Manufacturing associate jobs in San Buenaventura, CA - 156 jobs

Be visionary Teledyne Technologies Incorporated provides enabling technologies for industrial growth markets that require advanced technology and high reliability. These markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research. We are looking for individuals who thrive on making an impact and want the excitement of being on a team that wins. Job Description Job Summary Under the general supervision of the fab manager, the Semiconductor Wafer Processing Technician performs hands-on technical tasks in a cleanroom environment to support wafer fabrication and processing. This role involves operating and maintaining semiconductor processing equipment, monitoring workflows, and collaborating with other technicians and engineering to ensure high-quality production and continuous improvement. This is a second shift position from 2:30pm to 11:00 pm M-F. Key Responsibilities Perform wafer-level processing steps such as wafer cleaning, photolithography, deposition, and etching Operate and maintain semiconductor fabrication tools, ensuring compliance with safety and cleanliness protocols Maintain detailed records, including SPC charts and data entry for products and equipment Use metrology tools (optical microscopes, laser confocal, profilometry) to inspect wafers and verify process results Collaborate with engineers and technicians to troubleshoot issues and implement corrective actions Support continuous yield improvement and equipment qualification efforts Maintain accurate logs of tests, trials, and production runs Work in an ISO Class 6 cleanroom and adhere to 6S principles Follow cleanroom protocols and handle chemicals safely Inspect and disposition nonconforming products Qualifications High School Diploma or equivalent 2+ years of experience in semiconductor wafer processing or related technical field preferred Familiarity with cleanroom protocols and semiconductor fabrication equipment preferred Basic computer skills (Word, Excel, PowerPoint); experience with MES systems a plus Must be able to communicate clearly and read/write in English. Preferred Skills Strong attention to detail Effective communication skills Ability to work effectively in a collaborative team-oriented environment Initiative and problem-solving mindset Physical Requirements Ability to stand and walk for extended periods (up to 8-10 hours per shift) Frequent bending, stooping, and reaching to handle wafers and equipment Manual dexterity for handling small, delicate components and precision tools Ability to lift and carry items up to 25 lbs (e.g., wafer cassettes, chemical containers) Comfortable working in full cleanroom gowning (coveralls, gloves, mask, eye protection) Visual acuity for detailed inspection under microscopes and metrology tools Tolerance for repetitive tasks and working in controlled temperature/humidity conditions Salary Range: $42,800.00-$57,100.000 Pay Transparency The anticipated salary range listed for this role is only an estimate. Actual compensation for successful candidates is carefully determined based on several factors including, but not limited to, location, education/training, work experience, key skills, and type of position. Teledyne and all of our employees are committed to conducting business with the highest ethical standards. We require all employees to comply with all applicable laws, regulations, rules and regulatory orders. Our reputation for honesty, integrity and high ethics is as important to us as our reputation for making innovative sensing solutions. Teledyne is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age, or any other characteristic or non-merit based factor made unlawful by federal, state, or local laws.

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

Business Unit: MCS Cell Culture Group Employment Type: Contract Duration: Initial 3 months with possible extensions or conversion to FTE based on performance. Rate: $30 - $34/hour W2 Posting Date: 2/14/2024. Notes: Only qualified candidates need apply. Fully onsite in Thousand Oaks, CA. SWING SHIFT 1:00 PM to 12:00 AM (midnight). Also flexibility to work various shifts (day, swing, graves, weekends, holidays, 5x8hrs, 4x10hrs, 3 or 4x12hrs) 3 Key Consulting is hiring! We are recruiting a MCS Manufacturing Associate for a consulting engagement with our direct client, a leading global biotechnology company. Job Description: The Manufacturing Process Technician will work in a dynamic production environment at the client's Thousand Oaks site supporting development, clinical, and launch activities. Under general supervision, the technician will perform operations in the Manufacturing area. Operations will be performed according to Standard Operating Procedures (SOPs). Top Must Have Skill Sets: GMP experience Safety oriented Experience in manufacturing environment is a plus*. Day to Day Responsibilities: 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. Basic Qualifications: Bachelor's degree OR Associate degree and 4 years of experience OR High school diploma / GED and 6 years of experience Available to work various shifts (day, swing, graves, weekends, holidays, 5x8hrs, 4x10hrs, 3 or 4x12hrs) 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. Mechanically inclined Why is the Position Open? Supplement additional workload on team. Red Flags: Not willing to work shift Not willing to be fully onsite at USTO Interview Process: WebEx. 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

