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Outstanding precision medical parts manufacturing company has immediate openings for Deburring Bench Technicians to be responsible for performing all secondary operations using a microscope and hand tools in the production of precision machined parts used in the medical device industry. Key Responsibilities: Reads and interprets Process Sheet to determine sequence of secondary production processes. Inspects and measures precision metal parts for conformity to specifications. Removes burrs from precision metal parts using microscope and hand tools. Harperizes precision metal parts as specified on Process Sheet. Displays strong organizational and time management skills with the ability to handle several assignments at one time. Uses and operates most hand tools and equipment necessary to perform the job. Maintains lot trace ability, log sheets, and good housekeeping practices at all times. Maintains a working knowledge of safety policies and regulations to ensure duties of self and others are performed in a safe manner. Qualifications: High school diploma or equivalent and/or vocational training. 1-2 years manufacturing work experience. Ability to use in process inspection tools. Ability to occasionally lift 10 - 20 pounds. Employee stands, sits and walks frequently. Ability to use both hands in a repetitive motion for up to 6 hours per day. Specific vision abilities required by this job include close vision, peripheral vision, depth perception, and the ability to adjust focus. Schedule available: 1st Shift: 5:30 am - 2:00 pm (1 opening) $18.50/hr 1st Shift: 6:00 am - 2:30 pm (1 opening) $18.50/hr 2nd shift: 1:30 pm - 10:00 pm (1 opening) $18.50/hr + 10% shift diff = *$20.35/hr* 3rd Shift: 10:00 pm - 6:30 am ( 2 opening) $18.50/hr + 20% shift diff = *$22.20/hr* 3rd Shift: 9:30 pm - 6:00 am ( 1 opening) $18.50/hr + 20% shift diff = *$22.20/hr* Join us as a Deburring Bench Technician where your expertise will contribute to our commitment to excellence in manufacturing! Job Type: Full-time Pay: $18.50 - $22.20 per hour Benefits: * Health insurance Work Location: In person
DPI Direct is a *fast-growing, technology-driven print service provider* with facilities in San Diego and Las Vegas. We specialize in offset, digital, large format, label, packaging, and fulfillment solutions, serving major biotech, retail, and manufacturing companies as well as national and international online PSP partners. As we continue to expand, we are looking for a highly skilled *Prepress Technician* to join our growing team and contribute to our reputation for quality, innovation, and customer service excellence. *Position Title:* Full-Time, Pre-Press Associate with strong communication and multi-tasking skills. Our Prepress Associates set the foundation for successful printing production. *Compensation:* DOE *Benefits:* 401k, Medical, Dental, Vision and PTO *Hours:* M-F / 8am-4:30pm *Position Summary* The Prepress Technician is responsible for preparing, reviewing, and processing digital files for high-quality print production. This role ensures accuracy, efficiency, and color consistency while supporting smooth handoff to press and digital workflows. The ideal candidate has strong technical expertise, thrives in a fast-paced environment, and is eager to grow with us. *Key Responsibilities* * Review, preflight, and prepare customer files for print (offset, digital). * Ensure proper file setup including bleed, trim, color profiles, fonts, and image resolution. * Perform color corrections, trapping, imposition, and proofing as required. * Create print-ready PDFs and impositions using tools such as *Adobe Creative Suite, PitStop, Preps.* * Generate digital and hard proofs for customer and internal review. * Communicate with project managers, sales, and production teams to clarify artwork issues and ensure accuracy. * Troubleshoot file or RIP issues to prevent downtime in production. * Maintain G7 color standards and support consistent output across devices. * Collaborate with pressroom and digital operators to ensure smooth transition from prepress to print. * Support workflow automation initiatives and continuous improvement in prepress processes. *Qualifications* * *5+ years of hands-on prepress experience in a commercial print shop.* * *Must have strong proficiency in Adobe InDesign and the full Adobe Creative Suite (Illustrator, Photoshop, Acrobat).* * Deep knowledge of preflight, imposition, trapping, and *RIP software Kodak Prinergy.* * Strong background in G7 color management and ICC profiles. * Experience with digital print workflows (HP Indigo, Ricoh, Xerox, etc.) strongly preferred. * Ability to handle multiple projects under tight deadlines with minimal supervision. * Strong attention to detail, accuracy, and quality control. * Effective presentation, communication and problem-solving skills. * Ability to work well with all levels of management & team * Able and willing to work extended hours during peak season *What We Offer* * Competitive pay based on experience. * Comprehensive benefits package (Medical, Dental, Vision, Life Insurance, Supplemental Insurance, 401k, PTO, Holiday Pay, and Discount Perks). * A supportive team environment with cutting-edge print technology. *Education:* Minimum High School Diploma or GED / Associates Degree in Graphic Design or Higher Preferred. Job Type: Full-time Pay: $24.00 - $27.00 per hour Benefits: * 401(k) * Dental insurance * Health insurance * Life insurance * Paid time off * Vision insurance Work Location: In person
