Manufacturing technician jobs in Wake Forest, NC - 550 jobs

Job Title: Metrology Technician Job Type: Full-time, Monday-Friday Pay rate: $90,000- 110,000 (DPE) TMI Calibration, established in 1991, is an ISO/IEC 17025-accredited laboratory offering comprehensive calibration, repair, and asset management services for test equipment. With multiple full-service labs across the U.S., TMI specializes in providing automated and on-site calibrations, clean room certifications, and custom solutions. Position Overview: We are seeking experienced Metrology Technicians with demonstrated knowledge in metrology and the calibration of Pressure, Temperature, and Physical test equipment. In this role, you will ensure the accuracy and reliability of measurement instruments, applying a keen eye for detail and strong organizational and communication skills. This position is part of Onsite Technical Services (OTS), embedded at our customer location in Clayton, NC. Responsibilities: Calibrate and repair temperature, pressure, conductivity, humidity, pH, TOC, flow, mass, and frequency measuring equipment, including process and utility instrumentation. Participate in systematic problem solving, cross-functional investigations, and metrology-related projects. Support, train, and mentor lower-level team members. Accurately document all activities, including work orders, calibration reports, and process confirmations. Review and confirm calibration documentation for accuracy and compliance with corporate and local standards. Operate and maintain calibration working standards with care and expertise. Identify and escalate safety, quality, staffing, or personnel issues as necessary. Maintain aseptic clean room certification and follow all safety and environmental requirements. Support other department roles and execute work according to schedule and department plan. Requirements and Skills: Associate's degree (engineering or science) required, or HS diploma with 6 years of calibration experience. 4 years of relevant metrology/calibration experience and understanding of instrumentation & control systems. Competencies in calibration, instrumentation & controls, electro-mechanical systems, and electronics. Experience with electronic calibration management systems (SAP, Blue Mountain RAM, ProCal, MAXIMO, etc.). Ability to read and apply schematics, wiring diagrams, and other technical documents. Systematic problem-solving, troubleshooting, logical task planning, and strong organizational skills. High attention to detail with accurate documentation. Basic computer skills; excellent communication skills for team collaboration. U.S. Citizen or Permanent Resident status required. Benefits: TMI offers comprehensive benefits including Health, Vision, Dental, and Life insurance 401(k), Paid time off, Referral program, and more! We are an Equal Opportunity Employer TMI is an Equal Opportunity and Affirmative Action Employer.

Morrisville, NC Responsibilities: Able to Understand, Retain, and effectively apply On the Job training instruction Consistently follow processes and procedures to operate compliantly within a controlled environmental manufacturing space Read and Understand Assembly drawing and assembly instructions to correctly and efficiently assemble products Distinguish differences in sub-component parts based on part number and visual inspection Perform in-process inspections per applicable specifications or work orders, including inspection of input and output materials, packaging integrity Performs labeling and packaging activities Consistently adhere to assembly methodology of accept / reject criterion Interact with Quality Assurance personnel to ensure product quality and address any non-conformity detected Report problems with quality, processes, equipment, or materials to the Team Lead and or Supervisor Utilize approved tools and fixtures as required in a safe and efficient way Complete line clearance, scrap records, training records, and other documentation as required Maintain batch records for traceability purposes in accordance with company documented standards Maintain a clean and organized work area to facilitate manufacturing functions Other duties as assigned by the Supervisor and or Team Lead Essential Functions Ability to read and comprehend procedures written in English Ability to complete paperwork accurately in English Ability to work safely around chemicals and equipment Ability to stand or sit for long periods of time Ability to do repetitive work, requiring strong dexterity and hand/eye coordination Ability to lift up to 40 lbs Desired Education & Experience: High school diploma or equivalent Previous Work experience within a controlled environmental space preferred Previous assembly experience preferred Ability to lift up to 40 lbs Work Environment: • Work is normally performed in a climate-controlled office environment and throughout a heated manufacturing and warehouse facility • The noise level in the work environment is usually low to moderate

Accentuate Staffing is assisting a global leader and manufacturer of high-tech automation solutions, who is hiring a skilled Automation Engineering Technician to join their team in Morrisville, NC. This role is ideal for a hands-on problem solver who enjoys working with advanced machinery, traveling to customer sites, and providing exceptional technical support. Every day brings new challenges as you troubleshoot, install, and upgrade highly specialized equipment used in cutting-edge industries. Responsibilities Perform service visits at customer locations across the U.S., providing troubleshooting, maintenance, and upgrades on high-tech machinery. Support equipment installations and commissioning activities at customer sites worldwide. Receive hands-on training with machines and systems both at the U.S. location and at the company's headquarters in the Netherlands. Assist assembly and service teams when working onsite at the Morrisville facility. Complete system modifications, repairs, and performance checks to ensure equipment reliability and customer satisfaction. Document service activities and communicate technical findings clearly to internal teams and customers. Requirements Associate degree or higher in Mechatronics, Mechanical Engineering, Electrical Engineering, or related technical field. 3-5+ years of experience in a technical service or industrial machinery environment. Must have automation experience. Strong mechanical, electrical, and/or electronic troubleshooting abilities. Proficiency with diagnostic tools, safety protocols, and complex machinery. Excellent communication skills and a customer-focused mindset. Valid passport with at least 6 months of remaining validity; ability to travel up to 70% Must work fully onsite in Morrisville, NC (no hybrid/remote options; relocation not provided).

