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Company: IPS Group, Inc. is a design, engineering and manufacturing company focused on wireless telecommunications and parking technologies. IPS manufactures its products locally and has been delivering world-class solutions to the telecommunications and parking industries for over 25 years. The company is best known for its patented credit card-enabled, solar powered parking meter and web-based management system. Job Description We are currently seeking a reliable, hard-working technician/fabricator for our expanding operation. In this role, you will be a part of our metal fabrication team, ensuring our production goals are met in a realistic time frame while adhering to standards for safety and quality. You will need to be punctual, able to perform repetitive physical tasks, and lift 65 lbs. unassisted. Machine Shop Tech II is responsible for performing various tasks to set up, operate, monitor, and troubleshoot production machines/equipment. Will also be responsible for inspecting parts to specifications, making machine adjustments and tool changes to maintain quality specifications. Machine Shop Tech II utilizes specialized machines and tools on a day-to-day basis to complete advanced fabrication/manufacturing projects. This is a group environment where team cooperation is a required skill. Essential Duties and Responsibilities Demonstrate professionalism Follow all written and verbal instructions Adhere to safe work practices and guidelines Attend all safety and production trainings Work cooperatively with production team(s) Ensure production standards are maintained Perform necessary tasks for proper equipment startup and shutdown Operate machinery/ tools/ devices with caution and care Alternate operation of multiple types of equipment day-to-day for quality production and minimal unplanned stops Fabrication and manufacturing projects involving engineering drawings Utilization of specialized tools and equipment Metal finishing (using power tools to deburr and shape production parts as needed) Participation in daily department cleanup Maintain a safe and organized work area Maintain general hygiene and sanitation standards Qualifications and Skills High school diploma or equivalent required Math, reading, writing, verbal communication skills Capable of reading and understanding production documents and safety manuals Understanding of industry technology, including specialized tools/equipment Previous experience working in industry Comply with all safety guidelines (non-negotiable) Physically capable of manual labor (lifting, bending, reaching, ) Able to lift 65 unassisted Able to stand for 8 hours (with breaks) Position Type/Expected Hours of Work This is a full-time position. Hours of work are Monday through Friday, 7:00 a.m. to 3:30 p.m., 40 hours per week. Other Duties Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities are subject to change. Work Environment The work environment described here is representative of those that an employee encounters while performing the essential functions of this job. Reasonable accommodation may be provided to enable individuals with qualified disabilities to perform the essential functions. The position is in the factory and involves sitting, standing, walking, lifting, manipulating materials for long periods of time throughout the day in an indoor environment that is organized and typically free of hazardous materials. Note: The above statements are not intended as an exhaustive list of all responsibilities, duties and skills required of personnel in this classification. Nothing in the job description restricts IPS Group, Inc. from the right to change, assign, or reassign duties and responsibilities at any time for any reason. Furthermore, they do not establish a contract for employment as this is an "At-Will Employer." It is the policy of IPS Group, Inc. not to discriminate against any applicant for employment, or any employee because of age, color, sex, disability, national origin, race, religion, sexual orientation, or veteran status. Benefits: 401(k) 401(k) matching Dental insurance Health insurance Life insurance Paid time off Vision insurance Job Type: Full-time Salary range: $22 - $27/hr. An Equal Opportunity Employer—M/F/D/V
Salary Range: $93,000 - $101,000 POSITION SUMMARY The Quality Engineer is responsible for driving process excellence and executing strategic quality initiatives. Reporting directly to the Quality Director, this role does not manage people but serves as the ultimate champion and owner of quality processes. The ideal candidate acts as a cross-functional conduit of quality—collaborating with co-manufacturers (co-mans), vendors, and internal teams during plant trials, managing non-conformances, and ensuring audit readiness. ESSENTIAL FUNCTIONS Reasonable Accommodations Statement To accomplish this job successfully, an individual must be able to perform, with or without reasonable accommodation, each essential function satisfactorily. Reasonable accommodations may be made to help enable qualified individuals with disabilities to perform the essential functions. Essential Function Statements Deviation Management: Review, investigate, and assess planned and unplanned process deviations; partner with teams to identify true root causes and implement robust corrective and preventive actions (CAPAs). Supplier Quality Investigations & SCARs: Issue, manage, and execute Supplier Corrective Action Reports (SCARs) for co-manufacturers and raw material/packaging vendors; perform diligent follow-ups to ensure timely containment, resolution, and compliance. Non-Conformance Tracking: Monitor, investigate, and follow up on Non-Conformance Reports (NCRs) from inception to final disposition, ensuring defective materials or products are properly segregated and tracked. SOP Training: Develop training materials and conduct regular employee training on Standard Operating Procedures (SOPs) to guarantee plant-wide alignment with regulatory guidelines and internal quality benchmarks. Plant & Packaging Trials: Serve as the on-the-floor quality conduit during plant trials and new packaging trials; provide real-time quality oversight, evaluate process capabilities, and document findings to ensure seamless scaling. Should be involved in new equipment or process validation in collaboration with R&D and Manufacturing Engineering counterparts. Audit Representation: Actively participate in, prepare documentation for, and support internal, third- party, and regulatory quality audits. Initiative Execution: Assist the Quality Director in rolling out corporate quality initiatives, continuous improvement projects, and data-driven quality programs across the organization. POSITION QUALIFICATIONS Competency Statement(s) Problem Solving & Root Cause Analysis: Proficient in structured problem-solving methodologies (e.g., 5 Whys, Fishbone diagrams, 8D) to resolve complex process issues. 