Quality control technician jobs in Maryland

Description: : A Square Group (ASG) is a Minority Woman Owned, Physician owned small business with over 15 years' experience in federal government contracting. ASG provides a broad range of healthcare, intelligence, and defense technology-related, services such as software development and integration, mobile apps, AI/ML, Analytics, Data Science, Bigdata, DevSecOps, Digital transformation, Cloud, and Cybersecurity. ASG is CMMI Level 3 certified for Development and Services and holds ISO certifications 9001:2015, 20000-1:2011, and 27000:2015. Job Description: We are seeking a highly skilled Primary Technical Control Facility Lead to manage the operation and maintenance of a Tech Control facility in a DoD environment. The ideal candidate will have expertise in managing cryptographic facilities, overseeing technical teams, and maintaining network infrastructure to ensure secure and efficient communications. What You Will Do: Maintain the operational status of a Tech Control facility, including the management of encryption devices, switches, and network operation consoles. Oversee and supervise technical control employees in day-to-day activities and responsibilities similar in size and scope as outlined in the project requirements. Provide leadership in the operational direction, restoration, and maintenance of transmission paths and facilities. Develop, implement, and maintain technical procedures and documentation to ensure smooth facility operations. Monitor and control the operational aspects of the Tech Control facility, ensuring that all systems remain fully operational. Collaborate with senior management and provide updates on facility status, performance, and ongoing improvements. Support Tier 2 Tech Control Helpdesk functions and ensure compliance with DISAC 310-175-9. Supervise the maintenance and troubleshooting of network components and systems. Oversee the planning and coordination of upgrades and improvements to the facility's technical infrastructure. Ensure that operational and security standards are met in accordance with DoD regulations. Requirements: What We Need: Bachelor's Degree in a related field. Minimum five (5) years of experience managing and operating cryptographic facilities. Demonstrate knowledge in maintaining the operational status of a Tech Control facility. Knowledge of Tech Control equipment such as Switches, Encryption devices, Network Operation Consoles, and Circuits. Demonstrated successful working knowledge and supervision of tech control employees in efforts similar in size and scope as referenced under this Call Order. Demonstrated ability for oral and written communication with the highest levels of management. Must have knowledge in operating and maintaining Tier 2 Tech Control Helpdesk functions and DISAC 310-175-9. Ability to provide technical directions and supervision, in coordinating, restoring, and reporting functions necessary for effective maintenance of transmission paths and facilities. Knowledge of industry accepted standards and best practices related to Information Management Operations and with ITSM best practices. Knowledge in handling and managing incidents and service requests for activities such as changes, problems, configurations, and requisitions for equipment and services. Clearance Level: Active TS/SCI Clearance. Additional Information: At ASG, we value diversity and always treat all employees and job applicants based on merit, qualifications, competence, and talent. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Applicants in need of special assistance or accommodation during the interview process or in accessing our website may contact us by sending an email to ******************. We will treat your request as confidentially as possible. In your email, please include your name and preferred method of contact, and we will respond as soon as possible. Perks: At ASG, we want you to be well and thrive. Our benefits package includes: Healthcare Benefits Paid Time Off 401k Matching Employee Referral Bonus Education Assistance Learning and Development resources EOE, including Disability/Veterans

Summary/Objective: The Technical Service/Quality Control Technician implements and complies with quality assurance methods and procedures to ensure products and materials are produced in accordance with specifications. Essential Functions: Perform specimen tests of concrete from random loads or for special jobs or mixes; prepare test reports as required. Oversee unique jobs to ensure product standards are met, i.e., jobs that have restrictive specifications or require large quantities of material to be delivered. Perform aggregates and batch plants tests including daily graduation and moisture tests on all concrete being produced for State and spec projects. Certify concrete loads being delivered to "spec" jobs in accordance with SHA specifications; check loads for proper procedure and time of mixing. Perform quality assurance tests on trial batches of new concrete mix designs under close tolerance conditions and make adjustments until mixture meets specifications. Troubleshoot problems with customers, analyze and evaluate specific conditions, situations, quantities, etc., and provide appropriate resolution. Provide technical assistance and training to plant managers, equipment and yard operators, and drivers when requested. Perform laboratory tests including gradation, moisture, lightweight particles and specific gravity tests on aggregates. Select samples for materials that need certification by an outside laboratory or that are beyond the department capability. Transport these samples to the testing agency. Perform additional tasks such as cleaning facilities to ensure safety and cleanliness, moving equipment and materials, and completing tasks for other positions when incumbent is absent. Assist the Technical Services Manager and Assistant Manager as needed. Other duties as assigned. JOB SPECIFICATIONS Work Environment: Work time will be split between indoors/office and outdoors/field Exposure to dust and fumes/offensive smells. Exposure to chemicals such as concrete, chemical admixtures. Close proximity to moving mechanical parts. Noise level will be moderate to loud. Physical Demands: Lift a maximum weight of 50 lbs., repetitively lift 50 lbs., carry approximately 50 lbs., and push/pull approximately 75-100 lbs. Reach overhead and reach away from the body. Minimal kneeling, squatting and climbing may be required. Sit 3 hours per day, stand 5 hours per day, and walk 2 hours per day. ADDITIONAL QUALIFICATIONS Experience: Laboratory testing experience in ready-mix concrete or aggregates preferred. Special Skills: Written communication, verbal communication, and basic mathematical skills. Ability to use a computer and iPad, including Microsoft Office. Ability to use the company dispatching system. Ability to compute basic material calculations. Excellent interpersonal skills. Able to exhibit a high level of confidentiality. Excellent organizational skills. Must be able to identify and resolve problems in a timely manner. Certifications: Valid Driver's License. ACI Level 1 certification (must be obtained within 1 year of assuming position). Industry Related Experience or Skills: Background in concrete, construction, mining operations or building materials (preferred). Education Required: High School Preferred Education: N/A Bilingual in Spanish Preferred: Yes Interested in future opportunities with Chaney? Join our Talent Community to get alerts about newly posted positions. Click here to sign up!

