Manufacturing associate jobs in San Buenaventura, CA

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 Requirements: * Bachelor of Science (B.Sc.) with 0-3 years of applicable biopharma experience or Associate degree with 2+ years of applicable biopharma experience or High school diploma with 3+ years of applicable biopharma experience Preferred Qualifications: * Ability to follow verbal and written instructions * Problem solving skills * Detail oriented * Team player * Ability to work with minimal supervision * Strong communication skills * Understanding of Aseptic Behaviors / Techniques * Experience in biomanufacturing environments Work Environment: * Work is generally performed in a Good Manufacturing Practice (GMP) facility. A GMP facility is governed by regulatory agencies in which there are specific requirements for hygiene and acceptable clothing. The following items are restricted when accessing the GMP manufacturing area: * Makeup, painted nails * Hair products (spray, gel, wax) * Perfume and cologne * Jewelry (rings, watches, bracelets, fitness bands, necklaces, and facial/ear piercings, etc.) * Donning of gowns requires ability to physically don gowns while balancing in a cleanroom environment * Personal Protective Equipment is required to perform certain tasks (i.e., latex/nitrile gloves, respirators and or masks, goggles, plant dedicated scrubs/shoes, full body gown that covers all exposed skin) * Subject to extended periods of standing, to include crouching / kneeling (8 plus hours) while being donned in applicable PPE * Required to handle biohazardous and hazardous material via direction of Standard Operating Procedures Physical Requirements: * Medium work that includes moving, lifting, pushing and or pulling objects up to 50 pounds * Medium work that includes pushing and or pulling equipment with up to 50 pounds of force assisted by wheels * Must be willing and able to bend, stoop, squat, crawl, twist, climb ladders, and wear a respirator * Position requires a combination of standing in the manufacturing environment and walking around the facility * Open to work various shifts as needed * Required to work weekends and holidays 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 Requirements: Bachelor of Science (B.Sc.) with 0-3 years of applicable biopharma experience or Associate degree with 2+ years of applicable biopharma experience or High school diploma with 3+ years of applicable biopharma experience Preferred Qualifications: Ability to follow verbal and written instructions Problem solving skills Detail oriented Team player Ability to work with minimal supervision Strong communication skills Understanding of Aseptic Behaviors / Techniques Experience in biomanufacturing environments Work Environment: Work is generally performed in a Good Manufacturing Practice (GMP) facility. A GMP facility is governed by regulatory agencies in which there are specific requirements for hygiene and acceptable clothing. The following items are restricted when accessing the GMP manufacturing area: Makeup, painted nails Hair products (spray, gel, wax) Perfume and cologne Jewelry (rings, watches, bracelets, fitness bands, necklaces, and facial/ear piercings, etc.) Donning of gowns requires ability to physically don gowns while balancing in a cleanroom environment Personal Protective Equipment is required to perform certain tasks (i.e., latex/nitrile gloves, respirators and or masks, goggles, plant dedicated scrubs/shoes, full body gown that covers all exposed skin) Subject to extended periods of standing, to include crouching / kneeling (8 plus hours) while being donned in applicable PPE Required to handle biohazardous and hazardous material via direction of Standard Operating Procedures Physical Requirements: Medium work that includes moving, lifting, pushing and or pulling objects up to 50 pounds Medium work that includes pushing and or pulling equipment with up to 50 pounds of force assisted by wheels Must be willing and able to bend, stoop, squat, crawl, twist, climb ladders, and wear a respirator Position requires a combination of standing in the manufacturing environment and walking around the facility Open to work various shifts as needed Required to work weekends and holidays 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 (*******************).

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.