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

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

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

Manufacturing Thousand Oaks, California, US + Added - 08/01/2026 Apply for Job Pay Rate Low: 25 | Pay Rate High: 30 Our client, a renowned leader in the field of biotechnology, is revolutionizing the use of living cells to create groundbreaking biologic medicines. We are excited to announce a fantastic opportunity to join the team! We are seeking a dynamic individual who is eager to contribute their expertise and drive their mission forward. **Title:** GMP Manufacturing Associate (Multiple openings!) **Location:** Thousand Oaks, CA **Schedule:** Day Shift (12-hour shifts) Day Shift: 7:00 AM - 8:00 PM **Pay:** $25-30/hr Contract to hire (Benefits Included!) **Job Summary** : The Associate of Manufacturing will work in a dynamic production environment at the clients Thousand Oaks Drug Substance plant supporting development, clinical, and commercial 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-scale 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 deviation records - Drafting and revising documents (SOPs, MPs) - Working around high-pressure systems and occasionally working around heavy equipment - Available to work various shifts (Days, Swings, Graves, Weekends, Holidays, 5x8hrs, 4x10hrs, 3 or 4x12hrs) as dictated by the production schedule **Preferred Qualifications:** Bachelors Degree in Biology and/or Life Sciences Mechanically inclined Basic Qualifications: Bachelor degree OR Associate degree and 4 years of experience OR High school diploma / GED and 6 years of experience INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Job Description QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you'll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA. Responsibilities: Perform hands-on operations including equipment setup, cleaning, and sanitization Prepare buffers and media per Manufacturing Procedures (MPs) and SOPs Follow GMP documentation (SOPs, MPs) with strict adherence to safety and compliance Perform and monitor critical processes, including basic troubleshooting Conduct in‑process sampling and operate analytical equipment Execute washroom activities, including cleaning small and large-scale production equipment Maintain an organized and clean workspace Work in a clean‑room environment while wearing steel‑toe shoes, full gowning, hairnet, and gloves Documentation & Quality Initiate quality reports Assist in reviewing documentation such as equipment logs and batch records Identify, recommend, and implement improvements related to routine functions Perform operations in the Manufacturing area, specifically for Purification processes. Operations will be performed according to Standard Operating Procedures (SOPs) while complying with GMP standards in safe manner Qualifications: College degree (science-based preferred) Alternatively: Relevant industry or laboratory experience may be considered in place of a degree Experience in biotech, pharmaceutical, or regulated manufacturing environments Science-based background (laboratory, manufacturing, or related field) Familiarity with: SOP adherence, GMP or GLP principles and General laboratory or manufacturing Willing to commit to shift rotations. Schedule: Day Shift or Graveyard Shift (12-hour shifts) Day Shift: 7:00 AM - 8:00 PM or Graveyard Shift: 7:00 PM - 8:00 AM Schedule Structure: Front-half and back-half schedules Includes alternating weekends off Initial training will take place on day shift Candidates will transition to assigned shift after training Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law. Powered by JazzHR vSVe01RKrz

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

Fresh-Squeezed Legacy, Bold New Chapter Tropicana Brands Group is a $3B startup aiming to revolutionize the beverage category. Formed in 2022 as a joint venture between PAI Partners and PepsiCo, our portfolio includes iconic brands like Tropicana, Naked, KeVita, Izze, Copella, and Punica. With over 76 years of global leadership in the orange juice category, we're committed to preserving this legacy while driving innovation in other areas. From reimagining orange juice to creating functional smoothies and driving afternoon refreshments, we are striving to become the undisputed global leader in fresh and chilled beverages. Your Next Pour: The Opportunity Tropicana Brands Group is looking for a Production Operator to support our Supply Chain Team. This role will be responsible for activities such as unloading tankers, bins, drums, driving forklifts, pallet jack, floor scrubber, cleaning, sanitation, material handling, ect. Tropicana is looking for a critical thinker with exceptional communication, influencing and relationship management skills who thrives in a fast-paced environment. . Additional responsibilities will include: * Operates and monitors machinery used in the production process * Verifies conformance to quality standards at all levels ( raw, finished, ingredients, storage, and transportation conditions) * Performs autonomous maintenance activities such as preventative maintenance, lubrication, center lining, 5s and defect identification, sources of contamination. ect. * Participate in periodical activities such assisting with the cycle counts and physical inventories * Performs duties and responsibilities within the guidelines of plant's programs and initiatives (i.e.: SFTPM) * All other duties as assigned by managemet The Perfect Blend: Experience * Minimum 1 year of recent work experience in a manufacturing facility, food production preferred Foundational Ingredients: Requirements * Must be located in Oxnard, CA surrounding area or willing to relocate for the duration of employment * Willingness to be onsite at the manufacturing facility on a full-time basis * Must be able to perform physical tasks for the duration of the shift, including standing, walking, bending, reaching, and lifting/moving items weighing 50 pounds or more * Must be legally authorized to work in the United States without the need for employer sponsorship now or in the future * High School Diploma, GED or equivalent * Knowledge of basic math & problem solving * Must be able to utilize manufacturing software * Ability to operate equipment and machines in an industrial environment * Ability to perform work within established guidelines in a safe manner * Ability to work independently and in teams * Must be able to obtain forklift certification Benefits TBG is pleased to offer you a comprehensive benefits package which includes medical, dental, vision, company provided life, STD and LTD insurance. In addition, you may also elect to participate in voluntary life, accident, hospital, and critical illness coverages. The hourly pay for this position is $24.51.

