Quality control analyst jobs in Concord, NC

No Visa Sponsorship: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. The Senior Microbiologist is a critical technical resource in the QC Microbiology laboratory supporting the manufacturing of sterile injectable products. This position is responsible for independently performing and overseeing complex microbiological testing and environmental monitoring (EM) in compliance with cGMP, USP, FDA, and internal quality standards. This position is in a fast-paced, FDA regulated environment in the Pharmaceutical Industry. This role is mainly responsible for completing deviation investigations, OOS/OOT and CAPA development related to EM and microbiological testing. Maintains spreadsheets and databases to track and monitor department/company data, KPIs and metrics. Accountable for QC Microbiology inventory control including ordering materials, maintaining stock and resolving material complaints as needed. This role will serve as a Subject Matter Expert (SME) to provide guidance and support junior microbiologists. Train team members in aseptic technique, microbiological methods, EM sampling, and good documentation practices. Participate in the qualification of microbiology lab equipment. Identify and implement continuous improvement opportunities to optimize workflows in the quality control microbiology laboratory. OVERALL JOB RESPONSIBILITIES: Operational Excellence: Models the principles and behaviors of Glenmark and ensures personnel follow the company code of conduct. Communicate progress, status, and roadblocks as required. Drive projects, assignments, and complete presentations within timelines and budgets. Create and maintain relevant metrics for department/site. Spreadsheets and databases will be leveraged for departmental and company metrics, presentations, and data/testing tracking/verification. The Senior Microbiologist is responsible for keeping these sheets and databases up to date. Ability to perform routine testing of samples submitted to the laboratory as appropriate. Schedules and participates in cleaning, inventory, and maintenance tasks in the lab. Supports inventory management and ordering/stocking of all QC department laboratory supplies. Ensures laboratory equipment is in compliance with procedures and GLP requirements. Troubleshoots laboratory issues related to all instrumentation. Recommends potential corrective and/or preventive actions and implements these actions within the laboratory. Performs GMP review of test data to ensure that test results meet all specifications. Trends data and analyzes trends to proactively mitigate equipment and reagent performance issues. Verifies laboratory equipment and associated equipment logs to ensure proper operation Stakeholder: Preparation, review and approval of sampling matrix and hold time schedule Conducts and communicates results of lab investigations when test results fall outside pre-established specifications (OOS). Performs routine equipment maintenance. Performs maintenance of spare parts inventory, calibrations and supervises third party maintenance and repair when necessary. Establishes good working relation with contract laboratories. Supports in the development of methods transfer and validation, troubleshooting, cross validation, IQ/OQ/PQ protocols. Supports activities regarding audits of suppliers and contract labs in support of vendor certification program. Conducts statistical evaluation of the manufacturing and inspection process and training QC staff. Ensure that all equipment is calibrated. Responsible to develop and validate new test procedures Perform data analysis, compile data and generate reports for management review. Review lab test data and their integrity and adherence to SOPs and cGMP. Compliance: Maintain current knowledge of regulatory and industry standards, trends and advancements. Responsible for ensuring compliance to systems and procedures in the EM/Microbiology laboratory and cleanroom areas. And prepare the lab for internal and external audits. Support Continuous Improvement initiatives by providing support on updating SOPs, WIs, and OJT Complete and maintain certified investigator training requirements. Perform investigation of the quality events assigned using root cause analysis tools, maintain timelines for closure of investigations and identify/initiate CAPAs Complete and maintain status as a certified trainer Ensure Quality Systems are compliant with cGMPs and internal/external regulations and procedures Evaluates and assists in the implementation of new changes at the site, including providing training on an as needed basis Provide support to collect and prepare EMPQ reports, EM Trend reports, QMR board presentations with associated documentation. Performs regular self-audits of the Microbiology and EM laboratory areas (including storage areas) and assists/leads activities to address audit findings. Stakeholder: Works collaboratively with other department stakeholders to ensure the services provided to the site are developed, tested, and delivered according to established procedures and regulations. Innovation: Supports purchasing QC EM laboratory supplies. Makes sound, well considered decisions to make the most of available funds and resources. Monitors lab supply costs and looks for ways to work with suppliers to reduce consumables cost when appropriate. Consults with management, when appropriate, about laboratory supply variances. Demonstrates the ability to assess upcoming laboratory supply needs and prepare accordingly. Makes realistic and actionable plans to address supply chain issues. Maintains the QC department ordering system to reduce costs and waste due to expiry. Keeps current on physical and computerized tracking systems for materials and supplies. Safety: Appropriately utilizes PPE (Personal Protective Equipment) as required to perform routine and non-routine laboratory duties Education: KNOWLEDGE, SKILLS AND ABILITIES: Minimum BS/BA in Pharmaceutical Sciences, Chemistry, Biology Experience: Minimum of 3+ years in a pharmaceutical environment Strong organizational skills. Displays the ability to prioritize work and manage multiple tasks independently. Excellent written communication and technical writing skills. Clearly demonstrates competence in the selection and use of root cause analysis tools and techniques (e.g., 5 Whys, Pareto Analysis, 5M +E). Displays strong interpersonal skills and ability to work with all levels of an organization. Clearly expresses ideas (verbal and written) and demonstrates the ability to apply a quality mindset when completing Microbiology/EM laboratory tasks. Demonstrates the ability to read, understand, author, redline and execute standard operating procedures (SOPs). Displays ability to achieve Glenmark Monroe QE investigator certifications for product/process/testing/facility issues with product and non-product impact. Exhibits both analytical and problem-solving skills. Proven ability to problem solve/troubleshoot and provide solutions for laboratory issues. Able to assess safety and environmental risks to ensure laboratory tasks adhere to EHS management system. The ability to work independently and within team structure and on multiple projects, with flexibility to adapt to changing priorities is required. This candidate must be a technical expert and have excellent written and oral communication as well as interpersonal relationship skills. Ability to lift 30 lbs.' and work within different extreme temperature / humidity environments as encountered in the various Incubator conditions.

🌟 Flexible Schedule | Weekly Pay | Career Growth 🌟 Are you detail-oriented, love helping others succeed, and looking for a role that combines independent work with team leadership? Join Spotless Cleaning Services as a Quality Control Specialist and be part of a growing company where your voice matters and your work makes a real impact. 🧼 Who We Are At Spotless Cleaning Services, we're more than a cleaning company - we're a team on a mission to make life easier for our clients and more meaningful for our employees. Since 2006, we've built a reputation for trust, quality, and care, and our team is at the heart of everything we do. When you join Spotless, you're not just getting a job - you're stepping into a long-term career path where you can grow from technician to team lead, trainer, or supervisor. 💼 What We Offer Flexible daytime schedule Weekly pay via direct deposit Paid training and ongoing support Sign-on & referral bonuses Paid travel time + mileage reimbursement Paid vacation All cleaning supplies & equipment provided Positive team culture with leadership that listens 👀 About the Role: Quality Control Specialist You'll be responsible for ensuring our cleaning standards are met across homes and offices, supporting technicians in the field, and being the bridge between clients and the company. This role is perfect for someone who is organized, dependable, and passionate about quality service. This position also involves stepping in to clean when needed - especially to support the team or ensure quality standards are met. 👉 Previous experience supervising teams and working in a fast-paced environment is required. 🔑 Key Responsibilities: Visit job sites to ensure high cleaning standards are being followed Provide on-the-spot coaching and support to technicians Communicate professionally with clients and the office team Track key details (supplies, key codes, customer notes, etc.) Perform walkthroughs and quality checks Help maintain a high client satisfaction rate Lead by example and help train new hires as needed Step in to assist with cleaning duties when necessary 📍 Service Areas: Mooresville | Huntersville | Cornelius | Denver | Charlotte 💬 What Our Team Says: “I love working here because the people care. Management supports us and celebrates our achievements. It's not just a job-it's a place to grow.”- Maria, Team Member since 2018 ✨ Ready to Join a Team That Values You? Take the next step in your career. Apply today and help us keep Spotless a name clients trust and employees are proud to represent.

