Manufacturing associate jobs in Compton, CA - 386 jobs

A growing apparel company is seeking a detail-oriented Production Associate to join their team.. This role is ideal for someone experienced in mass-market apparel production who can manage multiple styles, communicate effectively with factories, and ensure accurate, on-time delivery. Key Responsibilities: • Manage and track a high volume of apparel styles from development through delivery • Liaise between factories, design, and sales teams to ensure clear communication • Review and spec production samples; provide detailed fit and construction comments • Communicate revisions and approvals to factories and cross-functional partners • Approve final production samples and ensure quality standards are met • Coordinate sample send-outs and maintain organized tracking across all milestones • Support overall production timelines and workflow management Qualifications: • 3-5 years of apparel production or product development experience • Mass-market background required; experience with accounts • Category experience in men's, boys', or young men's preferred (juniors acceptable)- Mass Market • Strong understanding of garment specs, construction, and fit approvals • Excellent organizational and communication skills • Ability to manage multiple priorities in a fast-paced environment • Proficiency in Microsoft Office; PLM experience is a plus • Must be able to work onsite in Los Angeles

About Bobrick Headquartered in North Hollywood, CA, Bobrick is a global leader in stainless steel commercial washroom accessories with more than 100 years of innovation. Founded in 1906, Bobrick pioneered the world's first lavatory-mounted soap dispenser and has grown into a mid-sized, privately owned enterprise with trusted brands like Koala Kare. Today, Bobrick operates eight manufacturing facilities across the U.S., Canada, the U.K., and India, serving customers in over 125 countries worldwide. Job Summary Bobrick is hiring a Manufacturing Associate (Partition Finisher) for the first shift (5:30am - 2:00pm shift) in North Hollywood, CA. This is a great opportunity for those in the field of Wood Working, Cabinetry, Construction, or a closely related field. Under the guidance of a team leader or supervisor, you will assist with cutting and fabricating materials such as particle board, plywood, plastic laminate, and phenolic panels to required dimensions. You'll learn to safely operate a variety of shop equipment including panel saws, cut-off saws, routers, drills, drill presses, and glue application machines while producing quality parts that support daily production needs. Additional tasks include performing housekeeping and some preventative maintenance. This position is well-suited for someone looking to build hands-on manufacturing skills in a supportive, team-oriented environment. Job Responsibilities: Work closely with other department members in a fast paced environment. Handle phenolic and laminate material to finish and drill components. Operate and perform general maintenance on machines and equipment regularly. Use a variety of material handling equipment, including forklifts, as needed. Maintains production and quality standards. Reports, and contributes to problem solving in order to correct or prevent quality defects and errors. Assists senior level department positions in packaging, gluing and finishing components. Loads, unloads and organizes materials in the department as required. Uses drills and fixtures to attach leveling devices, t-nuts, and inserts. Prepares headrails for shipment as required. Submits suggestions for departmental, process and safety improvements. Maintains work area in a neat and orderly manner. Works in accordance with all safety standards. Uses a variety of material handling equipment, including forklifts as needed. Utilizes RF Scanners to scan labels and track job information. Under close supervision, checks toilet compartment components for final finish and appearances, and files out blemishes or scratches to ensure quality standards. Minimum Requirements: High school diploma or general education degree (GED). Some shop or industrial woodworking experience preferred. Ability to read, write and follow verbal and written instructions in English. Must possess basic math skills. Must be able to read a tape measure. Capable of using routers, files and other shop equipment as directed and trained. Must be able to organize own work and determine sequences of operations. Location: North Hollywood, CA Schedule: M-F, 5:30am - 2:00pm (overtime required based on business needs) Pay: $21.50 - $24.00 Benefits: Medical Dental Vision 401(k) Retirement Plan Life and AD&D Long- and Short-Term Disability Insurance Flexible Spending Account (FSA) Health Savings Account (HSA) Paid time off for vacation, sick and personal days Parental Leave Educational Assistance Program Employee Assistance Program Pet Insurance Why Join Bobrick? You'll find the stability of a long-established company with the growth opportunities of a trusted industry leader. We offer an inclusive culture, competitive benefits, and the chance to contribute to sustainable solutions that make a difference worldwide. Join us to grow your skills and contribute to a company built on innovation, integrity, and sustainability. Together, we're shaping the future of washroom design, one project at a time. Legacy & Leadership - 100+ years as a global washroom solutions leader Purpose-Driven Impact - Products that improve hygiene, accessibility, and sustainability worldwide. Growth Opportunities - Training, mentorship, and career advancement. Inclusive Culture - Collaborative, respectful, and diverse workplace Sustainability Commitment - Supporting green building and environmental stewardship. Global Stability - Privately held, established brand with global presence. Bobrick's Culture: We view our culture as a competitive advantage and a foundation for continued success. Our positive and supportive culture encourages our people to do their best work every day. Bobrick respects work-life balance, has a strong commitment to employee development and attributes its success to five core values and their alignment with its employees, suppliers, sales representatives, distributors and other channel partners. We are dedicated to: Do the right thing: Conduct all aspects of business honestly, ethically, and responsibly. Offer the best value: Provide products and services which best meet each customer's needs. Treat everyone with dignity and respect. Embrace all backgrounds and experiences, promote equity, and be inclusive. Help each employee develop and achieve their potential. Foster a fearless and trusting culture. Continuously improve everything we do.

