Manufacturing Associate jobs at The Timken Company - 1713 jobs

As a Production Associate, you will assemble all types of hermetic seals to specified production standards and various tasks related to the day-to-day operations. Qualifications: * Perform a variety of tasks including but not limited to assembly of parts at specified production levels maintaining quality standards at all times. * Provide feedback and take corrective action whenever conditions exist preventing achieving quality, performance and production standards. * Perform assigned duties with minimal supervision. * Acquire proficiency in maintaining quality/production standards in one job function for which you are trained. * Perform other duties as assigned by supervisor or management. Requirements: * High school graduate preferred but not required. * Basic math skills and ability to read and write English preferred. * Good vision (natural or corrected), excellent hand dexterity in both hands. * Knowledgeable with operating tools and equipment necessary to consistently perform and achieve top quality products. * Ability to repeatedly lift objects weighing 5 to 10 Lbs. and occasionally up to 20 Lbs. * Repeated standing, walking and bending are required. * Ability to perform in a production environment with unusual conditions such as high volume noise level and dust. * Available to work overtime if necessary, including weekends. * Attend training sessions as required to meet standards of job related activities relating to all Sealtron applications. * Participate in cross-training efforts interfacing with other departments to acquire additional skills and knowledge for advancement. Compensation Employee Type: Hourly Salary Minimum: $35,000 Salary Maximum: $40,000 Incentive: No Disclaimer: Where a specific pay range is noted, it is a good faith estimate at the time of this posting. The actual salary offered will be based on experience, skills, qualifications, market / business considerations, and geographic location. For more information on AMETEK's competitive benefits, please click here. AMETEK, Inc. is a leading global provider of industrial technology solutions serving a diverse set of attractive niche markets with annual sales over $7.0 billion. AMETEK is committed to making a safer, sustainable, and more productive world a reality. We use differentiated technology solutions to solve our customers' most complex challenges. We employ 21,000 colleagues, in 35 countries, that are grounded by our core values: Ethics and Integrity, Respect for the Individual, Inclusion, Teamwork, and Social Responsibility. AMETEK (NYSE:AME) is a component of the S&P 500. Visit ************** for more information. We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class. Individuals who need a reasonable accommodation because of a disability for any part of the employment process should call ****************. Nearest Major Market: Cincinnati

As a Production Associate, you will assemble all types of hermetic seals to specified production standards and various tasks related to the day-to-day operations. Qualifications: Perform a variety of tasks including but not limited to assembly of par Production Associate, Production, Associate, Manufacturing

**Production Specialist | Entry-level** Job Type: Full Time, Hourly Pay Range: Starting at $18.28 an hour and Earn up to $23.65 an hour Shift(s) Available: NIGHT shift of 12 hours, 4 days on 4 days off. Ability to work overtime including weekends, holidays, or different shifts with advance notice as needed. Apply Now! Text ADMCHAT to 53827 **Why Join?** + Benefits Start First Day + Medical, Dental, Vision, and Prescription Drug Insurance + Health and Wellness Incentives + Paid Vacation and Holidays + 401K/ESOP, pension with ADM matching contributions + Flexible Spending Accounts (FSAs) + Short & Long-Term Disability + Company Paid Life Insurance and Voluntary Life Insurance for Employees,' Spouse and Children + Parental leave (paternity/maternity) + Employee Assistance Program (EAP) + Tuition Reimbursement + Advancement Opportunities + Weekly Pay + Perks at work (discount program with several companies) **Summary** This is an entry-level position which will be in a union workforce. We are looking for high potential individuals ready to take on challenges and responsibilities within our Chattanooga, TN Oilseeds Paper facility. This position reports to the Department Supervisor in the department the employee is working in. You will gain knowledge of the facility, general department knowledge, and handle tasks through completion of tasks and look for ways to improve the process and personal performance. Production Specialists are expected to perform a variety of jobs, tasks or duties as assigned under limited supervision. **Essential Job Functions:** + Work in a fast-paced environment to complete various processes including weighing, bagging, packing, unpacking, labeling, and storing products and sanitizing around facility (sweeping, compressed air cleaning) + Maintain, monitor and adjust equipment + Utilize computer systems to input and record data as required in regards to safety, sanitation, maintenance, and processing equipment operation + Operating equipment associated with the loadout and unloading process for bulk materials including trucks and/or rail cars, forklifts, skid steers, utilizing scales, pumps, conveyor, etc. + Interact regularly with peers and management to pursue continuous improvement of facility operations and promote a teamwork focused environment + Understand and adhere to ADM's Safety, Environmental Compliance and Food Quality and goal of achieving a zero-injury culture. + Maintaining a safe and clean work environment + Exhibit regular and prompt attendance and maintain attendance record in accordance with company policy + Always exhibit a professional image; maintain a positive and supportive attitude + Other duties as assigned **Requirements:** + Must be 18 years or older + Must be eligible to work in the United States without visa sponsorship + Ability to understand and effectively communicate in English (verbal/written) + High School diploma or equivalent + Basic computer skills (Word and Excel) + Experience in production and/or similar military environment (preferred) + Knowledge of Good Manufacturing Practices preferred **On-the-Job Training Requirements:** + Complete ADM safety, food safety, quality, and environmental training + Participate in company planned operations training **Working Conditions** + Ambient conditions - Work area is, typically, a non-air-conditioned production environment. Hot or cold Temperatures, all seasonal elements, both indoors and outdoors + Atmosphere: Dust and odor + Must be able to work around noise levels that may reach or exceed 85 decibels and require use of hearing protection for most of the work shift + Company provided protective clothing required: Uniforms, hardhats, earplugs, safety glasses, hair restraints, steel-toed shoes, gloves, and safety harness may be required based on task performed; employees are required to wear all required PPE (Personal Protective Equipment) (i.e., hard-hats, safety glasses, earplugs, uniforms, and steel-toed boots) in addition to job specific PPE requirements. *Employees in roles that require respirators will need to be clean shaven. **Physical Requirements** + Ability to move about or to a work site by ascending/descending stairs, bending, kneeling and prolonged periods of standing and sitting, stooping, bending, kneeling, or squatting frequently + Ability to operate equipment or machinery that may be located at different heights; may require work on ladders, scaffolding or other work at heights or in confined spaces + Ability to lift and transport materials and equipment weighing up to 40 pounds on a frequent basis, up to 55 pounds on an occasional basis and up to 50 pounds overhead + Requires ability and willingness to wear respirators + Ability to traverse up to two (2) miles during the course of a workday **Work Hours** + Ability to work overtime including weekends, holidays, or different shifts with advance notice as needed + Rotating shift of 12 hours, 4 days on 4 days off. Ability to work overtime including weekends, holidays, or different shifts with advance notice as needed. ADM requires the successful completion of a background check. REF:104952BR **Req/Job ID:** 104952BR **City:** Chattanooga **State:** TN - Tennessee **Ref ID:** \#LI-DNI **:** **About ADM** At ADM, we unlock the power of nature to provide access to nutrition worldwide. With industry-advancing innovations, a complete portfolio of ingredients and solutions to meet any taste, and a commitment to sustainability, we give customers an edge in solving the nutritional challenges of today and tomorrow. We're a global leader in human and animal nutrition and the world's premier agricultural origination and processing company. Our breadth, depth, insights, facilities and logistical expertise give us unparalleled capabilities to meet needs for food, beverages, health and wellness, and more. From the seed of the idea to the outcome of the solution, we enrich the quality of life the world over. Learn more at ************ **\t:** **\#IncludingYou** Diversity, equity, inclusion and belonging are cornerstones of ADM's efforts to continue innovating, driving growth, and delivering outstanding performance. We are committed to attracting and retaining a diverse workforce and create welcoming, truly inclusive work environments - environments that enable every ADM colleague to feel comfortable on the job, make meaningful contributions to our success, and grow their career. We respect and value the unique backgrounds and experiences that each person can bring to ADM because we know that diversity of perspectives makes us better, together. We welcome everyone to apply. We are committed to ensuring all qualified applicants receive consideration for employment regardless of race, color, ethnicity, disability, religion, national origin, language, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law **:** Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. If hired, employees will be in an "at-will position" and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. The pay for this position is expected to be: **:** $20.42

