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Cali Cream Homemade Ice Cream is the California brand you want to be part of now. We are not your typical ice cream or dessert shop. We are hunting for the fun, energetic, enthusiastic, and dynamic people that can keep up with our culture of fun and enthusiasm. We pride ourselves in having the most enthusiastic ice cream connoisseurs in the biz and we know it comes from the team collaboration and constant development of new flavors. We are looking for creative people in both quality of service and quality of food. Cali Cream Homemade Ice Cream is made one batch at a time with detailed love and care that you would make in your grandmas kitchen. If you are looking to run your own kitchen in a collaborative way, here is that opportunity that comes once in a lifetime. If you are looking for an amazing opportunity to grow your skills with a growing brand and an amazing organization - then hit the apply button. Ice Cream Maker *Responsibilities* Prepare the day to ensure an efficient service and production Follow recipes, controls, portion and presentation specifications as set by the Cali Cream standards and share ideas and feedback on how to improve where needed Maintain high standard and consistency of ice cream and presentation, ensuring that each bite represents the flavor our guest is desiring Maintain in-depth knowledge of nutrition, common allergies, dietary restrictions and food terminology Rotate, store, and use all food products to maintain freshness Prepare ice cream flavor list each day to ensure that supply is meeting the demands of our guest Track and report food waste Stock inventory and give feedback on the quality standards of the inventory Ability to operate our specially designed production equipment Maintain clean and orderly service and production area Comply with established safety and sanitation standards Share ideas on new flavor recipes and creation ideas that you have or are hearing from our guest Be Open minded and able to stay one step ahead Inventory control and ordering Have a PASSION for what you DO and CREATE *Qualifications* Able to work in a high energy and fast paced work environment Able to perform quality work efficiently Requires a good sense of prioritization and organizational skills Able to multi-task while maintaining a sense of urgency Accuracy and high attention to detail Able to work as part of a Team, both giving and receiving feedback Must be dependable and timely Able to work a flexible schedule Weekends, holidays and evenings required Possess a clear understanding of weights and measures Possess knowledge of safe food-handling, sanitary kitchen conditions and proper hand washing techniques *Skills* Able to lift 15-55 lbs. Able to stand, walk, lift, twist and bend for up to 8 hours a day Able to climb stairs while carrying 15-55 lbs. *Shift* AM/PM Shifts Part-time Full-time *Experience Level* If your life experiences have built a passion for greatness, that is all the experience we need. Job Type: Full-time Pay: From $19.00 per hour Benefits: * 401(k) * Employee discount * Flexible schedule * Health insurance * Paid time off Application Question(s): * How many hours are you looking for? * Tell me more about your food prep experience? * If hired how long would you stay with us? Shift availability: * Night Shift (Required) * Day Shift (Required) Work Location: In person
Carlsbad, 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 Lead, Manufacturing Operations is responsible for serving as the subject matter expert and operational lead within GMP manufacturing operations supporting biologics production. This role provides day-to-day directional leadership, coordination, and training for manufacturing personnel involved in upstream and downstream processing activities, including cell culture expansion, bioreactor operations, harvest, purification, filtration, and bulk drug substance manufacturing. The Lead supports batch execution, training, process troubleshooting, documentation review, and operational readiness activities. The Lead, Manufacturing Operations will primarily be responsible for manufacturing operations of Train 2. Train 2 is a production line going from vial thaw in initial thaw and expansion to a 500L production reactor, followed by harvest, to finishing operations in downstream. Example Plan Shifts/Training Schedule: - First 2 weeks: 8 hour shifts, M-F - Next 1-2 months: 10 hour shifts, Mon-Thurs - After 90 days: 12 hour shifts, Sun-Tues & Alternating Wednesdays Schedule is subject to change based on needs. Responsibilities Manufacturing Operations Individual Skills Provide hands-on training for upstream staff to ensure compliance with 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. Perform upstream 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. Monitor processes and results and troubleshoot issues as they arise to ensure process success. Lead and guide associates through process and workflow improvement initiatives. Lead batch readiness activities such as general planning and coordination, material requests and transfer, and material and equipment staging. Setup, operate and maintain downstream bioprocessing equipment including AKTA ready column chromatography skids, FlexAct automation skids, large scale filtration skids, and analytical instruments such as SoloVPE. Perform downstream 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. Enforce cleanroom standards for cleanliness and order Direct floor operations for multiple projects simultaneously. Make adjustments as necessary to adhere to production schedules. Cross-train on various tasks including autoclaving of assemblies, formulation of buffers, and Downstream operations to support overall success of the Biologics group. Represent departmental activities as needed, including project teams and task forces. Review GMP records for completeness, accuracy, and compliance on a daily basis in conformance with regulatory requirements. Draft, revise and 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. Manufacturing Operations Leadership Lead day-to-day execution of upstream and downstream GMP manufacturing activities. Coordinate manufacturing floor activities and provide real-time direction to manufacturing associates during campaign execution. Support media and buffer preparation, inoculum expansion, bioreactor operations, harvest, chromatography, UF/DF, sterile filtration, and bulk drug substance filling. Ensure activities are performed according to approved batch records, SOPs, and production schedules. Provide hands-on training and