Quality control inspector jobs in San Diego, CA - 248 jobs

TekWissen is a global management consulting, technological service and outsourcing company delivering technology-driven business solutions to meet the strategically driven objectives for our numerous clients. Job DescriptionTitle/Role Sr. QA Engineer ( Quality Assurance) Location San Diego, California Type Fulltime **Also we are open for h1b transfer with good benefits** Responsibilities Creation, maintenance, and execution of both blackbox and whitebox tests Creation/evolution of QA infrastructure, processes, tools, harnesses, environments, etc. Scripting/automation Developing JUnit tests in Java Leading a team of QA engineers for delivering fast paced projects. Position Requirements 4+ years QA, development or performance engineering experience 2+ years scripting / automation experience. Java experience preferred 2+ years hands-on UNIX / Linux experience for Application Server infrastructures. Includes installation, performance assessment of applications, WAR file installation, Tomcat configuration, n-tier application server architectures Ability to use and develop tests for automated test tools/processes Previous experience in wireless data applications a strong plus Must have experience with server-side or backend/API testing Must be capable and willing to perform the entire range of QA activities, from high level planning to lowest level test execution Must have ability to thrive in a fast pace, dynamic startup environment Experience and Education Good knowledge/experience of Oracle or mysql DB Scripting languages: Unix shell, Perl, Awk, Python, etc. Web interface tools (e.g. cgi, html, etc) System operation, monitoring, tuning Linux/Redhat and/or UNIX mandatory Good knowledge of HTTP protocols Experience with Media (video/audio) testing is plus B.S. or equivalent experience Additional InformationThanks and regards Direct: ************ Email: chris@tekwissen dot com

About Us When you work at Chugach Government Solutions (CGS), you join a proud legacy of supporting missions while sustaining culture. The federal division of Chugach Alaska Corporation, CGS has been supporting critical missions as a government contractor for over 25 years. Our focus is to support facility maintenance, IT/technical services, construction and education. We are proud to have built, and continue to foster, an incredibly talented team spanning across the globe in hundreds of different fields - each team member proud to serve our country with first-class business services, while also making a difference for our Chugach shareholders. At CGS, empowering employees is a part of our core, and that focus is one of the ways we build and foster high-performing teams. We empower our employees through competitive compensation and benefits package, professional growth opportunities, truthful communication, and more! If you are looking for an opportunity to serve something bigger than yourself; if you want your day job to be one that creates meaningful value; if you are looking for an environment that highly values employees and respects individual differences - then Chugach Government Solutions may be the right fit for you! Job Overview Under the direction of the Task Order Manager, the Quality Control Inspector is responsible for conducting inspections to ensure compliance with contract requirements and Quality Control and Safety Plans. Pay Rate: $26.74/hourly Work Model: Onsite Responsibilities Essential Duties & Job Functions: * Review all site work to verify compliance in accordance with applicable plans and procedures. * Inspect and diagnose problems to determine corrective actions/repairs. * Inspect work in progress and finished work for discrepancies in accordance with the QC and applicable Safety Plans, and contract requirements.Complete necessary inspection reports and documentation required to support findings. * Assist in preparing Safety incident and hazard reports as required. * Maintains accurate administrative records. * Review all site work to verify compliance in accordance with applicable plans and procedures. * Respond to emergency site maintenance as required. * Ensures proper housekeeping practices are strictly observed. * Maintain open communications with personnel. * Performs other duties as assigned by the supervisor. * Other duties as assigned. Accountable For: * Tools and equipment within his or her possession. * Using PPE when required. * Timely completion and accuracy of all work. * Working closely and harmoniously with fellow workers. * Adherence to all Safety rules and regulations. Job Requirements Mandatory: * Working knowledge of Microsoft Programs, including but not limited to: Outlook, Word, PowerPoint, and Excel or equivalent software program. * Understanding of Government contracts, correspondence, reports, and records. * Knowledge of generally accepted standards of workmanship in custodial services. * Excellent communication skills, both oral and written. * Excellent organizational skills. * Mature judgment and ability to work with little or no supervision. * Ability to communicate ideas effectively with personnel at all levels. * United States Citizen. * High School Diploma or Equivalent. * Ability to pass pre-employment background check and drug screen. * Must be able to read, write, and speak English fluently. * Valid driver's license with excellent driving record (Must provide current driving record). * Ability to obtain access to U.S. Government Installations through the Defense Biometric Identification System (DBIDS). Preferred: * 2 yrs custodial experience. * Two-year degree in Safety, Industrial Hygiene, or a related field or broad experience in the same or similar areas. * Bilingual - Spanish Working Conditions: * Work is performed indoors and outdoors. Outdoor work is subject to temperature extremes and inclement weather conditions. * Work hours are subject to change, with overtime, weekend and/or holiday work as needed. * Subject to hazards that may cause personal bodily harm; diseases, cuts, bruises, burns, common cold, influenza, dust odors and elevated noise levels. * Tasks may be performed on uneven, inclined, hard and soft carpeted floors, cement structures and surfaces. * While performing duties of this job, the employee is occasionally required to stand and/or walk for long periods of time, sit, use of hands and fingers, handle, or feel objects, tools or controls, reach with hands and arms, climb stairs, climb ladders, balance, stoop, kneel, crouch or crawl, talk, hear, or smell. The employee must occasionally lift and/or move up to 35 pounds. Specific vision abilities required by the job include close vision. May be required to operate regular and specialized vehicles. Physical Requirements: * Must be able to lift to 50 lbs. * Must be able to climb stairs and ladders as required. * Must be able to load/unload materials, tools, and equipment. * Involves walking, bending, stooping, twisting, and reaching. Reasonable Accommodation: CGS will provide reasonable accommodations, according to applicable state and federal laws, to all qualified individuals with physical or mental disabilities. In compliance with the ADA Amendments Act (ADAAA), if you have a disability and would like to request an accommodation in order to apply for a position with Chugach Government Solutions or any if its subsidiaries, please email ******************. Equal Employment Opportunity: Chugach is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, gender, sexual orientation, gender identity or expression, age, pregnancy, disability, genetic factors, protected veteran status or other characteristics protected by law.

