Entry level manufacturing jobs in San Diego, CACreate job alerts

Job Description Test Packaging Lab Technician WESTPAK, Inc. San Diego 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 35 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 develop our employee-owned company with stewardship and integrity while continuing to make lives better. WESTPAK is looking for an experienced Test Technician to support our testing operations. We offer a competitive compensation package that includes ESOP shares, 401 (k) match, health benefits, various supplemental health packages, and pet insurance for your furry loved ones. A Test Technician candidate will: • Ensure project accuracy and quality through document control, standard operating procedures, and auditing., • Conduct required client testing to Quality Systems or Standard Operating Procedures., • Perform testing duties and documentation within the designated workday hours according to WESTPAK requirements, • Ensure customer objectives are met through proactive communication, documentation, and customer service., • Conduct testing with a high degree of integrity and data accuracy., • Conduct testing per WESTPAK quality processes and procedures with minimal non-conformance occurrences., • Record, collect, and organize all necessary documentation (equipment list, instrumentation, data) for each test conducted., • Maintain WESTPAK 5S and various site standards and expectations., • Accurately perform data entry, including customer contact records., • Assist on various duties and projects as assigned by the manager., • Fast learner and ability to communicate clearly., • Demonstrates strong accountability., • High focus on customer service, and willing to go above and beyond to get the job done., • Organized and impeccable follow-through skills are a must., • Work collaboratively with colleagues., • High school education required or GED equivalent, associate’s or bachelor’s preferred., • 1-3 years of working experience in a testing laboratory, manufacturing, or production environment preferred, • Ability to read and interpret documents such as protocols, industry specifications, and procedures, • Experienced in working within a documentation and process-based environment, • Understanding packaging fundamentals, • General tool knowledge (hand tools and light power), • Possess a strong work ethic and a high level of professionalism, • Proficient in the Microsoft Office suite and general computer literacy Principals only. We are not accepting any resumes or support from outside vendors. Please refrain from unsolicited marketing for the role. *This position is posted as a "Temp to Hire" position that will require 3-6 months of probationary evaluation before consideration to move into a full-time role." Monday - Friday 7AM - 3PM

Job Description Job title : Engine Mechanic I Client : Aerospace Industry Duration : 06 months Location : San Diego, CA 92121 Shift : 2nd Shift - 12:00 PM - 8:30 PM Description: • This entry-level role supports the disassembly, inspection, repair, and assembly of aero-derivative gas turbine engines. You will work under the guidance of senior mechanics or subject-matter experts, gaining hands-on training and technical experience in aerospace manufacturing. Responsibilities: • Participate in on-the-job training (OJT) to learn turbine engine maintenance procedures, • Assist in disassembling and assembling aero-derivative engines, • Review technical documents, tools, and visual aids before and during operations, • Perform basic inspection and support manufacturing processes, • Ensure compliance with Environmental, Health, Safety, and Quality procedures, • Demonstrate punctuality and commitment to scheduled shifts Qualifications: • High school diploma or GED required, • Technical education in a relevant field preferred, • Hands-on experience with gas turbine engines (preferred), • Familiarity with manufacturing principles and data systems, • Must be legally authorized to work in the U.S. (citizen or Green Card holder)#ZRCompany DescriptionAs a leading contract, contract-to-hire and professional placement firm, Three Point Solution understands the importance of aligning our client with the right resource at the right time. We are committed to the highest caliber of service that will benefit our clients, candidates and employees. Unlike large, corporate style recruiting firms, we commit to individualized attention that uniquely positions us to bridge the communication gap between recruiter, employer and candidate. Our goal is to cultivate and maintain true partnerships with our clients and candidates.As a leading contract, contract-to-hire and professional placement firm, Three Point Solution understands the importance of aligning our client with the right resource at the right time. We are committed to the highest caliber of service that will benefit our clients, candidates and employees. Unlike large, corporate style recruiting firms, we commit to individualized attention that uniquely positions us to bridge the communication gap between recruiter, employer and candidate. Our goal is to cultivate and maintain true partnerships with our clients and candidates.