Who YOU are and what YOU can become The Quality Technician/Designated Supplier Quality Representative (DSQR) will have responsibility of all Quality functions for 2nd shift Assembly and as DSQR, is responsible for the inspection and acceptance of hardware / end item deliverables on behalf of the customer. The individual will be responsible for ensuring all engineering and regulatory requirements are met to ensure customer satisfaction. The Quality Technician/ DSQR will be a part of a cross-functional technical and operations team to focus on achieving business objectives. Who WE are and where WE are going At ST Engineering MRAS, our employees have amazing opportunities to work on advanced technologies and systems that support thousands of customers and millions of people worldwide every day. From the first flight across the Pacific Ocean to developing highly complex structures for the most popular aircraft in the world, we have come a long way always with a can-do approach to problem solving while delighting customers with our high say-do ratio. We are looking for people with innovative ideas and the drive to help us grow into the future. A pioneer in the production and assembly of complex aerostructures including aircraft and rocket components, engine nacelle systems, thrust reversers and advanced composite products, we apply the latest digital technologies and automation in composite design and manufacturing that are second to none. What YOU will do * Manages all Quality functions for assembly program supporting 2nd shift operation. * Review and accept hardware on behalf of customers prior to delivery as DQSR, including generation of conformance certificates and all acceptance documentation. * Obtain and maintain FAA certification to provide Aircraft On Ground (AOG) support. * Acts as the Point of Contact for 2nd shift inspectors. * Assists with development of Root Cause/Corrective Action with some guidance using established RCCA tools (PFMEA, DMAIC, Apollo, 5 WHYs, 8D, etc.). * Provide Quality support and assistance with Inspection personnel while performing First Article inspections. * Processes all Nonconformance Items and Workflows in a timely manner. * Solicits weekly prioritization of tasks and deliverables that align with business objectives. What YOU must bring to Succeed High school diploma / GED with at least 2 years experience in Manufacturing or Quality. Knowledge of Aerospace / DOD / assembly line experience is highly preferred. * Acquire and maintain multiple customer representative certifications for acceptance of hardware. * Knowledge and experience for problem solving techniques such 5 why's, Fishbone, Process mapping, etc. to identify root cause and define CAPA. * Must be able to work 1st shift for three months before transitioning to 2nd shift. * This position involves access to export-controlled technology which requires U.S. Person status or government authorization. A 'U.S. Person,' as defined by 22 C.F.R. §120.62, includes U.S. citizens, U.S. nationals, individuals lawfully admitted for permanent residence (green card holders), and individuals granted asylum or refugee status in the United States. To be considered for this position, you must either be a U.S. Person or fall within a legally recognized export control exception or authorization. If hired, you will be required to provide valid proof of such status. Desired Characteristics: * Strong oral and written communication skills. * Strong interpersonal and leadership skills. * Willingness to support business needs as required to meet company objectives. * Maintain customer required inspection reports. * Work with Program QE on resolution of customer identified quality issues. * Perform inspections across all stages of production. * Strong analytical, problem solving, and root cause analysis skills. * Ability to multitask and handles tasks with competing priorities effectively. * Demonstrated ability to work independently with minimal supervision. * Detail oriented and strong computer skills. * Preferred minimum of 1 year of experience in Production Quality. * Working knowledge of PPAP and APQP, AS9145, ISO9000 / AS9100 At ST Engineering - MRAS, we offer great rewards, competitive pay, career advancement and growth opportunities. Estimate salary range for this role $52,300 to $75,900 per year. ST Engineering considers several factors with extending job offers, including but not limited to candidates' key skills, relevant work experience, education/training/certification, job level, and work location. Base salary is only one component of our competitive Total Rewards package. ST Engineering - MRAS Benefits: As a full-time employee of ST Engineering- MRAS, you are eligible for our benefits package including: * Medical, Dental, and Vision coverage starting from start date * Health Flexible Spending Accounts * Free Onsite Gym with weekly fitness classes * Immediate 401k vesting * Educational Assistance * Life Insurance * Paid Time off (Permissive for exempt staff) Employment Notice: Background and Drug Screening Requirements As part of our commitment to maintaining a safe and secure workplace, successful completion of a background check and drug screening is a mandatory condition for employment. All offers of employment are contingent upon satisfactory results from these screenings. It takes diverse talent to solve real-world problems. ST Engineering is deeply committed to building a workplace community where inclusion is valued, and everyone feels welcomed. We're proud to consider all qualified applicants for employment without regard to race, color, religion, sex, pregnancy, family status, marital status, sexual orientation, national origin, disability, age, or veteran status, or any other legally protected grounds. So, bring us your personal experience, your perspectives, and your background. It's through our differences that innovative changes are made. ST Engineering is committed to providing reasonable accommodations to qualified individuals with disabilities in the employment application process. To request an accommodation, please contact our Talent Strategies team at ************, or by email at ***********************. Nearest Major Market: Baltimore Apply now "

Job Description About Us At Tate we are passionate about everything we do. As an independent brand operating within Kingspan Group, a global plc group of companies, Tate has been recognized worldwide as an industry leader in the development and manufacture of data center infrastructure solutions and commercial office raised access floors, for over 60 years. With revenues of over $420m and growing, Tate plays a pivotal role in offering expertise in cutting edge design engineering in order to craft solutions, by working collaboratively with clients as a trusted partner. Tate continues to grow and expand, operating multiple manufacturing and commercial sites across the US, Europe, the Middle East, Asia, and Australia. We are excited about our fresh, dynamic, and inclusive team of experts working on new innovations and forward-thinking designs, as we remain a market leading player within our industry. We continue to invest heavily in the best available manufacturing tools and equipment needed to adhere to Tate's world class standards and in keeping with our Planet Passionate sustainability strategy, our focus is on having minimal climate impact. We are excited by potentially welcoming you as part of our team as we continue to grow on a worldwide scale. About the Role We are looking for a Quality Technician 1 to join our team at our Baltimore, MD facility. The Quality Technician 1 is responsible for quality inspection for all products to ensure they conform to all applicable company and quality standards. This position will test products after, in process, and in final stages to ensure quality levels are met. Note: This Position is for 2nd Shift. Hours are Monday-Friday 2pm-1030p What You'll Do Ensures all test equipment is properly maintained and calibrated Performs routine & job specific load performance tests to ensure compliance with published specs. Performs incoming inspections on products received from vendor. Has a working knowledge of all equipment and machinery within the facility. Performs daily in process quality audits on products on production floor. Performs testing needed for qualifications of new or revised products. Maintains updated certified testing reports on standard products. Assists with continuous improvement of product and manufacturing processes to improve quality, reduce costs, and ensure product quality objectives are met. As assigned by supervisor, visits job sites to identify problems and recommends solutions. Maintains good housekeeping and follow established safety procedures. Performs other duties as assigned or directed by Team Leader/Supervisor. Follows all policies, procedures, and work instructions including Employee Handbook, Standard Operating Procedures (SOPs), Manufacturing Operating Procedures (MOPs), Job Safety Analysis (JSAs), and Safety Manual. Maintains awareness of individual contribution to and impact of the quality, safety, environmental, and product compliance policies and activities; reports all quality issues, unsafe acts, and unsafe conditions to the proper personnel. Additional Expectations Remain compliant with the Code of Conduct and Policies which includes the Kingspan Group Compliance Policy. Ensure that all duties related to product compliance are adhered to in accordance with the Product Compliance Policy, Laws, Regulations, and market demands. Responsible for all tasks to achieve compliance goals and demands of the Compliance Management System. Must raise concerns related to the Compliance Management System to their supervisor, manager, or any member of the Leadership Team, or through the confidential whistle blower service. What You'll Bring High school diploma or GED; or equivalent experience. Must be able to lift up to 50 lbs. unassisted. Must be able to stand, walk, bend, stoop or crouch for at least an 8-hour shift. Must be computer literate, including proficiency with Microsoft Office Products. Ability to use various tools and measuring instruments such as calipers, micrometers, tape measures, dial indicators, feeler gauges, etc. and verify all test equipment is in calibration and maintained in good working order. Strong shop-floor orientation. Knowledge of aluminum cutting and milling operation is a plus. Must be able to work in a fast-paced working environment with accuracy and integrity. Strong written and verbal communication skills. Detail-oriented. Three (3) plus years manufacturing experience. Employee Benefits Career Scope and Advancement: As we grow, new positions and career opportunities arise, offering accelerated paths for the right candidates, locally and globally. World of Wellness Philosophy: We empower you to take charge of your health and well-being. You'll have access to a wide range of medical, dental, and vision benefits, along with personalized guidance from a “Health Advocate.” We also offer other supplemental options, including 401k, legal, disability, and theft insurance, to ensure your financial wellness. Corporate Social Responsibility: Through Planet Passionate we are determined to reduce our manufacturing carbon (CO2e) emissions to as close to zero as technically possible, together with halving carbon intensity in our primary supply chain. We are very involved in our community, and you will have ample opportunities to support us in creating a better world. Skills Development: Given the dynamic pace of our business and a strong collaborative environment, your new role will be diverse and multifaceted - allowing you to be more versatile and develop a broader skill set. Mentorship and development: At Tate, we don't believe in hierarchy, we work together as one team for one common goal. You will have access and exposure to our senior leaders and experts for learning in your role, and additionally mentorship for the future. Culture: We have a great team culture, highly collaborative, supportive, and social. Together we innovate, collaborate, take ownership, and strive for excellence. Tate is an equal-opportunity employer. We encourage applications from candidates of all backgrounds and experiences. Stay connected with us on LinkedIn for insights into life at Tate. Join us in our mission to make a difference through exceptional solutions.