The successful Quality Assurance Manager (QAM) candidate will be responsible for understanding, implementing, and maintaining the entire quality system, maintaining and acquiring certifications, communicating with internal and external customers, engaging and developing best practices, eliminating non-conformance risk situations, tracking of quality data for review and support of continuous improvement goals. Reports to: President Shift: Day from 7:00a - 3:30p Job Type: Full-time Pay: $33.65 - $43.26 per hour Expected hours: 40 per week Benefits: * 401(k) * Dental insurance * Employee assistance program * Health insurance * Life insurance * Paid time off * Professional development assistance * Referral program * Retirement plan * Vision insurance Application Question(s): * How many years experience do you have functioning as Management Representative for ISO Related Audits? * How many years experience do have inspecting sheet metal products? Education: * Associate (Required) Experience: * working in QA Manufacturing: 8 years (Required) * implementation/maintenance of ISO:9001:2015: 4 years (Required) * Statistical Process Controls: 3 years (Required) * Receiving, in-process & Final Inspection: 3 years (Required) * rocess Failure Mode and Effects Analysis (PFMEA): 3 years (Preferred) * Lean manufacturing/Six Sigma Technique: 1 year (Preferred) * implementation/maintaining in AS 9100 Rev D: 4 years (Required) * First Article & PPAP Submission: 3 years (Preferred) License/Certification: * ASQ Certification (Preferred) Ability to Commute: * San Diego, CA 92121 (Required) Work Location: In person
*Folder / Stitcher / Cutter / Inserter / and Inkjet Operators * *1) Paper Cutter Operator* * Experience Required: 1-2 years of experience operating Programable Polar 45” and Saber 36” paper cutters. * Full Time, Part Time, or Temp On-Call positions available * Pay Range: $20 - $27/hr. *2) Bindery Operator* * Working knowledge of bindery or mailing equipment required. * Folders / Stitcher / Cutters / Plow folders / Inserters / Inkjets * Full Time, Part Time, or Temp On-Call positions available * Pay Range: $20 - $27/hr. Full Time, Part Time or Temp On-Call positions available. Comprehensive benefits package including: Medical, dental and life insurance, and a 401(k)-retirement plan Job Types: Full-time, Part-time, Contract, Temporary Pay: $20.00 - $27.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Health insurance * Life insurance * Paid time off * Vision insurance Work Location: In person
*Who are we?* *APPLIED MEMBRANES is an INDUSTRY LEADER in RO Expertise and Membrane Applications Since 1983™. Applied Membranes, Inc. is a manufacturer and distributor of Reverse Osmosis Membranes, Systems and Components, both commercial and residential. We have been manufacturing Reverse Osmosis Systems, RO Membranes and Water Filtration Components under the AMI label for over 40 years. From residential to 1 MGD size and in standard to custom engineered designs, AMI RO, NF, UF, MF and EDI Systems are used in many different applications from Water Reuse, Brackish and Sea Water to Ultrapure Water with thousands of installations world-wide.* *AMI Products have earned an industry-wide reputation for their high quality and superior performance.* *Our Certified Water Experts and Engineers can create custom solutions to solve virtually any water treatment challenge. From feed water report analysis, detailed drawing and budgetary proposals, prototype and pilot testing, to system startup, our technicians are involved every step of the way to ensure the success of the project. With hundreds of membrane and system designs in production, we are also a leading manufacturer of standard solutions and welcome the opportunity to standardize any design for large volume production.* *With over 8 million membrane elements rolled and twenty thousand water treatment system installations, we have the real-world experience needed to ensure the success of any project. Committed to continual improvement, we treat every challenge as a learning experience. Our products designs and material selection reflect decades of knowledge gained where it most counts: from actual operation and performance in the field.