7/2/26 Process Ownership & Autonomy: Demonstrated ability to manage, monitor, and optimize complex quality processes independently without requiring direct oversight of personnel. Collaboration & Influence: Exceptional interpersonal skills to act as a collaborative partner and quality conduit between internal operations, co-manufacturers, and external vendors. Detail-Oriented & Compliance-Driven: Uncompromising focus on documentation accuracy, regulatory standards, and meticulous record-keeping. Project Management: Ability to prioritize multiple moving parts—such as simultaneous plant trials, open NCRs, and supplier follow-ups—while meeting critical deadlines. SKILLS & ABILITIES Education: Bachelor's degree in Engineering, Quality Management, Food Science, Chemistry, or a related technical discipline is required. ASQ Certified Quality Engineer (CQE) or equivalent quality certification is highly desirable. Experience : 3–5 years of direct experience in a quality engineering or quality assurance role within a manufacturing environment. Proven experience working within regulated industries (e.g., dietary supplements, food manufacturing, pharmaceuticals, or medical devices). Hands-on experience managing vendor relationships, co-manufacturers, and executing SCAR/NCR workflows. Computer Skills: High proficiency with Quality Management Systems (QMS) and Enterprise Resource Planning (ERP) software (e.g., SAP). Advanced knowledge of Microsoft Office Suite (particularly Excel for data tracking, Word for SOP drafting, and PowerPoint for training delivery
How will you make an impact? The Lead Manufacturing Technician, based in San Clemente, CA will be responsible for the completion of the scheduled production and management of preventative maintenance. The Lead will ensure proper documentation (cGMP and GDP), open/close jobs in MRP system, and provide feedback and updates to Management and Engineering. This position will also prepare components, build assemblies, and bulk drug formulations. All activities will be performed with good documentation practices (GDP) in accordance with current good manufacturing practices (cGMPs) and quality system regulation (QSR) medical device good manufacturing practices (GMP) requirements. Additional tasks will include performing the following: Filing, capping, and crimping operations Packaging and labeling operations Sampling Visual inspections Documentation and data input into materials requirement planning (MRP), Batch Records (BRs), and Device History Record (DHR) Track clean room, environmental chambers, and equipment preventive maintenance (PMs) What will you do? Manage the operation schedule, project schedule, and adjusts the schedule and resources accordingly Supervise production technician(s) to optimize quality and output Ability to perform all activities outlined for a Manufacturing Technician as needed Verify all documentation is followed and completed accurately (cGMP, QSR, and GDP) Manages Oracle to open and close jobs Manages inventory requests and reconciliation for accuracy Revise documentation to ensure accuracy and compliance Communicate feedback to engineering on Non-Standard Build Requests, Validation builds, Clinical builds, etc. How will you get here? To be successful in this role, you will need to have the following: Industry (medical device, pharmaceutical, and/or biotechnology) and educational experience. 8 – 10 years’ experience with high school diploma 6 – 8 years’ experience with associate degree in science or engineering 4 - 6 years’ experience with bachelor’s degree in science or engineering It is highly desirable to have experience working in and maintaining a clean room in accordance with GDP, cGMPs, and QSR standards. #GKOSUS Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible. Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company focused on developing and commercializing novel therapies for the treatment of glaucoma, corneal disorders, and retinal diseases. Our mission at Glaukos is to truly transform vision by pioneering novel, dropless therapies that can meaningfully advance the standard of care and improve the lives of patients suffering from chronic, sight-threatening eye diseases. Innovation is at the core of everything we do, and we are resolute in our commitment to challenge conventional thinking with new treatment alternatives that are supported by real science, robust clinical evidence, and an unrelenting focus on patients. Our constant pursuit of game-changing technologies that disrupt legacy treatment paradigms is encapsulated in the Glaukos mantra “We’ll Go First,” which articulates our willingness to take chances, our determination to forge new ground, and our commitment to continuous improvement in all that we do. Our company completed an initial public offering in June of 2015, and our shares are traded on the New York Stock Exchange under the ticker symbol “GKOS”. Our global headquarters is in Aliso Viejo, California with additional locations in San Clemente, California, and Burlington, Massachusetts. Glaukos Corporation is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. All offers of employment are contingent upon the successful completion of a background check, including successfully passing a drug screen, based on the position and local regulations.