We're looking for people who put their innovation to work to advance our success - and their own. Join an organization that ensures a more secure world through connecting and protecting our customers with inventive electrical solutions. Job Description We're looking for people who put their innovation work to advance our success - and their own. Join an organization that ensures a more secure world through connecting and protecting our customers with inventive electrical solutions. What YOU WILL EXPERIENCE IN THIS POSITION: Provide quality assurance support and lead root cause problem solving activities that are aligned to improve internal and external quality levels, supporting overall customer satisfaction of our products. This position is a development track to a quality engineering position, by providing structured involvement with quality engineering responsibilities. * Lead problem solving activities for both product and manufacturing processes, with assistance from Quality Engineer * Perform process validations, in-process inspections, and monitoring, analyzing the quality of manufacturing processes and products * Provide support to design, manufacturing, and quality engineering functions for data collection, analysis, product review, and process capabilities * Understand, adhere to, and develop processes compliant with the Quality Management Systems (QMS) objectives, as well as train other personnel to adhere to QMS standards * Disposition NCR product and assign appropriate resolution * Provide formal documented FAI reports suitable for customer or internal use as required * Determine and use appropriate measuring tools and equipment to verify dimensional and functional requirements * Effectively communicate with appropriate areas as needed, (Operations, Supply, Manufacturing Engineering, Design, Quality, Customer Service, Production Planning, Logistics, etc.) * Lead and/or assist in supporting the activities that maintain the calibration status of inspection, test, and measurement equipment * Perform other related duties as assigned You have: Academics: * High school diploma or GED * American Welding Society (AWS) Certification as Certified Welding Inspector (optional) * Ability to read blueprints. GD&T knowledge is a plus. Previous experience in or with: * 2+ years working in the quality/manufacturing field * Ability to use measurement tools and techniques - strongly preferred * Strong knowledge and understanding of charting and process control methods preferred * Experience with Quality Management Systems (QMS) preferred Skills: * Strong written, verbal, and interpersonal communication skills * Attention to detail and ability to prioritize tasks is key to being successful in this role * Must be able to interpret order requirements, drawings, and draw conclusions * Ability to use precision measuring equipment (e.g., calipers, micrometer, paint mill gauges, etc.) * Skilled in identifying root causes of routine problems/issues and the ability to develop recommendations for resolution * Ability to interpret and apply Quality Systems / ISO procedures and documentation * Comfortable using computer systems and software including MS Office Applications Abilities to meet the physical and environmental demands: * Lift up to 50lbs * Stand and walk frequently * Operate hand tools * Work primarily indoors where there is frequently noise of 85 dB and occasional exposure to chemical hazards (solvents) WE HAVE: * A dynamic global reach with diverse operations around the world that will stretch your abilities, provide plentiful career opportunities, and allow you to make an impact every day * nVent is a leading global provider of electrical connection and protection solutions. We believe our inventive electrical solutions enable safer systems and ensure a more secure world. We design, manufacture, market, install and service high performance products and solutions that connect and protect some of the world's most sensitive equipment, buildings and critical processes. We offer a comprehensive range of systems protection and electrical connections solutions across industry-leading brands that are recognized globally for quality, reliability and innovation. * Our principal office is in London and our management office in the United States is in Minneapolis. Our robust portfolio of leading electrical product brands dates back more than 100 years and includes nVent CADDY, ERICO, HOFFMAN, ILSCO, SCHROFF and TRACHTE. Learn more at ************** * Commitment to strengthen communities where our employees live and work * We encourage and support the philanthropic activities of our employees worldwide * Through our nVent in Action matching program, we provide funds to nonprofit and educational organizations where our employees volunteer or donate money * Core values that shape our culture and drive us to deliver the best for our employees and our customers. We're known for being: * Innovative & adaptable * Dedicated to absolute integrity * Focused on the customer first * Respectful and team oriented * Optimistic and energizing * Accountable for performance * Benefits to support the lives of our employees Pay Transparency nVent's pay scale is based on the expected range of base pay for this job and the employee's work location. Employee pay within this range will be based on a combination of factors including knowledge, skills, abilities, experience, education, and performance. Where federal, state, or local minimum wage requirements exist, employee pay will comply. Compensation Range: $23.90 - $44.40 Per Hour Depending on the position offered, employee may be eligible for other forms of compensation, such as annual incentives. Benefit Overview At nVent, we value our people and their health and well-being. We provide a broad benefits package with meaningful programs for eligible full-time employees that includes: * Medical, dental, and vision plans along with flexible spending accounts, short-term and long-term disability benefits, critical illness, accident insurance and life insurance. * A 401(k) retirement plan and an employee stock purchase plan - both include a company match. * Other supplemental benefits such as tuition reimbursement, caregiver, personal and parental leave, back-up care services, paid time off including volunteer time, a well-being program, and legal & identity theft protection. At nVent, we connect and protect our customers with inventive electrical solutions. People are our most valuable asset. Inclusion and diversity means that we celebrate and encourage each other's authenticity because we understand that uniqueness sparks growth.

Under the direction of the Quality Assurance Manager, the Quality Inspector will maintain quality standards by approving incoming materials, in-process production, finished products, and recording the results. Essential Job Functions (primary duties and outputs of position) Inspect at receiving and in-process inspection. Complete operation sheet with stamping and dating for controlled production. Maintain lot traceability. Interpret production schematics, specification and/or blueprints. Perform final inspection of complex assemblies or first article inspection. Administer prescribed inspection procedures, set up and checks. Perform visual inspections on production bench-assembled components and subassemblies for conformance. Predetermine electrical and/or mechanical standard, specification or tolerances. Maintain gauges in working order. Provide training to other employees. Safety Follow safe work practices, participate in safety training as required, and report any unsafe condition or accident. Quality Employees are responsible to understand and support the quality policy and the appropriate elements of the quality management system for their areas of work, reduce, eliminate, and prevent quality deficiencies including escapes. Initiate action to prevent the occurrence of nonconformities related to product, process, and quality system. All employees have the responsibility and authority to identify quality deficiencies, elevate any concerns for action within or related to our quality system and processes. Communication Communicate effectively in English, both verbally and in writing. Maintain effective and constructive working relationships with others both internally and externally. Prepare effective reports and presentation of departmental information. Requirements Education/Work Experience Requirements Must have high school diploma or GED. 3 or more years' experience in manufacturing QA inspection. Must be able to operate standard inspection devices and/or elementary testing equipment. Able to test subassemblies. Ability to read and understand wiring diagrams; schematics, blueprints. Ability to read and interpret drawings and follow verbal and written job instructions. Able to pass IDC-J-STD-001 on IPC A610. Experience working in a controlled environment where lot traceability is required. Computer experience (using Excel) for data collection. Physical/Travel Requirements This position requires bending, walking, and standing, typing and lifting a maximum of 25 lbs. No travel required. Salary Description $20-25/Hour

SeeScan is seeking a detail-oriented PCB/PCBA Quality Inspector to perform visual and mechanical inspections of printed circuit boards (PCBs) and printed circuit board assemblies (PCBAs). Compensation is $25 to $35 hourly. This range represents a good faith estimate based on the qualifications we expect to find in a successful candidate. Actual compensation offered may be less or greater than this estimate based on a variety of factors, including, but not limited to, our assessment of your ability to bring value to our organization. We offer * A position within an established company that has over 40 years of experience * Medical, dental, and vision coverage * Traditional and Roth 401(k) investment options, with partial company matching contribution * Flexible Paid Time Off plan with no cap or "use it or lose it" requirement In your application, include your resume and a thoughtful cover letter explaining why you are the ideal candidate for this position. We are looking for a long-term, in-house teammate to join us, not a contractor or consultant. In this position, you will * Perform incoming, in-process, and final inspections of PCBs and PCBAs according to drawings, assembly instructions, and applicable standards * Inspect solder joints, component placement, polarity, and labeling using magnification tools and microscopes * Review and interpret engineering drawings, BOMs, and schematics * Identify, document, and report nonconformances, assisting with root cause analysis and corrective actions * Collaborate with manufacturing engineers and technicians to address rework, repair, and process improvements * Ensure all inspection results and quality data are accurately recorded * Maintain a clean, organized, and safe work environment * Support calibration and maintenance of inspection tools and equipment Your background * 3+ years of experience in electronic assembly inspection, preferably in a manufacturing or OEM environment * Familiar with electronic components, assemblies, and soldering processes * Able to read and interpret schematics, assembly drawings, and BOMs * Experience using inspection tools such as microscopes, calipers, and multimeters About you * Excellent attention to detail and accuracy * Strong communication skills, with the ability to work collaboratively in a team-oriented environment * Comfortable working in a fast-paced manufacturing environment About SeeScan Beneath the ground and below the water's surface is a world out of sight. Whether it's the inside of a pipe, or a maze of the buried services that keep our world running, or the deepest places of the ocean, our mission is to create products that help our customers see. Dating back more than 40 years to our founder's garage, we are an original equipment manufacturer in San Diego, CA that builds diagnostic, utility locating, and harsh-environment oceanographic equipment from the ground up. And as leaders in our industries, we provide ongoing support and parts services to ensure that our equipment is never short of the best. At SeeScan, you'll be part of a group of people who bring passion and energy into everything they do. We value the individual contributions all of our employees make and invest in the tools and training they need to find success and professional growth. We do our best to empower the right people to take on new opportunities, and our culture promotes transparency, integrity, and continuous learning. Notes * No recruiters, contractors, or consultants, please * No relocation assistance or visa sponsorships available for this position * SeeScan is an Equal Opportunity Employer

