Manufacturing associate jobs in Corpus Christi, TX

Job Posting Start Date 10-20-2025 Job Posting End Date 01-02-2026Flex is the diversified manufacturing partner of choice that helps market-leading brands design, build and deliver innovative products that improve the world.A career at Flex offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but don't meet every bullet point, we encourage you to apply and join us to create the extraordinary.Job Summary To support our extraordinary teams who build great products and contribute to our growth, we're looking to add a Manufacturing Technician located in Dallas, Texas. Reporting to the Operations Excellence Manager, the Manufacturing Technician role is responsible for supporting production operations, process improvement, and product quality within a lean manufacturing environment. Products related to Relay Panels, Low Voltage Switchgear, Substation Buildings and Fabrication. Shift: 6:00 AM - 2:30 PM What a typical day looks like: Work closely with engineers, operators, and quality teams to set up equipment, conduct tests, perform troubleshooting, and ensure consistent manufacturing performance Maintain production standards and implement lean methodologies Support continuous improvement initiatives to optimize efficiency, reduce waste, and enhance product reliability Support Lean Implementation on the Shop Floor by assisting engineers in deploying 5S, standardized work, visual management, and workplace organization to improve safety, quality, and efficiency Conduct Time Studies and Process Observations to identify non-value-added activities, bottlenecks, and improvement opportunities within production lines Collaborate with Engineers and Operators to develop and sustain standardized work instructions, ensuring consistent performance and training alignment across shifts Participate in Kaizen Events and Continuous Improvement Projects, contributing hands-on support in process mapping, problem-solving, and implementation of quick wins Assist in Equipment Set-Up, Calibration, and Process Optimization to ensure machines run efficiently and within defined process limits, reducing downtime and variation Perform Root Cause Analysis and Corrective Actions for process deviations or quality issues using structured problem-solving tools (5 Whys, Ishikawa diagrams, PDCA) Support Visual Factory Development by maintaining dashboards, production boards, and andon systems that communicate real-time status and improvement metrics Perform rework and quality testing related to the production of parts, components, subassemblies and final assemblies in products related to Relay Panels, Low Voltage Switchgear and Substation Buildings The experience we're looking to add to our team: High school diploma or equivalent 4-6 years of experience as a manufacturing technician or related field Physical Requirements: Regularly required to stand, walk and reach with hands and arms Must be able to lift up to 10 pounds at a time Must have manual dexterity to handle small components Must have excellent hand-eye coordination Ability to differentiate between colored wires, tabs, and electronic components Must wear PPE, such as gloves, safety glasses, hard hat, and ear protection, while working on the production floor What you'll receive for the great work you provide: Full range of medical, dental, and vision plans Life Insurance Short-term and Long-term Disability Matching 401(k) Contributions Vacation and Paid Sick Time Tuition Reimbursement Job CategoryProduction Engineering Is Sponsorship Available? NoFlex is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. We do not discriminate based on: age, race, religion, color, sex, national origin, marital status, sexual orientation, gender identity, veteran status, disability, pregnancy status, or any other status protected by law. We're happy to provide reasonable accommodations to those with a disability for assistance in the application process. Please email accessibility@flex.com and we'll discuss your specific situation and next steps (NOTE: this email does not accept or consider resumes or applications. This is only for disability assistance. To be considered for a position at Flex, you must complete the application process first).

At Diamondback Industries, we are more than just a manufacturing company. We are a team of dedicated professionals who take pride in creating amazing, dependable, and consistent products that our customers can rely on. As the market leader in Energetics and innovator of the disposable setting tools, we are committed to providing the highest quality products and exceptional customer experience. Watch this in-depth, behind the scenes video from Titans of CNC Machining to see more! We understand that our success is a direct result of our team's hard work and dedication, which is why we offer full benefit packages (we cover almost 90% of the monthly cost!), 401k matching, and paid time-off to all of our employees. So, if you're looking for an exciting opportunity to join a rapidly expanding team, look no further than Diamondback Industries. UP to $16.50 per hour! Full benefits package & overtime opportunities! ENERGETICS MANUFACTURING ASSOCIATE Job Specifics: Duties are light-weight lifting and may include assembling, mixing, packing, and boxing materials. Work hours are Monday - Friday, 6:30 a.m. to 4:30 p.m. (Every other Friday may be a shorter work day) Working in a team environment, inside with one hour for lunch. We have one work location in Crowley/Fort Worth area convenient/close to I-35 or the Tollway. *Drug testing is required before hire and you must pass a standard ATF background check within the first 60 days. Must pass Bureau of Alcohol, Tobacco, Firearms, and Explosives (ATF) background check. *Compensation based on experience and years of service

Job Description "Bridging Innovation to Cure "Developing and manufacturing your cell therapies from benchtop to bedside" Cellipont Bioservices is growing, and we are looking for a Manufacturing Associate I who believe in the potential bridging client's discoveries to patient cures and who want to challenge the status quo and take Cellipont and its clients to the next level. The Manufacturing Associate I is an entry level role and will be responsible for assisting in the planning and timely execution of manufacturing operations for a cGMP-compliant state-of-the-art cell processing/clinical manufacturing facility with emphasis on primary cell isolation and cell culture in an aseptic processing environment. The Manufacturing Associate I is responsible for following the standard practices outlined for the operation of the facility in accordance with the regulatory requirements for the manufacture of materials for our clinical studies, clinical trials and products. THE ROLE Assists the operation of a state-of-the-art GMP cell manufacturing plant in accordance with FDA, ISO, Environmental Health & Safety, Human Resources, EMA regulations and other Quality System regulations, as applicable Ensures production area, processes and procedures are maintained in compliance with internal and external compliance and operating standards Conduct ancillary activities in support of processing functions, e.g. lab and equipment cleaning and maintenance, inventory management and stocking, preparing shipping/packaging materials Maintains a strong culture of safety, quality, accountability, cost efficiency, on time delivery and customer service Ensures facilities are maintained in a continuous state of readiness. Identifies and mitigates risks for the operation and timely brings to the attention of a supervisor. Ensures relevant manufacturing data are captured appropriately and accurately for supporting regulatory filings for clinical trials Inform Supervisor of equipment needs and supplies required to avoid interruption in processes tagging out/equipment for recalibration. Routine monitoring and troubleshooting of equipment, with appropriate escalation if necessary. Other tasks as assigned THE CANDIDATE Bachelors Degree in Life Sciences preferred, with demonstrated technical experience in Bioprocessing, Cell Line Engineering or Tissue Engineering. 0-1+ years of direct experience in cell manufacturing/commercial biologic drug manufacturing operations in a GMP environment 0-1+ years of direct experience working within manufacturing operations and leading by example; capable of helping to train other manufacturing technicians Understanding of GMP and GDP requirements Excellent time management and organizational skills, demonstrated ability to manage and prioritize multiple projects and meet deadlines Able to demonstrate willingness to problem solve and/or diagnose process/product/equipment problems Excellent oral and written communication skills. Strong technical writing ability required Must be highly motivated, follow oral and written instructions, communicate effectively, think logically, and thrive independently and/or in a fast-paced team environment Must be proficient in Microsoft Word and Excel. Experience in Microsoft Projects, Visio, and preferred Ability to work flexible hours and inconsistent schedules as necessary to meet production demands and timelines PHYSICAL DEMANDS While performing the duties of this job, the employee is frequently required to stand and/or sit for extended periods. The employee is occasionally required to walk; have high levels of hand/finger dexterity; climb or balance and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 25 pounds WORK ENVIRONMENT While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts; biological materials or caustic cleaning chemicals; strong magnets; and sensitive calibrated equipment. Noise level in the work environment is usually moderate A marginal amount of the work is completed in a clean-room environment; employees may be expected to work in clean room conditions for up to 4-6 hours at a time. While working in the area the gowning requirements are safety goggles, shoe covers, hood, gown, mask, boots and gloves. Working conditions can include standing for long periods of time. POSITION BENEFITS Opportunities for career growth within an expanding team Defined career path and annual performance review & feedback process Cross-functional exposure to other areas of within the organization Robust benefit package designed for unique Health & Wellness needs, including coverage for your furry family members 401K strong employer match Tuition Reimbursement Employee Referral Bonuses Flexible work schedules and PTO based on role/level, increasing 1 PTO day each year and paid holidays Gain experience in the cutting-edge cell therapy space "At Cellipont Bioservices, we look for candidates with an innate desire to serve. Our "family" approach ensures you will get the mentorship you need to develop a satisfying career here!" Notice to Agency and Search Firm Representatives Cellipont Bioservices is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Cellipont Bioservices employee by a third-party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Cellipont Bioservices. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral.

