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WESTPAK exists to make lives better. From the products we test that are used by global consumers, to the people and communities we invest in, our purpose is to improve the lives of those around us. For over 40 years, WESTPAK has been a trusted testing partner for a diverse industry. Sustaining that level of consistency requires a core ingredient, our great people. From the tenured employees who value the lasting bonds and share their wealth of knowledge, to our new employees who bring in new perspectives and opportunities; we continue to evolve our employee-owned company with stewardship and integrity while continuing to make lives better. It is the responsibility of every WESTPAK employee to contribute to a positive work environment through cooperative and professional interactions with co-workers, customers, and vendors. We are seeking a Packaging Test Engineer I - EIT who will conduct and support package testing. The ideal candidate will exhibit strong personal attributes and behaviors that will be instrumental for growth as a Packaging Test Engineer. This is a very hands-on active role with physical demands to support client testing. We offer a competitive compensation package that includes ESOP (Employee Stock Ownership Plan) shares, 401k match, health benefits, various supplemental health packages, and pet insurance for your furry loved ones. A Packaging Test Engineer I will: Independently conduct package testing defined by but not limited to ASTM, and ISTA standards, customer requirements, and WESTPAK’s Quality Management System. Examples of test inputs include transit, sterile barrier package integrity, and shelf-life testing. Perform testing duties within the designated workday hours according to WESTPAK requirements to ensure customer objectives are met through proactive communication, documentation, and customer service. Analyze and interpret data to identify deviations and provide client insight. Ensure project accuracy and quality through document control, standard operating procedures (SOPs), and auditing. Maintain responsive customer communication in email and in person regarding testing services provided, test status, updates, and results. Maintain WESTPAK 5S and various site standards and expectations. Requirements for Eligibility B.S. degree in Packaging or packaging emphasis, Mechanical or Industrial Engineering, or equivalent technical education degree. 2-5 years of working laboratory experience in conducting product and package testing is preferred. Ability to read and interpret documents such as protocols, industry specifications (ASTM and ISTA), and procedures. Understanding packaging fundamentals. Possess a strong work ethic and a high level of professionalism. Proficient in Microsoft Office suite and general computer literacy. Math skills: Intermediate to advanced algebra, statistics and geometry. Personal / Professional Attributes Fast learner and ability to communicate clearly Demonstrate strong accountability and integrity High focus on customer service, plus be willing to go above and beyond to wow the customer Organized and impeccable follow-through skills Work collaboratively with colleagues Able to create innovative solutions to complex problems The above statements are intended to describe the general nature and level of the work being performed by the employee assigned to this position. There are no exhaustive lists of all duties and responsibilities, knowledge, skills, abilities, physical job demand, and working conditions associated with this position. The anticipated salary range for this position is $32-34 per hour depending on experience with company-wide bonus incentives and Employee Stock Ownership Participation. Principals only - We are not accepting any resumes or support from outside vendors. Please refrain from unsolicited marketing for the role. The pay range for this role is: 32 - 34 USD per hour(San Diego)
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: The GDP Clerk is responsible for daily batch record review, reconciliations & job receipts in SYSPRO. Essential Duties and Responsibilities: • Batch record review (daily): • Review PBR for GDP (Good Documentation Practices). • Verify all raw material used on the job Syspro and make any necessary transactions. • Reconcile the gelatin used on the job to the gelatin tags attached to the PBR. • Creation of job receipt in SYSPRO and submission of PBR (Production Batch Record) to QA. • Work with Operations to correct all documentation errors prior to release to QA. • Reconcile the gelatin jobs to the bulk. • In collaboration with the Production lead, review and reconcile gelatin batch records. • Apply Encapsulation Fee to all jobs on a daily basis. • Update Encapsulation Fee report on a daily basis. • Initiate low yield NCR's. • Adherence to HACCP and Food Defense. Qualifications: • Good communication skills both written and verbal • Ability to set priorities, be flexible, multi-task, and meet deadlines • Ability to develop and maintain professional relationships with internal and external stakeholders. • Experience working with ERP systems and SYSPRO experience preferred. • Working knowledge of cGMPs and FDA regulations • Highly organized and detail-oriented with the ability to work effectively in a fast-paced work environment. Education/Experience: • High School Diploma or GED equivalent. • Minimum of 3 years relevant work experience. 