How will you make an impact? The Lead Manufacturing Technician, based in San Clemente, CA will be responsible for the completion of the scheduled production and management of preventative maintenance. The Lead will ensure proper documentation (cGMP and GDP), open/close jobs in MRP system, and provide feedback and updates to Management and Engineering. This position will also prepare components, build assemblies, and bulk drug formulations. All activities will be performed with good documentation practices (GDP) in accordance with current good manufacturing practices (cGMPs) and quality system regulation (QSR) medical device good manufacturing practices (GMP) requirements. Additional tasks will include performing the following: Filing, capping, and crimping operations Packaging and labeling operations Sampling Visual inspections Documentation and data input into materials requirement planning (MRP), Batch Records (BRs), and Device History Record (DHR) Track clean room, environmental chambers, and equipment preventive maintenance (PMs) What will you do? Manage the operation schedule, project schedule, and adjusts the schedule and resources accordingly Supervise production technician(s) to optimize quality and output Ability to perform all activities outlined for a Manufacturing Technician as needed Verify all documentation is followed and completed accurately (cGMP, QSR, and GDP) Manages Oracle to open and close jobs Manages inventory requests and reconciliation for accuracy Revise documentation to ensure accuracy and compliance Communicate feedback to engineering on Non-Standard Build Requests, Validation builds, Clinical builds, etc. How will you get here? To be successful in this role, you will need to have the following: Industry (medical device, pharmaceutical, and/or biotechnology) and educational experience. 8 – 10 years’ experience with high school diploma 6 – 8 years’ experience with associate degree in science or engineering 4 - 6 years’ experience with bachelor’s degree in science or engineering It is highly desirable to have experience working in and maintaining a clean room in accordance with GDP, cGMPs, and QSR standards. #GKOSUS Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible. Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company focused on developing and commercializing novel therapies for the treatment of glaucoma, corneal disorders, and retinal diseases. Our mission at Glaukos is to truly transform vision by pioneering novel, dropless therapies that can meaningfully advance the standard of care and improve the lives of patients suffering from chronic, sight-threatening eye diseases. Innovation is at the core of everything we do, and we are resolute in our commitment to challenge conventional thinking with new treatment alternatives that are supported by real science, robust clinical evidence, and an unrelenting focus on patients. Our constant pursuit of game-changing technologies that disrupt legacy treatment paradigms is encapsulated in the Glaukos mantra “We’ll Go First,” which articulates our willingness to take chances, our determination to forge new ground, and our commitment to continuous improvement in all that we do. Our company completed an initial public offering in June of 2015, and our shares are traded on the New York Stock Exchange under the ticker symbol “GKOS”. Our global headquarters is in Aliso Viejo, California with additional locations in San Clemente, California, and Burlington, Massachusetts. Glaukos Corporation is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. All offers of employment are contingent upon the successful completion of a background check, including successfully passing a drug screen, based on the position and local regulations.
General Atomics Aeronautical Systems, Inc. (GA-ASI), an affiliate of General Atomics, is a world leader in proven, reliable remotely piloted aircraft and tactical reconnaissance radars, as well as advanced high-resolution surveillance systems. We are looking for a First Shift Electrical Quality Inspector to join our Poway, CA team. Under general direction, this position is responsible for receiving, in-process and final inspections of electronic/electrical cables, wiring, printed circuit boards (PCB), printed wiring assembly components, assemblies, and system installations in accordance with engineering requirements using associated drawing, schematics and parts lists. Maintains proper records of tests and inspections and configuration of systems under tests. Uses hand tools, small power tools, and various measuring and testing devices in performing job duties. Monitors and verifies quality in accordance with statistical process or other control procedures, and may perform source inspections. May recommend and develop inspection procedures. May act as a lead while providing guidance and direction to less experienced staff. DUTIES AND RESPONSIBILITIES: Visually inspects electronic circuit boards, cables, and assemblies. Performs in-process and final inspection or tests of major components, subsystems and systems. Verifies proper records of tests and inspections. Performs inspection of installed equipment into control shelters. Performs source inspections in supplier facilities, in-house inspection, and follow up. Interfaces with and assists customers' inspectors during their on-site source inspection. Interface with manufacturing, quality engineering, software engineering, and procurement for corrective actions and inspection criteria. May recommend and develop inspection procedures for all electrical product types when requested. May act as the inspection leader when requested. Provides guidance, training, and direction to other staff. 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. Other duties as assigned or required. 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 high school diploma, technical trade school training or equivalent and five or more years experience in electronics inspection and testing, preferred experience with printed circuit board assembly, cable assembly and electromechanical assembly. Familiar with IPC 610 Standards and soldering inspection. AOI programming skills preferred. Must be customer focused and possess: Ability to read and interpret a variety of complex engineering drawings, specifications, work instructions and manuals. Complete knowledge of inspection equipment Basic knowledge of IPC standards for acceptability of electronic assemblies and MIL standards for soldering and assembly requirements. Ability to perform complex mathematical calculations. Skills to maintain the flow of work within the unit. Good interpersonal skills and written communication skills to interface with employees and to identify, document and resolve non-compliance issues. Basic computer skills. The ability to work both independently and in a team environment is essential as is the ability to work extended hours as required. Ability to obtain and maintain a DoD security clearance is required. Job Category Quality Experience Level Mid-Level (3-7 years) Workstyle Onsite Full-Time/Part-Time Full-Time Hourly Pay Range Low 56,180 Pay Range High 83,518 Travel Percentage Required 0% - 25% Relocation Assistance Provided? No US Citizenship Required? Yes Clearance Required? No Search Jobs at | General Atomics and Affiliated Companies
