResponsibilitiesParticipate in requirements, design, and review meetings.Execute test strategy, test plan, and risk assessment leading to successful implementation and timely project completion.Create, maintain, and execute test cases/test scripts (manual/automated) for the user stories developed to build new features and product functionality.Develop test scripts to verify workflow functionality and REST API’s.Create and execute SQL queries to verify data integrity.Report, track, and escalate anomalies discovered during testing and ensure closure on the issues.Collaborate with cross-functional teams to ensure timely and effective testing, as part of a regular release schedule.Ability to work proactively, independently, or as part of a team on multiple tasks and projects, and quickly learn new technologies.Strong organizational, problem-solving, and analytical skills.Excellent written and verbal communication; inclusive of technical documentation skills.Ability to integrate and apply feedback in a professional manner.Ability to prioritize and drive to results with a high emphasis on quality.Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork. Support and comply with the company’s Quality Management System policies and procedures. Regular and reliable attendance. Ability and means to travel between Redwood City locations.Ability to travel 5% of working time away from work location, may include overnight/weekend travel.QualificationsMinimum QualificationsBachelor’s Degree in Computer Science or related field; or High School Degree/General Education Diploma and 4 years of relevant experience in lieu of Bachelor’s degree.5+ years of experience with web-based enterprise application testing and technical/domain expertise in CRM solutions.2+ years of experience using tools like SOAPUI, JMeter, Selenium, TestNG.2+ years of experience working in an Agile/Scrum-like environment.Demonstrated ability to perform the Essential Duties of the position with or without accommodation. Authorization to work in the United States without sponsorship.Preferred QualificationsExperience testing web services and/or REST API using JSON/XML.Working knowledge of CI/CD framework.Knowledge of SDLC processes.Experience in SaaS, SaMD, or Cloud environments.Experience in SOA environments. Experience in working in a regulated environment (e.g., SOX, HIPAA, CLIA, GCP, and/or FDA). #LI-SS1We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to age, color, creed, disability, gender identity, national origin, protected veteran status, race, religion, sex, sexual orientation, and any other status protected by applicable local, state or federal law. Applicable portions of the Company’s affirmative action program are available to any applicant or employee for inspection upon request.

Location: San Jose, CADescription: Android Quality Engineer Location: Cincinnati, OH/San Jose, CA/Charlotte, NC/Boca Raton, FL/Chicago, IL/Portland, OR Duration: 12+ Months contract to hireAbout UsWe're committed to delivering exceptional experiences to our customers through our Ecommerce App. As an Android Quality Engineer, you'll play a critical role in ensuring the quality and reliability of our native Android components and experiences. From navigation features to user interfaces.Responsibilities Design, develop, and maintain native Android automation tests that validate key functionalities within the Ecommerce App. This includes navigation and informational features that guide and inform our customers. You'll also empower customers by ensuring seamless selection of grocery preferences (delivery or pickup). Collaborate with our software team to test new and existing native components and experiences during sprint and release events. Write clean, maintainable code for automation scripts, test cases, and release processes. Build and maintain the automation suite for the Android platform, closely monitoring the build pipeline to ensure optimal test performance. Provide manual testing support on the Android platform when required. Offer subject matter expertise during new feature planning and development. Document how-to instructions, setup guides, and reports for shareholder and partner teams. Investigate root causes of defects and document repeatable steps for reproduction. Champion effective communication practices by collaborating with Product, Design, Development, and other QA teams. Qualifications 3+ years of experience in software development and testing, with a focus on the Android platform. Strong proficiency in Android application development using Java or Kotlin. Hands-on experience with Android testing frameworks, including Espresso, UI Automator, and Appium. Familiarity with continuous integration and delivery pipelines (e.g., Jenkins, CircleCI, GitHub). Excellent problem-solving skills and attention to detail. Knowledge of Accessibility and Security: Testing apps for accessibility and ensuring they are secure from vulnerabilities. Effective communication and collaboration skills. Ability to translate requirements, wireframes, and mock-ups into test cases executed in the automation platform. Strong problem-solving abilities, detail-oriented, and comfortable working both independently and within a team. Thanks, Kris JonesThe Judge Group Contact: [email protected] job and many more are available through The Judge Group. Find us on the web at www.judge.com

Job Title: Software Quality Engineer for Andriod Level 3Location: RemoteJob Type: Contract C2C / W2Job Description:Qualifications:• Looking for 8+ years testing experience• 3+ years of experience in software development and testing, with a focus on the Android platform.• Strong proficiency in Android application development using Java or Kotlin• Hands-on experience with Android testing frameworks such as Espresso, UI Automator, and Appium.• Experience with continuous integration and delivery pipelines (e.g., Jenkins, CircleCI, Github).• Excellent problem-solving skills and attention to detail.• Knowledge of Accessibility and Security: testing apps that are accessible to everyone and secure from vulnerabilities is important.• Excellent communication and collaboration skills• Can translate requirements, wireframes and mock-ups into test cases that are executed in the automation platform• Strong problem-solving skills, detail oriented, works well in a team and individually.