Career CategoryOperationsJob Description 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. Pilot Plant Manufacturing Associate What you will do Let's do this. Let's change the world. In this vital role you will execute a variety of production and technology related operations in the Downstream (Purification) area of their large-scale pilot plant. The pilot plant delivers data and material to support process development of early and late stage clinical biologic molecules. The plant also prototypes and develops new technologies to support advancement of Amgen's equipment and operations for current and future biologic facilities. This Associate will perform hands on operations of purification equipment. The purification equipment typically includes large scale chromatography, various types of filtration, ultrafiltration /diafiltration and equipment cleaning. In addition, the applicant may participate in new product introductions, technology transfer, experiment design, equipment commissioning, and equipment design. The applicant will communicate results through authoring standard operating procedures, detailing results in electronic lab notebooks, manufacturing procedures, presentations, or meeting notes. This role will analyze data, process results, summarize findings, and identify challenges to future commercial processes Must be able to work both Day (7:30am - 4:30pm) and Swing Shift (2:30pm - 11:30pm). Shifts rotate roughly every 3 months based on business needs. Ability to lift and move up to 25 lbs. Completing a variety of production-related operations in a large-scale facility, including but not limited to chromatography, UF/DF, and viral filtration. Performing supporting activities such as equipment set-up/cleaning and running analytical instruments Performing ‘hands-on' work in the plant. Ensuring documentation accurately reflects operations performed, implementing area improvements (efficiency and safety) applying lean principles, and participating in operations meetings. 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 an individual with these qualifications. Basic Qualifications: High school diploma / GED and 2years of Manufacturing, Scientific or Operations experience; Or Associate's degree and 6 months of Manufacturing, Scientific or Operations experience; Or Bachelor's degree Preferred Qualifications: Bachelor's degree and previous bio-processing/biotech experience Strong verbal and written communication skills. Analytical, project management, and continuous improvement skills. Ability to work off hours or non-standard shifts. 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

**Country:** United States of America ** Onsite **U.S. Citizen, U.S. Person, or Immigration Status Requirements:** The ability to obtain and maintain a U.S. government issued security clearance is required. U.S. citizenship is required, as only U.S. citizens are eligible for a security clearance **Security Clearance Type:** DoD Clearance: Secret **Security Clearance Status:** Active and existing security clearance required after day 1 At Raytheon, the foundation of everything we do is rooted in our values and a higher calling - to help our nation and allies defend freedoms and deter aggression. We bring the strength of more than 100 years of experience and renowned engineering expertise to meet the needs of today's mission and stay ahead of tomorrow's threat. Our team solves tough, meaningful problems that create a safer, more secure world. We have an opening for a Production Worker 4 in our Class 7 Clean Room Facility in Goleta, California, that is involved in the packaging of IR detectors for high-reliability space, military, and commercial applications. We need a skilled electro-mechanical technician in support of a variety of program processes as assigned by management. The selected candidate will be working with critical dewars and subassemblies. **What You Will Do** + Must be able to work extended periods of time in an environmentally controlled area (cleanroom). + Technicians are required to communicate in English and must be able to understand written and verbal instructions in English. + The ability to use a computer to access work instructions, perform data entry, and complete on-line training is required. + You must wear company provided Personal Protective Equipment (PPE) and strictly follow all safety-related processes, procedures, and protocols. + Tasks may require the ability to push a cart, extend arms above shoulder height, and be able to visually inspect small parts. + Tasks may include working with chemicals (epoxies, adhesives, solvents, etc.) and following rigorous disciplined methodologies and instructions. + This is a 1st shift, onsite position. **Qualifications You Must Have** + Typically requires HS diploma (or equivalent, e.g. G.E.D in the US) or vocational/ technical education in related discipline with a minimum of 4 years of relevant experience. + Minimum of four years' relevant experience in manufacturing or operations. + Experience using general lab equipment like microscopes and small hand-held tools (tweezers, screwdrivers, etc.) + U.S. Citizenship status is required, as this position will require the ability to access U.S. only data systems. **Qualifications We Prefer** + Experience using manual or automated wire bonders or tab bonders as well as pull testing equipment. + Previous experience working in a cleanroom, around ESD sensitive parts is a plus. + Experience with FOD and FOD reduction methods. **What We Offer** Our values drive our actions, behaviors, and performance with a vision for a safer, more connected world. At RTX we value: Safety, Trust, Respect, Accountability, Collaboration, and Innovation. _Relocation assistance not provided for this position._ **Learn More & Apply Now!** Please consider the following role type definition as you apply for this role. Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance employees, as they are essential to the development of our products. _The salary range for this role is $31-$35/hour. The salary range provided is a good faith estimate representative of all experience levels. RTX considers several factors when extending an offer, including but not limited to, the role, function and associated responsibilities, a candidate's work experience, location, education/training, and key skills._ **_As part of our commitment to maintaining a secure hiring process, candidates may be asked to attend select steps of the interview process in-person at one of our office locations, regardless of whether the role is designated as on-site, hybrid or remote._** Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement. Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company's performance. This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply. RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window. _RTX is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans' Readjustment Assistance Act._ **Privacy Policy and Terms:** Click on this link (******************************************************** to read the Policy and Terms Raytheon Technologies is An Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age or any other federally protected class.