"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive. Join a rapidly expanding global company, where diverse perspectives and experiences come together in a collaborative environment. Here, you'll find a workplace that values both collective success and your individual contributions-offering long-term opportunities to grow and make an impact. Your Role: 3rd Shift Position - 10 PM to 6:30 AM Sunday night to Friday morning This position requires knowledge and ability to perform duties related to the manufacturing of drug products in a cleanroom environment, aseptic, device and assembled products utilizing reliable methods according to established procedures. Your Profile: Responsibilities Completes training modules regarding cleaning and sanitization methods for aseptic environments, this includes but is not limited to the use of germicidal/bactericidal/veridical/ agents, isopropyl alcohol, Sporklenz, Minnteck etc. Completes training modules regarding gowning techniques for the entrance to and from ISO 5/6 designated areas. Performs set up activities and operates aseptic filling machines. Perform cleaning activities post fill. Ability to assess the process performed, and if necessary, stop a line to insure a quality product. Ensures good document practices in the recording, maintenance, reviewing and organizing of batch records, forms, documents and logbooks for responsible areas. Assists other team members in manufacturing areas when needed. Maintain good work place organization and housekeeping. Responsible for adhering to applicable SOP, GMP and ISO rules and regulations related to the position. Train and instruct personnel to perform tasks following appropriate SOPs. Any and all other related duties as assigned by immediate supervisor. Required Knowledge, Skills and Abilities Good oral and written communication skills Good team and problem solving skills Initiative and manual dexterity Ability to stand continuously for two or more hours while wearing proper gowning materials Ability to work safely and use all material moving equipment in a safe manner Basic math skills Ability to work overtime as necessary Required Education and Experience High school graduate or equivalent A minimum of 4+ years of aseptic filling operator experience Pharmaceutical industry experience helpful Experience with cGMP and aseptic gowning for ISO 5/6 helpful Target Pay Range: $27-30/hour + 15% Differential when working on 3rd Shift Your Benefits: Medical, Dental Vision Life, Accident, Disability Voluntary Life, AD&D, Pet 401K Founded in 1873 in Zofingen, Switzerland, Siegfried has grown into a global network of 13 sites across three continents. With a team of more than 3,800 highly skilled professionals, we take the innovations of our pharmaceutical customers to industrial scale and manufacture safe drugs for patients worldwide. As a fully integrated CDMO, Siegfried is one of the few organizations today that can carry out the development and manufacturing of APIs and finished dosage forms under one roof. This unique combination of know-how and experience makes us the most trusted partner in the pharmaceutical industry.

ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. We envision a day when we no longer fear cancer, but can conquer it, thanks to the biological wonder that is the human immune system. Our scientists are working to develop novel therapies that harness that inherent power by amplifying both branches of the immune system, attacking cancerous or infected cells today while building immunological memory for tomorrow. The goal: to reprogram the patient's immune system and treat the host rather than just the disease. Why ImmunityBio? * ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases. * Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern California. * Work with a collaborative team with the ability to work across different areas of the company. * Ability to join a growing company with professional development opportunities. Position Summary The Associate, Manufacturing is responsible for supporting biological manufacturing. All functions and roles of the manufacturing process are required to be performed with adherence to cGMP and GDP to ensure successful, quality operations. Essential Functions * Performs manufacturing activities according to cGMP guidelines, including batch record execution and review, product and equipment changeover, manufacturing equipment troubleshooting, issue resolution. * Execute process operations in accordance with dynamic production timeline. * Ensures safety and cGMP compliance in manufacturing area at all times * Communicate transparently with management on all manufacturing related activities * Utilize Cell culture expansions and aseptic techniques * Develop and author necessary supporting cGMP documentation that supports all Cell Culture manufacturing processes. * Maintain aseptic gowning qualification status and participate in semi-annual media fills. * Engage cross-functionally with other departments in order to stream-line all operations supporting cGMP manufacturing. * Cross-train on and assist with multiple cell lines operations as required. * Contribute to and develop process improvement initiatives with all Cell Culture manufacturing equipment and operations. * Assist and/or execute ordering of material and ensure that equipment and materials are available for production runs. * Adhere to Standard Operating Procedures (SOPs) and cGMP guidelines. * Maintain and sustain all organizational training profile requirements. * Performs ad-hoc and cross-functional duties and/or projects as assigned to support business needs and provide developmental opportunities. Education & Experience * Bachelor's degree in chemical engineering, genetics, molecular biology, biotechnology, microbiology, biochemistry, or a related field is required * Relevant industry or research experience is preferred * Bio-Manufacturing experience is preferred Knowledge, Skills, & Abilities * Attention to detail, cleanliness, physical and mental flexibility * Good perception to implement what has been learned, following guidelines precisely * Understanding and application of safety and quality requirements * Solid adherence to cGMP * Ability to successfully work in a team environment with effective communication skills * Hands on approach to learned skills * Team player with good communication skills * Skill in Microsoft Word, Excel, and PowerPoint * Ability to read, understand and apply Standard Operating Procedures (SOPs) and Manufacturing Batch Records (MBRs) Working Environment / Physical Environment * This position works onsite and depending on location may need to travel to other buildings * This position works in a lab environment * Must have ability to perform work while wearing the appropriate gowning material for cleanroom environments and work under aseptic conditions in a class 100 environment (BSC). * Ability to work on unscheduled days occasionally to support the dynamic production schedule and relevant timelines. * Ability to manage up to fifty (50) pounds at a time and stand for extended periods of time while wearing appropriate clean room gowning material and appropriate personal protective equipment is required This position is eligible for a discretionary bonus and equity award. The hourly base pay range for this position is below. The specific rate will depend on the successful candidate's qualifications, prior experience as well as geographic location. $31.25 (entry-level qualifications) to $35.00 (highly experienced) per hour The application window is anticipated to close on 60 days from when it is posted or sooner if the position is filled or closed. ImmunityBio employees are as valuable as the people we serve. We have built a resource of robust benefit offerings to best support the total wellbeing of our team members and their families. Our competitive total rewards benefits package, for eligible employees, include: Medical, Dental and Vision Plan Options • Health and Financial Wellness Programs • Employer Assistance Program (EAP) • Company Paid and Voluntary Life/AD&D, Short-Term and Long-Term Disability • Healthcare and Dependent Care Flexible Spending Accounts • 401(k) Retirement Plan with Company Match • 529 Education Savings Program • Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks • Paid Time Off (PTO) includes: 11 Holidays • Exempt Employees are eligible for Unlimited PTO • Non-Exempt Employees are eligible for 10 Vacation Days, 56 Hours of Health Pay, 2 Personal Days and 1 Cultural Day • We are committed to providing you with the tools and resources you need to optimize your Health and Wellness. At ImmunityBio, we are an equal opportunity employer dedicated to diversity in the workplace. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law.

