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With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing. Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely. We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services. We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient. The Manufacturing Associate I will primarily be responsible for performing all aspects of biologics production in a single use facility, including cell vial thaw and inoculum train expansion inside a Bio-Safety Cabinet, operation of wave and stirred-tank bioreactors up to 2000 L, clarification and sterile filtration, and master cell bank fills. In addition, this role will include operation of chromatography skids in conjunction with multi-use and single-use columns, processing intermediates by depth filtration, ultrafiltration and diafiltration, and performing bulk drug substance fills. Responsibilities Operate under cGMP manufacturing conditions Ensure compliance to training on all activities prior to GMP execution. Adhere to appropriate gowning procedures required for working in Class 10,000 and Class 100,000 cleanrooms Perform operations in a bio-safety cabinet using aseptic technique and maintain asepsis of all closed container sterile processes Setup, operate and maintain bioprocessing equipment including single-use bioreactors up to 2000 L, large scale filtration skids, and automated filling machines and analytical instruments for cell culture such as Nova Bioprofile and Vi-Cell systems Perform production activities including thawing of cell stocks, inoculum train expansions, cell culture maintenance in bioreactors, depth and sterile filtration, and master cell bank and bulk drug substance fills Setup, operate and maintain bioprocessing equipment including AKTA ready column chromatography skids, FlexAct automation skids, large scale filtration skids, and analytical instruments such as SoloVPE Perform production activities including depth filtration, purification by affinity, ion exchange, and hydrophobic interaction chromatography, viral inactivation and filtration, tangential flow filtration, sterile filtration, and bulk drug substance fills Troubleshoot process related issues as they arise Inventory manufacturing lab supplies and ensure items are properly stocked. Participate in batch readiness activities such as general planning and coordination, material requests and transfer, and material and equipment staging Maintain cleanroom standards for cleanliness and order Conduct activities in support of production schedules as directed by senior staff Work effectively and efficiently in a team environment Communicate effectively with clients, supervisors, colleagues, and staff, and provide status of floor operation to leads on a regular basis Support multiple projects simultaneously Cross-train on various tasks including formulation of media and buffers, and operations to support overall success of the Biologics group. Review GMP records for completeness, accuracy, and compliance on a daily basis in conformance with regulatory requirements Review manufacturing SOPs, master batch records, specifications, and other applicable cGMP documentation Adhere to quality standards set by regulations and Abzena policies, procedures, and mission Operate to the highest ethical and moral standards Perform additional duties as assigned Qualifications 1 – 2 years cell culture experience in a GMP pharmaceutical/biotech environment role with a technical degree or equivalent combined years of both Demonstrate knowledge and understanding of cGMPs and how they apply to responsibilities. A proven ability to confidently compute basic arithmetic operations. FLSA: Non-Exempt Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
ABOUT THE BRAND: Callaway Golf Company is a premium golf equipment, gear and apparel company with a portfolio of global brands, including Callaway Golf, Odyssey, TravisMathew, and OGIO. Through an unwavering commitment to innovation and premium craftsmanship, Callaway designs, manufactures, and sells high-performance golf clubs, golf balls, apparel, bags, and other accessories—setting the standard for performance in the game of golf. Our Mission: To create demonstrably superior and pleasingly different products powered by innovative technology and premium craftsmanship enabling golfers of all abilities to play their best and find more joy in the game. Our company is a blend of experience and diverse backgrounds, and together we look to leave the past behind while moving the game forward. For more information, please visit https://www.callawaygolf.com JOB OVERVIEW Under direct supervision, the Source Inspector is responsible for assisting daily product and process audits (using approved procedures, standards, and specifications), product disposition and/or measuring supplier compliance. ROLES AND RESPONSIBILITIES Assists in conducting, reviewing and reporting on audits. Assist in identifying, organizing, and summarizing evidence to support conclusions about compliance to standards (such as PCPs) to SI Lead and Supervisor. Assist in identifying, documenting, recommending, disposition of non-conforming products. Assist with the maintenance of product quality standards documentation and physical samples. Assist with the data collection, reporting and analysis of defects. Assist to maintain the equipment, tools and facilities, keeping sufficient material and supplies. Support SI Leads, Supervisor, and engineering on data collecting, data entry, and data analysis. Process SI daily inspection data into SAP system. TECHNICAL COMPETENCIES (Knowledge, Skills & Abilities) Understanding of production processes (assembly, inspection, packaging, material handling). Knowledge of quality standards and requirements contained in them. Knowledge of general audit terminology. Understanding of variation and common and special causes. Able to understand new product