Job Title: Engine Mechanic II Location: San Diego, CA 92121 Duration: 6 months Contract SHIFT: 12:00 PM to 08:30 PM Pay Rate: $24.00/hr. - $30.00/hr. Qualifications: 2ND SHIFT POSITION: Qualifications • Technical Education in related field., • Hands on experience with gas turbine engines (preferred)., • Familiar with the manufacturing principles; planning, data systems etc., • Must have High School diploma, or equivalent., • Must be a US citizen or Green Card holder per FAA requirements. Responsibilities: • This entry-level position requires the incumbent to learn, read, comprehend and perform a variety of basic manufacturing methods to support disassembly, repair and assembly of aero-derivative engines under the guidance of an experienced Engine Mechanic, Subject-Matter Expert (SME), Lead or Leader., • Actively participates in OJT by learning and applying manufacturing techniques and knowledge to support disassembly, repairing and assembly of aero-derivative engines., • Assists Engine Mechanics with preparing and visually inspecting parts, tools, reviewing sketches and technical information., • Performs basic manufacturing, disassembly and assembly of aero-derivative gas turbine engines., • Work as scheduled, on time and every day., • Observe the "Three Circles" with particular focus on client Values., • Adherence to all Environmental, Health, Safety and Quality Policies and Procedures., • All other duties assigned by Leadership.

Job Description Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. The Position The Clinical Research Associate (CRA) provides support to Study Lead(s) in clinical study planning, execution and management. The primary purpose of the position is to support the COM/Study Lead in study set-up, execution, oversight, and closeout activities in compliance with the clinical protocol, regulatory requirements, ICH GCP guidelines and governing policies & procedures. Responsibilities • Routinely monitor TMF inspection readiness for assigned studies, • Collect and/or review Essential Documents from investigational sites, • Review informed consent documents for accuracy and completeness, • Support investigator identification, feasibility, and activation activities, • Review monitoring visit reports for accuracy and completeness, • Perform periodic data reviews as requested by Study Lead, • Prepare and present updates at team meetings as assigned by Study Lead, • Provide guidance and training to junior level team members as assigned by management, • Participate in process improvement projects including SOP/WI development, • 2 years in clinical research, • 1 year onsite monitoring/site management experience, • Experience managing/supervising vendors preferred, • 4-year college degree All applicants must have authorization to work in the US for a company. California Applicant Privacy Policy

Job Description Millennium Health, based in Rancho Bernardo, is a leading health solutions company that delivers timely, accurate, clinically actionable information to inform the right treatment decisions for each patient at the right time. The company shares a unified belief that everyone has the right to safe and effective medicine and aims to deliver on that idea by providing clinicians with effective tools and information to reach that goal. We have an opening on our Lab Operations Team for a Supervisor, Lab Specimen Processing. Schedule: Tuesday - Saturday. Tuesday - Friday 6am start. Saturday 9am start. The Lab Specimen Processor Supervisor is responsible for managing the Lab Specimen Processor staff and the pre-analytical functions of specimen opening, lab support, test entry, aliquoting, centrifugation, batching and racking to ensure that all operational procedures and processes are followed including regulatory compliance within the laboratory. ESSENTIAL FUNCTIONS The following are intended to be examples of the accountabilities for which the person in this position is responsible. This position description is not intended to be complete or all-inclusive and does not preclude management from assigning other or related functions for which the individual has demonstrated competency through performance. • Manage the day-to-day activities of the Lab Specimen Processors including time and attendance, work schedules, time off requests, performance evaluations and disciplinary actions., • Plan, coordinate and supervise all functions within the laboratory including specimen opening, lab support, test entry, aliquoting, centrifugation, batching and racking., • Provide leadership, guidance, coaching and mentoring for all staff through regularly scheduled one-on-ones., • Initiate and conduct progressive disciplinary process when appropriate; involve HR as needed., • Responsible for training, scheduling, budgeting, supply maintenance and coordination with department administration and additional laboratory staff., • Ensure services being completed are of the best accuracy and are being carried out in an efficient manner within the standards and guidelines of current accreditations., • Responsible for being aware of safety issues and work in a safe manner in the lab at all times., • Understand the flow of the specimen through the lab and how each cell influences the flow of the specimen. Identify and implement process improvements., • Monitor employees’ productivity and take appropriate action to minimize overtime., • Knowledgeable of CAP regulatory requirements and other clinical laboratory audits and procedures., • Ensure appropriate training and competencies are met., • Ensure preventive maintenance on equipment and printers and promptly reports issues/problems., • Ensure audit-readiness in the lab at all times and follows up on issues/concerns associated with visits from regulatory/accrediting agencies., • Assist during internal and external laboratory inspections, to ensure compliance with applicable federal, state and local regulations and company standards., • Ensure Laboratory Occurrence Management (LOM) forms are completed for anomalies; organize and implement corrective action procedures as necessary., • Review accuracy of employee timecards and approve timecards daily., • Interview prospective Laboratory Specimen Processor employees., • Attend organizational meetings with team leads and provide feedback and updates to department., • Review and approve SOPs for the department. Ensure that SOPs are current., • Provide for the development and growth of Leads. Remains aware of evolving needs and opportunities, showing flexibility in doing whatever is appropriate to support the Company’s success. Pursues educational opportunities to maintain advanced and up-to-date knowledge in the field. Performs all other related duties as required and assigned and understands that the items in this description are not all-inclusive. Requirements EDUCATION • High School Diploma required., • 1-3 years of supervisory/management experience within a clinical lab, biotech or manufacturing industry highly preferred., • Experience managing a large staff (25+) preferred., • Excellent communication skills with the ability to interact professionally with all levels of management and staff., • Flexibility and ability to multi-task in a fast-paced environment, operating well in a team setting., • Ability to set own goals and expectations while meeting company’s goals., • Effective attention to detail with high degree of accuracy., • Proficient and able to meet deadlines., • Possesses proven team building skills with training knowledge/background., • Proficient in MS office applications (Outlook, Word, Excel, PowerPoint)., • Should have demonstrable comfort in the office environment., • Must handle daily changes well and be flexible in an ever changing environment., • Ability to ensure HIPAA, Confidentiality and Compliance policy, procedures, and standards are always adhered to., • Ability to ensure administrative, physical and technical cyber security controls are always adhered to. ESSENTIAL PHYSICAL & MENTAL REQUIREMENTS: • Standing (20%), sitting (20%), walking (60%) and lifting up to 20 lbs., • Physical requirements will vary depending on departmental needs., • The employee is expected to read and understand SOPs., • The employee should be able to convert SOP instructions into work-related tasks., • The employee must be able to perform simple calculations as required in SOPs., • The employee must be able to use judgment when there is a deviation in the system and effectively communicate any discrepancy to his/her Supervisor., • Must be able to speak in front of small to large groups. ADDITIONAL PHYISCAL & MENTAL REQUIREMENTS: • The employee is regularly exposed to a fast-paced environment, therefore must be able to thrive in this type of setting., • Withstand moderate amounts of stress and the ability to work in an environment where the noise level is usually moderate., • Must be able to work an extended schedule as needed., • Due to occupational work with saliva/oral swab specimens, there is a low risk of exposure to tuberculosis. As part of Millennium Health’s Tuberculosis Exposure Plan, all laboratory personnel have the opportunity to be screened for tuberculosis free of charge. POTENTIAL HIRING RANGE: • $67,000-$75,000 Apply for this job

