Quality assurance technician jobs in Delaware - 164 jobs

Contribute to ensuring high-level of product and process quality for one of NKT's Business Lines NKT is on a growth journey, and we are expanding our Group Quality team with a new member to support our business line for high-voltage power cable solutions. Are you a quality professional with a commitment to ensuring quality and processes? Do you want to enhance our quality standards, ensure that we continue to meet our customers' expectations and contribute to a greener world? Secure, optimize and improve our process and product quality standards As a Group Quality Lead, you will provide optimized support to our stakeholders within the Solutions (SOL) Business Line, ensuring high-quality product and process outcomes. Working closely with local teams, you will ensure the implementation and execution of both Group and Local quality strategies to ensure compliance to NKT's management system. Serving as a key point of contact, you will offer guidance, facilitate best-practice sharing, and provide direct support across our two high-voltage power cable manufacturing sites in Cologne, Germany, and Karlskrona, Sweden. Your main tasks will be to: * Develop and support the implementation of NKT's global and local quality strategy, executing and validating the effectiveness of initiated processes. * Facilitate, support, and monitor problem solving methods, process improvements to ensure that key performance indicators are met. * Identify, initiate, and execute improvement activities, identify quality and process synergies across the sites and implement best-practices. * Support in implementing a governance with key stakeholders by directing steering committees and coordinating quality councils * Enhance and professionalize the global quality culture by promoting continuous improvement and best practices * Act as a quality partner to local and group stakeholders, ensuring alignment on quality objectives and initiatives * Act as the primary liaison between the local organizations to address quality issues in real-time * Conduct risk-based internal audits to ensure compliance with internal standards, customer requirements, and industry regulations You will join an international and collaborating team. We are open to flexible locations close to our offices in Cologne (Germany) or Karlskrona (Sweden). Being present at our sites, supply direct (shopfloor) support, stakeholder management, collaborating with our local teams and creating long-lasting internal and external relationships is key in this role. Frequent international travelling between both sites is to be expected (approx. 70%). Experienced quality professional You have a multi-site experience meaning you can deal with different cultures and different level of stakeholders within our sites in Europe. You work well within a team as well as efficiently manage your own tasks, are motivated, bring a solution-oriented mindset and have great communication skills (both written and verbal). High level of integrity and professionalism, stakeholder management skills, collaborative approach and the ability of setting priorities is also key for this position. The ability to make sense of problems and define follow-up steps that lead to effective solutions are what we expect from you. You also have: * Bachelor's degree in electrical or mechanical engineering or equivalent * 5 Years+ of leadership experience in Quality or Process within a manufacturing industry * Experience in power cable manufacturing industry is beneficial * Certifications in Lean Six Sigma and ISO9001:2025 (internal) auditor * Experience in risk management tools as Failure Mode & Effect Analyses (FMEA) * Problem solving skills with experience in Ishikawa, 5-Why, 8D or equivalent * Project management skills is beneficial * Fluency in English. Swedish or German language is considered beneficial Contribute, develop and grow NKT is committed to fostering a diverse organization and a culture where people from different backgrounds can thrive and are inspired to perform at their best. We believe that a diverse organization enables sustainable performance, and that an inclusive and welcoming culture makes for a better place to work. We offer the possibility to join an international company, an important seat within Group Quality Team and exciting career opportunities. Read more about our offer and listen to some voices of NKT Connectors here! We will review applications continuously but we recommend you to apply no later than 8th of February. Please apply with an English version of your resume. Personality and cognitive tests might be included in the recruitment process. If you have any questions regarding the position or have any inquiries about the recruitment process please reach out to Angelina Nilsson, Global Talent Attraction Specialist ************************. Please note that due to the GDPR regulations we cannot accept any applications via e-mail. Union representatives Sveriges Ingenjörer - Christian Fisch, +46 455 56 380 Unionen - Joakim Wikström, +46 734 070 243 Ledarna - Roger Jönsson, +46 455 55 911 Be a Connector of the green tomorrow! #LI-AN1 #LI-Hybrid About NKT NKT connects a greener world with high-quality power cable technology and takes centre stage as the world moves towards green energy. NKT designs, manufactures and installs low-, medium- and high-voltage power cable solutions enabling sustainable energy transmission. Since 1891, NKT has innovated the power cable technology building the infrastructure for the first light bulbs to the megawatts created by renewable energy today. NKT is headquartered in Denmark and employs 6,000 people. NKT is listed on Nasdaq Copenhagen and realised a revenue of EUR 3.3 billion in 2024. We connect a greener world. ***********

Established in 1991, Collabera has been a leader in IT staffing for over 22 years and is one of the largest diversity IT staffing firms in the industry. As a half a billion dollar IT company, with more than 9,000 professionals across 30+ offices, Collabera offers comprehensive, cost-effective IT staffing & IT Services. We provide services to Fortune 500 and mid-size companies to meet their talent needs with high quality IT resources through Staff Augmentation, Global Talent Management, Value Added Services through CLASS (Competency Leveraged Advanced Staffing & Solutions) Permanent Placement Services and Vendor Management Programs. Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence. Collabera offers a full range of benefits to its employees including paid vacations, holidays, personal days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance, Disability Insurance. Job Description Job Title: Quality Technician Location: Newark, DE 19713 Duration: 6 months Shift: 12 hour shifts (3 days on, 3 days off; 4 days on, 4 days off) Perform various properties testing of composite materials and generate reports used for batch acceptance Qualifications Must have previous technical testing experience in a lab. Must have experience with state of the art technical test technology. Experience with tensile testing and quality dimensions. Additional Information If you are interested and want to apply, Please contact: Himanshu Prajapat ************ **********************************