MACOM designs andmanufactures semiconductor products for Data Center, Telecommunication and Industrial and Defense applications. Headquartered in Lowell, Massachusetts,MACOM has design centers and sales offices throughout North America, Europe and Asia. MACOM is certified to the ISO9001 international quality standard and ISO14001 environmental management standard. MACOM has more than75 years of application expertise with multiple design centers, Si, GaAs and InP fabrication, manufacturing, assembly and test, and operational facilitiesthroughout North America, Europe, and Asia. Click here to view our facilities. Inaddition, MACOM offers foundry services that represent a key core competencywithin our business. MACOM sells anddistributes products globally via a sales channel comprised of a direct fieldsales force, authorized sales representatives and leading industrydistributors. Our sales team is trained across all of our products to give ourcustomers insights into our entire portfolio. MACOM is seeking a self-motivated and enthusiasticsemiconductor manufacturing Technician for our Wafer Fab operations. The ManufacturingTechnician will report to the manufacturing team and perform specific manufacturing tasks on the production floor. Key Responsibilities: Perform a variety of functions in the production of semiconductor devices in a cleanroom (class 1000 and class 10000) environment. Set-up, operate, load, and monitor specialized equipment to ensure quality products are produced. Responsible for monitoring equipment operation, inspecting final product, cleaning the work environment, and performing data entry. Execution towards Daily planning goals for operation. Ability to do multi-task. Capable of running multiple tools. Handle semiconductor wafers and die in clean room environments (Class 1000 and Class 10000) Familiar with FOD, contamination and ESD management Capable of using digital and optical microscopes and other wafer/die inspection tools. Knowledge of wafer, microelectronic and hybrid assembly processes and manufacturing processes Using ERP, shop floor control and the automated tracking tools to status daily production. Understands process flow and areas of impact. Requires minimal instructions (works independently without direction) on daily work. Receives general instructions on new processes. Performs non-standard work on 50% of assigned tools/processes. Required Qualifications and Experience: Must have high school diploma or equivalent and at least 5 years priormanufacturing experience in semiconductor wafer fabrication. Ability to sit or stand for 12 hours at a time with the flexibility to workday or night shifts for training purposes. Ability to work Night shift. Hours 6pm-6am. Compressed work week Solid computer and math skills. Comfortable working with automated equipment Good communication skills, both written andoral; ability to read and write effectively. Comfortable working around chemicals. Ability to multi-task and approachtasks with detail-oriented manner. Required to wear a cleanroom gownsand/or proper safety personal protective equipment. Great work ethic and ability to workwell with others. The ideal candidate will have a general knowledge of electronics manufacturing, with a strong aptitude and interest in working with automated and manual assembly equipment as well as the communication skills required to work with engineering Due to ITAR regulations, only candidates who are U.S. Persons (U.S. citizens, U.S. nationals, lawful permanent residents, or individuals granted asylum or refugee status) will be considered for this position. Work on one of our 12 hour compressed work weeknight shifts (6:00pm to 6:00am), or day shifts (6:00am to 6:00pm). All shifts alternate working 3, 12-hour shifts one week (36 hours) and 4, 12 hours shifts the following week (48hours). Shifts will work either Sun, Mon, Tue alternating Wed or Thu, Fri, Sat alternating Wed. EEO: MACOM is an Equal Opportunity Employer committed to a diverseworkforce. MACOM will not discriminate against any worker or job applicant onthe basis of race, color, religion, sex, gender identity, sexual orientation,national origin, age, disability, genetic information, veteran status, militaryservice, marital status, or any other category protected under applicable law. Reasonable Accommodation: MACOM is committed to working with and providingreasonable accommodations to qualified individuals with physical and mentaldisabilities. If you have a disability and are in need of a reasonableaccommodation with respect to any part of the application process, please call+1-978-###-#### or email [email protected]. Provide your name, phone number andthe position title and location in which you are interested, and nature ofaccommodation needed, and we will get back to you. We also work with current employeeswho request or need reasonable accommodation in order to perform the essentialfunctions of their jobs Benefits: This position offers acomprehensive benefits package including but not limited to: • Health, dental, and vision insurance. • Employer-sponsored 401(k) plan. • Paid time off. • Professional development opportunities.

Extron is a leading developer and manufacturer of professional AV hardware and software solutions which serve the ever-changing needs of organizations around the world as they strive to better communicate. Each Extron product is carefully engineered to provide best-in-class performance, intuitive operation, and exceptional reliability. At Extron, the passion for our products is evidenced by our company culture, which encourages innovation and provides opportunities for individual career growth. Our teams develop and release over 100 new products a year and continue to grow our vast patent portfolio. Qualified Candidates will have the following requirements: Minimum 5 years experience as manufacturing or maintenance technician. Associate degree in mechanical or manufacturing technologies or equivalent technical schooling preferred. Machine Shop tools experience preferred. (Familiar with Bridgeport Milling machine, Lathe, Drill Press, Engraver, Welding etc). Able to fabricate or modify parts using drills, calipers, cutters, saws, etc; Able to drill or tap holes in specified equipment/fixture locations to mount units or to provide openings for elements, wiring, or instruments. Able to lift and transport material, equipment and tools as needed. Loading and unloading of production materials to/from trucks and warehouse racks may be required at times. Basic knowledge of electrical systems / electronics, a plus. Soldering and assembly skills preferred. Ability to read and interpret schematics, diagrams, complex drawings and manufacturing process instructions. Experience in troubleshooting and isolating/identifying root cause of failure. Able to keep accurate records of time spent on each item and any problem encountered and to enter data into record keeping system as necessary. Able to perform Preventive maintenance on Production Equipment, including rivet runs, electric/pneumatic screwdrivers and other assembly tools. Able to test, troubleshoot, and repair electro-mechanical equipment. Provide verbal/written recommendations for process improvements. Excellent communication skills, both written and verbal. Strong attention to details, highly organized, and computer literate. Ability to work well in a fast-paced professional office/lab environment, working independently and as a team member. Assembly work will be required as need, to support the production department.

