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Veridiam is a strategic manufacturing partner with over 60 years of experience serving the aerospace, industrial, medical, and nuclear markets. Our roots were formed in the exacting nuclear and aerospace industries, expanded into Medical where we have supplied critical components to a global customer base. We currently provide elegant solutions across a broad range of customers and diverse markets. At Veridiam we recognize that talent is at the forefront of our organization and define who we are in today's industry. POSITION SUMMARY Use standard measuring equipment to perform inspections of fabricated parts; perform various dimensional and visual inspections of materials and products; and report results of inspections. ESSENTUAL DUTIES AND RESPONSIBILITIES Set-up and perform mechanical and electronic dimensional inspection of various products. Perform receiving, in-process and final visual and dimensional inspection on all product lines. Set-up and operate air gage equipment to measure products. Calibrate mechanical and electronic inspection equipment. Utilize sampling plans as required by the specification. Analyze and report inspection results. Perform various laboratory tests including, but not limited to, surface roughness tensile and hardness testing. Perform routine maintenance of equipment and tooling, including preventive maintenance and maintaining cleanliness of equipment and work area. Detect, identify and segregate non-conforming product. Follow instructions related to enhanced/additional inspections. Maintain clean and orderly work environment. Demonstrates ability to appear for work on time, follow directions from a supervisor, interact well with co-workers, understand and follow work rules and procedures, comply with company policies and procedures, goals and objectives, and accepts constructive feedback. Other duties as assigned, requested or needed. POSITION REQUIREMENTS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals to perform the essential functions. Education and Experience: High school diploma or General Education Development (GED). Minimum five (5) year’s aerospace and metal material inspection experience or equivalent of education and experience. Prior experience with visual and manual dimensional inspections. Knowledge, Skills and Abilities: Proficient knowledge of visual and dimensional inspection methods. Proficient knowledge of geometric dimensioning and tolerancing (GD&T). Knowledge of and ability to operate CMM. Ability to understand and follow standard operating and safety procedures. Ability to prioritize and handle workflow. Read and comprehend verbal and written instructions. Proficient knowledge of and ability to use measuring tools such as micrometers, rulers, calipers, and gauges, PI tape ring, pin gages tape measure. Ability to measure and read dimensional tolerance tools and equipment. Ability to view details in close range. The above statements are intended to describe, in broad terms, the general functions and responsibility levels assigned to this classification. Management has the right to change duties at any time to meet business needs. Pay Rate: The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience with the industry, education, geographic location, etc. Veridiam is an Equal Employment Opportunity/Affirmative Action Employer. Veridiam will recruit, hire, train and promote persons into all jobs without regard to age, race, color, religion, ancestry, medical condition, sex, sexual orientation, gender identity, national origin, status as a veteran or status as an individual with a disability or any other characteristic or classification protected by law. Access to our facility (and, therefore, employment) is restricted under the International Traffic in Arms Regulations (ITAR) and/or Export Administration Regulations (EAR) to U.S. Citizens, lawful permanent residents of the United States and properly licensed foreign persons. Applicants receiving a conditional offer of employment will be required to provide information to determine whether they are subject to these regulations and, if so, to assess their country of chargeability for export control purposes. 2nd shift 1 p.m. - 9:30 p.m.
