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Overview Join our dynamic team in Escondido, CA, as a CNC Set Up Operator! We are looking for a skilled individual who is passionate about precision machining and eager to contribute to our innovative manufacturing processes. In this role, you will be responsible for setting up and operating CNC machines to produce high-quality parts that meet our customers' specifications. If you thrive in a fast-paced environment and enjoy working with cutting-edge technology, we want to hear from you! Responsibilities Set up and calibrate CNC machines according to specifications and production requirements. Load raw materials and tooling into the machines, ensuring proper alignment and secure fastening. Monitor machine operations to ensure consistent quality and adherence to production standards. Perform routine maintenance and troubleshooting on CNC equipment to minimize downtime. Inspect finished products for quality assurance, making adjustments as necessary. Document production processes and maintain accurate records of machine settings and outputs. Collaborate with team members and supervisors to optimize production efficiency and resolve any issues. Qualifications High school diploma or equivalent; technical degree or certification in machining is a plus. Proven experience as a CNC operator or similar role, with a strong understanding of CNC machinery. Familiarity with CAD/CAM software and blueprints. Strong attention to detail and commitment to producing high-quality work. Ability to work independently and as part of a team in a fast-paced environment. Excellent problem-solving skills and mechanical aptitude. Willingness to work flexible hours, including overtime as needed.
Overview We are seeking a dedicated and skilled Assembler II to join our dynamic team in Carlsbad, CA, 92010. In this role, you will play a crucial part in the assembly process, ensuring that our products meet the highest quality standards. If you have a passion for hands-on work and thrive in a collaborative environment, we want to hear from you! Responsibilities Assemble components and subassemblies according to specifications and blueprints. Conduct quality checks to ensure all products meet established standards. Utilize various hand tools and machinery safely and effectively. Collaborate with team members to improve assembly processes and efficiency. Maintain a clean and organized workspace to promote safety and productivity. Document assembly processes and report any issues to the supervisor. Participate in training and development activities as required. Qualifications High school diploma or equivalent; technical certification is a plus. Minimum of 2 years of experience in assembly or manufacturing roles. Strong attention to detail and ability to follow instructions accurately. Proficient in using hand tools and basic machinery. Good communication skills and ability to work well in a team environment. Ability to lift up to 50 pounds and stand for extended periods. Basic computer skills for documentation and reporting.
*Steel Traditions LLC — Vista, CA* *Full-Time* Steel Traditions manufactures premium custom steel windows and doors for luxury residential and commercial projects. We are seeking a highly organized, hands-on *Final QC & Shipping Manager* to take ownership of every project during the final stages of production and ensure that nothing leaves our facility incomplete, improperly documented, or unprepared for installation. This is *not simply a shipping position* and it is not primarily a fabrication position. This person serves as the final checkpoint between production and the customer. The right candidate is someone who notices details, follows through without being chased, communicates clearly with production teams, and is comfortable stopping a shipment when something is not right. What You’ll Own You will take responsibility for projects as they move through the final stages of production, including Final QC, QC Wall, packaging and shipping. Your responsibilities will include: * Inspect every completed steel window and door before it is approved for packaging. * Verify paint finish, glass, silicone, weatherstripping, hardware, alignment, operation and overall workmanship. * Function-test operable windows and doors, including handles, locks, rollers, pivots, thresholds, door bottoms and specialty hardware. * Record required QC photos and operational videos and ensure documentation is uploaded to the correct project records. * Verify every installation kit against project requirements, including hardware, fasteners, stops, guides, sweeps, touch-up materials and specialty components. * Maintain accurate QC forms, shipping checklists, packing lists, labels and project verification records. * Verify project numbers, unit numbers, QR codes, shipping sequence and installation labels before units leave the facility. * Inspect packaging to ensure finished products, glass, hardware and accessories are adequately protected for transportation. * Coordinate loading sequence and shipping readiness with Operations. * Identify missing hardware, incomplete work and production roadblocks *before they become shipping emergencies*. * Communicate priorities and deficiencies clearly to Operations and the appropriate production departments. * Track shipping errors, missing components, field issues and warranty callbacks and help identify root causes. * Maintain an organized Final QC and shipping area. * Provide clear daily status updates on projects approaching shipment. Most importantly, *you will have the authority to stop a shipment that does not meet Steel Traditions' quality or completeness standards.