AXILLON AEROSPACE is a leading provider of complex, highly engineered composite and polymer solutions for demanding commercial and defense applications. Comprised of six, purpose-built centers of excellence throughout the USA and Mexico, each strategically focused on serving specific markets across aerospace engines and airframes, as well as munitions, radomes, antennas and fuel containment. JOB SUMMARY: The Quality Inspector inspects a range of components, parts and/or products for the area assigned as prescribed by all applicable specifications and quality assurance Instructions. Identifies moderately difficult quality issues in design, process or other inefficiencies to meet quality requirements. ESSENTIAL DUTIES AND RESPONSIBILITIES: Conducts examinations and quality control inspections on products, materials and components at various stages of the production process to ensure compliance with established quality and reliability standards. Participates in analysis statistical data from processes to either confirm compliance with established standards or identify deviations from standards. Performs visual inspections of soldered connections, mechanical inspections of electronic and electro-mechanical assemblies and subassemblies. Prepares and completes all necessary documentation for reporting. Acceptance/rejection of inspected and/or tested items. Identifies design, process or other inefficiencies and reports quality concerns and issues. Performs routine quality inspections on engineering designs, assemblies, piece parts, final assemblies and tooling. Conducts Internal audits and corrective action follow ups. Other responsibilities as assigned. Regular, consistent and punctual attendance is required. May need to work nights and weekends, variable schedule(s) and additional hours as necessary. JOB SPECIFICATIONS: Education: High School Diploma or equivalent. A Secondary Certificate combination of relevant education and work experience that will allow successful performance of job expectations. Certifications: Vocational training, apprenticeships, or the equivalent experience in related field. Experience: 2- 5 years of relevant experience. Skills: Ability to follow established job instructions and procedures with minimal supervision. Able to apply a systematic QA approach while using existing procedures to solve a range of technical issues. Skilled at measuring and using test equipment as prescribed by job assignment. Capable of following instructions and applying processes and procedures to standard routine tasks Must be able to interpret and follow written and verbal instructions, including engineering drawings, charts, diagrams, and sketches. Proficient computer skills. Please note that the salary range information is only applicable for California. Compensation is based on a variety of factors, candidate experience, qualifications, location as well as market and business considerations. Pay Range: $20.10/hour- $30.10/hour. Axillon is an Equal Opportunity and Affirmative Action Employer. Axillon is committed to ensuring equal employment opportunities for all job applicants and employees. Employment decisions are based upon job related reasons regardless of race, ethnicity, color, religion, sex, sexual orientation, age, national origin, disability, gender identity, genetic information, veteran status, or any other status protected by law. This position is subject to meeting export compliance eligibility requirements. This position requires use of information which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. 'Green Card Holder'), Political Asylee, or Refugee. (“Minority / Female / Disability / Veteran / VEVRAA Federal Contractor”) If you would like more information about Equal Employment Opportunity as an applicant under the law, please go to Know Your Rights: Workplace Discrimination is Illegal (eeoc.gov) and Genetic Information Discrimination

Rock West Composites, Inc. has an exciting opportunity for a Quality Inspector. Rock West Composites, Inc. is an engineering and manufacturing company dedicated to providing innovative solutions for commercial and government customers. This position is located at our San Diego, CA HQ facility and reports to our Quality Manager. Position Summary: The Quality Inspector inspects a range of components, parts and/or products for the area assigned as prescribed by all applicable specifications and quality assurance instructions. Inspector will identify moderate to difficult quality issues in design, process or other inefficiencies to meet quality requirements. Essential Function: Conduct detailed inspections of mechanical, metal, and composite materials, parts, and assemblies using precision measuring tools such as calipers, micrometers, height gauges, and mylars. Perform and document First Article Inspections (FAI) per AS9102 standards, including the creation of Forms 1, 2 & 3 and ballooning requirements (experience with DISCUS software is a plus). Perform final inspections, review customer requirements, and compile complete documentation packages. Support in-process inspections and monitor production area processes to ensure quality compliance. Accurately document inspection results, work instruction changes, and nonconforming conditions with clear, concise reports. Interpret mechanical and composite drawings, specifications, and requirements with a high degree of proficiency. Conduct receiving inspections for materials and parts outsourced for special processing. Participate in internal audits and cross-functional continuous improvement initiatives. Experience with Articulating Arm or CMM inspection using Verisurf is a plus. Non-Essential Functions: Other duties as assigned. Required Education and Experience: 2 years+ of experience in an aerospace manufacturing environment with AS9100 compliance. Strong knowledge of precision measurement tools and quality inspection techniques. Ability to work independently and lead a team in a fast-paced production environment. Excellent attention to detail and documentation skills. Experience with AS9102 First Article Inspections preferred. CMM and Verisurf experience is a plus. US. Person under 22 CFR 120 (due to ITAR Restrictions Perks and Benefits: 100% Employer Paid Medical and Dental Annual Bonus 401K - 5% match Employee Stocks Option Program 9/80 work schedule 8- paid Holidays PTO: Max. 4-weeks after 5 years of employment $2,500 tuition reimbursement Compensation: The hourly pay range for this position falls within $25-$30. The final compensation will be determined based on experience, skillset, and other factors permitted by law. Why should you want to work with us? Rock West Composites cares about our employees! Not only do we offer great benefits to our full-time employees (Medical & Dental 100% employer paid, Vision, Paid Time Off and 401K match), we offer a fun and friendly working environment! Rock West Composites is an Equal Opportunity Employer. It is the policy of the company to provide equal opportunity for all employees and applicants for employment without regard to race, color, religion, religious creed, ancestry, gender, pregnancy, sex, sexual orientation, transitioning status, gender identity, gender expression, national origin, age, genetic information, military and veteran status, marital status, medical condition, mental disability, physical disability, or any other basis protected by local, state, or federal law. EEO is the law. We also prohibit compensation discrimination under all applicable laws. Certain positions require meeting the U.S. Person definition in 22 CFR 120.62. ITAR Requirement: To conform to U.S. Government export regulations, applicant must be a (i) U.S. citizen or national, (ii) U.S. lawful, permanent resident (aka green card holder) as defined by 8 U.S.C. 1101(a)(20), (iii) Refugee under 8 U.S.C. 1157, or (iv) Asylee under 8 U.S.C. 1158, Must be authorized to work in the U.S. without the company's immigration sponsorship now or in the future. Rock West Composites will not offer immigration sponsorship for this position. Rock West Composites will not seek an export authorization for this role. Rock West Composites maintains a Drug and Alcohol-Free Workplace. Depending on state law and the nature of the position, candidates who receive a conditional offer of employment may be required to complete a drug screening. Rock West Composites may also conduct drug and alcohol testing based on reasonable suspicion, post-incident, or for safety-sensitive positions as permitted by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact ************.