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. Physical demands require sitting for extended periods of time, walking, bending, reaching, carrying, and occasionally lifting and/or moving objects up to 25 pounds. Specific vision abilities required by this job include Close vision, Peripheral vision, and the ability to adjust focus. While performing the duties of this job, the employee is occasionally required to use hands to finger, handle, or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl and talk or hear. CAPTEK is an equal employment opportunity employer. In order to provide equal opportunities to all individuals, employment decisions will be based on merit, qualifications, and abilities, not on any mental or physical disability. We comply with the law regarding reasonable accommodation for disabled employees and applicants. We do not discriminate on the basis of actual or perceived race, color, national origin, ancestry, sex (which includes pregnancy, childbirth, breastfeeding and medical conditions related to pregnancy, childbirth or breastfeeding), reproductive health decisions, gender, gender identity, gender expression, religious creed, disability (mental and physical) including HIV and AIDS, medical condition (cancer and genetic characteristics ), genetic information, age, marital status, sexual orientation, military and veteran status, or any other characteristic protected by federal, state or local law. Our management team is dedicated to this policy with respect to recruitment, hiring, placement, promotion, transfer, training, compensation, benefits, employee activities and general treatment during employment. Thank you for your interest in joining the CAPTEK team. You will be contacted shortly if your application is selected.
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. With limited supervision, this position is responsible for supporting engineering and manufacturing as a liaison to expedite the design and development process. Evaluates and resolves complex engineering related production problems related to manufacturing, design, quality and material engineering. Serves as an external spokesperson through correspondence with vendors and subcontractors to ensure delivery dates and company objectives are met. Exercises considerable latitude in determining objectives and approaches to assignments and develops solutions to complex problems. This position involves the exercise of independent judgment and discretion about matters of significance. JOB DUTIES & RESPONSIBILITIES: Ensures parts and purchase requisitions are processed through the system in a timely manner. Ensures delivery dates are met by maintaining frequent contact with all critical subcontractors and vendors. Analyzes engineering specifications and drawings. Confers across functional areas to provide and obtain technical information. Coordinates and monitors the design and development process by making periodic visits to various departments such as manufacturing shops, quality assurance, sales, MRB cribs, planning, purchasing, manufacturing engineering and electrical engineering. Coordinates engineering priorities for manufacturing issues, and ensures schedule parity. Advises management of the status of work in progress and identifies potential production problems. Ensures rapid disposition of engineering holds and lift orders. Coordinates Manufacturing Service Request activities by resolving priority schedule conflicts among engineering departments due to shop capacity limitations and resolving shop capacity issues with manufacturing and planning. Reviews and recommends resolutions for open engineering issues affecting sales orders. Alerts planning department to open engineering issues that may affect manufacturing. Alerts engineering departments to sales order activity which may affect outstanding work. May function in an advisory or leadership role and provide direction and guidance to less experienced staff. Maintains the strict confidentiality of sensitive information. 11.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. 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 or master's degree in business, planning, or a related discipline and ten or more years progressive experience in planning, coordinating, and scheduling production operations with a bachelor's degree or eight or more years experience with a master's degree. Equivalent professional experience may be substituted in lieu of education. Must demonstrate an extensive understanding of planning and production operation theories, concepts and principles and experience demonstrating a broad application of those concepts. Must possess leadership skills including organizing, scheduling, conducting, and coordinating work assignments to meet project milestones or established completion dates. Must possess: Ability to identify issues, analyze and interpret data and develop innovative solutions to a variety of complex problems. Excellent analytical, verbal and written communication skills to accurately document, report, and present findings. Excellent interpersonal skills to influence and guide others. Ability to contribute to the development of new processes or systems and communicate new concepts. Excellent computer skills. The ability to work independently or in a team environment is essential as is the ability to work extended hours and travel as required. Job Category Contracts/Sub Contracts/Purchasing Experience Level Senior (8+ 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
Overview Join our dynamic team in Carlsbad, CA, as a General Production team member! We are looking for motivated individuals who thrive in a fast-paced environment and are eager to contribute to our production goals. In this role, you'll be an essential part of our operations, ensuring that our products meet the highest standards of quality and efficiency. If you're ready to roll up your sleeves and make a difference, we want to hear from you! Responsibilities Assist in the setup and operation of production machinery and equipment. Monitor production processes to ensure quality standards are met. Perform routine maintenance and troubleshooting on production equipment. Package and label finished products for shipment. Maintain a clean and organized work area to promote safety and efficiency. Collaborate with team members to meet daily production targets. Follow all safety protocols and guidelines to ensure a safe working environment. Qualifications High school diploma or equivalent preferred. Previous experience in a production or manufacturing environment is a plus. Ability to work in a fast-paced environment and adapt to changing priorities. Strong attention to detail and commitment to quality. Excellent communication and teamwork skills. Basic mechanical aptitude and problem-solving skills. Willingness to work flexible hours, including overtime if needed.