* *AMI's state of the art ISO 9001:2015 and NSF certified facility features the most sophisticated manufacturing and testing equipment technologies in the industry. Above all else, quality and customer satisfaction are our highest priorities. We implement rigorous performance and integrity testing to ensure our products are achieving optimum performance, using internal test standards that exceed the published requirements. From design control to in process quality checks to final QC, quality control is built into every point from design to production to release and shipment.* *WHO ARE WE LOOKING FOR?* *Systems Technicians -Mechanical Assembly who are responsible for the assembly of various types of mechanical equipment from verbal and written instructions.* *Essential Duties and Responsibilities* * *Prepares work to be accomplished by studying assembly instructions, blueprint specifications, and parts lists; gathering parts, sub-assemblies, tools, and materials.* * *Positions parts and sub-assemblies by using templates or reading measurements.* * *Assembles components by examining connections for correct fit; fastening parts and sub-assemblies.* * *Verifies specifications by measuring completed component.* * *Resolves assembly problems by altering dimensions to meet specifications; notifying supervisor to obtain additional resources.* * *Keeps equipment operational by completing preventive maintenance requirements; following manufacturer's instructions; troubleshooting malfunctions; calling for repairs.* * *Maintains safe and clean working environment by complying with procedures, rules, and regulations..* * *Conserves resources by using equipment and supplies as needed to accomplish job results.* *Experience & Skills:* * *Experience in the water industry highly desired.* * *Skilled with PVC piping fabrication and installation.* * *Experienced with tubing assembly and installation for metallic and non-metallic tubing systems.* * *Experience working with water pumps, valves, and piping systems for commercial and industrial water purification.* * *Prefer strong mechanical aptitude and experience in a manufacturing setting.* *Education: Minimum of a high school diploma or equivalent* Job Type: Full-time Pay: $20.00 - $25.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Health insurance * Paid time off * Vision insurance Ability to Commute: * Vista, CA 92081 (Required) Ability to Relocate: * Vista, CA 92081: Relocate before starting work (Required) Work Location: In person
*Who are we?* APPLIED MEMBRANES is an Industry Leader in RO Expertise and Membrane Applications Since 1983™. Applied Membranes, Inc. is a manufacturer and distributor of Reverse Osmosis Membranes, Systems and Components, both commercial and residential. We have been manufacturing Reverse Osmosis Systems, RO Membranes and Water Filtration Components under the AMI label for over 40 years. From residential to 1 MGD size and in standard to custom engineered designs, AMI RO, NF, UF, MF and EDI Systems are used in many different applications from Water Reuse, Brackish and Sea Water to Ultrapure Water with thousands of installations world-wide. AMI Products have earned an industry-wide reputation for their high quality and superior performance. Our Certified Water Experts and Engineers can create custom solutions to solve virtually any water treatment challenge. From feed water report analysis, detailed drawing and budgetary proposals, prototype and pilot testing, to system startup, our technicians are involved every step of the way to ensure the success of the project. With hundreds of membrane and system designs in production, we are also a leading manufacturer of standard solutions and welcome the opportunity to standardize any design for large volume production. With over 8 million membrane elements rolled and twenty thousand water treatment system installations, we have the real-world experience needed to ensure the success of any project. Committed to continual improvement, we treat every challenge as a learning experience. Our products designs and material selection reflect decades of knowledge gained where it most counts: from actual operation and performance in the field. AMI's state of the art ISO 9001:2015 and NSF certified facility features the most sophisticated manufacturing and testing equipment technologies in the industry. Above all else, quality and customer satisfaction are our highest priorities. We implement rigorous performance and integrity testing to ensure our products are achieving optimum performance, using internal test standards that exceed the published requirements. From design control to in process quality checks to final QC, quality control is built into every point from design to production to release and shipment. *Who are we looking for?