I am working with a top company in the Medical Device space and they are building out their Supplier Quality team! They are looking for someone who is an experienced Senior Supplier Quality Engineer, skilled with class II and III devices. This role will focus both on NPD and Sustaining and this person will be responsible for leading their Supplier Quality Program. Responsibilities:Project ManagementSupplier Quality AuditsChange ControlIQ / OQ / PQ Continuous Improvement and Assesment of Supplier ProcessesSCAR Supplier qualifications and approval process as well as selecting new suppliersQualifications: Preferred PMP CertifiedASQ CQE Six Sigma Black Belt ASQ CQA 5+ years of experience in Supplier Quality in an ISO 13485 environment

Job Description There's no pledge more important than the one we make to look after our environment, and we're committed to helping you do exactly that! Join us as we strive to ensure a sustainable future for our communities and the world we live in. Become part of our global network of skilled engineers, scientists, auditors, planners and environmental specialists, all working together to leave this world better than we found it. Who are we looking for? GHD has an exciting opportunity for a Full-Time Air Quality Engineer in our West Region. The position will be located in Irvine, CA. We offer a professional, yet welcoming, culture based on our core values of Teamwork, Respect, Safety, and Integrity. We also provide accelerated professional development through hands-on experience, mentorship, and training via our GHD Business School. In an ever changing world, it requires creativity and innovation to stay ahead. We're seeking the curious, those who are stimulated by fresh thinking and a desire to shape our communities in new, positive ways. As part of a truly global team, working on complex and rewarding projects, you'll be at the forefront of driving change. See what the power of commitment can do for you. Working with an energetic and high performing team, this position offers a variety of work and will see you involved in: Collaborate with clients and colleagues meet to deadlines on unique and challenging projects. Work in self-directed role on air quality projects spanning a variety of disciplines including: air quality permitting, dispersion modeling, emissions reporting, regulatory compliance, audits, and more. Conduct air quality impact analysis with SCREEN3 and AERMOD. Communicate complex regulatory issues and concepts to technical and non-technical clients and project teams Support air quality compliance management in multiple industries, including: chemical/petro-chem, refining, electrical utility, petroleum refining, and manufacturing. What you will bring to the team: B.S. degree in Environmental Engineering, Science or a related field; M.S. preferred. 2-5 years of air quality permitting, compliance and/or modeling experience; consulting experience preferred. Knowledge of air quality rules, regulations and agency structure in Texas and surrounding states. Air dispersion modeling experience with SCREEN3 and AERMOD preferred. Experience with initial applications, renewals and revisions for variety of permitting mechanisms, including, but not limited to: Title V, NSR, NNSR, PSD, GHG, Standard Permit, and Permits by Rule. Ability to effectively communicate with other technical professionals, clients, and regulatory officials in person and in writing. Proficiency in relevant software. Take on some of the world's toughest challenges - with everyone at GHD backing you every step of the way! We'll give you control over your career, empower you to find innovative solutions and help you create a lasting impact. See where your commitment could take you with GHD. EEO Statement US: As a multicultural organization, we encourage individual achievement and recognize the strength of a diverse workforce. GHD is an equal opportunity employer. We provide equal employment opportunities to all qualified employees and applicants without regard to race, creed, religion, national origin, citizenship, color, sex, sexual orientation, gender identity, age, disability, marital status or veteran status. Salary Range: $74,980-$112,470 based on experience. #li-km1About Us Take on some of the world's toughest challenges - with GHD supporting you every step of the way. We'll give you control over your career, empower you to find innovative solutions and help you create a lasting impact. See where your commitment could take you with GHD. Our Pledge to You At GHD, we don't just believe in the power of commitment, we live and breathe it every day. That's why we pledge to empower our people to make a positive impact. Combining our deep technical expertise with the capabilities of our clients and partners, we respond to some of the most complex challenges facing our planet today. See where your commitment could take you. That's the #PowerOfCommitment Who we are GHD is a global professional services company that leads through engineering, architecture, and construction expertise. We are an employee-owned company with over 11,000 diverse and skilled individuals, across more than 200 offices spanning five continents. The Power of Commitment is our brand promise. It's what makes us different. We are bound to our stated vision and determination to address humanity's most urgent needs: to make water, energy and urbanisation sustainable for generations to come.

