Manufacturing Associate Jobs in Irvine, CA

Kinovate Life Sciences, Inc. established in 2004 in Oceanside, California. A wholly owned subsidiary of Nitto Denko Corporation (*************** Kinovate was spun-off from Oceanside, CA based R&D facility Nitto Denko Technical Corp (**************** with a mission to provide the highest quality materials to niche life science markets worldwide. Since its inception, Kinovate has grown to become the market leader in solid support in the oligonucleotide synthesis field. We are bringing the most creative minds in science and technology to develop medical discoveries and breakthroughs. Our customers are well-known in the biotechnology industry. We are in a growth phase within ISO work environment and leading towards a GMP Certification. KLS is seeking extraordinary people to join the team. KLS is proud to be an equal employment opportunity employer. Why Work Here Great place to work. Small subsidiary of large international company headquartered in Japan. Generous discretionary bonuses. Health, dental, vision, life, and disability insurance effective from date of hire. Additional benefits include 401(k), 3 weeks vacation in your first year, 12 paid yearly holidays, 5 paid sick days, tuition reimbursement and more. JOB SUMMARY: Under direct supervision, partner with manufacturing leadership to provide tactical services in the production of commodities for the organization. Partner with a variety of departments across a cross-functional organizational matrix, e.g., Quality Assurance (QA) /Quality Control (QC) and Supply Chain (SC). Work within a Good Manufacturing Practices (GMP) environment and the International Organization of Standardization (ISO) manufacturing environment. Follow Standard Operating Procedures (SOP's) ensuring no deviations occur during the manufacturing endeavor. ESSENTIAL DUTIES and/or RESPONSIBILITIES: 1. Reviews production schedule to determine what raw materials to assemble including any consumables for the manufacturing of all products and batches sizes. Ensures pre-production data meet the customer specifications and Quality Assurance (QA) requirement before proceeding to manufacturing batches. 2. Sets-up equipment and prepares labs to manufacture products based on SOPs and the production schedule. 3. Assures daily, weekly, and monthly productivity goals are met by the production department. 4. Authenticates product data information by using strong attention to details such as, but not limited to, the production schedule, SOPs, serial numbers, lot numbers, expiration dates, log reports and checklists. 5. Keeps accurate records of all transactions throughout product cycle, including any revisions or updates during the process. 6. Evaluates work for accuracy and completeness in accordance with SOPs and Manufacturing Best Practices. Identifies deviations in process to improve quality and safety of manufacturing. 7. Contributes to quality, safety and lean manufacturing policies, processes or procedures including sustaining a clean workstation and area in accordance with 5S standards. 8. Recognizes and supports continuous improvement efforts with production management team to streamline production procedures. 9. Works with QA team to implement the quality policies and goals and draft production-related procedures, as necessary. 10. Other duties as assigned. MINIMUM EDUCATION and/or EXPERIENCE: 1. Bachelor's degree in Biochemistry, Chemistry, or related field; and three (3) to five (5) year's directly related experience or equivalent combination of education and experience. 2. Experience in failure investigations and prevention, a plus. KNOWLEDGE, SKILLS and/or ABILITIES: Working knowledge of pharmaceutical and chemical manufacturing industry concepts, as well as SOPs, including, documenting manufacturing processes consistently and accurately. Ability to work with other departments across the organization to achieve goals. Familiarity with operating production equipment including reactors, stirrer, vacuum pumps, and vacuum ovens and automated manufacturing methods and understanding of workflow processes. Ability to work with a high volume of data with a high-level of accuracy, strong attention to detail and good follow-up and follow-through while doing repetitive tasks. Work independently as well as in a small and/or large group and foster cooperation in a team environment using interpersonal skills to document working knowledge. Strong application of critical thinking skills along with problem solving and creative skills to identify manufacturing issues for continuous improvement. Strong multi-tasking skills, flexibility in responding to rapidly changing, dynamic processes and demands/pressures in a fast-paced environment. Strong ability to verbally communicate across functional organizational groups, provide high-level customer service through effective interpersonal skills. Basic Microsoft Office Suite software applications such as Excel, Word, Power Point, and other enterprise software applications such as Net Suite, etc. Ability to read and interpret documents such as SOPs, safety rules, written instructions, checklists, and reports. Write clear processes, manuals and reports for management review and present technical information in understandable terms and respond to questions from groups of customers, employees and/or public. Understanding of KLS Quality Management System and EHS policies. PHYSICAL DEMANDS and/or WORK ENVIRONMENT: (Typical physical demands and the work environment characteristics an employee must meet and encounter while performing the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.) Sit for 30%-40% of time at a desk doing sedentary reports, research, work with computer and interfacing with others on the manufacturing floor. Must be able to stand/walk frequently up to 6 hours in a day. Ability to occasionally lift/carry items up to 30 pounds as well as overhead. Ability to push/pull carts or pallet jacks loaded with raw materials, work in progress and finish goods occasionally up to 3 hours in a day. Ability to grasp objects with a force up to 30 pounds.

Exciting Opportunity: Manufacturing Technician Are you passionate about making a difference in the medical device industry? Join our innovative team as a Diagnostic Instrument Assembler and contribute to the development of cutting-edge diagnostic instruments! Job Description: Assemble Diagnostic Instruments: Work alongside engineers to assemble diagnostic instruments compatible with consumable cartridges. Electrical Assemblies: Assemble electrical components, PCBs, and electrical wiring Materials Management: Prepare and manage materials inventory. Organize and Maintain: Keep your work area organized and maintain supplies. Independent Work: Perform tasks independently with minimal supervision. Safety First: Ensure a safe work environment, especially when handling chemicals and equipment. Operate Equipment: Use test equipment efficiently. Testing and Troubleshooting: Apply your skills in testing and troubleshooting electronics. Special Projects: Assist with special projects and additional duties as assigned. Experience: Medical Device Experience: Preferably experienced in the medical device industry. Assembly Skills: Skilled in assembling diagnostic instruments and/or molded consumables. Electrical Hardware: Experience with PCB assembly, electromechanical builds, and instrumentation maintenance. Testing and Troubleshooting: Proficient in testing and troubleshooting electronic components.