General Atomics Aeronautical Systems, Inc. (GA-ASI), an affiliate of General Atomics, is a world leader in proven, reliable remotely piloted aircraft and tactical reconnaissance radars, as well as advanced high-resolution surveillance systems. Under general supervision and with intermittent review, this position supports program engineering and manufacturing by serving as a liaison between the engineering and manufacturing departments. Reviews and monitors program development progress and expedites critical path components and processes to maintain schedule. Evaluates and resolves engineering related production problems related to manufacturing, design, quality and material engineering. Maintains physical control of program assets. May negotiate lead times with suppliers and manage schedules for timely delivery. This position involves the exercise of independent judgment and discretion about matters of significance. DUTIES AND RESPONSIBILITIES: Identifies issues in engineering and manufacturing and utilizes resources for resolution. Reviews engineering specifications and drawings. Confers across functional areas to provide and obtain technical information. Coordinates delivery schedule of raw materials and sub-assemblies from contractors. Monitors and reports on progress of manufactured parts required for project. Assists in and/or monitors the design and development process by coordinating between various engineering and manufacturing departments. Coordinates engineering support for manufacturing requirements and ensures schedule parity. Maintains project specific prototype inventory control. Coordinates Manufacturing Service Request activities by resolving priority schedule conflicts. Monitors and analyzes open engineering issues affecting sales orders. Alerts planning department to open engineering issues that may affect manufacturing. Alerts engineering departments to sales order activity that may affect outstanding work. May conduct periodic program engineering/manufacturing planning meetings. Maintains the strict confidentiality of sensitive information. Responsible for observing all laws, regulations and other applicable obligations wherever and whenever business is conducted on behalf of the Company. Expected to maintain a productive and safe working environment in accordance with established operating procedures and practices. Additional Functions: Other duties as assigned or required. 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 bachelor's degree in business, planning or a related discipline as well as three or more years of progressive experience in planning, coordinating and scheduling production operations. May substitute equivalent experience in lieu of education. Must have a general knowledge of production and engineering support principles and concepts and a general understanding of practices, techniques, and standards. Must be customer focused and possess: the ability to use independent analysis and judgment in developing solutions to a variety of non-routine problems of moderate scope and complexity excellent verbal and written communications and presentations skills to accurately document and report findings to a variety of audiences excellent interpersonal skills to influence and guide employees, managers and external parties excellent computer skills Ability to work independently or in a team environment is essential as is the ability to travel as required. Ability to obtain and maintain a DoD Security Clearance is required. Job Category Material and Production Control Experience Level Mid-Level (3-7 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? No US Citizenship Required? Yes Clearance Required? Desired Clearance Level Secret Search Jobs at | General Atomics and Affiliated Companies
General Atomics Aeronautical Systems, Inc. (GA-ASI), an affiliate of General Atomics, is a world leader in proven, reliable remotely piloted aircraft and tactical reconnaissance radars, as well as advanced high-resolution surveillance systems. The Quality Engineer serves as the Process Owner for the Internal Manufacturing Process Audit Program and is responsible for maintaining the audit process, procedures, work instructions, and associated documentation to ensure compliance with company and industry quality requirements. This role develops and delivers instructor-led training for internal process auditors, evaluates auditor competency through supervised audits, and formally qualifies new auditors based on established performance criteria. The Quality Engineer develops and manages the annual risk-based audit schedule, conducts process audits, monitors corrective actions, and drives continuous improvement of the audit program. The Quality Engineer also provides regular reporting on audit program performance, including schedule compliance, audit metrics, and corrective action status to leadership. Additionally, the role supports organizational readiness for special process compliance by conducting gap assessments against Nadcap requirements, collaborating with PRI/Nadcap on Critical Process Auditor training initiatives, and providing technical guidance and recommendations to senior management to strengthen manufacturing process compliance and audit effectiveness DUTIES AND RESPONSIBILITES: Identifies and recommends design or manufacturing changes and enhancements. Determines technical objectives for quality assurance as well as approaches to completing projects. Creates or recommends design, dimensional or manufacturing process changes to improve products and reduce costs. Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment. Participates in functional testing and/or inspection of equipment and systems. Audits quality systems for deficiency identification and correction. Implements solutions to complex problems occurring internally and at vendor facilities. May prepare statistical analysis reports, specifications and other technical documents. Interprets and adapts quality standards and government regulations. Acts as company contact with suppliers, customers and regulatory personnel to resolve quality issues. Delivers technical presentations. Provides project direction to other staff members. 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. Other duties as assigned or required. 