* What This Position Is — and Is Not The Final QC & Shipping Manager is responsible for *verification, organization, coordination and accountability*. A separate QC Wall & Finishing Technician supports the hands-on work of installing hardware, setting up units, making adjustments, cleaning, preparing units for inspection and packaging. You may occasionally assist hands-on when necessary, but your primary responsibility is making sure the overall Final QC and shipping process is being completed correctly. What We’re Looking For We are looking for someone who is: * Extremely organized and detail-oriented. * Comfortable working in a manufacturing/shop environment. * Mechanically inclined and able to understand how windows, doors and hardware should operate. * Able to read shop drawings, checklists and project documentation. * Comfortable using computers, tablets, photos and video as part of the QC process. * Strong at following a project through multiple steps without losing details. * Able to communicate professionally with production employees and management. * Comfortable identifying deficiencies and requiring corrections. * Able to prioritize several projects with competing deadlines. * Dependable, steady under pressure and willing to take ownership. * Capable of physically inspecting, operating and working around large steel window and door assemblies. Experience in *quality control, manufacturing, windows and doors, glazing, architectural metals, construction, shipping/logistics or fabrication* is strongly preferred. Success in This Role Success is measurable. We expect the Final QC & Shipping Manager to drive toward: * Zero missing hardware or installation kits. * Zero shipments released with known defects. * 100% completion of required QC documentation. * 100% operational testing of operable products before packaging. * Accurate shipping and installation labels. * Fewer field-service trips caused by preventable shop errors. * Fewer shipping discrepancies and missing components. * Better communication of problems before shipping deadlines. * Continuous improvement of the Final QC and shipping process. Our existing position description explicitly treats documentation as part of manufacturing and says a project isn't complete until its documentation is complete. I think that philosophy belongs prominently in the advertisement because it screens for the kind of person you actually need. Why This Role Matters Our products are custom-built for high-end projects and can represent a significant investment by our customers. A missing piece of hardware, undocumented defect, incomplete installation kit or improperly prepared shipment can result in expensive field visits and construction delays. The Final QC & Shipping Manager is the *last person responsible for catching those problems before the product becomes the customer's problem.* Steel Traditions would rather delay a shipment than knowingly ship an incomplete or defective product. Pay: From $26.00 per hour Expected hours: 40.0 per week Benefits: * 401(k) * Paid time off Work Location: In person
JOB DESCRIPTION About Jubilant Radiopharmacies At Jubilant Radiopharmacies, we support patient care by producing and delivering high-quality radiopharmaceutical products that help clinicians diagnose and treat disease. Our teams work with purpose, collaboration, and a strong commitment to safety and compliance. We value people, empower growth, and encourage a culture where individuals can do their best work. Jubilant Radiopharmacies is proud to becertified as aGreat Place to Work®, recognizing our commitment to a respectful, supportive, and people-first culture. Role Overview We are seeking a Site Quality Lead to help ensure our radiopharmaceutical manufacturing operations meet FDA, cGMP, and internal quality standards. In this role, you will oversee quality systems, provide support to sterile manufacturing operations, and partner closely with operations, QC, and corporate quality teams. This position is an excellent fit for someone who is detail-oriented, knowledgeable in quality compliance, and motivated to improve processes that directly impact patient safety. Key Responsibilities Maintain and improve quality