Production Specialist | Entry-level Job Type: Full Time, Hourly Pay Range: Starting at $18.28 an hour and Earn up to $23.65 an hour Shift(s) Available: NIGHT shift of 12 hours, 4 days on 4 days off. Ability to work overtime including weekends, holidays, or different shifts with advance notice as needed. Apply Now! Text ADMCHAT to 53827 Why Join? Benefits Start First Day Medical, Dental, Vision, and Prescription Drug Insurance Health and Wellness Incentives Paid Vacation and Holidays 401K/ESOP, pension with ADM matching contributions Flexible Spending Accounts (FSAs) Short & Long-Term Disability Company Paid Life Insurance and Voluntary Life Insurance for Employees,' Spouse and Children Parental leave (paternity/maternity) Employee Assistance Program (EAP) Tuition Reimbursement Advancement Opportunities Weekly Pay Perks at work (discount program with several companies) Summary This is an entry-level position which will be in a union workforce. We are looking for high potential individuals ready to take on challenges and responsibilities within our Chattanooga, TN Oilseeds Paper facility. This position reports to the Department Supervisor in the department the employee is working in. You will gain knowledge of the facility, general department knowledge, and handle tasks through completion of tasks and look for ways to improve the process and personal performance. Production Specialists are expected to perform a variety of jobs, tasks or duties as assigned under limited supervision. Essential Job Functions: Work in a fast-paced environment to complete various processes including weighing, bagging, packing, unpacking, labeling, and storing products and sanitizing around facility (sweeping, compressed air cleaning) Maintain, monitor and adjust equipment Utilize computer systems to input and record data as required in regards to safety, sanitation, maintenance, and processing equipment operation Operating equipment associated with the loadout and unloading process for bulk materials including trucks and/or rail cars, forklifts, skid steers, utilizing scales, pumps, conveyor, etc. Interact regularly with peers and management to pursue continuous improvement of facility operations and promote a teamwork focused environment Understand and adhere to ADM's Safety, Environmental Compliance and Food Quality and goal of achieving a zero-injury culture. Maintaining a safe and clean work environment Exhibit regular and prompt attendance and maintain attendance record in accordance with company policy Always exhibit a professional image; maintain a positive and supportive attitude Other duties as assigned Requirements: Must be 18 years or older Must be eligible to work in the United States without visa sponsorship Ability to understand and effectively communicate in English (verbal/written) High School diploma or equivalent Basic computer skills (Word and Excel) Experience in production and/or similar military environment (preferred) Knowledge of Good Manufacturing Practices preferred On-the-Job Training Requirements: * Complete ADM safety, food safety, quality, and environmental training * Participate in company planned operations training Working Conditions Ambient conditions - Work area is, typically, a non-air-conditioned production environment. Hot or cold Temperatures, all seasonal elements, both indoors and outdoors Atmosphere: Dust and odor Must be able to work around noise levels that may reach or exceed 85 decibels and require use of hearing protection for most of the work shift Company provided protective clothing required: Uniforms, hardhats, earplugs, safety glasses, hair restraints, steel-toed shoes, gloves, and safety harness may be required based on task performed; employees are required to wear all required PPE (Personal Protective Equipment) (i.e., hard-hats, safety glasses, earplugs, uniforms, and steel-toed boots) in addition to job specific PPE requirements. *Employees in roles that require respirators will need to be clean shaven. Physical Requirements Ability to move about or to a work site by ascending/descending stairs, bending, kneeling and prolonged periods of standing and sitting, stooping, bending, kneeling, or squatting frequently Ability to operate equipment or machinery that may be located at different heights; may require work on ladders, scaffolding or other work at heights or in confined spaces Ability to lift and transport materials and equipment weighing up to 40 pounds on a frequent basis, up to 55 pounds on an occasional basis and up to 50 pounds overhead Requires ability and willingness to wear respirators Ability to traverse up to two (2) miles during the course of a workday Work Hours * Ability to work overtime including weekends, holidays, or different shifts with advance notice as needed * Rotating shift of 12 hours, 4 days on 4 days off. Ability to work overtime including weekends, holidays, or different shifts with advance notice as needed. ADM requires the successful completion of a background check. REF:104952BR

Job DescriptionBenefits: 401(k) 401(k) matching Competitive salary Dental insurance Health insurance Paid time off Training & development UCS/Spirit - Sporting Goods Manufacturer - Pole Vaulting Poles We are seeking a Manufacturing Associate to join our team! You will operate and maintain industrial production and processing machinery. Responsibilities: Operate, Monitor, Adjust, and Repair specialized industrial machinery Perform routine preventative maintenance Respond to work order requests in a timely fashion Adhere to all safety policies and procedures Qualifications: Previous experience in manufacturing, machinery or other related fields preferred (not required) Mechanical aptitude and troubleshooting skills Familiarity with industrial tools and equipment Ability to handle physical workload Attention to detail Professional attitude Strong work ethic and reliability Organized and Professional Communicative and work well with others Self-Starter who can take instruction UCS/Spirit is a composites manufacturer specializing in producing the highest performing vaulting poles in the world since 1987. We are a family business looking to grow our team with an associate who takes pride in their work and wants to join our skilled team. Vaulting pole production is very specific, so we are looking for someone who is willing to learn new skills, working in a team environment. The job will require being on your feet, lifting, reaching, pulling, pushing etc. Previous manufacturing experience helps but is not necessary. We are looking for candidates who wants to grow with our business for many years ahead. We are offering competitive pay depending on experience plus benefits, paid holiday and overtime opportunities. Apply in person 8am-2pm 2180 Meridian Blvd, Minden, NV 89423 Minimum of 2 work references Competitive pay plus benefits and paid holidays Overtime Opportunities available