*Manufacturing Chemist II* *Location:* Carlsbad, California *Schedule:* Full-Time, On-site (Monday – Friday) *Compensation:* $79,200 – $89,400 annual base salary _(depending on experience, skills, and internal equity)_ *Diagnostics That Make a Difference* At *Lumos Diagnostics*, we develop, manufacture, and distribute innovative point-of-care diagnostic solutions that deliver actionable results when they matter most. We’re seeking a *hands-on Manufacturing Chemist II* to join our growing Carlsbad team. In this role, you’ll spend most of your time in the lab—preparing formulations, running experiments, and ensuring that every batch meets the highest standards of quality and performance. You’ll play an essential role in bridging scientific concepts with scalable manufacturing processes that make real-world impact in healthcare. This position is ideal for someone who thrives in a laboratory setting, enjoys solving problems through experimentation, and takes ownership of their work from concept through production. *What You’ll Do* * Prepare, test, and optimize *diagnostic reagent, buffer, and solution formulations* to improve stability, performance, and scalability. * Perform *hands-on laboratory work*, including mixing, pipetting, measuring, and performing analytical testing such as pH, viscosity, appearance, and stability. * Support *scale-up activities* from bench to manufacturing, maintaining precision and documentation at every stage. * Identify root causes of variability and drive *continuous process improvements* in formulation and production. * Collaborate with R&D, Manufacturing, and Quality teams to support *design transfer* and ensure compliance with ISO 13485 and Good Manufacturing Practices. * Draft, review, and maintain *standard operating procedures, batch records, and work instructions*. * Assist in *validation activities* and ensure equipment is qualified and properly maintained. * Provide technical support and mentorship to junior chemists or technicians. *What We’re Looking For* * *Bachelor’s degree* in Chemistry, Biochemistry, Chemical Engineering, or a related field, with *2–4 years of experience* in a laboratory or manufacturing environment; or a *Master’s degree* with *1–3 years of experience*. * Proven *hands-on laboratory experience* in a regulated environment (GLP, GMP, or ISO 13485). * Demonstrated ability to perform *formulation and process development* with strong attention to detail and data integrity. * Experience supporting *process validation, technology transfer, or production scale-up*. * Strong problem-solving skills and ability to work independently in a fast-paced, collaborative environment. * Excellent documentation and communication skills. *Preferred Experience:* * *Protein conjugation* to gold or latex particles. * Experience with *immunoassay, lateral flow*, or point-of-care diagnostic technologies. * Familiarity with *Lean principles, Design of Experiments, or Six Sigma* methodologies. *Why Join Lumos Diagnostics* * Be part of a *mission-driven company* advancing diagnostic solutions that improve lives. * Work in a *collaborative, supportive environment* built on our values: * *Take Ownership, Engage Openly, Act with Integrity, and Move Together.* * Opportunity to work hands-on in a growing team with meaningful exposure to cross-functional projects. * Competitive compensation, comprehensive benefits, and opportunities for growth and development.*How to Apply* To be considered for this position, please submit your resume and ensure *all screening questions are fully answered*. Job Type: Full-time Pay: $79,200.00 - $89,400.00 per year Benefits: * 401(k) matching * Dental insurance * Employee assistance program * Employee discount * Flexible schedule * Flexible spending account * Health insurance * Health savings account * Life insurance * Paid time off * Parental leave * Professional development assistance * Referral program * Tuition reimbursement * Vision insurance Application Question(s): * Do you have a Bachelor’s degree or higher in Chemistry, Biochemistry, Chemical Engineering, or a related scientific field? * Do you have at least two years of hands-on experience working in a laboratory or manufacturing environment? * Have you worked in a regulated environment such as Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), or ISO 13485? * Do you have experience preparing, testing, or optimizing formulations, buffers, or reagents? * Have you performed analytical testing such as pH, viscosity, or stability measurements? * Have you participated in process scale-up, validation, or technology-transfer activities? * Do you have hands-on experience with protein conjugation to gold or latex particles? * Are you comfortable spending the majority of your workday performing hands-on laboratory work? * Do you have experience maintaining accurate documentation, such as standard operating procedures, batch records, or work instructions? * Have you worked with cross-functional teams such as R&D, Quality, or Engineering to troubleshoot or improve processes? * Are you willing to wear appropriate personal protective equipment (PPE) and follow safety and contamination-control procedures at all times? * The compensation range for this position is $79,200 – $89,400 per year (depending on experience, skills, and internal equity). Are you comfortable with this compensation range? * Are you able to work on-site at our Carlsbad, California facility Monday through Friday? Education: * Bachelor's (Required) Work Location: In person