Overview Join our dynamic team in Carlsbad, CA, as a Production Operator! In this role, you will play a crucial part in our manufacturing process, ensuring that our products meet the highest quality standards. We’re looking for someone who is detail-oriented, enjoys working in a fast-paced environment, and is eager to contribute to our success. If you’re ready to take on new challenges and grow with us, we want to hear from you! Responsibilities Operate and monitor production equipment to ensure efficient and safe operation. Perform routine quality checks on products to maintain high standards. Assist in troubleshooting equipment issues and perform minor repairs as needed. Maintain a clean and organized work area to promote safety and efficiency. Collaborate with team members to meet production goals and deadlines. Document production data accurately and report any discrepancies. Follow all safety protocols and company policies to ensure a safe working environment. Qualifications High school diploma or equivalent; additional technical training is a plus. Previous experience in a manufacturing or production environment preferred. Strong attention to detail and ability to follow instructions precisely. Basic mechanical skills and ability to troubleshoot equipment. Excellent communication and teamwork skills. Ability to lift up to 50 lbs and stand for extended periods. Willingness to work flexible hours, including overtime as needed.
The Senior Engineer I, Pharmaceutical, based in San Clemente, CA is responsible for development/pilot, clinical, and commercial manufacturing for pharmaceutical/combination products. The candidate supports the in-house manufacturing and contract manufacturing (CMOs) for development/pilot, clinical, and commercial campaigns. The candidate plays a key-role on the team including a hands-on role partnering with technicians to manufacture as needed. Additionally, the candidate will partner with R&D, CMC, QA, and Regulatory on the following: Development/study protocols, execution, and reports Execute equipment and facility qualification Technology transfer Device History Record (DHR) and Master Batch Record (MBR) authoring and revisions Standard Operating Procedures (SOP) and Work Instructions (WI) authoring and revisions Support submission filings What will you do? Manufactures development, pilot, clinical, verification/validation, stability study campaigns, and commercial production whether internal or at CMO (hands-on as needed). Troubleshoots and performs investigations for process and equipment. Participate in development of completed per project plan with defined milestones, which are defined by the project engineer, but approved by the team and management. Organize internal and external activities and technicians to support manufacturing campaigns including all component and final product deliverables for accuracy and schedule. Ensures all pharma product development, manufacturing regulations, and quality requirements are met. Partners with Quality to ensure the Quality System (NCRs, deviations, CAPA, supplier notification (SCAR), ECOs, change controls, etc) documents appropriately comply with pharma product regulations. Responsible for equipment, process, and product verifications and validations (IQ, OQ, PQ, pFMEA, MVP, and PV). Supports the stability studies for the pharma projects. Responsible for applying fundamental and advanced (depending on level) engineering principles, concepts, theories and techniques to solve complex problems related to product development / design and manufacturing while following company standard practices and procedures, and related specification. Develops robust manufacturing processes that meet Corporate/Operations objectives for cost, quality, manufacturability, vendor quality, capacity, robustness, simplicity, validation, through put, etc., while meeting all regulatory, quality, and commercial requirements. How will you get here? Bachelor’s degree in Engineering or Science with 5-8 years direct clinical and/or commercial GMP experience within a pharmaceutical or biotechnology environment Experience in clean room GMP/GLP environments (ISO 5-ISO 8) Strong combination of technical, business, and project management skills Developing processes, equipment, specifications, procedures, training, etc. at pilot/ clinical/commercial scale(s) Working with Purchasing/Supply Chain/Materials Management groups and component/API/excipient/raw material vendors to manage pharmaceutical component purchasing, inventory, and manufacturing supply With limited direction from department director or Vice President including limited or no guidance on task development. Work may be reviewed for accuracy and overall content upon completion. Lead projects and investigations with limited guidance. Organization and authoring of documentation (development, manufacturing, validations, studies, builds, components, etc.) that meets pharma and medical device GMP requirements in preparation for submission filings Success in developing scaled up process/equipment and transfer from Pilot to Clinical/Commercial Production. Providing cGMP and GDP manufacturing documentation and hands-on