Manufacturing helper jobs near me - 87 jobs

Job Description Oberfields, part of The QUIKRETE Companies, LLC the leading packaged cement and concrete products producer, has an immediate opening for a highly motivated 1st Shift Manufacturing Associates for our Obetz, OH facility. To Apply: Click on the “apply” button to get started or apply in-person (4033 Alum Creek, Obetz, OH 43207)! What we offer Competitive pay Annual bonus plan Paid vacation 11 Paid holidays Growth & Development opportunities (nationwide) 401(k) with company match Medical and prescription drug coverage Dental and vision coverage Health savings and flexible spending account Life insurance and disability coverage Employee Discounts (internal and external products and services) Why apply: Career Growth: Be part of an industry leader renowned for world-class design, manufacturing, sourcing, and distribution, and take your career to the next level. Team Collaboration: Join a team-oriented environment where collaboration is not just a buzzword but a priority. About the Role: Forklift Operation Using Hand Tools Adhering to Safety Procedures. Cleaning and maintaining equipment and work areas. Loading and unloading materials and supplies. Sets up forms in the manufacturing production process of concrete products. Handling and moving heavy construction materials. Following safety protocols and wearing appropriate protective gear. Adhering to quality control standards to ensure the production of high-quality concrete products. Any other miscellaneous tasks assigned by management at any given time and in any given area About You: We Require: An understanding and respect for Safety Compliance Attention to detail to deliver product quality Dependable and on time Ability to thrive in a team environment Manufacturing Experience a plus Comfort with Lifting up to 50 Pounds Comfort working around Industrial Machinery *Your offer may be contingent upon passing a drug-screen and pre-employment testing for this role!*

You will be the Multi-Functional Manufacturing Associate Manager for the Manufacturing Operations team. Our team is responsible for delivering high‑performance missile systems on schedule while maintaining the highest engineering, quality, and cost standards. What You Will Be Doing As the Multi-Functional Manufacturing Associate Manager you will be responsible for executing dynamic strategies to ensure on‑time missile deliveries that meet all engineering and quality requirements while controlling costs. Your responsibilities will include, but are not limited to: * Lead day‑to‑day operations of a multi‑functional work group. * Provide direction to exempt and non‑exempt salaried personnel in accordance with company policies. * Manage manpower planning, employee assessment, training, work assignments, and performance evaluations. * Partner closely with ESH to enforce safety and environmental policies. * Assist in developing strategies and coordinating activities that drive cost‑effective production. Why Join Us The ideal candidate is a collaborative, forward‑thinking leader who thrives in a fast‑paced, mission‑critical environment. This role offers the chance to influence missile manufacturing excellence, work with cutting‑edge technology, and make a tangible impact on national security. We are committed to supporting your work‑life balance and overall well‑being, offering flexible scheduling options. Learn more about Lockheed Martin's comprehensive benefits package here. Further Information About This Opportunity This position is in Troy. Discover more about our Troy, Alabama location. MUST BE A U.S. CITIZEN - This position is located at a facility that requires special access. The selected candidate must possess an active Secret clearance to start. Basic Qualifications: Experience and success in leading manufacturing and/or production teams proven capability to manage budgets and schedules Excellent communication skills with presentation to various size groups Proficient use of computing resources including MS Office applications. Bachelor's degree from an accredited institution or equivalent experience/combined education with professional experience Must obtain an interim clearance prior to starting and have the ability to obtain a secret clearance. Candidate must be able to pass a Bureau of Alcohol, Tobacco, Firearms and Explosives ("ATF") background check to obtain approval to be an "employee possessor" (of explosives or other ATF-regulated items) as defined by ATF regulations. Failure to obtain and retain employee possessor status may result in revocation of an offer and loss of employment. Desired Skills: Eight or more years of related experience. Manufacturing and/or defense industry experience. Lean/Six Sigma Green Belt or Black Belt Certified. Working knowledge and previous experience managing cost, quality, and schedule metrics. Interest and ability in contributing to growth of team and team members. Excellent oral, active listening, and written communications skills. Security Clearance Statement: This position requires a government security clearance, you must be a US Citizen for consideration. Clearance Level: Secret Other Important Information You Should Know Expression of Interest: By applying to this job, you are expressing interest in this position and could be considered for other career opportunities where similar skills and requirements have been identified as a match. Should this match be identified you may be contacted for this and future openings. Ability to Work Remotely: Onsite Full-time: The work associated with this position will be performed onsite at a designated Lockheed Martin facility. Work Schedules: Lockheed Martin supports a variety of alternate work schedules that provide additional flexibility to our employees. Schedules range from standard 40 hours over a five day work week while others may be condensed. These condensed schedules provide employees with additional time away from the office and are in addition to our Paid Time off benefits. Schedule for this Position: 4x10 hour day, 3 days off per week Lockheed Martin is an equal opportunity employer. Qualified candidates will be considered without regard to legally protected characteristics. The application window will close in 90 days; applicants are encouraged to apply within 5 - 30 days of the requisition posting date in order to receive optimal consideration. At Lockheed Martin, we use our passion for purposeful innovation to help keep people safe and solve the world's most complex challenges. Our people are some of the greatest minds in the industry and truly make Lockheed Martin a great place to work. With our employees as our priority, we provide diverse career opportunities designed to propel, develop, and boost agility. Our flexible schedules, competitive pay, and comprehensive benefits enable our employees to live a healthy, fulfilling life at and outside of work. We place an emphasis on empowering our employees by fostering an inclusive environment built upon integrity and corporate responsibility. If this sounds like a culture you connect with, you're invited to apply for this role. Or, if you are unsure whether your experience aligns with the requirements of this position, we encourage you to search on Lockheed Martin Jobs, and apply for roles that align with your qualifications. Experience Level: Experienced Professional Business Unit: MISSILES AND FIRE CONTROL Relocation Available: Possible Career Area: Manufacturing Type: Full-Time Shift: First