* *Welder* Responsible for the assembly of systems frames/skids and any other welding required within the company. *Essential Duties and Responsibilities* 1. Weld and assemble stainless steel high pressure piping for large systems 2. Finish all welds and prepare frames for outsource to powder coating using grinders and other equipment 3. Make any weld or cutting modifications to the frame/skid on the Systems production floor, as required *Minimum Qualifications* *Experience & Skills:* 5 years similar welding experience required. Knowledge of aluminum, steel, stainless steel materials; welding with both TIG and MIG welding equipment. Ability to work with common hand tools. Ability to work with table saws, hand power saws, table and hand power grinders. Excellent communication skills, both verbal and written. Ability to read blueprints. Knowledge to metallurgy. Knowledge of various welding techniques, including TIG, MIG, arc and oxy-fuel welding. Knowledge of manual and mechanical welding techniques. *Welding certification required.* *Education* Minimum of a high school diploma or equivalent. Job Type: Full-time Pay: $30.00 - $34.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Health insurance * Paid time off * Vision insurance Experience: * Welding: 5 years (Required) License/Certification: * Welding Certification (Required) Shift availability: * Day Shift (Required) Ability to Commute: * Vista, CA 92081 (Required) Work Location: In person
*Overview* Aurora Spine, headquartered in Carlsbad, California, designs, develops, and manufactures high-quality minimally invasive spinal implants. We are a small, dedicated team passionate about innovation and precision in spinal technology. We’re looking for a motivated CNC Machine Shop Assistant to support our growing manufacturing operations. This role is ideal for someone eager to learn and gain hands-on experience. *Responsibilities* * Operate CNC 5-axis milling machines and equipment * Perform visual inspections and report defects * Load raw materials into machines * Assist with material handling, part cleaning, counting, and deburring * Support assembly tasks * Maintain a clean and safe workspace * Perform additional duties as needed *Qualifications* * High school diploma or equivalent * Reliable and committed to company values of honesty, integrity, and respect * Motivated learner with enthusiasm to grow and adapt * Ability to follow instructions and safety protocols * Physical ability to stand, walk, and use hands frequently during shifts * Able to lift up to 22 lbs as required * *Preferred:* Prior machine shop experience * Strong attention to detail *Schedule Requirements* * Flexible evening and weekend scheduling is a must *Why Join Aurora Spine?* Be part of an innovative team that’s shaping the future of spinal technology. At Aurora Spine, you’ll gain valuable hands-on experience, training, and the opportunity to contribute to meaningful advancements in healthcare. Job Types: Full-time, Part-time, Temp-to-hire Pay: $18.00 - $23.00 per hour Expected hours: 30 – 40 per week Benefits: * 401(k) matching * Dental insurance * Flexible spending account * Health insurance * Health savings account * On-the-job training * Paid time off * Retirement plan * Tuition reimbursement * Vision insurance Work Location: In person
Description: Kumquat Biosciences is committed to the discovery and development of innovative drugs to transform cancer treatments. Kumquat brings together an accomplished management team and distinguished scientific founders to translate innovative research to novel therapeutics. Our team has a proven track record of drug discovery and development, having played pivotal roles in the discovery of multiple clinical-stage compounds as well as an approved drug for the treatment of cancers and immune-mediated inflammatory diseases. We are currently seeking a highly motivated, creative CMC drug substance professional to join our CMC team in San Diego. This candidate will report to the senior director and head of CMC. This candidate is expected to work closely with Kumquat internal discovery and development teams as well as external CRO/CDMO companies to drive programs into early and late clinical development. This is a position with responsibility for synthetic route design and scouting, process development and manufacturing. The ideal candidate will have an in-depth understanding in all aspects of modern synthetic chemistry, process development, and non-GMP/GMP manufacturing. A strong team player who is detail-oriented and has the desire to learn and understand life-cycle product management concepts and practice is essential. The candidate will have the opportunity to work on multiple programs within the company’s pipeline which comprises potentially first-in-class approaches & novel-novel targets. Role responsibilities Evaluate available candidate synthetic routes and develop stage appropriate route modification and process optimization strategies. Select external CRO/CDMO partners based on project needs and the external parties’ technical capabilities, quality system, and track records. Prepare RFPs and evaluate proposals based on the targeted product quality, project timeline, and budget. Plan and oversee drug substance process optimization, GMP manufacturing, and stability evaluation. Track process development/validation history and manage CMC drug substance related documents in support of life cycle of quality improvement and regulatory filing/updates. Work closely with a cross-functional team within and outside of the CMC department to align with key stakeholders (CMC, clinical, quality assurance and regulatory, etc.). Author and review CMC drug substance related sections for regulatory filing and annual updates. Stay current on industry trends and regulatory requirements to ensure delivery of quality products under non-GMP and GMP environments. Prepare and communicate research results in both oral and written format. Supervise junior CMC Drug Substance team members. Contribute to a fast-paced, dynamic, data-driven scientific culture that embraces innovation and excellence. Requirements: Ph.D. or M.S. in chemistry, chemical engineering, pharmaceutical science, or related discipline with at least 10 years of related experience (title for this position will be commensurate with the candidate’s experience and qualifications) Strong synthetic organic chemistry knowledge and problem-solving skills. In-depth knowledge of industry practices in drug substance manufacturing and supply. Desire and ability to maintain constructive working relationship with the CMC analytical development team and the CMC drug product team. In-depth knowledge of cGMP regulations and compliance. Track record of accomplishment in managing CMC drug substance projects at early and late development stages. Direct experience with small molecule API NDA filing is preferred. Ability to enable external CRO/CDMO to achieve project goals on time and under budget. Strong written and communication skills, good problem-solving abilities, and an ability to work effectively with a diverse team of co-workers in a dynamic environment. Kumquat Biosciences offers an attractive salary and benefits package, including equity incentives. Salary Description: $185k-$250k
General Atomics (GA), and its affiliated companies, is one of the world’s leading resources for high-technology systems development ranging from the nuclear fuel cycle to remotely piloted aircraft, airborne sensors, and advanced electric, electronic, wireless and laser technologies. General Atomics Electromagnetic Systems (GA-EMS) designs and manufactures first-of-a-kind electromagnetic and electric power generation systems. GA-EMS’ expanding portfolio of specialized products and integrated system solutions support critical fleet, space systems and satellites, missile defense, power and energy, and process and monitoring applications for defense, industrial, and commercial customers worldwide. We have an exciting opportunity for an Electromagnetic Aircraft Launch System (EMALS) and Advanced Arresting Gear (AAG) Production Project Manager to join our team located in Rancho Bernardo, CA. The Production Project Manager plays a critical role in meeting financial business objectives and delivering hardware and contractual documentation for the EMALS and AAG systems. This position is responsible for overseeing and coordinating the operational aspects of one or more production project(s) that may involve hardware, firmware, and/or software, and teams of 10-75 project members. DUTIES & RESPONSIBILTIES: Deliver EMALS and AAG hardware and documentation per contract requirements and business objectives. Provide leadership, direction, and guidance to employees working on assigned projects. Effectively communicate project expectations and assign tasks/priorities to team members and stakeholders in a timely fashion. Assign and monitor work of project management staff, providing technical support and direction when necessary. Create project plan(s) and manage resources to ensure project schedule, budget, quality, and specification goals are attained. Oversee and monitor project schedule, timelines, and milestones to meet delivery goals. Assess project issues and develop solutions to meet production, quality, and customer-satisfaction goals and objectives. Responsible for decisions which have an impact on outcomes and where failure to complete assignments will typically result in serious delays and expenditure of additional resources. Develop and deliver progress reports, proposals, requirements documentation, and presentations. Develop mechanisms