This position operates on a night shift 2-2-3 schedule. The Manufacturing Associate I/II (Manufacturing Associate) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Manufacturing Associate must follow written, approved procedures and forms to ensure all work is conducted “Right First Time” (RFT) following Good Manufacturing Practice (GMP), including good documentation practices, and/or Good Laboratory Practice (GLP). As needed, the Manufacturing Associate will work individually or on teams to author standard operating procedures (SOPs) or Master Batch Records (MBRs); write corrective and preventive actions (CAPAs); and specify, commission, and qualify new equipment. The Manufacturing Associate will be responsible for upstream unit operations (seed expansion, bioreactor operations, cell culture harvest). The Manufacturing Associate will have a working knowledge of upstream processing equipment (incubators, biosafety cabinets, bioreactors, cell counters, blood gas analyzers, metabolite testing equipment). Additionally, the manufacturing associate will have knowledge of general bioprocessing equipment such as filters, filter integrity testers, balances, pumps, pH/conductivity meters, and disposable technologies (disposable bags, sterile tubing welders, tubing sealers). Following task execution, the Manufacturing Associate will review the executed production records and logbooks to ensure GxP compliance. The Manufacturing Associate will execute daily tasks and maintain strict accordance with manufacturing records, SOPs, and GMP. Staff will maintain a sense of ownership of the production processes, the manufacturing environment, and the facility. Staff will work cross-functionally with QA, MS&T, facilities, engineering, supply chain, IT, AFS, and other key departments to ensure startup and ongoing manufacturing operations are successful, reliable, and compliant. A proven Manufacturing Associate will demonstrate the following qualities: learning agility, orientation toward action, results driven, team player, strong attention to detail, and superior integrity and accountability. Position Responsibilities Manufacture bulk intermediates and drug substances per manufacturing batch records in compliance with quality, company policies, and current regulations Perform operations in a cleanroom environment, applying controls to ensure aseptic processing, including gowning and cleaning procedures Document each task involving manufacturing records and logbooks following GDP at the time of execution Utilize and perform maintenance on equipment per applicable SOP Ensure all materials are issued and accounted for during the execution of a record Demonstrate, apply, and ensure understanding of cGMP and how it applies to specific tasks and responsibilities Participate and be accountable for workplace organization Position Requirements Manufacturing Associate II- Bachelor's degree in a related scientific or engineering discipline and 2-5 years' experience in related cGMP manufacturing operations; or high school diploma and 4-6 years' experience, or equivalent Basic knowledge of upstream processing- cell culture or fermentation Experience in single-use platform technology is preferred *Please note: this is a night shift opportunity and will be eligible for a shift differential on top of listed salary* Salary Range: $24-$31.25/hour Salary range provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidate's qualifications and experience and may be outside this range. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, Sabbatical program, 401K matching with 100% vesting in 60 days and employee recognition programs. KBI Biopharma is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must inform KBI Biopharma of their vaccination status and must submit their vaccination status. All vaccinated employees are required to provide proof of their COVID-19 vaccination, with a COVID-19 vaccination which has been granted FDA approval or Emergency Use Authorization. KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply. I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary. I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

Additive Manufacturing Technicians will be responsible for the operation of 3D LBPF metal printers, including CAD model review, build preparation. Tuesday - Saturday, 8:00 am - 4:30 pm Sunday - Thursday, 8:00 am - 4:30 pm PRINCIPAL RESPONSIBLITIES Principal responsibilities for the position include the following. Other duties may be assigned as necessary. Full operation of 3d metal printers. Includes machine unload, setup, operation, maintenance and general upkeep and troubleshooting. CAD model review, build preparation and general software support for metal printers. Reviewing model drawings and processing requirements and creating device records. Aid in post-processing steps done on common shop equipment (micro-blasting, grinding wheel, deburring tools). Aid in testing of verification samples on hydraulic and electronic test frames. Support R&D engineers during testing of devices for other purposes. Follow all appropriate safety precautions, including usage of PPE and maintaining lab cleanliness. Visual inspection of manufactured goods as part of quality-controlled process. EDUCATION High school diploma or GED Some college education is preferred. Preference given to technical training and degree work. EXPERIENCE Strong attention to detail Ability to work in a regulated industry, including adherence to proper paperwork protocols and good quality practices. Ability to routinely lift 35 lbs during a shift Ability to be standing for 3+ hours during a shift Strong visualization skills TOOLS AND EQUIPMENT Position may involve the use of: Basic hand tools Direct Metal Printers Polymeric 3D Printers Media Blasting Cabinet Testing Frames Cleaning and Inspection Equipment Respirator and fire-retardant PPE MATERIALS HANDLING / EXPOSURE Position will involve handling of ultra-fine, medical grade, metallic powder. May involve handling of other raw materials and waste material applicable to the manufacture of medical devices. SUPERVISORY RESPONSIBILITIES Position does not have supervisory responsibilities. PHYSICAL ACTIVITIES Position requires the ability to intermittently lift and carry up to 35 pounds and to operate while wearing a full-face respirator, protective clothing, eye protection, and/or hearing protection. A respirator fit test will be required prior to working with a respirator. Position may require extended periods of standing, extensive work with the operator's hands and tools, as well as occasional squatting, kneeling, and working with a ladder. WORKING CONDITIONS Working conditions include standard office and laboratory conditions as well as conditions of a machine shop. Machine shop conditions may include noise, dust, and elevated temperatures. restor3d is an equal opportunity employer

************************************************* xmlns="********************************* The PCX Manufacturing Technician supports a variety of engineering and production activities including equipment set-up and validation of new equipment, development and implementation of process improvements, process troubleshooting, monitoring of process data, assistance with creating and updating of process documentation, prototype execution, and assistance with preparation for new product introductions. The Manufacturing Technician is responsible for completing all assigned work according to specifications in a high quality and safe manner. The Manufacturing Technician assists and advises other employees in the assembly and production of switchgear and other electrical systems. Manufacturing Technicians understand and participate in the PCX quality program, to include KANBAN inspection scheduling and in-process inspections, and are knowledgeable in the project process flow, working with the engineering department during project planning and execution. They are required to follow the instructions of the electrical supervisor and suggest improvements. Specific Position Requirements: Must follow PCX safety guidelines and requirements Able to read, interpret, and understand blue prints and electrical schematics Develop detailed understanding of processes and equipment to identify and solve process issues through troubleshooting, data analysis, and collaboration with stakeholders across the Engineering, Operations, Maintenance, and Quality teams Support process validation projects by aiding with set-ups, engineering studies, and related testing Provide administrative support such as developing and updating manufacturing documentation and tracking and reporting on process performance Support execution of projects including DMAIC, LEAN, 5S, cost reduction and process improvement initiatives Install and connect power supply wiring, control wiring, cables, conduit, and electrical apparatus for machines and equipment following diagrams, schematics, or blueprints Inspect jobs upon completion and ensure areas are clean Ensure that equipment is in safe operating condition Follow established safety procedures and techniques to perform job duties Must verify conformance of work to specifications Must exhibit quality workmanship that adheres to engineering and customer specifications Adheres to PCX Quality Management System and ISO9001 standards Works in a timely, efficient manner to meet all daily performance objectives Maintains tools and equipment in proper working condition Must be able to read and understand posted bulletins, regulations, rule books, manufacturer manuals, and work instructions Must be able to work in a team environment which requires cooperating with others, offering help when needed, and maintaining positive work relationships Complete Time Reporting Sheets Report inventory use as required Able to lift 50# consistently Ability to work 10 hours per day and weekends as required Must have a valid Driver's License Background check and drug-screen are required