Join our high-impact manufacturing team as a Manufacturing Associate III at Endologix! WHO WE ARE: Endologix LLC is a California-based global medical device company dedicated to improving patients' lives through innovative therapies for the interventional treatment of vascular disease. Our therapeutic portfolio addresses clinically relevant unmet needs, spanning from abdominal aortic aneurysms to lower limb peripheral vascular disease. We are committed to delivering excellent clinical outcomes through precision in product design, advanced manufacturing, and comprehensive physician training-supported by industry-leading clinical evidence. At Endologix, we're driven by purpose, innovation, and the opportunity to make a lasting impact in vascular health. What sets us apart is not just our technology, but our culture. At Endologix, we foster a collaborative, mission-driven environment where every team member plays a vital role in advancing patient care. We value integrity, tenacity, and innovation-and we support our people with the tools, trust, and training they need to grow and continuously learn. If you're passionate about making a meaningful impact in healthcare, you'll find purpose and belonging here. ABOUT THE ROLE: We're looking for a talented Manufacturing Associate III to join our high-impact manufacturing team. In this role, you'll be responsible for the efficient and accurate assembly of high-quality medical devices in compliance with approved Manufacturing Process Instructions (MPIs), Standard Operating Procedures (SOPs), and quality standards. This role requires a strong understanding of medical device manufacturing processes and a commitment to continuous improvement. The Associate III serves as a technical resource on the production floor, assisting in troubleshooting line issues, identifying root causes, and recommending corrective actions. In addition, this individual actively contributes to process improvement initiatives, supports training of junior team members, and collaborates cross-functionally with Engineering, Quality, and other support functions to ensure smooth production flow and compliance with regulatory requirements. Responsibilities WHAT YOU'LL DO: * Assemble medical device products using small hand tools, calibrated instruments, microscopes, measurement devices, and test fixtures. * Ensure full compliance with Endologix policies, procedures, and quality standards, including safety regulations, environmental protocols, and required stretching exercises. * Maintain cleanroom and controlled environment integrity through proper attire and adherence to controlled environment practices. * Perform in-process quality checks and promptly report any safety, quality, or process-related concerns. * Identify and escalate unacceptable materials and sub-assemblies to Engineering and/or the Supervisor. * Ensure complete compliance with Endologix Quality and Regulatory policies and Core Values. * Take ownership of product quality by strictly following manufacturing instructions and completing quality records accurately. * Adhere to Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP). * Collaborate with supervisors, engineers, and technicians to troubleshoot line issues and implement process improvements. * Understand and use production terminology and demonstrate awareness of common manufacturing defects and their impact. * Exhibit flexibility by performing effectively across multiple assembly stations with minimal errors. * Participate actively in Lean Manufacturing and 5S initiatives to enhance efficiency and workplace organization. * Demonstrate knowledge of Lean principles and apply them to daily operations. * Proactively engage cross-functional resources to resolve production issues. * Read and interpret engineering drawings, specifications, and method sheets accurately. * Enter data into electronic systems as required for documentation and tracking. * Serve as a certified trainer for manufacturing processes; train and mentor other production employees. * Provide coaching and guidance to peers on standard operating procedures and assembly techniques. * Support supervisors as needed, including participating in leadership tasks and line coordination. * Perform other duties as assigned by supervisor. Qualifications WHAT YOU'LL BRING: Education: * High school diploma or equivalent required; associate or technical degree preferred. Experience: * 3-5 years of experience in a regulated manufacturing environment, preferably in the medical device industry. * Experience working within a clean room environment. * Lean & 5S experience desired. Skills/Competencies: * Strong attention to detail and ability to follow complex instructions and procedures. * Demonstrated ability to troubleshoot line issues and work independently with minimal supervision. * Effective communication skills and the ability to collaborate within a team environment. * Familiarity with lean manufacturing principles and continuous improvement methodologies is a plus. HOW YOU'LL SHOW UP: All In: Bring full commitment to everything you do. Support one another, hold yourself accountable, and take ownership of your work. Move with urgency, deliver on your promises, and lead with boldness and passion. Act with Integrity: Prioritize ethics and transparency in every decision. Earn trust by being honest, respectful, and dependable - working diligently to uphold the confidence of your colleagues, customers, and communities. Tenacious: Meet challenges head-on with resilience and resolve. Stay focused, push through obstacles, and consistently look for solutions, not excuses. Pioneering: Challenge the status quo and embrace innovation. Develop new ideas, test bold solutions, and pave the way for others - driving progress through curiosity and creativity. WHAT WE OFFER: At Endologix, we know that great work starts with great people - and people do their best when they feel valued and supported. That's why we offer competitive pay, solid benefits, career growth, a culture that genuinely cares, and the flexibility you need to thrive both at work and at home. But more than that, we offer purpose. You'll be part of a team that's making a real impact on patients' lives. When you join us, you're not just taking a job, you're building a meaningful career with a team that's invested in your success. The compensation package includes: * Hourly rate of $25.00/hr-$30.00/hr * Discretionary bonus * Equity participation as approved by Board of Directors (4-year vesting schedule) * Comprehensive health, dental, and vision insurance plans * Generous PTO and holiday schedule * 401(k) retirement plan with company match Plus: * Employee wellness initiatives and mental health support * Collaborative and inclusive company culture focused on impact and innovation * Opportunities for career growth and internal mobility OUR COMMITMENT TO DIVERSITY & INCUSION: Endologix LLC. is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