for monitoring project progress and problem solving with project management, line management, and the customer. Interpret and administer policies, processes and procedures that impact project(s). Collaborate across management and project team to expand services and potential business opportunities. May participate in, lead segments of, or provide overall management for the request for proposal (RFP) process to generate new business. Maintain the strict confidentiality of sensitive information. Responsible for ensuring all laws, regulations and other applicable obligations are observed wherever and whenever business is conducted on behalf of the Company. Responsible for ensuring work is accomplished 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.51096 Job Qualifications: Typically requires a Bachelors or Masters in manufacturing, engineering, or related technical field and eleven or more years of progressively complex experience in the project administration experience with at least five of those years in project management. May substitute equivalent experience in lieu of education. Experience with Government contracts, lean manufacturing process, quality documentation, and/or Cost Account Management is highly desired. Must demonstrate an extensive understanding of project management processes and procedures, planning and scheduling methods, and budget management as well as the ability to organize, schedule, and coordinate workloads to meet established milestones and budgets. Must possess: The ability to initiate, plan, and manage simultaneous projects; The ability to identify issues, analyze and interpret data and develop solutions to a variety of non-routine matters of diverse scope and nature; Strong communication, leadership, presentation, and interpersonal skills are required to enable an effective interface with other departments, all levels of management, professional and support staff, customers, potential customers, and government representatives; Must be proficient at managing teams to ensure all activities are completed on time and within budget; Hands-on experience with Earned Value Management System requirements and metrics is required; Customer focused, must be able to work on a self-initiated basis and in a team environment, and able to work extended hours and travel as required. Must hold or be able to attain a Secret clearance for potential cybersecurity requirements Salary:$90,930 - $162,788Travel Percentage Required 0 - 25Relocation Assistance Provided Not Provided US Citizenship Required? YesClearance Required? Desired Clearance LevelSenior (8+ years) WorkstyleOnsite
Summary The Senior Specialist DDIT OPS, Automation Engineer will oversee and lead the IT/OT team to ensure reliable 24/7 operations of the manufacturing plant, providing technical support, system maintenance, and issue resolution to minimize downtime and optimize plant performance. About the Role Major accountabilities: IT/OT Team Leadership & Incident Management: Lead the IT/OT team in managing and resolving incidents promptly, ensuring seamless plant operations and minimizing downtime. Support Automation CSV Activities: Support Computer System Validation (CSV) efforts to qualify production lines for the new site, ensuring all automation systems comply with regulatory and operational requirements. Vendor Coordination: Partner with equipment and system vendors to qualify and install PLCs, Environmental Monitoring Systems (EMS), Building Management Systems (BMS), and other automation technologies. Qualification Protocols: Develop, review, and execute qualification protocols—including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ)—in alignment with company and regulatory standards. Troubleshooting and Issue Resolution: Diagnose, troubleshoot, and resolve issues during qualification and commissioning phases to ensure timely project delivery and compliance. 24/7 Operational Support: Deliver continuous technical support for automation systems post-startup to ensure uninterrupted production and rapid response to system failures. IT Systems & Infrastructure: Plan, deploy, and maintain IT infrastructure, including setting up new environments, installing virtual machines, and configuring network switches. Cybersecurity: Implement and monitor cybersecurity best practices to protect IT/OT systems, safeguard critical data, and ensure compliance with corporate security standards. The salary for this position is expected to range between $108,500 and $201,500 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves. Minimum Requirements: Bachelor’s degree in Engineering (Electrical, Controls, Chemical, Mechanical, or related discipline) required. 