The Manufacturing Specialist 1 performs manufacturing support activities to ensure compliant and reliable production. This manufacturing facility will be 24/7 operational and the role may require to be flexible with working hours and shift rotation. Company Overview FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof. We're looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we're proud to cultivate a culture that will fuel your purpose, energy, and drive-what we call Genki. Ready to shape the future of medicine? Let's transform healthcare together! Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh's thriving tech scene, making it the perfect blend of community and opportunity. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: *************************************************** Job Description What You'll Do * Supports trouble shooting including acting as a process subject matter expert (SME) for their process respective area(s) * Coordinates Batch Planning including process template creation, import and management of preventative maintenance (PMs) * Maintains current and accurate documentation, ensuring timely updates of records (redlines and process improvements) * Coordinates of non‐batch activities including Changeover, PMs and column packing * Assists in inventory management and offers support in utilizing SAP for effective manufacturing operations * Supports tech transfer within manufacturing domain * Ensures compliance and safety procedures are followed in manufacturing environment * Manages, performs, initiates, or supports change management records, investigations, corrective and preventive actions (CAPAs) and continuous improvement (CI) activities * Identifies and/or drives improvement projects in drug substance manufacturing * Assists and supports inspections and audits. Provides support to ensuring compliance within the manufacturing environment * Other duties as assigned Basic Requirements * High School Diploma/GED and 10 years of related experience OR * Associate's degree, preferably in life sciences or engineering with 8 years of direct experience OR * Bachelor's degree preferably in life sciences or engineering with 6 years of direct experience OR * Equivalent Military experience/training Preferred Requirements * Strong cGMP manufacturing operations experience * Understanding of operations sequence and cadence of activities * Prior experience in updating and creating manufacturing documents per schedule * BioWorks or BTEC Capstone cGMP coursework preferred WORKING CONDITIONS & PHYSICAL REQUIREMENTS * Ability to discern audible cues * Ability to ascend or descend ladders, scaffolding, ramps, etc. * Ability to stand for prolonged periods of time * Ability to sit for prolonged periods of time * Ability to conduct activities using repetitive motions that include wrists, hands and/or fingers * Ability to conduct work that includes moving objects up to 10 pounds * Will work in heights greater than 4 feet To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid. EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBN_****************).

Full-time Description Maintains a territory and has thorough knowledge of products and provides various operational support with service and maintaining of large production copiers. Essential Duties and Responsibilities: Service Ricoh, Konica Minolta production and some midrange copiers in customer's office. Must be able to train customer on the operation of the equipment including all options. Manage a full field of assigned territory. Must be able to connect, print, scan and update firmware from laptop computer. Maintain good customer relations through visits or telephone communications. Ensures the timely and accurate preparation of reports. Performs periodic inspections of vehicle parts stock and tool bag. Provides assistance to management as required. Must stay informed of all updates, such as bulletins and firmware along with other technical developments for all production models. Coordinates service installs/setups with delivery personnel, management, sales personnel and customer support. Must be able to communicate professionally with customers to understand their printing and copying needs and how to achieve these goals for the customer. Minimum of 5 year experience servicing production equipment. Requirements Physical Requirements Must be able to carry at least 30 to 50 lbs. Job will require bending, squatting, kneeling, pushing/pulling and moving/lifting various equipment. Driving company vehicle to customer locations Qualifications: Requires two-year Associates degree in Electronics or two to four years' experience in related electronic field. Must have experience with large production copiers. Must pass basic electronic skills test.

Working at Freudenberg: We will wow your world! Responsibilities: Monitor and control the production process to ensure optimal efficiency and quality output Ability to set-up production line for start-up as well as all style changes required Monitor material specifications and make required adjustments to produce first quality material Inspect and observe line function from raw material input to quality material output, identifying deviations in process and/or equipment and communicating issues to maintenance or management Conducts regular quality inspections to identify any deviations or issues in the production process Practice lean manufacturing principles to drive continuous improvement and operational excellence Demonstrates a deliberate focus on safety, quality, continuous improvement Performs other job duties as assigned Qualifications: High school diploma or equivalent; technical degree or certification preferred Manufacturing experience with preference in plastics extrusion, nonwovens or paper manufacturing. Excellent teamwork and communication skills Strong attention to detail and ability to follow procedures Excellent problem-solving skills Experience entering information into production database as well as ERP system Must be able to read a ruler and understand fractions, and demonstrate basic math skills Must be able to work well with others and in a diverse workforce environment Forklift experience required. Ability to lift and/or move up to 50 pounds Prolonged periods of standing Ability to sit, stand for the majority of the shift The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law. Freudenberg Performance Materials LP (USA)