specifications and shop floor work instructions. Basic level skill in any e-mail application, MS Word and Excel, and basic level skill in power point. Basic level skill in raw data collecting and various quality tools (histograms, cause-and-effect diagrams, pareto charts, and run charts) Understand and apply basic conflict management techniques, effective listening skills, and assertive communication methods. Strong initiative to complete assignments. EDUCATION AND EXPERIENCE At least 3 years of High School / Technical School Diploma required Minimum 1 year experience as a process and product auditor/inspector in a manufacturing setting, preferably golf club assembly. DE&I and EEOC: Inclusion & Diversity: As a purpose-led, performance driven company, we strive to foster a culture of belonging based on respect, connection, openness and authenticity. We are committed to building and maintaining a workplace that celebrates the diversity of our associates, supporting them to bring their authentic selves to work every day. If your experience is close to what we’re looking for, please consider applying. Experience comes in many forms, skills are transferable, and passion goes a long way. We know that diverse backgrounds and experiences make for the best problem-solving and creative thinking, which is why we’re dedicated to adding new perspectives to the team and encourage everyone to apply. We look forward to learning more about you. ARE YOU READY TO MAKE THE TURN? APPLY TODAY! 0.00 - 0.00 - 0.00 USD Hourly
Position Summary: The Project Engineer coordinates and ensures the completion of projects and ensures work is in line with customer and regulatory requirements. This is a 100% onsite position at our Vista, CA facility. Relocation assistance and visa sponsorship is not offered. Essential Duties and Responsibilities: Review and monitor program progress and expedite critical path and processes to maintain schedule Assure product and process quality by designing inspection methods, establishing standards and confirming manufacturing processes. Provide support for QA, Supply Chain and suppliers about drawing interpretation, manufacturing methods, inspection methods, etc. Evaluate non-conforming materials, including analyzing the non-conformance for fit, function, safety, and reliability, and communicating with QA, Supply Chain and suppliers, as required. Completing Engineering Changes with supporting substantiation and drawing changes as required for product improvement. Provide support for customers and operators regarding our products. Participate in design reviews for supplier changes, product changes and/or improvements for production parts. Perform reviews of first article inspections and documentation for dormancy and supplier changes of production parts. Review and provide feedback to suppliers on the manufacturing process plans for production parts. Develop test plans for production parts. Design tooling and/or fixtures to aide in the inspection of production parts. Required participation in internal training as needed to perform the duties assigned to this role. Other related duties may be assigned. Estimated Salary Range: $90-135k Requirements: Minimum Qualifications (Knowledge, Skills and Abilities) Required composite fabrication experience. (Layup, Curing, Assembly) U.S. Person status required do to export control Bachelor's Degree in engineering or related field, or combination of education and work experience 10 years aerospace, mechanical design, and or manufacturing experience is required. Strong attention to detail Capable of standing and or sitting for extended periods of time Ability to communicate effectively with coworkers and the management team. Must be well organized, flexible, and able to work in a fast-paced manufacturing environment Must thrive in a team-oriented and deadline-driven environment Ability to verbally communicate, read and comprehend written and verbal instructions in English Familiarity and skill with interpreting technical drawings and blueprints Experience using 3D CAD software (Pro-Engineer, SolidWorks, etc.). Knowledge of Geometric Dimensioning & Tolerance and Standard Measurement & Test Equipment for Aerospace products is preferred. Knowledge of conventional aerospace manufacturing methods is preferred. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. Strong organizational skills, ability to multitask and prioritize as necessary, with minimal supervisory direction. Must possess a high level of commitment to quality and customer satisfaction. Highly skilled in MS Office programs- Excel, Word, Outlook, Power Point and Adobe Acrobat Physical Demands and Work Environment The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodations may be made. While performing the duties of this job, the employee is regularly required to stand; walk; reach with hands and arms; climb or balance and stoop, kneel, crouch, or crawl. Constant specific vision abilities required include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus. The employee may occasionally lift and /or move up to 25 pounds. The employee sits for extended periods of time at a computer station or work desk and is exposed to typical office environment conditions and noise levels. Required to wear Personal Protective Equipment (PPE) when working on the manufacturing floor where the employee may be exposed to moving mechanical parts and is occasionally exposed to high, precarious places; fumes or airborne particles; outside weather conditions; extreme heat and risk of electrical shock. The noise level in the manufacturing floor is usually loud. Pay Transparency In order to support the Fair Compensation Strategy by the US Govt., HR Dept., clients are required to adhere to "Pay Transparency Law"; in the impacted states; that have mandated the employers to list the salary ranges in Job advertisements or postings for job opportunities and Job promotions.