The Manufacturing Associate works as part of the manufacturing team to deliver high quality therapeutics. This role is focused on processing of cell therapy technologies where Aseptic Processing is of the utmost importance. This role contributes to the successful delivery of released product in support of clinical trials and commercial production. Company Overview At FUJIFILM Biotechnologies California, we're driving the future of medicine with the expertise to produce life-changing cell therapies like T-cell and CAR T immunotherapies. Working with pioneering biotech partners, our teams manufacture innovative treatments that improve lives. Join us at our advanced Thousand Oaks facility, where you'll make a tangible impact on groundbreaking therapies. We offer a collaborative, flexible workplace and a vibrant culture driven by passion and energy-what we call Genki. If you're ready to reimagine the future of healthcare, let's create something extraordinary together. Our campus is in Thousand Oaks, California, an exceptional place to live with great schools, natural beauty, outdoor activities, and proximity to Los Angeles and Santa Barbara. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: *************************************************** Job Description Responsibilities: * Performs Aseptic operations in a Grade A environment * Support production in an aseptic environment. * Executes on production batch records and work orders according to SOPs and protocols. * Generates work orders. * Assist in all areas of cell therapy and all related duties as required including (stocking, tracking inventory, material movement, maintaining metrics, filling out log sheets, and other special projects). * Assists in manufacturing batch record review. * With supervision, initiates deviations and participates in root cause investigations and CAPA. * Drafts and revises SOPs/ WINs/ BRs. * Execute SAP transactions. * Execute media batching. * Routine maintenance and cleaning of rooms and equipment. * Identifies and implements continuous improvements. * Perform tasks in a manner consistent with the safety policies, quality systems, and GMP * Adhere to all safety protocols and procedures. * Execute visual inspection of final drug product. * Will be managing D space during production (sample handoff, material ingress as needed, print documents as needed). * Assist the team with maintaining an up-to-date working inventory for the equipment/supplies * Document and review appropriate paperwork, daily logs, and documentation per Good Documentation Practices, to include electronic documentation * Participate in a detailed training program and develop training plan * Maintain inventory of equipment and supplies * Identifies and implements continuous improvements * Perform tasks in a manner consistent with the safety policies, quality systems, and GMP requirements * Adhere to all safety protocols and procedures Qualifications: * Bachelor's Degree in science based discipline; or Associate degree with 2+ years of applicable biopharma cell therapy or cell culture experience; or High school diploma with 5+ years of applicable biopharma cell therapy or cell culture experience. * Relevant technical writing experience with Biopharma Standard Operating Procedures (SOPs) or applicable academic mediums (i.e. reports, papers, essays). Preferred Qualifications: * Ability to follow verbal and written instructions * Problem solving skills * Detail oriented * Team player * Ability to work with minimal supervision * Strong communication skills * Understanding of Aseptic Behaviors / Techniques * Experience in biomanufacturing environments Work Environment: * Work is generally performed in a Good Manufacturing Practice (GMP) facility. A GMP facility is governed by regulatory agencies in which there are specific requirements for hygiene and acceptable clothing. The following items are restricted when accessing the GMP manufacturing area: * Makeup, painted nails * Hair products (spray, gel, wax) * Perfume and cologne * Jewelry (rings, watches, bracelets, fitness bands, necklaces, and facial/ear piercings, etc.) * Donning of gowns requires ability to physically don gowns while balancing in a cleanroom environment * Personal Protective Equipment is required to perform certain tasks (i.e., latex/nitrile gloves, respirators and or masks, goggles, plant dedicated scrubs/shoes, full body gown that covers all exposed skin) * Subject to extended periods of standing, to include crouching / kneeling (8 plus hours) while being donned in applicable PPE * Required to handle biohazardous and hazardous material via direction of Standard Operating Procedures Physical Requirements: * Medium work that includes moving, lifting, pushing and or pulling objects up to 50 pounds * Medium work that includes pushing and or pulling equipment with up to 50 pounds of force assisted by wheels * Must be willing and able to bend, stoop, squat, crawl, twist, climb ladders, and wear a respirator * Position requires a combination of standing in the manufacturing environment and walking around the facility * Open to work various shifts as needed * Required to work weekends and holidays Salary and Benefits: * For California, the base salary range for this position is $27.50-34.50 per hour. Compensation for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience, location, etc.). * Medical, Dental, Vision * Life Insurance * 401k * Paid Time Off LI-#Onsite EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (*******************).

The Asahi Kasei Group operates with a commitment of creating for tomorrow. Our business sectors, Material, Homes, and Health Care, contribute to the development of society by anticipating the changing needs of those around the world. We look for candidates that offer a fresh perspective and a variety of skills to help us achieve our commitment.Bionova is a rapidly growing, biologics CDMO focused on developing and manufacturing recombinant protein products using mammalian cell culture processes. Our business success is built on bringing together top scientific talent, arming them with the best available tools, and setting them loose in an agile, energized culture focused on solving difficult client problems. Because our success depends on our ability to exceed our clients' expectations, we look for candidates with an innate desire to serve. Adaptability and an interest in transformative action are also common attributes among our team. Bionova became a subsidiary of Asahi Kasei Medical in May 2022, a division of Tokyo-based Asahi Kasei Group. This acquisition has enabled Bionova to greatly accelerate growth of the business, both in capacity of current service offerings and expansion into new service offerings. Company: Bionova Scientific LLC Job Description: Company Summary: Bionova is a rapidly growing, biologics CDMO focused on developing and manufacturing recombinant protein products using mammalian cell culture processes. Our business success is built on bringing together top scientific talent, arming them with the best available tools, and setting them loose in an agile, energized culture focused on solving difficult client problems. Because our success depends on our ability to exceed our clients' expectations, we look for candidates with an innate desire to serve. Adaptability and an interest in transformative action are also common attributes among our team. Position Summary: The Manufacturing Associate will actively contribute to the manufacturing projects at the Bionova Scientific West Warren site. As part of the Cell Culture/Manufacturing group, you will have opportunities to work on wide-ranging set of projects for troubleshooting and investigations, system and workflow implementation, and tech transfers of processes into a GMP mulit-product manufacturing facility. The role will provide hands-on execution of complex experiments in a team setting. The role will support GMP and manufacturing activities. Essential Duties and Responsibilities: Executes with oversight of qualified staff complex unit operations including but not limited to media prep; cell culture thaw, expansion, and end of production banking; operation of single-use bioreactors, process monitoring and harvest operations. Performs internal support activities such as maintenance of analytical equipment, stocking of consumables, discarding expired reagents, material coordination and weigh and dispense. Maintains own training within compliance and trains other GMP associates upon completion of trainer qualification. Support in equipment troubleshooting, pilot scale material generation, non-GMP tox material generation and GMP upstream manufacturing activities. Author/review/approve technical documents such as tech transfer protocols and reports, experimental plans, production batch records, training materials, manufacturing SOPs, and regulatory filing documents per project needs. Documents work according to cGMP and cGDP. Adheres to established regulations and follows cGMP established by site. Maintain cleanroom standards, practices, and housekeeping according to SOPs. Recognize any minor issues from the equipment and any affiliated documentation and take appropriate corrective action within scope. Notify leads/managers of issues and discrepancies immediately. Assess impact of issues and non-conformities to products and projects as they pertain to product safety and efficacy or project milestones. Evaluate new technologies and innovations to improve operational efficiency or expand cell culture capabilities. Contributes to quality activities such as investigations and area walk-throughs and support authoring deviations, CAPA, change control. Other duties as assigned to ensure appropriate compounding practices Working Conditions: This position required to work in a lab/office setting. The role requires walking, standing, stooping, kneeling, and crouching. The employee must occasionally lift and or move up to 20 pounds independently. Qualifications Minimum of Associate degree with 1-2 years of relevant experience, or combination of experience and relevant advanced degree, preferably in biopharma manufacturing role. Must have bioreactor operations experience. Understanding of mammalian cell culture performance is required. Working knowledge of cGMP compliance as it pertains to procedures, processes, and manufacturing Experience with process monitoring software and equipment software (UNICORN, Pi Historian) Creative thinker that can identify better and more efficient methods to address issues and gaps Demonstrate ability to work independently and on cross-functional teams. Ability to handle more than one task at a time, while maintaining attention to detail and working in a fast-paced environment. Strong analytical skills and attention to detail. Flexible mindset for a dynamic environment. Flexibility with work hours to meet business needs, including weekends and holidays, as needed. Compensation Range: The base compensation range for this role is between $25 and $30 an hour. However, the actual compensation may vary depending on your experience and qualifications. Health Benefits and Program: Bionova offers health benefits at a subsidized rate. Healthcare, Dental, and Vision insurance Life Insurance and Disability Program: 100% covered by Bionova. Retirement Plan (401K) Up to 8% of Employer Match Paid time off up to two weeks 10 days of Holidays and 5 days of Sick Leave. As an equal opportunity employer, Asahi Kasei believes a diverse workforce will provide us with the ability to continuously support the changes in the economy, society, and environment.