Kincell Bio engineers cells into therapies . With manufacturing facilities located in Research Triangle Park, NC and Gainesville, FL, Kincell Bio is a contract development and manufacturing organization (CDMO) with the mission to streamline CMC development, apply expertise in analytical and process development and GMP manufacturing, testing and release from early clinical to pivotal studies and product launch. Kincell Bio is focused on supporting innovative companies developing immune cell therapies, including autologous and allogeneic CAR-T, TCR, TILs, Tregs and CAR-NK technologies. We offer challenging career opportunities, competitive benefits, and an environment that recognizes and rewards performance. For more information, please visit our website at ******************* Kincell is seeking a highly motivated Manufacturing Specialist who will be a key contributor to a dynamic and collaborative Manufacturing team. As a Manufacturing Specialist, you will have the responsibility to ensure initiatives related to production readiness and compliance are optimized and executed appropriately in the areas of cGMP production. This position will directly support manufacturing for all production-related activities. You will work with cross-functional teams to identify and implement meaningful corrective actions arising from deviations and audit observations. In addition, you will be operating automatic and manual cell therapy equipment with a variety of complexities in CAR-T, CAR-M, or CAR-NK processes in accordance with standard operating procedures and policies as needed. You will perform quality control analyses as required to complete in-process batches and identify variations. You will be trained in handling hazardous materials and emergency procedures since you will be handling leukapheresis cellular materials. As part of manufacturing operations, you will be a team member who is relied on to have a good understanding of procedures, techniques, tools materials, and equipment to help support cGMP activities at the Gianesville, FL site. Your work and decision-making will be team-based and will focus on the prioritization of workflows centered on the process and available resources. You will follow standard operating procedures to complete tasks which may vary in scope, complexity, and timing. Patients need colleagues like you who take pride in their work and look for successful outcomes. You will help ensure patients have the therapies they need when they need them. You will be operating cell therapy process equipment of varying complexity with different processes in accordance with standard operating procedures. Essential Duties and Responsibilities Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position. This list contains the major duties and requirements of the job and is not all-inclusive. Incumbent(s) may be expected to perform role-related duties other than those contained in this document. Subject Matter Expert in drug-product (DP) aseptic filling, sterility assurance, and isolator operations within a regulated cGMP biotechnology manufacturing environment. Demonstrated hands-on proficiency with closed and open aseptic processing, including cell-therapy manipulation, cell culture, G-Rex expansion, formulation, and final DP fill execution. In-depth operational knowledge of GMP isolators (ISO 5 unidirectional airflow, positive pressure control, glove-integrity assurance, and environmental control strategies). Provides direct manufacturing floor leadership and execution support, actively participating in GMP processing, aseptic interventions, equipment setup, batch readiness walkthroughs, and deviation prevention strategies. Authors and reviews SOPs, Work Instructions, Master Batch Records, and validation documents to ensure clarity, traceability, and regulatory alignment (FDA, EU Annex 1, and internal QMS governance). Manage deviations, change controls, and CAPAs, applying 5M/5-Why/RCA methodologies and validated risk-management tools (FMEA, RPN scoring, impact assessments, and control-strategy design to ensure compliance with internal procedures and regulatory requirements. Provide support for all related start-up and continuous improvement activities related to operational readiness and operational excellence, including procedure creation, revision, equipment qualification and validation. Collaborates with QA, QC Microbiology, MSAT, Engineering, and Supply Chain to drive operational readiness, equipment qualification, data integrity, and continuous improvement for clinical and commercial manufacturing campaigns. Provides manufacturing and operational guidance and recommendations in a professional and collaborative manner to internal and external stakeholders. Maintaining personal responsibility with Personal Protective Equipment (PPE) Proficient in Microsoft Word, Excel, PowerPoint, and other standard applications used in technical field. Qualifications The requirements listed below are representative of the knowledge, skill, and/or ability required to perform this job successfully. Required: B.S degree in Natural Sciences (i.e, Biology, Chemistry, etc.) or Engineering (Chemical, Biomedical, etc.) and 5-7+ years of manufacturing experience. Must have direct isolator or aseptic DP fill execution experience supporting sterility-critical operation. Must be able to work onsite daily and be willing to have a flexible schedule to support a multi-shift operation that covers nights and weekends as needed. Ability to work independently and stay on task in a fast-paced environment without direct supervision. Experience supporting clinical manufacturing campaigns, regulatory inspections, and aseptic process validation in isolator-protected suites. Knowledge of cell and gene-therapy workflows, isolator contamination-control strategy, metric systems, and process-measurement scale-ups. Must have experience in drafting and reviewing technical documents with high technical writing skill. Provides consistently prompt, efficient, dependable, and highly skilled services. Understands, selects, and uses appropriate risk management and root cause analysis tools. Takes initiative in making improvement suggestions to promote operational goals. Applies Quality concepts and company policies to resolve issues of moderate complexity in an effective manner. Reflects solid understanding of strategies and goals and can take part in major parts of projects or provide expert service. Recommends improvements to on-going processes and projects. Facilitates designing processes with Quality built in from the beginning. Identifies, and uses good judgement to handle out-of-compliance situations. Good listening and communication skills. Positive approach and highly collaborative persona. Must be able to lift bags and/or containers of media of up to 40+lbs. Manage personal time and professional development. Maintain accountability for your own outcomes and prioritized workflows. Preferred: M.S degree in Natural Sciences (i.e, Biology, Chemistry, etc.) or Engineering (Chemical, Biomedical, etc.) and 3-5+ years of manufacturing experience Have knowledge of cell and gene therapy processing, the metric system, and scales. Excellent project management skills to ensure projects and goals are met in a timely manner. Travel Requirements N/A Location This is an office-based position located at the RTP, NC site. #LI-Onsite Kincell Bio provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable, federal, state, and local laws. Kincell Bio complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. NOTE TO EMPLOYMENT AGENCIES: Kincell Bio values our relationships with our Recruitment Partners. We will only accept resumes from those partners who have been contracted by a member of our Human Resources team to collaborate with us. We are not responsible for any fees related to resumes that are unsolicited or are received without contract.

The Advanced Cellular Therapeutics (ACT) Facility is a Good Manufacturing Practices (GMP) facility focused on expansion and manipulation of human cells for clinical phase 1 applications, specifically including applications involving chimeric antigen receptor (CAR) T cells. The ACT Facility also manufactures Master Cell Banks (MCBs) used in the production of clinical grade gamma retrovirus vector for use in CAR T clinical trials. Is Time Limited Yes If Yes, Appointment Length 11 months Wolfpack Perks and Benefits As a Pack member, you belong here, and can enjoy exclusive perks designed to enhance your personal and professional well-being. As you consider this opportunity, we encourage you to review our Employee Value Proposition and learn more about what makes NC State the best place to learn and work for everyone. What we offer: * Health Insurance for Temporary Employees * Enhance your career with LEAD courses * Attend non-revenue generating sporting events for free. Attain Work-life balance with our Childcare discounts, Wellness & Recreation Membership, and Wellness Programs that aim to build a thriving wolfpack community. Disclaimer: Perks and Benefit eligibility is based on Part-Time or Full-Time Employment status. Eligibility and Employer Sponsored Plans can be found within each of the links offered. Department Information Job City & State Chapel Hill, NC Department System Information Classification Title Temporary-Service Maintenance Working Title UTS- Temporary GMP Manufacturing Technician at UNC Chapel Hill Position Information Requirements and Preferences Work Schedule Monday-Friday, 8:00 AM-5:00 PM Other Work/Responsibilities Other duties as needed Minimum Experience/Education * Relevant bachelor's degree (or foreign degree equivalent) and 3 or more years of relevant experience in substitution. Department Required Skills * Perform cell culture activities within an ISO 7 clean room environment in compliance with Good Manufacturing Practices (GMP). * Work aseptically in a Biological Safety Cabinet (BSC) to ensure product integrity and prevent contamination. * Execute cell counting, assess cell viability, and perform related in-process testing to support the manufacturing of patient-specific cellular therapy products. * Follow established Standard Operating Procedures (SOPs) and batch records accurately, documenting all activities in accordance with GMP requirements. * Make routine manufacturing decisions within defined procedures to support timely and compliant production of patient products. * Demonstrate sound judgment by recognizing when to seek guidance, escalate issues, or request support from manufacturing leadership or quality personnel when questions or deviations arise. * Collaborate effectively with cross-functional teams to ensure safe, consistent, and high-quality manufacturing operations. Preferred Years Experience, Skills, Training, Education * Assist with maintaining appropriate inventory levels of materials and supplies within clean rooms and controlled release spaces, ensuring proper storage, labeling, and documentation in accordance with GMP requirements. * Support a variety of manufacturing-related tasks as needed to meet operational demands, including preparation, cleanup, and coordination of materials and equipment. * Lead or support validation projects for manufacturing systems, equipment, and processes, including documentation, execution, and data review activities. * Participate in continuous improvement initiatives to enhance manufacturing efficiency, compliance, and product quality. * Collaborate with manufacturing, quality, and facilities teams to ensure validated systems remain in a state of control. Required License or Certification N/A Valid NC Driver's License required? No Commercial Driver's License Required? No Recruitment