systems, including CAPA, change control, deviations, complaints, and document control. Support internal and external audits, including FDA inspections and customer audits. Ensure timely completion of quality events and implementation of effective corrective actions. Monitor compliance with 21 CFR Part 212 and applicable USP chapters. Review batch records, QC data, and manufacturing documentation for accuracy and compliance. Perform batch trend tracking and upload batch information required by customers. Support regulatory submissions and responses to health authority inquiries. May serve as the Radiation Safety Officer. Collaborate with Production and QC teams to ensure aseptic processing standards are met. Support root cause analysis and write investigation reports for quality events. Participate in environmental monitoring review, trending, and sterility assurance activities, including media fill validations. Develop and deliver GMP and compliance training. Write and update SOPs, protocols, and reports in alignment with regulatory expectations. Identify and implement process improvements that enhance quality and operational efficiency. Partner with Corporate Quality, Supply Chain, Radiation Safety, Engineering, and Operations to support site readiness and compliance. Qualifications Bachelor’s degree in a scientific discipline (e.g., Chemistry, Biology, Pharmacy, Engineering). 3+ years of experience in pharmaceutical quality assurance or quality compliance, preferably in sterile or radiopharmaceutical manufacturing. Strong knowledge of FDA regulations, cGMP, and quality systems. In-depth understanding of GxP regulations, FDA 21 CFR Part 11, 21 CFR Part 211, 21 CFR Part 212, USP <825>, and global data integrity standards. Experience with electronic systems such as LIMS, MES, ERP, or CDS. Strong communication, organization, analytical thinking, and technical writing skills. Ability to work independently and manage multiple priorities effectively. Ability to collaborate well with cross-functional stakeholders. Benefits We offer competitive compensation, an annual performance bonus, generous vacation, and 401K matching. Equal Employment Opportunity Statement Jubilant Radiopharmacies is an equal opportunity employer. We are committed to building a diverse and inclusive workplace where all employees feel valued and supported. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other legally protected status.
GROW WITH US: Tandem Diabetes Care creates new possibilities for people living with diabetes, their loved ones, and their healthcare providers through a positively different experience. We’d love for you to team up with us to “innovate every day,” put “people first,” and take the “no-shortcuts” approach that has propelled us to become a leader in the diabetes technology industry. STAY AWESOME: Tandem Diabetes Care is proud to manufacture and sell the Tandem Mobi system and t:slim X2 insulin pump with Control-IQ+ technology — an advanced predictive algorithm that automates insulin delivery. But we’re so much more than that. Our company’s human-centered approach to design, development, and support delivers innovative products and services for people who use insulin. Because many of our own team members live with diabetes, or have a loved one impacted by diabetes, the work is personal, and we are committed to the cause. Learn more at tandemdiabetes.com A DAY IN THE LIFE: Quality Assurance Associates at Tandem perform inspection and release of manufacturing goods during the manufacturing process by conducting routine and non-routine verification and review of in-process and finished products under general supervision and according to Quality Test Procedures (QTP) & Standard Operation Procedures (SOPs). Compiles data for documentation of test procedures and may assist with report preparation. A Quality Assurance Associate at performs In-process, Final Inspection and Final Approval of Product : Reviews and approves manufacturing Design History Records (DHRs), associated test reports and records and reports abnormalities. Verifies training and other records for compliance to specifications. Assists with resolving non-conformances occurring with in-process and finished products. Provides quality oversight of manufacturing process/final packaging. Updates departmental spreadsheets and statistics. Assists in revising DHR’s, work instructions, SOP’s, process risk documents, etc. Maintains department documentation and inventory of retained materials. Reviews and approves manufacturing records such as test reports and 5S log-sheets. Assists with calibration/preventive maintenance (PM) program: Checks PM logbooks on manufacturing equipment for completeness and accuracy. Verifies area equipment is within calibration specifications. - May assist with Incoming Inspections as required. - Assists with Internal audits and participates in 3rd party audits. - Confirms completion of required training plan before assuming job responsibilities. WHEN & WHERE YOU’LL WORK: On-Site: This role is on-site four days a week at our San Diego office due to the nature of the work involved. Schedule: This position has a schedule of 2:30 pm - 1:00 am (PT) Monday-Thursday. Please note that this a temporary position. As a temporary employee you will be employed through a staff agency partner. Benefits during your temporary assignment may be provided by the staffing agency. Access to Tandem sponsored benefits is contingent upon conversion from temporary to regular full-time status. Conversion is determined based on business need and job performance. WHAT YOU’LL NEED: Associate’s degree or combination of education and applicable job experience. Bachelor’s degree preferred. 