I am looking for Plastic Injection Operators and assemblers at a Newbury manufacturing plant. The job involves removing parts from a plastic injection press or assembling parts after they are produced. The shifts are 1st shift-6am-2:30am Monday through Friday 2nd shift-3pm-11:30pm Monday through Friday 3rd shift-11:30pm-7am Sunday through Thursday The positions are interim to direct. Money goes up once you are hired in. All applicants must live within 30 minutes of the plant and have their own transportation. All applicants will be drug screened and criminal backgrounds will be checked. #MID001

We make and supply medicines and vaccines all around the globe and our teams own every production stage, from creating quality products at our manufacturing sites to designing effective supply forecasting and regulatory inspections; all powered by digital, data and analytics. We operate at impressive scale, producing over 1.7 billion packs of medicine and 767 vaccine doses in 2021. We continue to modernize, so we can launch even more new products at speed whilst turbo-charging delivery across our entire portfolio through our relentless focus on quality, safety, and service. The way we work will change. For some, the shift in technology and products will be revolutionary. Our R&D pipeline demands a new kind of supply chain, and we need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of automation and robotics so we can work smarter together. As a Biopharm Manufacturing Associate II, you will perform production operations including fermentation or cell culture operations, preparation of solutions, chromatographic separation, filtration and concentration operations, autoclave and parts washing of process assemblies, and area cleaning/upkeep. Will be responsible for completing daily manufacturing tasks, and increasing competency in different production areas over time. Will participate in safety and compliance initiatives, as well as investigations. Will engage in the GSK Production System to continuously improve safety, quality, and schedule/cost performance. The purpose of this role is to be a part of a dynamic, multi-tiered operations team that brings life changing and life saving medicine to patients around the world. They will demonstrate GSK Values (Patient Focus, Transparency, Respect, & Integrity) and Expectations (Courage, Accountability, Development, & Teamwork) on a daily basis by engaging positively with team members and production support groups. Under the direction of senior personnel, the biopharmaceutical manufacturing associate II performs a variety of largescale production operations, interacting with automated equipment and monitoring/processing data. Will be responsible for completing daily manufacturing tasks, and increasing competency in different production areas over time. They will participate in safety and compliance initiatives, investigations, and help solve technical and organizational problems while working with different teams of experts. Will work within these teams to continuously improve safety, quality, and schedule/cost performance. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Demonstrate GSK Values - Patient Focus, Transparency, Respect, and Integrity - in every interaction, in every work task, and with every responsibility of the job role. Live GSK's Expectations of Courage, Accountability, Development, and Teamwork to achieve high performing behaviors in the workplace. With good documentation and data integrity practices, safely and compliantly completes and documents daily manufacturing tasks per standard operating procedures, batch document instructions, and logbooks Proactively works with senior staff to achieve competency in production operations Supports in cross-functional activities, such as engineering actions, validation actions and Tech Transfer actions, including proactive safety and compliance input prior to execution. Primarily these activities are within the production suite, but sometimes require out of suite or off-site work (i.e. FAT support) Monitors equipment and critical process parameters, and escalates any issues or abnormalities and participating the resulting troubleshooting activities Strives to maintain a high level of competency with current and emerging digital platforms (SAP, EBR, AR/VR, etc) By learning the production schedule and assessing it daily, proactively ensures all processing equipment and necessary materials are adequate and available to set the team up for success Transparently participates in investigations that are the result of safety or compliance issues. Why you? Basic qualifications: BS/BA degree, with cGMP manufacturing experience OR an Associate's degree from Montgomery county community college in Biotechnology or related technical field with cGMP manufacturing experience OR High School degree, 1+ years of cGMP manufacturing experience. Preferred Qualifications: Demonstrated level of high performance Strong verbal and written skills The ability to work well in a team environment Must be able to follow detailed processing instructions as well as accurately documenting all necessary documentation Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at ************************ where you can also request a call. Please note should your inquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a Recruitment FAQ guide. Click the link where you will find answers to multiple questions we receive GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at *********************************

