Manufacturing Associate Jobs in Lakewood, CA

include, but are not limited to: Locates and positions parts to be processed, by following blueprints and Standard Work Instructions. Works at station as member of manufacturing group producing one or more specific parts to meet production requirements. Locates and positions parts in specific areas and secures them in place. May solders parts by following schematic, blueprint, and Standard Work Instructions to produce increasingly more complex parts. Verifies dimensions or appearance of part after process using basic measuring tools and gauges. Ability to dimensional aspects with related test fixture. Performs related duties, which may be assigned, from one area task to another at area supervisor's requirements. Qualifications Soldering. Blueprint and/or schematic reading. Finger dexterity manipulating small parts. Hand-eye coordination. Ability to verify process of part per final blueprint. Effective communication skills in English with the ability to read, speak, and understand English. Education/ Previous Experience High school education or general education degree (GED), A minimum of one year of manufacturing experience, or equivalent combination of education and experience. Work environment and Safety Equipment Requirement The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of the job. While performing the duties of this Job, the employee is regularly required to sit for long periods and stand to perform work. The employee is required to reach with hands and arms and talk or hear. The employee must be able to lift, push, pull or move up to fifty (50) pounds or more with assistance. Specific vision abilities required by this job include close vision, color vision, peripheral vision and ability to adjust focus. Occasionally required to lift up to 30 lbs. Regularly required to sit, stand, bend, reach and move about the facility. Safety glasses, shop coat/apron, proper shoes. Occasional exposure to shop element such as noise, dust, odors and fumes.

DAY SHIFT - 8-4:30 Sunday to Thursday OR Tuesday to Saturday IMPORTANT: Please tailor sourcing to experience in CHEMICAL ENGINEERING/ ENGINEERING/BIOLOGY/CHEMISTRY. This is still entry level. Academic experience is fine!! Must be flexible and available for week end and holiday work (I.E Tuesday-Saturday or Sunday-Thursday) MCS Mfg Associate MCS Manufacturing Associate - EW Job Description The Associate of Manufacturing will work in a dynamic production environment at the Client 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 manufacturing plant environment wearing steel toe shoes, lab coat, safety glasses 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, weekends, holidays) as dictated by the production schedule 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.

Production Operators Key Qualifications & Preferred Backgrounds Education & Professional Background: Minimum Education: High school diploma or vocational school certificate, with priority given to candidates in the following fields: Mechanical Engineering (e.g., mechanical maintenance, equipment calibration). Automation & Electrical Engineering (e.g., PLC programming, servo systems). Industrial Electronics (e.g., circuit troubleshooting, sensor calibration). Note: While higher qualifications (e.g., associate/bachelor's degrees) are advantageous, practical experience and technical certifications (e.g., PLC technician license) are equally valued. Core Skills & Responsibilities: Equipment Operation: Operate production machinery (e.g., automated assembly lines, CNC machines) and monitor parameters (e.g., temperature, pressure). Troubleshoot mechanical/electrical faults (e.g., conveyor belt jams, PLC communication errors). Technical Expertise: Basic understanding of PLC systems (e.g., Siemens S7, Mitsubishi FX series) for process adjustments. Familiarity with pneumatic/hydraulic systems (e.g., valve adjustments, pressure testing). Quality & Safety: Adhere to ISO 9001 standards for product quality and OSHA safety protocols. Perform routine maintenance (e.g., lubrication, filter replacement) to minimize downtime. Preferred Certifications: PLC Programming Certification (e.g., Allen-Bradley, Omron). Electrical Safety Training (e.g., NFPA 70E compliance). 6S/Lean Manufacturing training for workplace optimization. Career Advancement Pathways Skill-Based Tiers: Junior Operator → Senior Operator (requires mastering 3+ equipment types). Technical Specialist (e.g., PLC troubleshooting expert, automation lead). Leadership Roles: Transition to Production Supervisor or Shift Manager with cross-departmental collaboration experience. Physical Requirements: Capable of working in confined spaces, at heights, or in high-noise environments. Flexibility to respond to emergency calls during non-working hours. General Requirements for All Roles Adaptability: Willingness to work in shifts and adapt to dynamic production demands. Safety Awareness: Commitment to PPE use and adherence to factory safety protocols. Continuous Improvement: Proactive mindset to optimize utility efficiency and reduce operational costs.