Career CategoryQualityJob DescriptionJoin Amgen's Mission of Serving Patients At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the Amgen FleX batch facility will combine the latest in single use technologies with traditional stainless steel equipment to allow for maximum flexibility in operations The FleX Batch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it will also integrate sustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027. Specialist-Manufacturing Investigations What you will do Let's do this. Let's change the world. In this vital role, you will be a key member of the team that investigates major deviations in the Amgen North Carolina Biologics Drug Substance Manufacturing plant. You will communicate and interface between the GMP manufacturing teams and stakeholder groups including, Process Development, Facilities & Engineering, Automation, EHSS, and Quality. This position is responsible for ensuring deviation investigations are successfully conducted and documented while driving improvements in the investigation process. Manage Major deviation investigations, including assembling investigation teams, leading root cause analysis, development of CAPAs, and compliant documentation of all findings. Drive improvements to the investigation process. Present investigations to regulatory inspectors, internal auditors, and management. Clearly communicate investigation progress to impacted areas and leadership. Coordinate and effectively lead cross-functional teams through complex investigations, and complete milestones on-schedule. Present complex topics to large and small groups at various levels and quickly understand and clearly communicate complex issues. Build effective relationships across functions. Navigate through ambiguity and provide a structured problem-solving approach. Apply inductive and deductive reasoning in the investigation process Clear and concise technical writing Use Operational Learning Team strategies to promote open collaboration with staff to maximize investigation findings. Develop tracking tools to ensure on-time closure and proactive review of deviation investigations. What we expect of you We are all different, yet we all use our unique contributions to serve patients. The collaborative investigator we seek has a biologics Drug Substance manufacturing and investigations background with strong cross-functional project management and communication skills as well as the below qualifications. Basic Qualifications: High school diploma / GED and 10 years of Quality Control experience OR Associate's degree and 8 years of Quality Control experience OR Bachelor's degree and 4 years of Quality Control experience OR Master's degree and 2 years of Quality Control experience OR Doctorate degree Preferred Qualifications: 5+ years related work experience (manufacturing, process development, or quality assurance) in biotech or pharmaceutical industry with progressively increasing responsibility Experience with compliance, problem-solving, simple and complex root cause analysis tools (5-whys, fishbone, Kepner Tregoe Problem Analysis , Design of Experiment etc.) critical thinking, project management, and quality systems. Degree in Science or Engineering Experience leading complex investigations Experience using Veeva QMS for Deviation investigations and CAPAs Demonstrated project management ability Experience presenting to inspectors during regulatory inspections and internal audits. Excellent written and verbal communication skills Ability to work in a team matrix environment and build relationships with partners Strong interpersonal skills What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now and make a lasting impact with the Amgen team.careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected 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. . Salary Range 114,990.00 USD - 139,433.00 USD

The Manufacturing Specialist 1 performs manufacturing support activities to ensure compliant and reliable production. This manufacturing facility will be 24/7 operational and the role may require to be flexible with working hours and shift rotation. Company Overview FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof. We're looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we're proud to cultivate a culture that will fuel your purpose, energy, and drive-what we call Genki. Ready to shape the future of medicine? Let's transform healthcare together! Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh's thriving tech scene, making it the perfect blend of community and opportunity. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of “giving our world more smiles.” Visit: *************************************************** Job Description What You'll Do Supports trouble shooting including acting as a process subject matter expert (SME) for their process respective area(s) Coordinates Batch Planning including process template creation, import and management of preventative maintenance (PMs) Maintains current and accurate documentation, ensuring timely updates of records (redlines and process improvements) Coordinates of non‐batch activities including Changeover, PMs and column packing Assists in inventory management and offers support in utilizing SAP for effective manufacturing operations Supports tech transfer within manufacturing domain Ensures compliance and safety procedures are followed in manufacturing environment Manages, performs, initiates, or supports change management records, investigations, corrective and preventive actions (CAPAs) and continuous improvement (CI) activities Identifies and/or drives improvement projects in drug substance manufacturing Assists and supports inspections and audits. Provides support to ensuring compliance within the manufacturing environment Other duties as assigned Basic Requirements High School Diploma/GED and 10 years of related experience OR Associate's degree, preferably in life sciences or engineering with 8 years of direct experience OR Bachelor's degree preferably in life sciences or engineering with 6 years of direct experience OR Equivalent Military experience/training Preferred Requirements Strong cGMP manufacturing operations experience Understanding of operations sequence and cadence of activities Prior experience in updating and creating manufacturing documents per schedule BioWorks or BTEC Capstone cGMP coursework preferred WORKING CONDITIONS & PHYSICAL REQUIREMENTS Ability to discern audible cues Ability to ascend or descend ladders, scaffolding, ramps, etc. Ability to stand for prolonged periods of time Ability to sit for prolonged periods of time Ability to conduct activities using repetitive motions that include wrists, hands and/or fingers Ability to conduct work that includes moving objects up to 10 pounds Will work in heights greater than 4 feet To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid. EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBN_****************).