Since its spin-off in September 2025 AUMOVIO continues the business of the former Continental group sector Automotive as an independent company. The technology and electronics company offers a wide-ranging portfolio that makes mobility safe, exciting, connected, and autonomous. This includes sensor solutions, displays, braking and comfort systems as well as comprehensive expertise in software, architecture platforms, and assistance systems for software-defined vehicles. In the fiscal year 2024 the business areas, which now belong to AUMOVIO, generated sales of 19.6 billion Euro. The company is headquartered in Frankfurt, Germany and has about 87.000 employees in more than 100 locations worldwide. Job Description The position requires Manufacturing Associate II (Rework/Production Operator) being an active participant in an autonomous manufacturing team, actively providing and implementing ideas to improve their process. Manufacturing Associate II operators are expected to maintain their trainings and skill for reworking the product in compliance with industry standards with highest quality. Perform a wide variety of electronic rework tasks including soldering, swapping parts, populating the PCB, and verify the quality of rework per IPC (Institute for Interconnecting and Packaging Electronic Circuits) standards Perform standard work instructions given by Quality department, refer drawings, process change notifications to repair or modify assemblies. Stay up to date with IPC (610 H, 7711/7721), AOI (Automated Optical Inspection), and X-Ray certifications. Identify essential soldering aids, soldering tips and associated consumables and maintain necessary inventory. Follow established safety, production, and quality procedures Participate in the team's daily start-up communications meeting, assigns work, and establishes job rotation Maintain personal training documentation/status including any on-the job training Follow defined Standard Work Instructions (SWI) and provide input for improvement Perform workstation audits and inspections and follow-up on abnormalities Ensure individual compliance for all established policies and procedures Determine and react if operating conditions become abnormal Actively preserve normal conditions of equipment and/or processes Ensure team achieves daily 5S+1, Quality, Delivery, Kaizen, and Cost goals Employ various problem-solving techniques (5 Why, 8 D, Cause and Effect, and Fishbone Diagrams, etc.) to drive problems to permanent corrective action Participate in teams Kaizen activities to ensure continuous improvement within the work cell Full-Time (4 days working, 4 days off): B Shift Qualifications High School Diploma or GED Must be 18 years of age 0-2+ years of manufacturing or logistics experience required. Legal authorization to work in the U.S. is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening Relocation will not be provided 2+ years' experience as a rework technician working on electronics and circuit boards with maintaining the highest quality Ability to work with minimal supervision and strong time management skills Ability to read, write and speak English Preferred Qualifications: (Not required, will provide training) Experience working in a manufacturing environment Experience manufacturing electronic or semi-conductor products 5 years' experience as a rework technician working on electronics and circuit boards with maintaining the highest quality Physical Requirements: Position requires the ability to sit and stand for up to 10+ hours per day (and working with microscope Ability to lift up to 40 pounds unassisted. Must be able to Push, Pull Reach, Twist, Turn, Stoop, Walk, Stand for up to10+ hours. Additional Information All your information will be kept confidential according to EEO guidelines. EEO / AA / Disabled / Protected Veteran Employer. AUMOVIO offers equal employment opportunities to all qualified individuals, without regard to unlawful consideration to race, color, sex, sexual orientation, gender identity, age, religion, national origin, disability, veteran status, or any other status protected by applicable law. In addition, AUMOVIO complies with government regulations where they apply. To be considered, you must apply for a specific position for which AUMOVIO has a current posted job opening. Qualifying applications will be considered only for the specific opening(s) to which you apply. If you would like to be considered for additional or future job openings, we encourage you to reapply for other opportunities as they become available. Further, AUMOVIO provides reasonable accommodations to qualified individuals with a disability. Ready to take your career to the next level? The future of mobility isn't just anyone's job. Make it yours! Join AUMOVIO. Own What's Next. EEO-Statement: EEO / AA / Disabled / Protected Veteran Employer. AUMOVIO offers equal employment opportunities to all qualified individuals, without regard to unlawful consideration to race, color, sex, sexual orientation, gender identity, age, religion, national origin, disability, veteran status, or any other status protected by applicable law. In addition, as a federal contractor, AUMOVIO complies with government regulations, where they apply, including affirmative action responsibilities for qualified individuals with a disability and protected veterans. To be considered, you must apply for a specific position for which AUMOVIO has a current posted job opening. Qualifying applications will be considered only for the specific opening(s) to which you apply. If you would like to be considered for additional or future job openings, we encourage you to reapply for other opportunities as they become available. Further, AUMOVIO provides reasonable accommodations to qualified individuals with a disability. Ready to take your career to the next level? The future of mobility isn't just anyone's job. Make it yours! Join AUMOVIO. Own What's Next.