At a top Biopharmaceutical company, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Manufacturing Associate at our Thousand Oaks, CA site. Here, you will be a vital contributor to our inspiring, bold mission, and have the opportunity to grow within a thriving company. Summary: The Manufacturing Associate is provided general direction of the Manufacturing Lead and overall direction of the Supervisor, the Manufacturing Associate is responsible for executing all processes in the production area while strictly adhering to CGMP, environmental health and safety guidelines and any other related regulations all in the Drug Product (Formulation/Filling) team. This is a perfect entry level position for those with minimal experience or want to gain further career advancements within the Biotech industry! Title: Manufacturing Associate I/II Location: Los Angeles, CA - Onsite Pay: $23-$25/hr. Duration: 12 months w/ potential for extension Multiple Shifts Available: Wed-Sat 12PM - 10:30PM (OT after 8 hours of work) Wed-Sat 6AM - 4:30PM and Sun - Wed 12PM - 10:30PM Responsibilities: Participate in bulk formulation, aseptic filling, Lyophilization, and capping operations. Executes processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Clean, set up, operate, and teardown of equipment such as tanks, filtration systems, filling lines, lyophilizers, etc. Operate general production equipment such as an autoclave, filter integrity testers, temperature probes, pH and conductivity meters, CIP skids, etc. Receive and distribute supplies into the manufacturing areas. May perform other duties as assigned. Set up operations, daily maintenance, and breakdown of simple/routine equipment. Gain qualification to perform CIP, SIP autoclave, small parts preparation. Identify processing gaps and assist with implementation of new technologies. Perform minor to moderate troubleshooting. Draft simple to moderate DCRs and complete minor NCR investigations. May perform other duties as assigned. Must Haves: Highly motivated, proactive, and enthusiastic team player with demonstrated history of flexibility. Ability to work independently, collaborate cross-functionally, and utilize resources efficiently. Ability to troubleshoot, demonstrate problem solving skills, and multitask while paying attention to timelines and priorities. Able to work effectively and efficiently in a team environment. Able to provide feedback for operations & elevate concerns as needed. Actively seeks opportunities for personal growth and development and monitors progress toward achieving development goals. Excellent organizational, interpersonal, verbal, and written communication skills Proactively assists others in accomplishing work. Listens carefully and is receptive to feedback from others. General knowledge with cGMP manufacturing, regulatory regulations and requirements is a plus. Education/Experience: High school diploma or equivalent required; bachelor's degree preferred. No minimum years of experience required; 1-2 years preferred. Work Environment: The overall physical exertion of this position requires medium to heavy work. May be required to gown frequently and balance when gowning into clean areas. May be exposed to dust, gases, chemicals, liquid Nitrogen, and fumes. May require respiratory protection. May be required to work with biohazards such as: bloodborne pathogens or medical waste. Will require entering a 2-8 degree Celsius & -60-degree Celsius freezer to store and retrieve materials and various chemicals in support of manufacturing such as IPA, 500ppm sodium hypochlorite. Able to work in controlled or clean room environments requiring special gowning. May require the use of special visual or auditory protective equipment. Required to follow gowning requirements and wear protective clothing over the head, face, hands, feet, and body. No make-up, jewelry, contact lenses, nail polish or artificial fingernails may be worn in these work environments. May be required to manage hazardous waste in compliance with company procedures & State/Federal/Local hazardous waste regulations. Duties may include identifying, handling, and generating, accumulating, storing, labeling, and on-site transporting of hazardous wastes. May be required to work overtime, a weekend day, holidays or be assigned to a different shift. May work and have exposure to hot, cold, wet environment/conditions. May be required to work in confined areas; may be required to work around moving equipment and machinery. May be required to work at heights above floor level. May be required to climb (use step stools and ladders) or kneel up to 1 hour. May be required to walk, stand, or bend at the neck/waist for over 4 hours May be required to reach above/below the shoulder between 3-4 hours May be required to lift up to 50lbs; Lifts per shift are up to 100 times. May be required to carry up to 50lbs; Carry distance of up to 6 feet; Carries per shift are up to 100 times. May require simple grasping & pushing/pulling with hands/arms between 3-4 hours; power grasping for over 4 hours; fine manipulation between 1-2 hours.