Join our team to play a pivotal role in mitigating tech risks and upholding operational excellence, driving innovation in risk management. As a Tech Risk & Controls Lead in Cybersecurity & Tech Controls, you will be responsible for identifying, and mitigating compliance and operational risks in line with the firm's standards. You will also provide subject matter expertise and technical guidance to technology-aligned process owners, ensuring that implemented controls are operating effectively and in compliance with regulatory, legal, and industry standards. By partnering with various stakeholders, including Product Owners, Business Control Managers, and Regulators, you will contribute to the reporting of a comprehensive view of technology risk posture and its impact on the business. Your advanced knowledge of risk management principles, practices, and theories will enable you to drive innovative solutions and effectively manage a diverse team in a dynamic and evolving risk landscape. Job responsibilities Manage horizontal execution of outsourcing controls. Ensure accurate monitoring, transparent reporting and issue/risk escalation with leaders and partners Ensure compliance with firm wide outsourcing policy and/or standards Identify, escalate and implement solutions for identified issues and risks along business stakeholder decisions. Demonstrate superior judgment to mitigate risk impacts to the operational processes: Reputation, Regulatory, Legal, Operational, and Financial. Collaborate with stakeholders in a consulting role to add value and address unresolved critical problems and exposures Develop and maintain key contacts and working relationships with various areas within Enterprise Technology, Controls peer groups, and CTPO Ensure timely escalation of key risks and issues to management and interested stakeholders Represent the Third Party and IAS Oversight team in various governance, legal, and controls forums Required qualifications, capabilities, and skills 5+ years of experience or equivalent expertise in technology risk management, information security, or related field, emphasizing risk identification, assessment, and mitigation Familiarity with risk management frameworks, industry standards, and financial industry regulatory requirements Proficient knowledge and expertise in data security, risk assessment & reporting, control evaluation, design, and governance, with a proven record of implementing effective risk mitigation strategies Demonstrated ability to influence executive-level strategic decision-making and translating technology insights into business strategies for senior executives Familiarity with outsourcing risk and processes, implementing policies/standards, and risk management Ability to coordinate engagement with key stakeholders and proficiency in cross-functional frameworks Strong understanding of controls framework and compliance standards Adaptability to thrive in a fast-paced, collaborative, team-oriented, cross-functional environment Self-motivated and confident decision-maker with the ability to lead, challenge and influence change where necessary Synthesizes data quickly and communicates analysis succinctly and professionally Preferred qualifications, capabilities, and skills CISM, CRISC, CISSP, or similar industry-recognized risk and risk certifications are preferred Ability to maintain professional documentation for internal and external reporting purposes Demonstrated knowledge/background in internal control philosophies

Are you passionate about ensuring compliance and patient safety in the medical device industry? At Hologic, we are seeking a Clinical QA Specialist to play a critical role in the investigation and reporting of potential and actual adverse events, as well as other regulatory reporting activities. In this role, you'll collaborate with cross-functional teams, including Technical Service, Marketing, Sales, and Regulatory, to ensure timely and thorough documentation, analysis, and reporting. If you thrive in a fast-paced, collaborative environment and have a strong background in regulatory compliance and quality assurance, this is your opportunity to make a meaningful impact on healthcare innovation. Knowledge: Comprehensive understanding of FDA Quality System Regulations, ISO 13485, EU Medical Device Regulation, and ISO 14971 for risk management. Strong knowledge of medical procedures and the expected and potential outcomes related to Hologic's product portfolio. Familiarity with post-market surveillance requirements, adverse event reporting, and health risk assessments. Awareness of regulatory reporting processes, including MedWatch reports, notified body communications, and external notifications. Skills: Proven ability to independently collect, analyze, and assess information associated with adverse events and determine appropriate next steps. Effective communication skills to interact with internal teams, sales personnel, customers, patients, and regulatory agencies. Strong organizational skills to ensure timely documentation, reporting, and follow-up of adverse events and regulatory submissions. Analytical skills to support and lead investigations, including CAPAs, nonconformances, and other quality system processes. Experience in developing metrics and quality reports related to reportable events and identifying potential excursions. Ability to innovate and improve processes to enhance efficiency and compliance with post-market surveillance requirements. Proficient in leading or participating in internal and external audits, inspections, and assessments. Behaviors: Proactive and detail-oriented, ensuring compliance with regulatory requirements and internal procedures. Collaborative and team-oriented, fostering strong relationships across functions to support investigations and reporting activities. Customer-focused, ensuring communications and responses are timely, accurate, and aligned with patient safety goals. Resilient and adaptable, thriving in a fast-paced and evolving environment. Problem-solving mindset, with a commitment to driving resolution and continuous improvement in quality processes. Experience: Bachelor's degree in Medicine, Nursing, Biomedical Engineering, Electromedical Engineering, or a related field. Risk Managers will also be considered. 5+ years of experience in a similar role, preferably within the medical device or healthcare industry. Hands-on experience with adverse event reporting, regulatory communications, and health risk assessments. Proven track record in supporting or leading CAPAs, nonconformances, and quality investigations. Why join Hologic? We are committed to making Hologic the destination for top talent. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career. The annualized base salary range for this role is $83,000 - $129,700 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, education, business needs and market demand. Agency and Third-Party Recruiter Notice Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition, Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered. Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans. #LI-NT1

Join our team to play a pivotal role in mitigating tech risks and upholding operational excellence, driving innovation in risk management. As a Tech Risk & Controls Lead in [Insert LOB and/or Sub LOB], you will be responsible for identifying, and mitigating compliance and operational risks in line with the firm's standards. You will also provide subject matter expertise and technical guidance to technology-aligned process owners, ensuring that implemented controls are operating effectively and in compliance with regulatory, legal, and industry standards. By partnering with various stakeholders, including Product Owners, Business Control Managers, and Regulators, you will contribute to the reporting of a comprehensive view of technology risk posture and its impact on the business. Your advanced knowledge of risk management principles, practices, and theories will enable you to drive innovative solutions and effectively manage a diverse team in a dynamic and evolving risk landscape. Job responsibilities Ensure effective identification, quantification, communication, and management of technology risk, focusing on root cause analysis and resolution recommendations Develop and maintain robust relationships, becoming a trusted partner with LOB technologists, assessments teams, and data officers to facilitate cross-functional collaboration and progress toward shared goals Execute reporting and governance of controls, policies, issue management, and measurements, offering senior management insights into control effectiveness and inform governance work Proactively monitor and evaluate control effectiveness, identify gaps, and recommend enhancements to strengthen risk posture and regulatory compliance Required qualifications, capabilities, and skills Formal training or certification and 5+ years of experience in technology risk management, information security, or related field, emphasizing risk identification, assessment, and mitigation Familiarity with risk management frameworks, industry standards, and financial industry regulatory requirements Proficient knowledge and expertise in data security, risk assessment & reporting, control evaluation, design, and governance, with a proven record of implementing effective risk mitigation strategies Demonstrated ability to influence executive-level strategic decision-making and translating technology insights into business strategies for senior executives Preferred qualifications, capabilities, and skills CISM, CRISC, CISSP, or similar industry-recognized risk and risk certifications are preferred