At a top Biopharmaceutical company, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Manufacturing Technician at our Los Angeles, CA site. Here, you will be a vital contributor to our inspiring, bold mission, and have the opportunity to grow within a thriving company. Summary: The Manufacturing Technician is responsible for maintaining, cleaning, preventing maintenance repairs, and overall being within a GMP environment. This is a perfect entry level position for those with minimal experience or want to gain further career advancements within the Biotech industry! Title: Manufacturing Technician I Location: Glendale, CA - Onsite Duration: 6 months potential for extension/conversion Multiple Shifts Available: Overnight Weekend Fri-Sat-Tues 10PM - 10:30AM and Swing M-F 2PM-10:30PM Responsibilities: Perform process equipment cleaning and organization within the Pre-viral department. Maintain GMP area housekeeping (per GMP compliance) such as cleaning walls, floors, doors, drains, windows, and other general surface areas. Empty trash containers and maintain an adequate amount of cleaning supplies. Perform removal of hazardous waste. Supports all local manufacturing operations. Supply components, small parts, tubing, etc. Complete relevant paperwork following GDP/GMP guidelines. Manually clean all portable equipment, small parts, plastic tubing, and equipment. Receive and distribute supplies into the production area as necessary. Manual 5 step cleaning & automated cleaning Details on the cleanings: chemicals used bleach, 500 ppm, liquinox Type of cleaning: cleaning small parts in a sink subjecting to different waters; mostly stainless steel parts Qualifications: Attention to details when weighing chemicals to make cleaning solutions Experience in GMP environment and good documentation process Able to assist with prioritization of assignments in order to maximize support for the Fractionization production area. Must have good written and verbal communication skills and understanding of cGMP regulations. Familiarity with pharmaceutical production equipment including but not limited to CIP. Must be able to read and follow detailed written instructions. Good interpersonal skills and be able to work effectively and efficiently in a team environment. This position requires shift, weekend, and holiday work. Overtime may be required at times. The incumbent must work in a cleanroom environment wearing special garments. Additionally, personal protective equipment must be worn due to safety requirements. Knowledge of basic chemical and biological safety procedures. Requires AA degree or high school diploma with 0-2 years related manufacturing experience. Ability to read, write, speak English and communicate effectively. Should possess basic math skills. Previous work-related experience is preferred. Some college experience is preferred. Education: Must have 1-3 years experience w/ GED or High School Diploma Recent College graduates with a Science Background are highly recommended to apply Knowledge of GMP/SOPs in Manufacturing setting

The Technician performs fundamental tasks within a GMP environment in support of more complex manufacturing operations. The Tasks include, but are not limited to, cleaning and maintaining the work place so that it meets the standards for controlling bioburden levels; cleaning operating equipment per applicable procedures so that it meets the standards established to prevent product contamination and maintaining records/logs neatly and accurately and in accordance with current standard procedures. The technician performs job tasks in a safe manner while following specific department safety rules. 6:30 AM-3:00 PM Monday-Friday Primary Responsibilities: Responsible for equipment setup and operation in a biologics processing environment for plasma derived pharmaceuticals Detailed cleaning of equipment/facilities to MSP/cGMP standards. Complete technical training profile as required. Strict adherence to Dept. Safety Rules Bulk processing and filtration involving monitoring processing parameters (i.e. pH, weights, separation, assay results..) Perform real-time documentation during the production run. Responsible for equipment setup and operation in a biologics processing environment for plasma derived pharmaceuticals Additional Responsibilities: English fluency both verbal and written. Accurate documentation skills is a must Basic computer skills Mechanical aptitude Ability to work well with others in a team environment is essential. Self-starter with the ability to work independently and use good judgment. Must be able to handle multiple priorities. Must be proactive, results oriented, and have strong attention to detail Knowledge, Skills, and abilities: Accurate documentation and attention to detail oriented. Education: High school diploma or GED required. Associates Degree or Bachelors degree preferred. Manufacturing, or experience in pharmaceuticals/biologics processing in a GMP Experience: 1-2 years experience in a manufacturing environment Occupational Demands: Ability to lift/push 50 lbs. All work is preformed in a clean room (sanitized) manufacturing environment and must gown up. Must be able to work in a cold environment , job requires bending or standing for prolonged periods.

12 month Contract Pay rate: $25-33 /hr W2 Onsite only US Citizenship required Performs functions associated with all manufacturing operations, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components, subassemblies and final assemblies. Uses sophisticated programs to collect and evaluate operating data to conduct on-line adjustments to products, instruments or equipment. Determines and may assist in developing methods and procedures to control or modify the manufacturing process. Works with engineers in conducting experiments.

Job Details Entry 0T534 CA - El Monte, CA Undisclosed N/A Full Time High School $17.46 - $23.62 Hourly None 2nd Shift Manufacturing 2nd Shift: 2:00 p.m. to 10:30 p.m. Who We Are: The Gill Corporation is one of the world's largest manufacturers of honeycomb, high performance floor panels, cargo compartment liners and original equipment for passenger and freighter aircraft. The company also excels in many other types of reinforced plastics including interior sandwich panels for creating structures such as aircraft galleys and bulkheads, honeycomb core and related products. Summary: We are looking for individuals with or without prior experience in production assembly. High attention to detail, accuracy, efficiency and a team player are key qualities to be successful in this role. Responsibilities: Primarily responsible for laying up panels and liners prior to the work order to load and unload into the press and assembling precut material slices (Balsa, Aluminum, Nomex) into panels or liners. Will check core accuracy according to work order and that orders are properly signed off on. Prepare and stage all left over materials to be returned back to warehouse. Ensures all materials used are within shelf-life requirements. Makes sure housekeeping is being maintained and all containers are properly labeled. Qualifications: Minimum 1-year Manufacturing experience (Assembly/Machine Operating/Warehouse) Basic PC Computer Skills Must be able to lift, push & pull a minimum of 50 lbs. Ability to reach, grab, pull and stand for entirety of shift. A minimum composite score of 240 on the Wonderlic Basic Math Skill Test is required. Benefits offered: Full range of medical benefits, dental, vision Life Insurance 401(K) and Profit Sharing Paid Vacation, Sick Leave and 10 Paid Holidays Tuition Reimbursement Employee discounts to theme parks, attractions, shows and more! Shift differentials ITAR Requirement: This position requires access to information that is subject to compliance with the International Traffic Arms Regulations (“ITAR”) and/or the Export Administration Regulations (“EAR”). In order to comply with the requirements of the ITAR and/or the EAR, applicants will be asked to provide specific documentation to verify U.S. person status under the ITAR and the EAR. A “U.S. person” according to their definition is a U.S. citizen, U.S. lawful permanent resident (green card holder), or protected individual such as a refugee, or asylee. The Gill Corporation is an Equal Opportunity Employer . Applicants for all job openings are welcome and will be considered without regard to race, religious creed, color, age, sex, gender identity, gender expression, genetic information, sexual orientation, national origin, religion, marital status, medical condition, physical or mental disability, military service, pregnancy, childbirth and related medical conditions, or any other classification protected by federal, state, and local laws and ordinances. The Gill Corporation provides reasonable accommodations to qualified individuals with disabilities in accordance with the Americans with Disability Act and applicable state and local law. If you require an accommodation in the application process, please notify the Human Resources Department.