San Diego, CAManufacturing – Manufacturing /Full Time /On-Site With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing. Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely. We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services. We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient. The Manufacturing Associate I will primarily be responsible for performing all aspects of biologics production in a single use facility, including cell vial thaw and inoculum train expansion inside a Bio-Safety Cabinet, operation of wave and stirred-tank bioreactors up to 2000 L, clarification and sterile filtration, and master cell bank fills. In addition, this role will include operation of chromatography skids in conjunction with multi-use and single-use columns, processing intermediates by depth filtration, ultrafiltration and diafiltration, and performing bulk drug substance fills. Responsibilities Operate under cGMP manufacturing conditions Ensure compliance to training on all activities prior to GMP execution. Adhere to appropriate gowning procedures required for working in Class 10,000 and Class 100,000 cleanrooms Perform operations in a bio-safety cabinet using aseptic technique and maintain asepsis of all closed container sterile processes Setup, operate and maintain bioprocessing equipment including single-use bioreactors up to 2000 L, large scale filtration skids, and automated filling machines and analytical instruments for cell culture such as Nova Bioprofile and Vi-Cell systems Perform production activities including thawing of cell stocks, inoculum train expansions, cell culture maintenance in bioreactors, depth and sterile filtration, and master cell bank and bulk drug substance fills Setup, operate and maintain bioprocessing equipment including AKTA ready column chromatography skids, FlexAct automation skids, large scale filtration skids, and analytical instruments such as SoloVPE Perform production activities including depth filtration, purification by affinity, ion exchange, and hydrophobic interaction chromatography, viral inactivation and filtration, tangential flow filtration, sterile filtration, and bulk drug substance fills Troubleshoot process related issues as they arise Inventory manufacturing lab supplies and ensure items are properly stocked. Participate in batch readiness activities such as general planning and coordination, material requests and transfer, and material and equipment staging Maintain cleanroom standards for cleanliness and order Conduct activities in support of production schedules as directed by senior staff Work effectively and efficiently in a team environment Communicate effectively with clients, supervisors, colleagues, and staff, and provide status of floor operation to leads on a regular basis Support multiple projects simultaneously Cross-train on various tasks including formulation of media and buffers, and operations to support overall success of the Biologics group. Review GMP records for completeness, accuracy, and compliance on a daily basis in conformance with regulatory requirements Review manufacturing SOPs, master batch records, specifications, and other applicable cGMP documentation Adhere to quality standards set by regulations and Abzena policies, procedures, and mission Operate to the highest ethical and moral standards Perform additional duties as assigned Qualifications 1 – 2 years cell culture experience in a GMP pharmaceutical/biotech environment role with a technical degree or equivalent combined years of both Demonstrate knowledge and understanding of cGMPs and how they apply to responsibilities. A proven ability to confidently compute basic arithmetic operations. $45,000 - $60,000 a year FLSA: Non-Exempt Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
San Diego, CAManufacturing – Manufacturing /Full Time /On-Site With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing. Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely. We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services. We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient. As a member of the manufacturing team at Abzena, you will be responsible for executing daily task in strict compliance with manufacturing batch records, SOP’s, and Good Manufacturing Practices (GMP). You will take ownership of the production process, facility, and environment to ensure smooth operations. Additionally, you will collaborate cross-functionally with key departments, including QA, MS&T, Facilities, and others to support successful and compliant manufacturing activities and responsibilities. Responsibilities Operate under cGMP manufacturing conditions. Ensure compliance to training on all activities prior to GMP execution. Adhere to appropriate gowning procedures required for working in Class 10,000 and Class 100,000 cleanrooms. Perform operations in a bio-safety cabinet using aseptic technique and maintain asepsis of all closed container sterile processes. Ensures right-the-first-time performance of all process steps. Perform production activities including depth filtration, purification by affinity, ion exchange, and hydrophobic interaction chromatography, viral inactivation and filtration, tangential flow filtration, sterile filtration, and bulk drug substance fills. Escalate process related issues as they arise Inventory manufacturing lab supplies and ensure items are properly stocked. Participate in batch readiness activities such as general planning and coordination, material requests and transfer, and material and equipment staging. Maintain cleanroom standards for cleanliness and