One of Insight Global's largest pediatric healthcare clients is seeking a Clinical Laboratory Quality Assurance Supervisor to join their laboratory group at the main hospital in Wilmington, DE. This person will ideally specialize in blood bank operations and ensure compliance with CAP, AABB, and CLIA standards (among others) by leading inspection readiness, managing quality systems, and working hands-on with technologists and inspectors during audits. This role oversees document control, competency programs, and corrective actions, while maintaining a strong floor presence to guide workflows, validate processes, and resolve issues in real time. The supervisor drives continuous improvement, supports training, and serves as the primary liaison during inspections to uphold patient safety and regulatory excellence. This candidate will have a hand in preparing the laboratory for upcoming expansion this year and will be expected to serve as the subject matter expert for inspections and regulatory guidelines. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to ********************.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: **************************************************** Skills and Requirements Bachelor's degree. 5+ years of experience as a Blood Bank Technologist or Generalist with specialization in Blood Banking. Thorough knowledge of inspection process & laboratory guidelines (ex/ CAP, CLIA, COLA, AABB) Excellent communication skills, ability to articulate guidelines and processes between techs and leadership. Previous experience serving as point person for inspections via CAP, CLIA, COLA, JCo, or additional clinical laboratory guidelines. Leadership or supervisory level experience. Senior or Lead Blood Bank experience.

The QC Microbiology Lead will manage all microbiology laboratory activities at WuXi STA's drug product manufacturing site in Middletown, DE. This role is responsible for establishing, maintaining, and continuously improving GMP-compliant microbiological testing programs for drug product manufacturing, including environmental monitoring (EM), water system monitoring, bioburden, endotoxin, and identification testing. The QC Microbiology Lead will play a key role in site startup by building the micro lab infrastructure, qualifying equipment, and establishing EM programs. In steady-state operations, this role will ensure timely execution of microbiology testing to support manufacturing, product release, cleaning validation, and regulatory readiness. Responsibilities Microbiology Laboratory Leadership • Lead the setup and daily operations of the QC Microbiology laboratory for drug product manufacturing, ensuring alignment with corporate quality standards. • Oversee procurement, installation, qualification, calibration, and maintenance of microbiology equipment including biosafety cabinets (BSCs), incubators, autoclaves, particle counters, endotoxin testing systems, and microbial identification instruments. • Develop, implement, and maintain SOPs, test methods, and microbiological procedures in compliance with ICH, USP , , , , EP, and JP requirements. • Establish and manage workflows to ensure microbiological testing supports manufacturing and packaging schedules. Method Transfer, Validation, and Testing Support • Lead microbiological method transfers and validations from WuXi STA global R&D sites and client facilities for drug product testing. • Ensure robustness, reproducibility, and regulatory compliance of validated microbiology methods. • Oversee and review microbiology data for environmental monitoring (EM), water system monitoring, bioburden, endotoxin, and microbial identification testing. • Provide microbiological support for process validation, cleaning validation, and contamination control strategy implementation. • Provide timely review and approval of microbiological data to meet batch release and stability program timelines. Regulatory Compliance • Ensure all analytical testing meets FDA, EMA, and ICH regulatory requirements for drug product QC. • Maintain compliance with data integrity principles (ALCOA+), ensuring accurate and complete documentation. • Prepare microbiology teams for client and regulatory inspections, acting as the primary microbiology SME during audits. • Monitor industry trends, regulatory updates, and compendial changes, ensuring methods and procedures remain compliant. Technical Leadership • Act as SME for microbiological techniques including EM, endotoxin testing (USP ), microbial limits testing (USP /), microbial identification, and water system monitoring. • Lead troubleshooting of complex microbiological issues, overseeing root cause analysis and CAPA implementation. • Collaborate with QC Analytical and QC Operations to optimize sample management, workflows, and shared resources. • Identify and recommend new microbiological technologies or automation to improve efficiency, accuracy, and throughput. People Management & Leadership • Build, lead, and develop the microbiology laboratory team, defining roles, responsibilities, and performance expectations. • Provide coaching, technical training, and career development opportunities for team members. • Conduct regular performance evaluations, manage staffing levels, and ensure adequate coverage for operations. • Foster a culture of accountability, collaboration, and continuous improvement within the team. Qualifications • PhD in Microbiology or related field preferred; Master's or Bachelor's degree with extensive relevant experience will also be considered. • Minimum 7 years of microbiology QC experience in GMP-regulated drug product manufacturing, with demonstrated leadership or supervisory responsibilities. • Proven expertise in microbiology method transfer, validation, and compendial testing for finished dosage forms. • Strong understanding of ICH, USP , , , , EP, JP, FDA, and EMA regulatory requirements for drug product QC. • Demonstrated ability to manage teams in a fast-paced manufacturing environment with multiple client projects. 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 based on disability This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management. We can recommend jobs specifically for you! 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 Click here to get started.

Do you believe that quality is not a coincidence, but the result of responsibility, accuracy and real teamwork? Then you're the perfect fit for us! In Quality assurance, you don't just count numbers and check processes. You will help to ensure that our products leave the factory reliably, safely and with pride. If it's important to you that every move counts, you like to think for yourself and value good teamwork, we look forward to getting to know you! Apply now! Become part of our team and make a difference before it becomes visible. Contract type Temporary Workload 100% Working time model 2-shift operation Start of employment as of now Bell Deutschland GmbH & Co. KG Osterschepser Straße 40 26188 Edewecht Calculate route Language German What we offer Work-life balance We offer 30 vacation days, a flexitime system and special leave for important events such as marriage, birth or relocation. In addition, you do not work on 24 December and 31 December. Professional development opportunities Expand your knowledge with extensive training programmes, high-quality courses at the Coop Training Centre and a wide range of personal development opportunities such as mentoring and coaching. Health Your well-being is important to us: Benefit from our health management programme and subsidised fitness subscriptions - for health and fun during your leisure time. Fair wages and social benefits Receive anniversary bonuses and attractive rewards for employee referrals. We also offer various corporate benefits (discounted online shopping offers) and a company pension scheme. At our plant in Schiltach, we also offer monthly vouchers (e.g. supermarket, petrol station) and free lunch. Your tasks * Carrying out process checks on the lines during production * Checking the metal detectors * Creating labels * Taking and labelling retained samples, chemical and microbiological samples, tasting samples * Regularly carrying out cleaning checks and checking intermediate cleaning * Determining and checking tare weights, entering into checkweighers What you bring with you * Initial experience in the food and/or Quality assurance sector is desirable * Communication and teamwork skills, ability to work under pressure, assertiveness * Reliability and diligence * Confident knowledge of and compliance with hygiene regulations * Assertiveness * Willingness to work shifts and weekends * Computer skills are desirable