Huntsman is seeking a Production Operator supporting the Advanced Materials Division located in Los Angeles, CA . This position will report to the Production Manager. Job Scope This role involves Huntsman is currently recruiting for a Production Operator for our chemical manufacturing site in Los Angeles, CA. As a flexible and motivated team member, you will operate plant equipment and chemical processes safely and efficiently to production output. The Production Operator, the primary responsibility is gaining knowledge and in-depth understanding of the production process and its supporting operations and applying that knowledge to achieve the desired outcome of efficient production. The ideal candidate shall be responsible for all unit functions including housekeeping necessary to maintain a safe and efficient operation. In summary, as the Production Operator, you will: Safely handle chemicals and chemical processing equipment (vessels, mixers, reactors, dischargers, etc) for the manufacture of epoxy and polyurethane type formulations for aerospace, electronics, tooling, etc. Processes incorporate heating, cooling, vacuum, pressure, nitrogen purging and exothermic reactions Applicant must be able to follow instructions precisely as written (in English) as well as verbally and adhere to all safety precautions and PPE (personal protection equipment) requirements Shift work is required Good housekeeping is essential along with motivation for high quality Working knowledge of basic mathematics and science/engineering is necessary. Use of a forklift and physical handling of drums is common The role also includes the filling of containers and cleaning of equipment and tools The individual should be able to work independently as well as part of a team, following instructions and completing tasks as assigned by Supervisor/Lead Operator Must be accurate and precise. Assist employees in accomplishment of Huntsman company goals Participate in and complete company-required training programs Participate in Environmental, Health and Safety initiatives as set forth by the company Qualifications You must possess the below minimum qualifications to be initially considered for this position. Preferred qualifications are in addition to the minimum requirements and are considered a plus factor in identifying top candidates. The candidate must have an unrestricted right to work for Huntsman in the United States. Minimum Qualifications High School diploma or equivalent, such as GED required 3 or more years of related experience in a manufacturing facility, preferably a chemical formulation plant You must be approved/cleared by the State and Federal to extend applicable to work with controlled chemicals that Huntsman utilizes at the site You must be willing and able to work any of the three shifts (1st, 2nd, or 3rd) based on business needs: 1st Shift Hours: 6:00 a.m. - 2:30 p.m. 2nd Shift Hours: from 2:00 p.m. - 10:30 p.m. 3rd Shift Hours: from 10:00 p.m. - 6:30 a.m. Skills and knowledge Follow instructions and perform other duties as may be assigned by supervisor Excellent communication skills as position interface with various departments and contractors Dealing with ambiguity and priority setting Proven understanding of day-to-day business activities, reporting and operations Computer literacy Ability to work well with others and works well in a team setting Able to communicate clearly with line supervisors and management Working Environment Starting rate for Production Operator is $35.00/hr. plus $2.00/hr. shift differential for hours worked from 2:00pm-6:00am. The compensation range reflects the Company's reasonable expectation at the time of posting. We consider a number of business-related factors when making individual compensation decisions including, but not limited to, education, experience and training. Step progression available based on qualification - minimum of 12 months prior to associate qualifying. Huntsman offers outstanding benefits which start from Day One. Competitive healthcare, dental, and vision. One additional week of paid time off - on top of vacation. 401k - Huntsman automatically contributes 6% of eligible pay, regardless of employee contribution. In addition to the 6% non-discretionary contribution, Huntsman will match $1 for every $1 you contribute up to a maximum match of 4% of eligible pay. Huntsman is proud to be an equal opportunity workplace and is an affirmative action employer. We provide equal employment opportunities (EEO) to all qualified applicants for employment, without regard to race, color, religion, sex, national origin, disability status, protected veteran status, gender identification, sexual orientation and/or expression or any other characteristic protected by law in every location in which we have facilities national or local. Please refer to ****************************************************** for Company's Data Privacy and Protection information. All unsolicited resumes presented by recruitment agencies are treated as pro bono information or service. Huntsman is aware of a scam involving fraudulent job offers. Huntsman does not make job offers until after a candidate has submitted a job application and has participated in a face-to-face interview. Please be advised that emails from Huntsman always end in “@huntsman.com” , and that any job offer that requires payment or requires you to deposit a check is likely a scam. If you have questions about any open positions at Huntsman, please visit our Careers website at ******************************************** Additional Locations:

About Us At Quaker Houghton, we are experts in the development, production and application of industrial process fluids, lubricants and coatings for the manufacturing industry. We have been an integral part in the growth of the world s largest industrial and manufacturing companies from aerospace and automotive to primary metal and energy. Today, we have a global presence, with our corporate headquarters located in Conshohocken, PA. Quaker Houghton is a global publicly traded company with a unique collaborative culture that supports career growth for its colleagues and offers competitive compensation and benefit programs. Position Summary: Coordinate activities of all contract manufacturing activities to ensure that orders are delivered on time, within specifications and at minimal cost. Must be bilingual in Spanish and English Job Responsibilities: Assist Contract Manufacturing (CM) Manager in Negotiating Contract Manufacturing rates, including preparation of bid packets. Work with product management & Supply Chain Department (SCD) team to ensure adequate contract manufacturing capacity in accordance with strategic plan. Works with SCD and Quality Assurance to qualify new contract manufacturers. Acts as a buyer of raw materials for various contract manufacturing sites Manage the storage of raw materials and finished goods at contract manufacturing sites by setting stocking levels and doing periodic cycle counts, and select carriers for transport. Provide leadership for resolution of raw material, shipping or other operational problems to ensure minimum costs and prevent delays. Monitor performance by tracking costs and other metrics on weekly, monthly and YTD basis; investigate and respond to CPR s; identify and implement corrective actions and process improvements. Make required transactions in JDE, including Item Setups, bill of material (BOM) and routings. Compile, store, and retrieve production data; produce reports for position customers as needed. Establish and maintain good working relationships with position customers, and meet customer needs. Assist CM Manager to implement policies and procedures and recommend improvements. Investigate all billing and invoice discrepancies from the contract manufacturers and /or related suppliers. Ensure timely processing of CM orders & shipments. Assist with contract manufacturing site audits, as needed, based on the audit schedule. This includes auditing safety and environmental practices Assist CM Manager in maintain contract manufacturing records as to comply with ISO and SOX requirements. Education, Experience, Training and Skills: Bachelor s degree (B. A. or B.S.) in related technical discipline preferred. Persons with an education less than a degree must demonstrate successful related experience and/or training in the area of contract manufacturing. Minimum 2 years relevant experience. Must have successful work experience in a manufacturing environment, preferably related to manufacturing of chemical products or technical knowledge of manufacturing and equipment. Experience with JDE or similar Enterprise software, and experience with shipment of hazardous goods and DOT requirements is also preferred. Work Environment: While performing the duties of this job the employee is frequently required to sit, stand and walk; use hands to finger or handle; reach with hands and arms; talk and hear. The vision requirements include close vision, distance vision and peripheral vision. Must be able to travel by automobile and air to visit contract manufacturing sites in MX, USA and CA. Must be able to don and wear personal protective equipment (PPE) as required by work environment and/or job task (example but not limited to: full/half respirator, safety glasses, goggles, gloves, and steel toes boots). Must be able to traverse oily, slippery or uneven terrains. While performing the duties of this job the employee is generally working in an office environment. Occasionally exposed to moving mechanical parts; high, precarious places; fumes or airborne particles; toxic or caustic chemicals and risk of electrical shock, slippery surfaces, and occasionally exposed to loud noise levels. Quaker Houghton is an equal opportunity employer committed to creating a diverse workforce. Quaker Houghton provides equal employment opportunity for all qualified candidates. Quaker Houghton does not discriminate against any candidate for employment based on race, color, religion, sex, gender, gender identity or expression, affectional or sexual orientation, pregnancy, age, creed, ancestry, national origin, citizenship, marital or domestic partnership or civil union status, veteran s status, physical/mental disability, genetic information, or any other category protected by U.S federal, state, and/or local employment law. Furthermore, Quaker Houghton is committed to providing reasonable accommodations to qualified candidates with physical and/or mental disabilities. Applicants with a disability who need assistance applying for a position may email ************************ .

