Quality assurance manager jobs in California

4+ years of testing experience working as a test lead on large scale Salesforce implementation projects. Experience in large-scale implementation projects in State/Local Government/Federal is required. Minimum 2+ years of hands-on experience working as a Lead for UAT full cycle implementation. Responsible for the design, documentation, and execution of automated and manual test cases, and scripts across all stages of the software development life cycle (Agile/SCRUM). Strong in analyzing business requirements and specifications developing of test plans, test scripts, and test cases, and executing them Ability to coordinate with Clients, Business Analysts, and Tech teams. Bachelor's degree is required.

Localization QA III Duration: Contract We are seeking a skilled Localization QA III to join our team in Cupertino, California. In this role, you will assist in localization efforts, coordinate localization QA, work with vendor testers both locally and internationally, and collaborate with multiple team members within the internal team. You will be responsible for creating QA plans, supporting QA efforts in the localization lab, fixing bugs, and ensuring the delivery of high-quality localized products in up to 40 languages simultaneously. The ideal candidate will have the ability to quickly identify and escalate issues while effectively communicating status updates to management. Responsibilities: Create and execute QA plans for localization projects. Support QA efforts in the localization lab. Identify, track, and resolve bugs to ensure high-quality localized products. Coordinate with vendor testers locally and internationally. Collaborate with internal team members to meet project deadlines. Effectively communicate project status and escalate issues as needed. Qualifications: Solid understanding of Localization Workflows, Software Development, and Software QA. Experience with content management databases and localization tools. Proven record of localization project management, testing, and bug tracking. Outstanding organizational and time-management skills. Ability to work independently in a global team environment. Excellent written and verbal cross-functional communication skills. Experience managing and delivering multiple projects within tight timeframes. High level of focus and meticulous attention to detail. Ability to identify and prioritize key deliverables and address blockers promptly. Flexibility, strong organizational skills, and adaptability to changing directions. Inventiveness, analytical skills, and a strong drive to learn and succeed. Preferred Skills: Competence working on iOS, mac OS, and other platforms, with familiarity with client products and services. Experience with scripting in Python and JavaScript. Native-level fluency in one or more languages besides English. Education and Experience: Bachelor's degree or equivalent experience in localization or QA. About PTR Global: PTR Global is a leading provider of information technology and workforce solutions. PTR Global has become one of the largest providers in its industry, with over 5000 professionals providing services across the U.S. and Canada. For more information visit ***************** At PTR Global, we understand the importance of your privacy and security. We NEVER ASK job applicants to: Pay any fee to be considered for, submitted to, or selected for any opportunity. Purchase any product, service, or gift cards from us or for us as part of an application, interview, or selection process. Provide sensitive financial information such as credit card numbers or banking information. Successfully placed or hired candidates would only be asked for banking details after accepting an offer from us during our official onboarding processes as part of payroll setup. Pay Range: $50 - $55 The specific compensation for this position will be determined by a number of factors, including the scope, complexity and location of the role as well as the cost of labor in the market; the skills, education, training, credentials and experience of the candidate; and other conditions of employment. Our full-time consultants have access to benefits including medical, dental, vision and 401K contributions as well as any other PTO, sick leave, and other benefits mandated by appliable state or localities where you reside or work. If you receive a suspicious message, email, or phone call claiming to be from PTR Global do not respond or click on any links. Instead, contact us directly at ***************. To report any concerns, please email us at ******************* GC1