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 bachelor’s or master’s degree in engineering or related discipline and six or more years of related experience with a bachelor’s degree or four or more years with a master’s degree. May substitute equivalent experience in lieu of education. Must be able to apply a detailed understanding of inspection methods and have strong knowledge of computer operations and applications. Must have a strong knowledge of concepts, techniques, and methods in a particular field of specialization. Must have the analytical ability required to develop creative solutions to complex quality issues and the skills required to present those solutions to internal and external contacts. Must be detail-oriented to accurately prepare statistical reports and technical documents in support of company objectives. Must have strong leadership skills to direct staff members and ensure project costs and schedules are maintained while representing the organization on technical quality assurance issues. Able to deliver effective technical presentations and work extended hours as required. Job Category Quality Experience Level Mid-Level (3-7 years) Workstyle Onsite Full-Time/Part-Time Full-Time Salary Pay Range Low 89,180 Pay Range High 155,825 Travel Percentage Required 0% - 25% Relocation Assistance Provided? No US Citizenship Required? Yes Clearance Required? No Search Jobs at | General Atomics and Affiliated Companies
*Job Overview* Garek Enterprises dba Alphacoat Finishing are seeking a dedicated and detail oriented Plater to join our manufacturing team in a dynamic industrial environment. As a Plater, you will play a vital role in preparing, coating, and finishing metal components to meet rigorous quality standards. Your expertise in surface preparation, coating application, and fabrication will ensure that our products are durable, visually appealing, and ready for assembly or installation. You must be knowledgeable of plating processes on aluminum, including electroless nickel, gold etc. The ideal candidate should also know how to run their own calculations ASF to determine the thickness of the electroplated layer deposited on the object, determined by the time of plating, and the amount of available metal ions in the bath relative to current density. If you are looking to work for a growing and empowering company, and you enjoy working in a fast-paced setting, then come and join our team at Alphacoat Finishing, a proud NADCAP certified employer. *Duties* * Prepare metal components by cleaning, degreasing, rinsing, masking, and performing other required surface preparation processes. * Rack and unrack parts for anodizing, plating, and related finishing operations. * Operate plating tanks, anodizing equipment, and related production equipment in accordance with established procedures. * Monitor and maintain plating process parameters, including bath chemistry, temperature, voltage, current density (ASF), and processing times. * Calculate plating requirements, including current density and plating thickness, to meet customer and engineering specifications. * Inspect completed parts for coating thickness, appearance, adhesion, color, and overall quality. * Use measuring and testing equipment to verify compliance with specifications. * Maintain accurate production, inspection, and quality records. * Perform routine equipment inspections and basic preventive maintenance. * Maintain a clean, organized, and safe work area following 5S and company housekeeping standards. * Safely handle chemicals and hazardous materials in accordance with company procedures, Safety Data Sheets (SDS), and applicable environmental regulations. * Wear required personal protective equipment (PPE) and follow all company safety policies. * Assist with other production-related duties as assigned. *Required Qualifications* * High school diploma or equivalent, or equivalent combination of education and experience. * Knowledge of metal finishing or plating processes. * Ability to read and interpret work instructions, engineering drawings, and specifications. * Basic math skills, including the ability to perform calculations related to plating operations. * Ability to accurately complete production and quality documentation. * Ability to work independently and collaboratively in a team environment. * Commitment to workplace safety and quality standards. *Preferred Qualifications:* * Three (3) or more years of experience in electroplating, anodizing, or metal finishing. * Experience with aluminum plating processes, including electroless nickel, gold, silver, or other specialty finishes. * Experience calculating current density (ASF), plating thickness, and plating times. * Experience working in an AS9100, NADCAP, ISO, aerospace, or other highly regulated manufacturing environment. * Experience with Lean Manufacturing or continuous improvement initiatives. *Physical Requirements:* * Stand and walk for extended periods during the workday. * Frequently use hands and arms to handle parts, tools, and equipment. * Lift, carry, push, or pull materials weighing up to *50 pounds*, with or without reasonable accommodation. * Frequently bend, stoop, reach, kneel, and twist. * Wear required personal protective equipment, including gloves, eye protection, face shields, aprons, and respiratory protection when required. * Work around chemicals, plating solutions, moving machinery, and production equipment while following established safety procedures. *Work Environment:* * Manufacturing and industrial environment. * Exposure to noise, chemicals, heat, humidity, and varying temperatures. * Use of personal protective equipment is required. * Overtime and weekend work may be required based on business needs. *Equal Employment Opportunity Statement:* Garek Enterprises dba Alphacoat Finishing is an Equal Opportunity Employer. We are committed to creating an inclusive workplace and making employment decisions based on qualifications, merit, and business needs. Qualified applicants will receive consideration for employment without regard to race, color, religion, creed, sex, pregnancy, childbirth or related medical conditions, gender, gender identity, gender expression, sexual orientation, national origin, ancestry, citizenship, age, physical or mental disability, medical condition, genetic information, marital status, military or veteran status, reproductive health decision-making, or any other status protected by applicable federal, California, or local law. Pay: $18.27 - $22.97 per hour Benefits: * Dental insurance * Health insurance * Paid time off * Vision insurance Work Location: In person