Our client, a leader in the healthcare and diagnostics industry, is seeking a dedicated and detail-oriented Quality Technician 3 to join their team. As a Quality Technician 3, you will be an integral part of the Quality Control Department supporting manufacturing testing and analytical processes. The ideal candidate will demonstrate precision, analytical thinking, and a proactive approach, which will align successfully within the organization. **Job Title:** Quality Technician 3 **Location:** Newark, DE **Pay Range:** $30.50 **Shift: 8:00am-4:30pm** **What's the Job?** + Perform analytical testing on instruments such as Titrator, Karl Fisher, UV-VIS, Spectrophotometer, and pH meter. + Conduct manufacturing-related testing on diagnostic equipment including Atellica, Dimension, DM Vista, SCS Stratus, and ADVIA Centaur. + Analyze large sets of test data, compiling, interpreting, and presenting findings through graphs and charts. + Perform routine inspections and preventative maintenance on analytical instruments to ensure optimal performance. + Follow established protocols and schedules, troubleshooting issues that may arise during testing processes. **What's Needed?** + 3-5 years of experience in a technical or laboratory environment, with a focus on analytical testing and instrumentation. + Knowledge of quality management systems, FDA, QSR, ISO, and IVDD standards. + Proficiency with MS Office, SAP, LIMS, and Siemens Clinical testing software. + Strong laboratory skills, including operation, maintenance, and troubleshooting of analytical instruments. + Excellent communication skills and the ability to work independently or as part of a team. **What's in it for me?** + Opportunity to work in a dynamic and innovative healthcare environment. + Engagement in meaningful work that impacts patient care and diagnostics. + Chance to develop technical skills and advance your career within a reputable organization. + Supportive team environment fostering professional growth. + Potential for full-time employment and career stability. If this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you! **About ManpowerGroup, Parent Company of: Manpower, Experis, Talent Solutions, and Jefferson Wells.** _ManpowerGroup (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands -_ **_Manpower, Experis, Talent Solutions, and Jefferson Wells_** _-_ creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2023 ManpowerGroup was named one of the World's Most Ethical Companies for the 14th year - all confirming our position as the brand of choice for in-demand talent. ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee's race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.

A confidential defense -industry organization is seeking skilled Manufacturing Technicians to join its advanced materials production team in Wilmington, Delaware. This role supports the manufacturing of products critical to defense and aerospace operations. Key Responsibilities Operate, monitor, and maintain manufacturing equipment to ensure optimal performance. Perform machine setups, process adjustments, and quality inspections. Monitor process controls and report any deviations or issues. Troubleshoot production problems and support routine maintenance. Document production output and maintain accurate inventory records. Follow strict safety and quality standards within a clean, climate -controlled facility. Qualifications High school diploma or GED required; associate degree or technical training a plus. 1+ year of experience in manufacturing, production, or a related technical field. Strong mechanical aptitude and familiarity with industrial safety standards. Ability to lift up to 50 lbs and remain on feet for extended periods. Basic computer skills and data entry proficiency. VantageClear or equivalent certification required for defense -industry compliance. Compensation & Benefits Pay: $22.00 - $30.00 per hour (based on experience). Comprehensive health, dental, and vision insurance. 401(k) retirement plan with company match. Paid time off (PTO), paid holidays, and overtime pay. On -the -job training with clear advancement opportunities. Safe, clean, and climate -controlled work environment.

**Are you looking to power the next leap in the exciting world of advanced electronics?** Do you want to help solve problems that drive success in the rapidly evolving technology and connectivity landscape? Then bring your problem-solving, passion, and creativity to help us power the next leap in electronics. At **Qnity** , we're more than a global leader in materials and solutions for advanced electronics and high-tech industries - we're a tight-knit team that is motivated by new possibilities, and always up for a challenge. All our dedicated teams contribute to making cutting-edge technology possible. We value forward-thinking challengers, boundary-pushers, and diverse perspectives across all our departments, because we know we play a critical role in the world enabling faster progress for all. Learn how you can start or jumpstart your career with us. Qnity's Tralee Park/Tralee Park Annex sites in Newark, DE has an exciting opportunity for multiple **Manufacturing Technicians** to join our team! We are immediately hiring for full-time employment. The Tralee Park/Tralee Park Annex facilities produces high performance Kalrez seals in a discrete part manufacturing environment. We have recently expanded our business by building an additional facility to support our production needs. For more than 50 years, Kalrez parts have demonstrated cost-effective solutions for high-performance sealing applications globally. To learn more about Qnity Kalrez go to: ******************************************** (*********************************** Qnity offers an excellent benefits package that includes a generous 401k match, health, dental insurance and paid vacation, a variable bonus plan, parental leave and much more! This position has generous compensation of $53,000.00 - $62,000.00 per year, based on years of experience in a manufacturing environment. Annual pay based on hourly wage, shift premium, and regularly scheduled overtime on set 12-hour rotating shift schedules. **RESPONSIBILITIES DESCRIPTION** Responsibilities include, but are not limited to: + Sets-up,monitorsand operates mills, extruders, presses, etc. ensuring quality and conformance with standard operating procedures. + Alwaysmaintainssafety and quality standards at all times. Initiates and follows emergency procedures when necessary + Routinely inspect and measure parts against specifications to ensure they are within allowed tolerances using variousmeasuringdevices + Operate fork trucks and motorized equipment + Perform basic maintenance + Perform area patrols to visually inspect,monitorequipmentand process conditions to ensure compliance with standard operating procedures and environmental regulations. **JOB QUALIFICATIONS** **The following are** **required** **:** + A minimum of a high school diploma or GED isrequired + Proficiencyin Microsoft applications, such as Word, Excel, and Outlook + Good communication, interpersonal, organizational, numerical, and analytical skills arerequired **Preferred Requirements for Some Roles:** + Knowledge and experience with Automated Process Controls (PLC system). + Ability to interpret blueprints or technical drawings + Process Safety Management (PSM) knowledge and experience + Knowledge and experience in continuous improvements in a manufacturing environment + Milling and Extrusion **Physical Requirements:** + Ability to wear personal protective equipment (PPE) & quality protective equipment including steel toe shoes, gloves, clean roomgarmentsand full-face respirator whenrequired. + Stand for extended periods of time whileoperatingmachinery + Lifting > 20-30 lb. occasionally **Shift:** You must be available for all shifts listed to be considered for this role. All shifts are assigned based on business needs and you will not have an option to select a specific shift. + 12- hour Rotating/Non-Rotating shifts: 6am-6pm, 6pm-6am + 8-hour shifts: 6am-2pm, 8am-4pm, 4pm-12am,10pm-6m,12am-8am + Must be able to work overtime whenrequired, per business need Join our Talent Community (*************************************************************** to stay connected with us! Qnity is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information (**************************************************** . Qnity offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page (*************************************************************************** . **We use Artificial Intelligence (AI) to enhance our recruitment process.**