qualification support for manufacturing personnel. Review GMP documentation for completeness, accuracy, and compliance. Support deviations, CAPAs, change controls, and quality events. Troubleshoot process, equipment, and operational issues. Champion EHS compliance and safe work practices. Partner with QA, QC, MSAT, Engineering, Facilities, Supply Chain, and Program Management. Team Leadership & Development Train Manufacturing Associates. Provide feedback and review of staff during performance evaluations. Facilitate onboarding and qualification of new employees. Promote a culture of safety, teamwork, accountability, and continuous improvement. Lead daily shift meetings, production reviews, and operational communications. GMP Compliance & Quality Ensure strict compliance with cGMP regulations, company procedures, and regulatory requirements. Review and verify batch documentation for accuracy and completeness. Support investigations, deviations, CAPAs, change controls, and quality events. Participate in internal audits, client audits, and regulatory inspections. Ensure proper documentation practices and data integrity standards are maintained. Process Execution & Technical Support Provide technical oversight for upstream and downstream operations. Support process transfers from development to GMP manufacturing. Assist in process validation, engineering runs, and GMP campaign readiness activities. Collaborate with MSAT, Process Development, and Engineering teams to improve process robustness and efficiency. Troubleshoot manufacturing and equipment-related issues. Safety & Operational Excellence Champion Environmental Health and Safety (EHS) compliance. Ensure safe handling of biological materials, chemicals, and manufacturing equipment. Lead risk assessments and support implementation of corrective actions. Drive Lean Manufacturing and continuous improvement initiatives. Monitor and improve key performance indicators (KPIs) including safety, right-first-time execution, batch success rate, and schedule adherence. Cross-Functional Collaboration Partner with Quality Assurance, Quality Control, Validation, Facilities, Engineering, Supply Chain, and Program Management teams. Support customer visits and client-facing manufacturing discussions as required. Ensure manufacturing readiness through effective planning and material coordination. Qualifications BA/BS degree that included laboratory work in a chemistry, biology, or related field. At least 3 – 4 years of purification experience in a GMP pharmaceutical/biotech environment role. Demonstrate knowledge and understanding of cGMPs and how they apply to responsibilities. Skilled in aseptic handling, including BSC operations to maintain the integrity of sterile systems. Skilled with using single-use technologies Strong technical and mechanical aptitude in bioprocessing. Knowledge of purification using column chromatography Experience leading, training, and coaching peers. Computer proficiency A proven ability to confidently compute basic arithmetic operations. Travel between Abzena sites (local San Diego CA facilities ) as needed. Physical Requirements Ability to stand for 1-2 hours at a time, sit for 2 to 3 hours at a time. Frequently lift and or move objects at least 30 pounds in weight. Stand/walk during entire length of shift. Use arms, hands and fingers to handle, feel or reach. Ability to climb, balance, stoop, kneel, crouch, or crawl. Visual abilities including near and far sight, color, peripheral vision, depth and ability to focus. $85,000 - $100,000 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 and identifying potential inconsistencies or verification signals in application materials based on available information. 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.
Carlsbad, 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 Lead, Manufacturing Operations is responsible for serving as the subject matter expert and operational lead within GMP manufacturing operations supporting biologics production. This role provides day-to-day directional leadership, coordination, and training for manufacturing personnel involved in upstream and downstream processing activities, including cell culture expansion, bioreactor operations, harvest, purification, filtration, and bulk drug substance manufacturing. The Lead supports batch execution, training, process troubleshooting, documentation review, and operational readiness activities. The Lead, Manufacturing Operations will primarily be responsible for manufacturing operations of Train 2. Train 2 is a production line going from vial thaw in initial thaw and expansion to a 500L production reactor, followed by harvest, to finishing operations in downstream. Example Plan Shifts/Training Schedule: - First 2 weeks: 8 hour shifts, M-F - Next 1-2 months: 10 hour shifts, Mon-Thurs - After 90 days: 12 hour shifts, Thurs-Sat & Alternating Wednesdays Schedule is subject to change based on needs. Responsibilities Manufacturing Operations Individual Skills Provide hands-on training for upstream staff to ensure compliance with 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. Perform upstream 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. Monitor processes and results and troubleshoot issues as they arise to ensure process success. Lead and guide associates through process and workflow improvement initiatives. Lead batch readiness activities such as general planning and coordination, material requests and transfer, and material and equipment staging. Setup, operate and maintain downstream bioprocessing equipment including AKTA ready column chromatography skids, FlexAct automation skids, large scale filtration skids, and analytical instruments such as SoloVPE. Perform downstream 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. Enforce cleanroom standards for cleanliness and order Direct floor operations for multiple projects simultaneously. Make adjustments as necessary to adhere to production schedules. Cross-train on various tasks including autoclaving of assemblies, formulation of buffers, and Downstream operations to support overall success of the Biologics group. Represent departmental activities as needed, including project teams and task forces. Review GMP records for completeness, accuracy, and compliance on a daily basis in conformance with regulatory requirements. Draft, revise and 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. Manufacturing Operations Leadership Lead day-to-day execution of upstream and downstream GMP manufacturing activities. Coordinate manufacturing floor activities and provide