Position Summary To safely and effectively run equipment related to HPP/Bottling/Packaging and Pack Out. Operator 2 will demonstrate the ability to run all machines within one department e.g. All machines associated with the Bottling department. Schedule Wednesday-Sunday, 5:00 AM - 1:30 PM Essential Duties and Responsibilities Including but not limited to: To run all machines safely and effectively within your department including but not limited to: Fillers, HPP’s, Labelers, Case Packers, Bundlers, Sleevers, Palletizers, etc. Plan to ensure you have the correct materials, equipment, and ingredients for each day. Communicate with your Shift Lead/Supervisor/Manager to advise of any issues/concerns. Communicate well with other employees. Follow all OSHA rules regarding safe machine operation. Keep your work area clean, organized, and safe always. Keep your work area clean, organized, and safe always Adhere to SOP, SSOP, GMP, and HACCP guidelines when in the plant. Ability to understand and follow verbal and written instructions related to safety, equipment operation, and daily work assignments. Regular and reliable attendance. Department Machine Bottling Depal GRX Unscrambler F4 F5 Shot Filler Carbonated Filler HPP HPP 1 - 2 HPP 3 - 4 Trines Sleever Packaging/Pack Out Bundlers (Dimac, KHS, SMI) Drop Packer Unscrambler Non-Essential Job Duties May perform similar and incidental duties as required. Job Qualifications Experience: 2+ years’ experience working in a manufacturing/warehouse environment Skills & Abilities Must have strong leadership skills. Problem solver skills Be able to work independently with moderate supervision Ability to think ahead. Responsibilities may require an adjusted work schedule, overtime, evening/weekend hours in order to meet deadlines. Ability to work cross-functional with other departments. Attention to detail and a commitment to maintaining high product quality. Flexibility to work in a fast-paced and dynamic production environment. Language Skills Ability to communicate, read, listen, and understand English. Bilingual is a plus. Working Environment Regular exposure to wet, cold manufacturing environments (temperatures as low as 35°F) Occasional exposure to dry warehouse spaces or freezer conditions (down to -10°F) Frequent exposure to high noise levels (above 85 dBA) Requires use of PPE including safety glasses, ear protection, gloves, and steel-toed footwear Physical Requirements Ability to stand and walk for the full duration of the shift Must be able to frequently lift/move hoses, equipment, and chemical containers weighing up to 50 lbs. Ability to push/pull up to 100 lbs. with continuous motion Must be able to bend, kneel, squat, climb stairs/ladders, and reach overhead regularly Must have sufficient hand strength and manual dexterity to operate sanitation tools and machinery Must be able to pass a pre-employment physical Compensation and Benefits Come thrive at Suja Life! We offer a competitive benefits package, including: Pay rates starting at $18.00-20.00 an 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 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. Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.
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 At Argonaut Manufacturing Services we value our employees and are proud to offer a comprehensive benefits package designed to support your well-being and financial future. Eligible employees enjoy: Medical, Dental, and Vision Insurance Company-Paid Life Insurance (1x Annual Salary) Voluntary Life Insurance Options Short-Term and Long-Term Disability Insurance Flexible Spending Account (FSA)Health Savings Account (HSA) 401(k) Retirement Plan with Company Matching 10 Days of Paid Time Off (PTO) 10 Paid Holidays Annually The pay range for this position is $36.00 - $40.00 per hour. Actual compensation will be based on factors such as location, skills, education, experience, and other relevant qualifications. Position Overview The Quality Systems Specialist will identify, document, and resolve quality issues, deviations, and non-conformances related to sterile drug product manufacturing operations. They will perform root cause analysis, assess risks, and determine Corrective and Preventive Actions (CAPA) to ensure strict compliance with FDA and cGMP standards. The Quality System Specialist will also participate in internal and external audits (client and supplier) and facilitate any corrective actions identified. The role is a key Quality contact at Argonaut and requires the ability to independently manage timelines and effectively communicate with team members, cross-functional stakeholders, and clients while helping to maintain site Quality Systems in a state of inspection readiness. This role is an on-site position Monday - Friday 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. Flexible start time between 7:00 am - 9:00 am with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance. Responsibilities and Duties Lead in-depth investigations into batch deviations, out-of-specifications, and product failures Oversee the analysis of customer complaints, review production history records, and interview personnel. Ensure that investigation documentation and manufacturing processes align with FDA, cGMP, ISO, and other relevant industry standards. Analyze and present quality data via metrics and reports to inform management decision-making. Assist other departments to successfully investigate and documents investigations. Complete accurate and thorough historical searches within quality system to identify similar events and determine trends. Lead quality training sessions as needed Participate in process improvements associated with investigations Support visual inspection of finished product Lead internal audit program and assist in hosting and responding to client and regulatory audits Other duties may be assigned Requirements and Qualifications Bachelor's degree in Life Sciences (Biology, Chemistry), Engineering, or a closely related field is strongly preferred Minimum four (4) years of experience in pharmaceutical or biotech manufacturing, heavily focused on GMP (Good Manufacturing Practices) and performing investigations. Strong analytical mindset, root-cause analysis skills, exceptional technical writing, and a solid working knowledge of FDA guidelines and ICH requirements. Must have a high attention to detail, and excellent communication skills Must be able to effectively communicate within the department and cross-functionally with other divisions Experience with MasterControl and NetSuite a plus Superior attention to detail, organizational skills, and the ability to multi-task in a time-line driven environment Ability to make decisions regarding quality of product and material Strong initiative and willingness to take ownership and drive projects to completion 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.