Kinovate Life Sciences, Inc. established in 2004 in Oceanside, California. A wholly owned subsidiary of Nitto Denko Corporation (*************** Kinovate was spun-off from Oceanside, CA based R&D facility Nitto Denko Technical Corp (**************** with a mission to provide the highest quality materials to niche life science markets worldwide. Since its inception, Kinovate has grown to become the market leader in solid support in the oligonucleotide synthesis field. We are bringing the most creative minds in science and technology to develop medical discoveries and breakthroughs. Our customers are well-known in the biotechnology industry. We are in a growth phase within ISO work environment and leading towards a GMP Certification. KLS is seeking extraordinary people to join the team. KLS is proud to be an equal employment opportunity employer. Why Work Here Great place to work. Small subsidiary of large international company headquartered in Japan. Generous discretionary bonuses. Health, dental, vision, life, and disability insurance effective from date of hire. Additional benefits include 401(k), 3 weeks vacation in your first year, 12 paid yearly holidays, 5 paid sick days, tuition reimbursement and more. JOB SUMMARY: Under strategic leadership, sustain the improvement of the Quality Management Systems (QMS) and manages the development of quality assurance & systems staff. Utilize the following industry standards to drive high-quality products: Current Good Manufacturing Practice (cGMP), International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH), and International Organization for Standardization (ISO). Facilitate employee relations issues including coaching, mentoring, and disciplining including performance evaluation of employees. Provides strong leadership to motivate, guide and inspire employees to meet the organization's business objectives with production. Lead the implementation phase of MasterControl, ensuring successful implementation, and post-implementation management. ESSENTIAL DUTIES and/or RESPONSIBILITIES: Partners with leadership to develop the Quality Management System (QMS) and ensure it is compliant with relevant regulations, including ISO 9001, 21 CFR Part 210 and 211, ICH, and other applicable national and international regulatory guidelines.Ensure the QMS always remains in an auditable state. Oversees the daily operations of the QMS, ensuring it runs efficiently and in compliance with quality standards. This includes managing critical quality systems processes such as Incoming Raw Material Receipt, Raw Material Review/Disposition, Final Product Review/Disposition. Manages quality events and investigations including but not limited to Deviations, CAPA, Change Control, OOS, OOT, Customer Complaints, including leading and facilitating cross-functional meetings to ensure proper assessments and actions. Ensures QA review of Validation/Qualification activities including protocols, execution, and reports. Upholds timely response to events and on-the-floor QA support(MQA), including ensuring the MQA program is tracked and measurable. Leads the transition of QMS programs, such as Quality Events (Deviation, CAPA, Change Control, OOS, OOT), Audits and Supplier Qualification transition into Master Control, and serves as the System Administrator. Administers post-implementation management of MasterControl, including, but not limited to, system optimization, performing troubleshooting support, managing software updates, and continuously improving system functionality to meet evolving regulatory needs. Reports key metrics for QA Operations turnaround times and Quality Events. Contributes to the continuous improvement initiatives related to the QMS, collaborating with cross-functional teams to optimize quality processes. Analyze quality data and metrics to identify trends, root causes, and areas for process improvement within manufacturing and quality control activities. Develops standard operations and other quality documents related to QMS and ensure all documents meet regulatory requirements and internal standards. Supervises and develops a team providing guidance, training, and support to ensure compliance with regulatory standards and best practices. Mentors and develops a team of the QA team, fostering an environment of accountability and growth. Ensures cross-functional collaboration and provide effective leadership managing the QMS processes and ensures effective employee relations. Facilitates training initiatives to ensure that team members are adequately prepared to handle QMS functions and sustain a flexible workforce. Fosters a culture of continuous improvement, supporting staff development and efficiency improvements within the quality systems team. Conducts performance reviews for direct reports. Institutes timely corrective actions and interfaces with Leadership and HR in developing disciplinary actions up to and including terminations. Administers time-keeping functions to track absenteeism; approves timecards on a bi-weekly basis. SUPERVISOR RESONSIBLITIES: Quality Assurance Associate Quality Assurance Specialist Sr. Quality Assurance Specialist MINIMUM EDUCATION and/or EXPERIENCE: Bachelor's degree in a scientific discipline; and five (5) years' directly related experience in a Good Practice (GXP) or ISO manufacturing-controlled environment or equivalent combination of education and experience. Experience in transitioning from paper based to electronic QMS. KNOWLEDGE, SKILLS and/or ABILITIES: Working knowledge of pharmaceutical industry concepts, as well as analytical methods and writing skills, including documenting manufacturing processes, a plus. Familiarity in Lean or Six Sigma, a plus. Strong Knowledge of quality management principles and practices, including ISO 9001 and cGMP standards. Proficient in the use of quality management software with experience in implementing or managing MasterControl being highly desirable. Experience conducting technical investigations with formal root cause analysis tools. Prior supervisory experience, preferred. Knowledgeable of change control, validation/qualification, and method development and tech transfer. Strong knowledge of formal root cause analysis and risk assessment tools. Ability to lead or facilitate investigations and/or risk assessments. Strong application of critical thinking skills along with problem solving and creative skills to identify manufacturing issues for continuous improvement. Strong multi-tasking skills, flexibility in responding to rapidly changing, dynamic processes and demands/pressures in a fast-paced environment. Strong ability to verbally communicate across functional organizational groups, provide high-level customer service through effective interpersonal skills and conflict resolution, including communicating with equipment suppliers to obtain input on equipment modification and improvement. Microsoft Office Suite software applications such as Excel, Word, Power Point, and other enterprise software applications such as Net Suite, LIMS, and Familiarity with statistical analysis tools. Strong language skills with the ability to read, analyze and interpret general business periodicals, professional journals, technical procedures, or government regulations. Write clear processes, manuals and reports for management review and present technical information in understandable terms and respond to questions from groups of customers, employees and/or public. Work independently as well as in a small and/or large group and foster cooperation in a team environment using interpersonal skills to document working knowledge. Work in a detail-oriented environment with strong follow-up, follow-through, and organizational skills. CERTIFICATES and/or LICENSES: American Society for Quality Certified, a plus. Certified Quality Engineer, a plus. Certified Quality Auditor, preferred. PHYSICAL DEMANDS and/or WORK ENVIRONMENT: (Typical physical demands and the work environment characteristics an employee must meet and encounter while performing the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.) Works in a typical office environment with prolonged periods in front a computer entering or researching data. Regularly required to sit; use hands to finger, handle or feel and talk or hear. Availability and willingness to travel if required for audits, inspection, vendor management or if requested to visit or attend a business transaction as legal agent of the company. Must be able to work extended hours per the demands of the business.

📍 San Diego County, CA | Competitive Pay & Benefits The Opportunity A respected federal contractor is seeking a Construction Quality Control (QC) Manager to join their West Coast field operations team. You'll oversee QC programs for military and federal projects throughout San Diego County. This is an on-site leadership role suited for someone who thrives in compliance-driven environments and is committed to delivering projects to the highest standards of quality and safety. Key Responsibilities Plan, coordinate, and implement project-specific QC programs in line with contract requirements. Ensure documentation, reporting, and administrative tasks are completed accurately and on schedule. Cultivate strong client relationships and represent the company's mission, vision, and values on every project. Support field teams by monitoring work quality, enforcing compliance, and maintaining safety and environmental standards. Ideal Candidate Profile Bachelor's degree in Engineering, Architecture, Construction Management, or related field (or equivalent experience). 5-10 years of construction experience, including at least 2+ years in a dedicated QC Manager role. Current USACE CQM for Contractors certification required. Specialty inspection training, LEED certification, and OSHA 30/EM 385-1-1/CPR/First Aid certifications preferred (training available if needed). Strong computer skills; Vista/Viewpoint software experience a plus. Proven track record on military/federal or highly regulated projects. What's on Offer ✔ Salary $100K-$145K (DOE) ✔ Full benefits (medical, dental, vision, PTO, holidays) ✔ Vehicle allowance & bonus eligibility ✔ Career growth within a leading Design/Build federal contractor About the Company Our client is a full-service contracting and design firm with a primary focus on Department of Defense projects. Their mission is to deliver the best built environments while remaining the first choice of all stakeholders.

Hi, Everyone ******W2 CONTRACT ONLY***W2 CONTRACT ONLY***W2 CONTRACT ONLY****** 100% Closure & Long-term project, Immediate Interview Surely Job Title: QA / Test Coordinator Loc: San Francisco, CA( onsite) Contract : w2 Contract Note :8+ years exp , Job Details: Coordinate with business end users and offshore development team Create the test data for System test and Integration testing Prepare Test strategy Perform E2E Testing and create test Evidence Support UAT Thanks, Mahesh *********************** NOTE: Please share your updated resume to *********************** or can reach out me at ************.