We make and supply medicines and vaccines all around the globe and our teams own every production stage, from creating quality products at our manufacturing sites to designing effective supply forecasting and regulatory inspections; all powered by digital, data and analytics. We operate at impressive scale, producing over 1.7 billion packs of medicine and 767 vaccine doses in 2021. We continue to modernize, so we can launch even more new products at speed whilst turbo-charging delivery across our entire portfolio through our relentless focus on quality, safety, and service. The way we work will change. For some, the shift in technology and products will be revolutionary. Our R&D pipeline demands a new kind of supply chain, and we need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of automation and robotics so we can work smarter together. As a Biopharm Manufacturing Associate II, you will perform production operations including fermentation or cell culture operations, preparation of solutions, chromatographic separation, filtration and concentration operations, autoclave and parts washing of process assemblies, and area cleaning/upkeep. Will be responsible for completing daily manufacturing tasks, and increasing competency in different production areas over time. Will participate in safety and compliance initiatives, as well as investigations. Will engage in the GSK Production System to continuously improve safety, quality, and schedule/cost performance. The purpose of this role is to be a part of a dynamic, multi-tiered operations team that brings life changing and life saving medicine to patients around the world. They will demonstrate GSK Values (Patient Focus, Transparency, Respect, & Integrity) and Expectations (Courage, Accountability, Development, & Teamwork) on a daily basis by engaging positively with team members and production support groups. Under the direction of senior personnel, the biopharmaceutical manufacturing associate II performs a variety of largescale production operations, interacting with automated equipment and monitoring/processing data. Will be responsible for completing daily manufacturing tasks, and increasing competency in different production areas over time. They will participate in safety and compliance initiatives, investigations, and help solve technical and organizational problems while working with different teams of experts. Will work within these teams to continuously improve safety, quality, and schedule/cost performance. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Demonstrate GSK Values - Patient Focus, Transparency, Respect, and Integrity - in every interaction, in every work task, and with every responsibility of the job role. Live GSK's Expectations of Courage, Accountability, Development, and Teamwork to achieve high performing behaviors in the workplace. With good documentation and data integrity practices, safely and compliantly completes and documents daily manufacturing tasks per standard operating procedures, batch document instructions, and logbooks Proactively works with senior staff to achieve competency in production operations Supports in cross-functional activities, such as engineering actions, validation actions and Tech Transfer actions, including proactive safety and compliance input prior to execution. Primarily these activities are within the production suite, but sometimes require out of suite or off-site work (i.e. FAT support) Monitors equipment and critical process parameters, and escalates any issues or abnormalities and participating the resulting troubleshooting activities Strives to maintain a high level of competency with current and emerging digital platforms (SAP, EBR, AR/VR, etc) By learning the production schedule and assessing it daily, proactively ensures all processing equipment and necessary materials are adequate and available to set the team up for success Transparently participates in investigations that are the result of safety or compliance issues. Why you? Basic qualifications: BS/BA degree, with cGMP manufacturing experience OR an Associate's degree from Montgomery county community college in Biotechnology or related technical field with cGMP manufacturing experience OR High School degree, 1+ years of cGMP manufacturing experience. Preferred Qualifications: Demonstrated level of high performance Strong verbal and written skills The ability to work well in a team environment Must be able to follow detailed processing instructions as well as accurately documenting all necessary documentation Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at ************************ where you can also request a call. Please note should your inquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a Recruitment FAQ guide. Click the link where you will find answers to multiple questions we receive GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at *********************************

Site Name: USA - Pennsylvania - King of Prussia We make and supply medicines and vaccines all around the globe and our teams own every production stage, from creating quality products at our manufacturing sites to designing effective supply forecasting and regulatory inspections; all powered by digital, data and analytics. We operate at impressive scale, producing over 1.7 billion packs of medicine and 767 vaccine doses in 2021. We continue to modernize, so we can launch even more new products at speed whilst turbo-charging delivery across our entire portfolio through our relentless focus on quality, safety, and service. The way we work will change. For some, the shift in technology and products will be revolutionary. Our R&D pipeline demands a new kind of supply chain, and we need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of automation and robotics so we can work smarter together. As a Biopharm Manufacturing Associate II, you will perform production operations including fermentation or cell culture operations, preparation of solutions, chromatographic separation, filtration and concentration operations, autoclave and parts washing of process assemblies, and area cleaning/upkeep. Will be responsible for completing daily manufacturing tasks, and increasing competency in different production areas over time. Will participate in safety and compliance initiatives, as well as investigations. Will engage in the GSK Production System to continuously improve safety, quality, and schedule/cost performance. The purpose of this role is to be a part of a dynamic, multi-tiered operations team that brings life changing and life saving medicine to patients around the world. They will demonstrate GSK Values (Patient Focus, Transparency, Respect, & Integrity) and Expectations (Courage, Accountability, Development, & Teamwork) on a daily basis by engaging positively with team members and production support groups. Under the direction of senior personnel, the biopharmaceutical manufacturing associate II performs a variety of largescale production operations, interacting with automated equipment and monitoring/processing data. Will be responsible for completing daily manufacturing tasks, and increasing competency in different production areas over time. They will participate in safety and compliance initiatives, investigations, and help solve technical and organizational problems while working with different teams of experts. Will work within these teams to continuously improve safety, quality, and schedule/cost performance. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: * Demonstrate GSK Values - Patient Focus, Transparency, Respect, and Integrity - in every interaction, in every work task, and with every responsibility of the job role. Live GSK's Expectations of Courage, Accountability, Development, and Teamwork to achieve high performing behaviors in the workplace. * With good documentation and data integrity practices, safely and compliantly completes and documents daily manufacturing tasks per standard operating procedures, batch document instructions, and logbooks * Proactively works with senior staff to achieve competency in production operations * Supports in cross-functional activities, such as engineering actions, validation actions and Tech Transfer actions, including proactive safety and compliance input prior to execution. Primarily these activities are within the production suite, but sometimes require out of suite or off-site work (i.e. FAT support) * Monitors equipment and critical process parameters, and escalates any issues or abnormalities and participating the resulting troubleshooting activities * Strives to maintain a high level of competency with current and emerging digital platforms (SAP, EBR, AR/VR, etc) * By learning the production schedule and assessing it daily, proactively ensures all processing equipment and necessary materials are adequate and available to set the team up for success * Transparently participates in investigations that are the result of safety or compliance issues. Why you? Basic qualifications: * BS/BA degree, with cGMP manufacturing experience * OR an Associate's degree from Montgomery county community college in Biotechnology or related technical field with cGMP manufacturing experience * OR High School degree, 1+ years of cGMP manufacturing experience. Preferred Qualifications: * Demonstrated level of high performance * Strong verbal and written skills * The ability to work well in a team environment * Must be able to follow detailed processing instructions as well as accurately documenting all necessary documentation Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at ************************ where you can also request a call. Please note should your inquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a Recruitment FAQ guide. Click the link where you will find answers to multiple questions we receive GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at *********************************

ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers . If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post. Description: You will be the Multi-Functional Manufacturing Associate Manager for the Manufacturing Operations team. Our team is responsible for delivering high‑performance missile systems on schedule while maintaining the highest engineering, quality, and cost standards. What You Will Be Doing As the Multi-Functional Manufacturing Associate Manager you will be responsible for executing dynamic strategies to ensure on‑time missile deliveries that meet all engineering and quality requirements while controlling costs. Your responsibilities will include, but are not limited to: Lead day‑to‑day operations of a multi‑functional work group. Provide direction to exempt and non‑exempt salaried personnel in accordance with company policies. Manage manpower planning, employee assessment, training, work assignments, and performance evaluations. Partner closely with ESH to enforce safety and environmental policies. Assist in developing strategies and coordinating activities that drive cost‑effective production. Why Join Us The ideal candidate is a collaborative, forward‑thinking leader who thrives in a fast‑paced, mission‑critical environment. This role offers the chance to influence missile manufacturing excellence, work with cutting‑edge technology, and make a tangible impact on national security. Additional Qualifications/Responsibilities MUST BE A U.S. CITIZEN - This position is located at a facility that requires special access. The selected candidate must possess an active Secret clearance to start. Basic Qualifications: Experience and success in leading manufacturing and/or production teams proven capability to manage budgets and schedules Excellent communication skills with presentation to various size groups Proficient use of computing resources including MS Office applications. Bachelor's degree from an accredited institution or equivalent experience/combined education with professional experience Must obtain an interim clearance prior to starting and have the ability to obtain a secret clearance. **Candidate must be able to pass a Bureau of Alcohol, Tobacco, Firearms and Explosives (“ATF”) background check to obtain approval to be an “employee possessor” (of explosives or other ATF-regulated items) as defined by ATF regulations. Failure to obtain and retain employee possessor status may result in revocation of an offer and loss of employment. Desired Skills: Eight or more years of related experience. Manufacturing and/or defense industry experience. Lean/Six Sigma Green Belt or Black Belt Certified. Working knowledge and previous experience managing cost, quality, and schedule metrics. Interest and ability in contributing to growth of team and team members. Excellent oral, active listening, and written communications skills. Security Clearance Statement:This position requires a government security clearance, you must be a US Citizen for consideration. Clearance Level:Secret Other Important Information You Should Know Expression of Interest:By applying to this job, you are expressing interest in this position and could be considered for other career opportunities where similar skills and requirements have been identified as a match. Should this match be identified you may be contacted for this and future openings. Ability to Work Remotely:Onsite Full-time: The work associated with this position will be performed onsite at a designated Lockheed Martin facility. Work Schedules:Lockheed Martin supports a variety of alternate work schedules that provide additional flexibility to our employees. Schedules range from standard 40 hours over a five day work week while others may be condensed. These condensed schedules provide employees with additional time away from the office and are in addition to our Paid Time off benefits. Schedule for this Position:4x10 hour day, 3 days off per week Experience Level:Experienced Professional Business Unit:MISSILES AND FIRE CONTROL Relocation Available:Possible Career Area:Manufacturing Type:Full-Time Shift:First

Hourly Job Posting Template 030623 Manufacturing Associate Pay Rate: 24.53 Category/Shift: Hourly Full-Time ( 2nd Shift 3p-11p or 3rd Shift 11p-7a - Monday-Friday) Physical Location: Middletown Container 912 Nelbar St Middletown, Oh 45042 ************ The Job You Will Perform: * Counting and stacking finished product * Reading factory orders * Accurately reading gauges and other test equipment * Utilizing basic shop math, inspecting * Accurately completing quality and administrative documents and following directions * This person will also be assigned to clean-up functions such as blowing down the machine, wiping off shafts, cleaning ink systems, vacuuming and sweeping the machine area, as well as picking up and shredding scrap. The Skills You Will Bring: * Counting and stacking finished product * Reading factory orders . Manufacturing experience preferred

About Abeona Our Values: Patient First | Innovation | Integrity | Determination | Trust Join us in making cure the new standard of care. At Abeona Therapeutics, we exist for our patients and their caregivers; their needs guide our decision-making. We challenge ourselves to think differently, move quickly, and deliver solutions. We hold ourselves to the highest ethical and quality standards. We persevere with resilience and focus to achieve our mission. We build trust through humility, mutual appreciation, openness, and respect. Company Description Abeona Therapeutics Inc. is a commercial-stage biopharmaceutical company focused on developing cell and gene therapies for serious diseases. Notably, Abeona's ZEVASKYN (prademagene zamikeracel) is the first autologous cell-based gene therapy treating wounds in adults and pediatric patients with recessive dystrophic epidermolysis bullosa (RDEB). The company's cGMP manufacturing facility in Cleveland, Ohio, is dedicated to producing ZEVASKYN. Abeona's portfolio includes adeno-associated virus (AAV)-based gene therapies for ophthalmic diseases with unmet medical needs, and their novel AAV capsids aim to improve treatment outcomes for various debilitating conditions. Position Overview Abeona is looking for a Manufacturing Associate to join our team in Cleveland, OH. The successful candidate will be responsible for Manufacturing initiatives supporting multiple product pipelines. The candidate will be an integral part of a fast-paced group responsible for the manufacture of retroviral vector, autologous gene-corrected cell therapies, and clinical AAV gene therapies. Responsibilities will include executing protocols and manufacturing clinical material across multiple products as well as supporting process optimization work and document generation. The ideal candidate will have experience in production of biologics in a controlled cGXP setting. Strong aseptic and cell culture technique as well as collaborative work in a team is an integral part of this position. Schedule: The current manufacturing team schedule is Monday to Friday, with occasional weekend shifts. The manufacturing team will be transitioning into a 4-day work week with 10-hour shifts in the near future. These days will be Sunday - Wednesday and Wednesday to Sunday. Essential Duties and Responsibilities * Produce cell therapies in cGMP facility in conjunction with manufacturing production records (MPRs). * Execute studies in support of process optimization and validation. * Author, review, and provide technical support for manufacturing SOPs and MPRs. * Identify, suggest, and manage projects in parallel with manufacturing activities to reach set goals. * Ability to collaborate with others while maintaining a strong capability in independent, critical thought. * Strong organizational skills required. * Must be able to work as part of a team. * Contribute to activities that support safety and/or lab infrastructure. Qualifications * BS or equivalent in scientific discipline and min of 2-4 years related lab experience or MS or equivalent with 1-2 years of experience. * General biological lab experience. * Experience with mammalian and/or insect cell culture technology. * Familiarity with aseptic technique, cell culture, and cell counters is strongly preferred. * Previous GXP experience. * Experience with production processes for cell therapies and/or viral vectors or vaccines is highly preferred. * A strong background in the fundamentals and scale-up of production of biologic molecules strongly preferred. Additional Desired Skills and Abilities: * Advanced communication and organizational skills. * Advanced interpersonal skills and the ability to work with individuals across all organizational levels. * Attention to detail and accuracy. * Detailed record keeping and data documentation. * Demonstrated project management skills. * Ability to read, analyze, and interpret technical procedures, publications, intellectual property and/or government documents. * Working knowledge of GLP, GDP, GCP and GMP regulations and their ISO counterparts and ICH Guidelines. * High level of proficiency with Microsoft Office programs. * Less than 10% travel. Any travel will be reimbursed in accordance with company policy Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to experience prolonged sitting, some bending, stooping and stretching. Hand-eye coordination and manual dexterity sufficient to operate office equipment is required. A normal range of hearing and vision correctable to 20/20 is required. Occasional lifting of up to 50 pounds is required. Benefits Our values apply to how we view caring for each other as well. While the patient comes first, our employees are vital to making that happen, and so we strive to offer a competitive benefits package that includes: * Medical insurance coverage (multiple options to meet our employees' and their families' needs) * Dental and vision coverage * 401k match plan * Lifestyle spending account * Compensation (annual): $70,000 - $$73,700 (please note that this range includes annual salary and the maximum anticipated annual bonus) Visa Sponsorship Not Currently Available IMPORTANT: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