Description:• Act as a quality engineer for medical device QMS quality improvement activities, with a focus on design controls and risk management.• Provide oversight of quality improvement activities and ensure compliance with FDA 21 CFR Part 820, 21 CFR Part 4, ISO 13485, ISO 14971, and other applicable domestic/international regulatory requirements, including Gilead quality system requirements.• Plan and support implementation of approved quality improvement action items and deliverables.• Interface with internal stakeholders and contract manufacturers to address and resolve complex technical drug-device combination product, process, and quality issues. • Act as an escalation contact for complex and high impact quality issues, concerns and decisions.• Support strategic relationships with internal cross-functional teams and related CMOs.• Provide training as needed for cross-functional stakeholders.• Provide guidance and impact assessments for Change Control, including DHF/RMF assessments.• Write and/or implement changes to controlled documents (e.g., SOPs, specifications, test methods, etc.).• Anticipates shifts in industry trends and regulatory environment that will impact Gilead's business needs and positions the function to respond accordingly.• Collaborate with R&D during new combination product development and provide input into the design controls process.Knowledge & Skills:• Demonstrates understanding and application of QSR/GMP principles, concepts, best practices and standards in the US and internationally.• Can develop and improve complex concepts, techniques, and standards and new applications based on quality principles and theories.• Demonstrates strong knowledge of medical devices, combination products and general pharmaceutical manufacturing.• Can provide guidance to solving problems, uses Gilead Quality standards, regulations and industry best practices.• Demonstrates knowledge of industry best practices and trends.• Demonstrates excellent verbal, written, and interpersonal communication skills.Typical Education & Experience:• 3+ years of relevant experience in a GMP environment related field and a BS or BA. OR 4+ years of relevant experience and a MS.• Knowledge and experience in quality assurance for development of drug-device combination products• Previous experience with combination products is required, such as autoinjectors, co-packed kits, pre-filled syringes.• QA experience in both clinical and commercial combination products.• Strong project management and process improvement skills.• Demonstrates understanding of domestic and internal quality systems regulations to adopt best in class systems/processes and drive continuous improve• Knowledge of Six Sigma, Define-Measure-Analyze-Improve-Control (DMAIC) methodology, performance measures and quality improvement statistics is preferred.• Knowledge of Risk Management principles according to ISO 14971, including the use of risk management tools such as FMEA.About ActalentActalent 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.Diversity, Equity & InclusionAt Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:Hiring diverse talentMaintaining an inclusive environment through persistent self-reflectionBuilding a culture of care, engagement, and recognition with clear outcomesEnsuring growth opportunities for our people 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 process due to a disability, please email [email protected] for other accommodation options.

At Boeing, we innovate and collaborate to make the world a better place. From the seabed to outer space, you can contribute to work that matters with a company where diversity, equity and inclusion are core values. Were committed to fostering an environment for every teammate thats welcoming, respectful and inclusive, with great opportunity for professional growth. Find your future with us. JOB SUMMARY The Senior Supply Chain Quality Engineer champions drives improvements with suppliers using analysis and implements corrections and improvements using quality tools such as Process mapping, SPC, FMEA, Six Sigma, Kaizens, A3s, fishbones, root cause analysis etc. The Senior Supply Chain Quality Engineer monitors suppliers and ensures the management of the company's quality, process and/or business improvement efforts within the Supply Chain. He / She interfaces with Procurement / Purchasing to improve the relationship and performance with the supplier. The Senior Supply Chain Quality Engineer will visit suppliers and be heavily engaged in ensuring product conformance and craftsmanship from suppliers. The Senior Supply Chain Quality Engineer is also responsible for rate readiness assessments as well as approving and disapproving suppliers. SUMMARY OF JOB DUTIES - Essential Functions (Other duties and projects may be assigned or requested.) Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions The Senior Supply Chain Quality Engineer will visit suppliers and be heavily engaged in ensuring product conformance and craftsmanship from suppliers Monitors the performance of Suppliers Approves, disapproves suppliers Champions improvements with suppliers using analysis and implements corrections and improvements using quality tools Ensures the management of the company's quality, process and/or business improvement efforts within the Supply Chain. Performs rate readiness assessments with suppliers Interfaces with the supplier on program quality issues. Assists with supplier audits. Creates craftsmanship and inspection plans and drives requirements to suppliers Participates in MRB and CCB Reviews nonconformance reports with suppliers Assists with supplier audits GENERAL QUALIFICATIONS Education, Knowledge, and Experience Education: 4 year technical Bachelors degree required Experience: At least 1 years in the quality environment Skills: Proficient with Microsoft Office programs, Office, and with MRP systems. Advanced Excel skills Preferred Skills/Experience: Strong trouble shooting skills and communication skills. Advanced Spreadsheet building and Microsoft Office Skills. Ability to read engineering drawings, specifications and other related literature is necessary. Proficient with general quality systems and with the following tools: Process mapping, SPC, FMEA, Six Sigma, Kaizens, A3s, fishbones. Ability to communicate professionally with suppliers Other: Extended or irregular hours may be required. Travelling and visiting suppliers is a requirement. CERTIFICATES AND LICENSES ASQ Quality Engineer Certificate desired SUPERVISION PROVIDED TO THE POSITION Direction is provided for assignments in terms of desired outcome (goals), timing and budget. Work is reviewed or measured in terms of meeting organizational objectives and schedules. LEADERSHIP RESPONSIBILITY Has no direct reports, however, the Supply Chain Quality Engineer is expected to lead improvement and corrective action events and provide guidance to suppliers. PROBLEM SOLVING Develop and provide solutions to complex problems based on established precedents and are consistent with organization objectives. LANGUAGE SKILLS Ability to communicate effectively in English, both verbally and in writing.