Are you ready to be part of a company that's not just talking about the future, but actively shaping it? Join The AES Corporation (NYSE: AES), a Fortune 500 company that's leading the charge in the global energy revolution. With operations spanning 14 countries, AES is committed to shaping a future through innovation and collaboration. Our dedication to innovation has earned us recognition as one of the Top Ten Best Workplaces for Innovators by Fast Company in 2022. And with our certification as a Great Place to Work, you can be confident that you're joining a company that values its people just as much as its groundbreaking ideas. AES is proudly ranked #1 globally in renewable energy sales to corporations, and with $12.7B in revenues in 2023, we have the resources and expertise to make a significant impact as we provide electricity to 25 million customers worldwide. As the world moves towards a net-zero future, AES is committed to meeting the Paris Agreement's goals by 2050. Our innovative solutions, such as 24/7 carbon-free energy for data centers, are setting the pace for rapid, global decarbonization. If you're ready to be part of a company that's not just adapting to change, but driving it, AES is the place for you. We're not just building a cleaner, more sustainable future - we're powering it. Apply now and energize your career with a true leader in the global energy transformation. Position Overview We are seeking a highly detail-oriented and safety-driven FAA Part 107 licensed Remote Pilot with thermal imaging certification to serve as a dual-role QC Administrator and Drone Operator. This position supports construction and commissioning operations across utility-scale solar projects, combining aerial inspection capabilities with digital workflow management. The ideal candidate is experienced in both visual and thermal drone operations, and proficient in platforms such as Procore, SAP Fiori, Ironclad, and Drone Deploy. Key Responsibilities Quality Control Administration * Procore Auditing: Conduct regular audits of solar project documentation to ensure accuracy, completeness, and compliance with internal standards. * Fiori Task Management: Execute and monitor SAP Fiori workflows related to procurement, Quality Control personnel contracts, and operational tracking. * Ironclad Contract Oversight: Manage QC-related contract workflows, ensuring proper review, approval, and archiving. * Team Record Keeping: Maintain records of QC team certifications, training logs, and performance metrics. * 107 Pilot Credential Tracking: Verify FAA Part 107 pilot credentials and flight logs for compliance and operational readiness. Remote Drone Operations * Aerial Inspections & Documentation: Conduct scheduled and on-demand aerial inspections using Drone Deploy. Capture high-resolution imagery and videos to monitor construction progress, material placement, and site conditions. * Thermal Imaging Operations: Perform thermal scans to identify electrical hotspots, module defects, and performance issues. Collaborate with EPCs and AES QC teams to validate findings. * Data Management & Reporting: Upload, organize, and annotate imagery in Drone Deploy. Generate inspection summaries and maintain FAA-compliant flight documentation. * Compliance & Safety: Adhere to FAA Part 107 regulations, local airspace restrictions, and internal safety protocols. Conduct pre-flight checks and site-specific risk assessments. Qualifications Required * Valid FAA Part 107 Remote Pilot Certificate * Thermal Imaging Certification (e.g., FLIR Level I or equivalent) * Experience using Drone Deploy for mapping, photogrammetry, and reporting * Proficiency with drone platforms such as DJI Mavic 3 Enterprise, Matrice series, or similar * Strong understanding of aerial data processing, GIS, and thermal analysis Preferred * Experience in administrative tasks * Familiarity with commissioning documentation workflows * Knowledge of Procore, DroneDeploy, SAP Fiori, or similar platforms Work Environment * Remote operations via Drone Deploy platform with limited travel to sites as needed * Coordination with project engineers, commissioning specialists, and QC teams * Flexibility to support field schedules, including early morning or weekend operations for thermal accuracy AES is an Equal Opportunity Employer who is committed to building strength and delivering long-term sustainability through diversity and inclusion. Respecting all backgrounds, differences and perspectives enables us to improve the lives of our people, customers, suppliers, contractors, and the communities in which we live and work. All qualified applicants will receive consideration for employment without regard to sex, sexual orientation, gender, gender identity and/or expression, race, national origin, ethnicity, age, religion, marital status, physical or mental disability, pregnancy, childbirth, or related medical condition, military or veteran status, or any other characteristic protected under applicable law. E-Verify Notice: AES will provide the Social Security Administration (SSA) and if necessary, the Department of Homeland Security (DHS) with information from each new employee's I-9 to confirm work authorization.

The Quality Control Chemist reports directly to Quality Laboratory Management and plays a key role in supporting laboratory operations through accurate and timely testing. This position requires strong time management skills to meet testing deadlines and a willingness to learn laboratory processes, instrumentation theory, and troubleshooting techniques. Schedule: This position will be on a 2nd shift: Monday - Thursday 3:30pm - 11:30pm and Friday 1:30pm - 9:30pm. Key Responsibilities Testing: * Perform Release, Stability, and Special Request testing on finished products and raw materials in compliance with Standard Operating Procedures (SOPs), in-house methods, and compendial standards. * Execute in-house methods independently and accurately with minimal supervision. Team Collaboration: * Adapt to changes in testing schedules and support continuous improvement initiatives within the lab. * Assist in training new laboratory personnel and document training per established SOPs and Nutramax guidelines. Safety: * Maintain a safety-first approach and remain vigilant of surroundings while performing laboratory tasks. * Ensure all equipment used in testing is properly calibrated and maintained. General Duties: * Train on and operate various laboratory instruments, including but not limited to: Laboratory Balances, HPLC, GC, Automated Titrators, FTIR, UV/Vis Spectrophotometer, Polarimeter, Dissolution and Disintegration instruments. * Complete assigned projects within established timelines while balancing testing responsibilities. * Stay informed on updates from USP, FDA, and other regulatory bodies to ensure compliance with analytical standards and documentation practices. * Assist in investigating Out-of-Specification (OOS) results as needed. * Perform additional duties as required to support company objectives. * Communicate effectively across departments and work collaboratively within a team environment. * Maintain regular and reliable attendance. Skills Chemistry, Quality control, Laboratory, Gmp, Wet chemistry Top Skills Details Chemistry Additional Skills & Qualifications * Experience: 2-5 years in a laboratory setting, a cGMP environment. Familiarity with GC and/or LC instrumentation is preferred. * Skills: Strong interpersonal skills, self-motivation, and ability to work with individuals at all organizational levels. * Education: Bachelor's degree in Chemistry; concentrations in Biochemistry, Inorganic, Physical, or Polymer Chemistry are preferred. Experience Level Intermediate Level Job Type & Location This is a Permanent position based out of Lancaster, SC. Pay and Benefits The pay range for this position is $70000.00 - $80000.00/yr. Comprehensive Health Coverage: Competitive medical, dental, and vision plans for employees and their families. Educational Assistance: Opportunities for training and professional development to support career growth. Supportive Work Culture: A family-oriented environment that values faith, servant leadership, and collaboration. Community Engagement: Volunteer opportunities and mission trips organized by the company to give back locally and internationally. Employee Recognition & Perks: Birthday cards with gift cards, family days at the zoo, Thanksgiving dinners, and other thoughtful gestures. Work-Life Balance: A culture that prioritizes employee well-being and fosters a positive, supportive atmosphere. Workplace Type This is a fully onsite position in Lancaster,SC. 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 for other accommodation options.