About us SpaceManager Closet is the fastest growing companies in the closet and home organization solutions industry in Houston. At SpaceManager Closets, we pride ourselves on working hard, enjoying what we do, and exceeding our customers' expectations. This is an exciting opportunity for a carpentry and wood working pro! Multiple Cabinet Manufacturing Jobs SpaceManager Closets has become the top rated custom closets and home organization systems companies in Houston. SpaceManager values its ability to deliver the best customer service possible and it shows - we've won multiple service awards from Angie's List, Best Picks, Houzz and others. The amazing SpaceManager Team makes all of these accomplishments possible. The ideal person is hard working and teachable, with an eye for detail. Previous experience in carpentry, closet or cabinet industry is preferred. We are looking for Experience with woodworking hand tools - nail gun, table saw etc. Running Edgebanders, Beam Saws, and CNC . Packing and Final Assembly Quality Control and Inspection Qualifications: High-End Cabinetry Manufacturing Cabinetry Assembly/Finishing Touch Up Experience with numerous hardware accessories Cabinetry Adjustment Hardware Installation Candidates should have various woodworking experiences Experience working in a production environment Problem-solving & Critical thinking Great Attitude Highly Motivated Great people skills High Standard of Customer Service We will provide tools if needed Ability to lift 50+ lbs. SpaceManager Closets provides custom designed and manufactured, functional and stylish home organizational systems. We started out building custom closet organizer systems 20 years ago and have since expanded our offering to include expertly crafted custom closet systems, custom home office cabinets, custom pantry closets, custom garage cabinets, garage organizers and epoxy flooring, wall beds or murphy beds, custom entertainment centers, wine rooms and solutions for a host of other rooms and spaces. We work directly with homeowners on their specific projects, but we are also trusted by several home builders and commercial customers in the Houston area to be their exclusive provider of home organizational systems

Department: Manufacturing Reports to: Manager, Manufacturing CTMC is a pioneering biotech joint venture, formed by National Resilience and MD Anderson Cancer Center, located in the heart of the Texas Medical Center. Our mission is to accelerate cell therapies from bench to bedside. We offer a wide range of cell therapy modalities, including CAR-T, TIL, and TCR-T. Our expert team collaborates closely with MD Anderson's research and clinical faculty, bringing impactful cell therapies to cancer patients. Since inception in May 2022, our team has filed eight INDs and have received approval, without delay, demonstrating our commitment to delivering innovative treatments to patients with speed and precision. Our alliance with National Resilience enables us to remain at the forefront of biomanufacturing practices, leveraging advanced technology and processes to deliver exceptional results. Our growing, state-of-the-art, 60,000 sq. ft. industrial facility in the Texas Medical Center is staffed by an integrated team of industry veterans and academic scientists who are passionate about bringing life-saving cures to patients. Our unique joint venture structure, with two highly established partners, provides us with the financial stability and long-term horizon to achieve our organizational goals. At CTMC, we value our employees and offer a variety of development opportunities within our novel corporate structure to inspire professional growth and satisfaction. We foster a team-first culture and a balanced work-life environment to ensure our staff is energized and engaged in our mission to accelerate cell therapies from bench to bedside for patients who need them. If you share our passion for advancing the frontiers of medical science with innovative therapeutics and want to join a highly dedicated team committed to delivering novel cures to patients, we invite you to submit your application. We look forward to hearing from you and exploring how your skills and expertise can help us achieve our mission. Responsibilities Perform routine or non-routine cleaning, kitting, documentation, processing, and materials procurement for the manufacturing department. Maintain aseptic and model exceptional technique during processing to ensure quality and integrity of cellular drug products. Assist with training staff on proper operations and documentation in cGMP cleanroom facilities. Operate standard cleanroom equipment: Incubators, BSCs, and Centrifuges. Operate the following Cell Therapy equipment: CliniMacs Prodigies, G-Rexes, Incubators, Cell Stacks, Cue, or Lovos. Independently troubleshoot and triage cross-functionally with quality partners. Provide input to develop SOP's for new and incoming equipment. Provide input and assistance in executing training for cleanroom personnel cGMP, best practices and awareness training related to working in a cleanroom environment. Establish a culture of continuous improvement, collaborative spirit, and dedication to safe workplace practices. Execute master batch production records in a timely manner and maintain accurate documentation with FDA's Good Manufacturing Practices, ensuring ALCOA+ principles, with real-time documentation. Request and prepare materials for manufacturing operations while maintaining proper inventory levels in the cleanroom at all times. Provide support for routine maintenance activities, such as performing a daily, weekly, or monthly cleaning of the clean rooms when required. Ensure transparent communication with staff, teams, support functions, and site leadership team, operating as a liaison between junior staff and management. Meet and report key performance indicators in alignment with Cell Therapy Manufacturing and CTMC goals. Other duties as assigned. Qualifications/Skills Bachelor's degree in scientific field, or equivalent education and experience. 3+ yr.'s experience in a related manufacturing environment (cell therapy or biotech) required. 3+ yr.'s experience with standard cleanroom equipment: Incubators, BSCs, and Centrifuges required. 3 + yr.'s previous experience with one or more of the following Cell Therapy equipment: CliniMacs Prodigies, G-Rexes, Waves/Xuris, Incubators, Cell Stacks, Cue, or Lovos preferred. Proficient with Microsoft Office: Word, Excel, Outlook, PowerPoint, and Teams. Previous GMP Experience required. Previous experience performing accurate calculations and lab measurements required. Previous experience with technical writing required. Able to understand and follow personnel flows, cleaning procedures, gowning requirements and other procedures defining requirements necessary to ensure cGMP compliant operations of cleanroom facilities. Able to troubleshoot cell processing operations and equipment. Meticulous attention to detail in terms of documentation, following procedure SOPs, and performing functions as it pertains to the Batch Record. Able to train and lead junior level Associates on all aspects of the manufacturing process for which the individual is an SME. Able to work a flexible schedule including nights, weekends, and holidays with short advance notice. Working Conditions, Equipment, Physical Demands The incumbent in this position works in an office environment. The incumbent in this position will use the following equipment and shall have the following physical demands: Equipment- Computer, printer, fax, and telephone. Physical Demands- Frequent sitting, standing, walking Carrying packages and moving bins and boxes, lifting up to 10 lbs. The physical demands and work environment that have been described are representative of those an employee encounters while performing the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions in accordance with the Americans with Disabilities Act. The above job description is an overview of the functions and requirements for this position. This document is not intended to be an exhaustive list encompassing every duty and requirement of this position; your supervisor may assign other duties as considered necessary.