Job Title: Manufacturing and Production Positions Job Type: Temporary to Full Time About Us: iBoost Talent is a leading staffing agency dedicated to a talent first approach, with years of industry experience. iBoost supports all service models, contingent, temp-to-hire, direct hire, and our proprietary managed services offering Our mission is to simplify the job search process and provide thoughtful solutions for both job seekers and employers. If you're ready to explore your next opportunity, apply today. Job Summary: Join our dynamic team as a Manufacturing Worker in Raleigh, NC. We are actively seeking motivated individuals with experience in various manufacturing roles, including assemblers, machine operators, production technicians, and quality control inspectors. This is an excellent opportunity to advance your career in the manufacturing industry with a leading company known for its commitment to quality and innovation. Key Responsibilities: Assemblers: Assemble components and products according to specifications and quality standards. Material Handlers: Move, load, and unload materials and products within the facility. Production Workers: Assist in the production process, ensuring efficiency and adherence to safety protocols. Forklift Operators: Operate forklifts and other material handling equipment to transport goods safely. Maintenance Technicians: Perform routine maintenance and repairs on machinery and equipment. Inventory Specialists: Monitor inventory levels, conduct counts, and ensure accurate recordkeeping. Machine Operators: Set up and operate machinery, ensuring quality standards and production rates are met. Quality Control Specialists: Inspect products and processes to ensure compliance with company and industry standards. CNC Operators: Operate CNC machines, following blueprints and technical drawings to create precise components. Machinists: Use tools and machinery to fabricate, modify, and repair parts and components. Qualifications: High school diploma or equivalent; technical training or certifications in relevant fields are a plus. Previous experience in manufacturing or production roles is preferred but not required; we welcome entry level candidates. Strong attention to detail and commitment to quality. Ability to work in a fast-paced environment and adapt to changing demands. Good communication skills and ability to work effectively in a team setting. Willingness to work flexible hours, including overtime as needed. Physical Requirements: Ability to lift [insert weight] pounds and stand for extended periods. Comfortable working in a manufacturing environment with exposure to noise, dust, and varying temperatures. What We Offer: Competitive pay. Health, dental, vision, and life insurance Opportunities for career advancement and skill development. EOE Thank you for your interest in iBoost Talent, we are proud to be an Equal Employment Opportunity Employer and participate in the E-Verify eligibility confirmation program.

About the Company: Bell and Howell delivers technology-driven Automation Services and Automation Solutions that help businesses optimize performance, reduce downtime, and improve customer experiences. Our Automation Services bring a dedicated team of expert mechatronic service engineers completely covering North America and backed by our Integrated 360™ advanced technology enabling remote repair, diagnostics, automated SmartOps Dispatch™ and 24/7/365 technical assistance for our clients. We provide a comprehensive and certified level of support for thousands of diversified clients. Our Automated Solutions product portfolio consists of next-generation equipment delivering best-in-class performance enhancing workflow efficiency and elevating customer experiences across multiple markets including retail, pharmaceuticals, packaging, mail production, ecommerce and manufacturing - all backed by the best service in the industry. Position Title: Associate Manufacturing Technician Location: Durham, NC - ONSITE Summary: Reporting to the Manager, Manufacturing, the Manufacturing Technician supports operations by producing quality parts, sub-assemblies, assemblies, and systems of an electro-mechanical nature by assembling, measuring, and testing final product according to standard operating procedures, Manufacturing Instructions, and/or Quality Instructions. Provides technical assistance to other technicians and areas as required. Duties and Responsibilities: Prepares work to be accomplished by studying assembly instructions and diagrams; selecting appropriate parts/materials from inventory via parts (pick) list; gathering work tools. Verification and communication of accuracy of these pick lists. Produces quality machined parts and/or product by assembling parts, sub-assemblies, assemblies, and systems; setting-up various assemblies in accordance with engineering specifications and procedures; making adjustments; completing rework; inspection (measuring to exacting tolerances). Resolves assembly problems by testing/troubleshooting to the piece part level; running diagnostics using various testing equipment; (if required), verifying proper assembly techniques and function of each assembly and sub-assembly. Contributes to quality by training other technicians on proper assembly techniques (cross-training); participate in the development and completing quality checklists prior to acceptance; initiating and participating in defect and cost reduction process improvement efforts; communication of customer needs (internal and external) in a clear and concise manner. Initiating Corrective Action Requests and Problem Solution Logs as required. Contributes to manufacturing process by participating in projects and process improvements. Recommends process and design changes; for cost and process efficiency. Assists in keeping production on schedule by monitoring production status; highlighting areas of concern. Maintains safe and clean working environment by complying with procedures, rules, and regulations. Contributes to team effort by transporting, storing and delivery of components, painting, packaging and crating and by accomplishing related results in a cooperative and supportive manner. Key Relationships: Internal Operations Management, Design/process engineers, material planners, team members Background Requirements: Education, Experience, and Knowledge High School degree or equivalent plus 3+ years of experience in the manufacture/service of electro-mechanical devices. Familiarity with electro-mechanical test equipment or machine shop tools, gauges, and equipment; knowledge of principles of electricity. Advanced technical training preferred. Skills and Abilities: Strong mechanical and/or electrical aptitude; attention to detail Ability to carry out detailed written and/or oral instructions independently Clear and concise verbal and written communications Ability to problem solve; collect, and analyze data; prepare findings Ability to make independent decisions regarding troubleshooting Ability to accomplish the described duties through the use of appropriate hand, power, and testing tools/equipment Ability to lead/train others, receptive and supportive of team efforts Mental and Physical Requirements: Mental/Cognitive Requires reading and understanding written procedures and diagrams for assembly and test; analyzing and drawing conclusions; developing and implementing solutions to assembly problem Physical Requires walking; stooping; lifting to waist of up to 50 pounds to connect parts for assembly and storing, lifting to head up to 25 pounds. Requires standing and walking; talking and hearing; using hands to finger and feel objects; balancing. Requires stooping, kneeling, crouching; reaching with arms and hands. Requires close vision and depth perception; color vision to distinguish wiring and part numbers. Work is performed in a controlled manufacturing environment; noise levels within acceptable safety levels; some assembly performed in cramped areas. 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. Bell and Howell is an Equal Opportunity Employer. It is company policy to administer employment based solely on an individual's qualifications, ability and performance without regard to race, color, religion, gender identity, sex (including pregnancy, lactation, childbirth or related medical conditions), sexual orientation, age, national origin or ancestry, physical or mental disability, genetic information (including testing and characteristics), veteran status, uniformed servicemember status, marital status, or any other characteristic protected by federal, state or local law.