Job Description Primary Responsibilities Assemble, align, and adjust parts, components, or units according to specifications and follows established manufacturing procedures. Use hand tools, power tools, and other manufacturing assembly line equipment to assemble units. Tests and calibrates parts and mechanisms to ensure all components meet tolerances, product specifications, and quality standards. May repair or refit parts or units that fail tests or tolerance levels. Keeps daily labor tracking. Maintains a clean and organized work environment. Qualifications Ability to read and follow English verbal and written instructions Able to use measuring Tape and weighing devices: Scales Attention to detail Knowledge of basic math and computer skills Demonstrated ability to measure a metal or rubber part Occasionally may lift/push more than 50 pounds. Kirkhill, Inc. Competencies Customer Focus - Knows and understands the needs of internal and external customers. Is results oriented and works hard to consistently provide exceptional service. Ethics and Values - Adheres to an effective set of core values and beliefs and acts in accordance. Rewards the right values and disapproves of others. Problem Solving - Looks beyond the obvious to find effective solutions. Integrity and Trust - Widely trusted and seen as direct and truthful. Functional/Technical Skills - Possesses the skills to be effective in the job. Has the skills to perform the job at a high level of accomplishment. Listening - Practices active and attentive listening, able to hear others. Action-oriented - Full of energy, willing to take action. Composure - Cool under pressure, not knocked off balance by the unexpected, is a settling influence. Values Diversity - Supports fair and equal treatment for all. Kirkhill, Inc. is proud to be an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. All successful candidates must submit to post offer pre-employment physical examination, drug/alcohol screen and background check as a condition of employment. Job Posted by ApplicantPro

Job Description 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.

Job Description Join TLG Solutions, LLC as a Full Time Manufacturing Associate in Chatsworth, CA! As part of our dynamic team, you'll have the opportunity to work onsite and be at the forefront of our manufacturing operations. Your role will be crucial in ensuring that our production processes run smoothly and efficiently, making a direct impact on our product quality and customer satisfaction. With a competitive pay rate of $17.87/hr, you'll be fairly compensated for your hard work and dedication. If you're looking for a hands-on position in a fast-paced environment where your contributions are valued and recognized, this role is perfect for you. You will receive great benefits such as Medical, Dental, 401(k), Paid Time Off, Snack/Drink Room, and Employee Discounts. Apply now and take the first step towards a rewarding career with TLG Solutions, LLC! TLG Solutions, LLC: Our Mission Ready for a new adventure? If so, look no further! We are a licensed cannabis distillate company seeking a reliable individual to join our playful and unique production team. Find your inner light and spark up your skills and passions in an environment where individualism is encouraged, appreciated, and honored. We are an equal opportunity employer who believes and values the importance of providing meaningful opportunities for growth and development. What it's like to be a Manufacturing Associate at Manufacturing Associate As a Manufacturing Associate at TLG Solutions, LLC, you will play a pivotal role in organizing and managing all product parts and finished packages with precision and attention to detail. Your responsibilities will involve meticulously assembling and packing cannabis distillate products in adherence to our strict company standards. By ensuring that all manufactured products meet our high-quality and performance expectations, you will contribute significantly to our continued success and reputation as an industry leader in manufacturing. If you are a detail-oriented individual with a passion for maintaining excellence in all aspects of production, this position is an ideal fit for you. What we're looking for in a Manufacturing Associate To excel as a Manufacturing Associate at TLG Solutions, LLC, candidates must possess certain key skills and qualifications. Applicants must be at least 21 years of age and have a minimum of 2 years of working experience. While a High School Diploma is preferred, relevant experience will also be considered. The role requires individuals to be able to sit for extended periods of time, showcasing their endurance and commitment to the job. Candidates should demonstrate strong organizational skills and a keen eye for detail to manage product parts and packages effectively. Additionally, the ability to work collaboratively with team members, coupled with exceptional work ethics and moral standards, is crucial for success in this position. Knowledge and skills required for the position are: MUST BE AT LEAST 21 YEARS OF AGE 2+ years of working experience preferred High School Diploma Preferred Must be able to sit for extended periods of time Must be organized and detail-oriented Must be able to cooperate well with others Must possess excellent work ethics and morals Our team needs you! If you think this job is a fit for what you are looking for, great! We're excited to meet you! We perform background checks on all new hires.

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.