Job Description GROW WITH US AND STAY EXTRAORDINARY: Launch your career to new heights with Innoflight—one of San Diego’s fastest-growing Aerospace and Defense innovators. Here, visionary minds engineer the future of space technology through pioneering, compact, and cyber-secure solutions. From software-defined radios to cutting-edge cryptographic systems and avionics, everything we build powers the next era of New Space. Join our small, agile, and mission-driven team where your work has real impact and your growth has no limits. We’re not just reaching for the stars—we’re engineering them. Let’s innovate the infinite, together. A DAY IN THE LIFE: As a Mechanical Engineer I, you’ll support the design, development, and implementation of mechanical components and systems for spacecraft-related products. Working under the guidance of senior engineers, you’ll gain experience in CAD design, prototype builds, product testing, and documentation—while collaborating with cross-functional teams to ensure successful project execution. This entry-level role is the perfect opportunity to apply mechanical engineering principles to real-world aerospace projects and grow your technical expertise. WHAT YOU'LL DO: • Design & Development: Assist in the design and development of mechanical components and assemblies using CAD tools., • Prototyping & Testing: Support prototype builds, engineering testing, and early-stage design iterations., • Documentation: Create and maintain technical drawings, plans, and specifications with supervision., • Product Improvements: Participate in testing and experimentation to support design refinements., • Technical Writing: Write and maintain basic technical documentation for manufacturing and assembly., • Project Support: Assist in estimating project timelines and budgets with guidance., • Compliance: Ensure that designs meet basic compliance regulations., • Collaboration: Work with cross-functional teams, including electrical and software engineers., • Mechanical Engineering Principles: Applying academic knowledge to design, testing, and documentation., • Technical Problem-Solving: Analyzing design challenges and supporting practical solutions., • CAD & Tools: Using software such as SolidWorks or AutoCAD to create and refine designs., • Teamwork & Communication: Collaborating effectively across disciplines and communicating technical concepts clearly., • Bachelor’s Degree in Mechanical Engineering or a related field required., • 1 or more years of mechanical engineering experience, including internships and/or project-based work preferably in the aerospace industry., • Experience with CAD software such as SolidWorks or AutoCAD., • Knowledge of mathematical computing and analysis tools (e.g., MATLAB, Excel, LabView)., • Strong technical and problem-solving skills with the ability to analyze design challenges., • Effective communication skills, both verbal and written., • Ability to work collaboratively in a team environment and take direction from senior engineers., • Proficiency in Microsoft Office tools (Word, Excel, PowerPoint)., • 401(k) with 3% company match (automatic enrollment), • Comprehensive medical, dental, vision, HSA & life insurance, • 10 paid holidays + 120 hours PTO (starting in year one), • Flexible Work-Life Balance: Enjoy a 9/80 work schedule with every other Friday off—whether you use it to recharge, work on a passion project, or spend time with family, the choice is yours., • Continuous Learning & Development: We’re serious about professional development. From tuition reimbursement to internal "Ask Me Anything" sessions and weekly “Lunch & Learns,” we make learning a core part of the job. YOU SHOULD KNOW: Potential new employees must successfully complete a background check which includes criminal search, education certification and employment verification prior to hire. Applicants must be authorized to work for any employer in the U.S as you must have the ability to obtain a security clearance. We are unable to sponsor or take over sponsorship of an employment Visa. REFERRALS: We love a good referral! If you know someone that would be a great fit for this position, please share! A NOTE TO STAFFING AGENCIES: Innoflight does not accept unsolicited resumes from agencies, recruiters, or any third-party sources. Any such submissions will be considered property of Innoflight, and no fees will be paid in the event a candidate is hired from an unsolicited referral. To California residents applying for this job, please read Innoflight’s CCPA Notice: . #LI-Onsite Powered by JazzHR qsCAB6eCao