Country: United States of America Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: The ability to obtain and maintain a U.S. government issued security clearance is required. U.S. citizenship is required, as only U.S. citizens are eligible for a security clearance Security Clearance Type: DoD Clearance: Secret Security Clearance Status: Active and existing security clearance required after day 1 At Raytheon, the foundation of everything we do is rooted in our values and a higher calling - to help our nation and allies defend freedoms and deter aggression. We bring the strength of more than 100 years of experience and renowned engineering expertise to meet the needs of today's mission and stay ahead of tomorrow's threat. Our team solves tough, meaningful problems that create a safer, more secure world. We have an opening for a Production Worker 4 in our Class 7 Clean Room Facility in Goleta, California, that is involved in the packaging of IR detectors for high-reliability space, military, and commercial applications. We need a skilled electro-mechanical technician in support of a variety of program processes as assigned by management. The selected candidate will be working with critical dewars and subassemblies. What You Will Do Must be able to work extended periods of time in an environmentally controlled area (cleanroom). Technicians are required to communicate in English and must be able to understand written and verbal instructions in English. The ability to use a computer to access work instructions, perform data entry, and complete on-line training is required. You must wear company provided Personal Protective Equipment (PPE) and strictly follow all safety-related processes, procedures, and protocols. Tasks may require the ability to push a cart, extend arms above shoulder height, and be able to visually inspect small parts. Tasks may include working with chemicals (epoxies, adhesives, solvents, etc.) and following rigorous disciplined methodologies and instructions. This is a 1st shift, onsite position. Qualifications You Must Have Typically requires HS diploma (or equivalent, e.g. G.E.D in the US) or vocational/ technical education in related discipline with a minimum of 4 years of relevant experience. Minimum of four years' relevant experience in manufacturing or operations. Experience using general lab equipment like microscopes and small hand-held tools (tweezers, screwdrivers, etc.) U.S. Citizenship status is required, as this position will require the ability to access U.S. only data systems. Qualifications We Prefer Experience using manual or automated wire bonders or tab bonders as well as pull testing equipment. Previous experience working in a cleanroom, around ESD sensitive parts is a plus. Experience with FOD and FOD reduction methods. What We Offer Our values drive our actions, behaviors, and performance with a vision for a safer, more connected world. At RTX we value: Safety, Trust, Respect, Accountability, Collaboration, and Innovation. Relocation assistance not provided for this position. Learn More & Apply Now! Please consider the following role type definition as you apply for this role. Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance employees, as they are essential to the development of our products. The salary range for this role is $31-$35/hour. The salary range provided is a good faith estimate representative of all experience levels. RTX considers several factors when extending an offer, including but not limited to, the role, function and associated responsibilities, a candidate's work experience, location, education/training, and key skills. As part of our commitment to maintaining a secure hiring process, candidates may be asked to attend select steps of the interview process in-person at one of our office locations, regardless of whether the role is designated as on-site, hybrid or remote. Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement.Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company's performance.This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply.RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window. RTX is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans' Readjustment Assistance Act. Privacy Policy and Terms: Click on this link to read the Policy and Terms

Fresh-Squeezed Legacy, Bold New Chapter Tropicana Brands Group is a $3B startup aiming to revolutionize the beverage category. Formed in 2022 as a joint venture between PAI Partners and PepsiCo, our portfolio includes iconic brands like Tropicana, Naked, KeVita, Izze, Copella, and Punica. With over 76 years of global leadership in the orange juice category, we're committed to preserving this legacy while driving innovation in other areas. From reimagining orange juice to creating functional smoothies and driving afternoon refreshments, we are striving to become the undisputed global leader in fresh and chilled beverages. Your Next Pour: The Opportunity Tropicana Brands Group is looking for a Production Operator to support our Supply Chain Team. This role will be responsible for activities such as unloading tankers, bins, drums, driving forklifts, pallet jack, floor scrubber, cleaning, sanitation, material handling, ect. Tropicana is looking for a critical thinker with exceptional communication, influencing and relationship management skills who thrives in a fast-paced environment. . Additional responsibilities will include: Operates and monitors machinery used in the production process Verifies conformance to quality standards at all levels ( raw, finished, ingredients, storage, and transportation conditions) Performs autonomous maintenance activities such as preventative maintenance, lubrication, center lining, 5s and defect identification, sources of contamination. ect. Participate in periodical activities such assisting with the cycle counts and physical inventories Performs duties and responsibilities within the guidelines of plant's programs and initiatives (i.e.: SFTPM) All other duties as assigned by managemet The Perfect Blend: Experience · Minimum 1 year of recent work experience in a manufacturing facility, food production preferred Foundational Ingredients: Requirements Must be located in Oxnard, CA surrounding area or willing to relocate for the duration of employment Willingness to be onsite at the manufacturing facility on a full-time basis Must be able to perform physical tasks for the duration of the shift, including standing, walking, bending, reaching, and lifting/moving items weighing 50 pounds or more Must be legally authorized to work in the United States without the need for employer sponsorship now or in the future High School Diploma, GED or equivalent Knowledge of basic math & problem solving Must be able to utilize manufacturing software Ability to operate equipment and machines in an industrial environment Ability to perform work within established guidelines in a safe manner Ability to work independently and in teams Must be able to obtain forklift certification Benefits TBG is pleased to offer you a comprehensive benefits package which includes medical, dental, vision, company provided life, STD and LTD insurance. In addition, you may also elect to participate in voluntary life, accident, hospital, and critical illness coverages. The hourly pay for this position is $24.51.