order Conduct activities in support of production schedules as directed by senior staff. Work effectively and efficiently in a team environment. Communicate effectively with clients, supervisors, colleagues, and staff. and provide status of floor operation to leads on a regular basis. Support multiple projects simultaneously. Crosstrain on various tasks including autoclaving of assemblies, formulation of buffers, and Downstream operations to support overall success of the Biologics group. Perform manufacturing and process development activities for projects and products in collaboration with others. Review GMP records for completeness, accuracy, and compliance on a daily basis in conformance with regulatory requirements. Review manufacturing SOPs, master batch records, specifications, and other applicable cGMP documentation. Adhere to quality standards set by regulations and Abzena policies, procedures, and mission. Operate to the highest ethical and moral standards. Adjust to a flexible work schedule including weekend work, as needed. Perform additional duties as assigned. Qualifications A minimum of 2 years of experience in a GMP pharmaceutical/biotech environment role with a technical degree or equivalent combined years of both. Demonstrate knowledge and understanding of cGMPs and how they apply to responsibilities. Experience with aseptic handling, including BSC operations to maintain the integrity of sterile systems. Knowledge of purification using column chromatography Experience using single-use technologies, such as tube welding, tube sealing, and disposable systems A proven ability to confidently compute basic arithmetic operations. $60,000 - $80,000 a year FLSA: Non-Exempt Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
Manufacturing Technician I (1st Shift) Position Summary: Work Schedule: Monday-Friday from 7:30am-4pm 100% on-site (San Diego) Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO), and Catalent’s San Diego facility focuses on early-stage development of small molecule and peptide drug candidates from the bench to the clinic. This facility offers an array of services that support oral and injectable dosage forms that include preformulation testing, formulation and analytical development, cGMP manufacturing and clinical packaging, labeling, and worldwide distribution. Our San Diego location is the home of our Catalent Spray Drying technologies with downstream roller compaction capabilities to support the needs of our client’s most challenging compounds. The Manufacturing Technician I will be responsible for conducting Good Manufacturing Practices (cGMP) manufacturing of solid oral and liquid oral pharmaceutical dosage forms for Phase I and Phase II clinical trials. Daily responsibilities will include production equipment set up, weighing of materials, sieve and blending activities, spray drying, milling, granulation, mixing, roller compaction, submitting samples, encapsulation, tableting, coating and packaging. You will be a key member of a multi-site mission to deliver unparalleled service to our clients and quality drug products to the patients. The Role: Prepare materials, equipment and manufacturing suites for production Conduct GMP manufacturing of solid oral and liquid oral dosage forms Packaging and labeling of manufactured products Pre/postproduction cleaning of equipment, supplies and manufacturing area Follow Standard Operating Procedures (SOPs) and production batch records Responsible for accurate documentation in production batch records May also assist engineering with equipment validations, preventative maintenance, and cleaning verifications Other duties as assigned The Candidate: High School Diploma or GED equivalent is required No prior experience required. Some GMP experience in pharmaceutical or medical device manufacturing a plus. Physical Requirements: On an average 8-hour day this position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch, or crawl; talk and hear, smell and lift up to 40 pounds. Specific vision requirements including reading of written documents, visual inspection of materials and use of computer monitor screen frequently Pay: The anticipated salary range for this role in California is $40,000 to $46,000 annually. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states. Why you should join Catalent: Awesome employee activities: Movie Day, Monthly Birthday Celebrations, Friday Bagel Breakfast, On-site Fitness Center with machines, Sponsored Sports Teams, and several other company-sponsored events that encourages positive employee comradery, which contributes to effectively building positive employee relationships, overall creating a positive work environment. Environmentally friendly green initiatives with on-site practices as well as regularly participating in Beach Clean-up activities for community engagement. Defined career path and annual performance review and feedback process. Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives. Several Employee Resource Groups focusing on Diversity and Inclusion. Competitive salary with bonus potential. Generous 401K match and Paid Time Off accrual. Medical, dental and vision benefits effective day one of employment. 152 hours of PTO + 10 paid holidays. Positive and fast-paced working environment focusing on continually improving processes to remain innovative and dynamic. Tuition Reimbursement – Let us help you finish your degree or earn a new one! WellHub program to promote overall physical wellness. Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories. Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.