**Manufacturing Associate (Cell Specialist)** **Working at our Beavercreek Site** : GE Aerospace operations have been part of the Beavercreek community for over 70 years! Our Beavercreek facility manufactures gas turbine tubes, ducts, and manifolds, and also has complex machining, fabrication and investment casting capabilities. Product engineering, new product development and testing is performed on site. This facility also does repair and overhaul of tubes, ducts, and manifolds. We have been awarded OSHAS's highest safety rating. **Role Overview:** The Manufacturing Associate is responsible for supporting production processes, following written instructions and maintaining a safe workplace. Manufacturing duties will vary depending on work area. You may be operating a variety of tools such as: + Grinders + Gas torches, hot plates and irons + Hand gauges + Special-Purpose Machines (i.e., shot peen, seam welders, cut-off saws, wax injection, etc.) + Will move controls to adjust machine/equipment + Changes worn cutting tools, using wrenches + Will work with metal Types of roles that my be available, but not limited to: + May polish/deburr material + May operate a forklift and/ or tugger + May work in shipping or receiving + May be trimming/cutting up metal + Will be required to transfer from one type of machine/equipment to another as situation demands, as well as performing miscellaneous duties as directed by supervisory personnel. **Required Qualifications:** + High school diploma or General Education Degree (GED) + 2 + months experience with some light hand tools, i.e. minor home, or car repair, woodworking, shop class in school, etc. **Preferred Qualifications:** + Prior experience utilizing hand tools + General manufacturing experience + Team Player and willing to operate in a professional environment + Takes Pride in the work they are doing + Excellent attendance and punctuality history and availability to work overtime as needed + Able to work effectively when receiving general supervision (This involves performing routine assignments alone.) + Able to carry out operations according to set procedures or sequences. + Makes decisions based on experience & available data + Strives to meet or exceed job requirements + Ability to receive and act on constructive feedback **Additional Information:** + Wages $20.00 + per hour based on experience + $1.50/hr Shift Differential for 2nd & 3rd Shift + **Safety** . Your safety is important to us, so we provide most protective gear including hearing protection if needed. Strong safety focus with daily/monthly reviews and we have been awarded OSHAS's highest safety rating. GE Aerospace provides a $125 voucher towards the purchase of safety shoes as well as a voucher for safety prescription glasses if needed. + **Surroundings.** You'll be operating and working around moving machines - stand-up forklifts, mobile carts, cranes, etc. Due to normal machining operations there may be dust, fumes, or smoke (not over OSHA Permissible Exposure Levels (PEL)). + **Inclusive Culture.** Team oriented, ability to share ideas and make recommendations with peers and leadership + **Activity.** In addition to sitting and standing while operating equipment, some activities may require standing in one place for long periods, walking around, or climbing stairs. + **Temperature** . Most areas are climate controlled **Closing:** We strive to keep a fun and enjoyable shop atmosphere while maintaining the highest level of quality work output. We work together to make the impossible happen and we are looking for people like YOU to join us! We're looking for team-oriented individuals with the ability to share ideas and make recommendations with peers and leadership. _This role requires access to U.S. export-controlled information. Therefore, employment will be contingent upon the ability to prove that you meet the status of a U.S. Person as one of the following: U.S. lawful permanent resident, U.S. Citizen, have been granted asylee or refugee status (i.e., a protected individual under the Immigration and Naturalization Act, 8 U.S.C. 1324b(a)(3))._ **Additional Information** GE Aerospace offers a great work environment, professional development, challenging careers, and competitive compensation. GE Aerospace is an Equal Opportunity Employer (****************************************************************************************** . Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. GE Aerospace will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable). **Relocation Assistance Provided:** No GE Aerospace is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

Operates finishing machinery and equipment. Reads job specifications to determine machine adjustments and material requirements. Observes machine operation to detect product defects or machine malfunction. Measures product dimensions to determine accuracy of machine operation. Removes burrs, sharp edges, rust, or scale from product. Performs minor machine maintenance such as oiling machines or products. Operates any equipment needed to perform job. Performs related duties as assigned by supervision.