Job Description Production Laborer I M-F 6:00am - 2:30pm $19/hour Who we are Atkore is forging a future where our employees, customers, suppliers, shareholders, and communities are building better together - a future focused on serving the customer and powering and protecting the world. With a global network of manufacturing and distribution facilities, Atkore is a leading provider of electrical, safety and infrastructure solutions. Who we are looking for: We are currently looking for a Production Laborer I to be based out of Santa Paula, CA. Reporting to Production Supervisor, this person will be responsible for performing production work that includes assembling and disassembling parts, inspecting product to ensure quality as well as operating, tending, and cleaning the production area. The ideal candidate will have a one (1) year experience in a manufacturing setting. Experience in lean manufacturing or business system-based company is a plus. What you'll do: Assist with the production line Load and unload parts from machine Feed or place items onto equipment for processing Pull damaged or non-conforming parts off the line Install and uninstall tooling from product Cut and scrape waste material from parts Label, clean, pack or strap and wrap finished goods Must be able to remain in a stationary position during shift Perform Daily 5S in production work area to prevent safety hazards Be able to work with daily production schedule Take instruction from production line coordinator Read and understand the department metrics Knowledge of basic hand power tools Follow all Personal Protective Equipment (PPE) as required Continuously perform all required tasks in a safe manner, adhering to Atkore's established safety rules and procedures Be flexible and willing to adapt to change, be comfortable working in the constant changing environment Assist in meeting performance to meet Safety, Quality, Delivery, Cost and Innovation goals Attend monthly safety trainings, be an active participant in daily safety briefings, and provide feedback to improve safety program. Must embrace and foster an environment that supports our core values of Accountability, Teamwork, Integrity, Respect and Excellence. What you'll bring: One (1) year of production experience in a manufacturing setting Ability to maintain quality, safety, and effective control standards Ability to understand and follow safety procedures Ability to interpret and execute standard works Ability to read, sort, check, county and verify numbers / perform simple arithmetic Ability to detect problems and report information to appropriate personnel Ability to move objects weighing up to 50lbs Ability to multitask in a fast-paced work environment is a must Ability to familiarize and follow the 5S company program Ability to work independently and in a team when necessary. Good attendance and punctuality. Within 3 months, you'll: Complete your Atkore immersion program Understand your team and your role within the team and how it will help delivery Atkore's strategy Understand departmental standard work and Atkore's policies and procedures Understand department metrics Load and unload parts onto machine Cut/scrape waste material from product Install/Uninstall tooling from product Process and pack finished goods to next process Within 6 months, you'll: Ensure parts conform to specifications, by identifying nonconforming parts and pulling off the line Work efficiently as a team within the department to meet the daily target goal To detect problems and report information as necessary Within 12 months, you'll: Ensure full adherence to 5S practices Follow department standard work procedures, continuous quality improvement objectives, and safety and environmental policies. Atkore is a recipient of a Great Place to Work© certification and a Top Workplaces USA award! We're committed to creating an engaged and aligned workforce that drives collaborative culture. Our team strives for breakthrough results, stays focused on being standout leaders, and fully supports decisions of the Company. We consistently live the Atkore mission, strategic priorities, and behaviors, all in a way that's consistent with our core values. Together, we build strong leaders that continually endeavor to move us forward. Join our team and align yourself with an industry leader!