The Quality Control Technician inspects work performed by client employees, internal employees, or client subcontractors. Work is inspected for process and specification compliance against company/client guidelines. (This purpose is meant to be a guide. Duties may vary dependent upon client.) Essential Position Functions: * Inspect assigned work locations for compliance with client or company specifications and guidelines. * Inspections may include but are not limited to work safety, installation, and troubleshooting compliance. * Use appropriate testing equipment based upon client specifications. * Assist in preparing and developing inspection instructions and procedures. * Develop and create project specific checklists and standards. * Record and document inspection results and findings in applicable data sheets and forms. * Complete and submit inspection documentation to the appropriate supervisory personnel. * Ensure completion of inspections in a timely manner and track/report activities and metrics. * Drive safely to work sites and comply with all company/client safety standards. * Follow company/client standards by using related technical documentation. * Deliver feedback and supplemental training to employees/contractors as required. * Other duties assigned. Education and/or Experience: * High School diploma or GED preferred. * 2 or more years of relevant inspection experience from the telecommunications, construction, or utilities industries. Equivalent, applicable experience in lower level role may be substituted. * Must be proficient with a Windows and Android operating systems (proficiency with a tablet is preferred). * Must be proficient with Microsoft office applications (emphasis on Excel). * Must be able to read blueprints and other technical documentation. * Must be able to operate testing equipment relevant to the inspections such as an OTDR. * Experience with a major MSO or Telecom Operator is preferred. * Strong analytical and problem-solving ability required. * Ability to prioritize and complete assignments accurately and in a timely manner. * Able to effectively handle multiple priorities with a strong attention to detail in a fast-paced environment. * Strong interpersonal, organizational, oral and written communications skills. * Must be able to work alone, and with a team. * Must be able to pass a drug screen and criminal background check. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential duties of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. * Frequent walking, standing, sitting within the work area. * Lifting of up to 50 pounds less than one-third of the time. * Ability to sit/stand/walk for extended periods of time. * Ability to effectively communicate with employees, management, peers, et al. * Ability to work in extreme hot/cold environments for lengthy periods of time. Work Environment: The work environment characteristics described here are representative of those of a standard office environment. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. * Travel up to 100% required. * Ability to work in all temperatures, climates and weather conditions. * The work environment is that of being in the field. * The position requires working independently, as well as part of a team. * This position requires verbal and face-to-face contact with others daily. * Frequent use of a computer is necessary. * This position requires use of all general office equipment.

Fibrix is a leading manufacturer of precision crafted, nonwoven materials for the furniture and bedding, industrial, and craft markets. Work Schedule: Monday - Friday 5:00pm-4:00am (nights) $500 HIRING BONUS, WEEKLY INCENTIVE BONUS, MONTHLY/QUARTERLY ATTENDANCE BONUS OPPORTUNITIES DUTIES: Assist the operator(s) with bringing material out of the oven. Set loft and set cutting blades at slitter bank; make adjustments as needed. Set photo eye for length/width at computer panel per the schedule. Adjust range speed, blade cutting speed, and nip roller (to hold product in place). Perform quality checks during the production run filling out Quality Control Worksheets. Perform ILD (compression) checks to test density of product. Monitor quality of product during production run and notify operator(s) of any defects. Participate in the Continuous Quality Improvement Process. Other duties as assigned. QUALIFICATIONS: Must have manufacturing experience, non-wovens experience a plus Must be able to read a tape measure Must be able to climb steps up to catwalk Must possess the ability to bend, stoop, and lift 35+ pounds Must pay close attention to detail Must be able to walk and stand for an entire shift Must have cooperative attitude and good communication skills Must follow directions and instructions BENEFITS 401(k) & 401(k) Matching Bereavement Leave Dental Insurance Disability Insurance Employee Assistance Program Flexible Spending Account Health Insurance Hiring Bonus Incentive Bonus Life Insurance Paid Time Off Referral Program Vision Insurance

Blythe Development, headquartered in Charlotte, NC, is a licensed general contractor specializing in site work, road construction and golf course construction in North Carolina, South Carolina and Virginia. We are now 100% Employee Owned! The company, founded by twin brothers and Charlotte natives Jack and Frank Blythe in 1989. Blythe Development's operations include clearing, grading, storm drainage, sanitary sewer, waterline, curb and gutter, sidewalk, concrete paving, retaining walls, culverts, bridges, stone base and asphalt paving. Blythe Brothers Asphalt Company provides the asphalt services for Blythe Development Co. Blythe Development employs over 900 employees. This large, experienced workforce enables Blythe Development to self-perform 80% of site groundwork, which gives them greater control than competitors who must subcontract the bulk of the job. Blythe Brothers Asphalt is currently looking for a Roadway Quality Control Technician to join our growing team. The Roadway Quality Control Technician is responsible for monitoring all paving operations to ensure that the asphalt product being placed meets all contract specifications. The roadway quality technician must work and coordinate with paving personnel and project inspectors to ensure that contract specifications are being met. Once the paving work is completed, the roadway quality control technician is responsible for obtaining core sample specimens from the roadway and delivering them to the quality control laboratory for density testing. Excellent record keeping skills and being able to communicate effectively is a must for this position. This position will require availability from the candidate to work both day and night shifts, as well as weekends. Typical hours range from 40 to 70+ hours per week. Knowledge, Skills and Abilities Knowledge of proper use of equipment, hand and power tools, materials and supplies used in highway and heavy construction work in a safe manner to minimize the risk of injury, property damage or loss of life. Knowledge of first aid and applicable safety precautions. Ability to work independently and complete assigned tasks according to work schedule. Ability and willingness to communicate, follow instructions and transmit written and oral instructions. Ability to meet attendance schedule with dependability and consistency. Ability to work well with others. Comply with Blythe Brothers Asphalt LLC's policies and procedures including those outlined in the Employee Handbook. Physical Demands Regularly works near moving machinery/tools which requires good manual dexterity and multi-limb coordination, must be able to move quickly and have excellent stamina. Must be able to lift, push, pull or carry objects (over 80 lbs.), use legs, hips, shoulders, abdominal and lower back muscles to provide support over time without fatigue. This position will require the technician lift a core saw from the bed of a pickup truck and place it on the asphalt. This saw weighs approximately 80 lbs. Must be able to stand and/or walk for long periods of time and climb a ladder. This position will require the candidate to stand on hot asphalt mat for long periods of time. Ability to perform free of drugs and alcohol; including prescription drugs that may hinder the ability to perform the essential functions of the job. Meet the physical demands of the job with or without reasonable accommodation. General Laborers are required to be on their feet for long periods of time, either standing or moving throughout the work areas. If you require a reasonable accommodation to perform these essential functions of your position, you should talk to your supervisor or Human Resources. Sensory Demands Periodic exposure to dangerous and/or toxic substances and must wear necessary personal protection as a precaution to protect eyes, nose, and skin, etc. Regular exposure to dust, dirt, vehicle exhaust, asphalt, and noise, etc. Environmental Conditions Must be able to work in all types of weather and must be prepared for both extreme heat and cold conditions. Typical temperatures range from 30 degrees Fahrenheit to 105 degrees Fahrenheit. Other Position Related Items Must have a driving record that meets the company's requirements. The candidate must provide a trustworthy pickup truck capable of hauling asphalt coring equipment. Monetary allowance for vehicle and gas card provided. The Roadway Technician will be expected to work mainly in but not limited to, the Charlotte Metro area of North Carolina. Good communication skills are required. Good math skills are required. Ability to pass certification exams for a Roadway Quality Technician Certification in both NC and SC, training will be provided for the exams. All required tools (excluding a pickup truck) are provided. Position will require that the candidate provides good sturdy boots and workwear to protect their feet and extremities from the heat of the asphalt material. Benefits * Employee Stock Ownership Program * Paid Time Off * 401k + matching * Medical, dental, vision, life, disability, supplemental insurance programs An Equal Opportunity Employer Drug-Free Workplace