real-time direction to manufacturing associates during campaign execution. Support media and buffer preparation, inoculum expansion, bioreactor operations, harvest, chromatography, UF/DF, sterile filtration, and bulk drug substance filling. Ensure activities are performed according to approved batch records, SOPs, and production schedules. Provide hands-on training and qualification support for manufacturing personnel. Review GMP documentation for completeness, accuracy, and compliance. Support deviations, CAPAs, change controls, and quality events. Troubleshoot process, equipment, and operational issues. Champion EHS compliance and safe work practices. Partner with QA, QC, MSAT, Engineering, Facilities, Supply Chain, and Program Management. Team Leadership & Development Train Manufacturing Associates. Provide feedback and review of staff during performance evaluations. Facilitate onboarding and qualification of new employees. Promote a culture of safety, teamwork, accountability, and continuous improvement. Lead daily shift meetings, production reviews, and operational communications. GMP Compliance & Quality Ensure strict compliance with cGMP regulations, company procedures, and regulatory requirements. Review and verify batch documentation for accuracy and completeness. Support investigations, deviations, CAPAs, change controls, and quality events. Participate in internal audits, client audits, and regulatory inspections. Ensure proper documentation practices and data integrity standards are maintained. Process Execution & Technical Support Provide technical oversight for upstream and downstream operations. Support process transfers from development to GMP manufacturing. Assist in process validation, engineering runs, and GMP campaign readiness activities. Collaborate with MSAT, Process Development, and Engineering teams to improve process robustness and efficiency. Troubleshoot manufacturing and equipment-related issues. Safety & Operational Excellence Champion Environmental Health and Safety (EHS) compliance. Ensure safe handling of biological materials, chemicals, and manufacturing equipment. Lead risk assessments and support implementation of corrective actions. Drive Lean Manufacturing and continuous improvement initiatives. Monitor and improve key performance indicators (KPIs) including safety, right-first-time execution, batch success rate, and schedule adherence. Cross-Functional Collaboration Partner with Quality Assurance, Quality Control, Validation, Facilities, Engineering, Supply Chain, and Program Management teams. Support customer visits and client-facing manufacturing discussions as required. Ensure manufacturing readiness through effective planning and material coordination. Qualifications BA/BS degree that included laboratory work in a chemistry, biology, or related field. At least 3 – 4 years of purification experience in a GMP pharmaceutical/biotech environment role. Demonstrate knowledge and understanding of cGMPs and how they apply to responsibilities. Skilled in aseptic handling, including BSC operations to maintain the integrity of sterile systems. Skilled with using single-use technologies Strong technical and mechanical aptitude in bioprocessing. Knowledge of purification using column chromatography Experience leading, training, and coaching peers. Computer proficiency A proven ability to confidently compute basic arithmetic operations. Travel between Abzena sites (local San Diego CA facilities ) as needed. Physical Requirements Ability to stand for 1-2 hours at a time, sit for 2 to 3 hours at a time. Frequently lift and or move objects at least 30 pounds in weight. Stand/walk during entire length of shift. Use arms, hands and fingers to handle, feel or reach. Ability to climb, balance, stoop, kneel, crouch, or crawl. Visual abilities including near and far sight, color, peripheral vision, depth and ability to focus. $85,000 - $100,000 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 and identifying potential inconsistencies or verification signals in application materials based on available information. 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.
The Company Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Dexcom began as a small company with a big dream: To forever change how diabetes is managed. To unlock information and insights that drive better health outcomes. Here we are 25 years later, having pioneered an industry. And we're just getting started. We are broadening our vision beyond diabetes to empower people to take control of health. That means personalized, actionable insights aimed at solving important health challenges. To continue what we've started: Improving human health. We are driven by thousands of ambitious, passionate people worldwide who are willing to fight like warriors to earn the trust of our customers by listening, serving with integrity, thinking big, and being dependable. We've already changed millions of lives and we're ready to change millions more. Our future ambition is to become a leading consumer health technology company while continuing to develop solutions for serious health conditions. We'll get there by constantly reinventing unique biosensing-technology experiences. Though we've come a long way from our small company days, our dreams are bigger than ever. The opportunity to improve health on a global scale stands before us. Meet the team: At Dexcom our patient's satisfaction is at the heart of everything we do. We strive to enable people to take control of their health. This enrichment of life also extends our patient’s friends, families and significant others. The Industrial Engineering team plays an integral part in allowing the organization to achieve that goal. This requires a highly skilled candidate who moves fast, has an entrepreneurial spirit to create new solutions, a tenacity to get things done, will thrive in an environment of ambiguity and change, and can break down and solve complex problems. Joining our team will open you to a fun and professional work environment. You will get to partner cross-functionally across all organizations and each complex manufacturing processes that create the most accurate CGM on the market. You will have the ability to help design, analyze and improve our business systems and production systems to help achieve world class manufacturing. We are proud to foster a culture of personal and professional growth so come build your career with us! Where you come in: You will lead Process Design & Optimization for San Diego’s Product Innovation Center You will design an ideal Transfer Readiness