Castelion is bringing a new approach to defense development and production: one that focuses on short, iterative design cycles, rapid testing in development, and modern commercial manufacturing strategies for production at scale. We're designing, building, and testing next generation long range strike weapons systems to give America and its Allies a definitive edge and deter future conflicts. Avionics Manufacturing Specialist Castelion is looking for an Avionics Manufacturing Specialist, reporting to the Head of Avionics, to support the development of the systems that will be required for the design and build of long-range hypersonic strike vehicles. This will be a full-time, exempt position located in our El Segundo facility. As an Avionics Manufacturing Specialist, you will work closely with our engineering teams to execute highly technical electrical builds for our research vehicles, assist in advancing designs, and play a critical role in defining and maturing manufacturing, assembly and integration processes. Responsibilities Work with avionics engineering by rapidly iterating electronic components and cables Construct superior wire cables, perform PCB assembly rework, assemble, and test racks/systems, electro-mechanical units, engineering enclosures, and test equipment Create and record testing systems and cable diagrams according to engineer-selected testing gear Collaborate closely with engineering to transform concepts into reality Monitor one's own work progress against established standards and deliver all work on schedule Examine, interpret, and use drawings and regulated documentation and procedures Understand intricate cable harnesses, wiring diagrams, mechanical and layout drawings, and geometric dimensioning and tolerancing Verify flight hardware and thoroughly document outcomes Aid in developing manufacturing processes for initial production runs Contribute to projects aimed at increasing operational efficiency in the area Basic Qualifications 5+ years of avionics technician experience Experience reading PCBA schematics and execute rework Capability to rework 0201 SMD and BGA components in tight spaces Experience read wiring harness drawings to build and troubleshoot laboratory and flight articles Knowledge of and adherence to industry standards, such as IPC-610 and IPC-620 Proficient with test equipment such as multimeters, oscilloscopes, and signal generators. Demonstrated direct or indirect leadership Preferred Qualifications Experience in a research and development environment Previous involvement in a high-speed production environment, handling flight hardware Prior involvement in a high-output environment, involving hands-on experience in constructing cables, electro-mechanical devices, or building prototypes Ability to acclimate to frequently changing assignments and a fast-paced working environment Excellent communication skills, both written and oral, along with effective teamwork abilities Superb focus and attention to detail, with remarkable work efficiency and accuracy Experience with soldering PCBAs, including soldering in tight spaces such as 0402 packages and high-density ICs, installing jumpers, and performing dead-bugging Expertise in manufacturing and repairing intricate testing systems Familiarity with Atlassian tools such as SVN, Confluence, and JIRA Basic comprehension of electronic principles and theory Skills in project management Additional Requirements Must be willing to work extended hours and/or weekends as needed Must be able to travel up to 30% All employees are granted long-term stock incentives as part of their employment as Castelion. All employees receive access to comprehensive medial, vision, and dental insurance, and the company offers three weeks of paid time off per year. Leadership Qualities Bias to Action and Creative Problem Solving. Desire and experience questioning assumptions in ways that lead to break through ideas that are ultimately implemented. Successfully bring in applicable processes/concepts/materials from other industries to achieve efficiency gains. Ability to personally resolve minor issues in development without requiring significant support. High Commitment, High Initiative. A successful candidate will have a genuine passion for Castelion's mission and consistently look for ways to contribute to the company's technical goals and prevent hardware blockers. Ability to work in a fast paced, autonomously driven, and demanding atmosphere. Strong sense of accountability and integrity. Clear Communicator. Proactively communicates blockers. Trusted in previous roles to be voice of company with regulators, suppliers, gate keepers and customers. Capable of tactfully managing relationships with stakeholders to achieve company-desired outcomes without compromising relationships. Emails, IMs and verbal interactions are logical, drive clarity, and detailed enough to eliminate ambiguity. ITAR Requirements: To conform to U.S. Government export regulations, applicant must be a (i) U.S. citizen or national, (ii) U.S. lawful, permanent resident (aka green card holder), (iii) Refugee under 8 U.S.C. § 1157, or (iv) Asylee under 8 U.S.C. § 1158, or be eligible to obtain the required authorizations from the U.S. Department of State. Employment with Castelion is governed on the basis of competence and qualifications and will not be influenced in any manner by race, color, religion, gender, national origin/ethnicity, veteran status, disability status, age, sexual orientation, gender identity, marital status, mental or physical disability or any other legally protected status.