The Asahi Kasei Group operates with a commitment of creating for tomorrow. Our business sectors, Material, Homes, and Health Care, contribute to the development of society by anticipating the changing needs of those around the world. We look for candidates that offer a fresh perspective and a variety of skills to help us achieve our commitment.Bionova is a rapidly growing, biologics CDMO focused on developing and manufacturing recombinant protein products using mammalian cell culture processes. Our business success is built on bringing together top scientific talent, arming them with the best available tools, and setting them loose in an agile, energized culture focused on solving difficult client problems. Because our success depends on our ability to exceed our clients' expectations, we look for candidates with an innate desire to serve. Adaptability and an interest in transformative action are also common attributes among our team. Bionova became a subsidiary of Asahi Kasei Medical in May 2022, a division of Tokyo-based Asahi Kasei Group. This acquisition has enabled Bionova to greatly accelerate growth of the business, both in capacity of current service offerings and expansion into new service offerings. Company: Bionova Scientific LLC Job Description: Company Summary: Bionova is a rapidly growing, biologics CDMO focused on developing and manufacturing recombinant protein products using mammalian cell culture processes. Our business success is built on bringing together top scientific talent, arming them with the best available tools, and setting them loose in an agile, energized culture focused on solving difficult client problems. Because our success depends on our ability to exceed our clients' expectations, we look for candidates with an innate desire to serve. Adaptability and an interest in transformative action are also common attributes among our team. Position Summary: The Manufacturing Associate will actively contribute to the manufacturing and technology transfer projects at the Bionova Scientific Fremont location. As part of the Purification/Manufacturing group, you will have opportunities to work on a wide-ranging set of projects for troubleshooting and investigations, system and workflow implementation, and tech transfers of processes into the GMP manufacturing facility. The role will provide hands-on execution of complex experiments in a team setting. The role will support GMP and manufacturing activities. Essential Duties and Responsibilities: Execute, with oversight of qualified staff, complex unit operations including but not limited to chromatography, TFF, depth filtration, virus filtration, and buffer preparation in GMP manufacturing suites. Maintain own training within compliance. Support in equipment troubleshooting, pilot scale material generation, non-GMP tox material generation and GMP downstream manufacturing activities. Author/review/approve technical documents such as tech transfer protocols and reports, production batch records, training materials, manufacturing SOPs, and regulatory filing documents per project needs. Documents work according to cGMP and cGDP. Adheres to established regulations and follows cGMP established by site. Maintain cleanroom standards, practices, and housekeeping according to SOPs. Recognize any minor issues from the equipment and notify leads/managers of issues and discrepancies immediately. Contributes to quality activities such as investigations and area walk-throughs and support authoring deviations, CAPA, change control. Other duties as assigned and flexible to work in shifts Working Conditions: This position required to work in a lab/office setting. The role requires walking, standing, stooping, kneeling, and crouching. The employee must occasionally lift and or move up to 20 pounds independently. Qualifications Associate degree with 1-2 years of relevant experience, or combination of experience or relevant advanced degree, preferably in biopharma manufacturing role. Working knowledge of cGMP compliance as it pertains to procedures, processes, and manufacturing, preferrable Working knowledge of industry-standard purification processes (affinity, IEX, SEC, viral inactivation and filtration, depth filtration, TFF, UFDF, etc) and equipment (GE AKTAs, disposables), preferrable Experience with process monitoring software and equipment software (UNICORN, Pi Historian) Creative thinker that can identify better and more efficient methods to address issues and gaps Demonstrate ability to work independently and on cross-functional teams Ability to prioritize assignments and to manage multiple projects simultaneously. Compensation Range: The base compensation range for this role is between $25 and $30 an hour. However, the actual compensation may vary depending on your experience and qualifications. Health Benefits and Program: Bionova offers health benefits at a subsidized rate. Healthcare, Dental, and Vision insurance Life Insurance and Disability Program: 100% covered by Bionova. Retirement Plan (401K) Up to 8% of Employer Match Paid time off up to two weeks 10 days of Holidays and 5 days of Sick Leave. As an equal opportunity employer, Asahi Kasei believes a diverse workforce will provide us with the ability to continuously support the changes in the economy, society, and environment.

At a Glance Legrand has an exciting opportunity for a Flexible Associate to join the The Wiremold Team in West Hartford, CT. Perform fabrication and assembly operations to produce products of all kinds, including complex operations. What Will You Do? Major Responsibilities/Activities: * Fabrication and assembly activities include, but are not limited to, pressing, tapping, welding, sealing, labeling, stamping, counting, loading and unloading products and cartons and pallets. In addition, cutting to length and fabricating wires and assembling power/data devices into products including terminating connections and testing of assemblies or finished products. Taking direction from appropriate Group Leader or supervision. * Potentially packs, seals, and labels all raceway products utilizing tools and equipment as needed. Makes minor adjustments on assembling and packaging machines and small hand tools to maintain quality. Taking direction from appropriate Group Leader or supervision. * Uses a variety of hand tools, air screw drivers, tapping machines, automatic and semi-automatic machinery. * Records, maintains, and reports on materials handled, packed, stored, or transported using applicable company systems. * Places completed work in designated location, potentially using basic material handling equipment. * Loads and unloads work in process to machines required in their rotation, including restarts and resets as needed. * Maintains equipment and materials in good repair and maintains an orderly work area consistent with 5C practices and the Wiremold Production system. * Performs Total Preventive Maintenance (TPM) schedules and assignments as required for the tools, equipment and small machines used in the performance of this function. * Complies with all OSHA safety and Company safety procedures and works in a safe manner to insure both personal safety and safety to others. * Performs all assignments with attention to quality standards of workmanship. * Records quality and productivity information as necessary. * May work alone with periodic supervision or may work with a group depending on the products being assembled or the tools and equipment being operated. * Performs other work as directed by Group Leader or supervisor. Qualifications Minimum Requirements: * Must be authorized to work in the United States * Must be able to read, write, speak, and understand English fluently. High school education or equivalent. * Six (6) months prior experience in a manufacturing/warehouse environment, ideally involving wiring and assembly. Other consideration may be given for prior experience with corporations who highly utilize continuous improvement activities. * Must be able to use basic hand tools and measuring instruments. * Must demonstrate an ability to perform standard work processes. * Must be able to perform all work assignments within the classification in a rotation within the work cell/department, in a productive and efficient way, producing work of good quality. * Must be willing to cross train on all rotation assignments in the work cell/department. Essential Mental Functions: * Must be able to work from the paperwork, including but not limited to blueprint or standard work sheets, when the work assignment requires. * Must be able to solve mathematical equations. * Must have good organizing and prioritization skills Essential Physical Functions: Instructions: For the tasks, duties and responsibilities contained in this job description, check all physical aspects below that could be encountered on the job. PHYSICAL ASPECT FREQUENCY, AMOUNT, OR DESCRIPTION Physical Activity (check all that apply) x Bending body downward/forward by bending spine at the waist x Bending legs at knee to come to a rest on knee(s) x Bending the body downward/forward by bending leg/spine x Extending hand(s) and arm(s) in any direction x Standing, particularly for sustained periods of time x Moving about on foot, particularly for long distances x Raising objects from a lower to a higher position or moving objects horizontally from position to position x Picking, pinching, typing or working with primarily the fingers x Applying pressure to an object with the fingers and palm x Verbalizing detailed or important instructions to others accurately, loudly or quickly x Applying substantial movement/motion of the wrists, hands, and/or fingers in a repetitive manner Physical Requirements (check all that apply) o Exerting up to 20 pounds of force occasionally and/or a negligible amount of force frequently or constantly to lift, carry, push, pull or move objects, including the body. Sitting most of the time for sedentary work. x Exerting up to 40 pounds of force occasionally, and/or up to 20 pounds of force frequently, and/or a negligible amount of force constantly to move objects. Using arm/leg controls requiring exertion of forces greater than that required for sedentary work. Physical Surroundings (check all that apply) x Subject to inside environmental conditions, with protection from weather conditions but not necessarily from temperature changes. x Subject to sufficient noise to cause one to shout in order to be heard above the ambient noise level. x Subject to a variety of hazards including moving mechanical parts, electrical current, exposure to high heat or exposure to chemicals. x Subject to one or more of the following conditions: fumes, odors, dusts, mists, gases or poor ventilation. o No substantial exposure to adverse environmental conditions. Visual Acuity x Dealing with data and figures, accounting, transcription, computer terminal, extensive reading, visual inspection involving small defects/parts, operation or machines, using measurement devices, assembly or fabrication of parts at distances close to the eyes. Company Info About Legrand Legrand is the global specialist in electrical and digital building infrastructures. Our comprehensive offering of solutions for residential, commercial, and data center markets makes us a benchmark for customers worldwide. We harness technological and societal trends with lasting impacts on buildings with the purpose of improving life by transforming the spaces where people live, work, and meet with electrical and digital infrastructures and connected solutions that are simple, innovative, and sustainable. Legrand is a global, publicly traded company listed on the Euronext (Legrand SA EPA: LR). For more information, visit *********************** About Legrand North and Central America Legrand, North & Central America (LNCA) is a leader in the AV, Lighting & Controls, Electrical, and Data Center markets. LNCA offers comprehensive medical, dental, and vision coverage, as well as distinctive benefits like a high employer 401K match, paid time off (PTO) and holiday pay, short-term and long-term disability benefit plans, above-benchmark paid maternity and parental leave, bonus opportunities in accordance with the Company's incentive plans, paid time off to volunteer, and an active/growing Employee Resource Group network. For more information, visit legrand.us About Legrand's Electrical Wiring Systems Division Legrand's Electrical Wiring Systems (EWS) division provides the most complete line of residential, commercial, and industrial electrical wiring devices in the world. Through commitment to innovation and quality, EWS maintains the position of industry leader in wire and cable management and wiring devices categories, specializing in raceways, flexible floor, open space and outdoor power solutions, wire mesh cable trays and systems, and designer switches and outlets. With this comprehensive offering, EWS serves a range of exciting vertical markets, including commercial office and commercial interior, data centers, education, healthcare, hospitality, manufacturing, mixed-use developments and residential. For more information, visit legrand.us/electrical wiring devices ********************* ******************************** ************************************* ************************** NA Equal Opportunity Employer