training for operations Ability to author V&V and some DHF deliverables with guidance SolidWorks or Visio (drawings, flowcharts) experience Minitab or JMP (statistical analysis) experience Design of Experiments (DOE) experience Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible. These are just a few of the terms our employees use to describe their experiences as a part of the Glaukos family. Those may seem like big aspirations, but here at Glaukos, we recognize the deep significance and profound meaning that comes from knowing that we can make a meaningful difference by helping improve eyesight of people worldwide. And because we’re a rapidly growing company with a dynamic, fast-paced culture, individual employees are empowered with more diverse and enriching challenges that might not be possible at a larger company, and more fulfillment in knowing every person and every task is directly tied to making a difference in the life of others. We offer competitive salary (based on experience), bonus eligibility, medical/dental/vision, life insurance, stock options, 401(k) Employer Match, Employee Stock Purchase Program, generous time off & paid holidays as well as time-off to volunteer in the community, plus the opportunity to work for a company that is pioneering a new glaucoma treatment class! Moreover, Glaukos Corporation has been Certified as a Great Place to Work the last three years! 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. #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.
The Senior Engineer I, Pharmaceutical, based in San Clemente, CA is responsible for development/pilot, clinical, and commercial manufacturing for pharmaceutical/combination products. The candidate supports the in-house manufacturing and contract manufacturing (CMOs) for development/pilot, clinical, and commercial campaigns. The candidate plays a key-role on the team including a hands-on role partnering with technicians to manufacture as needed. Additionally, the candidate will partner with R&D, CMC, QA, and Regulatory on the following: Development/study protocols, execution, and reports Execute equipment and facility qualification Technology transfer Device History Record (DHR) and Master Batch Record (MBR) authoring and revisions Standard Operating Procedures (SOP) and Work Instructions (WI) authoring and revisions Support submission filings What will you do? Manufactures development, pilot, clinical, verification/validation, stability study campaigns, and commercial production whether internal or at CMO (hands-on as needed). Troubleshoots and performs investigations for process and equipment. Participate in development of completed per project plan with defined milestones, which are defined by the project engineer, but approved by the team and management. Organize internal and external activities and technicians to support manufacturing campaigns including all component and final product deliverables for accuracy and schedule. Ensures all pharma product development, manufacturing regulations, and quality requirements are met. Partners with Quality to ensure the Quality System (NCRs, deviations, CAPA, supplier notification (SCAR), ECOs, change controls, etc) documents appropriately comply with pharma product regulations. Responsible for equipment, process, and product verifications and validations (IQ, OQ, PQ, pFMEA, MVP, and PV). Supports the stability studies for the pharma projects. Responsible for applying fundamental and advanced (depending on level) engineering principles, concepts, theories and techniques to solve complex problems related to product development / design and manufacturing while following company standard practices and procedures, and related specification. Develops robust manufacturing processes that meet Corporate/Operations objectives for cost, quality, manufacturability, vendor quality, capacity, robustness, simplicity, validation, through put, etc., while meeting all regulatory, quality, and commercial requirements. How will you get here? Bachelor’s degree in Engineering or Science with 5-8 years direct clinical and/or commercial GMP experience within a pharmaceutical or biotechnology environment Experience in clean room GMP/GLP environments (ISO 5-ISO 8) Strong combination of technical, business, and project management skills Developing processes, equipment, specifications, procedures, training, etc. at pilot/ clinical/commercial scale(s) Working with Purchasing/Supply Chain/Materials Management groups and component/API/excipient/raw material vendors to manage pharmaceutical component purchasing, inventory, and manufacturing supply With limited direction from department director or Vice President including limited or no guidance on task development. Work may be reviewed for accuracy and overall content upon completion. Lead projects and investigations with limited guidance. Organization and authoring of documentation (development, manufacturing, validations, studies, builds, components, etc.) that meets pharma and medical device GMP requirements in preparation for submission filings Success in developing scaled up process/equipment and transfer from Pilot to Clinical/Commercial