Manufacturing Technician (Environmental Support) Join FUJIFILM Diosynth Biotechnologies in our new facility location - Thousand Oaks, California! Manufacturing Technician (Environmental Support) will report directly to the Senior Manager Manufacturing at the FUJIFILM Diosynth Biotechnologies California (FDBC) location. External US The work we do at FDB has never been more important-and we are looking for talented candidates to join us. We are growing our locations, our capabilities, and our teams, and looking for passionate, mission-driven people like you who want to make a real difference in people's lives. Join our new FDB facility in Thousand Oaks, CA and help manufacture the next cell therapy in partnership with some of the most innovative biopharma companies across the globe. We are proud to cultivate a culture that will fuel your passion, energy and drive - what we call Genki. Job Description The Environmental Support Technician works as part of the manufacturing team to deliver high quality therapeutics. This position contributes to the successful delivery of released product in support of clinical and commercial processes. Primary Responsibilities Perform the cleaning/sanitization of the manufacturing areas and equipment in accordance with all Company procedures. This requires the application of various disinfectants to floors, ceilings, walls, and equipment with use of proper cleaning equipment such as mops, wipes and associated tools Execute cleanings compliantly and safely without negative impact to the production schedule. This requires general agility to clean in difficult/hard to reach spaces Ability to achieve and maintain gowning qualifications as well as perform work in an aseptic environment This position will work in both an office and a manufacturing setting. When in the manufacturing area, staff may be exposed to various chemicals and biohazards. Additionally, there is potential for equipment hazards, strong odors, and other detergents/sanitizers Assist the team with maintaining an up-to-date working inventory for the equipment/supplies. Perform various 'housekeeping' activities. (i.e., keeping work areas clean, cleaning of equipment) Document and review appropriate paperwork, daily logs, and documentation per Good Documentation Practices Participate in a detailed training program and develop training plan Maintain inventory of equipment and supplies Assist in the evaluation of the current cleaning procedures/equipment and recommend changes to optimize the cleaning program 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 requirements Adhere to all safety protocols and procedures Essential Physical Requirements: 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 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 (all shift times are 4 am) 4 days a week /10 hours per day Shift (4 am - 02:30 pm, Sunday through Wednesday or Wednesday through Saturday) 5 days a week /08 hours per day Shift (4 am - 12:30 pm) Open to potential swing shift hours (10 am - 08:30 pm) 4 days a week /10 hours per day Shift (Sunday through Wednesday or Wednesday through Saturday) Required to work weekends and some holidays Qualifications High school diploma; or Associate degree Preferred Qualifications A minimum of 2 or more of related experience is preferred (work or schooling) Ability to follow verbal and written instructions Problem solving skills Detail oriented Team player Ability to work with minimal supervision Strong communication skills Strong demonstrated aseptic techniques

We are currently hiring for 2nd shift Manufacturing Associates (Partition Finisher) 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 close direction of the Lead and/or Supervisor, we are searching for individuals with the ability to pack pallets, finish components in the solid and laminate cells, and pass components through the hot press and glue spreader. Additional tasks include performing housekeeping and some preventative maintenance. 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. Schedule: M-F, 1:30 pm - 10:00 pm Pay: $21.00hr - $26.00 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 About the Company: Bobrick, headquartered in North Hollywood, CA, is the industry-leading manufacturer of Stainless Steel commercial washroom accessories with 100+ years of experience (back when it was a start-up, Bobrick invented the lavatory-mounted soap dispenser!). A mid-sized, privately owned company, Bobrick includes brands such as Koala Kare, operates 6 manufacturing facilities throughout the US and Canada, and conducts business in over 85 countries worldwide. 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 four core values and their alignment with its employees, suppliers, sales representatives, distributors and other channel partners. We are dedicated to: Conduct all aspects of business honestly, ethically, and responsibly. Offer the best value. Treat each employee with dignity and as an individual Continuously improve everything we do.

The Manufacturing Associate works as part of the manufacturing team to deliver high quality cell therapy materials during process transfers, routine production, and technology improvements. This position contributes to the successful delivery of released product in support of clinical trials and commercial production. Company Overview At FUJIFILM Diosynth 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 Reports to: Manufacturing Supervisor Function: Technical Operations (Manufacturing) Location: Thousand Oaks, CA SUMMARY OF POSITION: 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. MAJOR ACTIVITIES AND 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 BACKGROUND REQUIREMENTS (Education, Behavioral, Professional & Technical Capabilities Experience): Qualifications Bachelor of Science (B.Sc.) with 0-3 years of applicable biopharma experience; or Associate degree with 2+ years of applicable biopharma experience; or High school diploma with 3+ years of applicable biopharma experience 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: $29.50 to $33.50 per hour, depending on experience Medical, Dental and Vision Life Insurance 401k Paid Time Off To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid. *#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 (*******************).