Job Description Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. The Position The Sr. Clinical Research Associate (Sr. CRA) provides support to Study Lead(s) in clinical study planning, execution and management. The primary purpose of the position is to support the COM/Study Lead in study set-up, execution, oversight, and closeout activities in compliance with the clinical protocol, regulatory requirements, ICH GCP guidelines and governing policies & procedures. Responsibilities • Support assigned study teams with TMF set-up, maintenance, ongoing quality control reviews, and final reconciliation of study documents, • Routinely monitor TMF inspection readiness for assigned studies, • Assist Study Lead with investigational product and ancillary supplies management, accountability and reconciliation activities, • Collect and/or review Essential Documents from investigational sites, • Review informed consent documents for accuracy and completeness, • Support investigator identification, feasibility, and activation activities, • Review monitoring visit reports for accuracy and completeness, • Support Study Lead in preparing materials for study-wide meetings (eg investigator meetings, interim update meetings, data safety committee meetings, etc.), • Perform QC (formatting, spelling and grammar, accuracy, consistency) of study-level documents (master ICFs, study plans, manuals, CRFs/CRF completion instructions, etc.) in alignment with study protocols, • Contribute to the development of study-level documents ( study templates, manuals, guides, newsletters, etc.), • Provide updates on study/site status as needed to ensure timely study entry and updates are reflected on ClinicalTrials.gov or equivalent, • Perform periodic data reviews as requested by Study Lead, • Prepare and present updates at team meetings as assigned by Study Lead, • Support central/referral laboratory set-up and on-time activation (eg specifications, user manual) as delegated by the Study Lead, • Work closely with CRO to plan for execution of study start-up and ongoing study execution activities as assigned by the Study Lead., • Provide guidance and training to junior level team members as assigned by management, • Recommend modifications to SOPs/work instructions (WIs) when necessary to improve compliance or efficiency, • Participate in process improvement projects including SOP/WI development, • 5 years in clinical research and development, • 3 years onsite monitoring/site management experience, • Experience managing/supervising vendors, • 4-year college degree All applicants must have authorization to work in the US for a company. California Applicant Privacy Policy