Manufacturing Associate I In this job you will perform a variety of repetitive sub-assembly and/or assembly operations of basic complexity As a Manufacturing Associate I you will: * Prepare work to be accomplished by studying assembly instructions, blueprint specifications, and parts lists, gathering parts, subassemblies, tools, and materials * Position parts and subassemblies by using templates or reading measurements * Assemble components by examining connections for correct fit, fastening parts, and subassemblies * Assist in the building of prototypes and/or other basic assembly projects outside of normal production as needed * Maintain a safe and clean working environment by complying with procedures, rules, and regulations * Conserve resources by using equipment and supplies as needed to accomplish job results * Contribute to team effort by training others in the performance of basic assembly tasks as needed * Inspect all work and ensure it meets requirements before passing it on to the next operation * Document actions by completing production and quality forms * Assist in training new hires or current internal employees who have been newly assigned to this role. We are looking for someone who: * Has a High School diploma, GED or combination of work experience and skill development * Ideally has 0-1 years of experience working in a manufacturing environment * Must be able to safely use small hand and power tools * Must be able to read and interpret Drawings and Bills of Material * Must have basic computer skills * Must be able to understand and follow verbal and written instructions in English. * Is willing to cross-train and develop skills for Manufacturing Associate II roles, which may involve respirator fit and clean-shaven requirements. The physical demands of the job are: * Work is classified as Medium - Heavy Physical Demand Level (PDL) by the US Dept of Labor's Dictionary of Occupational Titles * Frequencies - Occasional (1-33%); Frequent (34-66%); Continuous (67-100%) * Lifting Demands: * Lift up to 75 pounds on an occasional basis floor to waist with assistance * Lift up to 40 pounds on a frequent basis floor to waist * Carry up to 40 pounds on an occasional basis up to 25 feet * Push/Pull up to 40 pounds on a frequent basis * Push/Pull more than 40 pounds on an occasional basis with assistance * Postural Demands: * Standing continuous * Walking continuous * Bending/stooping frequent * Squatting/kneeling frequent * Lifting frequent * Miscellaneous Demands: * Griping, manipulation, fingering continuous * Variable hand/power tool use frequent * Two-person tasks using assistive devices for lifting, pulling and pushing including engine stands hand trucks, pallet jacks, and hoists What we offer you: Pay Range starts at $20 per hour Please note the pay information shown above is a general guideline. Pay is based upon candidate skills, experience, and qualifications. G&W Electric offers a comprehensive benefits package that includes: * Medical, Dental and Vision Insurance * Short and Long-Term Disability * Life Insurance * Health club membership program and reimbursement * Employee Assistance Program * Tuition Reimbursement * 401 (k) * Annual Profit Sharing * Vacation * Air-conditioned/heated state-of-the-art manufacturing facility About G&W Electric Innovating since 1905, G&W Electric has grown into a global leader in engineered electrical power grid solutions. Working with us means joining a worldwide team of passionate manufacturing professionals striving to continually improve the technologies the world depends on to deliver safe, reliable electricity. Our culture is focused on employee success, so we foster an entrepreneurial environment that encourages everyone to thrive. Learn more about our company by watching this video:

Manufacturing Associate I In this job you will perform a variety of repetitive sub-assembly and/or assembly operations of basic complexity As a Manufacturing Associate I you will: * Prepare work to be accomplished by studying assembly instructions, blueprint specifications, and parts lists, gathering parts, subassemblies, tools, and materials * Position parts and subassemblies by using templates or reading measurements * Assemble components by examining connections for correct fit, fastening parts, and subassemblies * Assist in the building of prototypes and/or other basic assembly projects outside of normal production as needed * Maintain a safe and clean working environment by complying with procedures, rules, and regulations * Conserve resources by using equipment and supplies as needed to accomplish job results * Contribute to team effort by training others in the performance of basic assembly tasks as needed * Inspect all work and ensure it meets requirements before passing it on to the next operation * Document actions by completing production and quality forms * Assist in training new hires or current internal employees who have been newly assigned to this role. We are looking for someone who: * Has a High School diploma, GED or combination of work experience and skill development * Ideally has 0-1 years of experience working in a manufacturing environment * Must be able to safely use small hand and power tools * Must be able to read and interpret Drawings and Bills of Material * Must have basic computer skills * Must be able to understand and follow verbal and written instructions in English. * Is willing to cross-train and develop skills for Manufacturing Associate II roles, which may involve respirator fit and clean-shaven requirements. The physical demands of the job are: * Work is classified as Medium - Heavy Physical Demand Level (PDL) by the US Dept of Labor's Dictionary of Occupational Titles * Frequencies - Occasional (1-33%); Frequent (34-66%); Continuous (67-100%) * Lifting Demands: * Lift up to 75 pounds on an occasional basis floor to waist with assistance * Lift up to 40 pounds on a frequent basis floor to waist * Carry up to 40 pounds on an occasional basis up to 25 feet * Push/Pull up to 40 pounds on a frequent basis * Push/Pull more than 40 pounds on an occasional basis with assistance * Postural Demands: * Standing continuous * Walking continuous * Bending/stooping frequent * Squatting/kneeling frequent * Lifting frequent * Miscellaneous Demands: * Griping, manipulation, fingering continuous * Variable hand/power tool use frequent * Two-person tasks using assistive devices for lifting, pulling and pushing including engine stands hand trucks, pallet jacks, and hoists What we offer you: Pay Range starts at $20 per hour Please note the pay information shown above is a general guideline. Pay is based upon candidate skills, experience, and qualifications. G&W Electric offers a comprehensive benefits package that includes: * Medical, Dental and Vision Insurance * Short and Long-Term Disability * Life Insurance * Health club membership program and reimbursement * Employee Assistance Program * Tuition Reimbursement * 401 (k) * Annual Profit Sharing * Vacation * Air-conditioned/heated state-of-the-art manufacturing facility About G&W Electric Innovating since 1905, G&W Electric has grown into a global leader in engineered electrical power grid solutions. Working with us means joining a worldwide team of passionate manufacturing professionals striving to continually improve the technologies the world depends on to deliver safe, reliable electricity. Our culture is focused on employee success, so we foster an entrepreneurial environment that encourages everyone to thrive. Learn more about our company by watching this video:

The Asahi Kasei Group operates with a commitment of creating for tomorrow. Our business sectors, Material, Homes, and Health Care, contribute to the development of society by anticipating the changing needs of those around the world. We look for candidates that offer a fresh perspective and a variety of skills to help us achieve our commitment.Bionova is a rapidly growing, biologics CDMO focused on developing and manufacturing recombinant protein products using mammalian cell culture processes. Our business success is built on bringing together top scientific talent, arming them with the best available tools, and setting them loose in an agile, energized culture focused on solving difficult client problems. Because our success depends on our ability to exceed our clients' expectations, we look for candidates with an innate desire to serve. Adaptability and an interest in transformative action are also common attributes among our team. Bionova became a subsidiary of Asahi Kasei Medical in May 2022, a division of Tokyo-based Asahi Kasei Group. This acquisition has enabled Bionova to greatly accelerate growth of the business, both in capacity of current service offerings and expansion into new service offerings. Company: Bionova Scientific LLC Job Description: Company Summary: Bionova is a rapidly growing, biologics CDMO focused on developing and manufacturing recombinant protein products. As part of our business expansion plan, we are building a state-of-the-art facility that specializes in the development and manufacturing of Plasmid DNA. This facility will be equipped with cutting-edge technology and staffed by a team of highly skilled professionals who are dedicated to advancing the field of Plasmid DNA process development and manufacturing. Our business success is built on bringing together top scientific talent, arming them with the best available tools, and setting them loose in an agile, energized culture focused on solving difficult client challenges. Because our success depends on our ability to exceed our clients' expectations, we look for candidates with an innate desire to serve. Adaptability and an interest in transformative action are also common attributes among our team. Position Summary: Bionova is seeking for Manufacturing Associate, to support plasmid DNA production through upstream and downstream unit operations. This role executes GMP manufacturing processes, documents activities accurately, and supports a safe, compliant manufacturing environment. Essential Duties and Responsibilities: Execute GMP plasmid DNA upstream and downstream production activities within a GMP environment. More specifically, prepare and setup fermenters, centrifuges, mixing and filtration systems and chromatography skids. In addition, weigh and measure raw materials, and prepare media and buffer solutions Follow cGMP and cGDP practices, Maintain accurate and detailed records of all operations in accordance to the standard operating procedures (SOPs), work instructions and batch records. Ensure compliance with cGMPs and other regulatory requirements, including safety and quality standards. Perform routine equipment maintenance and troubleshooting of bioprocessing equipment. Assist in the identification and resolution of equipment issues that arise during production to ensure proper function and prevent downtime. Support manufacturing investigations and non-conformities to products that impact their safety and efficacy. Participate in process improvement initiatives to enhance efficiency, yield and product quality. Stay current with industry trends and best practices and participate in training program to develop new skills and knowledge. Communicate effectively with managers and team members to report production progress, issues, and improvements. Working Conditions: This position requires working in a lab/office setting. The role requires walking, standing, stooping, kneeling, and crouching. The employee must occasionally lift and or move up to 40 pounds independently. Qualifications: High School Diploma or GED required; Associate or bachelor's degree in Life Sciences preferred 1-3+ years of GMP manufacturing experience (biotech, pharma, or CDMO preferred) Hands-on experience with upstream operations or similar biological processes Ability to follow detailed procedures and work in a regulated environment Comfortable working in cleanroom/gowning environments As an equal opportunity employer, Asahi Kasei believes a diverse workforce will provide us with the ability to continuously support the changes in the economy, society, and environment.

JOB PURPOSE: The primary function of this position is the safe and efficient production of electrolyte solution within the facility using proven manufacturing techniques consistent with company policies. The incumbents are charged with the responsibility of delivering the plants goals of zero injuries and environmental releases while meeting all production goals. PRINCIPAL ACCOUNTABILITIES: Identify and take immediate steps to correct any unsafe working conditions. Utilize manufacturing knowledge and experience to proactively operate the plant in a safe, reliable and optimal manner. Under supervision, monitor process conditions, equipment and control system, including responding to alarms. Initiate and control manufacturing of chemicals in vessels, including changing of raw materials, monitoring batches, keeping records and operating process equipment according to Standard Operating Procedures (SOP) and Operating Discipline Principles and Practices. Utilize skills necessary to operate all equipment in the unit as required by operating/safety procedures. Initiate service requests and notify supervision regarding status of equipment malfunctions and troubleshoot process issues as needed. Perform safe-outs, lockout tagout and tryouts Set-up, operate, clean and monitor processing equipment. Complete production records and maintain a clean work environment. All other duties assigned by supervisor that fall within the realm of safe work practices. KNOWLEDGE/ EXPERIENCE/SKILLS: High school diploma required; technical training/education preferred college degree desirable. 1 year experience in a manufacturing environment with chemical experience a plus. Must possess applicable silver level WorkKeys scores - Applied Mathematics, Applied Technology, Locating Information, Reading for Information. Must be computer literate and competent in use of Microsoft Office (Excel, Word and Outlook) Problem solving skills to resolve quality or production problems that may arise. Technical ability to identify problems and resolve them, confidence in job knowledge to make critical operating decisions with supervision. Ability to work a rotating shift; weekends; holidays; overtime; and respond to callouts. Ability to obtain lift truck certification. Strong written and verbal communication skills Strong interpersonal skills including the ability to work as a team. PHYSICAL REQUIREMENTS: Perform all job functions and responsibilities in a safe and responsible manner. Moderate lifting, drum handling, use of stairs, ladders, tools, walking, bending, stooping, work outdoors and at heights, work on 2 _nd_ , 3 _rd_ and 4 _th_ floors; Must be able to lift 50 Lbs. Must be able to wear personal protective equipment and adhere to plant PPE requirements, including but not limited to, pass and keep up with air respirators fit test conditions (No facial hair that affects the seal or valve of the face piece - maximum one day's growth). Must be able to respond to visual and audible alarms. **The salary for this position is $26.81.** **Mitsubishi Chemical Group (MCGC) and any of our subsidiaries do not accept unsolicited resumes from individual recruiters or third-party agencies. No fee will be paid to third parties who submit unsolicited candidates directly to our hiring managers or HR team. No placement fees will be paid to any firm unless specifically invited on the search by the MCGC Talent Acquisition team and such candidate was submitted to the MCGC Talent Acquisition Team via our Applicant Tracking System.** EEO Statement All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status. Applicants with disabilities may be entitled to a reasonable accommodation under the Americans with Disabilities Act and/or other applicable laws. If you require accommodation due to a disability at any time during the recruitment and/or assessment process, please contact Talent Acquisition.