Join Amgen's Mission of Serving Patients At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. **Associate Manufacturing** **What you will do** Let's do this! Let's change the world! 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: + Performing drug product manual visual inspection 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) **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:** + Bachelor's degree OR Associate's degree and 6 months of GMP/GDP experience OR High school diploma / GED and 2 years of GMP/GDP experience **Preferred Qualifications:** + B.S. in a life science or related field + 2 years of work experience in a GMP environment + Ability to perform computer operations, such as ability to navigate in MS Office and Excel + Ability to operate specialized equipment and computers as appropriate to the individual area + Ability to adhere to regulatory requirements, written procedures and safety guidelines + Ability to evaluate documentation/data according to company and regulatory guidelines + Ability to interact with inspectors (internal and external) + Technical writing capabilities + Ability to organize work, handle multiple priorities and meet deadlines + Demonstrated written and oral communication skills + Presentation capabilities + Detail oriented as well as flexible and adaptable to changing priorities and requirements. **What you can expect of us** As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: + A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts + A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan + Stock-based long-term incentives + Award-winning time-off plans + Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies. 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.

Job Description Production Laborer I M-F 6am - 2:30pm $19.00/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: High school diploma or equivalent required. 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!

Operators are responsible for a variety of product assembly, inspection, testing, operation of equipment/tools and material/component processing tasks to meet production schedule requirements to the high-quality standard expected by Client. Essential Functions: Safely and efficiently meeting all production work requirements assigned to you by following operating procedures and work instructions. Trouble shoot problems quickly and efficiently, seeking advice where necessary. To produce the highest standard of quality products possible in accordance with the company's ISO 9001: 2015 procedures. Visually inspect products throughout the stages of production to identify defective parts, component orientation errors, missing components, or wrong part insertion. Initial testing for product conformity. Assist others to provide an organized and clean workplace including: all areas of the plant, workstations, equipment, walkways, and break rooms using 5S procedures. Participation in and implementation of continuous improvement projects. Other duties as assigned. Qualifications High school diploma or GED required. Experience working in a manufacturing or industrial setting preferred. Ability to read and comprehend written instructions, as well as, comprehend verbal instructions and effectively communicate verbally. Computer Familiarity. Ability to self-start yet take orders as directed. Ability to move and lift up to 25 pounds. Ability to sit or stand as required to perform essential functions. Consistent and punctual attendance required. Must be available to work assigned shifts and required overtime. Preferred Qualifications Brazing, soldering, mechnical calibration, and/or mechanical testing experience.

**Country:** United States of America ** Onsite **U.S. Citizen, U.S. Person, or Immigration Status Requirements:** U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract. **Security Clearance:** None/Not Required 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. **_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: U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract. Security Clearance: None/Not Required 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. Job Summary: A Production Worker S4 (Production Specialist) in the FPA area, operates equipment and performs processes to build hardware. Utilizes their advanced processing experience to trouble shoot and resolve issues with production support teams. Works closely with area leads to optimize area efficiency. Rigorously documents processes performed in electronic tracking systems. Executes tasks to ensure that equipment and processes being used are in control. May assist in outlining tasks and checking other's work for correctness. Routine work is performed without supervision. This is a 100% onsite position. 1st Shift - employee must start work after 5AM and before 12PM (PST), standard working hours are 6AM - 2:30PM and negotiable in Goleta, California. Responsibilities to Anticipate: Active participation in a Safety-First work environment. The ability to work in a class 100 cleanroom, in a full bunny suit, under yellow lights is required. Process Focal Plane Arrays (Hybridize, Wet Etch, Photomask, Fixturing, Hotplate processing, Surface treatment, Wire bond, Metrology, inspection etc.) to build hardware. Handle fragile hardware and manipulate small parts during processing. Rigorously follow written procedures and work instructions Document data on travelers and in the electronic database Utilize strong interpersonal communication skills with peers, leads, support teams and management. Cross train as necessary to improve area efficiency Execute specialized communications (pass downs) if operating during 2nd or 3rd shift hours. Basic Qualifications: High School Diploma or GED US Citizenship Minimum 4 years of production experience in cleanroom fabrication, assembly, manufacturing or equivalent. Has experience in MS Office (Excel) Preferred Qualifications: More than four years of production experience in cleanroom fabrication, assembly, manufacturing or equivalent. Experience in Hybridization, Thin Film Deposition, Photolithography, Wet Etch, or other cleanroom Focal Plane Array, fabrication work cells. Ability to work safely with chemicals and raw production materials. Ability to multitask. The flexibility to work occasional, voluntary overtime on weekends to meet the factory's needs is strongly desired. What We Offer: Whether you're just starting out on your career journey or are an experienced professional, we offer a total rewards package that goes above and beyond with compensation; healthcare, wellness, retirement and work/life benefits; career development and recognition programs. Some of the benefits we offer include parental (including paternal) leave, flexible work schedules, achievement awards, educational assistance and child/adult backup care. Additional Information: The salary range for this role is Goleta Ca, Zone 2 $25.65 - $48.11; however, Raytheon considers several factors when extending an offer, including but not limited to, the role 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