At Winchester Interconnect, we always do the right thing, the right way. Winchester Interconnect is committed to inspiring the most innovative teams. We foster a dynamic, inclusive environment that thrives on collaboration and continuous growth. We hire exceptional people, celebrate wins, empower employee growth, and provide opportunities to thrive. Winchester is where potential transforms into purpose, and every team member plays a vital role in shaping our shared success. Position Summary: We are seeking an experienced and technically driven Product Development Engineer with a background in Electrical or Chemical Engineering to support the development and manufacturing of high-performance wire and cable products. The ideal candidate will have a strong understanding of extrusion processes, cabling, shielding, and jacketing, and familiarity with the wire and cable interconnect market. This individual will play a key role in improving process capability, supporting new product introductions, and driving manufacturing excellence across our operations. Qualifications & Requirements: Bachelor's degree in Electrical Engineering, Chemical Engineering, Materials Science, or Mechanical Engineering. 3+ years of relevant experience in wire and cable or interconnect manufacturing. Hands-on knowledge of extrusion equipment, process controls, and polymer behavior. Experience with radiation polymer crosslinking, extrusion, braiding or metal armoring processes preferred. Strong analytical, troubleshooting, and data-driven problem-solving skills. Excellent communication skills and ability to work effectively across teams. Preferred Master's degree in Electrical Engineering, Chemical Engineering, Materials Science, or related field. Experience with fluoropolymer and high-temperature materials (e.g., FEP, PFA, ETFE,PU,PE). Familiarity with testing standards such as MIL-DTL, SAE AS22759, or UL cable specifications. Knowledge of process modeling or simulation for polymer extrusion or thermal processes. Proven ability to lead cross-functional technical projects or process transfers between facilities. Experience supporting regulated or high-reliability markets (e.g., Aerospace, Subsea, Space, Military) Our core values - Accountability, Collaboration, andEmpowerment(ACE) - are the foundation of how we operate and drive success. You will take ownership of your contributions, collaborate with a team that gets stuff done, and be empowered to innovate and pursue bold initiatives that drive our business forward. Are You Our Next ACE? Accountable for translating concepts into robust, reliable, and manufacturable designs. You will validate product performance through rigorous analysis and testing, ensuring all cost and quality targets are met. Ultimately, you are responsible for delivering engineering milestones on schedule and collaborating with cross-functional teams for a successful product launch. Collaborate with Product Management to design and transform market requirements and aesthetic concepts into functional technical designs. Working closely with Manufacturing and Quality Assurance, you will ensure designs are optimized for production and rigorously validated to meet all standards. You will also provide key technical updates to Project and Marketing teams to support a timely and successful product launch.. Empowered to drive the entire technical development process, from initial sketch to final production. This role gives you the autonomy to make critical design decisions, select the best materials and technologies, and manage project timelines. We trust you to be the engineering leader who ensures our products are innovative, robust, and successfully brought to market. Systems You'll Use: Google Enterprise ADP For a sneak peek into some of our benefits and to learn more about our career opportunities, click here https://www.winconn.com/jobs/. Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities. In addition to federal law requirements, Winchester Interconnect complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. Winchester Interconnect expressly prohibits any form of workplace harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. ***Candidate Inquiries Only-No Third-Parties*** Compensation: up to $140,00/annually DOE
*Quality Control Specialist* *Job Title: *Quality Control Specialist *Department: *Operations Department *Reports To: VP of Ops and MFG Ops Manger* *Salary/Pay Range:* $20.00-28.00 DOE As required by company need job hours may fall in one of the following: Full time: 30 - 40 hours /week (overtime may be required) JOB SUMMARY: Responsible for the organization, communication, and utilization of resources to efficiently complete the quality task assigned. Maintains quality standards by approving incoming materials, in process production, finished products, and recording quality results. Oversees and leads quality initiatives and trains other quality team members on all quality related procedures. RESPONSIBILITIES/ DAILY TASKS: Inspects incoming materials by confirming specifications, conducts visual and measurement tests, and inputs corresponding data into the system when required. * Participates in-process production by confirming specifications, conducting visual and measurement tests, and communicates any adjustments if necessary. * Inspects and approves finished goods by confirming specifications, performs a visual inspection, returns products for