Job Details Experienced Pocomoke City, MD Full Time $28.00 - $28.00 Hourly ManufacturingJob Posting Date(s) 07/02/2025 10/31/2025Description Responsible for performing quality control testing, creating technical reports on the specifications and outcomes of tests, products and processes. Responsible for all chemical manufacturing of Ricca's chemical inventory products. ESSENTIAL FUNCTIONS AND BASIC DUTIES: Act responsibly at all times to ensure the health, safety, and well-being of self, co-workers, visitors, neighbors, and property. This includes compliance with all RCC safety policies and procedures, and a working knowledge of government regulations, particularly hazardous material regulations. Schedule and assign daily testing based on the company's planning schedule to utilize available skills, knowledge and experience, labor hours, and lab equipment. Ensure that all assigned testing of finished products is conducted according to specified procedures and in a timely manner. Performing routine and non-routine analyses without supervision. Collect data and calculate Measurement Uncertainty Budgets for specified testing. Competently perform at least 95% of the types of analysis/testing. Make detailed observations, analyze data, and interpret results. Read and record data quickly and accurately and avoid perceptual errors in performing computations. Prepare Certificate of Analysis reports without errors. Review of data obtained for compliance with specifications and report abnormalities; including measurement uncertainty budgets for specified testing. Compile data for OOS investigations, documentation of test procedures, and abnormalities. Assist in technical complaint investigations and development of new methods and technologies. Participate and satisfy requirements for inter-laboratory round robin testing as well as ISO 17034 Proficiency Testing as required in order to maintain accreditation. Troubleshoot, calibrate and perform preventative maintenance on laboratory instruments and equipment and document events as required. Ensure inventory levels for laboratory supplies are kept current and are accurate. Stay abreast of ISO 17034 requirements and follow all RCC Standard Operating Procedures with special attention to those pertaining to the laboratory processes. Consistently meets/exceeds standards assigned within Functional Training Document (FTD) program. Any other tasks deemed necessary. Commitment to the organizations values; High Standards, Bias for Action, Teamwork, CustomerObsession, Trust, Accountability, Innovation and Growth & Learning. REQUIRED SKILLS: Good communication Critical thinking and problem-solving Time management Analytical Organizational skills Patience and determination Scientific and numerical skills EDUCATION AND EXPERIENCE: Bachelor's Degree in Chemistry or similar field, such as biology, engineering or physics. Three (3) to five (5) years of experience in quality control analytical laboratory or regulated manufacturing environment preferably in the chemical or pharmaceutical industry. Experience in handling and operating laboratory glassware and equipment for testing purposes. Working knowledge of ISO9001:2008 standards, cGMP/GLP regulation, and laboratory sample processes. Knowledge of ISO 17034 standard is a plus. This position requires a person to be able to speak, write and conduct business in English. This person shall also have sufficient eyesight to read business documents and properly fill out appropriate Quality System Records and Forms. This position should be able to understand and then follow written and verbal work instructions and quality system procedures without direct and constant supervision after the initial training period is successfully completed and documented. This position should have sufficient mental capacity to accommodate and successfully implement changes in work tasks and quality system changes when required. Strong organizational skills, meet deadlines, work independently and with the team with strong follow through, strong communication skills, both written and verbal and accuracy and attention to detail. WORK ENVIRONMENT: The physical environment may require the employee to work both inside and outside in heat/cold, wet/humid, and dry/arid conditions. This position may be working in the warehouse under various indoor environmental conditions, including supplemental heating in the winter months and without air-conditioning in the summer months. May be requested to work overtime and weekends. The position may occasionally be exposed to ruptured, leaking packages, some of which may contain Hazardous Materials. Where appropriate, proper safety equipment should be utilized and/or appropriate personnel notified. Frequently required to use personal protective equipment to prevent exposure to hazardous materials and chemicals. This job may require lifting of up to 50 pounds occasionally.

QUALITY TECHNICIAN The primary mission of this position is to help maintain the Quality Assurance Program relative to the production of armor products and includes activities related to setting and maintaining quality standards aligned with all appropriate regulations. POSITION RESPONSIBILITIES The Quality Technician handles a wide variety of situations and is primarily responsible conducting Quality Assurance (QA) for armor manufacturing to include the following responsibilities: GENERAL AUDITING & COMPLIANCE Inspection of incoming, in-process, and finished materials to include first article inspections and reporting, as required. Utilize Hardwire Production Database to log required inspection activities. Review and approve components and armor products to ensure proper quality and compliance standards are met. Promote reduction in process variation, contributing to continuous improvement. Review analytical results, protocols, reports and other documents as required. Investigate and resolve all routine quality issues identified during process or document reviews. QUALITY MANAGEMENT SYSTEM Maintain Quality Control equipment and gauge calibration programs to include internal calibration, scheduling of external calibration, and updating eMaint software, as necessary. Perform internal and external compliance audits, including focused and general audits of Operations and Quality Assurance areas against standards and ensure resolution of any identified issues. QUALITY RECORDS Review batch records and provide disposition (approval, rejection, etc.) to the armor material produced to ensure that all steps have been performed and verified where applicable, that all limits and specifications have been met and the raw materials and solutions have been tested and released. Ensure any deficiencies or deviations are shared with appropriate personnel through generation of Quality Deficiency Reports (QDR), Supplier Corrective Action Reports (SCAR) or Deviation Requests. OTHER Work with manufacturing group to optimize production processes including problem resolution and any necessary training. Provide support for design, manufacturing, and product launch efforts. Assist with coordination and disposition of RMAs (supplier and customer). Production, technical, and administrative duties as assigned. Job Knowledge, Skills and Abilities Ability to utilize measurement tools such as calipers, micrometers, and other key quality equipment to evaluate product conformance. Ability to read and interpret mechanical drawings. Ability to work independently and meet critical timelines. Proficient in interpreting and implementing appropriate regulations and laws. Demonstrated commitment to quality and safety. Ability to manage multiple priorities in a manufacturing setting and to easily adapt to changing situations. Excellent oral and written communication skills to effectively communicate with peers, management, and external contacts. Excellent working knowledge of computers and Microsoft Office Products, including Word, Project and Excel. Working knowledge of fundamental technical and quality concepts and applicable guidelines for ISO 9001, ANSI and other related standards. Proven understanding of manufacturing environment is preferred. Benefits for Full Time Employees Medical, Dental, Vision and Flexible Spending Account Employer-paid Group Term Life Insurance and Short Term Disability Insurance Paid time off Paid holidays 401K matching program Discretionary bonus program Education and Experience Quality assurance, quality control and/or compliance experience in a manufacturing environment is preferred. Physical Demands Required to lift up to 50 lbs. Regularly required to sit, stand, bend, reach and move about the facility. Work Environment Work performed in a combination of manufacturing and office environment. Exposed to shop elements such as noise, dust, odors, fumes, oils. FLSA Classification Non-Exempt