CPM Holdings, Inc. is a diversified leading global supplier of process equipment and engineered technologies that sustainably feed, fuel, and build a better world. With its growing family of 17 market-leading product brands, CPM serves a variety of industries including animal feed, consumer food, green energy, advanced materials, and sustainable packaging. Founded in 1883, CPM has 1,700 employees across 36 facilities on 4 continents with presence in 150+ countries. From the foods you eat to the fuels you require, CPM plays an important role in making the world more efficient and more sustainable. For more information, visit OneCPM.com. POSITION OVERVIEW (Job Summary): The QC Inspector will ensure that fabricated assembly components or finished goods manufactured at the CPM Lexington facility are in accordance with the current Acceptable Manufacturing Practices that meet internal specifications. This position will spend the majority of their time performing manual and automated quality assurance checks on in-process components and finished goods. Checks include but are not limited to: detailed visual and dimensional inspections of machined components, lasered and formed parts and welded assemblies. This will also include subassemblies for conformance to BOM's, Manufacturing Standard Work, QA Instructions, approved samples and engineering blueprints. PAY RANGE: $19.50/hr. to $24.00/hr. DOE ESSENTIAL JOB DUTIES: Confers with operators, supervisors and immediate supervisor (Manufacturing Engineer) to enforce quality standards. Uses a wide variety of gages, tools and other measuring devices. Performs visual and dimensional inspections/testing. Identifies, investigates and prepares Corrective Action Reports. Performing visual, 1st piece or full inspections on components, finished goods and physical testing. Maintains good housekeeping practices and performs duties in a safe and efficient manner so as not to inflict injury to self or others. Other duties, responsibilities and qualifications may be required and/or assigned as necessary. Responsible for monitoring production areas to ensure quality products are being produced and in compliance with: Visual Standards Dimensional Specifications Gauging Requirements Documentation Print Specifications Bill of Materials Quality Inspection Policies and Procedures ESSENTIAL SKILLS AND ABILITIES: The ability to prioritize work with minimal supervision and respond to internal demands in a timely fashion are critical requirements of this position. This position will report directly to the Manufacturing Engineer. Critical requirements for this job are: Strong organizational, interpersonal and communication skills Ability to prioritize incoming purchased items combined with in process jobs Ability to change priorities based on business needs with minimal notice Proficient with a wide variety of dimensional measurement equipment including calipers, coordinate measurement machine, micrometers, bore gages, inside micrometers, height gauges and fixed gages. Blueprint reading capability. Ability to read and interpret documents such as engineered drawings, procedure manuals, safety rules and operating instructions. Ability to add, subtract, multiply and divide in all units of measure using whole numbers, common fractions and decimals and ability to compute ratio and percent. Have a strong understanding of quality concepts and requirements. Must be able to read, write, speak, and understand fluent English. Must have a basic fundamental understanding of mathematics. Intermediate knowledge of MS Office Suite; Excel spreadsheets and Word documents. Able to demonstrate accuracy and thoroughness while completing work in a timely manner. Follows instructions and comply with policies and procedures. Must have good time management skills. Good housekeeping practices. Adapt to changes in the work environment. Flexible when having to change priorities. Excellent interpersonal skills are required to address quality compliance issues with other departments such as Planning, Production, Purchasing, Engineering, etc. Working knowledge of SAP is a plus. Ability to learn new applications as required. Must be safety and quality conscious. EDUCATION AND EXPERIENCE REQUIREMENTS: Experience in a machining, welding and fabrication environment is strongly suggested. This role will focus primarily and subcomponents for weldments, sub-assemblies and full assemblies for O.E.M Capital equipment. Candidates with a High School diploma or GED and a minimum of 2-3 years' QA experience in a manufacturing environment will be considered. PHYSICAL REQUIREMENTS: As a QC Inspector working with food processing equipment, there are certain physical requirements that you will need to meet to effectively perform your duties. Strength and Endurance: The job may involve lifting heavy objects, carrying equipment (up to 45 lbs.), and standing for long periods. Therefore, having physical strength and endurance is important. Manual Dexterity: Precise assembly of machinery parts often requires good hand-eye coordination and manual dexterity to handle tools and components with accuracy. Mobility and Flexibility: You may need to work in confined spaces, bend, kneel, crouch, or reach overhead to access different components of the equipment. Visual Acuity: Reading blueprints, inspecting parts, and ensuring proper alignment of components require good vision to perform tasks accurately. Hearing Ability: Being able to hear instructions and safety warnings in a noisy environment is crucial for maintaining a safe workplace. Safety Awareness: Awareness of safety protocols and the ability to follow safety guidelines to prevent injuries while working with potentially hazardous equipment. Stamina: The job at times may involve working long hours in physically demanding conditions, so having the stamina to sustain performance throughout the workday is important. Example, uncontrolled environments, hot in summers, cooler in winter. OTHER DUTIES: Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice. CPM Acquisition Corp. is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. CPM Acquisition Corp. offers competitive compensation and benefits, including paid holidays and vacations, 401k, medical/dental insurance, tuition assistance, and more.

JobID: 8801 JobSchedule: Full time JobShift: Day : As a 100% employee-owned contractor, when you work at Sundt, you're not just hiring on at a company, you're joining a culture. Because everyone at Sundt is part owner, you'll join a team of people who are deeply invested in their work. From apprentices to managers, we're passionate about the details and deliberate in everything we do. At Sundt we focus on building long-term prosperity for our clients, communities and employee-owners. We offer competitive pay, industry-leading benefits including a 401k and employee stock ownership plan, incentive programs for craft and administrative employees as well as training that focuses on your personal and professional growth. We're driven by skill, grit and purpose. Join us as we strive to be the most skilled builder in America Job Summary Basic Job FunctionsPosition is required to assist in the inspection, acceptance, and/or rejection of work performed in a particular discipline in compliance with applicable codes and/or specifications as dictated by quality programs and/or contract documents and specifications.Structural Inspection:Experience level must fall within the erection of structural steel. Must be able to work in elevated areas. Must have knowledge of AISC, AWS D1.1, and AWS D1.6 Codes. Must have knowledge of bolt?up inspection including bolt lot verifications using Skidmore?Wilhelm. Additionally, must have knowledge of architectural, insulation and lagging, grout and concrete placement, Epoxy anchor installation inspection. Must have CWI (Certified Welding Inspector) certification.Electrical and Instrumentation Inspection:Experience must fall in the installation of electrical and instrumentation components, including interconnecting wiring, cables, and tubing. Must be knowledgeable of ICEA, IEEE, ISA, NEC, NEMA, NESC, and NFPA Codes and standards.Mechanical Inspection:Experience level must fall in the setting and alignment of static and rotating equipment, equipment skids, coolers, tanks, and interconnecting process piping fabrication and installation. Must be able to use measuring tools such as micrometers, calipers, transits, etc. and be able to set up dial indicators and laser alignment devices.Piping Inspection:Experience level must fall in pipe installation inspection, including welding, supports, instrumentation, etc. Must have CWI (Certified Welding Inspector) certification. Key Responsibilities 1. Assists material handling personnel with required material storage and PM requirements as needed. 2. Communicates with others regarding inspections results and recommends corrective procedures. 3. Participates in activities to support the company's strategic planning efforts. 4. Participates in the preparation of Quality control ITP. 5. Performs control measuring and tests equipment. 6. Verifies the installation of the systems, components and equipment in accordance with the assigned discipline. Minimum Job Requirements 1. 1+ year construction practices 2. 1+ year in quality control inspection discipline 3. HS Degree Required 4. Proficient use of all Microsoft Office Suite programs Note: Job Description is subject to change at any time and may include other duties as assigned. Physical Requirements 1. Ability to wear personal protective equipment is required (including but not limited to; steel toed shoes, gloves, safety glasses, hearing protection, hardhat, vest, etc.) 2. May reach above shoulder heights and below the waist on a frequent basis 3. May stoop, kneel, or bend, on an occasional basis 4. May use telephone, computer system, email, or other electronic devices on a limited basis to communicate with internal and external customers or vendors 5. Must be able to comply with all safety standards and procedures 6. Occasionally will climb stairs, ladders, etc. 7. Required to use hands to grasp, lift, handle, carry or feel objects on a frequent basis 8. Will interact with people frequently during a shift/work day 9. Will lift, push or pull objects on an occasional basis 10. Will sit, stand or walk short distances for up to the entire duration of a shift/work day. Safety Level Safety-Sensitive Note: Jobs with the Safety-Sensitive designation are those that include tasks or duties that the employer reasonably believes could affect the safety and health of the employee performing the task or others such as operating a vehicle, operating equipment, operating machinery or power tools, repairing/maintaining the operation of any vehicle/equipment, the handling/disposal/transport of hazardous materials, or the handling/treatment/disposal of potentially flammable/combustible materials. Equal Opportunity Employer Statement: Sundt is committed to the equal treatment of all employees, and/or applicants for employment, and prohibits discrimination based on race, religion, sex (including pregnancy), sexual orientation, gender identity, color, age, disability, national origin, covered veteran status, genetic information; or any other classification protected by applicable Federal, state, or local laws. Benefit list: Market Competitive Salary (paid weekly) Bonus Eligibility based on company, group, and individual performance Employee Stock Ownership Plan & 401K Industry Leading Health Coverage Starting Your First Day Flexible Time Off (FTO) Medical, Health Savings, and Wellness credits Flexible Spending Accounts Employee Assistance Program Workplace Wellness Programs Mental Health Program Life and Disability Insurance Employee-Owner Perks Educational Assistance Sundt Foundation - Charitable Employee-Owner's program #LI-KW1