Employment Type: Contract Business Unit: Manufacturing Duration: 12 months with likely extensions Notes: Onsite 3 Key Consulting is hiring MCS Manufacturing Associate for a consulting engagement with our direct client, a leading global biopharmaceutical company. Job Description: The Associate of Manufacturing will work in a dynamic production environment at the client's Thousand Oaks Site supporting development, clinical, and launch activities. Under general supervision, employee will perform operations in the Manufacturing area. Operations will be performed according to Standard Operating Procedures (SOPs). Responsibilities include: Hands-on operations: set-up, cleaning, and sanitization of various manufacturing equipment Preparing buffers/media per defined manufacturing procedures (MPs) and standard operating procedures (SOPs) Following GMP documents (SOPs, MPs) with strict adherence to safety and compliance Performing and monitoring critical processes with the ability to perform basic troubleshooting Performing in-process sampling of equipment and operating analytical equipment Performing washroom activities: clean small and large scale equipment used in production activities Maintaining an organized and clean workspace Working in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves when performing all work Initiating quality reports Drafting and revising documents (SOPs, MPs) Identifying, recommending, and implementing improvements related to routine functions Assisting in the review of documentation for assigned functions (equipment logs, batch records) Performing activities that include periods of rigorous, repetitive work Working around high-pressure systems and occasionally work around heavy equipment Available to work various shifts (day, swing, graves, weekends, holidays, 5x8hrs, 4x10hrs, 3 or 4x12hrs) as dictated by the production schedule Basic Qualifications: Bachelor's degree OR Associate's degree and 4 years of Manufacturing /Operations experience OR High school diploma / GED and 6 years of Manufacturing /Operations experience Able to work in teams to complete operational tasks Able to take direction well, follow documents and policies at all times Able to take initiative Creates positive work environment through interactions with team members Able to regularly lift up to 35lbs, push and pull objects that require up to 50lbs of force, and work on your feet for long durations Able to perform the list of physical movements that may be necessary to perform daily functions on the production floor: bending, reaching above the head, climbing, kneeling, squatting, stooping, walking upstairs, and standing on portable stairs or ladders up to 6 feet off of the ground. Preferred Qualifications: Bachelor's Degree in Biology and/or Life Sciences Mechanically inclined Why is the Position Open? Staff Augmentation. Top Must Have Skills: Reliable Takes Initiative Safety minded Employee Value Proposition: Growth/ opportunity Red Flags: Spotty job history Interview process: Phone screen/interview. Virtual Panel Interview. We invite qualified candidates to send your resume to *****************************. If you decide that you're not interested in pursuing this position, please feel free to look at the other positions on our website ******************************* You are welcome to also share this opportunity with anyone you think might be interested in applying for this role. Regards, 3KC Talent Acquisition Team

Job Description QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you'll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA. Responsibilities: Perform hands-on operations including equipment setup, cleaning, and sanitization Prepare buffers and media per Manufacturing Procedures (MPs) and SOPs Follow GMP documentation (SOPs, MPs) with strict adherence to safety and compliance Perform and monitor critical processes, including basic troubleshooting Conduct in‑process sampling and operate analytical equipment Execute washroom activities, including cleaning small and large-scale production equipment Maintain an organized and clean workspace Work in a clean‑room environment while wearing steel‑toe shoes, full gowning, hairnet, and gloves Documentation & Quality Initiate quality reports Assist in reviewing documentation such as equipment logs and batch records Identify, recommend, and implement improvements related to routine functions Perform operations in the Manufacturing area, specifically for Purification processes. Operations will be performed according to Standard Operating Procedures (SOPs) while complying with GMP standards in safe manner Qualifications: College degree (science-based preferred) Alternatively: Relevant industry or laboratory experience may be considered in place of a degree Experience in biotech, pharmaceutical, or regulated manufacturing environments Science-based background (laboratory, manufacturing, or related field) Familiarity with: SOP adherence, GMP or GLP principles and General laboratory or manufacturing Willing to commit to shift rotations. Schedule: Day Shift or Graveyard Shift (12-hour shifts) Day Shift: 7:00 AM - 8:00 PM or Graveyard Shift: 7:00 PM - 8:00 AM Schedule Structure: Front-half and back-half schedules Includes alternating weekends off Initial training will take place on day shift Candidates will transition to assigned shift after training Quality Consulting Group, LLC 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, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law. Powered by JazzHR vSVe01RKrz

We are seeking a Manufacturing Associate, Downstream to join our multi-product manufacturing facility. This role plays a key part in downstream processing operations while adhering to cGMP requirements and established Standard Operating Procedures. The Manufacturing Associate will support production activities, documentation, equipment preparation, and materials coordination to ensure timely release of high-quality products. Our culture is built on Integrity, Adaptability, Innovation, Teamwork, and Passion, all driven by a shared mission to positively impact patients' lives. Key Responsibilities: Prepare and set up equipment and materials for scheduled production runs Plan and coordinate resources required for manufacturing processes Operate and maintain bioprocess chromatography skids Pack, unpack, clean, and maintain production-scale chromatography columns Perform antibody and enzyme purification using techniques such as Affinity, Size Exclusion, Ion Exchange, Hydrophobic Interaction chromatography, and Tangential Flow Filtration (TFF) Calibrate and test pH and conductivity meters Execute filtration processes, including sterile, ultrafiltration, and viral filtration Demonstrate strong aseptic techniques during all applicable operations Support aseptic filling activities, including media fills and qualification runs Maintain cleanroom cleanliness and equipment readiness Monitor and manage raw material inventory Ensure accurate and compliant GMP documentation Create, revise, and execute Batch Production Records, SOPs, protocols, and reports Lead or support independent projects as assigned Prepare media and buffer solutions for manufacturing processes Preferred Qualifications: Associate or Bachelor's degree, preferably with a focus in biology or chemistry Work Schedule: This is a full-time position working Monday through Friday, 8-hour shifts between 8:00 AM and 5:00 PM. Flexibility to work overtime, weekends, or holidays may be required based on business needs. KPG123