Job DescriptionJob Title: Quality TechnicianLocation: Laurel MDJob Type: 3-6 month contract Industry: [Manufacturing/Electronics/Defense] Job Summary:We are seeking a detail-oriented and experienced Quality Technician to join our team. The ideal candidate will possess an IPC-A-610 or IPC/WHMA-A-620 certification and will have hands-on experience inspecting electronic assemblies to industry standards. Experience operating and programming CMMs using PC-DMIS or similar software is highly desirable. Key Responsibilities:Inspect electronic assemblies and cable/wire harnesses in accordance with IPC 610 or IPC 620 standards.Perform visual inspections for soldering, component placement, wiring, and mechanical integrity.Utilize inspection equipment including microscopes, calipers, micrometers, and gauges.Operate and/or program Coordinate Measuring Machines (CMM) using PC-DMIS or similar software (a plus).Maintain accurate inspection records, reports, and quality documentation.Assist in root cause analysis and corrective/preventive action implementation.Collaborate with production, engineering, and quality teams to identify and resolve quality issues.Ensure compliance with company and industry quality standards. Requirements:IPC-A-610 or IPC/WHMA-A-620 Certification (required).2+ years of experience in a quality assurance or inspection role within a manufacturing environment.Experience with electronic assemblies, PCBAs, or cable/wire harnesses.Familiarity with CMM operation and PC-DMIS programming (preferred but not required).Strong attention to detail and documentation accuracy.Ability to interpret technical drawings and inspection criteria.Excellent communication and problem-solving skills. Preferred Qualifications:Experience in ISO 9001, AS9100, or similar regulated environments.Knowledge of statistical process control (SPC) and quality tools (e.g., Pareto, Fishbone).Proficiency with MS Office Suite.

Why Parker? A 30-year strong , manufacturing company Focused on growth, efficiency, and continuous improvement as a company Striving to provide opportunity, stability, & work-life balance for our employees Benefits 8-hour shifts Temperature controlled production floor 401(k) with company match Annual profit sharing Tuition Assistance Paid Holidays immediately after hire date Paid Vacation Medical, Dental, and Vision insurance Company-paid Short & Long-term Disability, AD&D, and Life Insurance Position Summary (A Day in the Life) The Quality Control Technician is responsible for performing routine inspections and audits by the means of visual and dimensional checks of the finished goods produced during the shift. This position will help monitor raw material defects; prepares defect reports to help continuously improve quality of supplied raw materials. The Quality Control Technician will assist the shift supervisor in the training and overview of the bottle inspectors to insure proper bottle inspection, and packing methods of the daily production produced during the shift. Primary Responsibilities Ensures all finished goods meet or exceeds the customer expectations in quality and shipping requirements. Helps production supervisors direct the shift activities regarding quality and training of all employees in the areas of quality control requirements, standards and procedures, and recognition of materials, which should be scrap vs, regrind. Follow quality control methods to ensure that all employees can identify product for rejects, rework, etc. and to ensure that all customers receive product, which meet or exceed the customers' standards. Performs quality checks (visual or dimensional) of product to assure container's meet or exceed customer requirements. Notifies shift supervisor when bottles do not meet customer specification, ensures that non-conforming material controls are effectively used. Conducts first article inspection, with appropriate documentation at start-up of production lines. During quality checks, complete shift quality inspection reports. Helps maintain quality specifications information regarding bottle drawings, pack patterns, packaging requirements, etc. Help monitor raw material defects; prepares defect reports and submits to management to help continuously improve quality of supplied raw materials. Help audit warehouse operations to ensure proper stacking and packing procedures to meet customer specifications. Help assure GMP, AIB and/or SQF regulations are followed during shift. Experience/Education Knowledge and/or willingness to learn the in-house inventory systems and general computer (PC) for all types of data entry, reports and internal communications. Requires constant visual attention; ability to discern flaws in containers. High-school diploma or equivalent required. Preferably a background/knowledge in Safe Quality Food (SQF) Program Physical Requirements Exerting up to 50 pounds of force occasionally, and/or up to 20 pounds of force frequently, and/or up to 10 pounds of force constantly to move objects. Growth Opportunities from here From this position, many people will move into roles such as, Lead/Trainers, Supervisors, or Mechanics ! Follow us on Social Media **************************************** ******************************************************

The Quality Technician is responsible for performing hourly inspections and providing support to ensure compliance with current Good Manufacturing Practice (cGMP) and internal procedures. The successful candidate will ensure overall compliance, including testing and methods in accordance with cGMP, and will inspect incoming components, in-process products, and finished products as per documented specifications. Responsibilities * Assist with the inspection of incoming components according to documented specifications. * Assist with the generation and approval of controlled labels using provided programs. * Record data and maintain accurate records in accordance with cGMP documentation practices for accuracy and completeness. * Retrieve documents using the EQMS computer system. * Troubleshoot quality concerns that may arise during the inspection of incoming components and report to the Quality Manager. * Verify the calibration of all inspection test equipment and maintain accurate records. * Perform data entry and retrieval using the computer system. * Work overtime, weekends, or alternate shifts as needed. * Assist in the generation and resolution of corrective and preventive action plans (CAPAs). * Assist in the documentation and resolution of nonconforming material reports and process discrepancy reports. * Ensure nonconformances are initiated and reported promptly. * Maintain work area orderliness and cleanliness. * Ensure test equipment is maintained and records are kept. * Ensure equipment is calibrated before use. * Communicate issues and procedures among multiple departments effectively. * Interact professionally with co-workers. Essential Skills * Knowledge of Current Good Manufacturing Practice (cGMP) Regulations for medical devices and pharmaceuticals. * Ability to manage daily activities to support business operations. * Ensure timely completion of paperwork in compliance with cGMP. * Determine root cause and develop corrective and preventive action plans for investigations, CAPA, and OOS issues. * Maintain operational efficiency and compliance with all test equipment and processes. * Provide necessary QA support for rapid commercialization of new products and processes. * Perform or assist in required cGMP validations. * Review in-process batch records and equipment notebooks daily. * Proficiency in Microsoft Excel, Word, and PowerPoint. * Serve as a backup for other QA Technicians as needed. * Excellent written and verbal communication skills for interdepartmental communication. Additional Skills & Qualifications * High School Degree with 3+ years of experience in the pharmaceutical industry. * Associate's degree preferred but not required. * Prior Quality Technician experience preferred. Work Environment This position involves working in a Liquid & Topical Manufacturing and Packaging environment. Full manufacturing and lab services include bottling, tubes, vials, pouching, form-fill-seal, kit assembly, and secondary packaging, within facilities totaling 184,000 square feet. The role requires physical activities such as climbing, walking, stooping, kneeling, and lifting up to 35 lbs. Employees may be exposed to inside and outside environmental conditions, including dust and chemicals, and warehousing environments. The work environment may include loud noise levels and requires appropriate attire to ensure safety and compliance. Job Type & Location This is a Contract to Hire position based out of EASTON, MD. Pay and Benefits The pay range for this position is $18.00 - $21.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in EASTON,MD. Application Deadline This position is anticipated to close on Dec 4, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

The Work Study - Tech Biology will participate in research activities with a specified mentor. This student may also assist with ordering and organizing shared laboratory research materials and maintaining the spaces and equipment in the Biological Sciences Research Laboratory. Essential Functions Complete relevant biological assays independently. Collect and analyze field samples and/or data relevant to the research project. Work with faculty mentor to design and implement experiments and/or protocols. Discuss and determine the future directions of the research project in consultation with the faculty mentor. Read and discuss research papers with mentor and potentially other students in the research laboratory. Work with faculty mentor to prepare scientific presentations/posters for dissemination of scientific results, as appropriate. Keep a detailed notebook on all lab functions performed Communicate with lab services and biology faculty members to keep lab stocked and to alert regarding waste removal.