Job Description Employment Type: Full-Time | Hourly | Non-Exempt Pay Range: $30.00 - $37.00 Who We Are Vigor Marine CM San Diego, a Vigor Marine Group company, builds on the proud legacy of Continental Maritime of San Diego (CMSD) to stand as a vital force on San Diego's working waterfront. As a certified Master Ship Repair Contractor for the U.S. Navy, our skilled professionals have successfully completed hundreds of ship repair and modernization projects for the Navy and Military Sealift Command. We perform maintenance and modernization on all classes of major surface vessels, including CVN, CG, and DDG, as well as amphibious ships such as LHD, LHA, LSD, LPD, and auxiliary ships. Our work spans a full range of Combatant, Hull, Mechanical and Electrical, and Habitability systems, supporting the readiness and mission success of the U.S. Fleet. Position Specifics Vigor Marine CM San Diego is currently seeking an experienced Quality assurance Inspector 3 to support our operations. The Quality Assurance Inspector (QAI) reports to the Quality Assurance Manager and is responsible for maintaining, implementing, and applying the Company's quality systems. The position works from blueprints, diagrams, customer specifications, drawing or inspection instructions and checklists. The QAI is the principal point of contact relative to customer inspection personnel and ensures the Company and Subcontractors comply with specification requirements and document results via the appropriate system of record. Minimum Requirements Strong background in quality assurance and environmental/health/safety programs Must be familiar with US Navy quality assurance requirements Must have demonstrated experience in execution and engineering support of test related functions Ability to plan and develop testing strategies based on extensive experience and judgement Ability to read technical drawings and interpret the Navy Engineering Operational Sequencing System (EOSS) Familiar with commonly used shipboard concepts, practices, and procedures Exceptional understanding of the NAVSEA Standard Items and associated military and commercial regulatory requirements Must be able to read and interpret work specifications, standards, and references Must be available for unscheduled extended work hours and non-standard workweeks Desire to learn new industry-related activities Superb communication and time management skills Computer skills in work processing, databases, and spreadsheets Ability to get along with and foster good relationships among peers, supervisory, and customer personnel US Citizenship is required The ability to acquire a DBIDS credential is required NBPI and/or NACE certification required Physical Requirements May be exposed to fumes, irritants, laser light, toxic chemicals, and potential electrical shock in an industrial or shipboard environment May involve gathering data while observing rotating or operating machinery Requires working in an industrial or shipboard environment Frequently moves throughout the yard Must be able to maneuver, ascend and descend stairs/ladders/ramps located inside various ships Ability to move more than 40lbs. May be exposed to rapid changes in microclimates, industrial processes, and other environmental factors while collecting data, providing direction, and observing performance of task teams Our Commitment The Vigor Marine CM San Diego Management Team is committed to providing the necessary structure, tools, and environment for our employees. We act in the economic best interests of our customers and our company, in a professional, honest, and sincere manner. Our mission is accomplished through unwavering commitment to the following principles: Teamwork Professional Conduct Integrity Total Quality Customer Satisfaction Open, honest communication at all levels Awareness of environmental issues Empowerment at every level Vigor Marine CM San Diego is an Equal Opportunity Employer of Veterans and individuals with disabilities. U.S. Citizenship may be required for certain positions. We offer excellent company-paid benefits and a savings plan. How to Apply In Person: Vigor Marine CM San Diego1995 Bay Front Street San Diego, CA 92113 Online: **********************************

Build Your Career. Build America's Future. Vulcan Materials Company is the nation's largest producer of construction aggregates and a major producer of aggregates-based construction materials including asphalt and ready-mixed concrete. When you join Vulcan, it's more than starting an exciting career - you get to make a difference for millions of people every day across the country. When you join Vulcan, you join a dynamic culture in which career development is encouraged, excellence is rewarded and diversity is valued. No matter the role or the location across the country, every member of the Vulcan team lives through the Vulcan Way: doing the right thing, the right way, at the right time. About The Job: This highly skilled position is critical for the efficient and safe operation of the quarry. The Plant Inspector is responsible for thoroughly inspecting all plant equipment, including crushers, screens, conveyors, and other machinery. This involves a deep understanding of how the entire operation functions, identifying potential problems before they occur, and prioritizing repairs to minimize downtime. What You'll Do: Safety and Compliance * Adhere to all safety regulations and protocols, including wearing appropriate PPE, and following MSHA/OSHA regulations. * Maintain a high level of situational awareness to prevent accidents and ensure the safety of yourself and others. * Report any safety concerns, incidents, or equipment malfunctions promptly. Preventative Maintenance Guidelines and Schedules * Assist in the develop and implement a robust preventative maintenance program, including: * Regular inspections of all equipment, including visual checks, lubrication checks, and performance assessments. * Identifying and addressing potential issues before they lead to breakdowns. * Scheduling and coordinating necessary repairs and maintenance activities. * Collaborate with plant management to prioritize repairs and maintenance activities to minimize downtime at operation. * Maintain accurate and detailed records of all inspections, repairs, and maintenance activities. Troubleshooting Equipment * Possess in-depth knowledge of quarry equipment, including crushers, screens, conveyors, wash plants, and other auxiliary equipment (e.g., generators, pumps, compressors) * Assist in troubleshooting equipment malfunctions quickly and effectively. * Assist in implementing strategies to improve equipment reliability and reduce overall maintenance costs. Skills You'll Need: Education: High school diploma or equivalent preferred. Experience: Experience in maintenance, preferably around heavy equipment and machines. Certifications/Licenses: Valid Driver's License Knowledge, Skills, and Abilities: * Strong understanding of safety protocols and MSHA/OSHA regulations. * Good communication and customer service skills. * Knowledge of quarry equipment and maintenance systems * Ability to work with others and manage time effectively. * Physical ability to climb up and down equipment and handle heavy loads. Critical Competencies: Inspecting and Evaluating Equipment: Inspecting all fixed plant equipment and structures to identify defects, upcoming problems, and potential root causes. Documenting/Recording Information: Entering and maintaining inspection findings in written or electronic/magnetic form. Communication and Collaboration: Providing information to supervisors, co-workers, and subordinates by telephone, in written form, e-mail, or in person. Evaluating Information: Using relevant inspection information and individual judgment to determine whether events or processes comply with regulations or standards. Organizational Culture Knowledge: Understanding of organizational culture dynamics and how they impact change efforts. Ability to promote cultural alignment and shift when necessary. Change Management: Strong understanding of change management principles, methodologies and best practices. Ability to develop and execute change strategies that drive successful organizational transformations. What You'll Like About Us: Great Company Culture: Our people share a competitive drive for excellence in an environment of trust, teamwork, open-mindedness, and communication. Safe: The industry leader in health and safety standards. We are committed to creating a safe work environment and protecting all employees and customers. Meaningful Work: What sets us apart is the work we do impacts our daily lives - and every employee contributes. Our aggregates produced are used to build roads, schools, hospitals, airports, and housing throughout the United States. Health Benefits: Medical, Dental, and Vision programs, plus much more. Rest and Relaxation: Paid vacation, personal floating days, and paid holidays. Prepare for the Future: 401(k) with company match and contribution. Training and Development: We see our development programs and helping our employees meet their goals as a key part of our business. Salary Range. The base hourly range for this role is between $30.00 - $40.00 per hour. This range is not inclusive of our discretionary bonus or equity package. When determining a candidate's compensation, we consider a number of factors, including skillset, experience, job scope, and current market data. Vulcan Materials Company is committed to employing a diverse workforce. You will receive consideration without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, gender expression, veteran status, or disability. You also have the right to be free from discrimination for medical needs arising from pregnancy, childbirth, or related medical conditions. The does not constitute an employment agreement between the employer and employee and is subject to change by the employer as the needs of the employer and requirements of the job change. The Company may at any time, in its sole discretion, modify or vary from anything stated in this job description, with or without notice.