Are you passionate about significantly improving the future of medicine? Do you believe that people are the most important asset of any company? If so, join AmplifyBio ! AmplifyBio is a leading contract research organization with a comprehensive range of services that span from being an outsourcing partner for discovery stage R&D work, a preclinical CRO performing safety efficacy and toxicology studies for small molecules and advanced therapies alike, and, most recently, an expansion into manufacturing services for cell, gene, and mRNA-based therapeutics. The AmplifyBio ecosystem is comprised of three distinct business units: ADOC (South San Francisco, CA)- Amplify's Discovery, Optimization, and Characterization laboratories: ASET (West Jefferson, OH) - Amplify's Safety, Efficacy, and Toxicology Site; and the most recently opened AMEC (New Albany, OH) - Amplify's Manufacturing Enablement Center. About AMEC New Albany, OH: Amplify Bio's Manufacturing Enablement Center provides customizable cGMP suites to enable advanced therapy manufacturing in a “hoteling model,” traditional contract development and manufacturing (CDMO) or a hybrid model. Partnering with AmplifyBio for manufacturing cell therapy, gene therapy, mRNA, plasmid, or other modality is quite different from a typical CDMO experience. The goal is to provide flexible solutions customized to client needs while bringing full expert partnership. At AmplifyBio drug developers will find an innovation-rich ecosystem designed to advance a diverse range and class of pharmaceutical products across development stages. Amplify Bio is seeking to hire a Manufacturing Associate (GMP) to join our growing team!!! The Manufacturing Associate is responsible for execution of manufacturing processes within a GMP-compliant facility specializing in cell and gene therapy production at AmplifyBio's Manufacturing Enablement Center ( AMEC ) Facility. This role involves working under the supervision of senior manufacturing personnel to ensure the successful production of therapeutic products while maintaining compliance with regulatory standards and quality requirements. The Manufacturing Associate will play an essential role in supporting manufacturing operations, ensuring compliance with regulatory standards, and contributing to the advancement of cell and gene therapy products for patient treatment. What You'll Do Here: Manufacturing Execution: Execute manufacturing processes according to established SOPs, batch records, and work instructions for the production of cell and gene therapy products. Perform tasks related to drug substance and drug product processing, including cell expansion, transfection, purification, formulation, and fill/finish operation. Prepare and operate equipment, such as bioreactors, centrifuges, chromatography systems, and filtration units, following safety and operational protocols. Documentation and Compliance: Complete manufacturing documentation accurately and in accordance with GMP regulations, including batch records, logbooks, and equipment usage logs. Participate in the review and revision of manufacturing documents and procedures to ensure compliance with regulatory requirements and continuous process improvement. Assist in investigations of deviations, non-conformances, and CAPA activities, contributing to the resolution and prevention of quality incidents. Quality Control and Assurance: Perform in-process testing and sampling to monitor critical quality attributes and parameters during manufacturing operations. Assist in maintaining inventory levels for raw materials, consumables, and reagents, ensuring availability for manufacturing activities while adhering to inventory management procedures. Support equipment qualification, calibration, and maintenance activities to ensure equipment reliability and compliance with regulatory standards. Continuous Improvement: Actively participate in continuous improvement initiatives to enhance manufacturing processes, efficiency, and product quality. Provide feedback on process improvements and assist in the implementation of best practices to optimize manufacturing operations. Team Collaboration: Collaborate effectively with cross-functional teams, including manufacturing, quality assurance, quality control, and MSAT, to achieve production goals and resolve operational challenges. Communicate clearly and proactively with supervisors and team members to ensure alignment on priorities, tasks, and project timelines. We Would Love to Hear from You If: Bachelor's or associate degree in biology, bioengineering, biotechnology, or related field; or equivalent combination of education and experience. Previous experience in a GMP manufacturing environment, preferably in cell and gene therapy or biopharmaceuticals, is desirable but not required. Demonstrated ability to execute operations in controlled aseptic environments. Knowledge of GMP regulations and documentation practices is advantageous. Strong attention to detail, organizational skills, and ability to follow standard operating procedures. Excellent communication and interpersonal skills, with the ability to work collaboratively in a team-oriented environment. Flexibility to adapt to changing priorities and willingness to work in a dynamic and fast-paced environment. Ability to work independently with minimal supervision and demonstrate initiative in problem-solving and decision-making. Willingness to work flexible hours, including weekends and holidays, as needed to support manufacturing operations. At AmplifyBio , we're committed to growing and empowering an inclusive community within our company and industry. Therefore, we hire and cultivate diverse teams of the best and brightest from all backgrounds, experiences, and perspectives across our organization. AmplifyBio is an equal opportunity employer, and we value diversity at our company. We don't discriminate on the basis of race, color, citizenship status, national origin, ancestry, gender (including gender expression and gender identity), sexual orientation, age, weight, religion, creed, physical or mental disability, marital status, veteran status, political affiliation, or any other factor protected by federal, state, or local law. Why You Will Love Working Here: We take the health and happiness of our employees seriously and consistently evaluate new ways to Amp up our benefits to provide an amazing place to work. From a wellness program to financial planning and legal assistance, we make sure to take care of our own. Health, Dental, and Vision insurance that starts on your first day at Amplify Bio ! Competitive Compensation Package We take work-life balance seriously and we back it up with a UNLIMITED PTO policy. Generous paid parental leave Wellness and Self-Care Programs 401(k) match Tuition Reimbursement EAP/work-life support system A fun work environment where everyone's voice matters. We are just getting started! More benefits on the way! An Opportunity to Change the World!!! When you join our team , you will be a part of groundbreaking work while collaborating with our clients, research scientists, study directors, lab technicians, and specialists across a variety of disciplines. The future for AmplifyBio is as great as the combination of our imaginations and actions, and we hold ourselves accountable for our choices and results. We have a bias for action, excellence, and, especially, the health and safety of our employees.

