Manufacturing associate jobs in Palmdale, CA - 234 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.

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

Manufacturing Associate - $19.00 to $22.00/hour Full-Time | On-Site | Hands-On Production | Team-Focused Environment We're hiring motivated Manufacturing Associates to join our growing production team. If you enjoy hands-on work, operating machinery, and being part of a team that values precision and performance, this opportunity is for you. As a Manufacturing Associate, you'll play an essential role in foam production operations - ensuring materials are processed, packaged, and delivered safely and efficiently. Job Responsibilities: Operate foam-processing equipment on the production floor Load materials, monitor machines, and follow product specs Inspect output for quality and report any defects Label, seal, and stack finished products for shipping Assist with basic equipment cleaning and maintenance Maintain a clean, organized, and safe work environment Support team goals and follow safety guidelines Qualifications: Prior manufacturing or warehouse experience preferred Able to stand, bend, and lift up to 50 lbs Focused, detail-oriented, and safety-minded Strong attendance and team cooperation Willing to work flexible or rotating shifts What We Offer: Hourly Pay: $19.00-$22.00 (based on experience) Full-time hours with optional overtime Paid training and hands-on experience Opportunity for long-term placement and growth Supportive team atmosphere and modern facility Learn more at alohahp.com or call us at **************. Apply today and bring your forklift skills to a team that moves with purpose.

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

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.

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 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.

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: Bachelor's degree or associate degree in related area 4 years of Manufacturing experience Knowledge GMP Manufacturing & Process Execution - Core focus: Safe, compliant execution of manufacturing operations. Experience in Quality, Compliance & Continuous Improvement - Core focus: Maintaining product quality and regulatory readiness. Teamwork, Communication & Operational Readiness- Core focus: Reliable performance in a fast-paced manufacturing environment. Shift: Wednesday to Saturday 6:00 am to 5:00 pm MUST be able commute to Thousand Oaks, CA 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.

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

ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers . If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post. At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Associate Manufacturing What you will do Let's do this! Let's change the world! In this dynamic role you will collaborate with multiple functions within the Thousand Oaks site on a routine basis in a dynamic environment (Quality Assurance, Quality Control, Engineering, Facilities, Maintenance, Process Development, Process Engineering, etc.) while developing a deep understanding of the manufacturing operations and planning activities within the facility. Responsibilities of the role include: Completing drug product filling activities, respectively Performing initial review of manufacturing batch records Maintaining a safe and compliant culture by identifying preventative measures Creating and/or revising standard operating procedures Leading continuous improvement initiatives, which may be cross-functional in nature Performing data analysis (e.g., SPC, CPV) of critical process parameters and making recommendations to Engineering and/or Process Development teams Developing finite schedule for tasks including, but not limited to unit operations Monitoring productivity and identifying countermeasures for issues impacting cycle time adherence Elevating critical and impactful events to management Applying appropriate systems for job duties (SAP, QMTS, and LIMS etc.) Supporting the introduction of new products and technologies into the facility Initiating and owning quality records, including but not limited to non-conformances (NC), Corrective/Preventative Actions (CAPA) Additional Qualifications/Responsibilities What we expect of you We are all different, yet we all use our unique contributions to serve patients. The Manufacturing professional we seek is a collaborative partner with these qualifications. Basic Qualifications: High school diploma / GED and 2 years of Manufacturing experience OR Associate's degree and 6 months of Manufacturing experience OR Bachelor's degree Preferred Qualifications: B.S. in a life science or related field 2 years of work experience in a GMP environment Ability to perform computer operations, such as ability to navigate in MS Office and Excel Ability to operate specialized equipment and computers as appropriate to the individual area Ability to adhere to regulatory requirements, written procedures and safety guidelines Ability to evaluate documentation/data according to company and regulatory guidelines Ability to interact with inspectors (internal and external) Technical writing capabilities Ability to organize work, handle multiple priorities and meet deadlines Demonstrated written and oral communication skills Presentation capabilities Detail oriented as well as flexible and adaptable to changing priorities and requirements. What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan Stock-based long-term incentives Award-winning time-off plans Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies. Salary Range 75,618.00 USD - 89,473.00 USD

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.

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.

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

ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers . If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post. What you will do Let's do this! Let's change the world! In this dynamic role you will collaborate with multiple functions within the Thousand Oaks site on a routine basis in a dynamic environment (Quality Assurance, Quality Control, Engineering, Facilities, Maintenance, Process Development, Process Engineering, etc.) while developing a deep understanding of the manufacturing operations and planning activities within the facility. Responsibilities of the role include: Completing drug product filling activities, respectively Performing initial review of manufacturing batch records Maintaining a safe and compliant culture by identifying preventative measures Creating and/or revising standard operating procedures Leading continuous improvement initiatives, which may be cross-functional in nature Performing data analysis (e.g., SPC, CPV) of critical process parameters and making recommendations to Engineering and/or Process Development teams Developing finite schedule for tasks including, but not limited to unit operations Monitoring productivity and identifying countermeasures for issues impacting cycle time adherence Elevating critical and impactful events to management Applying appropriate systems for job duties (SAP, QMTS, and LIMS etc.) Supporting the introduction of new products and technologies into the facility Initiating and owning quality records, including but not limited to non-conformances (NC), Corrective/Preventative Actions (CAPA) Additional Qualifications/Responsibilities What we expect of you We are all different, yet we all use our unique contributions to serve patients. The Manufacturing professional we seek is a collaborative partner with these qualifications. Basic Qualifications: High school diploma / GED and 2 years of Manufacturing experience OR Associate's degree and 6 months of Manufacturing experience OR Bachelor's degree Preferred Qualifications: B.S. in a life science or related field 2 years of work experience in a GMP environment Ability to perform computer operations, such as ability to navigate in MS Office and Excel Ability to operate specialized equipment and computers as appropriate to the individual area Ability to adhere to regulatory requirements, written procedures and safety guidelines Ability to evaluate documentation/data according to company and regulatory guidelines Ability to interact with inspectors (internal and external) Technical writing capabilities Ability to organize work, handle multiple priorities and meet deadlines Demonstrated written and oral communication skills Presentation capabilities Detail oriented as well as flexible and adaptable to changing priorities and requirements.

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.

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

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.