Introduction Werfen Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We're passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care. Overview Position Summary: The QC Technologist III is responsible for the execution of a broad range of bench test procedures used in raw material qualification, the testing of finished goods prior to release, the investigations of product performance, and for conducting routine validation studies, as well as assisting with routine maintenance of the Quality Control (QC) laboratory. The QC Technologist III works with cross-functional teams to resolve product performance issues and maintenance of QC Standard Operating Procedures (SOP) in compliance with applicable regulations and ISO standards. Additionally, QC Technologist III supports investigations and assists in trending and statistically analyzing finish product testing data. This is a temporary role lasting between 3 and 6 months, with the possibility of extension. The pay rate for this position is $29-$34/hr, depending on experience. Responsibilities Key Accountabilities Essential Functions: Perform and organize testing of biological raw materials and finished goods per relevant SOP with minimal supervision; subject matter expertise in at least one product line. Assist with planning of method, product and process validations on existing products; perform and organize testing as needed. Perform testing and prepare reports as required for environmental monitoring or investigation of out-of-specification results, as required. Perform testing and assist with preparation of reports for various special projects as deemed necessary by technical review team. Responsible for tracking relevant trends. Maintain proper laboratory housekeeping and supply levels in the QC laboratory, including submission of purchase requisitions and inventory adjustments. Document all test results and maintain product release records (including electronic records). Document existing product/process validation test results (including electronic records). Maintain product testing database and perform relevant statistical analyses associated with product specifications as specified in laboratory SOPs. As required, coordinate and assist with investigation and resolution of complaints, non-conforming material and product performance issues. Submit complex change orders to update procedures as required. As required, work cross-functionally to investigate and resolve issues deriving from finish product testing. Ensure and maintain compliance with the Company's quality system requirements through training and adherence to policies, procedures and processes. Other duties as assigned. Qualifications Minimum Knowledge & Experience Required for the Position: High school diploma required; Bachelor's degree in Science or equivalent experience preferred. A minimum of four (4) years previous Quality Control lab (QC) and/or Quality Assurance (QA) experience required; previous experience within a regulated medical device manufacturing or In-Vitro Diagnostic Device (IVDD) strongly preferred. Thorough understanding of Good Laboratory Practices (GLP) required. Practical experience with laboratory controls, internal audits, and lab training/maintenance. Phlebotomy certification a plus. Knowledge of FDA-GMP/QSR and ISO standards for quality. Excellent written and verbal communication skills. Ability to work independently and as part of a team. Proficiency with common laboratory techniques, such as pipetting and use of balances. Proficiency with Microsoft Office suite. Proficiency with Large Enterprise Resources Planning (ERP) and Laboratory Information Management (LIMS) systems preferred. Closing If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV. Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual's race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process, please contact ****************************** for assistance. We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7,000 employees around the world comprise our Werfen team. **************

Introduction Werfen Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We're passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care. Overview Position Summary: The QC Technologist III is responsible for the execution of a broad range of bench test procedures used in raw material qualification, the testing of finished goods prior to release, the investigations of product performance, and for conducting routine validation studies, as well as assisting with routine maintenance of the Quality Control (QC) laboratory. The QC Technologist III works with cross-functional teams to resolve product performance issues and maintenance of QC Standard Operating Procedures (SOP) in compliance with applicable regulations and ISO standards. Additionally, QC Technologist III supports investigations and assists in trending and statistically analyzing finish product testing data. This is a temporary role lasting between 3 and 6 months, with the possibility of extension. The pay rate for this position is $29-$34/hr, depending on experience. Responsibilities Key Accountabilities Essential Functions: Perform and organize testing of biological raw materials and finished goods per relevant SOP with minimal supervision; subject matter expertise in at least one product line. Assist with planning of method, product and process validations on existing products; perform and organize testing as needed. Perform testing and prepare reports as required for environmental monitoring or investigation of out-of-specification results, as required. Perform testing and assist with preparation of reports for various special projects as deemed necessary by technical review team. Responsible for tracking relevant trends. Maintain proper laboratory housekeeping and supply levels in the QC laboratory, including submission of purchase requisitions and inventory adjustments. Document all test results and maintain product release records (including electronic records). Document existing product/process validation test results (including electronic records). Maintain product testing database and perform relevant statistical analyses associated with product specifications as specified in laboratory SOPs. As required, coordinate and assist with investigation and resolution of complaints, non-conforming material and product performance issues. Submit complex change orders to update procedures as required. As required, work cross-functionally to investigate and resolve issues deriving from finish product testing. Ensure and maintain compliance with the Company's quality system requirements through training and adherence to policies, procedures and processes. Other duties as assigned. Qualifications Minimum Knowledge & Experience Required for the Position: High school diploma required; Bachelor's degree in Science or equivalent experience preferred. A minimum of four (4) years previous Quality Control lab (QC) and/or Quality Assurance (QA) experience required; previous experience within a regulated medical device manufacturing or In-Vitro Diagnostic Device (IVDD) strongly preferred. Thorough understanding of Good Laboratory Practices (GLP) required. Practical experience with laboratory controls, internal audits, and lab training/maintenance. Phlebotomy certification a plus. Knowledge of FDA-GMP/QSR and ISO standards for quality. Excellent written and verbal communication skills. Ability to work independently and as part of a team. Proficiency with common laboratory techniques, such as pipetting and use of balances. Proficiency with Microsoft Office suite. Proficiency with Large Enterprise Resources Planning (ERP) and Laboratory Information Management (LIMS) systems preferred. Closing If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV. Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual's race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process, please contact ****************************** for assistance. We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7,000 employees around the world comprise our Werfen team. **************

Job Description MPF Federal seeks a Quality Assurance Specialist/Quality Control Specialist to support the Naval Health Research Center (NHRC), Operational Infectious Diseases (OID) Directorate. Reporting to the Contract Program Manager and under the mentorship of the Sr. Laboratory Manager, this role oversees the Quality Management System, ensures compliance to regulatory standards, and makes continuous improvements. The NHRC OID is seeking a meticulous and proactive Quality Assurance/Quality Control Specialist to manage and maintain the integrity of critical research regulatory compliance and documentation. This vital role is responsible for ensuring the accurate and secure storage, retrieval, and control of all laboratory records, SOPs, batch records, and other essential documentation related to operational infectious disease research. The QA/QC Specialist will play a key role in supporting quality assurance efforts, maintaining regulatory compliance, and facilitating efficient data management practices. This position requires a strong understanding of quality systems, exceptional attention to detail, and the ability to collaborate effectively with cross-functional teams to ensure the highest standards of data quality and regulatory adherence. The OID Directorate conducts biosurveillance, clinical trials, research, and diagnostic testing to protect our warfighters, their families, and the homeland against infectious diseases and promote global health security. OID maintains a CLIP (Clinical Laboratory Improvement Program) and CAP (College of American Pathologists) accredited laboratory to support all categories of testing. Test specimens are collected and tested in accordance with their respective study protocols, and results are provided to the applicable sponsors, the Armed Forces Health Surveillance Center, local investigators and collaborators, ordering physicians, and county health units to guide proper responses that ultimately affect both the readiness of US forces and the safety of public health. COMPENSATION: $65-70k annually (this is a non-exempt hourly role) Responsibilities · Develops and maintains the Quality Management System (QMS), including the eQMS (MediaLab). · Ensures compliance with applicable regulatory standards (CLIP/CLIA, CAP, FDA, ISO); serves as primary contact for regulatory audits and help prepare and submit necessary documentation and responses. · Oversees and maintains the Internal Audit Program. · Oversees and maintains the Document Control and Record Retention programs, including maintaining a centralized documentation system for all records, ensuring that data and records are securely stored, easily accessible, and meet regulatory and organizational standards. · Oversee and maintain the nonconforming event system, including investigation of complaints, conducting root cause analyses for identified issues, and ensuring corrective and preventative actions (CAPA) are implemented effectively. · Provides training and orientation to new and existing laboratory staff on quality standards, regulatory requirements, and procedures. · Work with management to identify areas for process improvement and implement changes to enhance the quality of laboratory services. · Performs additional duties and responsibilities as assigned or directed by the supervisor, which may include attendance and participation in required training for the role. Requirements Qualifications A bachelor's degree in a science-related field. One or more years of quality assurance experience. Previous hands-on laboratory bench experience preferred. Knowledge of Regulations: Strong understanding of CLIA/CLIP/CAP regulations and other relevant federal and state guidelines. Quality Systems: Expertise in developing and implementing Quality Management Systems. Auditing Skills: Experience in conducting internal and external audits. Analytical Skills: Ability to analyze data, identify trends, and conduct root cause analyses. Communication Skills: Effective communication for reporting findings, training staff, and collaborating with teams and management. Attention to Detail: Meticulous approach to documentation, data review, and process monitoring. Ability to work effectively with cross-functional teams, including researchers, laboratory staff, and auditors. QA/QC Specialist to be able to help with any standardization of clinical trials documentations and SOPs if needed. US Citizenship and the ability to obtain and maintain a T3/Secret Clearance. Some positions or sites may require that the incumbent be fully vaccinated against COVID-19, and proof of vaccination may be required. Benefits MPF Federal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. We offer a competitive compensation package including a competitive salary, medical benefits, PTO, holiday pay and more.