Production. Providing cGMP and GDP manufacturing documentation and hands-on training for operations Ability to author V&V and some DHF deliverables with guidance SolidWorks or Visio (drawings, flowcharts) experience Minitab or JMP (statistical analysis) experience Design of Experiments (DOE) experience Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible. These are just a few of the terms our employees use to describe their experiences as a part of the Glaukos family. Those may seem like big aspirations, but here at Glaukos, we recognize the deep significance and profound meaning that comes from knowing that we can make a meaningful difference by helping improve eyesight of people worldwide. And because we’re a rapidly growing company with a dynamic, fast-paced culture, individual employees are empowered with more diverse and enriching challenges that might not be possible at a larger company, and more fulfillment in knowing every person and every task is directly tied to making a difference in the life of others. We offer competitive salary (based on experience), bonus eligibility, medical/dental/vision, life insurance, stock options, 401(k) Employer Match, Employee Stock Purchase Program, generous time off & paid holidays as well as time-off to volunteer in the community, plus the opportunity to work for a company that is pioneering a new glaucoma treatment class! Moreover, Glaukos Corporation has been Certified as a Great Place to Work the last three years! 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. #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.
*Overview* Join our dynamic team as an Automotive Upholsterer and bring vehicles back to life with expert craftsmanship and attention to detail! In this role, you will be responsible for reupholstering, repairing, and maintaining the interior furnishings of automobiles, including seats, panels, and other fabric or leather components. Your skills will help ensure each vehicle meets high standards of quality, comfort, and aesthetic appeal. This is an exciting opportunity for individuals passionate about automotive restoration, upholstery techniques, and manufacturing processes to showcase their talents in a fast-paced, rewarding environment. *Responsibilities* * Interpret technical drawings, blueprints, and specifications to accurately reupholster vehicle interiors according to manufacturer standards. * Use hand tools, pneumatic tools, power tools, sewing machines, and manual cutting equipment to cut fabric materials and assemble upholstery components. * Reupholster seats, door panels, dashboards, and other interior elements with leather or fabric materials while ensuring proper fit and finish. * Repair and maintain existing upholstery by replacing worn or damaged sections using appropriate techniques. * Handle heavy lifting safely during the removal and installation of large or bulky upholstery parts. * Apply woodworking skills when necessary for frame repairs or modifications within vehicle interiors. * Ensure all work complies with safety standards and quality control procedures throughout the manufacturing or auto restoration process. *Qualifications* * Demonstrated attention to detail with a focus on precision in upholstery work. * Proven experience in reupholstering using upholstery techniques specific to automotive interiors. * Skilled in the use of hand tools, pneumatic tools, power tools, sewing machines, and manual cutting equipment. * Knowledge of fabric materials such as leather and textiles used in vehicle interiors. * Ability to interpret technical drawings, blueprints, and specifications accurately. * Experience with woodworking or carpentry related to vehicle interior modifications is a plus. * Strong manual handling skills for heavy lifting tasks associated with automotive upholstery projects. * Familiarity with auto restoration processes or manufacturing environments is desirable. Join us in transforming vehicles into masterpieces of craftsmanship! We are committed to fostering a safe, inclusive environment where your skills can shine while delivering exceptional results for our clients. All positions are paid roles that support your growth as a professional upholsterer dedicated to excellence in automotive interior restoration and manufacturing. Pay: $23.00 - $31.00 per hour Benefits: * 401(k) * Dental insurance * Health insurance * Life insurance * Paid time off * Vision insurance Work Location: In person