Who we are. Dendreon is making the battle against cancer personal. Our flagship product PROVENGE (sipuleucel-T), was the first FDA approved immunotherapy for the treatment of metastatic castrate resistant prostate cancer and is made from the patient's own immune cells. If you are looking to positively impact the lives of patients, we want you to join our team. We have Immunotherapy Manufacturing Facilities located in Seal Beach, CA and Union City, GA. A sizeable Research & Development group based out of Seattle, WA, and a highly skilled Commercial team countrywide. Core Values: Put Patients First. Every day is a new opportunity to improve the lives of patients living with Act with Integrity. Be honest, transparent, and committed to doing what's right in every situation. Build Building trust takes time. Engage teammates, be candid and transparent. Over communicate and seek feedback. Raise the Harness continuous improvement, foster innovation and elevate our people. Drive Results. Be accountable and execute - we win together when everyone performs Your Role: Aseptic manufacturing and assembly of clinical and commercial human blood derived components in a clean-room environment (Class 10,000/ISO7, and Class 100,000/ISO8). Responsibilities Your Work: Weighs, measures and checks raw materials to ensure batches manufactured contain proper ingredients and quantities. Maintains records to comply with regulatory requirements and acts as subject matter expert for revisions or improvements to manufacturing documents. Works with other Cell Processing Associates utilizing good manufacturing practices during aseptic processing of clinical and commercial products using Standard Operating Procedures. Represents department in cross-functional teams, projects and GXP-related problem resolution. Posts weights and shipping charges, and prepares goods for final shipment. Prepares and maintains records of merchandise shipped. Prepares goods for final shipment and unpacks and checks goods received against purchase orders and invoices, maintains records of received goods, rejecting unsatisfactory items if necessary. Examines, stocks, and distributes GMP and non-GMP materials to inventory and manufacturing lines. Perform other duties as assigned Scope: Applies job skills and company policies and procedures to complete a wide range of tasks. Works on assignments that are moderately complex in nature where judgment is required in resolving problems and making routine recommendations. Normally receives general instructions on routine work, detailed instructions on new assignments. Uses ability as a skilled specialist in accordance with company policies and procedures to compete complex tasks in creative and effective ways. Works on assignments that are complex in nature where considerable judgment and initiative are required in resolving problems and making routine recommendations. May determine methods and procedures on new assignments and may provide guidance to other support personnel. Ability to be flexible and support all functions by readily responding to changing circumstances (i.e. shift changes) and business needs. Qualifications High school diploma with 3-5 years of stable work history OR Associates/Technical Degree. BA/BS degree in Science. No prior industry experience required. Experience in medical device, pharma or biotech preferred. Must be able to read and understand quality documents. Must be able to read, write and communicate fluently in English. Working Conditions and Physical Requirements: Ability to sit or stand for extended periods of time Intermittent walking to gain access to work areas Finger dexterity sufficient to use a computer and to complete paperwork activities Vision sufficient to use a computer, to read written materials and to complete paperwork activities; Hearing sufficient to communicate with individuals by telephone and in person Ability to lift up to 25 pounds. Limited exposure to (2ºC - 8ºC); (-20ºC); (-75ºC); (-196ºC) areas. Must have the ability to work around laboratories, manufacturing areas and equipment, and regularly lift 10 - 20 lbs and lift up to 50 lbs. May be required to work alternate shifts Ability to gown aseptically for work in Clean Room environments Job performed in a lab, office, or utility (noisy) environment Must have the ability to work around laboratories, manufacturing areas and equipment with exposure to blood, blood products or OPIM (other potentially infectious materials) while donning required personal protective materials.

Helpmates is seeking a Manufacturing Associate in the city of Cerritos.This role requires attention to detail, teamwork, and a commitment to quality in a fast-paced production environment. Schedule: Monday - Friday, 6:00 AM - 2:30 PM Pay Rate: $20/hr. Job Responsibilities: Perform quality tasks in a production setting Collaborate with team members to achieve shared goals (SQDC) Adapt to and promote changes in processes and workflows Deliver excellent customer service Communicate effectively in English, both verbally and in writing Operate a microscope proficiently Demonstrate dependability and the ability to work independently Maintain flexibility with work assignments as needed Approach challenges with a positive and solution-oriented mindset Foster a culture of continuous improvement Use and interpret various measuring devices accurately Perform basic soldering tasks when required Follow established procedures and processes precisely Contribute to a collaborative and supportive team environment Participate in continuous improvement initiatives Requirements: Soldering experience preferred Ability to learn, apply, and retain training Strong analytical and quality evaluation skills Positive attitude and commitment to company values Willingness to learn, adapt, and collaborate in a team environment Strong attention to quality and detail Effective communication and teamwork skills Basic math skills (addition and subtraction) Ability to follow company procedures and troubleshoot issues Education & Experience High school diploma, GED, or equivalent manufacturing experience If you’re detail-oriented, dependable, and ready to grow in a manufacturing role, apply today! #HSCE

Job Purpose Under general supervision, an assembler assembles components efficiently, safely and within budget. Key Responsibilities · Assemble components with the use of drawings, schematics or written work instructions. Work may include fitting or soldering parts together. Some assemblies require the use of adhesives and epoxies · Subassemblies or finished products in a manufacturing environment. Perform tests on electrical assemblies during the production process · Operate various power tools and occasional use of drill press · Loads and unloads signs · Completes daily time-ticket · Clean and maintain work area and equipment to provide a safe and organized work environment · Work safely to prevent on the job injuries following all safety regulations; including PPE (safety glasses, safety shoes, and on occasion gloves, dusk mask, or job specific safety equipment) · Interacts with other departments · Performs other related duties as assigned by management Skills Qualifications · Ability to deal effectively and tactfully with a wide variety of individuals in person · Ability to organize, prioritize and coordinate multiple work activities to meet critical deadlines, as well as working independently · Solid basic math skills · Strong work ethic with an enthusiastic, positive attitude, and the highest level of integrity · Good communication skills in order to receive and follow instructions and communicate to others necessary information pertaining to the production of signs · Maintain regular and timely attendance Education/Training/Experience · High School Diploma or GED · 1-2 years assembly experience preferred Note - Other duties, responsibilities and activities may change or be assigned at any time with or without notice. The above is intended to describe the general content of and requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities or physical requirements. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. PHYSICAL/MENTAL DEMANDS AND WORK ENVIRONMENT: The physical and mental demands described here are representative of those that must be met by employees to successfully perform the essential functions of this class. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Physical Demands Work is generally performed in a shop environment. While performing the duties of this class, the employee is regularly required to sit, walk, talk or hear in person, climb or balance; stoop, push, kneel, or crouch; smell; use hands and fingers to handle, feel or operate objects, tools or controls; and reach with hands or arms. The employee is often required to stand. Employees must frequently lift and/or move up to 50 pounds; occasionally up to 75 pounds and stand for full 8 + hour shift. Specific vision abilities required by this job include close vision, distance vision, color vision, depth perception and the ability to adjust focus. Work Environment The employee frequently works near moving mechanical parts, is exposed to cold or humid conditions and vibration. The employee is occasionally exposed to Epoxy, Silicone, Caulk, and Super Glue. The noise level in the work environment is frequently loud. We are an E-Verify employer. We conduct background and drug tests upon hire.