Job Description Operates finishing machinery and equipment. Reads job specifications to determine machine adjustments and material requirements. Observes machine operation to detect product defects or machine malfunction. Measures product dimensions to determine accuracy of machine operation. Removes burrs, sharp edges, rust, or scale from product. Performs minor machine maintenance such as oiling machines or products. Operates any equipment needed to perform job. Performs related duties as assigned by supervision.

Requisition ID 62926 Position Type (US) Full Time Workplace Arrangement #LI-Onsite We Are Kerry Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment. Where You'll Work Our Byesville, OH, USA plant is an integral part of our Beverage division, dedicated to processing and packaging fruit-based juice mixes, syrups, extracts, and other liquid ingredients. Kerry is on the lookout for career-oriented individuals to support the increasing demand for high-quality ingredients. You'll find yourself in a dynamic and enjoyable work setting! We take pride in our products that enhance food flavors, often featuring strawberry, banana, coconut, or lemon. Our team members are passionate about their community, their colleagues, and the outcomes we achieve daily. If you're seeking a manufacturing environment where you can develop a career and enjoy the process, our team could be the perfect fit for you! What You'll Do The Production Operators are responsible for completing processes to provide customers with fruit based, beverage specific syrups, sauces and extracts. Each position takes action in accordance with detailed instructions, following safe practices and operating within FDA and related regulations. Positions available include Blending - pulling raw materials, measuring and loading into 1500-to-4000-gallon hoppers. Filling - operating high speed equipment that fills bottles, or other containers with fluids, ensures labeling is aligned and packages are sealed. Downline - Operating finishing of line, ensuring alignment, product Lift Truck Operator - Transports raw materials and finished product, related duties. Our team members are committed to * Consistently communicating and collaborating with others. * Completing required training within deadlines. * Embracing and practicing safe work habits, following Kerry policies and procedures. * Participating in Kerry continuous improvement practices, development and implementation initiatives. * Participating in learning, development and cross-training initiatives. What You'll Need To Succeed * High School graduate or equivalent required, eighteen (18) years or older * Basic math skills, ability to calculate percentages accurately. * 6 mo. Manufacturing experience, preferably in a chemical or food processing facility. * 3 mo. Prior electric pallet jack operation and safety certification preferred. * Use of MS products required, SAP software preferred. * Ability to maintain a good attendance record and availability for overtime. * Must be self-motivated and conscientious. * Ability to work well with a team or other coworkers. * Mechanical aptitude and analytical skills to solve mechanical problems. * Ability to complete certification requirements What We Offer The pay rate for these positions starts at $17.34 per hour. Kerry offers a competitive benefits package, including medical, dental, vision, paid time off, a 401(k) plan with employee and company contribution opportunities, Employee Share Plan, Life, disability, and accident insurance. This job posting is anticipated to expire on February 16 2026. Kerry is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age disability, protected veteran status or other characteristics protected by law. Kerry will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditional upon the successful completion of a background investigation and drug screen. Additional information can be found at Know Your Rights Workplace Discrimination is Illegal (dol.gov). Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a "starter kit," investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name. Recruiter Posting Type DNI

Job DescriptionDescription: Interested in working for an industry leader? Since 1970, Anchor Manufacturing Group, Inc. has been providing exceptional quality stampings and welded assemblies to diversified industries with significant expertise in the automotive industry. With 350,000 square feet of manufacturing space and a stand-alone tool and die business, Anchor supplies the highest quality products to North American, European, and Asian OEM's as well as Tier I and Tier II manufacturers. Our core expertise includes small to large metal stampings and complex welded assemblies including Class A appearance trim, structural, exterior, interior, exhaust, N.V.H., ride control, seating, steering column, brake, chassis, and safety related components. Requirements: Must be able to lift 30 pounds Manufacturing experience preferred Forklift experience a plus Positive Attitude with a desire to learn and grow Team play Attention to detail, efficiency, and accuracy Accountability and responsible Must be able to communicate effectively Reliable transportation to and from work Must be able to read and speak English fluently Responsibilities Compliance - Comply with all the Anchor Principles and Guidelines, as well as Anchor policies and procedures. Work ability - Position, align, and secure workpieces against fixtures or stops on machine beds or on dies. Lubricate workpieces when needed. Operations Monitoring - Watching gauges, dials, or other indicators to make sure a machine is working. Quality Control Analysis - Conducting tests and inspections of products, services, or processes to evaluate quality or performance Time Management - Proper use of ERP System for logging of time, jobs, and quality checks Adaptability/Flexibility - Job requires being open to change (positive or negative) and to considerable variety in the workplace Safety - Operate machinery safely, report safety problems immediately, wear proper PPE. Handling and Moving Objects - Using hands and arms in handling, installing, positioning, and moving materials, and manipulating things. Attention to Detail - Job requires being careful about detail and thorough in completing work tasks. Teamwork - Work closely and cooperatively with the other Managers and Team Leads on day-to-day issues