We are currently looking for a 1st Shift, Quality Tech, Monday through Friday, to join our VALUES based organization. In this role you will focus on . Responsibilities: * Determine specifications and validate manufactured products and identify quality concerns * Thorough understanding of Work Order tickets & the ability to read and interpret Shop drawings and templates * Identify cause of errors, problems and/or defects * Assist in recommending and developing solutions to address quality concerns and to enhance quality/productivity * Discuss validation results with those responsible for products and recommend corrective actions Qualifications: * 3+ years production line experience in a manufacturing environment; experience as a millwork assembler or master carpenter is a plus. * Ability to follow oral and written communication from supervisor, lead or co-worker * The ability to see details at close range and match or detect differences between colors, including shades of color and brightness. * Must be able to read tape measure Specialty Building Products is the leading distributor of specialty building products in North America. SBP operates under the brands U.S. LUMBER, Alexandria Moulding, REEB Millwork, DW Distribution, Millwork Sales and Amerhart. We serve 45 states in the U.S. and 8 provinces in Canada from over 40 locations. Here at SBP we are a people first organization, our team is built upon strong culture and standards for success. We value your perspective and want to learn more about you with a commitment to laying the foundation for you to build a successful career with us. Join us and EVOLVE your Future at Specialty Building Products! Being a part of SBP you will be eligible for many benefits. Full-Time benefits would include: * Medical, Dental, Vision given on the 1st of the month following 30 days of employment * Company-Paid Life Insurance & Disability * 401(k) with Company Match * Company-Paid Time Off * Paid Holidays & Floating Holidays * Plus many more perks! Serving our communities, we are also committed to our core value of "using our influence to have a uniquely positive impact" on the people that we touch. Through our initiatives we encourage and incentivize our employees to aid fellow employees in need and to better serve our communities and the people we directly influence. We are proud to have the best team in our industry. We have experienced a tremendous amount of growth as a company. This growth has served not only our customer base but has also provided significant opportunities for advancement amongst our employees. Specialty Building Products is an equal opportunity employer. It is our policy of Specialty Building Products not to discriminate in hiring and employment on the basis of race, color, religion, national origin, sex, disability, age, military status, genetic information, or other protected class status in accordance with all applicable federal, state, and local laws.

Job Type: Full Time; Non-Exempt The Quality Control Technician will work cross-functionally to plan, organize, and recommend strategies to ensure products are developed successfully and in accordance with all specifications, SOP's, and GMP's. This position will be responsible for enforcing processing and manufacturing procedures, technology, and business practices documented in state-level SOPs, policies, forms, and batch records. This includes a complete understanding of the operation and maintenance for all equipment and HMI controls critical to finished good manufacturing. Also responsible for ensuring finished gummies meet formulation specifications, food safety guidelines, and established quality standards. Responsibilities: * Conduct inspections and audits to monitor and ensure traceability of product movement throughout the facility and to confirm established product quality requirements are achieved across all stages of production * Promptly communicate identified discrepancies to site and regional leaders and document accordingly * Advise operators of problems and follow up to ensure resolution; troubleshoot equipment issues and resolve efficiently to minimize production downtime * Investigate and participate in correction activities as directed * Assist with calibration, preventative, and routine maintenance of equipment * Continuously monitor processes to ensure sampling is appropriate to the product; color, flavor, weight, size, and appearance of the finished product meets specifications * Oversee QC for changeovers from one product or batch to another; ensure equipment and product continues to meet all specifications * Works with and trains new employees in all facets of finished goods manufacturing operation * Ensure work areas are maintained, organized, and in compliance with sanitary requirements * Accurately complete documentation and enter data to ensure compliance with internal and regulatory requirements; responsible for maintaining traceability in seed-to-sale and information management systems * Perform duties related to sampling and testing as required by production and staffing needs * Provide guidance on placement of operators and others on the production line * Possesses knowledge of the sanitation, safety, and requirements for food processing, handling, and storage in manufacturing of Gummy products * Responsible for CIP operation throughout all equipment used in the process to manufacture Gummy products * Maintain HACCP for all products and processes manufactured onsite * Lifts containers of in-process, finished, or waste products and transports within the facility as necessary * Perform all duties in compliance with safety rules, standard operating procedures and good manufacturing practices * Responsible for destruction of designated products * Maintain and enforce strict adherence to established safety and security procedures and report potentially unsafe conditions * Identify areas for quality control improvement and participate in problem solving activities to drive process improvements * Promote a culture of quality and change management * Additional duties and responsibilities will be assigned as necessary Education Requirements: * High school diploma or GED is required * Degree preferred in analytical chemistry or similar/related field Experience Requirements: * Minimum of 1 year working in a manufacturing or production based environment; experience in a GMP facility a plus * Analytical instrumentation experience preferred * Leadership or supervisory experience preferred Key Knowledge, Skills, and Abilities: * Fluent English skills to read/understand written instructions, manuals, and other information; to maintain a variety of written records, and to communicate effectively with and train, employees in a complex process * Fundamental arithmetic skills (addition, subtraction, division) to calculate weights, fills, etc * Computer skills, including keyboarding, standard functions, and data entry * Mechanical aptitude for troubleshooting and fixing equipment malfunctions, reading/understand gauges/controls/touch screen logic * Mechanical aptitude for troubleshooting and fixing equipment malfunctions * Perform duties that require constant attention to the manufacturing process Physical Requirements: * Ability to lift 50 pounds unassisted * Ability to stand/walk for most of shift * Ability to push/pull items weighing up to 100 pounds assisted * Ability to maintain attention and focus during manufacturing process * Manual dexterity to manipulate controls, disassemble/assemble equipment using a variety of hand tools. Environment: * Constant exposure to noise levels loud enough to require employees to wear hearing protection * Warm temperature levels, fumes, vibration, etc., enough to cause minor discomfort, oily/wet conditions * Employees to wear protective eyewear, hair nets, uniforms, steel-toed shoes, and gloves