Looking for individuals who have prior manufacturing experience in cosmetics, food products, aerospace, or electrical assembly. Our team has fun, and we make a great product that is very popular online. Through the interview and application process, we will identify the best part of the manufacturing process for you to assist in. Job duties may include: - Production Line - Ingredient Mixing - Picking, Packing, and Packaging - Material Handling Many positions require that you get a bit dirty, but we provide all the necessary gear to make the job comfortable for you. Requirements Previous manufacturing experience required. At least 6 months. Our job is different than general warehouse positions. Ability to read instructions in English Benefits - Increase in pay for learning new departments - Easy conversion process from temporary to permanent employee - Weekly pay - Product giveaways - Food often provided

Compunnel Software Group is a New Jersey based premier information technology consulting & services company into this market for nearly two decades now; with close to two decades of experience in IT Industry which includes consulting, development, e-learning etc. Our company is going through a tremendous growth spurt and we are now interested in personnel like you to augment the work force in the company. We have several projects starting that we are staffing for. If you think you would like to become a consultant for Compunnel Software Group Inc ., please send me an updated copy of your resume along with a detailed summary of your work experience. I need a phone number to contact you. I look forward to possibly working with you on these positions. We offer specialized services to our clients to meet their business objectives. Successful solutions that are valued by our clients are in industry areas such as pharmaceuticals, telecommunications, banking, finance, manufacturing, publishing and consumer products. Title: Manufacturing Associate/Assembly- 1st Shift Location: Chatsworth 9172 Eton Ave. Chatsworth CA 91311 United States Duration: 04 Months+ Interview: F2F Shift : 1st shift (7:00am - 4:00pm) Job Description: "*******MUST HAVE SOLDERING EXPERIENCE***** FLEXIBILITY - There may be times the selected candidates will help out in Shipping as needed. This group moves groups as needed for production reasons. The candidates must be flexible to float and help out between departments as needed. 1+ years of assembly experience and minimum GED/High School Diploma This is a short term assignment, it will not extend past the end of the year. Additional Information If you are interested you can call me at ************ / ************ Ext 1706

The role of a Manufacturing Associate I is crucial in maintaining the efficiency and effectiveness of the production process. They actively participate in meeting production targets and deadlines, which is essential in ensuring that the company can accurately and timely deliver customer orders. ESSENTIAL JOB FUNCTIONS Monitor machinery and equipment used in manufacturing, such as molded parts, to ensure products are made to specification. Remove the parts from the machine manually. Conduct visual inspections of the parts to check for pre-prescribed defects. Document inventory and quality management production data, including quantities produced, defects identified, and materials used. Correct certain defects, such as flash, using general tools based on engineering and quality feedback. Assemble subcomponents of products, following detailed assembly instructions. Package finished products for shipping, including labeling and preparing items according to customer orders. Maintain a clean and safe work environment by adhering to safety protocols and cleaning schedules. Participate in team meetings to discuss production goals and continuous improvement strategies and address concerns about the manufacturing process. Available to cover for other associates during their lunch and break times. * Other duties as required in support of the department and the company* SUPERVISOR RESPONSIBILITIES This role is purely as an individual contributor. QUALIFICATIONS To succeed in this job, an individual must satisfactorily perform each essential job function. The requirements below represent the required knowledge, skill, and ability. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. EDUCATION and EXPERIENCE A high school diploma or equivalent, e.g., vocational training, is required. Familiarity with standard manufacturing practices and equipment preferred. Experience in quality assurance (QA) and regulatory compliance preferred. Experience in basic troubleshooting of manufacturing processes preferred. Experience in the medical industries or molding businesses preferred. LANGUAGE REQUIREMENTS Excellent verbal and written communication skills in English. Conversational in any other language preferred. MATHEMATICAL SKILLS Basic arithmetic: add, subtract, multiply, and divide whole numbers. JOB SKILLS Familiar with Microsoft Office tools and SharePoint basics, eager to learn and expand proficiency. Basic knowledge of Continuous Improvement, Lean Manufacturing, and the 5S Methodology. Able to identify process deviations and product defects. Able to effectively allocate resources to ensure timely product delivery that meets the required specifications. Ability to set up, operate, and maintain equipment to ensure output meets established quality standards. Dependable and willing to work overtime when necessary. PHYSICAL DEMANDS The employee will regularly engage in activities such as using hands to finger, handle, or feel and communicating verbally. Additionally, the employee will frequently need to reach with hands and arms while standing and walking as part of the role. Occasional lifting and movement of objects weighing up to fifty (50) pounds may be required. This position also demands specific vision capabilities, including close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus. According to ADA regulations, reasonable accommodation will be provided to ensure that individuals with disabilities can perform the job's essential functions. WORK ENVIRONMENT A work environment in a plant is the physical and social setting where goods production occurs. Depending on the type of product, process, and plant, the work environment may vary in terms of noise, temperature, safety, and demand. Common characteristics of a work environment in a plant are the use of machinery and exposure to hazards such as chemicals, heat, dust, or noise, with a culture of teamwork, communication, and continuous improvement. ENVIRONMENTAL POLICY Carlisle Interconnect Technologies is dedicated to identifying and reducing the environmental impact of its operations, activities, and products. We are committed to complying with all applicable laws and other environmental regulatory requirements. We are also committed to preventing pollution and improving our environmental performance in all our global operations. This will be achieved through a comprehensive Environmental Management System that provides the framework for setting and reviewing Carlisle Interconnect Technologies' environmental objectives and targets. PERSONAL PROTECTIVE EQUIPMENT REQUIREMENTS ASTM F-2412-2005, ANSI Z41-1999, or ANSI Z41-1991 rated safety toe shoes in specific areas. Clear ANSI Z87.1 safety-rated glasses in specific areas. Hearing protection in specific locations. Ability to compile with JSA in specific areas. EXPORT COMPLIANCE DISCLAIMER This position includes access or potential access to ITAR and EAR technical data. Therefore, candidates must qualify as US Persons, defined as US Citizens or Permanent Residents (Green Card Holders). TRAVEL Travel is not required for this position. SALARY INFORMATION: According to the laws of several states, the hourly/salary range for this position falls between $17 and $19 per hour/annum. However, this salary information is merely a general guideline. When extending an offer, Carlisle Interconnect Technologies considers various factors such as the position's responsibilities, scope of work, candidate's work experience, education/training, essential skills, internal pay equity, and market considerations. I have read and understand the job description requirements and can fulfill the essential duties, responsibilities, and qualifications.