Process to smoothly transition between R&D and Operations You will analyze the current state process for how R&D builds get generate, approved and built You will establish Key Performance Indicators for business processes You will lead cross-functional workshops to ensure stakeholder alignment and changes are successfully adopted You will support organizational adoption of new processes through hands-on training, coaching and communication What makes you successful: You have prior experience in Medical Devices and understanding of ISO 13485, CFR and other applicable standards 8-10 years of experience across manufacturing operations and product development including sustaining, strategy, development, and support Experience with process/product development and ability to build a system from the ground up with an entrepreneurial spirit Expert facilitation and stakeholder management skills Strong in value stream mapping, process mapping, makigami You are a systems thinker and self-starter who thrives in a fast-paced environment Strong Project Management skills (PMP certified is preferred) Adaptable to shifting business needs Value teamwork, inclusion and have a respect for every individual What you’ll get: A front row seat to life changing CGM technology. Learn about our brave #dexcomwarriors community . A full and comprehensive benefits program. Growth opportunities on a global scale. Access to career development through in-house learning programs and/or qualified tuition reimbursement. An exciting and innovative, industry-leading organization committed to our employees, customers, and the communities we serve. Travel Required: 15-25% Experience and Education Requirements: • Typically requires a Bachelor’s degree in a technical discipline, and a minimum of 8-12 years related experience or Master’s degree and 5-7 years equivalent industry experience or a PhD and 2-4 years of experience. Please note: The information contained herein is not intended to be an all-inclusive list of the duties and responsibilities of the job, nor are they intended to be an all-inclusive list of the skills and abilities required to do the job. Management may, at its discretion, assign or reassign duties and responsibilities to this job at any time. The duties and responsibilities in this job description may be subject to change at any time due to reasonable accommodation or other reasons. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Dexcom’s AAP may be viewed upon request by contacting Talent Acquisition at talentacquisition@dexcom.com. If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please contact Dexcom Talent Acquisition at talentacquisition@dexcom.com. Meritain, an Aetna Company, creates and publishes the Machine-Readable Files on behalf of Dexcom. To link to the Machine-Readable Files, please click on the URL provided: https://health1.meritain.com/app/public/#/one/insurerCode=MERITAIN_I&brandCode=MERITAINOVER/machine-readable-transparency-in-coverage?reportingEntityType=TPA_19874&lock=true To all Staffing and Recruiting Agencies: Our Careers Site is only for individuals seeking a job at Dexcom. Only authorized staffing and recruiting agencies may use this site or to submit profiles, applications or resumes on specific requisitions. Dexcom does not accept unsolicited resumes or applications from agencies. Please do not forward resumes to the Talent Acquisition team, Dexcom employees or any other company location. Dexcom is not responsible for any fees related to unsolicited resumes/applications. Salary: $111,100.00 - $185,100.00
Become part of a team that champions wellness worldwide. CAPTEK® Softgel International is a global leader in the development and production of high-quality nutraceutical supplements. As a contract manufacturer organization (CMO), we collaborate with innovators from some of the world’s most successful brands. Summary: To monitor and care for the finished gelatin product. Ensure that all tracking log are maintained and executed for all gelatin receivers Essential Duties and Responsibilities: • Follows company policies, SOPs, cGMPs and GDP • Maintains a safe and clean work environment in the gelatin staging area • Must maintain all gelatin tracking logs throughout the shift • Assists the softgel encapsulation operators in finding and moving receivers to the correct location • Assists and check the softgel encapsulation operators connect the correct gelatin • With the assistant of a lead, check and record the viscosity when necessary. • Ensures that oldest lot numbers/ materials/gelatin batches are used first (FIFO) • Consistently monitors gelatin temperature throughout the shift • Make sure all gelatins left-over is accounted it for and documented on batch record. • Ensures that temperature probes are maintained, washed and ready to use for the following shift • Reports any damaged or broken tools, receivers and equipment to the manager • The ability to communicate and interact with other departments (nutrient, encapsulation, maintenance quality assurance etc.) • Executes proper shift change and communicates all information pertaining to the operator's area of responsibility • Anticipates and minimizes down time to ensure completion of order in a timely manner • Assists with janitorial duties as needed • Ensures work area is clean and organized at all times and mop at least once a day • Remove trash at the end of each shift • Communicates solutions and ideas on how to improve department to the department manager • Complies with company policies and procedures and maintains regular work attendance • Performs other duties as assigned Education/Experience: • Minimum High School Diploma or G.E.D. equivalent • Previous experience working with manufacturing equipment, preferred Supervisory Responsibilities: • N/A Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing 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 is occasionally exposed to work near moving mechanical parts; fumes or airborne particles and risk of electrical shock. The noise level in the work environment is usually moderate. Physical Demands: 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. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include Close vision, Peripheral vision and Ability to adjust focus. While performing the duties of this job, the employee is occasionally required to stand; walk; sit; use hands and fingers to handle, or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl and talk or hear Thank you for your interest in joining the CAPTEK team. You will be contacted shortly if your application is selected.