We are seeking a Manufacturing Technician II for a contract position lasting up to 6 months in Goleta, CA. The role involves testing, modifying, reworking, and repairing mechanical and/or electronic assemblies. Responsibilities + Fabricate and validate critical flight hardware, including mechanical assembly, electrical assembly, and flight Ground Support Equipment, following flight drawings, procedures, quality standards, and internal training. + Assist engineers in the manufacture and testing of flight/prototype hardware and in the development of test infrastructure, documentation of assembly, and test procedures. + Identify and communicate non-conformances to engineering and quality assurance. + Collaborate with facilities and maintenance to ensure timely maintenance and repair of production equipment. + Work with manufacturing engineering to optimize manufacturing orders and ensure process instructions are understood. Essential Skills + Proficiency in electronics, electrical systems, soldering, harnessing, blueprint reading, circuit testing, and the use of test equipment. + Experience with hand tools and power tools. + Mechanical experience and the ability to troubleshoot and work with engineers. + Intermediate computer skills, including Microsoft Office 365. Additional Skills & Qualifications + Ability to learn to read and work from diagrams, drawings, and detailed procedures. + Ability to learn how to operate electrical and non-electrical manufacturing equipment. + Ability to learn how to use hand tools, including crimpers, drills, taps, torque wrenches, power tools, and air tools. + Ability to learn how to work with adhesives, chemical cleaners, coating materials, and other commonly used chemicals in manufacturing. + High School Diploma, GED, or equivalent plus advanced training. + At least 2 years of prior experience working in an aerospace manufacturing setting in a similar position. + Strong mechanical aptitude, good fabrication skills, and general shop experience. + Ability to manage time to meet daily milestones and satisfy longer-term commitments to support projects. + Ability to stand, walk, use hands to finger, handle, or feel objects, tools, or controls, reach with hands and arms, and lift/move up to 50 pounds. + Specific vision abilities required, including close vision, distance vision, and color vision. Work Environment The work takes place in a cleanroom environment with hours from Monday to Friday, 6:30 AM to 3:00 PM. Occasional weekend work and late days may be required to meet shipping dates. Job Type & Location This is a Contract to Hire position based out of Goleta, CA. Pay and Benefits The pay range for this position is $25.00 - $32.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Goleta,CA. Application Deadline This position is anticipated to close on Feb 3, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Bring your passion for space! Redwire is accelerating humanity's expansion into space by delivering reliable, economical, and sustainable infrastructure for future generations. Redwire Space - Goleta, CA is the leading developer and provider of solar array systems to the global space market. The company's key products include Roll Out and Rigid Solar Arrays. The talented innovators in Goleta, CA are a leading developer and provider of satellite mechanisms, deployable structures and booms and deployable solar array systems to the global space market. The team is revolutionizing spaceflight and are currently being utilized on missions with NASA, the Department of Defense, and commercial space companies. With many more exciting projects on the horizon our team could use your curiosity, passion, talent and experience to help us Build Above. Summary We have a current opportunity for Contractor - Manufacturing Technician II for up to 6 months to join our team in Goleta, CA. The Contract - Manufacturing Technician performs testing, modifying, reworking, and repairing of mechanical and or electronic assemblies. Responsibilities Fabrication and validation of critical flight hardware, including mechanical assembly, electrical assembly, and flight Ground Support Equipment; per associated flight drawings, procedures, quality standards and internal training. Assist engineers in flight / prototype hardware manufacture / test infrastructure development, documentation of assembly, test procedures and other specified tasks. Identify and communicate non-conformances to engineering and quality assurance. Work with facilities and maintenance to ensure that production equipment is maintained and repaired in a timely manner. Work with manufacturing engineering to optimize manufacturing orders and ensure process instructions are understood. Ideal Experience High School Diploma, GED, or equivalent plus advanced training. At least 2 plus years prior experience working in an Aerospace manufacturing setting in a similar position. Strong mechanical aptitude, good fabrications skills and general shop experience. Intermediate computer skills including Microsoft Office 365. Must be able to work Mon-Fri, occasional weekends to meet shipping dates and some late days. Ability to stand; walk; and use hands to finger, handle, or feel objects, tools, or controls. Ability to reach with hands and arms. Ability to lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, and color vision. US Citizen or US Person as defined by ITAR regulations. Must be able to work the following shift: Mon-Fri 6:30 to 3:00pm Desired Skills: Ability to learn to read and work from diagrams, drawings, and detailed procedures. Ability to learn how to operate electrical and nonelectrical manufacturing equipment. Ability to learn how to use hand tools, including crimpers, drills, taps, torque wrenches, power tools and air tools. Ability to learn how to work with adhesives, chemical cleaners, coating materials and other commonly used chemicals used in manufacturing. Ability to take direction from multiple sources and manage time to meet daily milestones as well as satisfy longer term commitments to support projects. Some travel to local vendors and suppliers might be required. Grow with us as we innovate the next generation capabilities for a new era of space exploration! We offer a highly competitive benefits package along with a commitment to our core values of Integrity, Innovation, Impact, Inclusion, and Excellence. Pay Range $ 25.48 - $32/hour How We Determine What We Pay (Compensation Philosophy) Redwire determines pay for positions using local, national, and industry-specific survey data, for our locations throughout the US. We will evaluate external equity and the cost of labor/prevailing wage index, in the relative marketplace for jobs directly comparable to jobs within our company. For new hires, we strive to make competitive offers allowing the new employee room for future growth. Salaries will be based on the applicant's level of experience, education, and specialized knowledge and skills. Additionally, we consider the external market rate, the amount we have budgeted internally, and internal equity within the company for the same position. An employee/candidate with a stronger skill set will receive higher pay. Redwire is an Equal Opportunity Employer; employment with Redwire is governed on the basis of merit, 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. All offers of employment at Redwire are contingent upon clear results of a thorough background check and your ability to provide proof of eligibility to work in the US. Note that some positions will also require US citizenship or ability to obtain a security clearance due to requirements of a classified program. To conform to U.S. Government space technology export regulations, including the International Traffic in Arms Regulations (ITAR) you must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. Department of State. Learn more about the ITAR Click Here

