Manufacturing associate jobs in Huntington Park, CA - 442 jobs

At The Mogharebi Group (TMG), we take a partnership approach to our work, prioritizing understanding our clients' businesses and goals before developing tailored solutions. Our focus is on building long-term relationships and value creation, not just transactions. Through leveraging TMG's shared knowledge, clients sell and purchase multifamily assets with certainty. Role Description We are seeking a skilled marketing professional to join our team. In this position, you will collaborate closely with advisors, research, marketing leadership, and external vendors to translate data and content into compelling visual stories, manage multiple deadlines, and maintain organized, high-quality marketing assets using Adobe Creative Suite and related tools. Responsibilities: Design and produce a wide range of graphic marketing collateral including proposals, offering memorandums, brochures, email campaigns, social media graphics, online listings, presentations, and special projects Prepare creative drafts, layouts, and production files for internal review; implement edits and revisions based on feedback Ensure all materials align with company branding guidelines, quality standards, and production specifications Coordinate and prepare files for print and digital distribution, ensuring correct specs, formats, and file sizes Collaborate with internal teams-including advisors, research, and marketing leadership-to gather content and supporting materials Own day-to-day graphic design execution using Adobe Creative Suite (InDesign, Illustrator, Photoshop) from concept through final production Coordinate with external vendors such as photographers and printers; assist with cost estimates and production timelines Perform photo editing and retouching to ensure high-quality visual assets Prepare, upload, and maintain marketing assets and property listings across third-party commercial real estate platforms (e.g., CoStar, LoopNet, CREXi), ensuring accuracy, branding consistency, and up-to-date content Maintain and update website content, property listings, and digital assets within internal systems and third-party platforms Manage multiple projects simultaneously while meeting deadlines and maintaining high attention to detail Maintain organized digital file structures and support ongoing improvements to marketing workflows Can convert research-based data into a visually compelling story for presentations, market updates, infographics, graphs, etc. Minimum 2 years of experience in marketing production, hands-on graphic design, or related creative roles Proficiency in Adobe Creative Suite (InDesign, Illustrator, Photoshop) Working knowledge of Microsoft 365 (Excel, Word, PowerPoint) Strong attention to detail with excellent organization and time-management skills Excellent attention to detail and the ability to manage multiple projects simultaneously Ability to prioritize, multitask, and meet tight deadlines Experience with print production, vendor coordination, or web updates is a plus Ability to work independently and collaboratively Associate or Bachelor's degree in Design, Marketing, or a related field preferred Joining our team as a skilled Marketing Production Specialist offers an exciting opportunity to work in a dynamic environment where your skillset will be valued and further developed. Benefits: 401(k) Health, dental and vision insurance 15 days paid time off, 10 holidays observed Weekly Schedule: 1 day remote, 4 days in-office in Costa Mesa, CA

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.

Job DescriptionDescriptionWhat If You Could...…revolutionize the way the world experiences cannabis-one perfect pre-roll at a time-and get paid to innovate in a high-growth industry? We're seeking Production Assembly Associates to join our dream team in crafting top-tier pre-rolls, driving efficiency breakthroughs, and ensuring everyone has access to the best. If you're driven by innovation, grit, and a passion for pushing boundaries, this is your chance to scale with us What You'll Do Work the production line with speed, accuracy, and creative problem-solving to meet and exceed quality standards. Proactively identify ways to boost productivity and optimize workflows without compromising quality. Embrace flexibility in a fast-paced environment, including shifts, overtime, and adapting to new tech or processes. Handle repetitive packaging tasks (box assembly, packing, labeling) with precision and efficiency. Maintain a clean, safe workspace while championing safety innovations and team ideas. What You'll Bring A high school diploma or equivalent Ideally, 1+ year of experience in industrial production, manufacturing, or a related field-but we're open to eager learners with transferable skills. Flexibility for varying shifts, overtime, and evolving roles in a scaling company. Strong communication, a safety-first mindset, and collaboration on innovative solutions. Reliability, punctuality, and a positive, team-oriented attitude with a hunger for improvement. Physical Stuff Good manual dexterity and patience and ability to engage in repetitive tasks. Ability to learn and use various machines and hand tools. Capable of bending, reaching, twisting, pinching and lifting up to 50 lbs. Able to meet full scope of physical demands. What We BringMedical/Dental/Vision Insurance Paid Company HolidaysPaid Time Off Employee Assistance ProgramComplimentary Life Coach Pet Insurance