Work Your Magic with us! Start your next chapter and join EMD Electronics. Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. Everything we do in EMD Electronics is to help us deliver on our purpose of being the company behind the companies, advancing digital living. We are dedicated to being the trusted supplier of high-tech materials, services and specialty chemicals for the electronics, automotive and cosmetics industries. We foster a global collaborative organization made up of individuals who have the passion to win, obsess about the customer, are relentlessly curious and act with urgency. Together, we push the boundaries of science to make more possible for our customers. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Location: The US Customer Quality Manager, Semiconductor Materials is a remote role in the US preferably within one hour proximity to an EMD Electronics site (Carlsbad, CA, Sunnyvale, CA, Hillsboro, OR, Tempe, AZ, Austin, TX, Allentown, PA, Sheboygan Falls, WI). Approximately 10% domestic and international travel is required to meet business needs. Your Role: You will lead the next generation of semiconductor materials and equipment that power the digital age. This role blends technical leadership with strategic vision to drive innovations that improve performance, yield, and reliability in advanced manufacturing. You will collaborate with cross-functional teams and external partners to translate breakthroughs into scalable solutions. Together, you’ll shape the roadmap for future devices, systems, and applications that enable connectivity and intelligent technologies. Your role will be customer quality focused: Customer Quality in the US: Lead and manage successful completion of US based customers’ quality initiatives with a global and diverse workforce. Serve as the technical communication bridge between EMD sites globally and US customers to understand their needs and where EMD will help them advance their technology forward. This may include developing tactical and strategic roadmap items to address immediate and future needs. Own customer engagement between sites and customers for quality issues: enable site capabilities while ensuring sites meet developed rubrics and customer expectations. Collaborate with account team to deliver world class results to customers. Lead customer taskforces to ensure customer trust in EMD technical aptitude. Serve as the voice of US customers to global sites and supplier-quality teams for semiconductor materials, developing strategic, long-term relationships with regional customers to establish trust and position the company as a preferred partner. Foster and develop key broader industry relationships to enhance EMD Electronics' quality brand image and capabilities. Provide key input to technical and commercial risk analysis of new product and change implementation by participating in site change management review; provide support for customer PCN submission and approval. Review, approve, and communicate customer OCAP (Out of Control Action Plan) report provided by production site for product CoA OOC (out of control), OOB (out of boundary), OOS (out of specification), HH/HL (Historical high/Historical low) cases. Act as the key stakeholder in troubleshooting and problem solving of customer quality issues; Lead customer task forces, review and approve 8D report with high power factor corrective and preventive actions (CAPA). Develop automated visualizations and data dashboards to update status and key success indicators. Lead the success of semiconductor quality with customers in Korea. Who You Are Minimum Qualifications: Bachelor's degree in Engineering, Chemistry, Physics, Materials Science, or another technical discipline. 5+ yrs in chemical manufacturing, process engineering, control engineering, analytical chemistry, or semiconductor fabrication experience. 5+ yrs of successful customer engagement (semiconductor customer preferred). Preferred Qualifications: 5+ yrs of process or integration or yield engineering experience in semiconductor fabrication, preferably in Thin Films or SOD processes. Moderate to advanced statistical knowledge (SPC, t-test, ANOVA, single and multivariate statistical modeling). Proficient with data science/statistical software including JMP, Palantir Foundry, Python, and/or visualization tools such as Tableau. Excellent oral and written communication skills. Experience with process improvement, data automation, and data digitization. Demonstrated ability to remain objective with co-workers and work collaboratively with multiple internal stakeholders. Established success in contributing to the advancement of projects, project teams, and process improvements. In addition, Excellent time management and organizational skills with the ability to handle multiple activities and projects. Exhibited experience with Lean and/or Six Sigma projects or in data-driven process optimization projects. Experience in quality tools for problem solving (5Whys, segmentation, Model Based Problem Solving), FMEAs, continuous improvement (CI) activities, management of change (MOC), and document control systems. Ability to work with people from various backgrounds/cultures. Experience with ISO 9001 Quality Management Systems ISO9001 or IATF 16949 Internal Auditor Certification SAP experience Pay range for this position: $160,000 - $220,000 The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