Bring your passion for space! Redwire is accelerating humanity's expansion into space by delivering reliable, economical, and sustainable infrastructure for future generations. Redwire Space - Goleta, CA is the leading developer and provider of solar array systems to the global space market. The company's key products include Roll Out and Rigid Solar Arrays. The talented innovators in Goleta, CA are a leading developer and provider of satellite mechanisms, deployable structures and booms and deployable solar array systems to the global space market. The team is revolutionizing spaceflight and are currently being utilized on missions with NASA, the Department of Defense, and commercial space companies. With many more exciting projects on the horizon our team could use your curiosity, passion, talent and experience to help us Build Above. Summary We have a current opportunity for Contractor - Manufacturing Technician II for up to 6 months to join our team in Goleta, CA. The Contract - Manufacturing Technician performs testing, modifying, reworking, and repairing of mechanical and or electronic assemblies. Responsibilities * Fabrication and validation of critical flight hardware, including mechanical assembly, electrical assembly, and flight Ground Support Equipment; per associated flight drawings, procedures, quality standards and internal training. * Assist engineers in flight / prototype hardware manufacture / test infrastructure development, documentation of assembly, test procedures and other specified tasks. * Identify and communicate non-conformances to engineering and quality assurance. * Work with facilities and maintenance to ensure that production equipment is maintained and repaired in a timely manner. * Work with manufacturing engineering to optimize manufacturing orders and ensure process instructions are understood. Ideal Experience * High School Diploma, GED, or equivalent plus advanced training. * At least 2 plus years prior experience working in an Aerospace manufacturing setting in a similar position. * Strong mechanical aptitude, good fabrications skills and general shop experience. * Intermediate computer skills including Microsoft Office 365. * Must be able to work Mon-Fri, occasional weekends to meet shipping dates and some late days. * Ability to stand; walk; and use hands to finger, handle, or feel objects, tools, or controls. * Ability to reach with hands and arms. * Ability to lift and/or move up to 50 pounds. * Specific vision abilities required by this job include close vision, distance vision, and color vision. * US Citizen or US Person as defined by ITAR regulations. * Must be able to work the following shift: * Mon-Fri 6:30 to 3:00pm Desired Skills: * Ability to learn to read and work from diagrams, drawings, and detailed procedures. * Ability to learn how to operate electrical and nonelectrical manufacturing equipment. * Ability to learn how to use hand tools, including crimpers, drills, taps, torque wrenches, power tools and air tools. * Ability to learn how to work with adhesives, chemical cleaners, coating materials and other commonly used chemicals used in manufacturing. * Ability to take direction from multiple sources and manage time to meet daily milestones as well as satisfy longer term commitments to support projects. * Some travel to local vendors and suppliers might be required. Grow with us as we innovate the next generation capabilities for a new era of space exploration! We offer a highly competitive benefits package along with a commitment to our core values of Integrity, Innovation, Impact, Inclusion, and Excellence. Pay Range $ 25.48 - $32/hour How We Determine What We Pay (Compensation Philosophy) Redwire determines pay for positions using local, national, and industry-specific survey data, for our locations throughout the US. We will evaluate external equity and the cost of labor/prevailing wage index, in the relative marketplace for jobs directly comparable to jobs within our company. For new hires, we strive to make competitive offers allowing the new employee room for future growth. Salaries will be based on the applicant's level of experience, education, and specialized knowledge and skills. Additionally, we consider the external market rate, the amount we have budgeted internally, and internal equity within the company for the same position. An employee/candidate with a stronger skill set will receive higher pay. Redwire is an Equal Opportunity Employer; employment with Redwire is governed on the basis of merit, 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. All offers of employment at Redwire are contingent upon clear results of a thorough background check and your ability to provide proof of eligibility to work in the US. Note that some positions will also require US citizenship or ability to obtain a security clearance due to requirements of a classified program. To conform to U.S. Government space technology export regulations, including the International Traffic in Arms Regulations (ITAR) you must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. Department of State. Learn more about the ITAR Click Here