Position Summary The QA Floor Supervisor assures that the plant is compliant with food regulatory requirements and reports deficiencies or practices that could compromise food safety, quality, and food defense. Schedule: 9:00 AM – 5:30 AM, Sunday - Thursday Must be flexible for mandatory overtime as needed. Essential Duties and Responsibilities Must be able to perform all duties and responsibilities of: QA Tech 1 & 2 QA Lead Be able to cover all shifts. Cover QA Tech duties as necessary during call outs Perform special assignments as needed by the Quality Assurance Manager. Oversee the verification of CPPs, allergen controls, labeling accuracy and quality parameters, by ensuring product meets in process specifications. Assures that the plant is compliant with GMP, SQF and HACCP plans and reports deficiencies or practices that could compromise food safety, quality and food defense. Ensure floor coverage in all areas during breaks and lunches. Assign times for employee breaks and lunches to ensure proper coverage Investigate findings of non-conformities and report to QA Shift Manager Train new employees on QC roles and responsibilities Perform employee training verifications, proficiencies and evaluations Review Hold Log and complete dispositions. Place holds for necessary non-conformances. Food safety Culture observation audit and KPI reporting. Review QA paperwork at end of shift before submission for any necessary deficiencies. Participate in meetings as needed. Ability to understand and follow verbal and written instructions related to safety, equipment operation, and daily work assignments. Regular and reliable attendance. Responsibilities will require an adjusted work schedule, overtime, holidays, evening/weekend hours in order to meet deadlines. Qualifications & Requirements Education High School Diploma or equivalent (required) HACCP Certification (required; can be obtained after hire) Experience 1–2 years in Quality Assurance (preferred) 1–2 years in the food industry (preferred) Knowledge & Skills Knowledge of food safety regulations (preferred) Strong leadership and communication skills Proficient in computer use and basic software programs Excellent critical thinking and problem-solving abilities Flexible and adaptable to change; able to work independently with moderate supervision Skilled in delegating tasks and organizing floor duties Work Environment Warehouse and wet/cold storage environment with temperature at 35°F May work in confined spaces with noise levels exceeding 85 dBa Continuous use of required PPE, including safety glasses, ear protection, and steel-toed shoes Repetitive tasks and occasional interaction with loud machinery Physical Requirements Ability to stand for long periods, bend, climb stairs or ladders, and work in narrow areas Occasional lifting of up to 20 lbs. Ability to work at heights Periods of computer work and screen time Additional Requirements Report any food safety problems to the SQF Practitioner or Department Supervisor in a timely manner so that corrective actions may be performed. Compensation and Benefits Come thrive at Suja Life! We offer a competitive benefits package, including: Pay rates range from $26.00-$29.00 per hour Medical, dental, vision, life insurance, and more Paid Parental Leave – 12 Weeks at 100% Pay 401(k) match to help you plan for the future Paid time off: vacation, sick days & holidays Juice benefits: yes, we keep you fueled and refreshed! #INDHP #ZR Suja Life is proud to be an equal opportunity employer seeking to create a welcoming and diverse environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, ancestry, physical or mental disability, medical condition, marital status, genetics, age, or veteran status or any other applicable legally protected status or characteristic. The Company complies with all federal/local/state regulations regarding pay.
Introduction to the Job As a Production Engineer at ASML in San Diego, you help power the world’s chips. Your work improves the reliability and throughput of our extreme ultraviolet (EUV) light source manufacturing. You remove roadblocks, raise yield, and protect cycle time. As a Production Engineer, your impact shows up in stable tools, shorter lead times, and satisfied customers. Roles and Responsibilities You will solve production issues, qualify process changes, and drive continuous improvement. You will work with manufacturing, design engineering, and quality to build robust, scalable processes. This Production Engineer role is on-site in San Diego and supports a compressed 12‑hour shift schedule. Triage production issues to restore tool uptime quickly and safely. Develop and improve assembly and test processes for repeatable results. Design and run qualification tests for process and equipment changes. Analyze in-line and customer quality data using statistical methods. Lead root cause analysis and implement corrective and preventive actions. Prepare and present factory metrics on yield, cycle time, and capacity. Collaborate on design for manufacturability and new product introduction. Education and Experience You have a bachelor’s degree in mechanical engineering, electrical engineering, or computer engineering. Minimum of 1 year in a cleanroom or high-tech manufacturing environment. Strong hands-on skills with electromechanical systems and test equipment. Experience with Excel; familiarity with JMP, Minitab, or LabVIEW is a plus. Exposure to Python or basic scripting for data analysis is helpful. Knowledge of design of experiments (DOE) and lean manufacturing principles. Ability to read bills of material and follow controlled work instructions. Clear written and spoken communication across teams and shifts. Skills Working at the cutting edge of tech, you’ll always have new challenges and new problems to solve – and working together is the only way to do that. You won’t