*Quality Inspector* *Position Summary:* The Quality Inspector is responsible for performing receiving, in-process, first article, and final inspections to verify compliance with engineering drawings, customer requirements, industry standards, and company quality management system requirements. The position supports aerospace manufacturing operations through inspection, documentation review, and product acceptance activities. *Essential Functions and Responsibilities:* · Perform receiving, in-process, first article, and final inspections. · Interpret engineering drawings, specifications, and customer requirements. · Verify dimensional characteristics using precision measuring equipment. · Review material certifications, process certifications, and manufacturing records. · Complete inspection records and quality documentation. · Identify, document, and communicate nonconforming conditions. · Support corrective action and continuous improvement activities. · Maintain inspection equipment and work area in accordance with company procedures. · Comply with all quality, safety, and regulatory requirements. *Minimum Education:* · High school diploma, GED, or equivalent combination of education and experience. *Minimum Qualifications:* · Experience using precision measuring instruments. · AS9100 experience. · AS9102 First Article Inspection experience. · GD&T interpretation experience per ASME Y14.5. · Ability to read and interpret engineering drawings. · Basic computer proficiency. · Ability to perform inspection documentation and recordkeeping. *Preferred Qualifications:* · CMM experience. · Gear knowledge & inspection · ERP or manufacturing software experience. *Knowledge, Skills, and Abilities:* · Ability to read, write, speak, and understand English sufficient to perform job duties safely and effectively. · Ability to communicate professionally with employees, customers, suppliers, and auditors. · Ability to interpret engineering drawings and specifications. · Ability to perform mathematical calculations involving decimals, fractions, and basic geometry. · Ability to organize and prioritize multiple tasks. · Ability to maintain accurate records and documentation. · Ability to work independently and as part of a team. *Pay Range:* * $25.00-35.00/hr. *Equal Employment Opportunity Employer:* _We are an Equal Opportunity and Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race (including hair texture and hairstyles), color, religion, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity, gender expression, sexual orientation, national origin, ancestry, age, physical or mental disability, medical condition, genetic information, family care or medical leave status, military or veteran status, or any other characteristic protected by state or federal laws. We celebrate diversity and are committed to creating an inclusive environment for all employees._ Pay: $25.00 - $35.00 per hour Work Location: In person
*CNC LATHE MACHINIST* *Position Summary:* The CNC Lathe Machinist is responsible for setting up and operating Fanuc-controlled CNC lathes to produce precision aerospace components in accordance with engineering drawings, customer requirements, work instructions, and company quality management system requirements. The position supports turning operations through setup, operation, in-process inspection, documentation, and communication of machining or quality concerns. *Essential Functions and Responsibilities:* · Set up and operate Fanuc-controlled CNC lathes for production of precision machined components. · Review job travelers, drawings, setup sheets, tooling requirements, and inspection requirements before beginning work. · Load, verify, and run CNC programs in accordance with established procedures. · Install and adjust workholding, cutting tools, inserts, fixtures, and offsets as required. · Perform first-piece, in-process, and final dimensional checks using appropriate measuring equipment. · Make tool wear, offset, and minor process adjustments to maintain dimensional control. · Monitor machine operation, tooling condition, surface finish, and part quality throughout the manufacturing process. · Identify and communicate machining problems, tooling issues, nonconforming conditions, and process improvement opportunities. · Complete production records, inspection records, and other required documentation accurately and timely. · Maintain equipment, tooling, gauges, and work area in accordance with company procedures. · Comply with applicable safety, quality, and manufacturing requirements. *Minimum Education:* · High school diploma, GED, or equivalent combination of education and experience. *Minimum Qualifications:* · Experience operating CNC lathes in a manufacturing environment. · Experience with Fanuc CNC controls or similar CNC controls. · Ability to read and interpret engineering drawings and manufacturing documentation. · Experience using precision measuring instruments such as micrometers, calipers, indicators, bore gauges, and thread gauges. · Ability to perform basic CNC offset adjustments and tool wear compensation. · Basic computer proficiency and ability to complete production documentation. *Preferred Qualifications:* · Aerospace manufacturing experience. · Experience setting up CNC lathes independently. · Experience machining alloy steel, stainless steel, carburized or heat-treated materials, or other aerospace materials. · Experience working in an AS9100 or ISO 9001 quality management system. · Experience holding close tolerances and working from GD&T requirements. · Experience with gear, shaft, spline, or precision rotating component manufacturing. *Knowledge, Skills, and Abilities:* · Ability to read, write, speak, and understand English sufficient to perform job duties safely and effectively. · Ability to communicate professionally with supervisors, coworkers, engineering, quality, and production