Test, calibrates and repairs production machines and related subassemblies to written and/or oral specifications in a timely fashion . Responsible for meeting or exceeding quality and efficiency standards. Ensures quality and operation of work. Reads and interprets schematics and blueprints required to ensure proper calibration of machines. Timely and accurate testing and calibration of all electronic subassemblies and must clearly document results. Ensure that design, implementation, test and maintenance methods/processes are developed as well as executed in a manner, which supports all Client's Quality Standards. Perform other duties as required This will be first shift, with a start time of either 6am or 8am/40 hours a week. Duties & Responsibilities: Perform equipment maintenance both ongoing and preventative, repairs and process development in a Primary support to coaters, microscopes, pumps, and other equipment as required. Troubleshoot and repair of equipment. Support manufacturing engineering on technical projects. Perform equipment measurements and inspections based on written documentation. Follow all ESD requirements. Proficiency with all basic hand tools. Ability to work in a cleanroom environment with minimal supervision. Document equipment maintenance procedures. Perform measurements and inspections based on written documentation. Understand and follow all safety requirements of the equipment and processes in assigned area of responsibility. Ability to read and follow written specifications and/or procedures in all operations. Perform daily maintenance, both ongoing and preventative, of all equipment within assigned area. Ensure the use of the correct maintenance procedures and Checklists / Specs. Assist in the investigation and resolution of process problems within assigned area. Ensure that thorough documentation concerning equipment is properly recorded and tracked. Assist engineering and technicians to resolve production issues on a daily basis Work on special projects as requested. Ability to effectively participate in equipment installs, upgrades and improvements. Must be willing to work any shift and perform other related duties as directed. Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the basic knowledge, skills, and/or abilities required. Proficiency with electrical test equipment such as multimeters and microscopes. Ability to read and follow electro-mechanical assembly drawings, procedures and schematics. Ability to follow Client written procedures to maintain GMP compliance and ISO 13485 certification. Must have very good computer skills and knowledge. Must be detail oriented and work as a team with other technicians. Ability to communicate effectively with others, both written and verbally. Ability to self-manage required tasks to completion in a timely manner. Education: Associate Degree in Electronics Technology preferred to equivalent work experience. Experience: Minimum of 2 years working in a manufacturing/production environment. Minimum of 2-5 years of working experience performing intricate and/or heavy machine and equipment maintenance, troubleshooting, repair, testing needs assessment and ability to maintain continued support. Specialized Knowledge: Minimum of 2 years of experience working in a cleanroom environment preferred. Electrostatic Discharge (ESD) knowledge a plus. Working knowledge of Oracle application preferred. Additional Details: Must be able to repetitively lift and carry product weighing approximately 30 lbs. Additional Information All your information will be kept confidential according to EEO guidelines.

AAA Club Alliance is seeking a Quality Assurance Specialist to join our team. This position can be based at our offices located in Wilmington, DE, Lexington, KY, or Cincinnati, OH. This is a hybrid role and will require you to be on-site Tuesday, Wednesday, and Thursday. The primary duties of the Quality Assurance Specialist are: Collects and inputs survey results. Able to scrub and organize data for analysis. Monitors call content for technical knowledge and customer service. Responsible for reviewing survey data (Qualtrics), researching call data (Sales Force) and may require monitoring or evaluation(Genesys Cloud) of Contact Center agents and other operations associates to ensure that the professional and quality of information disseminated is correct. Provides input for improvement of methods and policies. Prepares reports summarizing performance relative to the monitoring program. Participates in regular calibrations with respective management staff. Responsible for providing weekly/monthly assurance reports to Analyst and Manager. Assists in the organization, review, evaluation and summarization of data to identify trends and opportunities for all business lines Minimum Qualifications: Associate's degree or equivalent. 2 years customer service and/or quality assurance experience. Possess a strong background in customer service, quality monitoring, report trending and analysis. MS office - working knowledge with Access and Excel. Willingness to become familiar with Automotive systems: Sales Force, Genesys and Reporting Qualtrics, BIA. At AAA, your success is our success. What we can offer you: The starting pay range for this position is $21.13 to $32.88. * The base pay range shown is a guideline for compensation and ultimate salary offered will be based on factors such as applicant experience and geographic location.* Comprehensive health benefits package. Up to three weeks of paid time off accrued during your first year. 401(K) plan with company match up to 7%. Professional development opportunities and tuition reimbursement. Paid time off to volunteer & company-sponsored volunteer events throughout the year. Other benefits include a free AAA Premier Membership, Health & Wellness Program, Health Concierge Service, Health & Life Insurance, Short Term/Long Term Disability. Full time Associates are offered a comprehensive benefits package that includes: Medical, Dental, and Vision plan options Up to 2 weeks Paid parental leave 401k plan with company match up to 7% 2+ weeks of PTO within your first year Paid company holidays Company provided volunteer opportunities + 1 volunteer day per year Free AAA Membership Continual learning reimbursement up to $5,250 per year And MORE! Check out our Benefits Page for more information ACA is an equal opportunity employer and complies with all applicable federal, state, and local employment practices laws. At ACA, we are committed to cultivating a welcoming and inclusive workplace of team members with diverse backgrounds and experiences to enable us to meet our goals and support our values while serving our Members and customers. We strive to attract and retain candidates with a passion for their work and we encourage all qualified individuals to apply. It is ACA's policy to employ the best qualified individuals available for all positions. Hiring decisions are based upon ACA's operating needs, and applicant qualifications including, but not limited to, experience, skills, ability, availability, cooperation, and job performance. Job Category: QA - Quality Control