Why Fibreworks Composites? Founded in 2009 by Guenther Steiner and Joe Hofmann, Fibreworks Composites is the largest privately-owned composite manufacturer in the U.S. In 2019, we expanded our capabilities with the launch of Composite Factory, an AS9100 / ISO-certified sister company serving the Aerospace, Aero Structures, Aviation, Defense, and Medical industries-sectors that demand the highest levels of traceability, certification, and quality. Rooted in motorsports, our team thrives in a fast-paced, precision-driven environment. We are fully vertically integrated, bringing engineering, machining, tool-making, and production under one roof to deliver advanced Composite Structures on tight timelines with unmatched quality. If you're looking to be part of a team that pushes boundaries and works with the most advanced technologies in the composites industry, this is where the future is being built! Position Overview : The Quality Control Inspector I is responsible for ensuring that materials and products being produced meet established quality standards through detailed inspection, testing, and measurement. The role involves closely following blueprints, specifications, and Standard Operating Procedures (SOPs) to maintain product quality and compliance. The Inspector will also handle the documentation of nonconformances, communicate inspection results to relevant parties, and play an active role in inventory and shipment management using an ERP system. Key Responsibilities : Conduct inspections on materials and products using hand-held measuring devices (rulers, calipers, micrometers) to ensure compliance with quality standards. Read and interpret blueprints, drawings, and specifications to verify product requirements and tolerances. Accept or reject products based on inspection results, ensuring quality standards are met. Record inspection results and test data; document nonconformances through the NCR process. Report inspection results to relevant personnel, providing feedback on product quality and necessary corrective actions. Follow Standard Operating Procedures (SOPs) for all inspections and testing to ensure consistency and regulatory adherence. Utilize ERP software to track parts from WIP to Finished Goods status and manage inventory. Monitor staged shipments. Experience with composite materials is a plus. Perform additional tasks related to quality control as assigned by management. What You Will Bring to the Team : High school diploma or equivalent required. Minimum of two (2) years of experience in a similar role. Strong understanding of quality control standards and testing techniques. Thorough knowledge of composite material manufacturing equipment and processes is a plus. Proficiency in MS Office products and MiniTab. Ability to perform basic math calculations, including measurements, calibrations, and specifications, essential for quality control testing. Experience using specialized tools and machinery for product testing. Ability to interpret blueprints, technical documents, and manuals to ensure products and components meet quality standards. Certification in Quality Control is preferred. Experience with electronic inspection equipment, such as Coordinate Measuring Machines (CMMs), is preferred. Must be a U.S. Citizen or lawful Permanent Resident in compliance with ITAR regulations. Our Investment in You: Comprehensive medical, dental, vision, and life insurance benefits. 401(k) matching after 6 months tenure Paid time off (PTO) for vacation and sick days Employee referral program Shift differential for 2nd shift employees Potential to earn quarterly discretionary bonuses based on company performance Discounts on select services/products Climate-controlled work environment Hours of Operation: Normal business hours: 1st Shift 7:00AM - 4:00PM, 2nd Shift 4:00PM - 1:00AM, Monday through Friday; and Split Shift 9:00AM - 8:00PM, Tuesday through Friday with occasional weekends and holidays as scheduled. Work Environment & Physical Requirements: Combination of indoor and outdoor activities with varying conditions Requires walking, standing, sitting, climbing, balancing, bending, reaching, handling, stooping, kneeling, and crouching Ability to lift/carry/push/pull up to 50 pounds May involve operating material handling equipment in a safe manner Work may include exposure to variable noise levels, fumes, airborne particles, hazardous chemicals, etc., requiring personal protective equipment Some positions may require working with small parts/components, necessitating excellent hand-eye coordination and manual dexterity Specific vision abilities required, including close vision, distance vision, peripheral vision, depth perception, and the ability to adjust focus Fibreworks Composites LLC is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability, genetic information, protected veteran status, or any other characteristic protected by applicable law.

Prime Beverage Group is looking for a team-oriented and passionate Analytical Lab Technician with the ability to carry out supervisory responsibilities in accordance with the company policies. The Analytical Lab Technician is responsible for monitoring, documenting, and controlling the quality of incoming ingredients and in-process liquid; maintaining records in accordance with applicable regulations and standards; producing laboratory results that are accurate, reliable, and timely; and releasing product to the filler in a timely fashion. The Lab Technician works closely with the Blending and Operations teams to maximize productivity, maintain food safety and trouble-shoot blending and production problems. It is expected that the Lab Technician will actively participate in continuous improvement efforts and contribute to the success of the Quality team and Operations overall by consistently meeting their metrics. A successful candidate will have attention to detail, knowledge of food safety standards, excellent wet chemistry and instrumental analysis skills, an understanding of liquid processing and strong problem-solving skills. This position reports directly to the shift Quality Supervisor. Position Responsibilities: • Maintain awareness of blending process and status of all fillers. • Minimize downtime and held product by actively coordinating with Blending and Operations teams to ensure that in-process liquid is in specification and released to the filler without delay. • Ensure correct recipe guidelines are followed and specifications for products are met during processing. • Perform analytical tests (HPLC, pH, density, brix, carbonation, titrations, dissolved oxygen, etc.). • Maintain, calibrate and trouble-shoot instruments. • Adhere to and enforce Good Manufacturing and Good Laboratory Practices. • Help to drive team success by meeting quality, production and schedule metrics and communicating effectively with team members and supervisors. • Assist with development and validation of new analytical methods/SOPs. • Benchtop trial new formulas. • Track laboratory consumables. • Collect and organize canning production samples (first, middle & last units). • Monitor raw materials, ingredients, and water for continued quality. • Participate in finished goods hold/release system. • Cross-train with quality control technicians. • Assist with resolving quality issues. • Other tasks as assigned. Position Requirements: • Ability to organize and coordinate diverse activities. • Works independently while understanding the necessity for communicating and coordinating work efforts with other employees. • Strong analytical chemistry knowledge and lab skills. • Problem solving skills; exercises good judgment in determining best method and procedure to be followed. • Must be able to lift to 25 pounds at times and inspect/swab under/around equipment. • Must be able to stand/be on their feet for the duration of the shift in a manufacturing environment which may be hot, cold, loud, etc. Education and Experience: • Bachelor's degree in chemistry, food science, engineering or equivalent. Equivalent experience considered. • HACCP and SQF certifications or experience, preferred. • Two to four of experience in a laboratory environment with similar functions, preferred. 06:00 (AM/PM) - 06:30 (PM/AM) 2-2-3 Schedule