About the Company Biolinq is a venture-backed digital health company developing a wearable biosensor platform that measures biomarkers important to the management of many clinical conditions including diabetes. This dynamic role is a part of a team of engineers and scientists developing a novel intradermal biosensor technology and the associated software data extraction and rendering SDK that will transform the way people manage their metabolic health. Job Purpose: The Senior Quality Control (QC) Specialist supports Biolinq's quality objectives by reviewing production records, ensuring documentation accuracy, and maintaining compliance with regulatory and internal standards. This role helps drive continuous improvement, supports audit readiness, and collaborates with cross-functional teams to uphold product quality throughout the production process. Duties and Responsibilities: Conduct thorough reviews of Device History Records (DHRs) to verify compliance with SOPs, work instructions, and regulatory requirements (ISO 13485, 21 CFR Part 820, etc.). Perform quality control inspections on products, including in-line checks, label verification, and final goods assessment. Lead regular production line audits, proactively identifying compliance risks and escalating issues as appropriate. Collaborate with Manufacturing and Quality teams to resolve discrepancies, implement corrective actions, and drive continuous improvement. Support audit preparation activities, including documentation review, gap analysis, and readiness assessments for production areas Document and report quality metrics related to DHR review and audit readiness. Ensure ongoing compliance with evolving regulatory and quality system requirements Performs additional duties as assigned. Requirements Qualifications: High school diploma or GED required. Bachelor's degree preferred 5-7+ years experience in a regulated medical device production environment Demonstrated expertise in DHR review, regulatory compliance, and audit preparation. Familiarity with Quality Management Systems, Enterprise Resource Planning systems, and equipment management tools (e.g., MasterControl, NetSuite/Oracle ERP, BMRAM). Ability to work collaboratively across departments Strong analytical skills, attention to detail, and problem-solving abilities. Excellent verbal and written communication skills. Working Conditions: Work is primarily performed in a production (Clean Room) and office environment. Physical Requirements: While performing the duties of this job, the employee is regularly required to stand; walk; sit; use hands to finger, handle or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, see, talk or hear in a standard office environment. Employee may occasionally lift/or move up to 15 pounds. BENEFITS Medical, dental, vision, health savings account, flexible spending account, life and long-term disability insurance, 401(k) plan, holidays, and PTO. At Biolinq we fully subscribe to the principles of Equal Employment Opportunity. It is our policy to provide employment, compensation, and other benefits related to employment based on qualifications, without regard to race, color, religion, national origin, age, sex, veteran status, genetic information, disability, or any other basis prohibited by federal, state or local law. In accordance with requirements of the Americans with Disabilities Act and applicable federal, state and/or local laws, it is our policy to provide reasonable accommodation upon request during the application process to applicants in order that they may be given a full and fair opportunity to be considered for employment. As an Equal Opportunity Employer, we intend to comply fully with applicable federal, state and/or local employment laws and the information requested on this application will only be used for purposes consistent with those laws. To the extent required by applicable law, The Company maintains a smoke- free workplace. As part of our efforts to ensure fair and equal pay based on merit, Biolinq supports pay transparency internally and during the recruitment process. The U.S. base salary range reasonably expected to be paid for this role is: $28.00 to $32.00 per hour. We may ultimately pay more or less than the posted range. Actual compensation packages are commensurate with experience and based on a variety of factors that are unique to each candidate including, but not limited to: skill set, depth of experience, education, certifications, and specific work location. The range displayed reflects the minimum and maximum target for new hire salaries for the job across the U.S. The total compensation package for this position may also include an annual performance bonus and/or other applicable incentive compensation plans. Biolinq also offers a comprehensive package of benefits including paid time off (vacation, holidays, sick time, parental leave), medical/dental/vision insurance, and 401(k) to eligible employees, subject to the terms and conditions of the applicable plans and any written agreement between the parties. Your recruiter can share more about the total compensation package during the hiring process. Please note: The information contained herein is not intended to be an all-inclusive list of duties and responsibilities of the job, nor are they intended to be an all-inclusive list of the skills and abilities required to do the job. Management may, at its discretion, assign or reassign duties and responsibilities to this job at any time. The duties and responsibilities in this job description may be subject to change at any time due to reasonable accommodation or other reasons. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please contact Biolinq Talent Acquisition at *******************

Job DescriptionDescription: Job Title: Quality Control Specialist III Company: Trimitron Corporation Position Type: Full-Time Equivalent (FTE) Trimitron Corp is seeking an experienced Quality Control Specialist III to provide advanced quality oversight, technical evaluation, and engineering support to the Naval Information Warfare Center (NIWC) Pacific's Positioning, Navigation, and Timing (PNT) Division. This senior-level role ensures that all products, processes, test activities, and fabricated components meet stringent Navy, DoD, and industry quality and safety standards. The ideal candidate brings hands-on experience with U.S. Navy navigation systems, strong technical problem-solving skills, and the ability to interpret engineering drawings, evaluate system performance, and support prototype development in a mission-critical environment. Key Responsibilities: Ensure all products, services, and engineering processes meet established quality, safety, and performance standards. Conduct inspections, testing, and evaluations of equipment, components, and fabricated models supporting PNT system development. Verify that testing processes operate effectively, safely, and in accordance with Navy and DoD requirements. Document findings, non conformances, and corrective actions with precision and clarity. Support quality audits, readiness reviews, and technical assessments for PNT-related systems. Technical & Engineering Support Apply engineering concepts and practical technical knowledge to support system testing, troubleshooting, and evaluation. Interpret engineering plans, schematics, and technical drawings to support quality assessments and fabrication activities. Contribute to the design and fabrication of test specimens, prototypes, and model components. Utilize Computer-Aided Drafting (CAD) tools to prepare shop drawings and support model construction. Ensure material specifications, fabrication methods, and engineering practices align with quality standards. Provide hands-on support to PNT engineers and program teams working on U.S. Navy navigation systems. Support system integration, prototype testing, and operational assessments for PNT technologies. Serve as a recognized technical resource in U.S. Navy navigation equipment and systems. Solve complex technical problems related to navigation systems, fabrication, testing, and quality processes. Provide technical insights and recommendations to engineering teams and government stakeholders. Support continuous improvement initiatives to enhance quality, safety, and system performance. Required Qualifications: TS/SCI security clearance (active). High School Diploma, GED, trade/industrial school graduate, or related military training. Three (3) years of professional experience solving technical problems. Training in engineering techniques, software design/maintenance, or related technical disciplines. Practical understanding of engineering concepts, quality standards, and safety requirements. Experience testing equipment to ensure safe and effective operation. Ability to interpret engineering plans, drawings, and technical documentation. Experience with CAD software, shop drawings, material specifications, and fabrication methods. Three (3) years of hands-on experience with U.S. Navy Navigation equipment and systems, including expertise in at least one of the following: - Systems Requirements - Operational Requirements - Test & Evaluation - Training Preferred Qualifications Recognized expertise or leadership in U.S. Navy navigation systems. Experience supporting NIWC, NAVWAR, NAVSEA, or other Navy technical programs. Familiarity with PNT technologies, navigation sensors, or maritime system integration. Why Join Trimitron Corp.? This position offers the opportunity to contribute to mission-critical defense projects, work alongside highly skilled professionals, and engage in challenging systems engineering tasks that directly impact national security operations. Benefits: We offer competitive pay and generous benefits including comprehensive medical insurance package, 401k with company match, employee assistance program and company paid benefits. Requirements:

Join our dynamic team in San Diego, CA, a hub for innovation and biotechnology, where you can leverage your skills in a thriving environment. We are seeking a dedicated professional to ensure the highest quality standards in our laboratory operations. Job Responsibilities Train and become proficient in all required techniques, operation of relevant equipment, and software packages associated with testing, data analysis, and data reporting. Work with human blood, human or mammalian cell culture, and/or animals and animal tissues as needed. Complete all assigned QC tests accurately and timely under supervision, following standard protocols or operating procedures. Prioritize daily workload and develop skills to work independently. Analyze data, report test results, and complete all required documentation and database entries as required by QC protocols or operating procedures. Calibrate and maintain equipment, reporting any issues to the QC Supervisor or Manager. Maintain logs and required documentation as necessary. Prepare lab supplies, reagents, and assist with laboratory maintenance as needed. Promote a safe work environment and provide recommendations for maintaining safety. Participate in Environmental, Health & Safety programs and address corrective actions when hazards are identified. Notify supervisor and Safety Officer(s) of all observed hazardous conditions or unsafe work practices. Keep abreast of the basic requirements for safety compliance in your area of work and comply with those requirements. Participate in group or intra-department teams and projects as required. Engage in assigned cross-training and perform other related duties and assignments as required. Education and Experience BS/BA in a related scientific discipline or some related college coursework with a minimum of 2 years of related experience in a biotech lab environment. Experience in an industrial or research laboratory preferred. Flow Cytometry experience required. Tissue Culture experience highly preferred. Knowledge and Skills Basic computer skills: MS Excel & Word. Knowledge of general laboratory safety. Effective interpersonal, written, and oral communication skills. Demonstrated ability to follow established policies/procedures, and ability to keep neat, accurate, and complete records and logs. Effective analytical and problem-solving skills.

Founded in 1952 and formerly known as Heery International Inc., the firm operates throughout the United States as part of Turner & Townsend. It specializes in project and program management for public sector organizations, with industry-leading experts in corporate, cultural, healthcare, justice, sports, K-12 education, higher education, aviation and government facilities. Recognized for service excellence by a broad spectrum of professional organizations and industry publications, the talented multidisciplinary team at Turner & Townsend Heery exceeds client expectations - adding value, best practice and expertise at every turn. The team's unique client-centric culture is integrated into each project and reflects a passion for the built environment and staying true to the client's vision. Job Description The QA/QC Senior Inspector will lead the effort for the client and provide, on-site inspection services to ensure all construction activities comply with client standards, project specifications, and contract requirements. The Inspector will monitor quality, safety, and environmental performance while preparing detailed inspection reports and supporting project documentation. Responsibilities: * Perform daily field inspections of construction activities and materials. * Verify compliance with project specifications, drawings, and client standards. * Prepare and maintain daily inspection reports, logs, and punch lists. * Track contractor manpower, equipment, and material deliveries. * Ensure compliance with sustainability and IRA-related construction mandates. * Support resolution of deficiencies and coordination of corrective actions. * SOX control responsibilities may be part of this role, which are to be adhered to where applicable. Qualifications * High school diploma required; associate or bachelor's degree preferred. * 10-15 years of construction inspection experience, preferably on federal projects. * Knowledge of GSA inspection protocols and federal construction requirements. * Certifications such as ICC, ACI, or equivalent strongly preferred. * Experience on large projects ($100M+) highly desirable. Additional Information The salary range for this full-time role is $130K-$150K per year. Ranges are determined by role and level and represent a good faith effort to provide a fair and equitable salary. This range is a reflection of base salary only, not of a total compensation package. Please note Turner & Townsend reserves the right to pay more or less than the posted range, depending on candidate's experience and qualifications. * On-site presence and requirements may change depending on our client's needs* * Qualified candidates with arrest or conviction records will be considered for employment in accordance with LA County ordinance and CA law. Our inspired people share our vision and mission. We provide a great place to work, where each person has the opportunity and voice to affect change. We want our people to succeed both in work and life. To support this we promote a healthy, productive and flexible working environment that respects work-life balance. Turner & Townsend is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees and actively encourage applications from all sectors of the community. Please find out more about us at ************************** and ********************** All your information will be kept confidential according to EEO guidelines. #LI-JS3 Join our social media conversations for more information about Turner & Townsend and our exciting future projects: Twitter Instagram LinkedIn It is strictly against Turner & Townsend policy for candidates to pay any fee in relation to our recruitment process. No recruitment agency working with Turner & Townsend will ask candidates to pay a fee at any time. Any unsolicited resumes/CVs submitted through our website or to Turner & Townsend personal e-mail accounts, are considered property of Turner & Townsend and are not subject to payment of agency fees. In order to be an authorised Recruitment Agency/Search Firm for Turner & Townsend, there must be a formal written agreement in place and the agency must be invited, by the Recruitment Team, to submit candidates for review.

Job Description Craft and Technical Solutions is an established Marine and Industrial Staffing Company with offices all over the country. We partner with businesses as well as jobseekers to place individuals into positions efficiently. We are currently in need of QA/QC Inspectors to join our team in San Diego, CA! Pay Rate: $24/hour Job Details: Perform basic inspection of shipbuilding and ship repair work in accordance with established policies to ensure compliance with technical requirements Performs other Quality Assurance tasks as assigned by supervisor/manager Ensure correct materials and proper fabrication and installation procedures are utilized during production processes Evaluate results from tests and inspections to determine acceptability with assistance as needed Basic understanding and ability to research technical documents including engineering drawings, specifications, standards, test procedures, work instructions, NAVSEA Standard Items, and contract requirements Basic understanding of the usage of calibrated equipment and ability to validate calibration of equipment, gauges, and tools used in production and inspection in accordance with established policies Basic ability to recognize and document nonconformance's per company policy Basic understanding of root cause analysis, corrective action, and preventative action practices Ability to learn and perform process audits and surveillances Drafts, reviews, and/or submits QA reports and technical documents Actively participates in implementing and monitoring continuous improvement initiatives to improve safety, improve quality, reduce cycle time, and reduce costs Brings complex issues to the attention of Supervision Requirements High School education or equivalent; Additional technical education or college education a plus Zero to four (0 - 4) years of Quality Assurance or related experience Knowledge of shipbuilding and repair operations a plus Ability to develop technical knowledge of ship construction and repair processes including welding, structural, machinery, electrical piping, ventilation, flushing and develop familiarity with various measuring instruments related to inspections. Computer literate; knowledge of Microsoft Word, Excel, Outlook, PowerPoint, and IFS Quality Modules a plus Good written and verbal communication skills, integrity, presentation skills, problem solving skills Positive attitude and determination to help others required Able to learn to read and understand blueprints, standard/specifications, regulatory body requirements, and ship specifications Must be a team player Benefits CTS, LLC offers a comprehensive benefit packet to eligible employees. Eligible employees may enroll in: Health Dental Vision Voluntary Life/Voluntary AD&D Short-Term Disability Long-Term Disability Hospital Indemnity Accident Critical Illness 401k Safety and responsible work practices are of paramount importance at CTS and are woven into the fabric of everything we do. We are committed to employee safety & development, the protection of the environment and the communities where we operate. We are ready to be a partner in your career success! Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform essential job functions. Craft and Technical Solutions, LLC has a consistent policy that requires an online application to be completed before we can further consider you as an applicant for this position. CTS is an EOE AA M/F/Vet/Disability