**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:** Performs a variety of functions associated with Dicing and Singulatulating Wafers, including preparing the product and tools, operating equipment, and inspecting and cleaning product after processing. **Primary Duties & Responsibilities:** + Process wafers on dicing saws + Perform routine operator maintence, and qualify tools after maintence + Familiarity with operation of metrology equipment requiring analysis of data + Maintain detailed records of tool tool usage and track usage of consumables + Ability to work in an ISO Class 6 cleanroom and familiar with 6S principles + Schedule and coordinate WIP for efficient movement of Production and Engineering priorities + Inspect and disposition nonconforming product **Job Qualifications:** + Experience operating ADT Saws + Attention to detail + Collaboration and teamwork + Initiative + Organizational and planning skills + SKILL: Applies acquired job skills and company policies and procedures to complete assigned tasks. + JOB COMPLEXITY: Works on assignments that are semi-routine in nature but recognizes the need for occasional deviation from accepted practice. + SUPERVISION: Normally follows established procedures on routine work; requires instructions only on new assignments. + EXPERIENCE: Typically requires a minimum of 1 - 2 years of related experience. + Must be able to communicate clearly and able to read and write using the English language. **_Applicants must be either a U.S. citizen, U.S. national, legal permanent resident, asylee, refugee or must be eligible to apply for and obtain the appropriate export control license from the U.S. Departments of State or Commerce._** **Salary Range:** $37,200.00-$49,600.000 **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. You may not realize it, but Teledyne enables many of the products and services you use every day **.** Teledyne provides enabling technologies to sense, transmit and analyze information for industrial growth markets, including aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, energy, medical imaging and pharmaceutical research.

We are seeking a reliable and detail-oriented Production Operator to join our plastic manufacturing team. In this full-time role, you will be responsible for operating machines, monitoring production lines, and ensuring that plastic parts and products are manufactured to quality standards. This is a hands-on position ideal for someone who thrives in a fast-paced, team-driven manufacturing environment. Machine Operation Set up and operate plastic molding, extrusion, or thermoforming machines based on production requirements. Monitor machines during operation to detect mechanical or processing issues. Adjust machine settings as needed to maintain product quality and consistency. Production Monitoring Inspect plastic products for defects, proper shape, color, and dimensions. Remove and dispose of defective items according to company procedures. Record production data including quantities produced, machine downtime, and materials used. Material Handling Load raw plastic materials (pellets, resins, additives) into machines. Safely transport materials and finished goods within the facility. Maintain clean and organized workspaces and production lines. Quality Control Use basic measuring tools (calipers, gauges, rulers) to check product specifications. Follow production checklists and quality guidelines to ensure compliance. Report quality issues to the supervisor or quality control team. Safety & Maintenance Follow all safety procedures, including proper use of PPE and machine lockout/tagout protocols. Perform routine cleaning and basic maintenance on equipment. Report any equipment malfunctions or hazards immediately. Team Collaboration Work cooperatively with other team members, supervisors, and maintenance personnel. Communicate issues or suggestions for improving productivity and safety.