*About Tensor ID* Tensor ID is a fast-growing machine vision, automation, and industrial inspection company specializing in advanced vision systems for manufacturing, packaging, distribution, and quality control environments. We design and support custom inspection systems using cameras, lighting, PLCs, encoders, barcode readers, OCR, AI, deep learning, and automation controls. Our systems help customers inspect labels, barcodes, print quality, cosmetic defects, product presence, package damage, OCR/OCV, traceability data, and complex production-line issues in real time. We work with major manufacturers, food and beverage companies, medical device companies, logistics operations, and OEM partners. We are looking for a driven Application Engineer who can support customer projects from concept through installation, testing, training, and long-term support. *Position Overview* The Application Engineer will work directly with customers, sales, engineering, and internal project teams to help design, test, configure, install, and support machine vision and automation systems. This role requires a hands-on technical person who enjoys solving problems, working with customers, and learning new technologies. This is not a desk-only role. The right person must be comfortable working in production environments, troubleshooting live equipment, communicating clearly with customers, and helping bring systems online under real-world conditions. *Key Responsibilities* * Support machine vision and automation projects from initial application review through final installation and customer acceptance. * Assist with camera, lens, lighting, barcode reader, encoder, PLC, and industrial PC configuration. * Test and validate inspection applications using vision software, AI tools, OCR, barcode grading, measurement tools, and defect detection methods. * Work with customers to understand inspection requirements, pass/fail criteria, production challenges, and system expectations. * Help prepare demonstrations, sample evaluations, feasibility testing, and application reports. * Support installation, startup, troubleshooting, SAT, training, and post-installation service. * Work with PLCs, I/O, sensors, encoders, reject devices, line triggers, and production-line timing. * Troubleshoot electrical, mechanical, networking, software, and communication issues. * Document project settings, wiring notes, inspection criteria, customer requirements, and support findings. * Communicate clearly with customers, vendors, and internal teams. * Support sales and engineering by identifying technical risks, system requirements, and recommended solutions. * Travel to customer sites as needed for installations, service, training, and project support. *Ideal Candidate* The ideal candidate is technical, hands-on, organized, and customer-focused. You do not need to know everything on day one, but you must be willing to learn quickly, take ownership, and work through problems until they are solved. You should be comfortable around industrial equipment, production lines, electrical panels, computers, cameras, sensors, and automation systems. You should also be able to explain technical information clearly to both engineers and non-technical customers. *Required Qualifications* * Experience in machine vision, automation, controls, electrical systems, industrial equipment, manufacturing support, or related technical fields. * Strong troubleshooting skills with the ability to diagnose problems logically. * Comfortable working with Windows PCs, industrial software, networking, IP addresses, Ethernet devices, and basic computer configuration. * Ability to read and understand basic electrical drawings, wiring diagrams, I/O layouts, and system documentation. * Strong communication skills with customers and internal teams. * Ability to work independently and as part of a project team. * Willingness to travel to customer sites as needed. * Professional attitude, strong work ethic, and attention to detail. *Preferred Experience* Experience with any of the following is a strong plus: * Machine vision systems * Industrial cameras, lenses, and lighting * Barcode readers and barcode grading * OCR/OCV inspection * AI, deep learning, or machine learning inspection tools * PLCs, I/O, sensors, encoders, and reject systems * Allen-Bradley, Omron, Siemens, or similar control platforms * Zebra, Omron, Teledyne DALSA, Cognex, Keyence, Matrox, or similar vision products * C#, Python, SQL, scripting, or software troubleshooting * Industrial networking, Ethernet/IP, TCP/IP, FTP, and device communication * Food, beverage, medical device, packaging, logistics, or manufacturing environments *What We Are Looking For* We are looking for someone who wants to grow with the company and become a key technical contributor. This position is a strong fit for someone who enjoys being hands-on, solving challenging problems, working directly with customers, and being part of a growing company in the machine vision and automation space. This role has room for advancement as Tensor ID continues to expand its machine vision platforms, AI inspection tools, automation systems, and customer base. *Why Join Tensor ID* * Work on real-world machine vision and automation projects. * Be part of a growing company with major expansion opportunities. * Gain hands-on experience with advanced inspection systems, AI vision tools, industrial automation, and customer applications. * Work directly with experienced machine vision professionals. * Have an impact on projects from concept through installation. * Opportunity to grow into a senior technical, project, or leadership role. *Compensation* Compensation will be based on experience, technical background, and overall fit. Benefits and additional details will be discussed during the interview process. *How to Apply* Please submit your resume and a brief summary of your experience with machine vision, automation, controls, manufacturing equipment, electrical systems, or related technical work. Tensor ID is looking for someone who can learn, take ownership, solve problems, and help deliver high-quality systems to our customers. Pay: $80,000.00 - $110,000.00 per year Benefits: * Health insurance * Paid time off Work Location: In person