AAA Club Alliance is seeking a Quality Assurance Specialist to join our team. This position can be based at our offices located in Wilmington, DE, Lexington, KY, or Cincinnati, OH. This is a hybrid role and will require you to be on-site Tuesday, Wednesday, and Thursday. The primary duties of the Quality Assurance Specialist are: * Collects and inputs survey results. Able to scrub and organize data for analysis. Monitors call content for technical knowledge and customer service. * Responsible for reviewing survey data (Qualtrics), researching call data (Sales Force) and may require monitoring or evaluation(Genesys Cloud) of Contact Center agents and other operations associates to ensure that the professional and quality of information disseminated is correct. * Provides input for improvement of methods and policies. Prepares reports summarizing performance relative to the monitoring program. Participates in regular calibrations with respective management staff. * Responsible for providing weekly/monthly assurance reports to Analyst and Manager. Assists in the organization, review, evaluation and summarization of data to identify trends and opportunities for all business lines Minimum Qualifications: * Associate's degree or equivalent. * 2 years customer service and/or quality assurance experience. * Possess a strong background in customer service, quality monitoring, report trending and analysis. * MS office - working knowledge with Access and Excel. * Willingness to become familiar with Automotive systems: Sales Force, Genesys and Reporting Qualtrics, BIA. At AAA, your success is our success. What we can offer you: * The starting pay range for this position is $21.13 to $32.88. * The base pay range shown is a guideline for compensation and ultimate salary offered will be based on factors such as applicant experience and geographic location.* * Comprehensive health benefits package. * Up to three weeks of paid time off accrued during your first year. * 401(K) plan with company match up to 7%. * Professional development opportunities and tuition reimbursement. * Paid time off to volunteer & company-sponsored volunteer events throughout the year. * Other benefits include a free AAA Premier Membership, Health & Wellness Program, Health Concierge Service, Health & Life Insurance, Short Term/Long Term Disability. Full time Associates are offered a comprehensive benefits package that includes: * Medical, Dental, and Vision plan options * Up to 2 weeks Paid parental leave * 401k plan with company match up to 7% * 2+ weeks of PTO within your first year * Paid company holidays * Company provided volunteer opportunities + 1 volunteer day per year * Free AAA Membership * Continual learning reimbursement up to $5,250 per year * And MORE! Check out our Benefits Page for more information ACA is an equal opportunity employer and complies with all applicable federal, state, and local employment practices laws. At ACA, we are committed to cultivating a welcoming and inclusive workplace of team members with diverse backgrounds and experiences to enable us to meet our goals and support our values while serving our Members and customers. We strive to attract and retain candidates with a passion for their work and we encourage all qualified individuals to apply. It is ACA's policy to employ the best qualified individuals available for all positions. Hiring decisions are based upon ACA's operating needs, and applicant qualifications including, but not limited to, experience, skills, ability, availability, cooperation, and job performance. Job Category: QA - Quality Control

There has never been a more exciting time to join our team! LaMotte Company is looking for a Production Technician who is hands-on, works well in a team environment, along with being an excellent team player with a positive attitude. We are looking for candidates who can grow, think, dream and execute with us. Our culture is results-oriented and we recognize that our people are our greatest asset. We invest to equip our teams with technology, healthy living options, team incentives, flex work schedules, and ongoing education and training opportunities. We value collaboration and personal initiative, and we are committed to ensuring employee satisfaction and success. If you are looking for a great career opportunity, come join our team. Our growing company is looking for high-energy employees to join our NEW facility in Newark, DE! Production Technician Duties and Responsibilities Safety Maintains a clean, safe work environment. Works safely, adheres to all safety policies & procedures; identifies, reports & helps eliminate hazards. Participates in workplace safety inspections and improvement kaizens. Quality Monitors equipment to ensure that products manufactured perform as designed and are appropriately reflected in QC/QA samples. Ensures that products manufactured meet specifications, such as lot numbers, manufactured date, expiration date, labeling, color, and other requirements. Ensures that products manufactured match “first article” representations. Verifies that the quantity of products per package meets specifications. Equipment Operation Operates various manufacturing equipment, while ensuring quality and conformance to standard operating procedures. Assists with equipment setup as needed. Performs routine and preventive maintenance and adjusts equipment as required. Ensures all product is labeled by batch record and expiration date on the label and on storage container for work in process. Ensures that all paperwork is completed accurately on the same day the work is done. Maintains inventory control of manufactured items and their raw materials and assures that there are adequate materials for daily work. Ensures that production rates and quality standards are being met and addresses any issues impeding such progress. Reports all major problems to the Shift Manager. Packaging Bags product and inserts desiccants. Heat-seals foil bags. Weighs bags to confirm accurate product quantity. Packs bags in boxes. Ensures proper labeling. Inspects product throughout the bagging operation. Works on a five-station work cell packaging products. Packs product in cases; seals, labels, and palletizes cartons. Reports all major problems to the Shift Manager. Qualifications: Ability to operate manufacturing equipment with training Good mechanical aptitude and manual dexterity Strong attention to detail and documentation Ability to multitask Good communication, judgment, decision-making, and troubleshooting skills Ability to work legally in the United States; No visa sponsorship/support Physical Requirements: Walking, standing, sitting, stooping, bending, reaching, climbing a step ladder Standing for extended periods of time while working at machines Transporting 50 lbs. occasionally Setting up, operating, and maintaining equipment Working in a clean, temperature and humidity-controlled environment. Compensation: $19.00/hr. and $1.00/hr. shift differential Benefits: Insurances: health, dental, vision, life, short-term disability, long-term disability, critical illness, and accident 401(k): The company provides 4% discretionary contributions each pay period and matches 25% up to the first 6% of employees' contributions each pay period Flexible Spending Account Employee Assistance Program Vacation Time Sick Time Holiday Pay Tuition Assistance Travel Assistance Corporate discounts for YMCA membership and AquaFit membership LaMotte Company, a 100+ year-old global industry leader in developing and manufacturing premier water testing solutions, employs 250+ employees at its existing manufacturing site in Chestertown, MD, and is opening a new manufacturing site due to expansive business growth. The new facility, located in Newark, DE will operate 24/7 and will employ 50+ employees within the first year and 100+ soon thereafter. We have an amazing culture and have been ranked as the Best Place to Work in Kent County, MD for the 3rd year in a row now!!! LaMotte is committed to a policy of Equal Employment Opportunity and will not discriminate against an applicant or employee on the basis of race, color, religion, creed, national origin or ancestry, sex, age, disability, military status, genetic information, sexual orientation, or any other legally recognized protected basis under federal, state, or local laws. Sunday - Saturday, rotating work days, 6:30 a.m. - 6:45 p.m. The work day is 12.25 hours, 11.75 hours paid. The employee will receive two paid 15-minute breaks and a 30-minute unpaid lunch.