5+ years of hands-on experience with control systems, including PLC, DCS, and MES platforms (e.g., Rockwell, Siemens, DeltaV, Syncade) within the pharmaceutical industry. Strong knowledge of Good Manufacturing Practices (GMP) and regulatory compliance requirements. In-depth understanding of Computer System Validation (CSV) and Commissioning & Qualification (C&Q) processes. At least 2 years of leadership experience managing automation teams, with a proven track record of troubleshooting system issues and driving timely resolutions. Strong expertise in IT infrastructure design and deployment to support OT systems. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards EEO Statement: The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. Accessibility & Reasonable Accommodations The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Division Operations Business Unit Universal Hierarchy Node Location USA State California Site Carlsbad Company / Legal Entity U061 (FCRS = US002) Novartis Services, Inc. Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No
Description:*Shift: *2nd *Schedule:* Monday - Friday, 2:00 PM - 10:30 PM *SUMMARY* The role of a Manufacturing Associate I is crucial in maintaining the efficiency and effectiveness of the production process. They actively participate in meeting production targets and deadlines, which is essential in ensuring that the company can accurately and timely deliver customer orders. *ESSENTIAL JOB FUNCTIONS* * Monitor machinery and equipment used in manufacturing, such as molded parts, to ensure products are made to specification. * Remove the parts from the machine manually. * Conduct visual inspections of the parts to check for pre-prescribed defects. * Document inventory and quality management production data, including quantities produced, defects identified, and materials used. * Correct certain defects, such as flash, using general tools based on engineering and quality feedback. * Assemble subcomponents of products, following detailed assembly instructions. * Package finished products for shipping, including labeling and preparing items according to customer orders. * Maintain a clean and safe work environment by adhering to safety protocols and cleaning schedules. * Participate in team meetings to discuss production goals and continuous improvement strategies and address concerns about the manufacturing process. * Available to cover for other associates during their lunch and break times. _*Other duties as required in support of the department and the company*_ *SUPERVISOR RESPONSIBILITIES* This role is purely as an individual contributor. Requirements:*QUALIFICATIONS* To succeed in this job, an individual must satisfactorily perform each essential job function. The requirements below represent the required knowledge, skill, and ability. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. *EDUCATION and EXPERIENCE* * A high school diploma or equivalent, e.g., vocational training, is required. * Familiarity with standard manufacturing practices and equipment preferred. * Experience in quality assurance (QA) and regulatory compliance preferred. * Experience in basic troubleshooting of manufacturing processes preferred. * Experience in the medical industries or molding businesses preferred. *LANGUAGE REQUIREMENTS* * Excellent verbal and written communication skills in English. * Conversational in any other language preferred. *MATHEMATICAL SKILLS* * Basic arithmetic: add, subtract, multiply, and divide whole numbers. *JOB SKILLS* * Familiar with Microsoft Office tools and SharePoint basics, eager to learn and expand proficiency. * Basic knowledge of Continuous Improvement, Lean Manufacturing, and the 5S Methodology. * Able to identify process deviations and product defects. * Able to effectively allocate resources to ensure timely product delivery that meets the required specifications. * Ability to set up, operate, and maintain equipment to ensure output meets established quality standards. * Dependable and willing to work overtime when necessary. *PHYSICAL DEMANDS* The employee will regularly engage in activities such as using hands to finger, handle, or feel and communicating verbally. Additionally, the employee will frequently need to reach with hands and arms while standing and walking as part of the role. Occasional lifting and movement of objects weighing up to fifty (50) pounds may be required. This position also demands specific vision capabilities, including close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus. According to ADA regulations, reasonable accommodation will be provided to ensure that individuals with disabilities can perform the job's essential functions. *WORK ENVIRONMENT* A work environment in a plant is the physical and social setting where goods production occurs. Depending on the type of product, process, and plant, the work environment may vary in terms of noise, temperature, safety, and demand. Common characteristics of a work environment