Unilock, North America's leading manufacturer of premier Architectural Concrete Paving Stones and Engineered Retaining Wall Systems, has immediate openings for Manufacturing Associates in our new state-of-the-art facility opening in Harrison, OH. Join the industry leader and a winning team by becoming part of a company that has worldwide recognition and stability. Wage: Starting at $18+ and up based on position, experience and skills Job Type: Full Time You can expect: * Bonus Program: * $100 - After 30 days of employment * $400 - After 6 months of employment * $500 - After 12 months of employment * Above average earnings * Paid Time Off, including Christmas Break * Semi-annual Performance Incentive Bonus Plan * Advancement - Opportunities for pay increases and promotions for high performers * 401(k) Plus Company Match * Generous Profit Sharing * Medical/ Dental/ Vision within 30 days of your date of hire * Life Insurance, Short-Term & Long-Term Disability - Company Paid * A safe and health-conscious work environment with ongoing training and support for all team members. All safety items and Personal Protection Equipment (PPE) is provided by Unilock. What you'll do * Operate a variety of different manufacturing equipment including batching systems, mixers, concrete press, packaging equipment and forklift operation * Quality control during all phases of the production process * Assist maintenance employees with simple tasks to maintain equipment * Clean machinery and maintain cleanliness in specified work areas * Participate within a team approach and family work environment that delivers excellence * Create products that enrich and improve the lives of our customers * Comply with all safety and health regulations * Must be available for both Day Shift and Night shift as required The ideal candidate will be reliable and motivated to succeed in a team-oriented environment. A career for which candidates with military service are encouraged to apply #INHPOH

Requirements EDUCATION REQUIREMENTS: High school graduate or G.E.D. equivalent. Must be able to read and write proficiently. EXPERIENCE REQUIREMENTS: Previous CNC experience preferred. Acceptable attendance record. Effective verbal and written communication skills. Demonstrated abilities in handling multiple priorities. Must have the ability to read tooling prints, micrometers, scales, indicators and other measuring devices. PHYSICAL REQUIREMENTS: Must be able to repeatedly handle up to 10-pound component parts during operations and up to 25-pounds with assistance as possible for change overs. Must be able to stand for long periods of time. Must be able to push loaded carts multiple times per day for short distances.

Join Our Team as a 3rd Shift Manufacturing Associate in Twinsburg, OH! - Urgently Hiring! Job Title: 3rd Shift Manufacuting Associate Pay: $18.25 per hour Hours: 10:00 PM to 6:00 AM, Sunday through Thursday Key Responsibilities Understanding and adhering to all safety procedures, including emergency stops, pinch points, and light curtains. Completing setup checklists and preparing work areas to ensure optimal operation. Correctly using banding and packaging tools while maintaining an organized supply area. Reading and following work orders, including special packaging instructions. Setting up carts and racks as needed and cutting and staging wood for efficient production. Blowing out tubes, packaging them properly, moving bundles, and verifying tags and stickers. Assisting with raft sizing changes and supporting the H-Coil Operator during roll changes. Maintaining a clean work area by removing coolant and ensuring adequate supply levels. Reviewing production schedules and inspecting tubes as they come off the mill while organizing, stacking, and packing them. Following all directions provided by the Cut Off Operator and Tube Mill Operator. Qualifications A high school diploma or GED, or equivalent experience. The ability to read safety rules, operating instructions, and work orders. Basic math skills, including fractions, decimals, and percentages. Capability to write simple reports and documentation. A reliable, safety-conscious mindset and keen attention to detail. Work Environment: Expect exposure to moving mechanical parts, occasional fumes or airborne particles, and a loud production environment typical of steel processing.

Manufacturing Associate ArtiFlex Manufacturing Group is a high-performing team that specializes in stamping, assembly, E-coat, and packaging. We manufacture automotive sheet metal body panels through large tonnage press stamping and welded assembly processes. We drive success through our commitment to being Innovative, Problem Solving, and Partners. ArtiFlex Manufacturing is known for using its unique set of capabilities to develop solutions for our customers and employing people with the willingness to step up to the fast-paced and innovative environment. We believe in serving our employees and unleashing their full potential. The ArtiFlex Manufacturing Group is ready to support and develop you! Apply today and start your journey in becoming an Innovative. Problem Solving. Partner." Benefits to working at ArtiFlex: * Paid Apprenticeship Programs, Tuition Assistance, Profit Sharing, On the Job Training, Free On-site Fitness Center, Referral Bonus, Employee Events, Great Medical, Dental and Vision insurance, Short- and Long-Term Disability, Life insurance, Vehicle Discounts, Weekly Pay, 401k, Paid Time Off, Holidays and more! Available Roles: * Paint and Pack Associate 1st Shift, Monday- Friday, from 5:15 am to 1:45 pm. Removes parts from paint line hooks, packs parts, loads parts into racks and bins, inspects parts for defects. * Paint and Pack Associate 1st Shift, Monday- Friday, from 7:00 am to 3:30 pm. Removes parts from paint line hooks, packs parts, loads parts into racks and bins, inspects parts for defects. * Automated Stamping Set up 1st Shift, Monday- Thursday, from 5:30 am to 4:00 pm. Operates and sets up presses, inserts sheet metal into presses, places parts in racks, tags racks for shipping or rework, completes box count sheets, inspects parts. * Laser operator 3rd Shift, Sunday- Thursday, from 7:15 pm to 5:45 am. Sets up, operates the lasers, pack parts, inspects parts for defects. * Automated Stamping Set up 3rd Shift, Sunday- Thursday, from 7:15 pm to 5:45 am. Operates and sets up presses, inserts sheet metal into presses, places parts in racks, tags racks for shipping or rework, completes box count sheets, inspects parts. Qualifications: * High School Diploma or Equivalent * Ability to lift 40 pounds unassisted * Able to stand for long periods of time * Ability to perform repetitive motions with arm, hand, shoulder, back (bend, twist, etc.) * Basic math skills. Job Location: * Performed on the plant floor.