About Rio Tinto: Rio Tinto is a leading global mining and materials company. We operate in 35 countries where we produce iron ore, copper, aluminum, critical minerals, and other materials needed for the global energy transition and for people, communities, and nations to thrive. We have been mining for 150 years and operate with knowledge built up across generations and continents. Our purpose is finding better ways to provide the materials the world needs-striving for innovation and continuous improvement to produce materials with low emissions and to the right environmental, social and governance standards. But we can't do it on our own, so we're focused on creating partnerships to solve problems, create win-win and meet opportunities. About Rio Tinto Lithium: On 5 March 2025, Rio Tinto completed the acquisition of Arcadium Lithium and combined it with its Rincon asset to form Rio Tinto Lithium, establishing Rio Tinto as a global leader in the supply of energy transition materials and one of the world's top lithium producers. Position Summary: Responsible for testing samples received into the Quality Control (QC) laboratory. Samples include raw materials, in-process samples and packaged final products. A variety of instrumentation is used including Inductively Coupled Plasma (ICP), Gas Chromatography (GC), Auto-titrators and coulometric Karl Fischer titration. Other equipment such as pH meters, ovens, balances, burettes, and calculators are also used. Essential Duties and Responsibilities: * Contribute towards the efficient running of the laboratory by helping with infrastructure duties such as restocking of supplies, cleaning of glassware, disposal of samples and managing sample retains. * Enter laboratory data into the LQM database, run interim and final reports to release samples for production use. * Standardize equipment prior to use * Train others in routine test methodology * Analyze samples in accordance with the prioritization plan. * Serve as First Aid responder to plant personnel. Assist PERT team in emergencies. * Perform other duties as assigned * Other duties as assigned. Education and Experience: * Bachelor's degree in a science discipline is required. * Ten years of experience in a laboratory setting is desired; this can be from college training in a laboratory science or equivalent laboratory experience. Knowledge and Skill Requirements: * Advanced understanding in acid/base titrations, Karl Fischer moisture, manual titrations, particle size, sieve analysis, and programming of automatic titrators * Basic computer skills involving Word, Excel, PowerPoint and Outlook are required. * Ability to read, understand and write technical documents (analytical procedures) is required. * Experience in Thermo LQM software is required. Ability to perform functions such as assisting production personnel in logging in samples, editing tests, and cancelling samples is needed. * Expertise in the use of Inductively Coupled Plasma instruments is needed. Able to calibrate and check for correct operation of ICP. Ability to review data, trouble-shoot and correct instrument problems. * Experience using SharePoint sites is needed. Skilled in different SharePoint sites used at Livent is needed (training, TOR reports, technology goals, etc.) * Must be qualified to run all tests outlined in the QC technician Individual Training Plan (ITP). * Must have experience dealing with air sensitive product line and be signed off on all of the methods used for BuLi samples. * Experience in cGMP (good manufacturing practices) is needed. Must be certified as able to analyze Pharmaceutical Carbonate samples. Must be approved to run all test methodology associated with Pharm Carb samples. * Ability to handle complex and challenging functions such as Cat Phosphate analysis and distillation of benzyl chloride. * Certified as a trainer in the majority of key tasks (ITP, Buli and Pharm Carb). * Must have a clear understanding of all Bessemer City production units and how QC analysis contributes to their production of material within specifications. * Understand and apply basic six sigma principles such as Kanban, Right First time, 5S, control charting Competencies: * Time management * Multi-tasking * Problem solving with respect to analytical methodologies and instrumentation. * Teamwork; able to get along with others * Demonstrated leadership ability * Ability to impart information to others; serve as a trainer * Proficient in troubleshooting and fixing most instrument issues Safety Requirements: (position and location specific) All employees are expected to carry out their work functions in a healthy and safe manner, to encourage and support safe work practices at all times, and to report and/or rectify any unsafe conditions that may come to their attention immediately. Physical Demands: (position and location specific) The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this Job, the employee is regularly required to sit and talk or hear. The employee is frequently required to walk and use hands to finger, handle, or feel. The employee is occasionally required to stand; climb or balance and taste or smell. The employee must occasionally lift and/or move up to [50] pounds. Specific vision abilities required by this job include close vision and color vision. Work Environment: (position and location specific) The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. While performing the duties of this Job, the employee is frequently exposed to toxic or caustic chemicals. The employee is occasionally exposed to wet and/or humid conditions; moving mechanical parts; fumes or airborne particles and outside weather conditions. The noise level in the work environment is usually moderate. Personal Protective Equipment - (position specific) Must wear PPE as required based on job duties or when traveling to locations where PPE is essential. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed above are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. RIO TINTO LITHIUM employs people across a broad range of occupations in locations across the world. We are looking for people to join us in creating, developing, and improving our products, our processes, and our markets. Employees enjoy competitive compensation, a menu of work/life benefits and opportunities to continue developing their skills and building their career. RIO TINTO LITHIUM is an Equal Opportunity Employer, EEO, AAE, MFDV and supports a drug free workplace.

Job Description Job Title: Welding Inspector Hourly Rate: Depending on Experience. About Us: We are a veteran owned contractor, providing project, maintenance, and outage support throughout the United States. Over the past 15 years we have proven to be a trusted partner for our clients while providing services that help power the world. Summary: We are looking for a skilled QA/QC lead. All applicants must be familiar with ASME Boiler and Pressure Vessel Code, welding processes, SMAW, GTAW and FCAW. Must have a valid CWI with a previous welding background. Familiar with NDT methods, visual, magnetic particle, liquid penetrant, radiography experience helpful. Responsibilities: Properly interpret client specifications, applicable codes and industry standards. Monitor all quality related activities on the project. Review quality inspection personnel qualifications and training requirements. Finalize specifications; conducting visual and measurement tests; rejecting and returning unacceptable materials. Adhere to all site and company rules, regulations, PPE requirements, etc. Use a computer to compile and submit daily reports, inspection reports, and inter-office communications. Pay attention to detail and be capable of recommending and approving repairs as well as performing visual inspections of completed work. Maintain a positive relationship between client, facility, customer, Authorized Inspector and Jurisdiction. Other duties as assigned. Qualifications: Experience working in an industrial setting (nuclear experience considered an asset). Proficient with standard computer software (MS Word and Excel) and be able to write detailed inspection reports while maintaining an organized system of files. 2-3 years of experience in Welding Inspection. Documented NDE experience a plus. VT, MT, PT, UTT Self-motivated with good written and verbal communication skills with a positive team-oriented attitude is required. Must have reliable transportation and be able to travel extensively and work variable hours. Able to pass background screens and drug/alcohol testing as required by our customers. TWIC card a plus. High School Diploma or GED Powered by JazzHR dc BFNICW51

Job Details Rock Hill, SC Plant - Rock Hill, SC Full Time 2nd ShiftDescription We are seeking a skilled, reliable Quality Control Laborer to join our growing company. In this position, you will be responsible for attaining production goals, and following all site health and safety regulations. A strong work ethic and attention to detail are essential. General Labor Duties and Responsibilities Follow project instructions from manager or supervisor Follow all health and safety regulations when operating machinery Ensure regulated and proper headgear, earplugs, gloves, safety glasses, and clothing are worn Complete all assigned tasks in a timely and efficient manner Safely operate a variety of tools including hand-held banders, banding tables, tagging guns, and hand tools Clean and clear debris and hazardous materials Ensure equipment and tools are cleaned and stored properly Verify lumber dimensions and counts Ensure compliance with Chemical Safety and SDS sheets General Labor Requirements and Qualifications Must be 18 years of age Ability to physically stand, bend, squat, and lift up to 40 to 60 pounds Ability to work outside in all weather Positive attitude and work ethic Basic Mechanical Functions Able to work independently or as an active member of a team Excellent interpersonal skills and communication with all levels of management Confined Space Entry training is a plus but not required Prior experience in a setting where mobile equipment and pedestrians interact is a plus but not required