Position Type - Full Time Education Level - High School Starting Pay - $16.00 Hourly WE ARE GROWING!! Production/Machine Operator Positions Monday - Thursday (First Shift 6:00am - 4:30pm) & (Second Shift 4:00pm - 2:30am) Every Expert Rotomolding Production Associate is a critical front-line position and directly impacts the company's sales, growth, and reputation for the highest quality products and service. A successful Production Associate will directly implement the strategies and processes required to provide the highest quality products for our customers. Summary Responsible for making sure procedures/essential functions are followed and communicate the daily issues and concerns. Team members will take responsibility for the tools, and roto machine to produce quality parts. Responsibilities Operate rotational molding machines to form plastic molds and other molded components Maintain proper safety of rotomolding machine and oven Proper loading of rotational molding machine Accurately measure, fill powder buckets and dispense raw materials Machine troubleshooting Operate various pneumatic and hand tools Ability to work at different workstations as per production needs Maintain a clean and safe working environment and optimize space utilization Follow quality service standards Follow all required safety regulations Perform additional duties as required Qualifications Working Conditions Must be able to lift 50 lbs Repetitive bending, stooping, pushing, pulling, standing and sitting Able to climb stairs repeatedly throughout the workday Must be able to withstand shop elements such as heat, noise, odors and dust Requirements High school diploma or general education degree (GED) Able to read and understand written and/or verbal instructions Must be able to accurately complete paperwork for workflow Basic math skills - addition, subtraction, multiplication, and division using whole numbers, common fractions, and decimals. Subject to satisfactory background investigation and drug screening

The Manufacturing Associate 3, Drug product is responsible for Component/Parts Preparation, Thawing and Formulation of Drug Substance, Sterile Filling and Visually Inspecting of Drug Product (DP). This role supports projects which influence manufacturing processes for Drug Product Manufacturing including training of new colleagues. Maintains compliance of cGMP documents and to assist in qualification of equipment and all aspects of startup of the DPFG facility. This manufacturing facility will be 24/7 operational and the role may require to be flexible with working hours and shift rotation Company Overview FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof. We're looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we're proud to cultivate a culture that will fuel your purpose, energy, and drive-what we call Genki. Ready to shape the future of medicine? Let's transform healthcare together! Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh's thriving tech scene, making it the perfect blend of community and opportunity. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: *************************************************** Job Description What You'll Do * Leads, executes and documents manufacturing processing steps and/or manufacturing support activities, process monitoring and control• Performs in-process testing (pH, conductivity, visual inspection)• Executes validation protocols according to cGMP Standard Operating Procedures (SOPs)• Maintains training to perform all required manufacturing activities• Assists and/or lead cycle counts and manage materials for the assigned manufacturing functional area• Performs Operations for all aspects of Drug Product (e.g., Parts Washer, Autoclave, Formulation, Filling, and Visual Inspection)• Assists the lead with tasks in manufacturing activities• Assists with the coordination of daily shift activities• This role may require shift work (weekend and potential for nights)• Performs other duties as assigned Basic Requirements * High School Diploma or GED with 4+ years of direct experience in cGMP manufacturing environment• Associate's Degree + 2 years direct experience in cGMP manufacturing environment OR• Bachelor's Degree, preferably Life Sciences or Engineering OR• Equivalent Military training or experience Preferred Requirements * Qualified Experience on unit operation (e.g., Parts Washer, Autoclave Operation, Compounding/Formulation, Filling with Isolator Technology, or Manual/Automated Visual Inspection) * BioWorks or BTEC Capstone cGMP coursework preferred WORKING CONDITIONS & PHYSICAL REQUIREMENTS * Be exposed to an environment that may necessitate respiratory protection * May work in Mechanical/Production spaces that may require hearing protection and enrollment in a hearing conservation program * Will work in environment operating a motor vehicle or Powered Industrial Truck * Ability to discern audible cues * Ability to inspect or perform a task with 20/20 corrected vision, visual acuity, including distinguishing color * Ability to ascend or descend ladders, scaffolding, ramps, etc * Ability to stand for prolonged periods of time * Ability to sit for prolonged periods of time * Ability to conduct activities using repetitive motions that include wrist, hands and/or fingers * Ability to operate machinery and/or power tools * Ability to conduct work that includes moving objects up to 33 pounds * Ability to bend, push or pull, reach to retrieve materials from 18" to 60" in height, and use twisting motions * Will work in heights greater than 4 feet To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid. EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBN_****************).

Manufacturing Associate (Glass) Wage: Starting at $17.00 (Depending on Experience) with Pay Rate Change Based on Evaluation *Bi-Weekly Pay via Direct Deposit Department: Production Summary Details: Local, Full-Time Schedule, Monday-Friday (Overtime Available Upon Orders) Day Shift Hours Available ( e.g. 8 a.m.-5p.m.) Production Floor Environment (Associates are lifting, moving and standing) Learn Flat Glass Manufacturing & Fabricating Cutting, Polishing, Tempering, Basic CNC Use Tape Measures, Glass Cutters & Other Tools Interested? Call us at ************ or apply through our site. What is Glaz-Tech Industries? Glaz-Tech Industries is a wholesale manufacturer and supplier of residential, commercial, & specialty glass with locations across 7 states. We offer the broadest product line in the flat glass industry including low-e products, laminated glass, tempered safety glass, tinted glass, reflective glass, and specializes in the manufacture of thermal efficient insulated glass units (Dual Pane Units). Why Glaz-Tech Industries? Competitive Pay with Annual Performance Reviews Health Insurance with Employer Contribution Medical, Dental, Vision, and Disability Insurance Company paid Life Insurance 401K Employer Plan Opportunity Paid Vacation and 6 Paid Holidays Training will be provided Employee Discount Program Opportunity to Grow into Supervisory Positions Summary Glaz-Tech is looking for an experienced glass fabricator at our Englewood, CO location . We are looking for a responsible, adaptable and self-driven individual looking to grow in the manufacturing industry. The job functions include fabricating, handling, and assembling glass panes that will be produced into dual pane windows, shower doors, table tops, mirrors, etc. The glass fabricator will use a variety of tools, machinery, and protective gear to ensure product is produced safely and to the highest quality. Responsibilities may include: Learning and using a custom CNC and production program to cut glass to required sizes. Reading production tags to correctly assemble dual pane windows. Organizing window panes onto transportation or storage racks. Loading completed product onto glass trucks for delivery. Requirements: Ability to safely lift 50-75 pounds Must be able to read a tape measure down to 1/8” Ability to physically stand for 8 hours per day. Ability to complete simple computer task. Ability to communicate in English Background Check/Drug Screen Qualifications: Must be 18 years or older High School Diploma or equivalent Authorized to work in the US Job Type: Full-time