2 year contract with Whiting Turner Company, one of the largest General Contractors in the US! Working on base at Travis AFB in Fairfield, CA. Must be local to NorCAL to apply, no relo candidates will be considered. Excellent potential to extend to 3 years, excellent potential to convert to permanent with Whiting Turner! Full benefits provided day 1 during the contract. We are seeking a highly qualified Quality Control Manager to oversee a renovation build project in Fairfield, CA to work onsite at Travis Airforce Base. The ideal candidate will have a 4-year engineering degree and a minimum of 5 years of experience working on federal projects. Experience with NAVFAC projects is highly desirable. Candidates must also possess CQM and OSHA 30 certifications. Responsibilities: - Develop and implement quality control processes and procedures to ensure compliance with federal regulations and project specifications - Conduct regular inspections and audits to identify and address quality issues - Collaborate with project managers, subcontractors, and other stakeholders to resolve quality-related issues - Provide training and guidance to project team members on quality control requirements and best practices - Maintain accurate records and documentation related to quality control activities - Communicate effectively with project stakeholders to address quality concerns and promote a culture of quality excellence REQUIRED SKILLS AND EXPERIENCE: - Bachelor's degree IS REQUIRED; non-negotiable per government requirement (end client) - Minimum of 10 years of experience in construction - Minimum of 2 years of experience as a Quality Control Manager and must be recent experience -Federal construction project experience -Experience working on a construction project with a minimum budget of $10M++ - CQM Certification is required - Cannot be an SSHO - must be only QCM NICE TO HAVE SKILLS AND EXPERIENCE: -Experience on NAVFAC project - OSHA 30 Compensation: $52.00/hr to $58.00/hr. Exact compensation may vary based on several factors, including skills, experience, and education. Benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.

Job Title: Manager of Quality Improvement Target Compensation Range: $95,000 - $105,000/year, depending on the relevant qualifications and experience. About Us: Astiva Health, Inc., located in Orange, CA is a premier healthcare provider specializing in Medicare and HMO services. With a focus on delivering comprehensive care tailored to the needs of our diverse community, we prioritize accessibility, affordability, and quality in all aspects of our services. Join us in our mission to transform healthcare delivery and make a meaningful difference in the lives of our members. SUMMARY: The Manager of Quality Improvement oversees critical medical management functions including Quality Management, Quality Improvement (QI), Risk Adjustment Factors, and Quality Assurance. This role serves as a key leader, responsible for advancing assigned areas toward enhanced capabilities and operational efficiency in alignment with Astiva's strategic plan, goals, and objectives. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following: Responsible for developing strategy, deploying systems, refining workflows, ensuring ongoing operational compliance, and consistently achieving results and metrics related to Quality Management, Quality Improvement (QI), and Quality Assurance. Maintains compliance with operational procedures and reporting standards to meet or exceed state and federal requirements. Works with senior management to establish a strategic vision for STARS improvement that aligns with Astiva's business planning process. Formulates strategies and carries out tactical plans aimed at enhancing HEDIS, CAHPS, HOS, and other STARS-related measures. Designs and supervises monitoring and reporting protocols to keep deliverables and budgets aligned with expectations. Annually reviews and updates the QI program, which includes evaluating its effectiveness, updating work plans, and revising Medicare policies and procedures for review and implementation. Develops quarterly processes for reporting on QI activity progress. Oversees the operations of the health plan's credentialing program. Guarantees adherence to all relevant federal, state, and local laws and regulations. Partners with internal departments to uphold compliance with the QI program and its policies. Prepares reports and facilitates discussion and action by the Utilization Management/Quality Assurance Committee and during Board of Directors Meetings. Collects, organizes, examines, and presents data regarding risk adjustment factors (RAF). Conducts comprehensive, concurrent, and retrospective reviews promptly. Develops and applies strategies to strengthen risk adjustment processes for accurate and thorough data collection. Performs audits focused on the precision and completeness of risk adjustment documentation. Recruits and retains skilled staff members to execute strategic and operational objectives, while managing succession planning and leadership development. Maintains regular communication with providers, members, employees, auditors, and regulators as needed. Regular and consistent attendance. Other duties as assigned. EDUCATION and EXPERIENCE: 7+ years senior-level Managed Care operations experience required Master's in Public Health, Health Science, or RN/NP/BSN licensure 5+ years QI experience at the plan level preferred Proven ability to build health plan QI programs Must be able to travel for work up to 5% of the time Experience with HMO, Medi-Cal/Medicaid, Medicare, insurance, or relevant government/public service preferred Board reporting and strategic planning experience preferred Experience overseeing delegated medical groups, IPAs, and contracted healthcare entities OTHER SKILLS AND ABILITIES: Conduct analysis and revise policies across all business lines for Quality and Population Health Management Programs. Demonstrate comprehensive expertise in HEDIS, STARS, RAF, HCC, and additional related quality and clinical care measures. Possess thorough knowledge of core functions within the health plan environment and effectively address associated challenges. Grasp primary objectives and systematically deconstruct them into actionable steps. Display exemplary leadership qualities to guide and influence teams. Apply advanced problem-solving, analytical, and organizational skills with careful diligence. Communicate effectively and professionally in both verbal and written formats. BENEFITS: 401(k) Dental Insurance Health Insurance Life Insurance Vision Insurance Paid Time Off

About Us: Pistola is redefining modern denim through craftsmanship and innovation, blending timeless style with forward-thinking design to create iconic, sustainable, and functional pieces that inspire confidence in every fit. As a Los Angeles-based contemporary apparel brand under KNG-Pistola and Daze-we're known for effortlessly elevated essentials with a clean, cool California aesthetic. **This position is based full-time onsite in our Vernon, CA HQ. Position Overview: As Quality Assurance Manager, you'll be the guardian of Pistola's product integrity-ensuring every piece we produce meets our exacting standards for fit, construction, and finish. From reviewing TOP, final audit reports and INDC samples, you'll lead the QA process with a sharp eye, technical expertise, and a collaborative approach to reporting back the issues found, to partnering closely with Production, Technical Design, Overseas QA teams and our vendor network. This role requires a balance of strategic oversight and hands-on involvement, ensuring our customers receive garments that embody Pistola's premium quality and effortless style. ** This role is based at our Los Angeles (Vernon) HQ and requires in-office attendance Monday through Friday. What You'll Do: Quality Standards & Inspections Continuously refine our QA procedures across all production stages, in-house and with vendor partners. If needed, help implement updates. Oversee and manage final inspections and INDC samples, verifying specifications, measurements, construction, and finishing, that aligns with brand standards Experience working with Inspectorio and being able to generate and analyze all KPI's. Team & Vendor Leadership Collaborate with our QA staff and inspectors, setting clear performance expectations and fostering a culture of accountability and excellence Partner with overseas factories to maintain consistent quality across all production runs by being able to implement company procedures and standard industry protocols to train vendors QC's to internally audit their own operation following our methods Provide constructive, actionable feedback to vendors and guide them toward corrective measures when issues arise Process Optimization & Problem-Solving Collaborate with Technical Design to analyze recurring defects and develop solutions that improve quality outcomes and manufacturing efficiency Maintain detailed inspection reports, defect logs, and quality metrics to inform decision-making and track performance trends Compliance & Safety Ensure all products meet regulatory requirements, including CPSIA, labeling, and brand compliance guidelines Ability to review and problem solve, third-party testing results What You Bring: 10+ years of quality assurance experience in apparel manufacturing is required (denim, RTW, or adjacent categories preferred) Deep understanding of garment construction, sewing techniques, pattern-making, and finishing methods Proficiency with AQL standards, inspection methodologies, and quality documentation Strong leadership skills with proven ability to inspire and direct a team in a fast-paced, deadline-driven environment Exceptional communication, organization, and analytical problem-solving abilities Proficiency in Microsoft Office and/or PLM systems; familiarity with RLM or similar apparel software a plus