About Bobrick Headquartered in North Hollywood, CA, Bobrick is a global leader in stainless steel commercial washroom accessories with more than 100 years of innovation. Founded in 1906, Bobrick pioneered the world's first lavatory-mounted soap dispenser and has grown into a mid-sized, privately owned enterprise with trusted brands like Koala Kare. Today, Bobrick operates eight manufacturing facilities across the U.S., Canada, the U.K., and India, serving customers in over 125 countries worldwide. Job Summary Bobrick is hiring Manufacturing Associates (Partition Finisher) for the second shift (1:30pm - 10:00pm shift) in North Hollywood, CA. This is a great opportunity for those in the field of Wood Working, Cabinetry, Construction, or a closely related field. Under the guidance of a team leader or supervisor, you will assist with cutting and fabricating materials such as particle board, plywood, plastic laminate, and phenolic panels to required dimensions. You'll learn to safely operate a variety of shop equipment including panel saws, cut-off saws, routers, drills, drill presses, and glue application machines while producing quality parts that support daily production needs. Additional tasks include performing housekeeping and some preventative maintenance. This position is well-suited for someone looking to build hands-on manufacturing skills in a supportive, team-oriented environment. Job Responsibilities: Work closely with other department members in a fast paced environment. Handle phenolic and laminate material to finish and drill components. Operate and perform general maintenance on machines and equipment regularly. Use a variety of material handling equipment, including forklifts, as needed. Maintains production and quality standards. Reports, and contributes to problem solving in order to correct or prevent quality defects and errors. Assists senior level department positions in packaging, gluing and finishing components. Loads, unloads and organizes materials in the department as required. Uses drills and fixtures to attach leveling devices, t-nuts, and inserts. Prepares headrails for shipment as required. Submits suggestions for departmental, process and safety improvements. Maintains work area in a neat and orderly manner. Works in accordance with all safety standards. Uses a variety of material handling equipment, including forklifts as needed. Utilizes RF Scanners to scan labels and track job information. Under close supervision, checks toilet compartment components for final finish and appearances, and files out blemishes or scratches to ensure quality standards. Minimum Requirements: High school diploma or general education degree (GED). Some shop or industrial woodworking experience preferred. Ability to read, write and follow verbal and written instructions in English. Must possess basic math skills. Must be able to read a tape measure. Capable of using routers, files and other shop equipment as directed and trained. Must be able to organize own work and determine sequences of operations. Location: North Hollywood, CA Schedule: M-F, 1:30pm - 10:00pm (overtime required based on business needs) Pay: $21.50 - $24.00 Benefits: Medical Dental Vision 401(k) Retirement Plan Life and AD&D Long- and Short-Term Disability Insurance Flexible Spending Account (FSA) Health Savings Account (HSA) Paid time off for vacation, sick and personal days Parental Leave Educational Assistance Program Employee Assistance Program Pet Insurance Why Join Bobrick? You'll find the stability of a long-established company with the growth opportunities of a trusted industry leader. We offer an inclusive culture, competitive benefits, and the chance to contribute to sustainable solutions that make a difference worldwide. Join us to grow your skills and contribute to a company built on innovation, integrity, and sustainability. Together, we're shaping the future of washroom design, one project at a time. Legacy & Leadership - 100+ years as a global washroom solutions leader Purpose-Driven Impact - Products that improve hygiene, accessibility, and sustainability worldwide. Growth Opportunities - Training, mentorship, and career advancement. Inclusive Culture - Collaborative, respectful, and diverse workplace Sustainability Commitment - Supporting green building and environmental stewardship. Global Stability - Privately held, established brand with global presence. Bobrick's Culture: We view our culture as a competitive advantage and a foundation for continued success. Our positive and supportive culture encourages our people to do their best work every day. Bobrick respects work-life balance, has a strong commitment to employee development and attributes its success to five core values and their alignment with its employees, suppliers, sales representatives, distributors and other channel partners. We are dedicated to: Do the right thing: Conduct all aspects of business honestly, ethically, and responsibly. Offer the best value: Provide products and services which best meet each customer's needs. Treat everyone with dignity and respect. Embrace all backgrounds and experiences, promote equity, and be inclusive. Help each employee develop and achieve their potential. Foster a fearless and trusting culture. Continuously improve everything we do.

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.

"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive. Join a rapidly expanding global company, where diverse perspectives and experiences come together in a collaborative environment. Here, you'll find a workplace that values both collective success and your individual contributions-offering long-term opportunities to grow and make an impact. Your Role: The Component Prep role is on 1st Shift (6 AM - 2:30 PM) This position requires knowledge and ability to perform duties related to the manufacturing of drug, aseptic, device and assembled products utilizing reliable methods according to established procedures. Your Profile: Responsibilities Completes training modules regarding cleaning and sanitization methods for aseptic environments, this includes but is not limited to the use of germicidal/bactericidal/veridical/ agents, isopropyl alcohol, Sporklenz, Minnteck etc. Completes training modules regarding gowning techniques for the entrance to and from ISO designated areas. Ensures the proper use of filter integrity testers. Surface sanitize/ sterilize equipment, supplies and tools required for Classified Area usage. Ensure equipment inventory is accurate and appropriated marked. Prepare equipment and components for autoclaving. Prepare tubing set assembly per drawings and procedures. Ensures good document practices in the recording, maintenance, reviewing and organizing of batch records, forms, documents and logbooks for responsible areas. Assists other team members in manufacturing areas when needed. Maintain good work place organization and housekeeping. Responsible for adhering to applicable SOP, GMP and ISO rules and regulations related to the position. Train and instruct personnel to perform tasks following appropriate SOPs. Any and all other related duties as assigned by immediate supervisor. Required Knowledge, Skills and Abilities Good oral and written communication skills Good team and problem solving skills Initiative and manual dexterity Ability to stand continuously for two or more hours while wearing proper gowning materials Ability to work safely and use all material moving equipment in a safe manner Basic math skills Ability to work overtime as necessary Required Education and Experience High school graduate or equivalent A minimum of 1 to 2 years of industry experience Pharmaceutical industry experience helpful Experience with cGMP environment helpful Target Pay Range: $23.50 - 25.50/hour Your Benefits: Medical, Dental, Vision, Life Voluntary Accident, Critical Illness, Hospital, Pet FSA, HSA 401K Founded in 1873 in Zofingen, Switzerland, Siegfried has grown into a global network of 13 sites across three continents. With a team of more than 3,800 highly skilled professionals, we take the innovations of our pharmaceutical customers to industrial scale and manufacture safe drugs for patients worldwide. As a fully integrated CDMO, Siegfried is one of the few organizations today that can carry out the development and manufacturing of APIs and finished dosage forms under one roof. This unique combination of know-how and experience makes us the most trusted partner in the pharmaceutical industry.