re-work, and confirms rework. * Documents and inputs all inspection results by inputting data into the Quality System. * Data entry on the ECO/ECR log and communicates with appropriate parties regarding current status and responsibilities. * Maintains measurement equipment and schedules calibration when necessary. * Maintains a safe working environment by following company standards and procedures, and complies with legal regulations. * Participates in maintaining the quality and organization of the company and reports any quality related issues in a timely manner. * Document quality activities/procedures as requested. * Trains and leads other quality team members in all quality related procedures and activities. * Other related tasks may be assigned such as counting, packaging, labeling or bagging the produced parts or the raw material in preparation for kitting. * Ability to work individually and / or within a team. QUALIFICATIONS: *Education/Experience* 12 months of quality related working experience. * ISO 9001 background/training preferred. *Knowledge, Skills and Other Abilities* * Adequate Math, Reading & Reasoning Ability – Ability to add, subtract, multiply, and divide. Ability to read and understand assembly instructions and interpret product drawings. Ability to understand to carry out instructions provided in written, oral, or diagram form. * Adequate understand in PC operations. * Knowledge of MS Office. * Strong Attention to Detail. * Individual is expected to have good verbal and written communications skills. * Able to train others and work in a team. * Organizational skills; Planning skills; Time Management skills. * Manual dexterity with the ability to maintain daily / weekly quota by working quickly and accurately. * Positive Attitude. * Ability to work overtime. _Physical Demands and Work Environment – The following physical demands and work environment characteristics are representative of those that must be met to successfully perform the essential functions of this job:_ Employee is regularly required to stand; walk; sit; use hands; reach with hands and arms; climb or balance; stoop, kneel, crouch or crawl; and talk or hear. The employee may be required to lift/and or more up to 20 pounds. Specific vision abilities required by this job include close vision, distance vision, peripheral vision, depth perception, ability to adjust focus and the ability to see color. While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts, work near ventilated and exhaust equipped soldering stations and some solvents and chemicals. The noise level in the work environment is usually moderate. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Job Type: Full-time Pay: $41,000.00 - $58,000.00 per year Benefits: * 401(k) * 401(k) matching * Dental insurance * Flexible spending account * Health insurance * Paid time off * Referral program * Vision insurance Work Location: In person
About BPS Bioscience BPS Bioscience is a leading provider of recombinant proteins, assay kits, and cell lines, specializing in supporting drug discovery across various research areas, including cancer, neurology, immunotherapy, epigenetics, and more. We are dedicated to advancing scientific discovery by offering high-quality products and services to researchers worldwide. Job Overview This role is responsible for the preparation, formulation, and packaging of biochemical reagents and assay components in compliance with ISO 9001:2015 standards. The ideal candidate will thrive in a fast-paced, quality-driven environment and demonstrate strong attention to detail, consistency, and documentation. Success in this role requires a team-oriented mindset, flexibility to adapt to shifting priorities, excellent interpersonal skills, and a commitment to high-quality work. Responsibilities: Reagent Preparation: Accurately retrieve, weigh, and mix raw materials and components according to department procedures. Labeling & Packaging: Dispense and label final products with precision, ensuring traceability and compliance with documentation standards. Documentation: Maintain accurate and complete records of manufacturing activities in both paper and electronic formats, in accordance with ISO 9001 standards. Inventory Management: Use ERP systems and Labguru ELN software to track material usage, manage inventory, and restock supplies. Workplace Organization: Maintain a clean and organized work area following 5S principles and safety protocols. Process Support: Assist in process development and scale-up activities for new reagent formulations, including troubleshooting and optimization. Cross-functional Collaboration: Work closely with QC, QA, and R&D teams to ensure product quality and support tech transfer initiatives. Other Duties: Perform additional tasks assigned to support production goals. Requirements: Bachelor’s degree in Biology, Chemistry, Biochemistry, or related field required. 0–2 years of experience in a manufacturing or laboratory setting, preferably in reagent or assay production. Familiarity with ISO 9001 or other quality systems is a plus. Strong organizational and communication skills. Benefits! 401k with 4% company match Medical/Dental/Vision health insurance plans Vacation and paid holidays Companywide lunches provided quarterly BPS Bioscience Inc. is an equal opportunity employer, without regard to race, color, religion, age, gender, sexual orientation, disability, or any other characteristic protected by applicable law.