Job Title: Quality Control Analyst-III Duration: 6+ Months Qualifications: - Bachelor's Degree in Chemistry or related field - Minimum 5 years of relevant pharmaceutical experience Responsibilities: - Perform complex testing and data evaluation - Perform complex Liquid/Gas Chromatography, UPLC, and other testing, and, as needed, troubleshoot issues - Participate in or assist with test method validations - Evaluate data for trends - Support supervisors in OOS Investigations and complete CAPA requirements - Interact with outside departments including attending meetings, providing updates, etc. - Coordinate testing performed at outside testing labs, raw materials, etc. - Maintain a detailed and accurate recording of activities and results on paperwork - Execute, author, and review SOPs, reports, protocols, investigations, change controls, and data summaries. Understand and use basic risk assessment and root cause tools - Train upon and understand methods, equipment and standard operating procedures - Provide training to others as needed. Attend internal and external training on related subjects, including both intra- and inter-departmental cross-training on new techniques and procedures - Support equipment upkeep - Prepare and order supplies, as necessary - Enter data into relevant data management systems. Perform tracking and trending of data as requested. Compile data and provide data summaries to management - Utilize a thorough understanding of regulatory and compliance guidelines for the pharmaceutical industry - Interact with other departments within the company for testing needs and scheduling - May lead departmental projects with the opportunity to participate in or lead cross-functional teams, including continuous improvement projects and new customer teams - May lead stability program including management of test points, reporting of data, and investigations of out of specification or aberrant stability results

In today's market, there is a unique duality in technology adoption. On one side, extreme focus on cost containment by clients, and on the other, deep motivation to modernize their Digital storefronts to attract more consumers and B2B customers. As a leading Modernization Engineering company, we aim to deliver modernization-driven hypergrowth for our clients based on the deep differentiation we have created in Modernization Engineering, powered by our Lightening suite and 16-step Platformation™ playbook. In addition, we bring agility and systems thinking to accelerate time to market for our clients. Headquartered in Bengaluru, India, Sonata has a strong global presence, including key regions in the US, UK, Europe, APAC, and ANZ. We are a trusted partner of world-leading companies in BFSI (Banking, Financial Services, and Insurance), HLS (Healthcare and Lifesciences), TMT (Telecom, Media, and Technology), Retail & CPG, and Manufacturing space. Our bouquet of Modernization Engineering Services cuts across Cloud, Data, Dynamics, Contact Centers, and around newer technologies like Generative AI, MS Fabric, and other modernization platforms. Job Title : Quality Assurance Automation Lead Location: Westlake Village, CA Ideal experience: Required - 10 years of hands-on experience in software testing including automation and Manual. Test automation with strong expertise in Web UI automation (Selenium, Playwright), API automation (RestAssured, Postman). Strong expertise in Java programming with TestNG/JUnit, execution, reporting, building reusable test frameworks, and integrating with CI/CD pipelines (Jenkins, GitLab CI, Azure DevOps). Ability to write SQL queries to set / retrieve the data for testing. Experience leading automation strategy and collaborating with cross-functional teams to embed quality in the SDLC. Bachelor's degree in computer science, information systems, or other technology-related field or equivalent number of years of experience Preferred: Strong understanding of SDLC and STLC methodologies, with hands-on experience in Agile/Scrum delivery models. Domain knowledge or experience in one or more industry verticals (e.g., Financial Services, Healthcare, Retail, Technology, etc.). Experience in designing and presenting automation strategies, frameworks, and results to stakeholders, including both technical and non-technical audiences. Exposure to cloud platforms (AWS, Azure, or GCP) and modern DevOps practices (CI/CD, containerization, microservices testing). Familiarity with performance testing, security testing, and test data management practices. Ability to multitask across various projects and initiatives, ensuring quality and timely delivery under dynamic priorities. Exposure to usage of AI tools like CURSOR, COPILOT, GEMINI in testing Why join Sonata Software? At Sonata, you´ll have an outstanding opportunity. The chance to use your skills and imagination to push the boundaries of what´s possible. To build never seen before solutions to some of the world's toughest problems. You´ll be challenged, but you will not be alone. You´ll be joining a team of diverse innovators, all driven to go beyond the status quo to craft what comes next. Sonata Software is an Equal Opportunity Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, national origin, gender identity, age, religion, disability, sexual orientation, veteran status, marital status, or any other characteristics protected by law.