J oin Immatics and shape the future of cancer immunotherapy ; one patient at a time! Immatics is at the forefront of immunotherapy innovation, working to harness the power of T cells to transform cancer treatment. Immatics is an exceptional clinical-stage biopharmaceutical company active in the discovery and development of T cells redirecting cancer immunotherapies. We use these powerful T cells to develop groundbreaking immunotherapies that target cancer cells. We are dedicated to transforming cancer treatment and improving patient outcomes through cutting-edge research and advanced TCR technology. Why Join Us? Innovative Environment: Help to pioneer advancements in cancer immunotherapy. Collaborative Culture: Be part of a diverse team dedicated to your professional growth. Global Impact: Contribute to therapies that make a lasting impact on patients globally. We are seeking a Manufacturing Associate II to support our CMC-GMP team. The Manufacturing Associate II will be responsible for performing complex, highly specialized and time sensitive technical cell manipulations and testing procedures on irreplaceable cellular products during clinical manufacturing. FLSA Classification: Hourly, Non-Exempt Schedule: 1230 - 2100; Monday to Friday; On-site Reports to: Associate Manufacturing Manager Location: 13203 Murphy Road Suite 100 Stafford, TX 77477 What You'll Do: As a Manufacturing Associate II, you will play a key role in supporting our manufacturing operations: Knowledge of current cGMP. Fulfill the operator and verifier roles in performing cell growth and manipulation procedures such as cell enrichment, cell culture, cellular product cryopreservation, cell product thaw/wash. Accurately perform procedures in compliance with FDA's Good Laboratory Practices, Good Manufacturing Practices, Good Tissue practices, as well as standards set by other accreditation agencies including but not limited to FACT, CAP, and CLIA. Adhere to ALCOAC++ and cGDocP requirements while accurately performing procedures and maintaining documentation in compliance with SOPs. Document deviations and events, notify supervisor and quality management personnel in timely manner, and assist in investigation of root cause and any required corrective actions. Responsible for aseptic handling of reagents and products to ensure the integrity and sterility of cellular products until final infusion to the patient. Must adhere to special cleaning and gowning requirements for the facility requiring specialized gowning such as masks, sterile jumpsuits, hair and shoe covers. Ability to work productively and to participate in a highly creative and fast-paced environment. Secondary Functions: Independently perform calculations to determine cell viability, dilutions, and cell concentrations. Completes all appropriate logs and trackers. Maintains GMP cleanliness: autoclaving, bleaching liquid waste, removing waste, general cleanliness and organization of the office and facility. Maintains knowledge regarding donor evaluation, screening and testing, labeling and product acceptability and release criteria. Conducts activities to support study plans, and IQ/OQ/PQs. Provide input or feedback regarding change controls, WI, SOPs, study plans, reports, deviations, OOS/OOE, and CAPA's as directed. Performs routine equipment maintenance and troubleshooting. Prepares and presents manufacturing summaries, as needed Required Experience and Education: Bachelor's degree in biology, Biochemistry, Biotechnology or another related field. Two (2) to Four (4) years of cell therapy manufacturing experience. Preferred Experience and Education: Bachelor's degree in biology, Biochemistry, Biotechnology or another related field. Four (4) years of cell therapy manufacturing experience. Competencies: Independent Working- routine tasks with limited supervision; non-standard tasks with close supervision. Communication- clear and efficient verbal and written communication; common courtesy; interaction mainly limited to own team (peers and supervisor) Problem Solving- ability to identify, deeply analyze and communicate problems; basic ability to develop suitable solutions. Critical Thinking- basic reflection on standard processes; identification of basic need and room for improvement within own or narrow scope. Initiative- high degree of initiative and intrinsic motivation to exceed basic expectations of own tasks and responsibilities. Organizational & Prioritization Skills- basic organization skills to structure own daily tasks according to predefined work packages, schedule and standard lab processes; prioritization in close interaction with supervisor. Coachability- receive pre-defined training essential for area of responsibility; high responsiveness to constructive criticism and basic ability to autonomously reflect on required improvements; timely implementation of suggested improvements. Leadership Skills, Training & Supervision- basic leadership skills for on-the-job trainings and guidance/support of (new) team members (e.g. providing and receiving feedback, empathy, honesty, reliability); train, instruct and coordinate E level; train D & C level during onboarding. Work Environment: Typical office environment with moderate noise levels (~20% of work hours). Uses phone, computer, office equipment and supplies on a regular basis. cGMP clean room spaces and facilities (~80% of work hours). Grade A/B/C/D GMP environment with associated facility noise levels. Uses cleanroom phone, computer, variety of equipment and reagent/supplies. General unclassified laboratory spaces, as needed. Common laboratory equipment and noise levels. While performing the duties of this job, the employee routinely handles blood components and is occasionally exposed to temperatures between -196°C and 40°C, liquid nitrogen, liquid nitrogen vapor, dry ice, and carbon dioxide. Travel required: Travel may be between the office building and manufacturing facility on a daily basis. Physical demands: Communicating Verbally - expressing or exchanging ideas by means of the spoken word to impart oral information to others to convey detailed spoken instructions or other workers accurately, loudly or quickly. Hearing - the ability to hear, understand, and distinguish speech and/or other sounds one-on-one, group or conference, telephone, and other sounds. Keyboarding - entering data or text into a computer or other machine by means of a keyboard. Devices include a traditional keyboard, 10 key-pad, touch screens and others. Lifting - raising or lowering an object (up to 25 lbs) from one level to another (includes upward pulling). Carrying is to transport an object - usually by holding it in the hands or arms but may occur on the shoulder. Near Visual Acuity - clarity of vision at approximately 20 inches or less (working with small objects, reading small print, including the use of computers). Pushing - Exerting force upon an object so that the object moves away from the object. Pulling - Exerting force upon an object so that the object moves toward the force. Sitting - remaining in a sitting position for at least 50% of the time. Standing/Walking - remain on one's feet in an upright position at a workstation. Stooping - occasional bending the body downward and forward by bending the spine at the waist - requiring full use of the lower extremities and back muscles. Work authorization/security clearance requirements: Legal eligibility to work in the United States is . Immatics participates in E-Verify and all new employees will be subject to the Department of Homeland Security requirements for employment. Affirmative Action/EEO statement: Immatics is an equal opportunity employer. All employment decisions including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs. We do not discriminate on the basis of race, color, religion, national origin, ethnicity, marital status, age, physical or mental disability, medical conditions, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. What do we offer? At Immatics, we believe in investing in our team's health, safety and well-being. Here's what you can expect if you join Immatics Comprehensive Benefits: Competitive rates for Health, Dental, and Vision Insurance 4 weeks of Paid Time off, granted up front each year and prorated for first and last year of employment. Sick Time Off - 56 hours 12 Paid Holidays 100% Employer-Paid Life Insurance up to at 1x annual salary, up to 100K ( club together) 100% Employer Paid Short- and Long-Term Disability Coverage 401(k) with Immediate Eligibility & company match… You are eligible for 401(k) plan participation as of your first paycheck. The company will match 100% of your contributions up to 3% of your base salary for the first two years of employment, 4% for years 2-3 of employment, and up to 5% of your salary from the fourth year onward of continued employment. Partially paid Parental Leave for eligible employees. (3 weeks) Additional voluntary employee paid coverages including Accident, Hospital Indemnity, and Critical Illness Employee Paid Identity Theft Protection and Pet Insurance. Professional Growth: Opportunities to work with leading experts in the field of T-cell immunotherapy. Company provided learning and development opportunities Fast paced, high demand collaborative and dynamic environment.