Duke University: Duke University was created in 1924 through an indenture of trust by James Buchanan Duke. Today, Duke is regarded as one of America's leading research universities. Located in Durham, North Carolina, Duke is positioned in the heart of the Research Triangle, which is ranked annually as one of the best places in the country to work and live. Duke has more than 15,000 students who study and conduct research in its 10 undergraduate, graduate and professional schools. With about 40,000 employees, Duke is the third largest private employer in North Carolina, and it now has international programs in more than 150 countries. Positional Summary Provide operational and technical support, in a part-time capacity, within Venue and Production Management (VPM) for lighting, audio, video, and other production systems. The VPM team is responsible for events and performances in campus theaters and mixed-use venues. Responsibilities include, but are not limited to, event setup and strike, operation of sound, lighting, and video systems, carpentry, and rigging and fly rail operation. Collaborate with artists, producers, designers, faculty, students, and other stakeholders to ensure the smooth, safe, and professional execution of events, typically held in campus venues over one or more days. Provide support across a range of performance and presentation spaces, including Page Auditorium, Reynolds Industries Theater, Sheafer Lab Theater, Griffith Film Theater, Baldwin Auditorium, and the Rubenstein Arts Center. Ensure all events are executed safely, on schedule, and in alignment with the highest standards of quality and excellence. Key Position Duties Event Production and Operations - 50% of Effort * Support the successful execution of events and performances by contributing to all aspects of Venue and Production Management operations. * Install, maintain, and program lighting, sound, stage, and video systems for theatrical, musical, and other live events, applying a thorough understanding of stagecraft and production technologies. * Operate lighting, sound, and stage equipment during rehearsals and performances, accurately following production cues and timelines. * Train, guide, and oversee others in the safe and effective use of technical theater systems and equipment, including, but not limited to, sound mixing and recording, theatrical lighting, scenic construction, rigging, projection, video, and stage machinery. Collaboration and Partnership - 25% of Effort * Work collaboratively with staff, faculty, students, and clients to ensure technical services align with event goals and artistic vision. * Coordinate with campus partners, external vendors, and production teams to verify technical specifications and event logistics. * Promote an inclusive, cooperative, and solutions-oriented working environment across all production activities. Leadership and Supervision - 20% of Effort * Lead and supervise production teams, including staff technicians, student workers, event users, and IATSE stagehands, ensuring safe and efficient backstage operations. * Oversee scheduling, call times, and break periods to maintain compliance with labor and safety standards while supporting overall production efficiency. * Uphold and model best practices in workplace and production safety, ensuring full adherence to university and industry regulations. * Support a culture of transparency, teamwork, and accountability within Venue and Production Management. Other- 5% of Effort * Perform related duties as assigned or required to meet departmental, Division and University goals and objectives, as assigned by their Supervisor, Director, or respective designees. Anticipated Pay Range: Duke University provides an annual base salary range for this position as USD $20.52 to USD $32.86. Duke University considers factors such as (but not limited to) scope and responsibilities of the position; candidate's work experience, education/training, and key skills; internal peer equity; as well as market and organizational considerations when extending an offer. Your total compensation goes beyond the dollars on your paycheck. Duke provides comprehensive and competitive medical and dental care programs, generous retirement benefits, and a wide array of family- friendly and cultural programs to eligible team members. Learn more at: ***************************** Minimum Qualifications: Minimum Education Work requires a thorough background in technical theatre normally acquired through a Bachelor's degree program in theatre or closely related field. Minimum Experience No experience beyond the degree is necessary; however, four years' experience in technical events support or theater production normally acquired through a special events technician or related position may be substituted for the degree. OR ANY OTHER EQUIVALENT COMBINATION OF RELEVANT EDUCATION AND/OR EXPERIENCE. Duke is an Equal Opportunity Employer committed to providing employment opportunity without regard to an individual's age, color, disability, gender, gender expression, gender identity, genetic information, national origin, race, religion, sex (including pregnancy and pregnancy related conditions), sexual orientation or military status. Duke aspires to create a community built on collaboration, innovation, creativity, and belonging. Our collective success depends on the robust exchange of ideas-an exchange that is best when the rich diversity of our perspectives, backgrounds, and experiences flourishes. To achieve this exchange, it is essential that all members of the community feel secure and welcome, that the contributions of all individuals are respected, and that all voices are heard. All members of our community have a responsibility to uphold these values. Essential Physical Job Functions: Certain jobs at Duke University and Duke University Health System may include essential job functions that require specific physical and/or mental abilities. Additional information and provision for requests for reasonable accommodation will be provided by each hiring department. Nearest Major Market: Durham Nearest Secondary Market: Raleigh

Benefits: Competitive salary Health insurance Paid time off Profit sharing Training & development Compensation and Benefits: Competitive Annual Salary Additional training/development opportunities Want to use your key eye for detail to full effect? While we can make the print look beautiful, it is often the installation of that print that can make or break the project. Primary Roles and Responsibilities: Complete site surveys prior to installation (to ensure the accuracy of measurements, etc.) Communicate with clients before, during, and after the installation (walk them through the process, timeframes, etc.); present a professional demeanor Install graphics to flat interior and exterior surfaces including walls, windows, floors, and ceilings Wrap vehicles (partial or full wraps) Cut and shape the graphics to fit each surface, heating and applying graphics, disassembling, and reassembling products during the application, using proper adherence and cutting techniques during the application Perform all necessary work to complete the installation; take photos of the work when completed Assist in production and finishing of graphics as directed. Work is both indoors and outdoors and requires everything from physical labor to detailed, artistic work Required Skills: 1+ years of experience installing a wide variety of large format sign and graphics projects such as dimensional letters, banners, post and panel signs, ADA signs, vinyl graphics (3M, Avery, Geek Wraps), vehicle lettering, and vehicle wraps, to name a few. Applicants should also have experience in Vinyl Production - Taping / Weeding / Masking Highly motivated with a great attitude; a problem-solver at heart Able to lift 30lbs and swing a 3lb hammer Compensation: $18.00 - $25.00 per hour Working at SpeedPro and in the large-format printing industry, gives you a chance to be creative. You will be hands-on, in the field, solving problems and meeting clients to make custom solutions every day. As a national brand, specializing in a variety of printed products, SpeedPro takes great pride in partnering with our long-term, satisfied clients. Our goal is to be considered an extension of each client's marketing team, and we collaborate with partners to determine the right solution for you and your business's end customer. At SpeedPro, we value the relationship between our clients and their customers and deliver quality work on time, every time. With a nationwide network of more than 130 studios, the same standard for excellence in printing, timeliness, and customer service is guaranteed. This is why we have an exceptional net promoter score with our clients of 96. Working at an independently owned and operated SpeedPro studio sets you up for a bright future. Studio employees experience a fast-paced work environment with new challenges and rewarding opportunities every day. If you are looking for a monotonous desk job, this is not the right job for you.