Macro-Z-Technology (MZT) is a leading construction company known for building exceptional projects through an unwavering commitment to its people. With a strong reputation in the Federal and Municipal construction markets, MZT has built everything from roadways and dams to multi-story building construction and complete facility renovations. With an in-house design department, we specialize in design-build projects. As a Quality Control Manager at MZT, you'll play a pivotal role in overseeing the successful completion of our construction projects. You will be responsible for managing the entire project lifecycle, which includes ensuring adherence to timelines, budget, and quality standards. You'll interface regularly with the Client, Client stakeholders, and other construction professionals to resolve project challenges. Your strong leadership, organizational skills, and construction expertise will be vital in driving the successful completion of projects that are safe, on-time, within budget, and leave the Client satisfied. We are looking for Quality Control Managers with experience working on Federal and Civil construction projects (roads/bridges, wastewater/sewer systems, railways, tunnels, dams, airports, etc.). While we appreciate candidates from other construction backgrounds only those with Civil construction experience will be considered. Company Culture MZT covers 100% of the premium for medical, vision, and dental insurance for you and your family because we want you to be well. You won't find this benefit anywhere else. MZT supports professional development. Whatever your growth goals are, we're here to provide support. We offer an incentive for you to get your PMP or CCM certification within your first six months of joining our team. MZT trusts your skills and expertise. We encourage our Construction Project Managers to exercise their judgment, explore innovative approaches, and seize opportunities for growth, while guided by our core values to delivering projects that align with our commitment to excellence. Teamwork is at the heart of everything we do. As part of our team, you will be an integral part of a collaborative and supportive environment. We value the power of collective knowledge and believe that together we can achieve remarkable results. You'll work directly with the company owner - your voice will be heard. Room for growth? You bet! Over 20% of MZT's key leaders started in the field. Job Summary We are seeking a dedicated and detail-oriented Quality Control Manager to oversee and enhance our quality assurance processes within the construction industry. The ideal candidate will possess a strong background in construction management and quality control, ensuring that all projects meet the highest standards of quality and compliance. This role involves analyzing data, conducting inspections, and collaborating with various teams to uphold our commitment to excellence. Responsibilities Develop and implement quality control procedures for construction projects. Conduct regular inspections on construction sites to ensure compliance with contract specifications. Analyze research data collection methods to improve quality assurance processes. Oversee the quality inspection of materials and workmanship throughout the project lifecycle. Collaborate with project managers and contractors to address any quality-related issues promptly. Prepare detailed reports on quality inspection findings and recommend corrective actions as necessary. Train and mentor staff on quality control standards and best practices. Stay updated on industry trends and regulations related to construction quality management. Qualifications Proven experience in construction management or a related field. Strong knowledge of quality control processes including construction inspection techniques, preparing documentation, and establishing best practices on the job site Experience working with Corp of Engineers MUST HOLD QCM/CQCM CERTIFICATION Ability to analyze complex data sets and derive actionable insights. Excellent communication skills, both written and verbal, for effective collaboration with teams. Detail-oriented with a strong focus on accuracy and compliance. Familiarity with relevant regulations, standards, and best practices in the construction industry. Ability to work independently as well as part of a team in a fast-paced environment. What We Offer Salary: $100,000 - $120,000 per year DOE Health, dental, and vision insurance premiums 100% paid for you and your dependents Life Insurance (100% premium paid by the company for the employee only) 401(k) with 100% match up to 4% of salary Paid time off Opportunity for bonuses based on performance Schedule Full time Hours vary, weekend work may be required In office or on-site where the project is located Must be willing to travel EEO We're dedicated to creating a respectful workplace that values diversity and offers equal employment opportunities for all qualified candidates. We celebrate our diverse team and ensure that every applicant is considered based solely on qualifications, without discrimination. We abide by the requirements of 41 CFR 60-741.5. This regulation prohibits discrimination against qualified individuals on the basis of disability, and requires affirmative action by covered prime contractors and subcontractors to employee and advance in employment qualified individuals with disabilities. VEVRAA/This contractor shall abide by the requirements of 41 CFR 60-300.5(a). This regulation prohibits discrimination against qualified protected veterans, and requires affirmative action by covered prime contractors and subcontractors to employee and advance in employment qualified protected veterans.

Serve as the contractor's designated Construction Quality Control Manager, responsible for overseeing and executing the Three-Phase Quality Control process (Preparatory, Initial, Follow-Up) in accordance with EM 385-1-1 and the project's approved CQC Plan. This role ensures all work is performed in line with contract requirements, technical specifications, and safety standards through consistent inspections, documentation, and collaboration with the USACE Quality Assurance team. Essential Duties & Responsibilities Manage the Contractor Quality Control (CQC) program and ensure full compliance with project specifications and contractual obligations. Organize and lead Preparatory, Initial, and Follow-Up meetings for each Definable Feature of Work (DFOW), maintaining all related documentation. Perform daily quality inspections and complete CQC Daily Reports using RMS 3.0. Confirm that materials, equipment, and deliveries match approved submittals and contract requirements. Coordinate with testing labs, third-party inspectors, and the Site Safety & Health Officer (SSHO) to maintain alignment between quality and safety efforts. Review shop drawings, RFIs, and submittals for accuracy and compliance prior to government review. Maintain up-to-date as-built drawings along with logs for deficiencies and corrective actions. Facilitate and record the Mutual Understanding Meeting and ongoing QC coordination meetings. Ensure corrective actions are implemented promptly and verified through re-inspection. Support onsite teams by confirming that workmanship meets established quality expectations. Provide training to subcontractors and field supervisors on CQC procedures, testing requirements, and documentation standards. Interface daily with USACE Quality Assurance representatives and government testing personnel. Maintain records of inspections, tests, re-inspections, and related documentation in accordance with EM 385-1-1. Submit recurring QC summary reports and assist with close-out documentation. Qualifications - Required Current USACE Construction Quality Management for Contractors (CQM-C) certification. At least 5 years of CQC experience on USACE or Federal construction projects of similar size and complexity. Strong working knowledge of EM 385-1-1, ACI 301, ASTM standards, and USACE QC requirements. Bachelor's degree in Construction Management, Civil Engineering, or equivalent field experience. Proficiency with RMS 3.0, Bluebeam, Prolog, and Microsoft Office applications. Excellent communication, documentation, organizational, and leadership abilities. OSHA 30-Hour Construction Safety certification. Ability to interpret construction drawings, specifications, and QC submittals. Qualifications - Preferred ACI Concrete Field Testing Technician Grade I or PE/CI certification. Background in cast-in-place concrete, post-tension systems, or structural parking projects. Experience working on design-build projects under Federal contracting. Understanding of LEED requirements and sustainable construction practices. Tools & Systems RMS 3.0, Prolog, Bluebeam, Microsoft Office Suite Coordination with accredited testing laboratories and project-specific QC templates.