Cerritos, CA, USA Req #11978 Thursday, April 3, 2025 **Company Information** Headquartered in St. Augustine, FL, with offices and manufacturing facilities all around the globe, Amphenol CIT is one of the world's leading designers and manufacturers of high-performance wire, cable, and medical devices. We provide complete interconnect solutions to industries like Aerospace, Military & Defense Electronics, Space, Medical, Test & Measurement, and Industrial. Our talented team of employees worldwide helps bring movies to your seat on airplanes, deliver mission-critical information from drones to the command office, transfer heart rhythm to paper, route communications from space, connect power to downhill oil drills, and get planes back in the air faster. At Amphenol CIT, we make the amazing possible. Take the next step to become an integral part of our team by applying today and kickstart your journey with us. **SUMMARY** The role of a Manufacturing Associate I is crucial in maintaining the efficiency and effectiveness of the production process. They actively participate in meeting production targets and deadlines, which is essential in ensuring that the company can accurately and timely deliver customer orders. **ESSENTIAL JOB FUNCTIONS** + Monitor machinery and equipment used in manufacturing, such as molded parts, to ensure products are made to specification. + Remove the parts from the machine manually. + Conduct visual inspections of the parts to check for pre-prescribed defects. + Document inventory and quality management production data, including quantities produced, defects identified, and materials used. + Correct certain defects, such as flash, using general tools based on engineering and quality feedback. + Assemble subcomponents of products, following detailed assembly instructions. + Package finished products for shipping, including labeling and preparing items according to customer orders. + Maintain a clean and safe work environment by adhering to safety protocols and cleaning schedules. + Participate in team meetings to discuss production goals and continuous improvement strategies and address concerns about the manufacturing process. + Available to cover for other associates during their lunch and break times. _*Other duties as required in support of the department and the company*_ **SUPERVISOR RESPONSIBILITIES** This role is purely as an individual contributor. **QUALIFICATIONS** To succeed in this job, an individual must satisfactorily perform each essential job function. The requirements below represent the required knowledge, skill, and ability. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. **EDUCATION and EXPERIENCE** + A high school diploma or equivalent, e.g., vocational training, is required. + Familiarity with standard manufacturing practices and equipment preferred. + Experience in quality assurance (QA) and regulatory compliance preferred. + Experience in basic troubleshooting of manufacturing processes preferred. + Experience in the medical industries or molding businesses preferred. **LANGUAGE REQUIREMENTS** + Excellent verbal and written communication skills in English. + Conversational in any other language preferred. **MATHEMATICAL SKILLS** + Basic arithmetic: add, subtract, multiply, and divide whole numbers. **JOB SKILLS** + Familiar with Microsoft Office tools and SharePoint basics, eager to learn and expand proficiency. + Basic knowledge of Continuous Improvement, Lean Manufacturing, and the 5S Methodology. + Able to identify process deviations and product defects. + Able to effectively allocate resources to ensure timely product delivery that meets the required specifications. + Ability to set up, operate, and maintain equipment to ensure output meets established quality standards. + Dependable and willing to work overtime when necessary. **PHYSICAL DEMANDS** The employee will regularly engage in activities such as using hands to finger, handle, or feel and communicating verbally. Additionally, the employee will frequently need to reach with hands and arms while standing and walking as part of the role. Occasional lifting and movement of objects weighing up to fifty (50) pounds may be required. This position also demands specific vision capabilities, including close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus. According to ADA regulations, reasonable accommodation will be provided to ensure that individuals with disabilities can perform the job's essential functions. **WORK ENVIRONMENT** A work environment in a plant is the physical and social setting where goods production occurs. Depending on the type of product, process, and plant, the work environment may vary in terms of noise, temperature, safety, and demand. Common characteristics of a work environment in a plant are the use of machinery and exposure to hazards such as chemicals, heat, dust, or noise, with a culture of teamwork, communication, and continuous improvement. **ENVIRONMENTAL POLICY** Carlisle Interconnect Technologies is dedicated to identifying and reducing the environmental impact of its operations, activities, and products. We are committed to complying with all applicable laws and other environmental regulatory requirements. We are also committed to preventing pollution and improving our environmental performance in all our global operations. This will be achieved through a comprehensive Environmental Management System that provides the framework for setting and reviewing Carlisle Interconnect Technologies' environmental objectives and targets. **PERSONAL PROTECTIVE EQUIPMENT REQUIREMENTS** + ASTM F-2412-2005, ANSI Z41-1999, or ANSI Z41-1991 rated safety toe shoes in specific areas. + Clear ANSI Z87.1 safety-rated glasses in specific areas. + Hearing protection in specific locations. + Ability to compile with JSA in specific areas. **EXPORT COMPLIANCE DISCLAIMER** This position includes access or potential access to ITAR and EAR technical data. Therefore, candidates must qualify as US Persons, defined as US Citizens or Permanent Residents (Green Card Holders). **TRAVEL** Travel is not required for this position. **SALARY INFORMATION:** According to the laws of several states, the hourly/salary range for this position falls between$17and$19per hour/annum. However, this salary information is merely a general guideline. When extending an offer, Carlisle Interconnect Technologies considers various factors such as the position's responsibilities, scope of work, candidate's work experience, education/training, essential skills, internal pay equity, and market considerations. I have read and understand the requirements and can fulfill the essential duties, responsibilities, and qualifications. AMPHENOL CIT RESERVES THE RIGHT TO MODIFY, INTERPRET, OR APPLY THIS IN ANY WAY THE COMPANY DESIRES. THIS IN NO WAY IMPLIES THAT THESE ARE THE ONLY DUTIES, INCLUDING ESSENTIAL DUTIES, TO BE PERFORMED BY THE EMPLOYEE OCCUPYING THIS POSITION. THIS JOB DESCRIPTION IS NOT AN EMPLOYMENT CONTRACT, IMPLIED OR OTHERWISE. THE EMPLOYMENT RELATIONSHIP REMAINS "AT-WILL." THE AFOREMENTIONED JOB REQUIREMENTS ARE SUBJECT TO CHANGE TO REASONABLY ACCOMMODATE QUALIFIED DISABLED INDIVIDUALS. Amphenol CIT is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status. For more information regarding EEOC requirements please visit **************************************************************** ***************************************************************************************************** Due to the nature of our business, the candidate must be able to legally work in the United States; we are unable to provide sponsorship. Position requires candidate to be a U.S. person as defined in ITAR, 22 CFR 120.15 (U.S. Citizenship or Resident Alien Status) and defined by 8 U.S.C. 1101(a) (20). Amphenol CIT participates in the United States Department of Homeland Security E-Verify program. The E-Verify program is a web-based employment eligibility verification system for newly hired employees operated by the U.S. Citizenship and Immigration Services. Any candidate that needs an accommodation or assistance with the application process should contact HR at ********************************** **Other details** + Pay Type Hourly + Cerritos, CA, USA <