Job Description The Manufacturing Associate will perform routine functions in one, or more, of the following areas: Clifford, UpGrade, Powder Coating, Welding, Saw, Hardware or Receiving. • Perform assigned duties while adhering to all site safety rules • Perform all assigned duties with maximum efficiency being utilized at all times • Perform all assigned duties while maintaining, or surpassing, defined quality expectations • Maintain clean work area as defined by plant housekeeping standards • All other duties as assigned Required Knowledge, Skills, and Abilities: • Regularly required to stand, climb stairs and move around the facility for up to 12 hours. • Ability to regularly lift and/or move up to 50 pounds and occasionally lift and/or move up to 70 pounds • Able to operate general tools/equipment that is necessary to perform the task that has been assigned. • Load/ unload, move fence materials • Ability to work in an environment that is often loud, dusty, and experiences extreme temperatures • Ability to be at work everyday, on-time as scheduled and complete the entire scheduled shift • Manage different stages of the production line by being actively involved in each procedure • Able to ensure quality control of the items being manufactured, making sure that meet the requirements from the WO and making sure that the finish good from that process meet the company quality standards. (visual inspection) • Must be able to perform clerical task to keep detailed record of WO and completions, must be able to organize WO by due date and priority, collecting all relevant documents required for employees to make a precise product. • Very good eye for detail, accountable, ability to work as part of a team. • Bi-Lingual (English/Spanish) is a plus • Able to work OT and weekends. Based on production demand requirement

Diasorin is a global leader in diagnostic solutions, pushing the boundaries of science and technology to create cutting-edge tools that improve healthcare worldwide. With a legacy spanning over 50 years, we've earned our reputation for excellence by developing innovative diagnostic assays and instruments that are trusted by healthcare providers around the world. Our broad offering of diagnostic tests and Licensed Technology solutions, made available thanks to ongoing investments in research, positions us as the player with the widest range of specialty solutions in the sector and identifies us as the "Diagnostics Specialist." Why Join Diasorin? * Impactful Work: When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world. * Global Reach & Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry. Diverse and Inclusive Culture: We believe in the strength of diversity, and our inclusive culture reflects this commitment. We value your unique perspective and offer a supportive, collaborative environment where everyone can thrive. Join Our Team: If you're passionate about innovation, diversity, and making a positive impact on healthcare, Diasorin is the place for you. We're looking for passionate and talented individuals who are ready to embrace new challenges and drive healthcare solutions forward. Are you ready to be part of a dynamic team that's shaping the future of diagnostics? Join Diasorin and become a catalyst for change in the world of healthcare. Apply today and be a part of our exciting journey toward a healthier, more connected world. Together, we can make an impact! Job Scope The Manufacturing Associate I, Reagents will be responsible for delivering manufacturing requirements against production schedule within a focused manufacturing operation and/or product segment. Work schedule may include alternate shifts, participating in manufacturing processes to support new product design transfer, stability program, process development, equipment validations, process validations and investigations and resolution of product/process issues and performing maintenance and calibration of Manufacturing measuring and monitoring devices as well as maintaining the integrity of work areas. Key Duties and Responsibilities * Deliver manufacturing requirements and attainment of production schedule for standard inventory, build-to-order, and contract manufacture market products. * Deliver manufacturing requirements for qualification/processing of incoming materials, production intermediates, and stability samples. * Deliver timely and accurate completion of manufacturing sections of process documentation and related business system transactions. * Perform scanning and archiving of quality records * Deliver timely and accurate completion of inventory cycle counts * Support design transfer and integration of new products and processes. * Support process development and process improvement projects. * Participate in the execution of equipment and process validations. * Support investigations and resolution of findings impacting the Reagent Manufacturing Organization identified through audits, non-conformances, corrective/preventive actions, or customer complaints escalation. * Deliver timely maintenance and calibration of assigned Manufacturing measuring and monitoring devices. * Monitor select non-inventory supplies, maintain focused supplies, and generate purchase requisitions as needed. * Maintain cleanliness and integrity of manufacturing laboratory and storage areas. * Participate in applicable departmental and interdepartmental training; maintain current and effective training to standard operating procedures, work instructions, and applicable changes affecting the Reagent Manufacturing. * Assist in establishing annual performance goals; fulfill performance goals * Maintain effective and professional multi-level organizational interfaces. * Maintain personal compliance and facilitate departmental compliance with the Quality System. * Adhere to safety, disposal, and gowning requirements * Other duties as assigned. Education, Experience, and Qualifications * Associate's Degree Associates degree or equivalent work experience in the field of Chemistry, Life Sciences, Biotechnology, or Medical Technology related field * 1+ Years At least 1 year of relevant experience in a Life Sciences, Chemistry, or Medical Technology related industry What we offer Receive a competitive salary and benefits package as you grow your career at DiaSorin. Join our team and discover how your work can impact the lives of people all over the world. Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status, and will not be discriminated against on the basis of disability. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and Canada and to complete the required employment eligibility verification document form upon hire. Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities. If you are a US or Canada candidate and require assistance or accommodation during the application process, please contact the North America Talent Acquisition Team at ********************* or ************** to request an accommodation. The above job description is intended to describe the general content, identify the essential functions, and set forth the requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Diasorin reserves the right to modify or amend this job posting as needed to comply with local laws and regulations. Please note that offers of employment at Diasorin may be contingent upon successful completion of a pre-employment background check and drug screen, subject to applicable laws and regulations. This position is not eligible for partnership with a third-party search firm vendor without expressed, written consent from the Diasorin Human Resources Department. Nearest Major Market: Austin