Corporate Overview Argonaut Manufacturing Services Inc. is a contract manufacturing organization (CMO) headquartered in Carlsbad, CA with over 100,000 square feet of manufacturing space across four locations. The company is dedicated to serving highly innovative companies in the biopharmaceutical and molecular diagnostics industries. Argonaut is a full service, cost-effective partner, providing complete solutions in the areas of formulation, filling and final kitting of reagents and consumables. Argonaut provides quality and regulatory expertise to assure the highest in quality manufacturing and supply chain excellence. Benefits and Pay Range Pay range for this position is $21.00 - $27.00 per hour, depending on experience. Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate. This is a temp to hire position. Position Overview The Manufacturing Technician II/III is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. The Manufacturing Technician is expected to fully participate in both departmental projects and any quality working teams which may be applicable. existing procedures. All of the specific requirements presented in this job description are applicable to the functional area in which it resides. This role is 100% On-Site, Monday - Friday 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. The scheduled start time for this position is either 6:00 AM or 12:00 PM, depending on business needs, with a consistent schedule once assigned. Any exceptions to the assigned schedule must be approved by the manager in advance. Responsibilities and Duties Ability to work within an ISO 13485 and cGMP production environment and ensure compliance with our quality system. Execute documentation based on cGMP and GDP procedures, as well as perform documentation review post manufacturing execution. Participate in Quality Working Teams and Continuous Improvement Teams. Visual inspection of lyophilized product and heat seals of packaging. Clean and sanitize manufacturing and associated support areas. Responsible for monitoring machinery and reporting alarms to lead technician or Supervisor. Conduct daily documentation review. Participate in Quality Working Teams and Continuous Improvement Teams. Operate large machinery and monitor automated. Employee may be required to manage hazardous wastes in compliance with company proceduresState/Federal/Local hazardous waste regulations. Duties may include identifying, handling, generating, accumulating, storing, labeling, and on-site transporting of hazardous wastes. Perform daily arithmetic calculations as it pertains to total volume and liquid concentrations. Perform daily unit conversions as it pertains to gravimetric and volumetric measurements. Operate production equipment such as pipettes, balances, pH meter and heat sealers. Monitor department equipment for proper operation that is within calibration. May perform safety and cGMP inspections or observations. Ensure compliance with SOP/cGMP and cGDP requirements. Assist in training/ leading of new team members in production activities. Assist in updating and new revision of standard operating procedures (SOP). May need to be an author for any MFG Non-Conformance Reports (NCR) and risk analysis memos. Receive and distribute supplies into the production area as necessary. Perform NetSuite transaction, issue material, completion and closing of work orders. This position may require local travel between company facilities within a short distance (approximately 3 miles) based on business needs. May assist with review of quality assurance logbooks. May perform other duties as assigned. Education Requirements Level II Bachelor's degree in a related field (Biotechnology, Molecular Biology, or Biochemistry) with at least 1 year of work experience at Argonaut or in manufacturing within a cGMP environment; Associate's degree in a related field; or High school diploma/equivalent with 3+ years of related manufacturing experience in a cGMP environment. Level III Bachelor's degree in a related field (Biotechnology, Molecular Biology, or Biochemistry) with 2+ years of work experience at Argonaut or in manufacturing within a cGMP environment; Associate's degree in a related field with 3+ years of related experience; or High school diploma/equivalent with 5+ years of related manufacturing experience in a cGMP environment. Required Skills and Knowledge Punctuality and reliable attendance required. Ability to read and follow detailed written instructions; strong verbal and written communication skills. Proficient in reading, writing, and conversing in English to understand cGMP manufacturing processes and SOPs. Knowledge of manufacturing production processes related to product integrity, including visual inspection of components and finished goods, manual and semi-automated packaging, and product labeling. Understanding of basic chemical and biological safety procedures. Basic knowledge of formulation, filling, and kitting operations and capabilities. Argonaut Manufacturing Services, Inc. is proud to be an equal opportunity employer committed to providing employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age or disability, or any other class protected by Federal, State or local laws. Argonaut complies will all employment eligibility verification requirements of the Immigration and Nationality Act and all must have the authorization to work in the US.
table.MiTabla { max-width: 1020px;!important Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. Manufacturing Technician I Monday – Friday 6:30AM – 3:00PM The Manufacturing Technician I performs fundamental tasks within a GMP environment in support of more complex manufacturing operations. The tasks include, but are not limited to, cleaning and maintaining the work place so that it meets the standards for controlling bioburden levels; cleaning operating equipment per applicable procedures so that it meets the standards established to prevent product contamination and maintaining records/logs neatly and accurately and in accordance with current standard procedures. The technician performs job tasks in a safe manner while following specific department safety rules. PRIMARY RESPONSIBILITIES: Responsible for equipment setup and operation in a biologics processing environment for plasma derived pharmaceuticals. Detailed cleaning of equipment/facilities to MSP/cGMP standards. Complete technical training profile as required. Strict adherence to Dept. Safety Rules. Bulk processing and filtration involving monitoring processing parameters (i.e. pH, weights, separation, assay results). Perform real-time documentation during the production run. ADDITIONAL RESPONSIBILITIES: English fluency both verbal and written. Basic math skills with proficiency in metric system. Accurate documentation skills are a must. Basic computer skills. Mechanical aptitude. Must be available to work any shift, including weekends. Ability to work well with others in a team environment is essential. Self-starter with the ability to work independently and use good judgment. Must be able to handle multiple priorities. Must be proactive, results oriented, and have strong attention to detail EDUCATION: High school diploma or GED required. Associates Degree or Bachelor’s degree preferred. Manufacturing, or experience in pharmaceuticals/biologics processing in a GMP environment is preferred. EXPERIENCE: 1-2 years’ experience in a manufacturing environment preferred. SKILLS & ABILITIES: Accurate documentation and attention to detail oriented. Usage of a 10-key calculator. OCCUPATIONAL DEMANDS: Ability to lift/push 50 lbs. All work is performed in a clean room (sanitized) manufacturing environment and must gown up. Must be able to work in a cold environment, job requires bending or standing for prolonged periods. This job description is accurate at the date of publication. It is intended to provide information essential to understanding the scope and general nature of the work performed by job holders within this position. This job description is not intended to be an exhaustive list of qualifications, skills, duties, responsibilities or working conditions associated with the position. Other duties may be assigned. #BiomatUSA The estimated pay scale for Manufacturing Technician I role based in California, is $18.70-$28.05 per hour. Additionally, the position is eligible to participate in up to 5% of the company bonus pool. We offer a wide variety of benefits including, but not limited to: Medical, Dental, Vision, life insurance, PTO, paid holidays and up to 5% 401(K) match and tuition reimbursement. Final compensation packages will ultimately depend on education, experience, skillset, knowledge, where the role is performed, internal equity and market data. We are committed to offering our employees opportunities for professional growth and career progression. Grifols is a global healthcare organization with employees in 30 countries focused on patient health and providing impactful results. Since our humble beginnings in 1909, Grifols has been a family company that prides itself on its family-like culture. Our company has more than tripled over the last 10 years, and you can grow with us! Third Party Agency and Recruiter Notice: Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate. Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws, including but not limited to, the California Fair Chance Act, the Los Angeles County Fair Chance Ordinance for Employers, and the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance. California Personnel Privacy Policy and Notice at Collection Location: NORTH AMERICA : USA : CA-Vista: USVISTA2 - Vista CA-980 Park Center Drive-AC Learn more about Grifols
Job Title: Material Handler / Warehouse Technician Location: Vista, CA Employment Type: Full-time Schedule: Mon–Fri, 7:00 AM–3:30 PM About Us: JifPak Manufacturing LLC., is a growing manufacturing company producing meat casings. We deliver high-quality products to customers nationwide and are committed to safety, continuous improvement, and on-time production. We’re seeking a dependable Material Handler / Warehouse Technician to support production and shipping by receiving, staging and moving raw materials, components, and finished goods. This role ensures production lines are supplied on schedule, inventory is accurate, and the manufacturing floor remains organized and safe. Key Responsibilities: Receive and inspect incoming raw materials and components; verify packing lists and PO quantities. Stage and deliver materials to production lines; assemble kits and replenish kanban/bin locations. Pick, pack, label, and stage finished goods for shipping per packing lists and quality requirements. Operate forklifts, pallet jacks, and other material handling equipment safely; maintain certifications. Perform cycle counts, physical inventories, and help reconcile discrepancies in ERP. Document material movements, lot numbers, serial numbers, and nonconforming material per procedures. Support production changeovers and expedite urgent material requests. Maintain clean, organized warehouse and production staging areas; follow all safety protocols. Assist with receiving inspections, basic quality checks, and return processing. Qualifications: Must speak, read, and write English 2+ year experience in manufacturing/material handling preferred. Forklift experience Comfortable lifting up to 50 lbs regularly and standing for extended periods. Basic computer skills; experience with ERP Strong attention to detail, reliability, and ability to work on a production schedule. Good communication skills and ability to follow documented procedures and quality standards. Compensation & Benefits: Pay $22.00–$25.00/hr depending on experience. Benefits: Medical, dental, vision, 401(k), paid time off. Overtime available during production peaks. 1st Shift: 7:00AM - 3:00PM
About Quantum Design For more than 40 years Quantum Design (QD) has been providing technology solutions to researchers in the fields of physics, chemistry, biotechnology, materials science, and nanotechnology. Established in 1982, Quantum Design is the leading commercial source for automated materials characterization systems offering a variety of measurement capabilities. QD instruments are found in the world's leading research institutions and have become the reference standard for a variety of magnetic and physical property measurements. Job Description: The Opportunity The Product Engineering Intern – Manufacturing Systems & Fixture Design will support Product Engineering initiatives focused on improving manufacturing efficiency, product quality, and workplace safety. This role will lead to the redesign of a critical flex circuit calibration probe used in the production of DynaCool and OptiCool systems. The selected candidate will work closely with engineers and technicians to develop hardware and software improvements that enhance calibration reliability, improve manufacturing yields, and eliminate identified safety risks associated with the cryogenic calibration process. This is an excellent opportunity for a hands-on engineering student interested in mechanical design, manufacturing processes, cryogenic systems, product development, and continuous improvement. Responsibilities Participate in the design, development, and testing of manufacturing fixtures and process improvements. Redesign the existing flex circuit calibration probe to improve reliability and operational safety. Incorporate secondary temperature-sensing capabilities to verify proper calibration conditions during testing. Develop or support software reporting tools that provide operator alerts when calibration conditions are outside acceptable limits. Design improved sealing mechanisms between the calibration probe and cryogenic vessel to prevent atmospheric contamination and ice formation. Evaluate and implement pressure-relief solutions to mitigate cryogenic safety risks. Create engineering documentation, test procedures, and operating instructions. Collaborate with engineers, technicians, and manufacturing personnel to validate designs and implement improvements. Participate in design reviews and present project recommendations to stakeholders. Support additional fixture and process-improvement projects as time allows. Qualifications Currently pursuing a bachelor's degree in engineering, physical sciences, chemistry, or a related field, with at least two years of coursework completed Experience with CAD software for mechanical design and assembly modeling Interest in manufacturing processes, product development, and continuous improvement Soft Skills Ability to take direction and incorporate feedback from technical mentors. Strong communication and teamwork skills. Ability to provide regular project updates and discuss technical progress. Comfortable presenting design concepts and recommendations in small-group design reviews. Strong organizational and problem-solving abilities. Self-motivated and eager to learn in a hands-on engineering environment. What You’ll Gain Hands-on experience in manufacturing and product engineering Exposure to fixture design, cryogenic systems, mechanical design, and process improvement Opportunities to work alongside experienced engineers and technicians Experience conducting design reviews and presenting engineering solutions Involvement in projects with measurable impact on manufacturing quality, efficiency, and safety Practical application of CAD, testing, validation, and engineering documentation skills Additional Information This position’s work mode is onsite. The employee will report to San Diego, CA This internship begins in Summer 2026 and may continue into the Fall semester based on business needs and the intern's availability Hourly: $30 - $35, actual compensation may vary based on education, experience, skills, and qualifications Quantum Design is an affirmative action and equal opportunity employer. All employment decisions, policies and practices are in accordance with applicable federal, state and local anti-discrimination laws. Quantum Design will not tolerate or engage in unlawful discrimination including any form of unlawful harassment, on account of a person's sex, age, race, color, religion, creed, sexual preference or orientation, marital status, national origin, ancestry, citizenship, military status, veteran status, handicap, disability, or membership in any protected group.