As a Laboratory Technician working onsite in the Resin QC Laboratory in Delaware, OH, you will be responsible for a variety of laboratory operations in quality assurance and research settings. In the QC team, you will validate raw material and finished good samples, identify result abnormalities, mitigate risk of defective material, and aid in the support of our continuous improvement and projects. Reporting directly to the Quality Laboratory Manager as a Laboratory technician you will be learner and collaborate within the QC team and across multiple teams. 3rd Shift: 11pm - 7am Key Responsibilities Troubleshoot batch QC result abnormalities Test all production samples - following SOPs as defined, performing test methods, and recording all test results Support project and continuous improvement work to help maintain project timelines Understand customer requirements and determine adjustments for batches Collaborate with other QC teams, production, and technical groups to independently disposition batches Maintain all laboratory equipment and perform required calibrations as assigned Use immediate production and project need to prioritize daily activities Maintain lab ancillary inventory, daily material stocking needs, and contribute to 6S Understand and maintain Delaware's Quality Management System requirements Support Departmental X matrix action items as assigned Complete development plans and develop RCA tasks as assigned Qualifications Bachelor's degree required Degree in Chemistry, Biochemistry, Chemical Engineering 1 year of academic or professional laboratory experience to apply laboratory methods. Work weekends as dictated by business need Work additional overtime as determined by business and project needs #LI-Onsite #Benefits - Medical, Dental, Vision, 401K PPG pay ranges and benefits can vary by location which allows us to compensate employees competitively in different geographic markets. PPG considers several factors in making compensation decisions including, but not limited to, skill sets, experience and training, qualifications and education, licensure and certifications, and other organizational needs. Other incentives may apply. Our employee benefits programs are designed to support the health and well-being of our employees. Any insurance coverages and benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents.

Demolition/Clean-Up Technician for Restoration Company! MUST HAVE VALID DRIVER'S LICENSE! Renowned leader in the restoration industry, specializing in fire, floods, water damage, tornadoes, wind damage, duct cleaning, bio-hazard clean-up, and mold remediation services. Key Responsibilities: Cut out drywall, pull up flooring, removal of all damaged materials. Perform pack outs and move backs with a team. Perform content restoration work for residential, commercial, and industrial properties. Determine salvageable and non-salvageable items within properties and document. Complete content cleaning using all methods. Perform physical labor associated with clean up activities, general on location cleaning and deodorization of personal property and structure. Must be able to lift 40-50 lbs. Respond swiftly to emergencies, including water and fire damage. Help with thorough assessments and the execution of restoration plans for a variety of damages. Operate and maintain specialized restoration equipment. Handle physical tasks such as water extraction, demolition, and site cleanup. Keep detailed inventories and ensure tools and vehicles are well-maintained. Provide exceptional service and clear communication to team mates. Comfortable working in diverse settings, including heights, tight spaces, and varying weather conditions. Position Requirements: Valid driver's license and reliability for on-call shifts, including nights, weekends, and holidays. Background in construction, restoration, or a related field is preferred. ICRC certification is a plus but not required. Job Type: Full-Time Temp-to-Permanent Pay: $16.00-$18.00 Per Hour Drug Test and Background Check Required. Equal Opportunity Employer: HTPR is an equal opportunity employer and prohibits discrimination and harassment based on race, color, religion, sex (including pregnancy), sexual orientation, national origin, disability, age, marital status, or genetic information. We are committed to providing employment opportunities to all individuals and comply with all applicable laws governing nondiscrimination in employment.

Reports to: Manager, Facility Operations or Supervisor, Production The Production Technician is responsible for all aspects of plant processing from post-crop harvest through packaging and labeling of the final product ready for customer sale as outlined by the management team and SOPs. These responsibilities include post-harvest tasks including the drying and curing stage all the way through trimming, packaging, and labeling the product. This position works in a timely manner and strives to increase productivity and acts with professional regard to the management and use of all production facilities and processing equipment. Pay: $16.00 Major Areas of Responsibility include: •Assists in the post-harvest plant processing of cannabis. •Fan leaf removal, harvest, drying, trimming, curing, weighing, packaging, labeling, recording, and inspection of product in addition to cleaning and sanitation. •Maintains a clean and organized work environment. •Transport harvested plants to drying room and hang to be dried. •Hand trims and/or operates a trimming machine to remove excess plant material. •Weighs, records, and shreds plants waste and adds a non-cannabis medium for compliant disposal. •Receives instructions and assists on tasks as delegated by management team. •Works in a quick and efficient manner. •Complies with all HR policies including confidentiality and non-disclosure. Minimum Qualifications (Skills, Knowledge & Abilities): •All applicants must be at least 21 years of age. •1-3 years of experience in production position; including hands-on production activities. •General knowledge of weights and measurement. •Evening/night/weekend work may be required. •Speed and precision with equipment and attention to detail. •Ability to multi-task and maintain work consistency on a daily basis. •High attention to detail. •Standing/sitting for long periods of time. Travel %: 0 FLSA status: Non-exempt Additional Abilities Required: •Exposure to pollen, dust, and plant particles due to the handling of raw plant materials. •The job requires physical activity, including prolonged sitting, standing, repetitive bending, climbing, and lifting or moving up to 50 pounds (or more with a coworker). Good visual acuity, hand-eye coordination, manual dexterity, and ability to perform repetitive motions with accuracy is required. The noise level in the work environment is usually moderate. Note: Nothing in this job description restricts the company's right to assign or reassign duties and responsibilities to this position at any time. Reasonable accommodations may be made in appropriate circumstances to enable individuals to perform the essential functions of the position. About The Cannabist Company (f/k/a Columbia Care) The Cannabist Company, formerly known as Columbia Care, is one of the most experienced cultivators, manufacturers and providers of cannabis products and related services, with licenses in 12 U.S. jurisdictions. The Company operates 77 facilities including 61 dispensaries and 16 cultivation and manufacturing facilities, including those under development. Columbia Care, now The Cannabist Company, is one of the original multi-state providers of cannabis in the U.S. and now delivers industry-leading products and services to both the medical and adult-use markets. In 2021, the Company launched Cannabist, its retail brand, creating a national dispensary network that leverages proprietary technology platforms. The company offers products spanning flower, edibles, oils and tablets, and manufactures popular brands including Seed & Strain, Triple Seven, Hedy, gLeaf, Classix, Press, and Amber. For more information, please visit ************************* Recognized for its comprehensive benefits, ongoing training opportunities and commitment to diversity and equity inclusion both internally and with external vendors, The Cannabist Company has earned a spot on mg Magazine's America's Top Cannabis Industry Employers list. The Cannabist Company provides full-time employees with an excellent benefits and compensation package including but not limited to competitive wages, paid holidays, vacation and sick time, 401K with company match, multiple health plan choices, dental, vision, pet and life insurances, 100% paid short-term disability, optional long-term disability insurance and more!