CHAGEE (pronounced CHAH-jee) is a modern teahouse with more than 7,000 locations globally. We are a global brand with proud roots in Yunnan, committed to bringing people together through tea. CHAGEE is awakening a modern tea movement, grounded in authentic heritage, fueled by cutting edge innovation, and crafted to nourish body and spirit. Position Overview: Elevate your career with CHAGEE as a Senior Quality Assurance Manager Through our stores across China, Asia Pacific, and the United States, we serve a staggering 100 million cups of tea monthly. CHAGEE is excited to expand its presence in the US market. This is your chance to be part of an exhilarating journey as we deliver the taste of authentic tea culture to America. What you'll do: Program Establishment & Leadership Design, implement, and maintain a company-wide Food Safety & Quality Management System for beverage QSR operations. Build robust HACCP/HARPC plans, allergen management, sanitation protocols, and preventive controls tailored to beverage production and service. Create documentation, training materials, and SOPs that can scale with growth. Regulatory & Ingredient Compliance Ensure all operations and products meet FDA, local health department codes, and applicable GFSI-benchmarked standards (e.g., SQF, BRC). Verify regulatory compliance of all ingredients, including allowable additives, nutritional labeling, and country-specific regulations for current and future markets. Quality Standards & Operations Define quality specifications for beverages, syrups, toppings, ice, and packaging materials (working in conjunction with PD/Equipment technical team) Establish sanitation and maintenance standards for beverage dispensing equipment, brewing systems, and ice machines. Implement cold chain monitoring from supplier to commissary to store to ensure product freshness and safety. Supplier & Co-Manufacturer Management Approve, audit, and monitor suppliers and co-manufacturers with a focus on beverage-specific raw materials. Maintain supplier scorecards and drive corrective actions when needed. Sensory & Product Consistency Partner with Product Development to create a structured sensory evaluation program for product launches, flavor consistency checks, and ongoing quality monitoring. Ensure uniform product quality across all stores through periodic sensory and operational audits. Training & Food Safety Culture Develop and deliver training programs for commissary staff, store managers, and operations teams. Foster a strong food safety mindset at all levels, from frontline to leadership. Incident Management Lead root cause investigations for customer complaints, product deviations, or food safety issues. Manage product recall and withdrawal processes when necessary. Data & Continuous Improvement Track KPIs, audit results, and consumer feedback to identify trends and opportunities. Recommend and implement improvements for efficiency, shelf life, and product consistency. Growth & Strategic Planning Build the QA/Food Safety function with a vision for future expansion into a Director-level leadership role. Provide guidance and mentorship to develop the QA team as the business scales. Experience you need to be successful: Bachelor's in Food Science, Chemistry, Biochemistry, Biology, Nutritional Science, or related field; Master's preferred. 10+ years in Quality Control and Food Safety, ideally in beverages and foods (QSR, RTD, CPG). This role is perfect for someone with a sharp eye for detail, critical thinking skills, and a passion for building systems that protect brand integrity and customer trust. You will be the architect and driver of our QA and Food Safety program, ensuring every beverage, ingredient, and process meets the highest standards of safety, quality, and consistency. You'll combine hands-on problem solving with a strategic mindset-moving seamlessly from investigating a store-level issue to shaping long-term quality frameworks. This is an ideal opportunity for someone who thrives in fast-paced, customer-focused environments, is confident in making data-driven decisions, and wants to see their work directly impact product quality and guest satisfaction. As our company grows, so will this role. The right candidate will have the opportunity to evolve from Senior Manager to Director, leading a full QA/Food Safety team and shaping the company's quality and safety strategy at a national or even global scale. What We Offer: Hybrid work schedule for a balanced life 401K with company match to secure your future Yearly bonus opportunity Comprehensive medical, dental, and vision insurance On-site fitness center and wellness programs Exclusive discounts at our tea locations, theme parks, and gyms Generous paid time off starting at 15 days, plus 7 federal holidays Opportunities for continuous education and scholarships Income protection including Disability, Life, and AD&D insurance Bereavement leave for those difficult times Who You Are: Join our team and be part of a brand that's as refreshing as our tea! We're excited to see how your talents will help us grow and create memorable experiences for our customers. The expected salary for this position is $121,750-$146,000. Your actual base compensation will be determined on a case-by-case basis and may vary based on considerations including (but not limited to): relevant knowledge and experience for this position, skills, education, certifications and more. Don't miss out on this incredible opportunity to be at the forefront of CHAGEE's expansion into the US market. Join us in shaping the future of premium tea culture and creating unforgettable experiences that will captivate American tea enthusiasts. Apply now and be part of something truly extraordinary! CHAGEE is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based on race, religion, color, national origin, gender, gender identity or expression, sexual orientation, age, marital status, veteran status, disability status, or any other protected characteristic under applicable law.

We are seeking a Junior Quality Engineer with strong experience in electrical or electro-mechanical assembly, PCBA, and wiring/harnessing to support our growing production environment. This role focuses on non-conformance management, MRB support, and hands-on problem solving not audits or mechanical assembly. The ideal candidate understands how to identify defects, document them clearly, and help drive disposition decisions by anticipating what is required to fix the issue. If you are confident in this space, PLEASE APPLY! You can clearly explain the MRB process and the lifecycle of a rejected part. You identify defects accurately and understand what goes into fixing them. You anticipate questions, gather the right information upfront, and reduce friction for engineering. You consistently drive non-conformance issues to closure and help keep production moving. Responsibilities: Experience in electrical or electro-mechanical assembly, PCBA inspection, wiring harness inspection/assembly, or similar hands-on environments. Familiarity with MRB or non-conformance processes: understanding what happens when a part is rejected and what steps occur from start to finish. Ability to go beyond inspection-someone who can identify a problem and drive it to completion. Understanding of how electrical components can fail and what typical rework or repair paths look like. Strong attention to detail and ability to anticipate what information engineers or technicians will need to disposition an issue. Comfortable working in fast-paced environments with incomplete information and ambiguity. Strong communication skills across engineering, operations, and quality. Nice-to-Have Qualifications Experience in aerospace or high-reliability industries. Familiarity with electrical quality standards (IPC-A-610, IPC/WHMA-620, etc.). Experience writing and processing defect tags or non-conformance reports. Exposure to electro-mechanical troubleshooting or rework processes.