About CTMC CTMC is a pioneering biotech joint venture, formed by National Resilience and MD Anderson Cancer Center, located in the heart of the Texas Medical Center. Our mission is to accelerate cell therapies from bench to bedside. We offer a wide range of cell therapy modalities, including CAR-T, TIL, and TCR-T. Our expert team collaborates closely with MD Anderson's research and clinical faculty, bringing impactful cell therapies to cancer patients. Since inception in May 2022, our team has filed eight INDs and have received approval, without delay, demonstrating our commitment to delivering innovative treatments to patients with speed and precision. Our alliance with National Resilience enables us to remain at the forefront of biomanufacturing practices, leveraging advanced technology and processes to deliver exceptional results. Our growing, state-of-the-art, 60,000 sq. ft. industrial facility in the Texas Medical Center is staffed by an integrated team of industry veterans and academic scientists who are passionate about bringing life-saving cures to patients. Our unique joint venture structure, with two highly established partners, provides us with the financial stability and long-term horizon to achieve our organizational goals. At CTMC, we value our employees and offer a variety of development opportunities within our novel corporate structure to inspire professional growth and satisfaction. We foster a team-first culture and a balanced work-life environment to ensure our staff is energized and engaged in our mission to accelerate cell therapies from bench to bedside for patients who need them. If you share our passion for advancing the frontiers of medical science with innovative therapeutics and want to join a highly dedicated team committed to delivering novel cures to patients, we invite you to submit your application. We look forward to hearing from you and exploring how your skills and expertise can help us achieve our mission. Responsibilities Perform routine or non-routine cleaning, kitting, documentation, processing, and materials procurement for the manufacturing department. Maintain aseptic and model exceptional technique during processing to ensure quality and integrity of cellular drug products. Assist with training staff on proper operations and documentation in cGMP cleanroom facilities. Operate standard cleanroom equipment: Incubators, BSCs, and Centrifuges. Operate the following Cell Therapy equipment: CliniMacs Prodigies, G-Rexes, Incubators, Cell Stacks, Cue, or Lovos. Independently troubleshoot and triage cross-functionally with quality partners. Provide input to develop SOP's for new and incoming equipment. Provide input and assistance in executing training for cleanroom personnel cGMP, best practices and awareness training related to working in a cleanroom environment. Establish a culture of continuous improvement, collaborative spirit, and dedication to safe workplace practices. Execute master batch production records in a timely manner and maintain accurate documentation with FDA's Good Manufacturing Practices, ensuring ALCOA+ principles, with real-time documentation. Request and prepare materials for manufacturing operations while maintaining proper inventory levels in the cleanroom at all times. Provide support for routine maintenance activities, such as performing a daily, weekly, or monthly cleaning of the clean rooms when required. Ensure transparent communication with staff, teams, support functions, and site leadership team, operating as a liaison between junior staff and management. Meet and report key performance indicators in alignment with Cell Therapy Manufacturing and CTMC goals. Other duties as assigned. Qualifications/Skills Bachelor's degree in scientific field, or equivalent education and experience. 3+ yr.'s experience in a related manufacturing environment (cell therapy or biotech) required. 3+ yr.'s experience with standard cleanroom equipment: Incubators, BSCs, and Centrifuges required. 3 + yr.'s previous experience with one or more of the following Cell Therapy equipment: CliniMacs Prodigies, G-Rexes, Waves/Xuris, Incubators, Cell Stacks, Cue, or Lovos preferred. Proficient with Microsoft Office: Word, Excel, Outlook, PowerPoint, and Teams. Previous GMP Experience required. Previous experience performing accurate calculations and lab measurements required. Previous experience with technical writing required. Able to understand and follow personnel flows, cleaning procedures, gowning requirements and other procedures defining requirements necessary to ensure cGMP compliant operations of cleanroom facilities. Able to troubleshoot cell processing operations and equipment. Meticulous attention to detail in terms of documentation, following procedure SOPs, and performing functions as it pertains to the Batch Record. Able to train and lead junior level Associates on all aspects of the manufacturing process for which the individual is an SME. Able to work a flexible schedule including nights, weekends, and holidays with short advance notice. Working Conditions, Equipment, Physical Demands The incumbent in this position works in an office environment. The incumbent in this position will use the following equipment and shall have the following physical demands: Equipment- Computer, printer, fax, and telephone. Physical Demands- Frequent sitting, standing, walking Carrying packages and moving bins and boxes, lifting up to 10 lbs. The physical demands and work environment that have been described are representative of those an employee encounters while performing the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions in accordance with the Americans with Disabilities Act. The above job description is an overview of the functions and requirements for this position. This document is not intended to be an exhaustive list encompassing every duty and requirement of this position; your supervisor may assign other duties as considered necessary.

Build a Career from the Ground Up - Join Western Pacific as a Manufacturing Associate At Western Pacific, we don't just build doors-we build careers. Our entry-level Manufacturing Associate role is where many of our current supervisors and managers got their start. We believe in mentoring, growing, and promoting from within-a philosophy that has helped shape a culture of loyalty, development, and long-term success. With over 40 years of leadership in the door and window distribution business, we're a family-owned and locally operated company that values dedication, teamwork, and individual growth. When you join us, you're joining a team that's invested in your future. Why This Role Matters: · You won't be the first to rise through the ranks-many of our leaders began in this exact position. · Our leadership team is hands-on, offering mentorship and support to those who show initiative and reliability. · As we continue to grow, entry points into our leadership pipeline are limited-this is your chance to get and build a career. · You give us your effort and dedication; we give you the tools, training, and opportunities to succeed. What You'll Do as a Manufacturing Associate: · Set up your work area at the start of your shift and maintain a clean, safe environment · Use hand and power tools to pre-hang doors and pull millwork for our customers · Machine and assemble interior and exterior door frames · Select and prepare the right components for each door build or millwork package · Inspect products to ensure top-tier quality · Support team operations and assist in other areas as needed Who You Are: · A team player with a positive attitude and strong work ethic · Comfortable with repetitive, detail-oriented tasks and hands-on assembly work · Able to lift up to 75 lbs. regularly and work on your feet for long shifts · Committed to safety, reliability, and showing up ready to contribute · College or High school diploma. GED accepted · Basic math and tape-measuring skills required · Prior woodworking or manufacturing experience is a plus-but not required Work Environment: You'll be working in a fast-paced manufacturing facility with exposure to machinery, dust, loud noise, and temperature fluctuations. We provide all necessary PPE and foster a culture of safety and teamwork. Expect to be on your feet for 8-10 hours a day, lifting and moving materials throughout your shift. Your Opportunity Starts Here: We believe that hard work should lead somewhere. If you're looking for more than just a job-if you're looking for a career with mentorship, advancement, and purpose-then this is your moment. Join Western Pacific and take the first step toward a future you can build with us. Apply today -openings are limited, and we're excited to meet our next great team member. Requirements Who You Are: · A team player with a positive attitude and strong work ethic · Comfortable with repetitive, detail-oriented tasks and hands-on assembly work · Able to lift up to 75 lbs. regularly and work on your feet for long shifts · Committed to safety, reliability, and showing up ready to contribute · College or High school diploma. GED accepted · Basic math and tape-measuring skills required · Prior woodworking or manufacturing experience is a plus-but not required Work Environment: You'll be working in a fast-paced manufacturing facility with exposure to machinery, dust, loud noise, and temperature fluctuations. We provide all necessary PPE and foster a culture of safety and teamwork. Expect to be on your feet for 8-10 hours a day, lifting and moving materials throughout your shift. Your Opportunity Starts Here: We believe that hard work should lead somewhere. If you're looking for more than just a job-if you're looking for a career with mentorship, advancement, and purpose-then this is your moment. Join Western Pacific and take the first step toward a future you can build with us. Apply today -openings are limited, and we're excited to meet our next great team member.