Assembly Operator (Manufacturing Associate) The Company Founded in 1946, HI-LEX is a leading supplier of window regulators, door modules, power lift gate systems, and mechanical control cables primarily serving the automotive industry, but also the power sports, marine, construction equipment, and medical device sectors. Headquartered in Takarazuka, Japan (near Osaka), and listed on the Tokyo Stock Exchange (TSE), HI-LEX employs more than 12,000 associates across its global footprint. Assembly Operator: The Job As an Assembly Operator, you be assisting in putting together the door module assembly and/or window regulator. You will be assigned a station at the line. It will be your duty to wait for the to come to you and complete your process for your station in a specific amount of time. Once you are finished, the part will move on to the next person in line. You will then wait for the next part to come to you, repeat the assembly process for your station with the next part, and so on. Assembly Operator Benefits 1 st shift: $17.25 2 nd shift: $18.25 (includes a $1.00 shift premium) PTO Company paid Holidays Company paid Short-Term Disability Company paid Basic Life Insurance Major Medical, Dental, and Vision insurance for you and eligible dependents, including HSA option, available, to start the 1 st of the month following 30 days of employment 401K, with employer match Optional FSA Optional Accident Insurance, Hospital Indemnity, and Critical Illness Optional Long-Term Disability Referral Bonuses Paid Parental Leave Tuition reimbursement Internal promotional opportunities, hourly and salary roles Assembly Operator Duties and Responsibilities: Perform work in safe manner, following all safety rules. Attach components in prescribed order to assemble product. Align, fit and secure components, using hand operations and fastening techniques for bench word. Assure component parts and finished assembly component with all quality checks required by the stations. Assure that component parts used are those required for the part that is being assembled. Assist all other operators on line. Perform the work of all stations on rotating basis as required by the company. Move parts from containers on the floor or other location to the containers in the work area. Sort and rework components on the assembly line or other locations to meet the quality requirements. Perform work in a safe manner, following all safety rules and keeps work area in a clean and orderly condition. Use hand tools, such as staple gun, hand pallet jack, wrapping machine, scale, computer, and printer, as necessary Perform other duties as necessary. Qualifications SPECIALIZED TRAINING, SKILLS, ABILITIES, EXPERIENCE: Use hand tools, staple gun, hand pallet jack, wrapping machine, scale, computer and printer PHYSICAL REQUIREMENTS / WORKING CONDITIONS: Office environment with noise from computer peripherals such as printers and disk drives. Also works in factory environment with noise from manufacturing environment. Exposure to moving equipment, parts and electrical shock. Possible serious injury due to carelessness around equipment. Sometimes lifts, carries or moves objects - weighing up to 35 pounds. Average weight limit is 3-5 pounds.

Assembly Operator The Company Founded in 1946, HI-LEX is a leading supplier of window regulators, door modules, power lift gate systems, and mechanical control cables primarily serving the automotive industry, but also the power sports, marine, construction equipment, and medical device sectors. Headquartered in Takarazuka, Japan (near Osaka), and listed on the Tokyo Stock Exchange (TSE), HI-LEX employs more than 12,000 associates across its global footprint. Assembly Operator: The Job As an Assembly Operator, you be assisting in putting together the door module assembly and/or window regulator. You will be assigned a station at the line. It will be your duty to wait for the to come to you and complete your process for your station in a specific amount of time. Once you are finished, the part will move on to the next person in line. You will then wait for the next part to come to you, repeat the assembly process for your station with the next part, and so on. Assembly Operator Benefits 1 st shift: $17.25 2 nd shift: $18.25 (includes a $1.00 shift premium) PTO Company paid Holidays Company paid Short-Term Disability Company paid Basic Life Insurance Major Medical, Dental, and Vision insurance for you and eligible dependents, including HSA option, available, to start the 1 st of the month following 30 days of employment 401K, with employer match Optional FSA Optional Accident Insurance, Hospital Indemnity, and Critical Illness Optional Long-Term Disability Referral Bonuses Paid Parental Leave Tuition reimbursement Internal promotional opportunities, hourly and salary roles Assembly Operator Duties and Responsibilities: Perform work in safe manner, following all safety rules. Attach components in prescribed order to assemble product. Align, fit and secure components, using hand operations and fastening techniques for bench word. Assure component parts and finished assembly component with all quality checks required by the stations. Assure that component parts used are those required for the part that is being assembled. Assist all other operators on line. Perform the work of all stations on rotating basis as required by the company. Move parts from containers on the floor or other location to the containers in the work area. Sort and rework components on the assembly line or other locations to meet the quality requirements. Perform work in a safe manner, following all safety rules and keeps work area in a clean and orderly condition. Use hand tools, such as staple gun, hand pallet jack, wrapping machine, scale, computer, and printer, as necessary Perform other duties as necessary. Qualifications SPECIALIZED TRAINING, SKILLS, ABILITIES, EXPERIENCE: Use hand tools, staple gun, hand pallet jack, wrapping machine, scale, computer and printer PHYSICAL REQUIREMENTS / WORKING CONDITIONS: Office environment with noise from computer peripherals such as printers and disk drives. Also works in factory environment with noise from manufacturing environment. Exposure to moving equipment, parts and electrical shock. Possible serious injury due to carelessness around equipment. Sometimes lifts, carries or moves objects - weighing up to 35 pounds. Average weight limit is 3-5 pounds.

Agility, Impact, Methodology. Do you exhibit these values and wish to be around others that do too? Do you thrive in fast-paced environments where agility, adaptability, and high standards go hand in hand? Are you driven to make a meaningful impact, whether through your work, your support of others, or your commitment to your community? Are you motivated by a disciplined, science-based approach that ensures consistent excellence, safety, and integrity in everything you do? If these statements resonate with you, Grand River Aseptic Manufacturing (GRAM) welcomes you to apply to join our community of dedicated individuals improving lives every day! Overview of this Position: The Aseptic Manufacturing Associate (AMA) is responsible for performing various routine manufacturing tasks following established procedures and cGMP regulations under guidance of a production supervisor and/or senior management. This primary location for this role is at our Front Avenue facility. The hours are from 6:00 pm to 6:00 am on Friday, Saturday, and Sunday. Non-Negotiable Requirements: A bachelor's degree OR a high school diploma and 2+ years relevant work experience in a manufacturing, medical, and/or laboratory environment is required for a Level I role. A bachelor's degree OR a high school diploma and 3+ years relevant work experience in a manufacturing, medical, and/or laboratory environment is required for a Level II role. Must also have experience working in a sterile manufacturing environment. A bachelor's degree OR a high school diploma and 4+ years relevant work experience in a manufacturing, medical, and/or laboratory environment is required for a Level III role. Must also have experience working in a sterile manufacturing environment. Qualification for use of a full-face respirator is required when working with hazardous chemicals. PAPR is required for working with hazardous chemicals during chemical dispense and addition activities. Preferred Requirements: Previous experience in pharmaceutical manufacturing or a laboratory environment is preferred. Responsibilities Include (but are not limited to): Perform equipment preparation, bulk drug formulation, and aseptic filling duties as needed. Accurately document data and complete batch records as needed. Perform cleaning and sanitization duties as instructed by the applicable procedure. Successfully complete facility's aseptic gowning and manufacturing qualification program. Perform duties in Grade 5, ISO 6, ISO 7, and ISO 8 cleanrooms. Full job description available during formal interview process. What sets GRAM apart from other employers: MEDICAL BENEFITS starting day 1: medical and dental, vision, life insurance, and disability benefits are available to you and your family on your first day of work, with the company paying for 75% of the cost! Once eligible for the 401(k) program, all your contributions are immediately 100% vested, and you are immediately vested in GRAM contributions as well. We also offer generous off-shift premiums! Paid VOLUNTEERISM starting day 1: GRAM encourages giving back to our community by offering 16 hours of paid volunteer time per calendar year! PTO: Full-time employees accrue up to 13 days of time off per calendar year. You choose how to use this time for your vacation, sick, or mental health needs! WELLNESS TIME OFF: Employees earn 1 hour of time off for every 30 hours worked to use how you choose. PAID HOLIDAYS: We offer 10 paid holidays per calendar year with immediate eligibility! PAY: Depends on Experience and is discussed during the interview process. If you meet the required criteria listed above, GRAM welcomes you to apply today!