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

Career CategoryManufacturingJob 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. Associate Manufacturing What you will do Let's do this! Let's change the world! In this dynamic role you will collaborate with multiple functions within the Thousand Oaks site on a routine basis in a dynamic environment (Quality Assurance, Quality Control, Engineering, Facilities, Maintenance, Process Development, Process Engineering, etc.) while developing a deep understanding of the manufacturing operations and planning activities within the facility. Responsibilities of the role include: Performing drug product manual visual inspection 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) 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: Bachelor's degree OR Associate's degree and 6 months of GMP/GDP experience OR High school diploma / GED and 2 years of GMP/GDP experience Preferred Qualifications: B.S. in a life science or related field 2 years of work experience in a GMP environment Ability to perform computer operations, such as ability to navigate in MS Office and Excel Ability to operate specialized equipment and computers as appropriate to the individual area Ability to adhere to regulatory requirements, written procedures and safety guidelines Ability to evaluate documentation/data according to company and regulatory guidelines Ability to interact with inspectors (internal and external) Technical writing capabilities Ability to organize work, handle multiple priorities and meet deadlines Demonstrated written and oral communication skills Presentation capabilities Detail oriented as well as flexible and adaptable to changing priorities and requirements. What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan Stock-based long-term incentives Award-winning time-off plans Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies. 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 73,359.00 USD - 85,625.00 USD

Country: United States of America Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract. Security Clearance: None/Not Required 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. Job Summary: A Production Worker S4 (Production Specialist) in the FPA area, operates equipment and performs processes to build hardware. Utilizes their advanced processing experience to trouble shoot and resolve issues with production support teams. Works closely with area leads to optimize area efficiency. Rigorously documents processes performed in electronic tracking systems. Executes tasks to ensure that equipment and processes being used are in control. May assist in outlining tasks and checking other's work for correctness. Routine work is performed without supervision. This is a 100% onsite position. **2nd Shift: 2PM - 10:30PM and negotiable in Goleta, California. This is an onsite position. Responsibilities to Anticipate: Active participation in a Safety-First work environment. The ability to work in a class 100 cleanroom, in a full bunny suit, under yellow lights is required. Process Focal Plane Arrays (Hybridize, Wet Etch, Photomask, Fixturing, Hotplate processing, Surface treatment, Wire bond, Metrology, inspection etc.) to build hardware. Handle fragile hardware and manipulate small parts during processing. Rigorously follow written procedures and work instructions Document data on travelers and in the electronic database Utilize strong interpersonal communication skills with peers, leads, support teams and management. Cross train as necessary to improve area efficiency Execute specialized communications (pass downs) if operating during 2nd or 3rd shift hours. Basic Qualifications: High School Diploma or GED US Citizenship Minimum 4 years of production experience in cleanroom fabrication, assembly, manufacturing or equivalent. Has experience in MS Office (Excel) Preferred Qualifications: More than four years of production experience in cleanroom fabrication, assembly, manufacturing or equivalent. Experience in Hybridization, Thin Film Deposition, Photolithography, Wet Etch, or other cleanroom Focal Plane Array, fabrication work cells. Ability to work safely with chemicals and raw production materials. Ability to multitask. The flexibility to work occasional, voluntary overtime on weekends to meet the factory's needs is strongly desired. What We Offer: Whether you're just starting out on your career journey or are an experienced professional, we offer a total rewards package that goes above and beyond with compensation; healthcare, wellness, retirement and work/life benefits; career development and recognition programs. Some of the benefits we offer include parental (including paternal) leave, flexible work schedules, achievement awards, educational assistance and child/adult backup care. Additional Information: The salary range for this role is Goleta Ca, Zone 2 $25.65 - $48.11; however, Raytheon considers several factors when extending an offer, including but not limited to, the role 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

Country: United States of America Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract. Security Clearance: None/Not Required 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. 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