Hybrid's humble beginnings started in 1997 in the back of a print shop designing, selling, and printing tee shirts. Today, Hybrid is a global apparel industry powerhouse in brand and licensing management. Hybrid provides its expertise and fully vertical operations capability - design, merchandising, development, sourcing, production, and distribution - to a broad suite of branded, licensed, generic, and private label partners. Hybrid's full-service apparel design and manufacturing expertise extends across the apparel category, including knits, woven tops, bottoms, tees, and accessories. As our organization has evolved, so has our philosophy of doing business. We have made concerted efforts to remove ourselves from the antiquated approach of other apparel manufacturers and doing things differently has been our focus. We are building a company ethos that breeds innovation, collaboration, integrity and excellence in customer service. What is my role? The Supervisor, Product Quality Assurance is responsible for overseeing all aspects of product quality and compliance across inbound shipments within the distribution center (DC) operations. This role ensures product quality standards are met through audits, documentation, and close communication with factories, customers, and internal teams. Additionally, this role drives process management and supports the launch of the inbound compliance chargeback initiative and program. The position requires strong organizational and communication skills, a proactive approach to quality leadership, and the ability to influence behavioral change in the way shipments are coming to Hybrid. What You'll Do Product Quality Control & Oversight Ensure finished goods are manufactured in accordance with the product specifications (measurements, fabric, trims and packing) and the quality of the workmanship meets all specified standards. Manage relationships with overseas factories to ensure all allocated orders are manufactured as per our Quality standards. Work closely with overseas mills and sewing factories, sourcing/production team, and other cross functional areas to continually escalate quality. Maintain QC records of pass/fail results and track performance, review factory scorecards and performance metrics, recommend corrective actions, and submit findings to the chargeback support team. Review and stay current with customers' QA manuals and quality standards. Communicate updates to factories and QC teams to ensure alignment with customer requirements Conduct QC audits at the Distribution Center and spot audits for specific customers as required; ensure audit findings are accurately documented and reported Partner with four team leaders and China QC personnel to maintain consistent product standards Inbound Quality & Compliance Ensure inbound shipments meet quality, compliance, and documentation standards Support the inbound compliance chargeback initiative and program Monitor vendor compliance and partner with stakeholders to reduce noncompliance issues Communicate with overseas and domestic factories regarding quality findings and follow up with best practices and methods to correct issues. Drive continuous improvement and behavior change in supplier and shipment quality practices Interact with cross-functional teams in order to achieve continued focus and improvement in the quality and safety of our products. Leadership & Collaboration Develop, coach, and support QC team members to ensure efficient workflow and high-quality output Serve as a liaison between domestic DC operations and the offshore (China) quality teams. Work together with our Domestic and Import Production teams and CSR team in the development and implementation on continual training, evaluation and improvement of our QA Team local and overseas. Other supervisory duties may be assigned in accordance with company needs What You'll Need 5-7 years' experience in apparel quality management. Experience must also include at least 2 years of product safety. Experience in apparel or consumer goods quality control is highly preferred Strong knowledge of QC inspection processes and standards Ability to effectively communicate to all levels within the organization and factory base. Ability to manage multiple functions and projects in a fast-paced environment Experienced in writing and implementing Quality standard operating procedures Capable of statistically driven performance and issue management Ability to organize work appropriately to meet and exceed department goals and objectives. Demonstrate ability to effectively train and educate all QA auditors and vendors Have a can-do/will-do/want-to-do attitude is a must. Display a consistently high level of detail in all aspects of work Detail-oriented with strong analytical and problem solving abilities Ability to travel to the Distribution Center in San Bernardino and domestic production factories as needed Hybrid Apparel is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.

Join Yorke Engineering, LLC, an Environmental Consulting leader in California that implements Environmental Engineering and Compliance solutions for our clients throughout California. Our mission is to solve environmental compliance problems for industrial and governmental/infrastructure facilities. We are a growing and dynamic organization of highly respected professionals. Yorke Engineering, LLC has assisted over 1,400 client organizations with their Air Quality and Environmental Compliance, Engineering, and Permitting needs. Our philosophy is to efficiently help government and industrial customers with the complex array of environmental laws and regulations. From simple permits to complex agency negotiations, from small companies to the largest of California's organizations, Yorke successfully solves our clients' Air Quality and Environmental challenges. Our team has over 1,000 years of combined environmental experience and consists of engineers and scientists that specialize in Air Quality, Waste, Water, CEQA, Safety, and Industrial Hygiene. We are looking for a sharp Mid to Senior level Air Quality Engineer/Scientist (Environmental Permitting and Compliance) to join our team in Northern CA. This is a full-time position at 40 hours per week from one of our Northern CA offices (Berkeley, San Francisco, or San Jose) during our normal business hours. We offer competitive salaries, a full benefits package including Paid Time Off, Holidays, Full Medical/Dental/Vision, along with a 401k program with a generous company match. Position Summary: The Mid to Senior level Air Quality Engineer/Scientist (Environmental Permitting and Compliance) performs professional engineering work, leading and executing the compliance and permitting functions in relation to Air Quality Regulations and Compliance. This candidate will be reviewing processes and equipment, analyzing permit-related technical and regulatory issues, and communicating those analyses within Yorke, the client organization, with government agencies and with the public at large. The work is challenging, broad in scope, and variable from project to project. The position involves effective communication, decision-making, and time management. The candidate performs other duties as required or assigned. The candidate's experience and qualifications we are seeking include: 5-15+ years of work experience in the Air Quality and/or Environmental industry in an engineering role (preferably in a consulting environment); Experience in the environmental services industry focusing on Air Quality services: Process and equipment review; Air quality permitting under BAAQMD, SCAQMD, SJVAPCD and other Air Districts, including Title V Permitting; RECLAIM implementation and reporting; Annual Emissions Reporting; Air Dispersion Modeling; Air Quality Assessments including Data Analysis and Emission Inventories; General Air Quality Compliance for facilities in CA. Ability to be an active team member on project teams towards project completion within project scope, budget and schedule and ensure quality work product and deliverables; Ability to work with clients, staff, and regulators through effective communication and expertise by fostering a collaborative environment without losing focus of quality; Proven track record or desire to engage in successful regulatory work in dealing with the SCAQMD, BAAQMD, SJVAPCD, EPA, CARB and/or other similar regulatory agencies; Experience or desire to work on-site at client facilities; Prepare reports and submissions in timely manner; Experience with handling highly technical data and technical data interpretation; Highly motivated to continue working in Air Quality environmental field and expand their knowledge and experience; CA Regulatory/Compliance experience is required. Job Requirements: B.S or M.S. degree in Chemical Engineering, Environmental Engineering, or Mechanical Engineering, or other relevant technical degrees from an accredited college (minimum GPA of 3.0); Ability to work collaboratively in a team fashion, handle several projects at once, prioritize work, and work efficiently; Desire to learn or developing technical expertise in environmental rules and regulations; Excellent oral and written communications skills; Experience in conflict resolution and crisis management; Track record of successful analysis, interpretation, and application of rules and regulations towards practical solutions; Ability to think critically and develop solutions; Software Knowledge: Strong Microsoft Excel, Word, Outlook, and Powerpoint skills (required); Microsoft 365 Applications, including Sharepoint (a plus) EIT, CPP or P.E. Certification (a plus).