With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing. Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely. We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services. We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient. The Associate II performs process development activities in collaboration with other individuals and departments to devise scalable and robust processes on accelerated timelines. Responsibilities Designs and executes process development experiments to develop a thorough understanding of operating and performance parameters and identifies promising areas for process improvements. Effectively analyses experimental results and designs and executes follow-up experiments that build upon previous results. Provides training to new personnel in specific technical processes, as needed. Performs process development activities for projects and products in collaboration with other individuals and departments. Actively participates in technical transfer of downstream purification processes from clients and between Process Development and other internal groups like Cell Line Development and MSAT/MFG. Actively participates in performing scale-up calculations across varying scales of the process — up to cGMP scale. Develops buffer formulations and makes buffers accurately according to protocols. Actively participates in the documentation of observations and collection of data for analysis. Participates in data management and the identification of trends in data and notification of scientists of possible impacts to processes and products. Conducts activities in support of production schedules and objectives as directed by senior staff. Troubleshoots challenging technical, experimental, and instrumental issues. Maintains detailed records to comply with regulatory requirements and assists with in-process testing. Maintains lab organization and cleanliness by regularly stocking supplies, scheduled cleanings, and managing supply inventory. Assembles and autoclaves tubing assemblies. Maintains cleanliness of specific equipment such as AKTA systems and biosafety cabinets. Maintains up-to-date knowledge of quantitative and qualitative analytical methods. Represents Process Development and its activities as needed during project team meetings, training, and evaluation of new technologies. As needed, assists with protein purification under cGMP standards for production of clinical trial material. Operates to the highest ethical and moral standards. Complies with Abzena's policies and procedures. Communicates effectively with clients, supervisors, colleagues and staff. Participates effectively as a team player in all aspects of Abzena's business. Adheres to quality standards set by regulations and Abzena policies, procedures, and mission. Performs other duties as assigned. Qualifications BS or MS degree in biological sciences, chemistry, chemical engineering, biotechnology, biochemistry or related fields with 3+ (BS) or 2+ (MS) years’ experience in the pharmaceutical or biotechnology fields. Strong knowledge of recombinant protein expression and protein purification strategies using a variety of chromatographic techniques. Strong knowledge in protein chemistry and analytical methods. Good understanding and extensive hands-on experience with AKTA systems and Unicorn software: Cytiva - Pure, Avant, Pilot, and Ready. Good understanding and extensive hands-on experience with centrifugation, depth filtration and TFF/UFDF. Knowledge of buffer formulation and preparation. Practical experience with cGMP manufacturing operations and fluency of regulatory regulations is desired. Comfortable in a fast-paced environment with minimal direction and able to adjust workload based upon changing priorities. Skilled with Microsoft Office suite. Ability to work effectively in a team environment and motivated to work on multiple and various tasks, when required. Skilled in problem solving and troubleshooting. Ability to safely operate production equipment in accordance with established practices. FLSA: Non-Exempt Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.
*Manufacturing Technician I – Temporary (90-Day Assignment)* *Location:* Carlsbad, California *Schedule:* Full-Time, Non-Exempt *Pay Range:* $20.05 – $22.36 per hour (depending on experience, internal equity, and alignment with market data) *Join a Team That Builds Diagnostics That Matter* At *Lumos Diagnostics*, every product you help assemble makes a difference in patient care around the world. We are seeking a motivated and detail-oriented *Manufacturing Technician I* to join our Carlsbad production team. *This is a 90-day temporary role with the possibility of conversion to a full-time position based on production needs, individual performance, and overall business conditions.