5 plus years’ relevant quality and/or manufacturing experience in a FDA regulated industry, preferably medical devices Experience with QSRs, QC testing methods and general knowledge of GMP requirements for production. Experience with lot release, document review, and in-process inspection. Deep understanding of GMP regulations and Process Controls, including document review, in-process and final acceptance criteria, identification and traceability requirements, and segregation of materials. Able to effectively share information and ideas within and outside of department in written or verbal form; able to put forth own ideas and gain understanding from others. Proficient at supporting effective interactions between team members and among cross-functional teams. Demonstrated ability to schedule and coordinate project priorities and resources and to produce high quality work. Proficient experience with MS Office suite (Word, Excel, Outlook). COMPENSATION & BENEFITS: The starting base pay range for this position is $22.50 - $24.00 per hour. Base pay will vary based on job-related knowledge, skills, experience and may also fluctuate depending on candidate’s location and the overall job market. In addition to base pay, Tandem offers a competitive compensation package that includes bonus and a robust benefits package. Tandem offers health care benefits such as medical, dental, vision available your first day, as well as health savings accounts and flexible saving accounts. You’ll also receive 11 paid holidays per year, a minimum of 20 days of paid time off (with accrual starting on day 1) and you will have access to a 401k plan with company match as well as an Employee Stock Purchase plan. Learn more about Tandem’s benefits here! YOU SHOULD KNOW: Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable state and local Fair Chance laws and regulations. A conditional offer of employment from Tandem is contingent upon successful completion of a pre-employment screening process comprised of a drug test (excluding marijuana) and background check, which includes a review of criminal history information. Tandem has good cause to conduct a review of criminal history information of candidates for this position, as this role may involve access to proprietary, sensitive and/or confidential information, including customer protected health information. This review is required to ensure that individuals in such roles uphold high standards of trust and integrity so as to protect the interests of our customers, employees, and stakeholders. SPONSORSHIP: Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. WHY YOU’LL LOVE WORKING HERE: At Tandem, we believe joy fuels excellence. That's why we've built a workplace that celebrates your achievements and supports your well-being. Our team thrives on pushing boundaries and fostering growth, all while maintaining a spirit of fun and camaraderie. This is just one of the ways we stay awesome! Explore the benefits and reasons to love Tandem at https://www.tandemdiabetes.com/careers. BE YOU, WITH US! We embrace the value that every single one of us brings to the table. But sometimes we forget that when we don’t meet 100% of a job description’s criteria – maybe you’re feeling that way right now? We encourage you to apply anyway. Because we want you to be you, with us. Tandem is firmly committed to being an equal opportunity employer and does not discriminate on the basis of age, disability, sex, race, religion or belief, gender identity or expression, marriage/civil partnership, pregnancy/maternity, or sexual orientation. We are an inclusive organization, and we welcome applications from a wide range of candidates. Selection for roles will be based on individual merit alone. REFERRALS: We love a good referral! If you know someone who would be a great fit for this position, please share! APPLICATION DEADLINE: The position will be posted until a final candidate is selected for the requisition or the requisition has a sufficient number of applications. Make a move that matters. Join Tandem Diabetes Care, where we're turning challenges into triumphs every day and where your talents will help shape a healthier, happier tomorrow. #LI-Onsite #LI-BC1