Job Description ABOUT THE ROLE The quality control group monitors, supports, and influences the design, configurations, and actual construction necessary to guide our design and production teams to manufacture high quality industry leading homes and components for our customers in accordance with regulatory requirements. The quality control inspector undertakes the inspection of materials, components, and final products to confirm adherence to quality, regulatory, and engineering specifications. He/she works collaboratively with production departments to identify ways to continuously improve production quality. The quality control inspector may work independently or under direct supervision executing specific process steps under continuous quality review and coaching as needed. ESSENTIAL DUTIES & RESPONSIBILITIES Works in a safe manner following all safety policies while performing job duties. Undertakes to maintain a safe and healthy work environment for all employees by identifying any safety standards, procedures, or regulations that are not optimally addressed. Maintains open communication with supervisor regarding safety concerns. Follows work orders and instructions in order to accurately and efficiently review the preparation and assembly of building components based on production area specifications and regulatory requirements including HUD specifications. Inspects incoming materials, in-process production, and finished products to ensure materials and products meet specifications, regulatory requirements, and applicable drawings; conducts visual and measurement tests; documents and communicates rejections of unacceptable items and required corrections; ensures defective products are not delivered to the customer. Works collaboratively with production supervisors, team leads, and line assemblers to discuss inspection results and provides guidance as needed. Documents inspection results by completing inspection reports and checklists; communicates any violations of the quality process or adherence to job performance requirements to Production Supervisors and QC Manager. Maintains a good attendance record and proactively communicates and coordinates with supervisors regarding attendance. Keeps inspection and measurement equipment operating by following operating instructions and notifying management when repairs are necessary. Assists in maintaining and keeping tools, machinery, and work area clean and organized. Performs various other job duties as assigned and needed. MINIMUM QUALIFICATIONS Must be 18 years of age. This can be a physically demanding job requiring the ability to lift 40+ pounds, to grip, work over head, pull at chest height, bend, stand, walk, kneel, crawl, push, pull, reach, climb and carry various materials and equipment. High school diploma and substantial experience in and clear understanding of the requirements and expectations across multiple production areas in a fabrication / manufacturing environment expected. Must have experience reading and interpreting schematics and excellent problem-solving skills. Experience in quality control Inspection preferred including building code knowledge, ability to gain an understanding of construction manuals, standards, regulations, and specifications regarding the products. Bilingual Spanish preferred. Ability to build effective relationships with fellow employees and supervisors including when providing constructive feedback and inspection results. Excellent written and oral communication skills required. Ability to handle multiple projects while maintaining attention to detail. Ability to work in a team, to be trained, and take direction. Flexible to work in a fast paced, changing environment. Not afraid to get dirty and handle tools/equipment daily. Must be able to pass a pre-employment drug screen.

SARSTEDT, a leading manufacturer and distributor of blood collection and medical devices, laboratory consumables and instrumentation, seeks a Quality Control Inspector. Shift: 2nd Shift Hours: 2:30 PM to 11:00 PM (Monday - Friday)/some Saturdays Department: Quality Control Summary Confirms the quality of Sarstedt products via visual, dimensional, and functional testing. Essential Duties and Responsibilities Collects and visually inspects random samples from various machines and assembly operations. Measures samples using calipers, indicator gages, and go/no go gages. Utilizes centrifuges, desiccators, and contact angle measuring devices for functional testing of products. Documents all inspections, measurements, and functional testing. Responsible for the initial assessment of product at production start, including visual inspection, measurements, functional testing, establishment of bag weights, and confirmation of line clearance. Documents and communicates product defects to the Quality Control Leadperson and appropriate Production staff. Responsible for the initial isolation of defective product. Weighs and records scrap as needed. Qualifications/Education and/or Experience/Language & Mathematical Skills/Computer Skills High school diploma or general education degree (GED); and three to six months related experience and/or training. Ability to measure and interpret dimensions using the metric system. Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of employees. Ability to calculate figures and amounts such as proportions, percentages, area, circumference, and volume. Ability to apply concepts of basic algebra and geometry. Ability to apply common sense understanding to carry out detailed but uninvolved written or oral instructions. Ability to deal with problems involving a few concrete variables in standardized situations. To perform this job successfully, an individual should have knowledge of Microsoft Excel Spreadsheet software and AS/400 programs. Physical Demands While performing the duties of this Job, the employee is regularly required to stand; walk; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. The employee is occasionally required to sit, stoop, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, color vision, depth perception and the ability to adjust focus. Work Environment While performing the duties of this Job, the employee is frequently exposed to moving mechanical parts. The noise level in the work environment is usually loud. Benefits SARSTEDT's benefits package includes a competitive salary, comprehensive job training, medical, dental and vision insurance, discounted YMCA gym membership, paid vacation, holidays and personal time, 401(k) matching as well as employer paid short and long-term disability and life insurance. SARSTEDT, Inc. is an Equal Opportunity Employer and does not discriminate against applicants due to race, ethnicity, gender, age, veteran status, or on the basis of disability or any other federal, state or local protected class. SARSTEDT, Inc. participates in E-Verify

Cosette Pharmaceuticals is a US based, diversified pharmaceutical company with a proven topicals and dermatology portfolio and a growing branded pharmaceuticals business. We are fully integrated, with a deep focus on internal R&D, high quality manufacturing standards and commercial sales excellence. We continue to diversify and expand through strategic partnerships, acquisitions and internal R&D. Our highly experienced leadership team are busy writing the next, most ambitious chapter of our story. Building on a 100+ year heritage, their shared vision of innovation will leverage the expertise of more than 350+ team members, and infrastructure to create remarkable new opportunities for the patients and physicians we serve every day. Cosette is headquartered in Bridgewater, NJ with 2 additional locations in the U.S. The South Plainfield, NJ office consists of an R&D Laboratory and other functional areas. The Lincolnton, NC site is a fully functioning, state of the art, manufacturing facility. Innovating every day.™ Basic Purpose: Sample Log-in, tracking, and organization within sample room. Assist QC Analysts with routine work. Essential Functions and Responsibilities: • Maintain sample databases for stability, raw materials, finished products, and customer complaints in Chemistry and/or Microbiology and perform clerical work associated with sample tracking. • Label glassware and prepare initial sample into appropriate containers. Discard expired samples and solvents appropriately. Operate autoclave for sterilizing medias and decontaminating microbiological waste • Perform basic physical testing, including pH, viscosity, specific gravity, color determination, etc. • Maintain an inventory of lab supplies. • Other duties as assigned by management. Knowledge, Skills, Qualifications and Physical Requirements: Education/Training/Work Experience: • A High School Diploma and a minimum of three (3) years of experience at a GMP facility • Demonstrated computer skills, including all Microsoft Office applications (Excel, Access, Word, etc.) • Demonstrated knowledge of cGMPs, Safety, OSHA, and 21 CFR regulations and requirements • Demonstrated ability to multi-task while meeting established deadlines. • Proven record of compliance with regard to safety, GDPs, and general performance • Ability to work in a team environment. • Organizational skills and attention to details a must. • Willingness to be flexible. • Willingness to learn new tasks. Specialized Knowledge and Skills: • Log all samples into the applicable database assuring accuracy and completeness of data and any accompanying paperwork. • Understands requirements from SOPs and general GDP, for labeling and media sterilization. Understands chemical handling hazards and/or microbiological hazards and discards waste in compliance with all requirements. • Assists QC Analysts in physical testing to ensure timely release of laboratory results. • Order supplies when needed and with cost-effective means and pro-actively inventory the lab for future needs. Equipment and Applications: • Microsoft Office Applications (Access, Word, etc.) • Analytical Balance • pH meter Work Environment and Physical Demands: • Gloves • Safety Glasses • Lab Coat • Respirator • Ability to occasionally lift up to 50 pounds Equal Opportunity Employment Providing “equal employment opportunity” is one of the most important people policies of Cosette Pharmaceuticals, Inc. Our goal is to do all that we realistically can to provide genuine equal employment opportunity to applicants and employees in all phases of our operation. It is the policy of this Company that there shall be no discrimination with respect to employment, or any of the terms and conditions of employment, because of an individual's race, creed, religion, color, national origin, citizenship, ancestry, age, gender identity or expression, affectional or sexual orientation, marital status, domestic partnership, familial status, atypical hereditary cellular or blood trait, disability (including AIDS and HIV infection), genetic information, liability for service in the United States armed forces or any other legally protected status. The Company is dedicated to ensuring that all employment decisions are in accordance with these principles of equal employment opportunity.