We are seeking a highly skilled Manufacture Process Engineer to lead and optimize manufacturing processes for Printed Circuit Board Assemblies (PCBA). This role is critical in ensuring high-quality, reliable, and cost-effective production through expertise in stencil design, soldering processes, wave solder profiling, conformal coating, and secondary operations. The ideal candidate will bring deep technical knowledge, hands-on experience, and a continuous improvement mindset to advance our PCBA manufacturing capabilities. ⚙ Key Responsibilities Process Development & Optimization Design, validate, and optimize stencil designs for solder paste application. Develop and maintain reflow soldering profiles, including vapor phase reflow processes, to ensure robust solder joints and minimize defects. Establish and refine wave soldering profiles for through-hole components. Define and implement secondary operations including press-fit connector installation, heat sink attachment, and mechanical assembly steps. Develop and oversee conformal coating processes to ensure environmental protection and product reliability. Create and enforce rework standards for soldering, ensuring compliance with IPC and industry best practices. Manufacturing Support Provide technical leadership to production teams in troubleshooting assembly issues. Collaborate with design engineering to ensure manufacturability of PCB layouts and component selection. Drive yield improvement initiatives and root cause analysis for process-related defects. Lead Corrective and Preventive Action (CAPA) initiatives to eliminate recurring issues and strengthen process robustness. Support new product introduction (NPI) by developing scalable and repeatable assembly processes. Quality & Compliance Ensure adherence to IPC-A-610, J-STD-001, IPC-7711/7721, and other relevant industry standards. Maintain documentation of process parameters, work instructions, and control plans. Partner with quality engineering to implement corrective and preventive actions (CAPA). Continuous Improvement Lead projects focused on automation, efficiency, and cost reduction. Evaluate and introduce new technologies, equipment, and materials to enhance PCBA processes. Train and mentor junior engineers and technicians in advanced assembly techniques. Qualifications & Experience Education: Bachelor’s degree in Mechanical Engineering, Electrical Engineering, Materials Science, or related field. Master’s preferred. Experience: Minimum 7–10 years in PCBA manufacturing engineering, with proven expertise in: Stencil design and solder paste application. Reflow soldering (including vapor phase reflow) and thermal profiling. Wave soldering process development and optimization. Conformal coating application and process control. Secondary operations (press-fit connectors, heat sinks, mechanical assembly). Rework and repair standards for solder joints. Root cause analysis and CAPA methodologies for troubleshooting and issue resolution. Strong knowledge of IPC standards (IPC-A-610, J-STD-001, IPC-7711/7721). Hands-on experience with SMT equipment, AOI/X-ray inspection, and process monitoring tools. Demonstrated success in NPI process development and scaling to volume production. Excellent problem-solving, analytical, and communication skills. Ability to lead cross-functional teams and drive process improvements in a fast-paced environment. Preferred Skills Experience with Design for Manufacturability (DFM) and Design for Test (DFT) principles. Familiarity with Lean Manufacturing and Six Sigma methodologies. Proficiency in CAD tools for stencil and fixture design. Knowledge of advanced soldering techniques (selective soldering, laser soldering). Strong project management and leadership capabilities. Benefits 401(k) 401 (k) matching Dental insurance Health insurance Vision insurance Paid time off
*About the job* *Company Description* Wintriss Engineering Corporation is an innovative technology company based in San Diego, California, specializing in automated surface vision inspection systems since 1989. The company serves a broad range of industries, including plastics, metals, nonwovens, paper, and coated or laminated composites. Its highly modular Web Ranger™ system helps customers improve product quality, reduce scrap and yield losses, and increase productivity. Wintriss focuses on tailored, industry 4.0-ready solutions that deliver measurable cost savings, positioning the company as a trusted expert in surface inspection. *Role Description* This full-time, on-site Production Electromechanical Technician role is based in San Diego, CA. The engineer will assemble, test, and troubleshoot electromechanical components and systems used in automated surface inspection equipment. Daily responsibilities include interpreting electrical and mechanical drawings, performing wiring and mechanical integration, and ensuring products meet performance, safety, and quality standards. The role involves collaborating with design engineers and production teams to resolve technical issues, implement process improvements, and support continuous optimization of manufacturing workflows. The candidate will also document procedures, maintain production records, and assist with training and support for production personnel. *Key Responsibilities* * Develop, implement, and continuously improve manufacturing processes for electro-mechanical and electronic assemblies. * Provide hands-on production support for medium- and large-scale power distribution and I/O control panels. * Design electrical control panels, operator interface panels, back panels, and mechanical enclosures using AutoCAD. * Create and maintain manufacturing drawings, wiring diagrams, assembly documentation, bills of materials (BOMs), and engineering documentation. * Partner with engineering and production teams to improve manufacturability, reliability, product quality, and cost efficiency. * Develop assembly procedures, work instructions, inspection criteria, and production test methods. * Troubleshoot manufacturing, quality, and field issues using structured root cause analysis techniques. * Design and develop production fixtures, tooling, and test equipment to improve manufacturing efficiency. * Ensure compliance with applicable industry standards, including IPC, MIL-STD, ISO, NEC, UL508A, and related requirements. * Support supplier selection, component sourcing, and technical evaluations. * Lead continuous improvement initiatives focused on quality, productivity, and cost reduction. *Required Qualifications* * Bachelor's degree in Mechanical Engineering, Electrical Engineering, Manufacturing Engineering, or equivalent technical experience. * Minimum of five years of manufacturing experience in industrial controls, aerospace, military, rugged