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

Cell Manufacturing Associate II - IPSC Cellular Therapy Production - (10032214) Description Join the forefront of groundbreaking research at the Beckman Research Institute of City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research. A Cell Manufacturing Associate II is available in the Cellular Therapy Production Center (CTPC). This is a fast-paced lab involved in cutting edge technology, research and clinical immunotherapeutic programs. New personnel will be trained in project specific techniques and procedures. As a successful candidate, you will:· Manufacture and test T cell products, under minimal supervision, following established SOPs in cGMP facility. · Conduct applications for aseptic techniques. · Passage, maintain and cryopreserve cell cultures (e. g. , T cell and tumor cell lines). · Assist in developing and adapting new manufacturing procedures and analytical methodology. · Cooperate with Quality Control (QC) and Quality Assurance (QA) groups to ensure the quality of product and cGMP compliance. · Assist in internal inspections and audits to ensure compliance with Federal Drug Administration (FDA) regulations and City of Hope and CTPC procedure requirements. Qualifications Your qualifications should include:· Bachelor's degree in biological science or related field, with at least 2 years of post-degree research experience or Master's degree in biological science or related field, with at least 1 year of post-degree research experience. · 6+ months of hands-on mammalian cell culture experience. · 6+ months of hands-on cGMP experience. · Biotechnology or pharmaceutical industry experience preferred. City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please CLICK HERE. Primary Location: United States-California-DuarteJob: ResearchWork Force Type: OnsiteShift: DaysJob Posting: Dec 1, 2025Minimum Hourly Rate ($): 33. 000000Maximum Hourly Rate ($): 50. 280000

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.

About New World Medical Founded in 1990, New World Medical is a mission-driven company focused on preserving and enhancing vision through innovative ophthalmic surgical devices, including the Ahmed Glaucoma Valve and Kahook Dual Blade. We partner closely with eye care professionals to deliver tools that improve clinical outcomes and patient care. Guided by our core values - Gratitude, Collaboration, and Impact, we strive to make a meaningful impact in eye health worldwide. In support of our global mission, we proudly donate surgical equipment to charitable organizations to expand access to quality eye care. Benefits starting Day One: Medical, Dental, and Vision Insurance 401(k) with Profit Share Bonus Opportunities Flexible Work Schedules Free Onsite Daily Lunches to foster team connection Career Development Program Tuition Assistance (after 1 year of service) Wellness & Employee Assistance Programs Company Events & Recognition And more! Be part of something meaningful-join the team at New World Medical. JOB SUMMARY: The Manufacturing Associate's responsibilities include but are not limited to: lifting 25lbs over 8 hours of continuous repetitive motion, using 10x microscope and magnifying glass for inspections, building product subassemblies, molding product subassemblies, final assemblies and final packaging, preparing and assembling material, setting up and operating production equipment in accordance with current good manufacturing practices and complying with regulatory and quality system procedures. ESSENTIAL JOB DUTIES AND RESPONSIBILITIES: Start up and shut down processing equipment Build product subassemblies and final assemblies Test products or subassemblies for functionality or quality Measure and record data associated with operating equipment Control machines and operate processes Set up and operate production equipment Assist engineering team in developing, building, or testing new product, processes or procedures Inspect subassemblies and finished products for quality using 10x microscope and magnifying glass Prepare materials for final packaging and package final product for delivery Plan and arrange work to meet production requirements Clean production equipment and/or work areas Provide information to supervisors and co-workers by telephone, in writing, email, or in person Requirements KNOWLEDGE, SKILLS AND ABILITIES: Ability to communicate in writing and orally with supervisors and co-workers Ability to read, write and understand information and ideas presented in writing Good record keeping and documentation skills Must adhere to all applicable regulations, and quality system procedures Able to work on a diverse team Ability to be cross-trained Flexibility and a team player Able to lift 25lbs EDUCATION AND EXPERIENCE: Minimum High School diploma, Associate's degree preferred 2+ years of laboratory experience, preferably in medical devices Must have experience working in cleanroom environment Lean manufacturing and/or Six Sigma certified, a plus Microscope experience, a plus PHYSICAL REQUIREMENTS: Must be able to remain in a stationary position for certain amount of time. Occasionally move about inside the cleanroom and travel to and from office buildings to access supply cabinets, setup and operate equipment, employee offices, office machinery, etc. This may include, but is not limited to, bending and walking. Must be able to operate a computer and other office productivity machinery, such as a computer printer, computer keyboard, calculator, etc. Ability to listen and speak with employees and vendors. Must be able to exchange accurate information in these situations. Occasionally lift up to 25 pounds and transport to other offices. This may be performed with reasonable accommodation. View and type on computer screens for certain amount of time. Must be able to read and manually conduct inspection processes and procedures with provided tools. Role may require performing functions within a controlled environment under standard gowning requirements for extended amount of time. This description reflects management's assignment of essential functions, it does not proscribe or restrict the tasks that may be assigned. Salary Description $21.50/hour plus 8% differential pay