Job Purpose Tired of being treated like a number instead of a person? You show up, put in the work, and hit your goals-but no one says thank you. No one notices when you stay late or go the extra mile. If you're ready for a workplace where effort actually matters and people have your back, Wisenbaker is ready for you. Your Mission: As a Manufacturing Associate, you're not just “on the line.” You're the heartbeat of our production. Your precision, hustle, and teamwork keep us on schedule and customers happy. You'll be trained, supported, and recognized-because you're not just filling a spot. You're building a future. This is hands-on work with real impact. If you take pride in doing things right and want to grow with a company that values hard work and loyalty, you've found your match. Primary Duties & Responsibilities What You'll Be Doing (And Owning Like a Pro): Operate machinery and tools to produce high-quality products Follow safety protocols and work instructions to meet daily targets Collaborate with your team to troubleshoot and solve problems Keep your workspace clean and organized Communicate any issues or improvement ideas-your voice matters here Qualifications & Required Skills What We're Looking For: Previous experience in manufacturing or production is helpful but not required; in cabinetry is a plus-but a strong work ethic is a must! A sharp eye for detail and the ability to work with speed and accuracy A willingness to learn new skills and follow instructions with precision Team-player mentality with the ability to work independently when needed Basic mechanical know-how and problem-solving abilities and tape measure reading About the Company Wisenbaker Builder Services is a family-owned industry leader in stylish, on-trend interior finishes for residential builders. As one of the nation's largest providers of flooring, cabinets, countertops, and window coverings, we take pride in delivering quality craftsmanship and exceptional service. Recognized as a Great Place to Work in 2024, we foster a collaborative and innovative environment where our team thrives. We believe in taking care of our people, offering competitive pay, profit sharing, health benefits, retirement plans, paid time off, and growth opportunities. At Wisenbaker, your success matters, and we're committed to helping you build a rewarding career. Job Type Full-Time

Production Specialists work in a dynamic, creative and fast-paced environment to create and assemble sign and graphic products for many different business applications. Creative work is performed within the FASTSIGNS Center sign production area that is fully equipped with top-of-the-line sign-making equipment. Position requirements include cutting printed graphics using a variety of wall cutters, saws, and Exacto blades, as well as applying the product to substrates. The Production Specialist may be required to work in the field performing installations to vehicles, and building interiors and exteriors using a ladder or mechanical lift system. Careful attention to detail utilizing work orders that outline specifics for each custom order is paramount. The ideal candidate will be self-motivated, with problem-solving skills who pays very close attention to accuracy and detail. Comprehensive training in all aspects of this position will be provided. If this describes you, we encourage you to apply! Compensation: $20,000.00 - $60,000.00 per year At FASTSIGNS, every day is unique and presents exciting opportunities, including new ways to use your talent and grow your skills. We have a large network of independently owned locations - both locally and internationally - who offer competitive pay and ongoing training opportunities. Are you ready to plan for your future? Discover your next career. Make your statement. Learn more by exploring the positions offered by FASTSIGNS centers. This franchise is independently owned and operated by a franchisee. Your application will go directly to the franchisee, and all hiring decisions will be made by the management of this franchisee. All inquiries about employment at this franchisee should be made directly to the franchise location, and not to FASTSIGNS Corporate.

In this role you would have the responsibility for performing various functions to manufacture and assemble jewelry items in a manufacturing environment. We offer skills training to teach you the skills you need to be successful - no prior jewelry manufacturing or assembly experience required. 1st Shift Schedule: Monday - Friday; 8 AM - 4:30 PM WHAT YOU WILL BE DOING * Perform manufacturing processes as needed in up to three (3) Manufacturing skills. Associate will be required to learn and achieve one (1) skill within 6 months of employment with no more than two (2) skill failures and a total of three (3) skills within 3 years of employment, with no more than three (3) skill failures. * NOTE: Opportunities for all skills training based on business need and meeting pre-requisites. ALL SKILLS Bench Finished Goods Prebench Handmade Hand Assembly Casting Mech Finish Mold Making - Basic Polish Gemstone Setting Wax Injection Rework Tree Setup Laser Operation WHAT YOU'LL NEED * Ability to read, write and speak English fluently including, but not limited to, verbally communicating with plant personnel regarding work processes and work assignments. * Ability to read and understand written work processes, safety instructions, forms, training materials, etc. * Ability to complete production forms. * Ability to perform basic formulas such as addition, subtraction, multiplication, division, counting and totals. * Ability to accurately determine weights and measurements. * Ability to pass a background check as well as an alcohol, controlled substance, and illegal drug screen that meets Company standards before beginning regular employment. Preferred Qualifications * Basic computer or tablet operating skills preferred.

Every day, Kelly Services connects professionals with opportunities to advance their careers.In addition to working with the world's most recognized and trusted name in staffing, Kelly employees can expect: Competitive pay Paid holidays Year-end bonus program Portable 401(k) plans Recognition and incentive programs Access to continuing education via the Kelly Learning Center Kelly Services is a U.S.-based Fortune 500 company.With our global network of branch locations, we are uniquely positioned to provide our customers with international staffing support and our employees with diverse assignments around the world. Job Description Food Manufacturing Associates - Garland, TX Available Shifts: 1st Shift: $9.50/hour - Monday-Friday 7 am - 3:30 pm 2nd Shift: $9.75/ hour - Monday's 10am to 9:30 pm Tuesday through Friday 3 pm to 11:30pm 3rd Shift: $10.00/ hour - Monday's 9pm - 7:30 am, Tuesday-Friday 11pm - 7:30 am This position generally works 40 hours per week, though hours scheduled can vary slightly with more or less hours based on production needs, weekends may be required. Duties: Food Manufacturing Associates are responsible for providing supplies, placing of package components into specified tray compartments, finished package inspection, grading for quality defects, placing finished packages into a carton, taping the carton and palletizing the cartons. All duties performed within specific quality/GMP procedures. Also responsible for keeping a clean workstation, which includes removing re-work and trash from the area. Responsible for inspecting packages exiting from the Mahaffey-Harder tray sealer for all packaging and observable supply defects. Identify and grade any rejects resulting from the Adco cartoner, including code date problems. Qualifications Requirements: Must have your own steel toed footwear Must be able to lift up to 25 lbs repeatedly Drug test and Background check required Production experience preferred, but not required Additional Information Important: Please call Azura Jalil at 520-235-8459 to phone interview. Leave a message with your name and phone number.

American Packing & Gasket (APG) is seeking a Manufacturing Specialist to join our dynamic production team. This role is responsible for fabricating, assembling, and inspecting precision components used in fluid sealing, conveyance, and industrial applications. You will work closely with our engineering and quality teams to ensure every product meets our high standards of accuracy, safety, and compliance. If you enjoy hands-on work, take pride in producing high-quality parts, and thrive in a fast-paced manufacturing environment, this position is for you. Key Responsibilities Manufacturing & Fabrication Operate machinery, cutting tools, and equipment to fabricate gaskets, seals, and other custom components to exact specifications. Follow CAD/CAM drawings, technical prints, and work instructions to ensure precision manufacturing. Utilize hand tools, dies, and templates for custom parts fabrication. Assembly & Production Perform light assembly of components, subassemblies, and finished products. Package and label finished goods per customer and quality requirements. Collaborate with cross-functional teams to ensure efficient production flow. Quality Control & Safety Inspect parts for dimensional accuracy, material integrity, and quality compliance. Document measurements, lot codes, and inspection results for traceability. Follow all safety protocols, including proper handling of materials and use of PPE. Collaboration & Continuous Improvement Communicate effectively with supervisors, engineers, and quality teams to resolve production challenges. Suggest improvements to processes and workflow to enhance productivity and reduce waste. Maintain a clean and organized work area in compliance with ISO 9001 standards. Requirements 1+ years of experience in manufacturing, assembly, or a related field. Basic mechanical aptitude and familiarity with hand tools and measuring instruments (calipers, micrometers, etc.). Ability to read and interpret technical drawings and work instructions. Strong attention to detail and commitment to quality. High school diploma or equivalent. Preferred Experience in gasket fabrication, plastics, industrial sealing, or light assembly environments. Familiarity with CAD/CAM systems or CNC equipment. Knowledge of ISO 9001 quality systems. Physical & Work Environment Requirements Ability to stand, walk, bend, and lift up to 50 lbs for extended periods. Comfortable working in a production environment with moderate noise and machinery. Willingness to wear required PPE, including safety glasses and gloves. Salary Description 15.00 per hour