Job DescriptionCenturum is seeking a Senior Acquisition Specialist to perform program analyst tasks required to support the Navy Catapult and Commercialization Readiness Program (CRP) at the NAVWAR Small Business Innovation Research (SBIR) Program Management Office. The individual will be responsible for the entry, validation, and configuration management of Navy Catapult and CRP program data on federal government information systems including, but not limited to, the DON Program Management Database (PMDB), S&T Alignment and Investment Reporting System (STAIRS), Flankspeed Teams and SharePoint tools, OneNote, and shared file resources. The individual will perform data validation and quality assurance activities to ensure the accuracy of data contained in these systems. The acquisition specialist will also be required to: • Conduct organizational studies and evaluations, design systems and procedures, conduct work simplification and measurement studies, and prepare operations and procedures manuals to assist management in operating more efficiently and effectively., • Support and draft program milestone related documentation to ensure compliance with all aspects of the DoD and SECNAV 5000 series directives., • Support the development of program acquisition documentation such as Acquisition Plans (APs), Acquisition Strategy Reports (ASR), Procurement Initiation Document (PID), Statement of Work (SOW), funding documents, contract awards, agreements, and Acquisition Program Baseline Agreements (APBA)., • Assess program procedures, practices, philosophies, and documentation for compliance with specifications, contracts, and mission requirements., • Attend, participate, support, analyze, provide input, develop, prepare and report on briefs, point papers, reports, correspondence, meetings, conferences, and review boards., • Utilize business and technical methodologies to provide support of hardware, software, and service acquisition and life cycle management., • Participate in meetings and support specified Program Integrated Product Teams (IPTs). Required Experience: • At least six (6) years of experience performing work related to the description above. Must have science and technology process experience., • At least six (6) years of experience in 2 of the following Defense acquisition areas: logistics, research and development, configuration management or systems analysis/design., • Demonstrated knowledge in one or more of the following areas: program management, systems engineering, system acquisition, financial management, test and evaluation or integrated logistics support., • Demonstrated knowledge, and/or familiarity with the DoD and SECNAV 5000 acquisition series, Federal and DoD acquisition regulations and PPBE process., • Demonstrated knowledge in risk analysis/risk management, • Demonstrated knowledge in developing a business plan, • Demonstrated knowledge in specialized and focused company management assessment recommendations. Preferred Experience:, • Over ten (10) years of experience performing work related to the description above. Must have science and technology process experience, preferably supporting the US Navy., • It least 6 years of experience to be related to Defense acquisition, preferably Navy, including logistics, research and development, configuration management or systems analysis/design., • Demonstrated knowledge in one of more of the following areas: system acquisition, acquisition documentation, configuration management, risk analysis and Government furnished equipment (GFE) or Government furnished information (GFI)., • At least six (6) years of experience related to manufacturing plans, configuration management, commercialization/transition, and audit preparations., • Demonstrated knowledge in one or more of the following areas: business planning, business development, or operational security review., • At least six (6) years’ experience in specialized and focused company management assessment recommendations. EOE M/F/Disability/Veteran Benefits Full-time employees are eligible for the following benefits enrollment from their date of hire: • Health Insurance - Centurum provides insurance for employee and dependent in a comprehensive package. Coverage for vision care is included. This option is available on a cost-sharing basis., • Dental Insurance - Available in conjunction with Health Insurance for an additional cost. Provides oral maintenance care for employee and dependent., • Basic Life Insurance - Company provided benefit for all full-time employees., • Supplemental Life Insurance - Optional life insurance coverage to employees at group rates., • Dependant Life Insurance - Optional coverage for dependents at a group rate., • Long Term Disability Insurance - Optional coverage available to employees at group rates., • Vacation and Sick Leave - Leave accrual is determined by length of service., • Holidays - The company observes ten paid holidays each year. Powered by JazzHR FAB5OmMIrp

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JOB TITLE: WAREHOUSE ASSOCIATEDEPARTMENT: PRODUCTIONSTATUS: FULL TIMEIMMEDIATE SUPERVISOR: WAREHOUSE SUPERVISORTHE SALVATION ARMY MISSION STATEMENT: The Salvation Army, an international movement, is an evangelical part of the universal Christian Church.Its message is based on the Bible.Its ministry

Two years of skilled, journey-level painting and traffic painting experience required. Should the level or location of the role change during the hiring process, the applicable base pay range may be updated accordingly.

In most jobs, everyone doesnt spontaneously erupt into applause and start raining down high-fives.At Buffalo Wild Wings, thats just a Thursday night.This is the place to start the next phase of your career.Whether you grow in our system here or your game-plan takes you elsewhere, we want you to have

No experience requited, hiring immediately, appy now.Our Freight Team works to ensure stores are stocked and ready for business.Responsible for unloading trucks and moving material through the store, they are an integral part of our business and the customer retail experience.The majority of these p

Sports Arena Blvd [Material Handler / Freight Handler] As a Warehouse Associate at Salvation Army U.Sort product efficiently and properly according to the standard of TSA policy; Inspect products for defects and damages; Identify product correctly and direct to proper department for processing; Coll