Job Purpose Under general supervision, an assembler assembles components efficiently, safely and within budget. Key Responsibilities · Assemble components with the use of drawings, schematics or written work instructions. Work may include fitting or soldering parts together. Some assemblies require the use of adhesives and epoxies · Subassemblies or finished products in a manufacturing environment. Perform tests on electrical assemblies during the production process · Operate various power tools and occasional use of drill press · Loads and unloads signs · Completes daily time-ticket · Clean and maintain work area and equipment to provide a safe and organized work environment · Work safely to prevent on the job injuries following all safety regulations; including PPE (safety glasses, safety shoes, and on occasion gloves, dusk mask, or job specific safety equipment) · Interacts with other departments · Performs other related duties as assigned by management Skills Qualifications · Ability to deal effectively and tactfully with a wide variety of individuals in person · Ability to organize, prioritize and coordinate multiple work activities to meet critical deadlines, as well as working independently · Solid basic math skills · Strong work ethic with an enthusiastic, positive attitude, and the highest level of integrity · Good communication skills in order to receive and follow instructions and communicate to others necessary information pertaining to the production of signs · Maintain regular and timely attendance Education/Training/Experience · High School Diploma or GED · 1-2 years assembly experience preferred Note - Other duties, responsibilities and activities may change or be assigned at any time with or without notice. The above is intended to describe the general content of and requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities or physical requirements. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. PHYSICAL/MENTAL DEMANDS AND WORK ENVIRONMENT: The physical and mental demands described here are representative of those that must be met by employees to successfully perform the essential functions of this class. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Physical Demands Work is generally performed in a shop environment. While performing the duties of this class, the employee is regularly required to sit, walk, talk or hear in person, climb or balance; stoop, push, kneel, or crouch; smell; use hands and fingers to handle, feel or operate objects, tools or controls; and reach with hands or arms. The employee is often required to stand. Employees must frequently lift and/or move up to 50 pounds; occasionally up to 75 pounds and stand for full 8 + hour shift. Specific vision abilities required by this job include close vision, distance vision, color vision, depth perception and the ability to adjust focus. Work Environment The employee frequently works near moving mechanical parts, is exposed to cold or humid conditions and vibration. The employee is occasionally exposed to Epoxy, Silicone, Caulk, and Super Glue. The noise level in the work environment is frequently loud. We are an E-Verify employer. We conduct background and drug tests upon hire.

RxSight is an ophthalmic medical technology corporation headquartered in Aliso Viejo, California that has commercialized the world s first and only adjustable intraocular lens (IOL) that is customized after cataract surgery. The company s mission is to revolutionize the premium cataract surgery experience by allowing surgeons to partner with their patients to achieve optimized results for every unique eye. OVERVIEW: The LAL Manufacturing Associate Technician, reporting to the Manager LAL Manufacturing, will focus on fully understanding the company's technology. After training in manufacturing procedures, the employee needs to be capable of executing each process step meeting time and quality standards. ESSENTIAL DUTIES AND RESPONSIBILITIES: Manufacturing Process: This individual will interact with the other functions including but not limited to Engineering, Quality, Warehouse, Planning, Chemistry and R&D. It is expected that this individual will have the depth and breadth of experience to contribute to the overall manufacturing of the LAL lenses. The LAL Manufacturing Associate Technician must complete the work with the highest Quality standards possible within the allowed time given to maintain the highest efficiencies. Employees may be expected to execute any of the following activities based on training and skillset: Cleanroom Activities: Gowning/Kanban Inventory Replenishment Cleanroom Monitoring Cleaning of Molds & Lens Holders Cleaning of lens caps & cases Haptic Cutting, polishing, cleaning, inspection, and sorting Label Production & application Tyek Pouching of Lenses Silicone Lens Molding Conducting lens testing according to established work instructions utilizing a variety of equipment such as: dimensional, optical and mechanical test benches, and OCT equipment. Haptic preparation & verification for molding Deflashing of Lenses Cleaning of Lenses Assisting in validation protocol execution. With guidance from engineering, performs tests, gathers test data and records results in accordance with manufacturing requirements. Training of manufacturing personnel on manufacturing process Supporting process improvement initiatives to enhance production efficiency, as well as ensure business continuity and regulatory compliance. Employees may also train and be asked to execute activities beyond this , while working toward a certification of an already established job description within the department function. Said training will be documented in accordance with quality system requirements and added to employee file as record of achievement. Additionally, employee may be certified to lead a process or set of processes, once proving they have mastery of the area and meeting the following criteria. This role places a higher level of responsibility for the individual to ensure proper training, execution, and mastery of processes within the area assigned. This does not place the employee in a supervisory role. Employee must prove to embody the following values to be considered for a certification: Qualification in areas of responsibility Respect (for self and others) Teamwork Sense of Urgency Customer Focus Professionalism Interpersonal communication Problem Solving Ability Certification is contingent on the following: Management discretion to train and select individuals as needed. Employees cannot have been involved in any human relations issue while at work within prior three months of petition for certification. Required Knowledge, Skills and Abilities: Microscope use, handling, and assembly of microscopic parts. Prior work inside a cleanroom environment. SUPERVISORY RESPONSIBILITIES: This job has no supervisory responsibilities. EDUCATION, EXPERIENCE, and TRAINING: Minimum of associate degree or three to five years related experience and/or training; or equivalent combination of education and experience on medical devices. Employee Training is completed per the training plan for this position as maintained in the document control system. The training requirements on TRN-10007 Insider Trading Policy, TRN-10008 Global Anti-Bribery and Anti-Corruption Policy and TRN-10009 Code of Business Conducts and Ethics must be diligently completed within 30 days from the hiring date and on an annual basis. CERTIFICATES, LICENSES, REGISTRATIONS: This job does not require certification, licensing, or registrations aside from the training and certification provided by RxSight. COMPUTER SKILLS: Baseline skills with Microsoft office applications (Word, Excel, Outlook, Teams), online spreadsheets (Smartsheet) and ERP system software (QAD) preferred. SALARY RANGE: $23.00 - $24.00 Per Hour