* If you enjoy working with your hands, thrive in a fast-paced, quality-driven environment, and want to be part of something meaningful, this is your opportunity. *What You’ll Do* * Assemble diagnostic cartridges, reagent kits, and related components following standard operating procedures and specifications. * Operate basic manufacturing and assembly equipment in a clean, controlled environment. * Follow established quality standards and production processes to ensure product consistency. * Maintain organized, safe, and clean work areas, including proper handling of materials and chemicals. * Accurately complete production records, work orders, and documentation. * Collaborate with team members to achieve daily production goals and support continuous improvement efforts. *What We’re Looking For* * *High School Diploma or GED* required. * *0–1 year of experience* in manufacturing, assembly, or a related technical field. * Ability to follow written and verbal instructions accurately. * Strong attention to detail and commitment to high-quality work. * Reliable, punctual, and able to work both independently and as part of a team. * Comfortable standing or walking for extended periods and lifting up to 50 pounds. * Experience in a regulated manufacturing or cleanroom environment preferred. *Why You’ll Love Working Here* * Be part of a mission-driven company advancing diagnostic solutions that improve lives. * Work in a collaborative, respectful environment built on our values: *Take Ownership, Engage Openly, Act with Integrity, and Move Together.* * Opportunity for full-time conversion based on performance and company needs. * Competitive hourly pay and valuable hands-on experience in the medical device industry. *Please Note:* In order to be considered for this position, *all screening questions must be fully answered* when submitting your application. Job Types: Full-time, Temporary Pay: $20.05 - $22.36 per hour Expected hours: 40 per week Benefits: * Employee assistance program * Employee discount Application Question(s): * Do you have 0–1 year of experience in manufacturing, assembly, or a related technical field? * Have you worked in a regulated manufacturing environment (for example, medical device or ISO 13485 environment)? * Have you ever worked in a cleanroom environment or followed Good Manufacturing Practices? * Are you able to stand or walk for extended periods and lift up to 50 pounds? * Are you able to follow written and verbal instructions accurately and complete required documentation such as batch records or standard operating procedures? * The schedule for this position is Monday through Friday, 7:30 AM to 4:00 PM, which is an 8-hour shift with a 30-minute unpaid lunch. Are you able to work this schedule? * The pay range for this position is $20.05 – $22.36 per hour, depending on experience, internal equity, and alignment with market data. Are you comfortable with this compensation range? * Have you consistently demonstrated dependable attendance and punctuality in previous positions? * Do you work well as part of a collaborative team environment? * Do you understand and agree that this is a temporary 90-day assignment, which may or may not convert to a full-time position depending on production needs, individual performance, and business conditions? Education: * High school or equivalent (Required) Work Location: In person
*GVI Inc.,* a subsidiary of Three Saints Bay, LLC, and a Federal Government Contractor industry leader, is seeking a *Field Engineer in San Diego, CA.* *Position Responsibilities:* * This engineer performs typical duties as: Design and test engineering activities in support of developing, updating, reverse engineering, and documenting printed circuit boards. Supports new capability engineering work, including design, evaluation, planning, testing and operation of C4ISR electrical, electronic, mechanical, and/or computer components, equipment and systems. Performs various tests and analyzes and documents results. Identifies and documents functional requirements. Reviews, writes, and provides updates to technical documentation. Analyzes research & development plans. Maintains current knowledge of relevant technologies as assigned. Participates in special projects as required. Position Requirements: * Bachelors in EE, ME, CE, CS, TM, IS, IRM, IT, Physics or other related field; Master’s in same. * 5 years C4ISR or other relevant experience in large system design, testing, installation, and analysis, using ILS data and risk/trade-off analysis of several systems. * Senior project management experience for planning, scheduling and execution of large programs. * Ability to learn new tools and processes quickly. * Hands on RF experience, networking experience, HiPot testing experience and spectrum analyzer experience. * Test software programming. Flying Probe program generation and debugging. Implement and verify relevant software upgrades. * Train, mentor, and support test and repair technicians. * Troubleshoot tester hardware and software issues by working with customer support to resolve. * Analyze and improve prototype, production yields and implement best practices for test and repair processes. Analyze failure data, summarize, and present analysis to stakeholders. Maintain backups of test programs and test data. Manage equipment by working with the facilities team and vendors to perform periodic calibrations and preventive maintenance. * Support testing process (time studies, data collection/analysis, special customer requests, etc.) for quotes, trials, and process improvements. Identify and recommend software solutions, cost reductions and quality improvements in repair operations. * Work closely with the Quality team to complete any First Article Inspection Reports or relevant Corrective and Preventive Actions, and submission of Technical Data Package to Configuration Management. Recommend appropriate hardware/software technology for optimizing the quality and efficiency. * Familiarity with operating machinery/robots