Work Hours: 8:00 AM to 4:30 PM, Monday through Friday Pay Range: $19 - $24 per hour Make the Right Connection-Build Your Career with Dixon! The Dixon Group is looking for a Quality Technician to join their Boss Division in Chestertown, MD! In this role, you will be responsible for in-process audits in production, inspecting and approving incoming materials, and managing calibration of gauges. This position is ideal for someone who takes pride in precision and has a strong background in inspection, measurement, and metrology. About Us: The Dixon Group is a global, family-owned manufacturing company with a history of over 100 years of operation in the U.S.A. Based in Chestertown, Maryland, with distribution centers located worldwide. The company has a diverse workforce and a strong values-based culture. As an innovator in the hose coupling industry, our mission is to provide real solutions for our customers while fostering a supportive and collaborative work environment. At The Dixon Group, we value the contributions of our Military Veterans and proudly employ our nation's heroes. Veterans are strongly encouraged to apply. What You'll Do: * Inspect and approve incoming materials, in-process production, and finished goods against engineering drawings and specifications. * Perform visual and dimensional inspections using height gages, calipers, micrometers, optical comparators, and other precision measurement tools. * Document inspection results through reports, logs, and database entries, including rework and scrap tracking. * Communicate nonconformances to affected parties and follow up for required adjustments. * Issue Corrective Actions where appropriate based on internal guidelines. * Maintain and manage all production gauges; performing in-house calibration where possible and coordinating third-party calibration when necessary. * Verify proper operation of gauges; manage inspection and repair as required. * Ensure compliance with company quality standards, safety practices, and regulatory requirements. * Maintain SOPs for the Quality department, making revisions and updates as needed. * Assist with auditing internal work procedures and making recommendations to address non-conformances. * Participate in continuous improvement efforts to enhance quality systems and reduce rework. What We're Looking For: * High school diploma or equivalent required; Associate degree in STEM or related coursework preferred. * 1-3 years of experience in a quality, inspection, engineering or manufacturing role is preferred. * Some experience in reading blueprints and using measurement tools is required. * Strong working knowledge of mechanical measurement equipment such as calipers, micrometers, height gauges and thread gauges. * Familiarity with engineering drawings, blueprints, and industry specifications such as ANSI, ASTM, API and 3A. * Familiarity with quality documentation, reporting, and data entry. * Detail-oriented, with strong organizational and communication skills. What We Offer: * Medical, dental, and vision insurance for you and your family * Competitive salary * Bonus programs * 401K retirement plan * Training opportunities * Tuition reimbursement * Paid vacation, PTO, and holidays * Gym reimbursements, and more! Join us and be a part of a team that values your contributions and supports your goals! The Dixon Group is an equal opportunity employer and complies with all applicable federal, state, and local fair employment practices and laws. Accordingly, to the fullest extent required by applicable law, The Dixon Group strictly prohibits and does not tolerate discrimination against employees, applicants, or any other covered persons. The Dixon Group is committed to protecting the privacy rights of its employees and job applicants to the fullest extent required by applicable law. To that end, personal information will be collected solely for those legitimate business purposes recognized by law, and then maintained in a manner consistent with all applicable laws and regulations pertaining to document retention requirements. The Dixon Group does not sell personal information to third parties, and does not share such personal information with third parties except when authorized by law to do so (e.g., in response to a lawful subpoena; mandatory tax reporting; etc.)

Job Description Quality Technician ???? Work Hours: 8:00 AM to 4:30 PM, Monday through Friday ???? Pay Range: $19 - $24 per hour Make the Right Connection-Build Your Career with Dixon! The Dixon Group is looking for a Quality Technician to join their Boss Division in Chestertown, MD! In this role, you will be responsible for in-process audits in production, inspecting and approving incoming materials, and managing calibration of gauges. This position is ideal for someone who takes pride in precision and has a strong background in inspection, measurement, and metrology. About Us: The Dixon Group is a global, family-owned manufacturing company with a history of over 100 years of operation in the U.S.A. Based in Chestertown, Maryland, with distribution centers located worldwide. The company has a diverse workforce and a strong values-based culture. As an innovator in the hose coupling industry, our mission is to provide real solutions for our customers while fostering a supportive and collaborative work environment. At The Dixon Group, we value the contributions of our Military Veterans and proudly employ our nation's heroes. Veterans are strongly encouraged to apply. ???? What You'll Do: Inspect and approve incoming materials, in-process production, and finished goods against engineering drawings and specifications. Perform visual and dimensional inspections using height gages, calipers, micrometers, optical comparators, and other precision measurement tools. Document inspection results through reports, logs, and database entries, including rework and scrap tracking. Communicate nonconformances to affected parties and follow up for required adjustments. Issue Corrective Actions where appropriate based on internal guidelines. Maintain and manage all production gauges; performing in-house calibration where possible and coordinating third-party calibration when necessary. Verify proper operation of gauges; manage inspection and repair as required. Ensure compliance with company quality standards, safety practices, and regulatory requirements. Maintain SOPs for the Quality department, making revisions and updates as needed. Assist with auditing internal work procedures and making recommendations to address non-conformances. Participate in continuous improvement efforts to enhance quality systems and reduce rework. ???? What We're Looking For: High school diploma or equivalent required; Associate degree in STEM or related coursework preferred. 1-3 years of experience in a quality, inspection, engineering or manufacturing role is preferred. Some experience in reading blueprints and using measurement tools is required. Strong working knowledge of mechanical measurement equipment such as calipers, micrometers, height gauges and thread gauges. Familiarity with engineering drawings, blueprints, and industry specifications such as ANSI, ASTM, API and 3A. Familiarity with quality documentation, reporting, and data entry. Detail-oriented, with strong organizational and communication skills. ???? What We Offer: Medical, dental, and vision insurance for you and your family Competitive salary Bonus programs 401K retirement plan Training opportunities Tuition reimbursement Paid vacation, PTO, and holidays Gym reimbursements, and more! Join us and be a part of a team that values your contributions and supports your goals! The Dixon Group is an equal opportunity employer and complies with all applicable federal, state, and local fair employment practices and laws. Accordingly, to the fullest extent required by applicable law, The Dixon Group strictly prohibits and does not tolerate discrimination against employees, applicants, or any other covered persons. The Dixon Group is committed to protecting the privacy rights of its employees and job applicants to the fullest extent required by applicable law. To that end, personal information will be collected solely for those legitimate business purposes recognized by law, and then maintained in a manner consistent with all applicable laws and regulations pertaining to document retention requirements. The Dixon Group does not sell personal information to third parties, and does not share such personal information with third parties except when authorized by law to do so (e.g., in response to a lawful subpoena; mandatory tax reporting; etc.)