in a plant are the use of machinery and exposure to hazards such as chemicals, heat, dust, or noise, with a culture of teamwork, communication, and continuous improvement. *ENVIRONMENTAL POLICY* Providien Thermoforming is dedicated to identifying and reducing the environmental impact of its operations, activities, and products. We are committed to complying with all applicable laws and other environmental regulatory requirements. We are also committed to preventing pollution and improving our environmental performance in all our global operations. This will be achieved through a comprehensive Environmental Management System that provides the framework for setting and reviewing Providien Thermoforming’s environmental objectives and targets. *PERSONAL PROTECTIVE EQUIPMENT REQUIREMENTS* * ASTM F–2412–2005, ANSI Z41–1999, or ANSI Z41–1991 rated safety toe shoes in specific areas. * Clear ANSI Z87.1 safety-rated glasses in specific areas. * Hearing protection in specific locations. * Ability to compile with JSA in specific areas. *TRAVEL* Travel is not required for this position. * SALARY INFORMATION* According to several states' laws, this position's salary range falls between *$17.25* and *$19.25* hourly/annually. However, this salary information is merely a general guideline. When extending an offer, Providien Thermoforming considers various factors such as the position's responsibilities, scope of work, candidate's work experience, education/training, essential skills, internal pay equity, and market considerations. Expected hours: 40 per week Benefits: * 401(k) * 401(k) matching * Dental insurance * Employee assistance program * Employee discount * Flexible spending account * Health insurance * Health savings account * Life insurance * On-the-job training * Paid time off * Parental leave * Professional development assistance * Tuition reimbursement * Vision insurance Work Location: In person
Scheduled Days & Hours: Monday-Friday, 1:00PM-9:30PM/FINISH, Occasional weekends as needed Wages: $25-30 per hour Location: San Marcos - At this time, we are only considering local candidates who are legally authorized to work in the United States. Relocation assistance is not available for this position. Ideal Candidate Criteria: The ideal candidate will be an experienced Journeymen Maintenance Mechanic wanting to cross train in a working plant environment. Job Duties: • Maintain various types of fluid packaging machinery in a food plant environment, including related auxiliary machinery. • Handling of chemicals for support equipment operation. Chemical testing of boiler feed water, condenser, cooling tower water, food-grade glycol, and plant process water • Fabrication and manufacturing of equipment for production needs: product and process piping, sanitary equipment, steam lines, chemical lines, pneumatic lines, etc. • Must be able to work overtime as needed. • Follow established programs, policies and practices to produce safe, quality foods that meets regulatory and company requirements. • Learn to weld if not already familiar, work with tools provided. • Prompt and regular attendance • Other duties as assigned. Skills Needed: Must have mechanical aptitude (auto or related is fine) and will be motivated, have a good attitude and be able to learn.???? Physical Requirements: While performing the duties of this job, the employee is regularly required to use hands to finger, handle, or feel; talk or hear and taste or smell. The employee is regularly required to stand; walk; reach with hands and arms; climb or balance and stoop. The employee must regularly push, pull; lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. Work Environment: While performing the duties of this Job, the employee is exposed to warm and humid conditions. The employee is regularly exposed to moving mechanical parts and vibration; occasionally fumes or chemicals and electricity. The noise level in the work environment is usually loud. Instructions: Employment is contingent upon results of a post-offer background check, drug test, functional assessment and physical. Instructions: Applicants may apply online at www.HollandiaDairy.com/Careers. Applicants who are unable to use the online system due to a disability should call the HR department to request an accommodation. Benefits: On day one, excellent medical, dental, vision, employer paid for long-term disability, life insurance (free up to $50k); various additional options to choose from Flexible Benefits account (FSA) for medical and dependent care Generous PTO (Paid Time Off) allowances and holiday pay 401(k) plan with employer matching Advancement and growth opportunities Fun employee and family events Employee gifts on birthdays & milestone anniversaries Safety bonuses and raffles Employee assistance program Hollandia Dairy is an EEO/AA/Disability/Vets Employer