* Early submissions are encouraged as applications will be reviewed on a regular and ongoing basis.* The City of Oxnard's Public Works Department is seeking a Power Production Operator with strong technical and customer service skills to be part of the Public Works team. This individual must be comfortable performing routine maintenance and preparing reports. The ideal candidate will have knowledge of operating procedures of heavy equipment maintenance. This position will be responsible for maintaining and assuring the proper work order of treatment plant enginators. Under general supervision, performs a variety of skilled tasks operating and maintaining enginators and ancillary equipment used for power production purposes; performs preventive maintenance, troubleshooting and repair; establishes and maintains work procedures and methods associated with assigned duties; performs related duties as required. WHAT YOU'LL DO: * Performs routine, preventive and emergency maintenance and repair of assigned treatment plant equipment. * Performs routine rounds and inspections of equipment. * Checks and records fluid levels, temperatures, pressures and vacuums. * Drains moisture traps and air receivers. * Flushes strainers and heat recovery systems drain lines. * Checks co-generation for import/export loading. * Adjusts and balances load-sharing voltages, amperes and hertz; records both electrical and mechanical readings. * Makes reports and keep log book records and equipment history cards up to date; coordinates with maintenance crew and operations crew * Draws oil samples, performs weekly, bi-monthly, quarterly, semi-annual, and annual preventive maintenance and complete work orders. * Removes watt hour and watt hour demand meters from service for annual calibration and reinstall. * Prepares annual reports. * Troubleshoots and make routing and emergency repairs; responds to emergency and standby calls. * Improves/Fabricates parts for installation of new components. * Demonstrates a full understanding of applicable policies, procedures and work methods associated with assigned duties. Payroll/Classification Title: Plant Maintenance Specialist SUPERVISION EXERCISED/SUPERVISION RECEIVED: Receives general supervision on routine items which are performed according to established standards and procedures and receives specific work instruction regarding non-routine matters and deadlines. DISTINGUISHING CHARACTERISTICS: This classification is distinguished from the Plant Maintenance Specialist, Senior in that it performs semi-skilled and skilled maintenance and repair work. WORK SCHEDULE: The Wastewater Power Production Operator work week is Sunday through Thursday, 7:30 a.m. to 3:30 p.m. Depending on the work assignment, staff may be assigned to shifts that are outside the standard City work hours. Additionally, this position requires the ability to work additional hours in response to workload peaks and changes in department needs, as well as perform on-call (standby) duties. This position is governed by the overtime provisions of the federal Fair Labor Standards Act and is eligible for overtime pay. ESSENTIAL DUTIES: This class specification represents only the core areas of responsibilities; specific position assignments will vary depending on the needs of the Department. * Performs skilled technical work in the maintenance, repair and/or operation of plant process and control equipment, pumps and/or lift stations; adheres to safety policies and procedures. * Performs scheduled preventative maintenance; calibrates and/or services equipment according to plans and specifications; assists with general operations work. * Monitors equipment and performs inspections; troubleshoots, diagnoses and addresses issues; schedules repairs; assists in general housekeeping tasks. * Prepares and submits reports; reviews parts, materials and equipment needs and initiates requests. * Assists with special projects; evaluates equipment failures; performs emergency repairs, as needed. POSITION SPECIFIC RESPONSIBILITIES MIGHT INCLUDE: Positions assigned to power production may be responsible for: * Operating and maintaining power production equipment; * Performing preventative maintenance; * Performing inspections, troubleshooting and repair work; * Recording and tracking data; * Preparing reports; Calibrating equipment. EDUCATION AND EXPERIENCE: * High School Diploma or GED * Three (3) years of related maintenance experience including specialized and directly related vocational training. LICENSING/CERTIFICATIONS: * Valid California Class C Driver's License with a satisfactory driving record. OTHER REQUIREMENTS: * Must be able to communicate in English effectively both orally and in writing. APPLICATION PROCESS: * Submit NEOGOV/Government Jobs on-line application. * Complete and submit responses to the supplemental questions, if required. * Upload resume, cover letter, proof of degree (transcript), or other requested documents. Your application may be rejected as incomplete if you do not include the relevant information in the online application and include the information only on the resume. Applications and/or Supplemental Questionnaires that state "see my resume" or "see my personnel file" are considered incomplete and will not be accepted. Cover letters and/or optional resumes are not accepted in lieu of a completed application. The list of qualified candidates established from this recruitment may be used to fill other full-time, part-time, and temporary assignments. There is currently one (1) full-time vacancy within the Public Works Department. Selected candidate(s) must pass a thorough background investigation. UNION MEMBERSHIP: International Union of Operating Engineers (IUOE) NOTE: For most positions, the City of Oxnard relies on office automation (Microsoft Office/Google) and web-based enabled tools, therefore candidates must be proficient and comfortable with computer use to perform functions associated with on-going work. Regular and reliable attendance, effective communication skills, and development of effective working relationships are requirements of all positions. Employees are required to participate in the City's direct deposit plan and are paid on a bi-weekly basis. This position requires a 12 month probationary period. Pursuant to California Government Code Section 3100, all public employees are required to serve as disaster service workers subject to such disaster service activities as may be assigned to them. EQUAL OPPORTUNITY: The City of Oxnard is an Equal Opportunity Employer and welcomes applications from all qualified applicants. We do not discriminate on the basis of race, color, religion, sex, national origin, age, marital status, medical condition, disability or sexual orientation. REASONABLE ACCOMMODATION: The City of Oxnard makes reasonable accommodations for individuals/people with disabilities. If you believe you require special arrangements to participate in the testing process, you must inform the Human Resources Department in writing no later than the filing date. Applicants who request such accommodation must document their request with an explanation of the type and extent of accommodation required. LEGAL REQUIREMENT: On the first day of employment, new employees must provide proof of citizenship or documentation of legal right to work in the United States in compliance with the Immigration Reform and Control Act of 1986, as amended. The City participates in E-Verify and will provide the federal government with you. Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, this employer is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue before the employer can take any action against you, including terminating your employment. Employers can only use E-Verify once you have accepted a job offer and completed the Form I-9. For more information on E-Verify, please contact DHS. ************ dhs.gov/e-verify If you have any questions regarding this recruitment, please contact Ashley Costello at **************************. NOTE: The provisions of this bulletin do not constitute an expressed or implied contract. Any provision contained in this bulletin may be modified or revoked without notice.