Job Title: Sr. Quality Engineer - Medical Device Type: 12-Month W2 Contract We're seeking an experienced Senior Quality Engineer to support the full product development lifecycle for implantable and electro-mechanical medical devices. The ideal candidate will have strong expertise in Design Controls, Risk Management (FMEA, Hazard Analysis), and Validation (TMV, IQ/OQ/PQ), ensuring compliance with FDA 21 CFR 820, ISO 13485, ISO 14971, and EU-MDR standards. Key Skills: • Design Control & Regulatory Compliance (ISO 13485, 21 CFR 820, EU-MDR) • Risk Management (FMEA, Hazard Analysis) • Electro-mechanical • Design Verification & Validation Testing • Process Validation (TMV, IQ/OQ/PQ) • Supplier Qualification & Design Transfer • Problem Solving / CAPA / Continuous Improvement. Preferred: • Experience with IEC 62304 and IEC 60601-1 • ASQ Certification (Quality/Reliability) • Strong communication & documentation skills. Qualification: • Bachelor's in Engineering/Science with 5+ years, or Master's with 3+ years in Quality/Engineering.

The Quality Manager will lead the quality assurance and control functions for manufacturing operations at the Valencia site. This role will oversee the quality system, ensure compliance with internal and customer requirements (including ISO/AS standards), drive continuous improvement of quality processes, and lead a team of quality professionals. The Quality Manager reports to the Director of Operations or VP of Operations and works closely with Production, Engineering, Supply Chain, and Sales to ensure that products meet or exceed customer and regulatory expectations. Key Responsibilities Develop, implement, maintain and continuously improve the site quality management system (QMS) consistent with standards such as ISO 9001:2015 and, where applicable, AS 9100 or other industry certifications. Lead and manage the quality team (inspectors, auditors, first-article, data-analysis) to ensure effective execution of quality assurance and control activities. Oversee incoming material inspections, in-process quality checks, first-article inspections, final inspections, audits, non-conformance management and corrective/preventive actions (CAPA). Interpret engineering drawings, specifications, GD&T, and customer requirements; collaborate with Engineering/Manufacturing to ensure manufacturability and design for quality. Monitor key quality metrics (scrap, rework, defect rate, customer returns, on-time quality shipments), report to senior management and drive improvement programs. Lead root cause investigations for major quality failures, coordinate cross-functional corrective actions, validate their effectiveness and integrate learnings into the process. Desired Skills and Experience The Quality Manager will lead the quality assurance and control functions for manufacturing operations All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

: The project includes construction of an aircraft refueling facility with an operations building, fuels laboratory, fuel farm, spill containment, Demolition of existing fuel farm site and incidental related work. The current schedule is for the Quality Control Manager to start approximately March 2026 and mobilize to site April 2026. The Quality Control Manager is responsible to implement and manage Quality Control Program per contract specifications and project QC Plan. Requirements : Work closely with the Project Superintendent and Project Manager coordinating quality with production. Manage and coordinate three phases of control for all features of work. Complete all associated report forms. Conduct Preparatory meetings and Initial inspections on all definable features of work. Conduct and keep minutes of the QC/Production Meeting. Observe and monitor daily field activities for compliance with the plans and specifications. Perform field testing as required. Be familiar with the EM 385-1-1, monitor field work for safety violations and inform the SSHO of any problems observed, take immediate action if necessary. Complete daily Quality Control Reports for submission to the Owner. Develop and maintain QC project files. Prepare, review and transmit submittals. Perform QC review and approve subcontractor submittals prior to transmitting to the Owner. Maintain the Submittal Register. Write RFIs in coordination with Project Supt. and Project Manager. Develop and maintain the Testing Plan and Log. Schedule testing and special inspections. Maintain reports of onsite and offsite quality control inspections and tests performed including work by suppliers and subcontractors. Schedule and manage QC Specialists and testing labs, verify work done by others. Keep a Rework list of work that does not comply with the contract requirements. Prepare punch lists and perform pre-final and final inspections; ensure punch list completion. Maintain As-Built drawings. Maintain weld log, weld field map with locations and elevations. Take and process progress photos. Perform and document a pre-pour checklist for concrete placements. Keep the Owner informed of onsite & offsite sampling/testing. Prepare project specific QC Plan and assist in Accident Prevention Plan and Environmental Protection Plan preparation. Perform additional assignments per supervisor's direction. Skills, Knowledge, Qualifications & Experience : Educational and experience requirements include: Experience with infrastructure projects including but not limited to medium voltage cabling, conductor splicing, insulators, grounding, lightning protection, transformers, switchgear, conductor lugs & terminations, underground duct banks, excavation, backfill, rebar, concrete, formwork, piping, welding, pumps, valves, painting & coating, instrumentation, pre-engineered buildings and commissioning. Familiar with U.S. Army Corps of Engineers EM 385-1-1 Safety and Health requirements. Minimum of 5 years of experience as a Superintendent, QC Manager, Project Engineer, or Construction Manager. Minimum 4 years as QC Manager. (Can be part of 5 years' experience in bullet above.) Computer skills to include Microsoft Office programs and Bluebeam or Adobe. Excellent organizational, supervisory and decision making/problem solving skills are essential. Advanced management or technical training preferred. Current USACE/NAVFAC CQM certification preferred. Experience with USACE, NAVFAC, and DoD construction contracts preferred. Familiar with eCMS, RMS, preferred. Bachelor's degree from accredited college or university in engineering or construction management preferred. Licensed Professional Engineer (PE) preferred. Work Environment: Work is performed on a construction site, typically in a construction trailer. This role routinely uses standard office equipment such as computers, phones, photocopiers, and filing cabinets. Physical Requirements: Must be able to access and navigate all areas of the construction site in all types of weather. Prolonged periods of standing and working outside. Prolonged periods of sitting. Must be able to lift to 40 pounds at times. Position Type and Expected Hours of Work This is a full-time, overtime exempt position. Days and hours of work will depend on production schedule. This Quality Control Manager, QCM, role is for the duration of the Bridgeport project and then relocating from project site to project site as Nova is awarded new projects. Typical projects are 1 -3 years in duration in locations both domestic and international. Between projects, the QCM may be assigned shorter term to one of the Nova offices, to another project, or remote from a home base for project support work as required. This position requires U.S. work authorization. Salary Range: $110K to $140K depending on experience, plus subsistence, auto allowance, benefit package, paid holidays, PTO (Paid Time off) and sick leave.