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

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

The primary responsibility of the Manufacturing Associate II is to ensure the successful completion of cell therapy products. Ensure all processes and procedures are followed in full compliance with cGMP, CFRs and site quality systems, policies, and procedures. The MFG Associate II will be part of a cohesive team responsible for the quality manufacturing of our products. General Responsibilities * Perform all tasks associated with the manufacturing of clinical drug product and follow the instructions described in standard operating procedures, protocols, training records and batch records. * Accurate and timely completion of documentation generated and required by protocols, training runs, standard operating procedures, and batch records. * Accurate and timely review of documentation generated during manufacturing production. * Adhere to tasks in a manner consistent with safety policies, quality systems, and cGMP requirements. * Work as part of a dedicated and committed team to execute cGMP production runs in close collaboration with support business units. * Adhere and maintain aseptic technique practices during processing of products to ensure the integrity, viability, and sterility of finish drug product. * Required to work in cleanroom environment (ISO 5/7) for prolonged periods of time; specialized gowning such as double gloves, hair net, masks, safety glasses, sterile coveralls and shoe covers. * Ability to perform cell counting (manual/automated), perform error free calculations of cell concentrations, dilutions. * Off hours or weekend work will be required at times depending upon the needs of the company. * Be flexible and adaptable to production schedule needs, procedural changes, batch record enhancements to ensure timely production is met. * Assist MFG leads and Senior Associates with sustaining inventory levels of supplies and monitors and tracks trends to identify gaps. * May lead continuous improvement projects. * Perform additional duties as needed. * The company reserves the right to add or change duties at any time Job Qualifications & Skills * Mid-level cell culture processing experience in handling and propagation of human primary cell. * BS degree in relevant Science or Engineering discipline preferred, plus 1-2 years of experience in biotech/pharma. * AA degree in relevant Science or Engineering discipline, plus 3-4 years experiences in biotech/pharma. * Well versed of cGMP regulations, 21CFRs and FDA guidance applicable to biologics and cell therapy. * Assist with implementation and support process improvement initiatives. * Consistent process execution to guarantee high quality output. * Good interpersonal, oral and written communication skills. Technical writing ability a plus. * Ability to be flexible, work off-shifts and extended hours as required. * Weekend work, holiday and/or Overtime may be required. * Capability to lift over 20lbs. * Candidates must be authorized to work in the U.S Benefits & Perks * Competitive compensation * Medical, Dental and Vision Insurance * Matching 401K * Business casual work attire

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.

Full-time Description 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 - Integrity, Accountability and Innovation, 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) Cell Phone & Home Office Stipends 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, Associates 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 11% differential pay

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: Executing drug product filling 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/GED + 2 years Manufacturing experience OR Associate's + 6 months Manufacturing experience OR Bachelor's 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, including remote and hybrid work arrangements, where possible Salary Range 73,359.00 USD - 85,625.00 USD