Dandy is transforming the massive and antiquated dental industry-an industry worth over $200B. Backed by some of the world's leading venture capital firms, we're on an ambitious mission to simplify and modernize every function of the dental practice through technology. As we expand our reach globally, Dandy is building the operating system for dental offices around the world-empowering clinicians and their teams with technology, innovation, and world-class support to achieve more for their practices, their people, and their patients. ENTRY LEVEL: NO EXPERIENCE REQUIRED! About the Role We are looking for entry level employees to join our growing manufacturing team! You will be responsible for operating our software(s) to ensure that orders are fabricated at the highest quality standards per customer deadlines. This role will require accurate shade distinction and color matching. If you're looking to help disrupt an industry status quo and take lead in building and scaling a “Gold Standard Department” per aggressive growth targets, this is the right place for you! We don't just want to offer you a job, we want to help you build a career by providing you with future opportunities for growth. Shift times: Day (6am-2:30pm) Swing (2pm - 10:30pm) Night (10pm-6:30am) What You'll Do Operate Quickly: Directly operate our software(s) to orient and properly support dental products (e.g., crown, bridge, abutment) in a fast-paced environment Drive Improvements: Serve as the go-to individual with firsthand insights on workflow, equipment, and capacity improvement opportunities to help drive high quality products Problem Solve: Roll up your sleeves to quickly troubleshoot and solve process, equipment and/or technology issues as you operate within a large scale and fast paced dental lab Quality Adherence: Uphold strict manufacturing quality standards (e.g., nesting operating procedures) and lead by example. High quality is key to efficient scalability! Collaborate: Work with other team members to identify and quickly address bottlenecks What We're Looking For High school diploma or GED equivalent 0-2+ years of experience in a fast-paced environment Must be able to read, write, speak and understand English Ability to sit for extended periods of time Passion for tackling problems and breaking them down into smaller manageable steps High level of comfort with digital tools and technology Very high attention to detail and organizational skills Team player attitude and willingness to help others to help the team exceed expectations Natural curiosity and ability to learn new concepts, tools, and workflows quickly Strong self-motivation, self-direction, and ability to prioritize Excellent communication and listening skills Bonus Points For Worked in a dental lab Outstanding professional references to share Relentlessly positive attitude, strong sense of humor, and the ability to have fun at work Req ID: J-271 For full-time positions, Dandy offers a wide range of best-in-class, comprehensive, and inclusive benefits tailored to each country where we operate. Our local benefits packages typically include healthcare, dental, mental health support, parental planning resources, retirement savings options, and generous paid time off-ensuring our team members are supported no matter where they live and work. Dandy is proud to be an equal-opportunity employer. We are committed to building a diverse and inclusive culture that celebrates authenticity to win as one. We do not discriminate on the basis of race, religion, color, national origin, gender, gender identity, sexual orientation, age, marital status, disability, protected veteran status, citizenship or immigration status, or any other legally protected characteristics. Dandy also fully complies with the Americans with Disabilities Act (ADA). We are dedicated to embracing challenges and creating an accessible, inclusive workplace for all individuals. If you require any accommodations for your interview or have any questions beforehand, rest assured that we will do everything we can to meet your needs. Visit Dandy Careers for more!

Houston, TX 77067 Temp to Hire We are seeking a reliable Manufacturing & Assembly Technician to cut materials, assemble components, and support daily production and shipping operations. This hands-on role requires attention to detail, the ability to follow directions, and physical stamina. The environment is fast-paced and non-climate controlled. Responsibilities Cut rubber materials using measuring tools and verbal/written instructions Complete 150+ lines per day with accuracy Operate tools and equipment for fabrication and light assembly Package and ship finished products as needed Perform quality checks and maintain accurate records Keep work area clean and organized (ISO 9001 environment) Required 1+ year experience in manufacturing or assembly Comfortable lifting 40-45 lbs occasionally (with assistance) Able to read technical drawings and use basic measuring tools Must pass a 7-year background check and drug test Forklift experience a plus No specific dress code-closed-toe shoes required Comfortable working in a non-climate controlled environment

Job Description Company Overview: Ethos Pet Brands is the parent company of Natural Balance and Canidae pet brands. By joining forces under Ethos Pet Brands, these premium pet food brands strengthen their commitment to delivering the highest quality nutrition. We believe in the power of strong brands to connect with pet parents and create meaningful experiences. Employees working in manufacturing will report to the shift manager. We are hiring employees on first, second, and third shifts. Due to the scope and needs of manufacturing operations, this position is an onsite-based position and is not eligible for remote work. The key responsibilities and duties of this position include, but are not limited to: Routine checks and preventative maintenance of equipment Efficient completion of final assembly and then packaging processes if required Startup and shutdown machinery as necessary Product labeling and inspection of final product, including correct bags, seals, etc. Maintaining cleanliness of equipment and work area according to 5S setup Reporting issues when they arise Quality checks of their equipment, process, or product in accordance with the site's quality requirements Other duties as assigned MINIMUM QUALIFICATIONS GED, High School diploma or equivalent Excellent written and verbal communication skills Able to multitask in a fast pace environment Able to be flexible and work overtime Good physical stamina and keen attention to detail Strong knowledge of heavy-duty and high-speed machinery Good understanding of production procedures and best practices Excellent knowledge of safety methods and hazard regulations Must work well with others and be a team player Must have experience in a manufacturing environment Must be willing to submit a background check and pre-employment drug screening Must be eligible to work in the US PREFERRED QUALIFICATIONS Ability to read manuals, blueprints, and handbooks Forklift certified ESSENTIAL FUNCTIONS Ability to push, pull, carry, or lift up to 50 lbs. Ability to remain in a stationary position for up to 8 hours Ascend/descend a ladder or stairs daily Ability to operate a computer and other office technology Occasionally position self to access low spaces Ability to observe details at close range Must be able to work in area with exposure to loud noises Ability to work safely in areas with hazardous equipment and materials Must be able to relay accurate information via multiple communication vehicles including verbal and written mechanisms Must be able to work in extreme hot and cold temperatures Ethos is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. All employment is decided on the basis of qualifications, merit, and business need.