Job Description Summary/Objective: The Technical Service/Quality Control Technician implements and complies with quality assurance methods and procedures to ensure products and materials are produced in accordance with specifications. Essential Functions: Perform specimen tests of concrete from random loads or for special jobs or mixes; prepare test reports as required. Oversee unique jobs to ensure product standards are met, i.e., jobs that have restrictive specifications or require large quantities of material to be delivered. Perform aggregates and batch plants tests including daily graduation and moisture tests on all concrete being produced for State and spec projects. Certify concrete loads being delivered to "spec" jobs in accordance with SHA specifications; check loads for proper procedure and time of mixing. Perform quality assurance tests on trial batches of new concrete mix designs under close tolerance conditions and make adjustments until mixture meets specifications. Troubleshoot problems with customers, analyze and evaluate specific conditions, situations, quantities, etc., and provide appropriate resolution. Provide technical assistance and training to plant managers, equipment and yard operators, and drivers when requested. Perform laboratory tests including gradation, moisture, lightweight particles and specific gravity tests on aggregates. Select samples for materials that need certification by an outside laboratory or that are beyond the department capability. Transport these samples to the testing agency. Perform additional tasks such as cleaning facilities to ensure safety and cleanliness, moving equipment and materials, and completing tasks for other positions when incumbent is absent. Assist the Technical Services Manager and Assistant Manager as needed. Other duties as assigned. JOB SPECIFICATIONS Work Environment: Work time will be split between indoors/office and outdoors/field Exposure to dust and fumes/offensive smells. Exposure to chemicals such as concrete, chemical admixtures. Close proximity to moving mechanical parts. Noise level will be moderate to loud. Physical Demands: Lift a maximum weight of 50 lbs., repetitively lift 50 lbs., carry approximately 50 lbs., and push/pull approximately 75-100 lbs. Reach overhead and reach away from the body. Minimal kneeling, squatting and climbing may be required. Sit 3 hours per day, stand 5 hours per day, and walk 2 hours per day. ADDITIONAL QUALIFICATIONS Experience: Laboratory testing experience in ready-mix concrete or aggregates preferred. Special Skills: Written communication, verbal communication, and basic mathematical skills. Ability to use a computer and iPad, including Microsoft Office. Ability to use the company dispatching system. Ability to compute basic material calculations. Excellent interpersonal skills. Able to exhibit a high level of confidentiality. Excellent organizational skills. Must be able to identify and resolve problems in a timely manner. Certifications: Valid Driver's License. ACI Level 1 certification (must be obtained within 1 year of assuming position). Industry Related Experience or Skills: Background in concrete, construction, mining operations or building materials (preferred). Education Required: High School Preferred Education: N/A Bilingual in Spanish Preferred: Yes Interested in future opportunities with Chaney? Join our Talent Community to get alerts about newly posted positions. Click here to sign up!

Job Title: Quality TechnicianLocation: Laurel MDJob Type: 3-6 month contract Industry: [Manufacturing/Electronics/Defense] Job Summary:We are seeking a detail-oriented and experienced Quality Technician to join our team. The ideal candidate will possess an IPC-A-610 or IPC/WHMA-A-620 certification and will have hands-on experience inspecting electronic assemblies to industry standards. Experience operating and programming CMMs using PC-DMIS or similar software is highly desirable. Key Responsibilities:Inspect electronic assemblies and cable/wire harnesses in accordance with IPC 610 or IPC 620 standards.Perform visual inspections for soldering, component placement, wiring, and mechanical integrity.Utilize inspection equipment including microscopes, calipers, micrometers, and gauges.Operate and/or program Coordinate Measuring Machines (CMM) using PC-DMIS or similar software (a plus).Maintain accurate inspection records, reports, and quality documentation.Assist in root cause analysis and corrective/preventive action implementation.Collaborate with production, engineering, and quality teams to identify and resolve quality issues.Ensure compliance with company and industry quality standards. Requirements:IPC-A-610 or IPC/WHMA-A-620 Certification (required).2+ years of experience in a quality assurance or inspection role within a manufacturing environment.Experience with electronic assemblies, PCBAs, or cable/wire harnesses.Familiarity with CMM operation and PC-DMIS programming (preferred but not required).Strong attention to detail and documentation accuracy.Ability to interpret technical drawings and inspection criteria.Excellent communication and problem-solving skills. Preferred Qualifications:Experience in ISO 9001, AS9100, or similar regulated environments.Knowledge of statistical process control (SPC) and quality tools (e.g., Pareto, Fishbone).Proficiency with MS Office Suite.