work in a silo. Instead, you’ll be part of a creative, dynamic work environment where you’ll collaborate with supportive colleagues. There is always space for creative and unique points of view. You’ll have the flexibility and trust to choose how best to tackle tasks and solve problems. To thrive in this job, you’ll need the following skills: Communicate clearly, listen actively, and build trust with teammates. Analyze data, spot trends, and make evidence-based decisions. Prioritize well in a fast-changing environment and meet commitments. Document processes with clarity and update work instructions promptly. Apply structured problem solving and statistical thinking. Collaborate across manufacturing, engineering, and quality functions. Take initiative, follow through, and ask for help when needed. Work safely in a cleanroom with full gowning and PPE. Support 12‑hour compressed shifts and on-site collaboration. Use basic automation or scripting to streamline reporting. Other Information The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee routinely is required to sit; walk; talk; hear; use hands to keyboard, finger, handle, and feel; stoop, kneel, crouch, twist, reach, and stretch. The employee is required to work in a cleanroom environment: full gowning (full body coveralls, hood, CR safety shoes, face mask, nitrile gloves and safety glasses. Working under ISO 9000/14000 standards). Operating/working around overhead cranes, fork trucks and motorized pallet movers. Working around lasers; working with ladders; working on platforms; and working around chemicals. The employee is occasionally required to move around the campus. The employee may occasionally lift and/or move up to 20 pounds. May require travel dependent on company needs. Specific vision abilities required by this job include close vision, color vision, peripheral vision, depth perception, and ability to adjust focus. Other work as needed This position operates on a compressed work week, working a 3-4-3 structure with 12 hour shifts. Available shifts are as follows 7am-7pm Sunday-Tuesday and every other Wednesday 7am-7pm Thursday-Saturday and every other Wednesday 7pm-7am Wednesday-Friday and every other Saturday 7pm-7am Sunday-Tuesday and every other Saturday Role within the Factory Responsibilities Must be willing to work in a clean room environment, wearing coveralls, hoods, booties, safety glasses and gloves for entire duration of shift. While performing the duties of this job, the employee routinely is required to sit; walk; talk; hear; use hands to keyboard, finger, handle, and feel; stoop, kneel, crouch, twist, reach, and stretch. The employee may occasionally lift and/or move up to 20 pounds. Can we be more specific: Must be willing to lift up to 20 pounds, pull 20 pounds at least once a day and spend the majority of time (greater than 90% less break time) on the floor working on tool sets, walking three to five miles a day, and/or standing/sitting for nine hours. Specific vision abilities required by this job include close vision, color vision, peripheral vision, depth perception, and ability to adjust focus. The current base annual salary range for this role is currently: $81,375-122,063 Pay scales are determined by role, level, location and alignment with market data. Individual pay is determined through interviews and an assessment of several factors that that are unique to each candidate, including but not limited to job-related skills, relevant education and experience, certifications, abilities of the candidate and pay relative to other team members. The Company offers employees and their families, medical, dental, vision, and basic life insurance. Employees are able to participate in the Company’s 401k plan. Employees will also receive eight (8) hours of vacation leave every month and (13) paid holidays throughout the calendar year. For more information, please contact the Recruiter or click on this link Compensation & Benefits in the US . All new ASML jobs have a minimum application deadline of 10 days. This position requires access to controlled technology, as defined in the United States Export Administration Regulations (15 C.F.R. § 730, et seq.). Qualified candidates must be legally authorized to access such controlled technology prior to beginning work. Business demands may require ASML to proceed with candidates who are immediately eligible to access controlled technology. Inclusion and diversity ASML is an Equal Opportunity Employer that values and respects the importance of a diverse and inclusive workforce. It is the policy of the company to recruit, hire, train and promote persons in all job titles without regard to race, color, religion, sex, age, national origin, veteran status, disability, sexual orientation, or gender identity. We recognize that inclusion and diversity is a driving force in the success of our company. Need to know more about applying for a job at ASML? Read our frequently asked questions . Request an Accommodation ASML provides reasonable accommodations to applicants for ASML employment and ASML employees with disabilities. An accommodation is a change in work rules, facilities, or conditions which enable an individual with a disability to apply for a job, perform the essential functions of a job, and/or enjoy equal access to the benefits and privileges of employment. If you are in need of an accommodation to complete an application, participate in an interview, or otherwise participate in the employee pre-selection process, please send an email to USHR_Accommodation@asml.com to initiate the company’s reasonable accommodation process. Please note: This email address is solely intended to provide a method for applicants to initiate ASML’s process to request accommodation(s). Any recruitment questions should be directed to the designated Talent Acquisition member for the position.