Asphalt Quality Control Technician - 2500037V Description Build Your Career. Build America's Future. Vulcan Materials Company is the nation's largest producer of construction aggregates and a major producer of aggregates-based construction materials including asphalt and ready-mixed concrete. When you join Vulcan, it's more than starting an exciting career - you get to make a difference for millions of people every day across the country. When you join Vulcan, you join a dynamic culture in which career development is encouraged, excellence is rewarded, and diversity is valued. No matter the role or the location across the country, every member of the Vulcan team lives through the Vulcan Way: doing the right thing, the right way, at the right time. We're Coming Back Together To Be Together 100% In Office & Onsite At Vulcan Materials, we believe that the heart of our success lies in the strength of our engagement, our connection, and our commitment to developing our people. We are excited to restore the collaborative in-person environment that fuels our innovation and growth. This move is not just about being physically present; it's about reigniting the spirit that comes from face-to-face interactions, fostering a collaborative, inclusive culture where every voice is heard and everyone thrives. What You'll Do:Ensure Quality Control. Conduct routine testing of in-process materials, raw materials, environmental samples, and finished materials to ensure quality control of products at the point of production, shipping, and arrival upon the job site. Adhere to testing methods, including American Society for Testing and Materials (ASTM), American Association of State Highway and Transportation Officials (AASHTO) and Department of Transportation (DOT). Document and Report Information. Complete all required reports in a timely and accurate manner, interpreting, documenting, and storing the results. Communicate test results in a timely manner to the supervisor and properly document in a database. Maintain Lab Standards. Ensure housekeeping standards are maintained in and around the lab. Troubleshoot problems and review basic product specifications. Inspect, calibrate, and maintain testing equipment periodically. Monitor Stockpile. Inspect stockpiles, materials sources, and truckloads at plant sites. Monitor the daily construction of the stockpile to ensure that segregation and contamination is kept to a minimum or eliminated. Notify management immediately if contamination is identified. Inspect Equipment and Structures. Conduct routine inspections of the plant equipment in order to ensure safe, reliable, and compliant operations to maximize production and minimize interruptions. Additional Responsibilities. Other duties as assigned. Qualifications Skills You'll Need: Experience. Prior training or experience in the materials testing field is preferred. Knowledge of general principles and practices of aggregate production is preferred. Travel. This role requires travel to various sites throughout Southern California. Must be willing to drive to these sites when needed and have a valid Driver's License. Safety Knowledge. Must display knowledge and awareness of construction and mining site hazards. Math Skills. Must possess good math skills and demonstrate the ability to perform simple to moderately complex arithmetic calculations. Technology Skills. Must have the ability to use computerized equipment and technology. Must be proficient in Microsoft Office Suite, Google, Oracle Business Environment, and other software packages relevant to the position. What You'll Like About Us: Great Company Culture. Our people share a competitive drive for excellence in an environment of trust, teamwork, open-mindedness and communication. Safe. Industry leader in health and safety standards. We are committed to creating a safe work environment and protecting all employees and customers. Meaningful Work. What sets up apart is the work we do impacts daily lives - and every employee contributes. Our aggregates produced are used to build roads, schools, hospitals, airports, and housing throughout the United States. Health Benefits. Medical, Dental, Vision programs, plus much more. Rest and Relaxation. Paid vacation, personal floating days, and paid holidays. Prepare for the Future. 401(k) with company match and contribution. Training and Development. We see our development programs and helping our employees meet their goals as a key part of our business. Salary Range: the base salary range for this role is between $27. 00 to $30. 00 per hour. This range is not inclusive of our discretionary bonus or equity package. When determining a candidate's compensation, we consider a number of factors, including skillset, experience, job scope, and current market data. Vulcan Materials Company is committed to employing a diverse workforce. You will receive consideration without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, gender expression, veteran status, or disability. You also have the right to be free from discrimination for medical needs arising from pregnancy, childbirth, or related medical conditions. NOTICE TO TEMPORARY STAFFING AGENCIES, PLACEMENT SERVICES AND PROFESSIONAL RECRUITERSVulcan Materials Company has an internal recruiting department. Please review our policy as it relates to the use of temporary staffing agencies, placement services and professional recruiters. Job: Quality Control Primary Location: California-San Diego Organization: GM - SO CAL Schedule: Full-time Job Posting: Dec 8, 2025, 11:31:21 PM

Job DescriptionQuality Control InspectorAre you passionate about ensuring the highest quality standards in the biotech industry? We are seeking a skilled and detail-oriented Quality Control Technician to join our reputable biotech diagnostic company. Location: CarlsbadPay Rate: $18 - $19.80/hr, contract Both 1st shift and 2nd shift available, Monday-Friday and weekends as needed Key Responsibilities: Perform routine and special inspections for visual, dimension, and functional assessments, ensuring adherence to inspection instructions. Document and report inspection findings, monitoring corrective actions for any identified issues. Execute product identification and traceability activities as required. Review, approve, and maintain Device History Records for all manufacturing functions, in compliance with relevant standards and regulations. Apply in-depth knowledge of QSRs/ISO and regulatory guidelines to daily tasks, ensuring quality standards are upheld. Monitor and comply with customer specifications and company quality assurance policies. Ensure proper calibration and maintenance of inspection equipment. Essential Functions: Conduct and document hourly inspections. Perform and document line clearance procedures. Carry out First Articles and Retention Samples, documenting and filing accordingly. Review, approve, and file documents for completeness and compliance. Work Environment:The work environment encompasses warehouse, laboratory, and manufacturing settings, where handling viral and bacterial hazards, potentially hazardous chemicals, and infectious bodily fluids and samples may occur. Flexible work hours may be required to meet project deadlines. Education, Skills & Experience: Minimum 6 months of Quality Control inspection experience required. Experience with Good Manufacturing Practice (GMP) Experience in a medical device high-volume manufacturing environment is strongly desired. Ability to read, interpret, and follow detailed procedures, instructions, and drawings. Solid understanding of QSRs/ISO standards. Demonstrated team-oriented interaction skills and professional behavior. Proficiency in word processing, data entry, and spreadsheet navigation. Familiarity with basic quality terms, definitions, and concepts. Understanding of traceability (product, material, and calibration). Basic math skills for determining appropriate sample sizes for inspection based on lot sizes. Problem-solving skills to identify processes and standards in need of improvement and initiate appropriate action. If you are driven by a commitment to excellence and have a passion for quality control in the biotech industry, we encourage you to apply. Join our dedicated team and make a significant impact on healthcare by maintaining the highest quality standards in our biotech diagnostic products.