Decima International is a professional services company, providing project management and controls services to clients in the United States and the Middle East. Our mission is to become the premier professional services provider across all industry sectors we are engaged in. To accomplish this, Decima International's founders established a simple yet powerful formula: Approach each client engagement as a partnership, create an environment that attracts the most talented professionals and allows them to flourish, and regulate growth to maintain excellence in our service standards. Decima International is a professional services company, providing project management and controls services to clients in the United States and the Middle East. Our mission is to become the premier professional services provider across all industry sectors we are engaged in. To accomplish this, Decima International's founders established a simple yet powerful formula: Approach each client engagement as a partnership, create an environment that attracts the most talented professionals and allows them to flourish, and regulate growth to maintain excellence in our service standards. If you are interested in a long and rewarding career working with high-profile clients on some of the most challenging projects in the world, then Decima is where you belong. At Decima, you will be able to explore incredible growth and professional development opportunities. We are looking for a driven and capable Civil Structure Architecture QA Inspector to support us with the development of multiple data center projects for one of the top technology clients in the world. This is a client-facing role that requires strong interpersonal, communication, and organizational skills, the ability to self-direct, client representation, and an emphasis on strong project management fundamentals. Must be able to manage multiple projects concurrently and across multiple regions. A strong background in data center development, design, engineering, controls, and operations requirements is a big plus. You will play an integral role in ensuring the implementation and management of the Quality Management System (QMS) in addition to the coordination, performance, and completion of all construction inspection and testing services of a project. The Civil Structure Architecture QA Inspector is accountable for the guarantee of the work performed, as well as meeting the project's contractual requirements set forth by the client. We are looking to bring in dedicated individuals with a passion for innovation and talent for multitasking in a fast-paced environment. We will help you grow, pursue, and fulfill what inspires you so we can make big impacts on the world, together. RESPONSIBILITIES Develop a sound knowledge of the project scope and requirements. Ensure compliance with stringent contract and owner quality requirements. Prepare comprehensive, project-specific QC plans. Review and verify material submittals for A/E and Client review. Verify delivered materials comply with approved submittals. Provide and review submittals, RFI logs, maintenance logs, and other project-related materials in a timely manner. Review and update QC punch lists and coordinate punch list completion with GC and subcontractors. Verify the implementation and operation of the quality assurance and control systems by planning and conducting internal quality audits and inspection of activities on site. Ensure implementation and continuous improvement in overall Quality Systems. Ensure that all contractual / company and local authority requirements for Quality, Health, Safety & Environment (HSE) requirements are complied with. Review, update, and verify the distribution of the Quality Management Procedure, Quality Manual, and related procedures for Infrastructure, MEP, Civil, and other subcontractors and divisions by the GC. Verify that GC implements adequate training/awareness of company personnel for Quality systems. Ensure that all non-conformance issues are promptly investigated, corrective and preventive actions are proposed/implemented, and are quickly closed out. Ensure that the contractual quality requirements of a project are fully communicated to all key personnel, so that their roles in fulfilling these requirements are fully understood. Ensure that all GC and subcontractors' quality systems and plans are acceptable to the company as applicable to the "Project Contract". Ensure that Subcontractors'/Suppliers' quality systems are implemented and effective. Ensure that the calibration of all inspection, measurement, and test equipment is conducted according to the defined schedule. Conduct reviews of the approved suppliers and subcontractors' list. Liaise with the General Contractor, Client, and Project Management team to ensure that all potential and actual quality issues are fully resolved. Establish a strong relationship with the GC and Client, and communicate with both technical and management-level personnel. Prepare PowerPoint decks and present to management on progress, findings, and recommendations. Review project plans, requirements, and specifications. Perform other related duties as required and assigned. QUALIFICATIONS Required Qualifications: 15+ years of construction quality management experience. Bachelor's degree in Civil, Structural, Architectural Engineering, or a related field. Experience with managing field engineering, inspection, and NDE related to all QA/QC functions. Ability to develop and manage non-conformance, deficiencies, and reporting programs, including root cause analysis. Experience in developing and monitoring of project QA/QC budgets. Ability to ensure that correct codes, standards, job specifications, project procedures, and federal and provincial regulations are properly identified, correctly specified in detail, and met or exceeded. Must have the ability to work within strict deadlines and under pressure while maintaining a professional demeanor. Experience working as a QA/QC Manager for large Commercial, Industrial, or Mission-Critical Facilities construction projects. An excellent understanding of construction Quality Management Systems (QMS). Experience developing various types of reports, targeting different audiences. Experience in client-facing positions. Demonstrated ability to understand technical and complicated construction programs and the ability to communicate progress to both technical and management-level personnel. Strong communication skills, including the ability to communicate with any audience clearly and accurately. Proficient in Microsoft Office programs. Preferred Qualifications: Project Management Professional (PMP) certification. Certified Construction Manager (CCM) certification. Strong background in data center development and construction. POSITION DETAILS: Location (On-site): Multiple Sites Dover, Delaware Shippingport, Pennsylvania Charleston, West Virginia Position: CSA QA Inspector Position Classification: Salary-based full-time hours Current US work permit required. This position does not offer sponsorship for employment (e.g., H-1B visa sponsorship or transfer not offered) PRODUCTIVITY TOOLS: Microsoft Office Microsoft 365 Decima International is an Equal Opportunity Employer who is committed to the safety and wellbeing of all. All qualified applicants will receive consideration for employment without regard to race, religion, creed, color, national origin, ancestry, sex (including pregnancy, childbirth, breastfeeding, or medical conditions related to pregnancy, childbirth, or breastfeeding), age, medical condition, marital or domestic partner status, sexual orientation, gender, gender identity, gender expression and transgender status, mental disability or physical disability, genetic information, military or veteran status, citizenship, low-income status or any other status or characteristic protected by applicable law. At Decima International, we offer a competitive salary package, including paid time off and performance-based bonuses. We also provide excellent medical, vision and dental insurance for our employees.