The Quality Control Chemist reports directly to Quality Laboratory Management and plays a key role in supporting laboratory operations through accurate and timely testing. This position requires strong time management skills to meet testing deadlines and a willingness to learn laboratory processes, instrumentation theory, and troubleshooting techniques. Schedule: This position will be on a 2nd shift: Monday - Thursday 3:30pm - 11:30pm and Friday 1:30pm - 9:30pm. Key Responsibilities Testing: + Perform Release, Stability, and Special Request testing on finished products and raw materials in compliance with Standard Operating Procedures (SOPs), in-house methods, and compendial standards. + Execute in-house methods independently and accurately with minimal supervision. Team Collaboration: + Adapt to changes in testing schedules and support continuous improvement initiatives within the lab. + Assist in training new laboratory personnel and document training per established SOPs and Nutramax guidelines. Safety: + Maintain a safety-first approach and remain vigilant of surroundings while performing laboratory tasks. + Ensure all equipment used in testing is properly calibrated and maintained. General Duties: + Train on and operate various laboratory instruments, including but not limited to: Laboratory Balances, HPLC, GC, Automated Titrators, FTIR, UV/Vis Spectrophotometer, Polarimeter, Dissolution and Disintegration instruments. + Complete assigned projects within established timelines while balancing testing responsibilities. + Stay informed on updates from USP, FDA, and other regulatory bodies to ensure compliance with analytical standards and documentation practices. + Assist in investigating Out-of-Specification (OOS) results as needed. + Perform additional duties as required to support company objectives. + Communicate effectively across departments and work collaboratively within a team environment. + Maintain regular and reliable attendance. Skills Chemistry, Quality control, Laboratory, Gmp, Wet chemistry Top Skills Details Chemistry Additional Skills & Qualifications + Experience: 2-5 years in a laboratory setting, a cGMP environment. Familiarity with GC and/or LC instrumentation is preferred. + Skills: Strong interpersonal skills, self-motivation, and ability to work with individuals at all organizational levels. + Education: Bachelor's degree in Chemistry; concentrations in Biochemistry, Inorganic, Physical, or Polymer Chemistry are preferred. Experience Level Intermediate Level Job Type & Location This is a Permanent position based out of Lancaster, SC. Pay and Benefits The pay range for this position is $70000.00 - $80000.00/yr. Comprehensive Health Coverage: Competitive medical, dental, and vision plans for employees and their families.Educational Assistance: Opportunities for training and professional development to support career growth.Supportive Work Culture: A family-oriented environment that values faith, servant leadership, and collaboration.Community Engagement: Volunteer opportunities and mission trips organized by the company to give back locally and internationally.Employee Recognition & Perks: Birthday cards with gift cards, family days at the zoo, Thanksgiving dinners, and other thoughtful gestures.Work-Life Balance: A culture that prioritizes employee well-being and fosters a positive, supportive atmosphere. Workplace Type This is a fully onsite position in Lancaster,SC. 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.

No Visa Sponsorship: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. The Senior Microbiologist is a critical technical resource in the QC Microbiology laboratory supporting the manufacturing of sterile injectable products. This position is responsible for independently performing and overseeing complex microbiological testing and environmental monitoring (EM) in compliance with cGMP, USP, FDA, and internal quality standards. This position is in a fast-paced, FDA regulated environment in the Pharmaceutical Industry. This role is mainly responsible for completing deviation investigations, OOS/OOT and CAPA development related to EM and microbiological testing. Maintains spreadsheets and databases to track and monitor department/company data, KPIs and metrics. Accountable for QC Microbiology inventory control including ordering materials, maintaining stock and resolving material complaints as needed. This role will serve as a Subject Matter Expert (SME) to provide guidance and support junior microbiologists. Train team members in aseptic technique, microbiological methods, EM sampling, and good documentation practices. Participate in the qualification of microbiology lab equipment. Identify and implement continuous improvement opportunities to optimize workflows in the quality control microbiology laboratory. OVERALL JOB RESPONSIBILITIES: Operational Excellence: * Models the principles and behaviors of Glenmark and ensures personnel follow the company code of conduct. * Communicate progress, status, and roadblocks as required. * Drive projects, assignments, and complete presentations within timelines and budgets. Create and maintain relevant metrics for department/site. * Spreadsheets and databases will be leveraged for departmental and company metrics, presentations, and data/testing tracking/verification. The Senior Microbiologist is responsible for keeping these sheets and databases up to date. * Ability to perform routine testing of samples submitted to the laboratory as appropriate. Schedules and participates in cleaning, inventory, and maintenance tasks in the lab. * Supports inventory management and ordering/stocking of all QC department laboratory supplies. * Ensures laboratory equipment is in compliance with procedures and GLP requirements. * Troubleshoots laboratory issues related to all instrumentation. Recommends potential corrective and/or preventive actions and implements these actions within the laboratory. * Performs GMP review of test data to ensure that test results meet all specifications. Trends data and analyzes trends to proactively mitigate equipment and reagent performance issues. Verifies laboratory equipment and associated equipment logs to ensure proper operation Stakeholder: * Preparation, review and approval of sampling matrix and hold time schedule Conducts and communicates results of lab investigations when test results fall outside pre-established specifications (OOS). * Performs routine equipment maintenance. * Performs maintenance of spare parts inventory, calibrations and supervises third party maintenance and repair when necessary. * Establishes good working relation with contract laboratories. * Supports in the development of methods transfer and validation, troubleshooting, cross validation, IQ/OQ/PQ protocols. * Supports activities regarding audits of suppliers and contract labs in support of vendor certification program. * Conducts statistical evaluation of the manufacturing and inspection process and training QC staff. * Ensure that all equipment is calibrated. * Responsible to develop and validate new test procedures * Perform data analysis, compile data and generate reports for management review. * Review lab test data and their integrity and adherence to SOPs and cGMP. Compliance: * Maintain current knowledge of regulatory and industry standards, trends and advancements. * Responsible for ensuring compliance to systems and procedures in the EM/Microbiology laboratory and cleanroom areas. And prepare the lab for internal and external audits. * Support Continuous Improvement initiatives by providing support on updating SOPs, WIs, and OJT * Complete and maintain certified investigator training requirements. Perform investigation of the quality events assigned using root cause analysis tools, maintain timelines for closure of investigations and identify/initiate CAPAs * Complete and maintain status as a certified trainer * Ensure Quality Systems are compliant with cGMPs and internal/external regulations and procedures * Evaluates and assists in the implementation of new changes at the site, including providing training on an as needed basis * Provide support to collect and prepare EMPQ reports, EM Trend reports, QMR board presentations with associated documentation. * Performs regular self-audits of the Microbiology and EM laboratory areas (including storage areas) and assists/leads activities to address audit findings. Stakeholder: * Works collaboratively with other department stakeholders to ensure the services provided to the site are developed, tested, and delivered according to established procedures and regulations. Innovation: * Supports purchasing QC EM laboratory supplies. Makes sound, well considered decisions to make the most of available funds and resources. Monitors lab supply costs and looks for ways to work with suppliers to reduce consumables cost when appropriate. * Consults with management, when appropriate, about laboratory supply variances. Demonstrates the ability to assess upcoming laboratory supply needs and prepare accordingly. Makes realistic and actionable plans to address supply chain issues. * Maintains the QC department ordering system to reduce costs and waste due to expiry. Keeps current on physical and computerized tracking systems for materials and supplies. Safety: * Appropriately utilizes PPE (Personal Protective Equipment) as required to perform routine and non-routine laboratory duties KNOWLEDGE, SKILLS AND ABILITIES: Education: * Minimum BS/BA in Pharmaceutical Sciences, Chemistry, Biology Experience: * Minimum of 3+ years in a pharmaceutical environment * Strong organizational skills. Displays the ability to prioritize work and manage multiple tasks independently. * Excellent written communication and technical writing skills. Clearly demonstrates competence in the selection and use of root cause analysis tools and techniques (e.g., 5 Whys, Pareto Analysis, 5M +E). * Displays strong interpersonal skills and ability to work with all levels of an organization. Clearly expresses ideas (verbal and written) and demonstrates the ability to apply a quality mindset when completing Microbiology/EM laboratory tasks. * Demonstrates the ability to read, understand, author, redline and execute standard operating procedures (SOPs). * Displays ability to achieve Glenmark Monroe QE investigator certifications for product/process/testing/facility issues with product and non-product impact. * Exhibits both analytical and problem-solving skills. Proven ability to problem solve/troubleshoot and provide solutions for laboratory issues. * Able to assess safety and environmental risks to ensure laboratory tasks adhere to EHS management system. * The ability to work independently and within team structure and on multiple projects, with flexibility to adapt to changing priorities is required. This candidate must be a technical expert and have excellent written and oral communication as well as interpersonal relationship skills. Ability to lift 30 lbs. and work within different extreme temperature / humidity environments as encountered in the various Incubator conditions.