*Overview* We are seeking a reliable, detail-oriented, highly organized Manufacturing Assistant to aid the Plant Superintendent to oversee our daily production operations and inventory movement within a fast-paced manufacturing facility. The ideal candidate will be responsible for ensuring that production goals are met while maintaining high standards of quality and safety. This role requires strong inventory FIFO control, daily cycle counts, manufacturing knowledge, and the ability to be self motivated. This role requires a strong command presence in a fast-paced manufacturing environment with focus on daily cycle counts, inventory accuracy, FIFO control, and resolving discrepancies. *Duties* * Supervise and coordinate daily manufacturing activities on the assembly line to ensure efficient workflow. * Experience with Inventory Control * Experience working in a factory or warehouse environment, particularly within an assembly line setting. * Ability to operate forklifts safely and efficiently (certification preferred). * Excellent leadership skills with the capability to motivate a diverse team. * Strong problem-solving skills with attention to detail in all aspects of production management. * Monitor production processes, troubleshoot issues, and implement solutions to optimize operations. * Ensure compliance with safety regulations and maintain a clean and organized work environment. * Collaborate with other departments to streamline processes and improve overall efficiency. * Maintain and record inventory levels of materials and supplies necessary for production. * Assist in developing and implementing standard operating procedures for various duties/responsibilities within the department. * Focus on maintaining accurate accounting and transfer of inventory between two local facilities. *Skills* Computer skills a must * Windows * Excel * Outlook * Strong experience with ERP systems * Strong organizational skills * Working knowledge of production, planning, shipping, and inventory functions * Supervisory experience * Forklift operator (desirable) * Driver license with clean driving record * Fluent English/Spanish Job Type: Full-time Pay: $20.00 - $24.00 per hour Benefits: * Dental insurance * Health insurance * Paid time off * Vision insurance Work Location: In person
*Overview* Join our dynamic manufacturing team as a Machine Operator and become a vital part of producing high-quality products with precision and efficiency. In this energetic role, you will operate a variety of manufacturing equipment, including Brown and Sharpe Screw machines, lathes, drill presses and fabrication tools, ensuring smooth production flow and adherence to safety standards. We are looking for motivated individuals who thrive in a fast-paced environment and are eager to develop their technical skills in machining and fabrication. Adjust inventory daily and perform cycle counts. *Responsibilities* * Set up, operate, and monitor various screw machines, lathes, drill presses to produce components according to specifications. * Read and interpret technical drawings, and CAD models to ensure accurate fabrication and assembly. * Operate and troubleshoot screw machine equipment to optimize machine performance. * Oversee four (4) work centers * Perform routine inspections using calipers to verify dimensions and tolerances. * Adjust machine settings based on production needs and quality standards to maintain efficiency and precision. * Conduct preventive maintenance on machinery and troubleshoot mechanical issues promptly to minimize downtime. * Handle materials safely using forklifts and other materials handling equipment within the manufacturing facility. * Maintain detailed documentation of production runs, machine logs, quality checks, and incident reports. * Ensure compliance with safety protocols and manufacturing standards at all times. *Requirements* * Proven factory or manufacturing experience operating machinery such as screw machines, lathes, drill press, or cold saws. * Strong mechanical knowledge with the ability to read technical drawings * Must be able to lift 30 pounds * Need a valid CA Driver License and clean driving record. * Ability to operate forklifts safely; forklift certification is preferred. * Skilled in using precision measuring instruments like calipers. * Knowledge of fabrication processes including welding, tooling setup, assembly line operations, and materials handling. * Basic math skills necessary for measurements, calculations, and troubleshooting during production processes. * Excellent attention to detail with a focus on safety standards in a manufacturing environment. * Ability to work effectively with hand tools, power tools, and basic shop equipment in a fast-paced factory setting. * Strong communication skills for documenting procedures and collaborating with team members. * Computer skills (Microsoft Suite, ERP) highly desired. * English/Spanish a plus! Job Type: Full-time Pay: $20.00 - $24.00 per hour Benefits: * Dental insurance * Health insurance * On-the-job training * Paid time off * Prescription drug insurance * Vision insurance People with a criminal record are encouraged to apply Work Location: In person
The application window is expected to close on: 05/01/2026Job posting may be removed earlier if the position is filled or if a sufficient number of applications are received. Meet the Team As Hardware Test& Packaging Engineer, you will help develop and support Cisco’s next generation component and packaging platform for Cisco's Silicon Photonics Integrated Circuits and chipsets. As a member of the platform team (engineering), you’ll be responsible for improving and supporting high-volume, automated optical assembly and test processes. Your Impact Design, Develop and Support • Work as part of platform team that develops tools and components for high-volume manufacturing to support, debug and improve tools and processes • Analyze data from Cisco’s automated packaging tools/processes to shape new projects targeting improvements in Cisco-designed high-volume manufacturing platforms • Recommend and implement test/assembly/process improvements, including cycle time reduction, and identify improvements required to maximize systems throughput and quality. • Design, build, and test prototypes of complex electromechanical assemblies to be used in automated manufacturing tools. Diagnostics Development& Lifecycle Management • Follow new tools, processes and components from development to production to ensure successful integration of new platform technologies. • Devise and perform complex tests needed during FA as part of development and continuous improvement. • Apply data analytics leveraging