Employment Type: Contract Business Unit: Pilot Plant Downstream Duration: 6 months with likely extensions 3 Key Consulting is hiring MCS (Manufacturing and Clinical Supply) Manufacturing Associate for a consulting engagement with our direct client, a leading global biopharmaceutical company. Job Description: The Associate of Manufacturing will work in a dynamic production environment at the client's Thousand Oaks Site supporting development, clinical, and launch activities. Under general supervision, employee will perform operations in the Manufacturing area. Operations will be performed according to Standard Operating Procedures (SOPs). Responsibilities include: Hands-on operations: set-up, cleaning, and sanitization of various manufacturing equipment Preparing buffers/media per defined manufacturing procedures (MPs) and standard operating procedures (SOPs) Following GMP documents (SOPs, MPs) with strict adherence to safety and compliance Performing and monitoring critical processes with the ability to perform basic troubleshooting Performing in-process sampling of equipment and operating analytical equipment Performing washroom activities: clean small and large scale equipment used in production activities Maintaining an organized and clean workspace Working in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves when performing all work Initiating quality reports Drafting and revising documents (SOPs, MPs) Identifying, recommending, and implementing improvements related to routine functions Assisting in the review of documentation for assigned functions (equipment logs, batch records) Performing activities that include periods of rigorous, repetitive work Working around high-pressure systems and occasionally work around heavy equipment Available to work various shifts (day, swing, graves, weekends, holidays, 5x8hrs, 4x10hrs, 3 or 4x12hrs) as dictated by the production schedule Basic Qualifications: Bachelor's degree OR Associate's degree and 4 years of Manufacturing /Operations experience OR High school diploma / GED and 6 years of Manufacturing /Operations experience Able to work in teams to complete operational tasks Able to take direction well, follow documents and policies at all times Able to take initiative Creates positive work environment through interactions with team members Able to regularly lift up to 35lbs, push and pull objects that require up to 50lbs of force, and work on your feet for long durations Able to perform the list of physical movements that may be necessary to perform daily functions on the production floor: bending, reaching above the head, climbing, kneeling, squatting, stooping, walking upstairs, and standing on portable stairs or ladders up to 6 feet off of the ground. Preferred Qualifications: Bachelor's Degree in Biology and/or Life Sciences Mechanically inclined Top Must Have Skills: 1. Chromatography Experience - At least 1 year experience preferred (HPLC/protein) 2. Biotech Process Development or Manufacturing experience. 3. Large Scale processing, buffer prep or media prep experience. 4. Must be able to work multiple shifts at 3 month intervals (Day and swing shift) Day to Day Responsibilities: Equipment set up, operating process equipment, buffer/media prep, equipment cleaning, sampling of in-process product pools and sample management in electronic sample management system. Red Flags: A candidate with an advanced degree may not fit well in this role (Masters degree or doctorate degree), not preferred. No BS degree in science with science background - biological/research experience Interview process: Phone screen followed by panel interview We invite qualified candidates to send your resume to *****************************. If you decide that you're not interested in pursuing this position, please feel free to look at the other positions on our website ******************************* You are welcome to also share this opportunity with anyone you think might be interested in applying for this role. Regards, 3KC Talent Acquisition Team