THE ROLE: * Travel Requirement: None * FLSA Status: Non-Exempt * Shift: 3rd shift 11pm-730am * Employment Category: Full Time - Regular * Pay Range: $21.00 to $25/hr. Generous Brands is dedicated to inspiring people to thrive through the power of vibrant nutrition through its leading brands, Bolthouse Farms, Evolution Fresh and our joint venture with Sambazon. Bolthouse Farms is the preeminent provider of chilled juice, smoothies, and protein drinks. Evolution Fresh - is the premier, cold-pressed juice brand and maker of the new Real Fruit Soda. Through our integrated partnership with Sambazon we produce and sell their high-quality Acaí beverages. Formerly known as Bolthouse Farms - Generous Brands was born out of the independence from its carrot operations and is poised to be the "World's Largest Beverage Start-Up." Currently we have 1000 employees located across the country at our hubs/facilities in Bakersfield, CA, Rancho Cucamonga, CA & Chicago, IL. You can connect with our brands on their socials - Bolthouse Farms (LinkedIn, Instagram and TikTok ) and Evolution Fresh (LinkedIn, Instagram and TikTok). WHAT YOU'LL BE RESPONSIBLE FOR IN THIS ROLE This position contributes to Evolution Fresh success by supporting and operating product packaging equipment in a juicing plant. Models and acts in accordance with Evolution Fresh guiding principles * Operates and maintains downstream secondary equipment * Replenishes raw materials on automated packaging equipment * Responds to stoppages on secondary packaging equipment and conducts troubleshooting, jam clearing and Cleaning * Performs changeovers on secondary packaging equipment and assists machine operator with changeover on primary packaging equipment * Responsible for quality checks on secondary packages, including lot coding and aesthetics * Assists machine operator with quality checks on primary packages, including lot coding, aesthetics, and seal Integrity * Tracks output from the palletizing equipment and responds to jams * Operates the supersack loading station * Demonstrates and understands safety as a core value and follows the key essentials to safety as set forth by our safety resolution; reinforces and coaches others to do the same * Understands and follows established safety guidelines, consistently complies with all safety procedures (e.g. PPE, Lock Out Tag Out) * Supports food safety, legality and quality programs * Maintains product quality through adherence to good manufacturing practices, Food Safety Preventative Controls, product specifications and quality procedures. Monitors and documents quality measures using analytical tools * Performs other duties as needed in support of business objectives and Evolution Fresh Mission & Values * Maintains regular and consistent attendance and punctuality WHAT WE'RE LOOKING FOR MINIMUM QUALIFICATIONS: * High School diploma/GED or equivalent experience * Production or distribution environment (1 year) * Operation of manual and automated packaging equipment (1 year) ADDITIONAL REQUIRED QUALIFICATIONS: * Basic math skills * Ability to follow verbal direction * Proficiency in Microsoft Windows and internet environments * Mechanical aptitude to make minor machine adjustments and clear jams in equipment * Ability to perform quality tests using analytical tools * Ability to gather, record on operational and quality metrics, through manual or automated systems * Ability to understand written policies and guidelines, specifications, and safety standards * Ability to work with a diverse team environment * Ability to work in accordance with safety, quality and sanitation standards, policies, and procedures * Ability to work variable shifts to support business needs PREFERRED QUALIFICATIONS: * Experience performing quality tests using analytical tools * Troubleshooting skills * Familiarity with food safety regulatory requirements and global standards including Preventive Controls for Human Food (FDA Code of Federal Regulations) and the Global Food Safety Initiative (GFSI). Experience with the GFSI certification schemes (i.e. BRC and/or or SQF) PHYSICAL DEMANDS: * O = Occasional (up to 25% of time) * F = Frequent (26%-74% of time) * C = Constant (75% or more of time) WHAT WE OFFER Our rich benefits packages are designed to support the health and well-being of both our eligible co-workers and their families. * Medical * Dental * Vision * Group Life and AD&D * Voluntary Life and AD&D * Group Short-Term Disability * Group Long-Term Disability * Flexible Spending Accounts * Employee Assistance Program * 401(k) * Paid Time Off EQUAL EMPLOYMENT OPPORTUNITY We are an equal opportunity employer committed to fostering a culturally diverse organization. We strive for inclusiveness and a workplace where mutual respect is paramount. We encourage applications from a diverse pool of candidates, and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, religion, sex, age, national origin, disability, sexual orientation, gender identity and expression, or veteran status. We will provide reasonable accommodations to qualified individuals with disabilities, as need, to assist them in performing essential job functions. REASONABLE ACCOMMODATIONS Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions. If you are interested in applying for employment with Generous Brands and need special assistance to apply for a posted position, or if you believe you do not meet any of the required qualifications of a posted position due to a protected disability and would like to explore the possibility of an accommodation, please contact our Talent Acquisition team at: ******************************* for additional support and guidance. RECRUITMENT AGENCIES: Generous Brands does not accept unsolicited agency resumes. Generous Brands is not responsible for any fees related to unsolicited resumes. #LI-YX1 #EvolutionFresh 3rd shift 11pm-730am

Collaborate with Innovative 3Mers Around the World Choosing where to start and grow your career has a major impact on your professional and personal life, so it's equally important you know that the company that you choose to work at, and its leaders, will support and guide you. With a variety of people, global locations, technologies and products, 3M is a place where you can collaborate with other curious, creative 3Mers. This position provides an opportunity to transition from other private, public, government or military experience to a 3M career. The Impact You'll Make in this Role As a Manufacturing Department Helper, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative people around the world. Here, you will make an impact by: * Maintaining cleanliness of work areas through different means such as shoveling, sweeping, wheelbarrow usage and/or bobcat, front loader and fork truck operation. Housekeeping duties include sweeping and shoveling crushed rock * Handling hazardous waste following appropriate plant procedures. Proper handling includes packaging, labeling, container inspection, and sealing * Obtaining and maintaining a valid PIV (Power industrial Vehicle) license * Operating heavy machinery and PIV's including, but not limited to Forklifts and Guzzler Trucks * Work in varying climate conditions. Your Skills and Expertise To set you up for success in this role from day one, 3M is looking for candidates who must have the following qualifications: * Possess a High School Diploma/GED or higher (completed and verified prior to start) from an accredited institution. * Work weekends, overtime, holidays, work any shift available, including, but not limited to, first, second, third and, short notice call-in as needed Applicants meeting the basic qualifications above may be required to take and pass 3M elected testing as a part of the selection process. Additional qualifications that could help you succeed even further in this role include: * Minimum of three (3) years of experience in manufacturing, construction, mechanical, and/or agriculture experience * SAP experience * Experience working in a mining environment * Experience operating a powered fork truck * Able to understand and follow both oral and written instructions Pay & Benefits: The starting rate of pay for this position is $26.88 and goes up to after 4 months of employment to $30.49. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate's relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental & Vision, Health Savings Accounts, Health Care & Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences, and Retirement Benefits, etc.). Additional information is available at: ************************************************************** Relocation Assistance: Is not authorized Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status). Supporting Your Well-being 3M offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, 3M regularly benchmarks with other companies that are comparable in size and scope. Resources for You For more details on what happens before, during and after the interview process, check out the Insights for Candidates page at 3M.com/careers. All US-based 3M full time employees will need to sign an employee agreement as a condition of employment with 3M. This agreement lays out key terms on using 3M Confidential Information and Trade Secrets. It also has provisions discussing conflicts of interest and how inventions are assigned. Employees that are Job Grade 7 or equivalent and above may also have obligations to not compete against 3M or solicit its employees or customers, both during their employment, and for a period after they leave 3M. Learn more about 3M's creative solutions to the world's problems at ********** or on Instagram, Facebook, and LinkedIn @3M. Responsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties. Pay & Benefits Overview: ************************************************************** 3M is an equal opportunity employer. 3M will not discriminate against any applicant for employment on the basis of race, color, religion, sex, sexual orientation, pregnancy, gender identity, national origin, age, disability, or veteran status. Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly. 3M Global Terms of Use and Privacy Statement Carefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at 3M are conditioned on your acceptance and compliance with these terms. Please access the linked document by clicking here, select the country where you are applying for employment, and review. Before submitting your application, you will be asked to confirm your agreement with the terms.