AI/ML for proactive problem detection and resolution • Ensure high standards of reliability, quality, and efficiency in all diagnostic work. Collaboration& Team Development • Partner with hardware, software, manufacturing, and product engineering teams to ensure alignment and successful program delivery. • Develop and execute project plans with predictability, quality and velocity. • Collaborate and travel to assure successful product deployment across a global environment Minimum Qualifications • Bachelors + 8 years of related experience, or Masters + 6 years of related experience, or PhD + 3 year of related experience. • Experience with photonic test or photonic assembly in a manufacturing environment • Ability to travel internationally to support projects/internal customers in theater Preferred Qualifications • Experience in hardware/software automation of photonics assembly/test. • Data analysis (SQL/JMP) in a semiconductor production environment • Knowledge of photonics, fiber optics and semiconductor lasers Why Cisco? At Cisco, we’re revolutionizing how data and infrastructure connect and protect organizations in the AI era – and beyond. We’ve been innovating fearlessly for 40 years to create solutions that power how humans and technology work together across the physical and digital worlds. These solutions provide customers with unparalleled security, visibility, and insights across the entire digital footprint. Fueled by the depth and breadth of our technology, we experiment and create meaningful solutions. Add to that our worldwide network of doers and experts, and you’ll see that the opportunities to grow and build are limitless. We work as a team, collaborating with empathy to make really big things happen on a global scale. Because our solutions are everywhere, our impact is everywhere. We are Cisco, and our power starts with you. Message to applicants applying to work in the U.S. and/or Canada: The starting salary range posted for this position is $134,300.00 to $195,400.00 and reflects the projected salary range for new hires in this position in U.S. and/or Canada locations, not including incentive compensation*, equity, or benefits. Individual pay is determined by the candidate's hiring location, market conditions, job-related skillset, experience, qualifications, education, certifications, and/or training. The full salary range for certain locations is listed below. For locations not listed below, the recruiter can share more details about compensation for the role in your location during the hiring process. U.S. employees are offered benefits, subject to Cisco’s plan eligibility rules, which include medical, dental and vision insurance, a 401(k) plan with a Cisco matching contribution, paid parental leave, short and long-term disability coverage, and basic life insurance. Please see the Cisco careers site to discover more benefits and perks. Employees may be eligible to receive grants of Cisco restricted stock units, which vest following continued employment with Cisco for defined periods of time. U.S. employees are eligible for paid time away as described below, subject to Cisco’s policies: • 10 paid holidays per full calendar year, plus 1 floating holiday for non-exempt employees • 1 paid day off for employee’s birthday, paid year-end holiday shutdown, and 4 paid days off for personal wellness determined by Cisco • Non-exempt employees** receive 16 days of paid vacation time per full calendar year, accrued at rate of 4.92 hours per pay period for full-time employees • Exempt employees participate in Cisco’s flexible vacation time off program, which has no defined limit on how much vacation time eligible employees may use (subject to availability and some business limitations) • 80 hours of sick time off provided on hire date and each January 1st thereafter, and up to 80 hours of unused sick time carried forward from one calendar year to the next • Additional paid time away may be requested to deal with critical or emergency issues for family members • Optional 10 paid days per full calendar year to volunteer For non-sales roles, employees are also eligible to earn annual bonuses subject to Cisco’s policies. Employees on sales plans earn performance-based incentive pay on top of their base salary, which is split between quota and non-quota components, subject to the applicable Cisco plan. For quota-based incentive pay, Cisco typically pays as follows: • .75% of incentive target for each 1% of revenue attainment up to 50% of quota; • 1.5% of incentive target for each 1% of attainment between 50% and 75%; • 1% of incentive target for each 1% of attainment between 75% and 100%; and • Once performance exceeds 100% attainment, incentive rates are at or above 1% for each 1% of attainment with no cap on incentive compensation. For non-quota-based sales performance elements such as strategic sales objectives, Cisco may pay 0% up to 125% of target. Cisco sales plans do not have a minimum threshold of performance for sales incentive compensation to be paid. The applicable full salary ranges for this position, by specific state, are listed below: New York City Metro Area: $168,800.00 - $277,400.00 Non-Metro New York state& Washington state: $148,800.00 - $248,200.00 * For quota-based sales roles on Cisco’s sales plan, the ranges provided in this posting include base pay and sales target incentive compensation combined. ** Employees in Illinois, whether exempt or non-exempt, will participate in a unique time off program to meet local requirements.
Dishwasher & Sanitation *Job Overview:* Ensuring the availability of clean utensils, molds, containers, etc. for the Production employees’ use. Preparing production and kitchen areas for next shift by cleaning equipment and cooking areas. *Responsibilities and Duties:* · Check that the warewasher is clean prior to starting shift. · Filling the warewasher with water and testing the chlorine concentration using a test strip. · Testing sanitizer solution using a test strip. · Putting liners on trash containers. · Filling the wash sinks with appropriate soap or sanitizing solution. · Cleaning and sanitizing utensils, molds, walls, and drains. · Cleaning and sanitizing static and small equipment. · Ensuring molds are dry for use in production. · Emptying trash containers and taking trash bags to bins throughout the production day and at end of shift. · Washing and cleaning carts. · Sweeping and mopping floor. · Filling in appropriate daily and weekly logs. · Must adhere to all safety, sanitation, good manufacturing practices and good housekeeping practices. Tipo de puesto: Tiempo completo Sueldo: A partir de $18.00 la hora Lugar de trabajo: Empleo presencial