electronics, or similar environments. * Hands-on experience designing and supporting electro-mechanical assemblies and enclosure systems. * Proficiency with AutoCAD for electrical panel layouts, enclosure design, and fabrication drawings. * Experience with electronic test equipment, including oscilloscopes, digital multimeters (DMMs), signal generators, and laboratory power supplies. * Experience designing, assembling, testing, or supporting industrial control panels and operator interface systems. * Safe operation of shop equipment, including drill presses, band saws, circular saws, and cutoff saws. * Knowledge of sheet metal fabrication, machining, wiring, mechanical assembly, and production testing. * Working knowledge of NEC requirements and UL508A standards for industrial control panels. * Experience creating and maintaining BOMs, routings, engineering change orders (ECOs), and manufacturing documentation. * Strong troubleshooting, analytical, and problem-solving skills. *Preferred Qualifications* * Experience with ruggedized or embedded electronic systems. * Background in industrial automation, control systems, or HMI panel design. * Familiarity with PCB assembly, electronics packaging, and circuit debugging. * Understanding of EMI/EMC design principles and environmental requirements for military and industrial electronic systems. * Familiarity with UL, CE, IEC 61439, and other applicable electrical safety standards. * Knowledge of global power distribution systems and grounding practices in North America, Europe, and Asia. *Core Competencies* * Electro-mechanical manufacturing * Mechanical design and drafting * Industrial control panel and enclosure design * AutoCAD, SolidWorks, or other 3D CAD software * Design for Manufacturing (DFM) and Design for Assembly (DFA) * Manufacturing process development * Root cause analysis and corrective actions * Engineering documentation and configuration management * Cross-functional collaboration * Hands-on production and shop floor support *Performance Objectives* *Success in this role will be measured by:* * Improvements in manufacturing efficiency and productivity * Increased first-pass yield and product quality * On-time production support and schedule adherence * Reduced defects, rework, and manufacturing costs * Successful implementation of new products into production * Continuous improvement initiatives that enhance manufacturability and operational performance *Physical Demands / Working Conditions* * General Office / Warehouse Environment, PC use * Lifting (occasional 50 lbs or less) * Stooping * Standing *Work Environment:* *This position requires a combination of office-based engineering work and hands-on support within a manufacturing environment. Responsibilities include supporting prototype builds, production operations, testing activities, and occasional interaction * Pay: $58,000.00 - $95,000.00 per year Benefits: * 401(k) * 401(k) matching * Dental insurance * Health insurance * Life insurance Work Location: In person
General Atomics Electromagnetic Systems (GA-EMS) designs and manufactures first-of-a-kind electromagnetic and electric power generation systems. GA-EMS’ expanding portfolio of specialized products and integrated system solutions support critical fleet, space systems and satellites, missile defense, power and energy, and process and monitoring applications for defense, industrial, and commercial customers worldwide. Under supervision, this position supports the manufacturing production process with focus on the design, development, and implementation of new or revised production processes for the efficient and economical fabrication of parts, components, sub-assemblies, and final assemblies. DUTIES AND RESPONSIBLITIES: Develops, implements, and maintains methods, operation sequence and processes in the manufacture or fabrication of parts, components, sub- assemblies, and final assemblies. Applies technical knowledge to analyze, investigate and resolve manufacturing and engineering related problems. Designs the sequence of production operations, specifying procedures for the fabrication of applicable tools and equipment, and adapting machinery. Collaborates with product design engineering on technical specifications that will best utilize equipment and manufacturing techniques. Investigates, dispositions and justifies product, drawing, and specification non conformances. Estimates manufacturing costs and determines time standards. Ensures that production processes and procedures are in compliance with regulations. Maintains records and reporting systems for coordination of manufacturing operations. Performs supplier audit and oversight as necessary to ensure conforming product being delivered. Communicates technical responses to supply base questions during proposal efforts, manufacturing efforts and post manufacturing efforts. Supports on-site supplier kick off meetings to discuss manufacturing plan, schedule and supplier deliverables. Assist with development, status and needs of the project plan to the Control Account Manager. Maintains the strict confidentiality of sensitive information. Performs other duties as assigned. Responsible for observing all laws, regulations and other applicable obligations wherever and whenever business is conducted on behalf of the Company. Expected to work in a safe manner in accordance with established operating procedures and practices. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. Job Qualifications Typically requires a bachelors in engineering or a related technical field . May substitute equivalent experience in lieu of education. The ideal candidate has exposure to welding, fabrication and machining. Degree in mechanical, aerospace manufacturing or industrial engineering is desired. Must have a solid understanding of manufacturing and engineering concepts, principles, and theory with technical experience demonstrating the application of those concepts while ensuring safety and regulatory compliance. Must possess the ability to understand new concepts quickly and apply them accurately throughout an evolving environment and organize work assignments to meet established timetables. Good communication, computer, documentation, presentation, and interpersonal skills are required, as well as the ability to work both independently and as part of a team. Ability to obtain and maintain DoD Secret Clearance is desired. Job Category Engineering Experience Level Entry-Level (0-2 years) Workstyle Onsite Full-Time/Part-Time Full-Time Salary Pay Range Low 56,820 Pay Range High 96,015 Travel Percentage Required 0% - 25% Relocation Assistance Provided? Yes US Citizenship Required? Yes Clearance Required? No Search Jobs at | General Atomics and Affiliated Companies