About Bobrick Headquartered in North Hollywood, CA, Bobrick is a global leader in stainless steel commercial washroom accessories with more than 100 years of innovation. Founded in 1906, Bobrick pioneered the world's first lavatory-mounted soap dispenser and has grown into a mid-sized, privately owned enterprise with trusted brands like Koala Kare. Today, Bobrick operates eight manufacturing facilities across the U.S., Canada, the U.K., and India, serving customers in over 125 countries worldwide. Job Summary Bobrick is hiring a Manufacturing Associate (Assembler) in our Soap Assembly department. Under close supervision, you'll perform standardized assembly tasks of varying complexity on soap dispensers and related subassemblies. This role is ideal for someone who enjoys hands-on work, takes pride in quality, and thrives in a team-focused, continuous improvement environment. Essential Responsibilities Under the direction of the Supervisor (or designee), you will: Assemble components into subassemblies and finished units on a production line or at individual workstations Use a variety of hand tools, power tools, and simple machines to complete assembly tasks Perform product tests at subassembly and/or final assembly stages, as required Complete repair and rework activities on units or subassemblies when needed Follow company standards for quality, workmanship, and production expectations Perform simple equipment or workstation set-ups Identify and report issues such as discrepancies or failures in materials, tooling, machinery, or processes Demonstrate the skills and performance level of an Entry-Level Assembler Understand and apply the Four Level Defect Grading System; actively report defects and contribute to problem-solving to prevent recurrence Work in compliance with workplace safety requirements and wear required PPE Maintain a clean, neat, and organized work area Qualifications: High school diploma or general education degree (GED); or equivalent combination of education and experience 6 months to 1 year of assembly experience Ability to read and interpret documents such as safety rules, operating and maintenance instructions, sketches/shop drawings and procedure manuals Must be able to operate specific equipment or tools and is required to comply with all safety rules and wear safety equipment Required to use arms and hands to handle, reach or feel objects, tools, or controls Must frequently lift and/or move up to 25 pounds Location: North Hollywood, CA Schedule: Monday - Friday 7:00am-3:30pm Pay: $19.18 - $22.00 per hour Benefits: Medical Dental Vision 401(k) Retirement Plan Life and AD&D Long- and Short-Term Disability Insurance Flexible Spending Account (FSA) Health Savings Account (HSA) Paid time off for vacation, sick and personal days' Parental Leave Educational Assistance Program Employee Assistance Program Pet Insurance Why Join Bobrick? You'll find the stability of a long-established company with the growth opportunities of a trusted industry leader. We offer an inclusive culture, competitive benefits, and the chance to contribute to sustainable solutions that make a difference worldwide. Join us to grow your skills and contribute to a company built on innovation, integrity, and sustainability. Together, we're shaping the future of washroom design, one project at a time. Legacy & Leadership - 100+ years as a global washroom solutions leader Purpose-Driven Impact - Products that improve hygiene, accessibility, and sustainability worldwide. Growth Opportunities - Training, mentorship, and career advancement. Inclusive Culture - Collaborative, respectful, and diverse workplace Sustainability Commitment - Supporting green building and environmental stewardship. Global Stability - Privately held, established brand with global presence. Bobrick's Culture: We view our culture as a competitive advantage and a foundation for continued success. Our positive and supportive culture encourages our people to do their best work every day. Bobrick respects work-life balance, has a strong commitment to employee development and attributes its success to five core values and their alignment with its employees, suppliers, sales representatives, distributors and other channel partners. We are dedicated to: Do the right thing: Conduct all aspects of business honestly, ethically, and responsibly. Offer the best value: Provide products and services which best meet each customer's needs. Treat everyone with dignity and respect. Embrace all backgrounds and experiences, promote equity, and be inclusive. Help each employee develop and achieve their potential. Foster a fearless and trusting culture. Continuously improve everything we do.

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.

Employment Type: Contract Business Unit: Manufacturing Duration: Initial 3 months with likely extensions Notes: Onsite 3 Key Consulting is hiring MCS (Manufacturing and Clinical Supply) Manufacturing Associate for a consulting engagement with our direct client, a leading global biopharmaceutical company. Job Description: The Associate of Manufacturing will work in a dynamic production environment at the client's Thousand Oaks Site supporting development, clinical, and launch activities. Under general supervision, employee will perform operations in the Manufacturing area. Operations will be performed according to Standard Operating Procedures (SOPs). Responsibilities include: Hands-on operations: set-up, cleaning, and sanitization of various manufacturing equipment Preparing buffers/media per defined manufacturing procedures (MPs) and standard operating procedures (SOPs) Following GMP documents (SOPs, MPs) with strict adherence to safety and compliance Performing and monitoring critical processes with the ability to perform basic troubleshooting Performing in-process sampling of equipment and operating analytical equipment Performing washroom activities: clean small and large scale equipment used in production activities Maintaining an organized and clean workspace Working in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves when performing all work Initiating quality reports Drafting and revising documents (SOPs, MPs) Identifying, recommending, and implementing improvements related to routine functions Assisting in the review of documentation for assigned functions (equipment logs, batch records) Performing activities that include periods of rigorous, repetitive work Working around high-pressure systems and occasionally work around heavy equipment Available to work various shifts (day, swing, graves, weekends, holidays, 5x8hrs, 4x10hrs, 3 or 4x12hrs) as dictated by the production schedule Basic Qualifications: Bachelor's degree OR Associate's degree and 4 years of Manufacturing /Operations experience OR High school diploma / GED and 6 years of Manufacturing /Operations experience Able to work in teams to complete operational tasks Able to take direction well, follow documents and policies at all times Able to take initiative Creates positive work environment through interactions with team members Able to regularly lift up to 35lbs, push and pull objects that require up to 50lbs of force, and work on your feet for long durations Able to perform the list of physical movements that may be necessary to perform daily functions on the production floor: bending, reaching above the head, climbing, kneeling, squatting, stooping, walking upstairs, and standing on portable stairs or ladders up to 6 feet off of the ground. Preferred Qualifications: Bachelor's Degree in Biology and/or Life Sciences Mechanically inclined Why is the Position Open? Staff Augmentation. Top Must Have Skills: 1) Mechanical and technical ability 2) Must be able to work all shifts 3) Must be able to understand GMP and compliance 4) Must take initiative Employee Value Proposition: Growth/ opportunity Red Flags: 1) Not local in distance to Amgen 2) No degree 3) If they are looking for research position, this is not it. 4) They need mechanical experience or show aptitude 5) Unable to work all shifts and be flexible (evenings, weekends, etc) Interview process: WebEx interview with hiring manager We invite qualified candidates to send your resume to *****************************. If you decide that you're not interested in pursuing this position, please feel free to look at the other positions on our website ******************************* You are welcome to also share this opportunity with anyone you think might be interested in applying for this role. Regards, 3KC Talent Acquisition Team