Employment Type: Contract Business Unit: Pilot Pland Downsteam Duration: 6+ months (with likely extensions and/or conversion to permanent) 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: Under general supervision, supports the execution of harvest and downstream purification process studies using pilot scale equipment including chromatography skids and filtration systems. Routine tasks include equipment preparation, operating chromatography and filtration systems, compounding media and buffer solutions, and sampling. Utilizes scientific principles in execution of experiments and analysis of experimental data. Carries out laboratory tasks per plan and procedure in a team environment. Documents data and process information in accordance to good documentation practices. Performs laboratory safety evaluations. Organizes and stocks laboratory supplies. Executes process/ equipment troubleshooting. Performs in-process testing using laboratory analyzers Why is the Position Open? Supplement additional workload on team. Top Must Have Skills: 1. Chromatography Experience - At least 1 year experience preferred 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. Basic Qualifications: Science or engineering degree and 0-2 years of experience Bachelors degree in Engineering or Science. 0-2 years of experience Ability to work evening/nights and occasional weekend work. (Evening/Night work is scheduled on a fixed duration rotation, subject to change). Preferred Qualifications: Prior hands-on experience in pilot-scale or large-scale cell culture or downstream purification process development or manufacturing operation. Experience with automated and computer-controlled biopharmaceutical process equipment. Knowledge of process data compilation and analysis. Demonstrated equipment troubleshooting skills. Excellent problem-solving capabilities and attention to detail. Experience of collaboration within and across functional areas and outstanding customer focus. Excellent written and verbal communication skills. Employee Value Proposition: The person in this role will do hands on bio processing using large scale purification equipment and managing purification samples. Red Flags: A candidate with an advanced degree may not fit well in this role (Masters degree or doctorate degree) Interview process: Video Skype Panel Interview We invite qualified candidates to send your resume to **************************. If you decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our website ******************************* You are also welcome to 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: Support the Cell Banking Group at client's site, working in a dynamic GMP-regulated production environment. Under general supervision, the associate will perform hands-on manufacturing operations while ensuring strict adherence to Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMPs). Set up, clean, and sanitize manufacturing equipment. Prepare buffers and media per defined Manufacturing Procedures (MPs) and SOPs. 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 equipment. Maintain an organized, clean, and compliant workspace. Follow GMP regulations, SOPs, and MPs with strict adherence to safety and compliance protocols. Work in a cleanroom environment, requiring full gowning (steel-toe shoes, cleanroom suit, hairnet, gloves, etc.). Identify, recommend, and implement process improvements for routine functions. Review documentation such as batch records and equipment logs. . Qualifications: Bachelor's degree in biology, Molecular Biology, or Biochemistry Preferably pharmaceutical industry experience. Open to candidates with strong lab skills and aseptic technique, even if their experience comes from internships or cross-industry backgrounds. Involves cell culture (passaging and expansion), media batching, cleaning biosafety cabinets, and SOP revisions. DAY SHIFT M-F 8-5 PM 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.

**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 - Cell Culture** **What you will do** Let's do this. Let's change the world. In this vital role you will perform operations for cell culture production. **Responsibilities:** + Hands-on operation, set-up, cleaning, and sanitization of bioreactors and various cell culture support vessels + Prepare buffers/media per defined manufacturing procedures (MPs) and standard operating procedures (SOPs) + Follow GMP documents (SOPs, MPs) with strict adherence to safety and compliance + Perform and monitor critical processes + Perform in process sampling of cell culture equipment and operate analytical equipment + Perform washroom activities; clean equipment, small to large scale, used in production activities + Work in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and latex gloves when performing all work + Draft and revise documents (SOPs, MPs) + Available to work various shifts (day, swing, graves, weekends, holidays, 5x8hrs, 4x10hrs) as dictated by the production schedule **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 employee with these qualifications. **Basic Qualifications:** + High school/GED + 2 years Manufacturing or Operations expereince OR + Associate's + 6 months Manufacturing or Operations expereince OR + Bachelor's **Preferred Qualifications:** + Bachelor's Degree in Biology and/or Life Sciences + Able to work in teams to complete operational tasks + Ability to take direction well, follow documents and policies at all times + Ability to take initiative + Create a positive work environment through interactions with team members + Mechanically inclined + Able to lift up to 50lbs and work on your feet for long durations **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, including remote and hybrid work arrangements, where possible **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. 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.

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: 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, recording process data in systems Under general supervision, employee will perform operations in the Manufacturing area. Operations will be performed according to Standard Operating Procedures (SOPs) while complying with GMP standards in safe manner. 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) Set up, clean, and sanitize manufacturing equipment. Performing and monitoring critical processes with the ability to perform basic troubleshooting Initiating quality deviation reports Conduct in-process sampling and operate analytical equipment. Execute washroom activities, including cleaning small- and large-scale equipment. Maintain an organized, clean, and compliant workspace. Qualifications: Associates degree Chromatography Experience - At least 1 year experience preferred - (protein separation) Biotech Process Development or Manufacturing experience - downstream purification area (process development, clinical manufacturing, protein purification, cell culture) Large Scale processing, buffer prep or media prep experience Team switches every quarter (4x/year). New hire will remain on days for first 2-3 months and then may switch to swings or stay on days. Rarely will work graves (maybe 2x/ year). All candidates must be open to working days and swing 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.