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

Join Amgen's Mission of Serving Patients 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! The Associate of Manufacturing will work in a dynamic production environment at the Amgen Thousand Oaks Drug Substance plant supporting development, clinical, and launch activities. Under general supervision, employees will perform operations in the Manufacturing area, specifically B23 Purification processes. Operations will be performed according to Standard Operating Procedures (SOPs). This Associate is responsible for hands-on operations, set-up, clean, sanitize and prepare media and buffers per procedure. Responsibilities include: * Perform and monitor critical processes * Complete routine validation protocols * Align with GMP's * Regularly draft and revise "routine" documents (e.g. MPs, SOP's, and technical reports) * Initiate Quality incidents * Identify and recommend improvements related to routine functions and implement after approval * Basic troubleshooting * Recognize and accurately report problems * Direct operators on critical processes * Assist in the review of documentation for assigned functions (e.g. equipment logs, routine area audits, 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 (days, swings, graves, weekends, holidays, 5x8hrs, 4x10hrs, 3 or 4x12hrs) as dictated by the production schedule * May train staff to perform hands-on tasks * May act as safety representative * May participate and represent group on cross-functional teams What we expect of you We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is an individual with these qualifications. Basic Qualifications: * High school/GED + 2 years of manufacturing or operations work experience OR * Associate's + 6 months of manufacturing or operations work experience OR * Bachelor's Preferred Qualifications: * Bachelor's degree in science or engineering * Knowledge of large-scale biotechnology operations such as purification, cell culture, aseptic processing, etc. * Knowledge of Single-use-Systems * CFR and Regulatory knowledge * Mechanical ability/expertise * Basic statistical mathematical skills * Ability to interpret and apply GMP knowledge * Understanding of analytical methods for manufacturing area * Demonstrated technical writing capability * Able to demonstrate project management skills and presentation skills * Ability to understand, apply and evaluate basic chemistry, biology and physical principles * Basic troubleshooting skills on production equipment * Experience with Delta V * Experience with lab equipment/testing 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. Apply now and make a lasting impact with the Amgen team. careers.amgen.com In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. Application deadline Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. Sponsorship Sponsorship for this role is not guaranteed. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. . 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.

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.

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: 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

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 Soap Dispensers 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: $18.75 - $21.00 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 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.

Employment Type: Contract Business Unit: Cell Culture Duration: Initial 3 months with likely extensions Notes: Onsite 3 Key Consulting is hiring a 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? Supplement additional workload on team. 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 Day to Day Responsibilities: Working in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves to support the manufacture of drug substance using SOP's. Employee Value Proposition: Extension is highly likely - unique knowledge and experience Red Flags: Not local in distance to Amgen No degree If they are looking for research position, this is not it. They need mechanical experience or show aptitude Unable to work all shifts and be flexible (evenings, weekends, etc) Interview process: Phone and Webex. 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.