RESPONSIBILITIES:Kforce's client, a growing and established Medical Device Company is seeking a Medical Device Software Quality Engineer in San Diego, CA. We are working directly with the Hiring Manager on this search assignment. The company offers a competitive compensation including base salary, annual bonus, and a generous Stock/RSUs Plan. The candidate must reside in the San Diego metro area. This position is Hybrid Remote.Responsibilities: Medical Device Software Quality Engineer will work with software teams to ensure that the software projects are meeting regulations and quality standards You will take ownership of software projects for regulatory compliance and champion for process excellence by driving their teams towards conformance at every stage of development Creates and reviews various software lifecycle project deliverables based on procedural requirements Performs risk analysis and is responsible for risk management activities determines, evaluates, and documents software risks from product design to post-launch Analyzes test results to ensure existing functionality and requirements are met, and if necessary, recommends corrective action Provides traceability analysis and traceability reports to ensure project requirements have been met Participates on the Software Review Board (SRB) to evaluate and disposition software anomalies As a Medical Device Software Quality Engineer, you will review and approve CO's as well as provides quality input to support closure (QMS updates, Procedural changes, etc.) Provides quality input to Complaint, FA, CAPA investigations and executes corrective actions when applicable Please note that this role will not be responsible for any software development or software testing; This is an FDA Medical Quality Engineering positionREQUIREMENTS: BS degree in Engineering, Biotechnology, or Computer Sciences or related field or equivalent combination of education and years of applicable experience At least 2-5 plus years of experience acting as a Medical Device Quality Engineer on software projects and guiding cross-functional teams towards compliance in an FDA-regulated industry Strong working experience in Risk Analysis and Risk Management is required Working knowledge of federal and other regulations including QSRs, ISO 14971, IEC 62304 Skilled at promoting team cooperation and a commitment to team success An understanding of the Software Development Lifecycle (SDLC) Knowledge of mobile app technologies is a plus but not required Visa sponsorship is not available for this position The pay range is the lowest to highest compensation we reasonably in good faith believe we would pay at posting for this role. We may ultimately pay more or less than this range. Employee pay is based on factors like relevant education, qualifications, certifications, experience, skills, seniority, location, performance, union contract and business needs. This range may be modified in the future. We offer comprehensive benefits including medical/dental/vision insurance, HSA, FSA, 401(k), and life, disability & ADD insurance to eligible employees. Salaried personnel receive paid time off. Hourly employees are not eligible for paid time off unless required by law. Hourly employees on a Service Contract Act project are eligible for paid sick leave. Note: Pay is not considered compensation until it is earned, vested and determinable. The amount and availability of any compensation remains in Kforce's sole discretion unless and until paid and may be modified in its discretion consistent with the law. This job is not eligible for bonuses, incentives or commissions. Kforce is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.

Will be responsible for assisting the Quality Manager in creating, maintaining and distributing documentation in accordance with the ISO9001 Quality Management SystemWill plan, manage and conduct internal audits and serve as a lead auditorWill also be responsible for root cause analysis and monitor corrective actionsMust have a least 2+ years of experience out of a Surface Mount Technology manufacturerISO Facility experience is required

A growing consulting firm in California is looking for an Air Quality Consultant to join their team. The individual will review processes, technical and regulatory issues, and execute permit functions for various clients to meet their compliance needs. This is a client-facing role and some travel will be required as part of the job. California air regulation experience is a must.The Role:Provide technical expertise, and develop, implement, and support programs and tools that help ensure proactive complianceEnsure that air quality programs, procedures, training, work practices, and controls are effectively implemented and developed up to client standardsConducts all necessary actions regarding Title V, Emissions Reporting, Green House Gas, RECLAIM implementation and reporting, technical and regulatory issues, etc.Build relationships and collaborate with employees at all levels, both within the organization and with external clientsThe Candidate:B.S. or M.S. Degree (preferably engineering or science-related)8+ years of work experience, particularly with air quality compliance/regulations.Experienced in air permitting and regulations, including; BAAQMD, SCAQMD & Title V.Working knowledge of federal and California state environmental regulations.Multisite or project management experience interfacing with regional stakeholders.