The Quality Technician is responsible for performing hourly inspections and providing support to ensure compliance with current Good Manufacturing Practice (cGMP) and internal procedures. The successful candidate will ensure overall compliance, including testing and methods in accordance with cGMP, and will inspect incoming components, in-process products, and finished products as per documented specifications. Responsibilities + Assist with the inspection of incoming components according to documented specifications. + Assist with the generation and approval of controlled labels using provided programs. + Record data and maintain accurate records in accordance with cGMP documentation practices for accuracy and completeness. + Retrieve documents using the EQMS computer system. + Troubleshoot quality concerns that may arise during the inspection of incoming components and report to the Quality Manager. + Verify the calibration of all inspection test equipment and maintain accurate records. + Perform data entry and retrieval using the computer system. + Work overtime, weekends, or alternate shifts as needed. + Assist in the generation and resolution of corrective and preventive action plans (CAPAs). + Assist in the documentation and resolution of nonconforming material reports and process discrepancy reports. + Ensure nonconformances are initiated and reported promptly. + Maintain work area orderliness and cleanliness. + Ensure test equipment is maintained and records are kept. + Ensure equipment is calibrated before use. + Communicate issues and procedures among multiple departments effectively. + Interact professionally with co-workers. Essential Skills + Knowledge of Current Good Manufacturing Practice (cGMP) Regulations for medical devices and pharmaceuticals. + Ability to manage daily activities to support business operations. + Ensure timely completion of paperwork in compliance with cGMP. + Determine root cause and develop corrective and preventive action plans for investigations, CAPA, and OOS issues. + Maintain operational efficiency and compliance with all test equipment and processes. + Provide necessary QA support for rapid commercialization of new products and processes. + Perform or assist in required cGMP validations. + Review in-process batch records and equipment notebooks daily. + Proficiency in Microsoft Excel, Word, and PowerPoint. + Serve as a backup for other QA Technicians as needed. + Excellent written and verbal communication skills for interdepartmental communication. Additional Skills & Qualifications + High School Degree with 3+ years of experience in the pharmaceutical industry. + Associate's degree preferred but not required. + Prior Quality Technician experience preferred. Work Environment This position involves working in a Liquid & Topical Manufacturing and Packaging environment. Full manufacturing and lab services include bottling, tubes, vials, pouching, form-fill-seal, kit assembly, and secondary packaging, within facilities totaling 184,000 square feet. The role requires physical activities such as climbing, walking, stooping, kneeling, and lifting up to 35 lbs. Employees may be exposed to inside and outside environmental conditions, including dust and chemicals, and warehousing environments. The work environment may include loud noise levels and requires appropriate attire to ensure safety and compliance. Job Type & Location This is a Contract to Hire position based out of EASTON, MD. Pay and Benefits The pay range for this position is $18.00 - $21.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in EASTON,MD. Application Deadline This position is anticipated to close on Dec 17, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Job Description At Curaleaf, we're redefining the cannabis industry with a strong commitment to quality, expertise, and innovation. As a leading global cannabis provider, our brands-including Curaleaf, Select, and Grassroots-offer premium products and services in both medical and adult-use markets. Join us at Curaleaf to be part of a high-growth, purpose-driven company that champions corporate social responsibility through our Rooted in Good initiative, supporting community outreach and positive change. Here, you'll have the opportunity to make a meaningful impact, drive innovation, and help shape the future of cannabis. Quality Control Technician Job Type: Full Time; Non-Exempt The Quality Control Technician will work cross-functionally to plan, organize, and recommend strategies to ensure products are developed successfully and in accordance with all specifications, SOP's, and GMP's. This position will be responsible for enforcing processing and manufacturing procedures, technology, and business practices documented in state-level SOPs, policies, forms, and batch records. This includes a complete understanding of the operation and maintenance for all equipment and HMI controls critical to finished good manufacturing. Also responsible for ensuring finished gummies meet formulation specifications, food safety guidelines, and established quality standards. Responsibilities: Conduct inspections and audits to monitor and ensure traceability of product movement throughout the facility and to confirm established product quality requirements are achieved across all stages of production Promptly communicate identified discrepancies to site and regional leaders and document accordingly Advise operators of problems and follow up to ensure resolution; troubleshoot equipment issues and resolve efficiently to minimize production downtime Investigate and participate in correction activities as directed Assist with calibration, preventative, and routine maintenance of equipment Continuously monitor processes to ensure sampling is appropriate to the product; color, flavor, weight, size, and appearance of the finished product meets specifications Oversee QC for changeovers from one product or batch to another; ensure equipment and product continues to meet all specifications Works with and trains new employees in all facets of finished goods manufacturing operation Ensure work areas are maintained, organized, and in compliance with sanitary requirements Accurately complete documentation and enter data to ensure compliance with internal and regulatory requirements; responsible for maintaining traceability in seed-to-sale and information management systems Perform duties related to sampling and testing as required by production and staffing needs Provide guidance on placement of operators and others on the production line Possesses knowledge of the sanitation, safety, and requirements for food processing, handling, and storage in manufacturing of Gummy products Responsible for CIP operation throughout all equipment used in the process to manufacture Gummy products Maintain HACCP for all products and processes manufactured onsite Lifts containers of in-process, finished, or waste products and transports within the facility as necessary Perform all duties in compliance with safety rules, standard operating procedures and good manufacturing practices Responsible for destruction of designated products Maintain and enforce strict adherence to established safety and security procedures and report potentially unsafe conditions Identify areas for quality control improvement and participate in problem solving activities to drive process improvements Promote a culture of quality and change management Additional duties and responsibilities will be assigned as necessary Education Requirements: High school diploma or GED is required Degree preferred in analytical chemistry or similar/related field Experience Requirements: Minimum of 1 year working in a manufacturing or production based environment; experience in a GMP facility a plus Analytical instrumentation experience preferred Leadership or supervisory experience preferred Key Knowledge, Skills, and Abilities: Fluent English skills to read/understand written instructions, manuals, and other information; to maintain a variety of written records, and to communicate effectively with and train, employees in a complex process Fundamental arithmetic skills (addition, subtraction, division) to calculate weights, fills, etc Computer skills, including keyboarding, standard functions, and data entry Mechanical aptitude for troubleshooting and fixing equipment malfunctions, reading/understand gauges/controls/touch screen logic Mechanical aptitude for troubleshooting and fixing equipment malfunctions Perform duties that require constant attention to the manufacturing process Physical Requirements: Ability to lift 50 pounds unassisted Ability to stand/walk for most of shift Ability to push/pull items weighing up to 100 pounds assisted Ability to maintain attention and focus during manufacturing process Manual dexterity to manipulate controls, disassemble/assemble equipment using a variety of hand tools. Environment: Constant exposure to noise levels loud enough to require employees to wear hearing protection Warm temperature levels, fumes, vibration, etc., enough to cause minor discomfort, oily/wet conditions Employees to wear protective eyewear, hair nets, uniforms, steel-toed shoes, and gloves Maryland Pay Transparency$20.50-$22.50 USD What We Offer: Career Growth Opportunities Competitive Pay and Benefits Generous PTO and Parental Leave 401(K) Retirement Plan Life/ Disability Insurance Community Involvement Referral Bonuses and Product Discounts Benefits vary by state, role type, and eligibility. Follow us on Social Media: Instagram: @curaleaf.usa Twitter: @Curaleaf_Inc LinkedIn: Curaleaf LinkedIn Curaleaf Holdings, Inc. (TSX: CURA) (OTCQX: CURLF) ("Curaleaf") is a leading international provider of consumer products in cannabis with a mission to enhance lives by cultivating, sharing, and celebrating the power of the plant. As a high-growth cannabis company known for quality, expertise and reliability, the Company, and its brands, including Curaleaf, Select, Grassroots, JAMS, Find and Zero Proof provide industry-leading service, product selection and accessibility across the medical and adult-use markets. Curaleaf International is the largest vertically integrated cannabis company in Europe with a unique supply and distribution network throughout the European market, bringing together pioneering science and research with cutting-edge cultivation, extraction, and production. Home | Curaleaf | Cannabis with Confidence Our Vision: To be the world's leading cannabis company by consistently delivering superior products and services and driving the global acceptance of cannabis. Our Values: Lead and Inspire. Commit to Win. ONE Curaleaf. Driven to Deliver Excellence. Curaleaf is an equal opportunity employer. Curaleaf recruits, employs, trains, compensates, and promotes regardless of race, religion, color, national origin, gender identity, sexual orientation, physical ability, age, veteran status, and other protected status as required by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Individuals adversely impacted by the war on drugs are encouraged to apply. Current Curaleaf employees should apply for open positions through our Internal Job Board, which can be accessed via the link on The Leaf.

The Quality Technician is responsible for performing hourly inspections and providing support to ensure compliance with current Good Manufacturing Practice (cGMP) and internal procedures. The successful candidate will ensure overall compliance, including testing and methods in accordance with cGMP, and will inspect incoming components, in-process products, and finished products as per documented specifications. Responsibilities * Assist with the inspection of incoming components according to documented specifications. * Assist with the generation and approval of controlled labels using provided programs. * Record data and maintain accurate records in accordance with cGMP documentation practices for accuracy and completeness. * Retrieve documents using the EQMS computer system. * Troubleshoot quality concerns that may arise during the inspection of incoming components and report to the Quality Manager. * Verify the calibration of all inspection test equipment and maintain accurate records. * Perform data entry and retrieval using the computer system. * Work overtime, weekends, or alternate shifts as needed. * Assist in the generation and resolution of corrective and preventive action plans (CAPAs). * Assist in the documentation and resolution of nonconforming material reports and process discrepancy reports. * Ensure nonconformances are initiated and reported promptly. * Maintain work area orderliness and cleanliness. * Ensure test equipment is maintained and records are kept. * Ensure equipment is calibrated before use. * Communicate issues and procedures among multiple departments effectively. * Interact professionally with co-workers. Essential Skills * Knowledge of Current Good Manufacturing Practice (cGMP) Regulations for medical devices and pharmaceuticals. * Ability to manage daily activities to support business operations. * Ensure timely completion of paperwork in compliance with cGMP. * Determine root cause and develop corrective and preventive action plans for investigations, CAPA, and OOS issues. * Maintain operational efficiency and compliance with all test equipment and processes. * Provide necessary QA support for rapid commercialization of new products and processes. * Perform or assist in required cGMP validations. * Review in-process batch records and equipment notebooks daily. * Proficiency in Microsoft Excel, Word, and PowerPoint. * Serve as a backup for other QA Technicians as needed. * Excellent written and verbal communication skills for interdepartmental communication. Additional Skills & Qualifications * High School Degree with 3+ years of experience in the pharmaceutical industry. * Associate's degree preferred but not required. * Prior Quality Technician experience preferred. Work Environment This position involves working in a Liquid & Topical Manufacturing and Packaging environment. Full manufacturing and lab services include bottling, tubes, vials, pouching, form-fill-seal, kit assembly, and secondary packaging, within facilities totaling 184,000 square feet. The role requires physical activities such as climbing, walking, stooping, kneeling, and lifting up to 35 lbs. Employees may be exposed to inside and outside environmental conditions, including dust and chemicals, and warehousing environments. The work environment may include loud noise levels and requires appropriate attire to ensure safety and compliance. Job Type & Location This is a Contract to Hire position based out of EASTON, MD. Pay and Benefits The pay range for this position is $18.00 - $21.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in EASTON,MD. Application Deadline This position is anticipated to close on Dec 5, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.