**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:** **Cleanroom Manufacturing Technician: As a Cleanroom Manufacturing Technician, you will process silicon wafers through automated and manual processes in an ISO Class 6 cleanroom. These processes include, lithography, plasma etch, thin film deposition, bonding, wet cleans and metrology. Wafers will be processed according to SOP and POR following our MES.** **At Teledyne FLIR, we have a simple but ambitious mission: to develop market-leading thermal and sensing technologies which enhance everyday life. From saving energy, to saving lives Teledyne FLIR is making a real difference in our world. Our products are used in a wide array of situations to rescue people in danger, detect criminals, conserve energy, navigate safely, provide security around the globe, and protect our environment.** **Primary Duties & Responsibilities:** **Process wafers according to workflows in the MES** **Enter data in SPC and equivalent databases** **Maintain high-level of cleanliness in lab** **Measure and record features on the wafer** **Report discrepant material** **Miscellaneous support functions, as necessary** **Job Qualifications:** **Basic computer skills - Outlook, Excel, Word** **Ability to work using hands and have good manual dexterity with attention to detail** **Must be able to communicate clearly and be able to read and write using the English language** **Desired skills:** **Familiarity with wafer processing** **Familiarity with operation of metrology tools** **Familiarity with Lean and 6S methods** **Familiarity with Camstar or equivalent** **Safe Chemical handling procedures** **Familiarity with Cleanroom and ESD procedures** **Applicants must be either a U.S. citizen, U.S. national, legal permanent resident, asylee, refugee or must be eligible to apply for and obtain the appropriate export control license from the U.S. Departments of State or Commerce.** ** ** **Salary Range:** $37,200.00-$49,600.000 **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. You may not realize it, but Teledyne enables many of the products and services you use every day **.** Teledyne provides enabling technologies to sense, transmit and analyze information for industrial growth markets, including aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, energy, medical imaging and pharmaceutical research.

We are seeking a dedicated and detail-oriented Production Operator to join our Aerospace Paint Department. This full-time role involves preparing, mixing, applying, and finishing aerospace-grade coatings on various components in accordance with strict industry standards and specifications. The ideal candidate will have experience in industrial painting or coatings, strong attention to detail, and a commitment to quality and safety in a controlled manufacturing environment. Key Responsibilities Surface Preparation Clean, sand, and prepare surfaces to ensure proper adhesion of aerospace coatings. Mask and unmask components as required, following specifications and blueprints. Paint Mixing & Application Accurately mix paint systems per technical data sheets and work instructions. Apply primer, topcoat, and specialty coatings using spray guns or other application tools. Quality Control Inspect parts visually and with measuring tools to ensure coating thickness, color, and finish meet aerospace standards. Document process steps and inspection results according to internal procedures and customer requirements. Equipment Operation Operate spray booths, curing ovens, and other related paint application equipment Perform basic equipment maintenance and ensure cleanliness of the work area. Process Documentation Maintain accurate production records and batch documentation in compliance with industry regulations. Follow written work instructions, standard operating procedures (SOPs), and safety protocols. Safety Compliance Adhere strictly to safety guidelines, including handling hazardous materials and wearing proper PPE. Work in accordance with OSHA, environmental, and aerospace industry standards. Team Collaboration Work closely with quality inspectors, supervisors, and team members to ensure on-time delivery and high-quality output. Communicate any defects, issues, or process improvements proactively.

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

Join Amgen's Mission of Serving Patients At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Associate Manufacturing What you will do Let's do this! Let's change the world! 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: * Performing drug product manual visual inspection 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) 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: * Bachelor's degree OR Associate's degree and 6 months of GMP/GDP experience OR High school diploma / GED and 2 years of GMP/GDP experience Preferred Qualifications: * B.S. in a life science or related field * 2 years of work experience in a GMP environment * Ability to perform computer operations, such as ability to navigate in MS Office and Excel * Ability to operate specialized equipment and computers as appropriate to the individual area * Ability to adhere to regulatory requirements, written procedures and safety guidelines * Ability to evaluate documentation/data according to company and regulatory guidelines * Ability to interact with inspectors (internal and external) * Technical writing capabilities * Ability to organize work, handle multiple priorities and meet deadlines * Demonstrated written and oral communication skills * Presentation capabilities * Detail oriented as well as flexible and adaptable to changing priorities and requirements. What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: * A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts * A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan * Stock-based long-term incentives * Award-winning time-off plans * Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies. 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 73,359.00 USD - 85,625.00 USD