personnel. · Ability to read and interpret engineering drawings, specifications, work instructions, routers, and related manufacturing documentation. · Ability to perform mathematical calculations involving decimals, fractions, basic geometry, and tolerances. · Ability to use computers or manufacturing systems to access work instructions, enter production information, and complete documentation. · Ability to understand feeds, speeds, tooling geometry, tool wear, and basic machining principles. · Ability to recognize chatter, taper, poor surface finish, tool failure, and other machining conditions. *Pay Range:* * $25.00-35.00/hr. *Equal Employment Opportunity Employer:* _We are an Equal Opportunity and Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race (including hair texture and hairstyles), color, religion, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity, gender expression, sexual orientation, national origin, ancestry, age, physical or mental disability, medical condition, genetic information, family care or medical leave status, military or veteran status, or any other characteristic protected by state or federal laws. We celebrate diversity and are committed to creating an inclusive environment for all employees._ Pay: $25.00 - $35.00 per hour Work Location: In person
Are you detail-oriented and enjoy working in a manufacturing environment? Our client is looking for a dependable individual who is eager to learn and has a strong attention to detail. Previous quality control experience is helpful, but not required-training will be provided for the right candidate with a solid manufacturing background. Responsibilities: Perform quality inspections on extruded carbon blocks and finished products. Complete quality inspection documentation for each machine and operator. Use measuring tools such as calipers, height gauges, and Go/No-Go gauges (training provided). Inspect products to ensure they meet quality standards. Maintain accurate quality records and documentation. Communicate with production and other departments as needed. Work in a manufacturing environment with daily exposure to carbon dust. Maintain a positive attitude and work efficiently to meet production deadlines. Work overtime when needed. Qualifications: Manufacturing experience preferred. Previous quality control experience is a plus, but not required. Strong attention to detail and ability to perform repetitive tasks accurately. Able to work independently and stay focused. Willingness to learn and be trained. Dependable with a positive attitude and strong work ethic. Position Details: Pay: $19.00 per hour Schedule: Monday–Friday, 6:00 a.m. to 2:30 p.m., with occasional Saturdays and overtime as needed. Type: Temporary-to-Hire
We are looking for a full time structural steel fabricator welder/fabricator/Installer that is D1.1 certified, and can weld 7018 in all positions proficiently, and has a 232 wire feed cert. Construction experience is a plus. A valid California drivers license is required. As well as a clean driving record. TEK Steel Inc. is a fabrication and welding company that focuses on fabricating structural steel columns, beams, and stair cases in custom homes in San Diego and Orange counties. We have been in business for 28 years, with a track record of excellence in custom structural steel fabrication. Available position: is a mix of shop fabrication of structural steel beams, columns and staircases and field work at construction sites. Where you will be tasked with installing steel columns and beams and field welding structural connections including full pen moment frames, welding nelson studs, saddles, connection plates etc. where you will be asked to read blueprints, measure, cut and weld structural steel components for columns and beams with a team of fabricators. Field work includes crane installations and field welding of structural steel components, including full pen moment frames that have to pass UT inspections. Field work is on active construction sites during the steel erection process, loading and off loading trucks with cranes or forklift, climbing ladders and bolting/welding steel components together, some projects may include carrying and lifting steel members that can weigh over 50 lbs, and other construction related tasks. Shop fabrication work includes cutting, torching, welding steel I Beams, tube steel, pipe to specific shop drawing specifications. Use of oxy/acetylene and plasma torches, band saws, grinders, iron worker, press break, drill press and a myriad of fabrication tools. Also could include primer painting completed parts. It would be a plus if you have a history of steel staircase fabrication. Mono stringer, dual stringer and cantilver style staircases. Health/Dental/Vision insurance and 401K programs are offered after probationary period has been completed. Job Type: Full-time Pay: $52,000.00 - $85,000.00 per year Benefits: * 401(k) * Dental insurance * Health insurance * Paid time off * Vision insurance Shift: * 8 hour shift Education: * High school or equivalent (Preferred) Experience: * Welding: 1 year (Preferred) License/Certification: * AWS D1.1 (Required) Work Location: In person