safely and efficiently. * Ability to read and understand technical drawings, datasheets, and written work instructions. * Oversee the installation, validation and development of new test equipment and processes. *Compensation: $90K - $150K* *Position is located in San Diego, CA. * VEVRAA Federal Contractor Three Saints Bay, LLC and its subsidiaries offer a team-oriented working environment and the opportunity to work with exceptional, dedicated industry professionals. We offer our employees a comprehensive benefits package and the opportunity to take part in exciting projects with government and commercial clients, both domestic and international. We are an Equal Opportunity Employer. We invite resumes from all interested parties without regard to race, color, sex, sexual preference, religion, creed, national origin, age, genetic information, marital or veteran status, disability, or any other category protected by federal, state, or local law. Job Type: Full-time Pay: $90,000.00 - $150,000.00 per year Benefits: * 401(k) * 401(k) matching * Dental insurance * Health insurance * Life insurance * Paid time off * Vision insurance Work Location: In person
***** Temporary Opportunity with the potential of conversion and/or extension **** Position: Production Associate Location: Temecula, CA 92590 Pay: $20-21/hr, 1st shift. *Job Description*: * Fill/dispense liquid and/or solid products into bottles/vials, using pipettes, pumps, spatulas, scoops, or automated equipment. * Safely and correctly execute filling operations * Perform procedures involving calculations and material measurements; collect and record data on batch records * Safely operate standard production and fill equipment * Correctly use of Biological Safety Cabinet (BSC) and Laminar Flow Work Stations * Use automated equipment such as auto-cappers and future production automation * Execute Aseptic Technique * Conduct support functions such as stocking and distributing supplies * Fill various containers with products of various materials and sizes * Use basic scientific laboratory equipment such as scales and fume hoods * Properly handle and dispose of biologically hazardous materials and chemically hazardous materials * Perform or assist in validations/verification of processes and equipment *Essential Job functions:* Packaging * Use automated equipment, such as auto-labelers, auto-baggers and future production automation * Conduct support functions such as stocking and distributing supplies * Apply labels to product, assemble kits and package products * Ensure quality is maintained by verifying information is correct and work is performed per procedures * Report any inconsistencies or non-conformances discovered during procedures * Responsible for verification and final product quality * Perform or assist in validations/verification of processes and equipment Filling * Fill/dispense liquid and/or solid products into bottles/vials, using pipettes, pumps, spatulas, scoops, or automated equipment. * Safely and correctly execute filling operations * Perform procedures involving calculations and material measurements; collect and record data on batch records * Safely operate standard production and fill equipment * Correctly use of Biological Safety Cabinet (BSC) and Laminar Flow Work Stations * Use automated equipment such as repeater pipette, liquid pump dispenser, auto-cappers and future production automation * Execute Aseptic Technique * Conduct support functions such as stocking and distributing supplies * Fill various containers with products of various materials and sizes * Use basic scientific laboratory equipment such as pipettes, scales, pH meters, fume hoods, and filters * Properly handle and dispose of biologically hazardous materials and chemically hazardous materials * Perform or assist in validations/verification of processes and equipment Additional Functions - Perform basic to very complex liquid and/or dry powder filling. - Identify low technical issues and troubleshoot/resolve as subject matter expert. - Utilize multiple databases to screen work orders and create job packet prior to release to shop floor. - Collaborate with support departments such as Quality, Distribution, and Data Management to resolve low complexity issues. - Maintain good documentation and laboratory practices. - Performs work within standard allotted time. - Support 6S program by conducting housekeeping at end of shift. - Use computer systems to collect information, troubleshoot, ERP transactions, etc. - Perform other duties as assigned. KNOWLEDGE, SKILLS & ABILITIES: --Lifting and moving up to 25 lbs --Proficient with use of pipettes, scales, and other basic laboratory equipment --Able to perform unit conversions and read, understand, and follow procedures --Highly collaborative and team oriented. --Ability to multi-task to meet manufacturing schedules. --Excellent organizational skills. --Effective verbal and written communication skills. --Attention to detail. --Analytical with the ability to troubleshoot and resolve issues. Education: High School Diploma Experience: Entry Level Qualifications: - 2 years of relevant lab tech experience in biotech or related industry OR applicable skills MilliporeSigma is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to his/her Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because he/she made a good faith report of discrimination. Job Types: Full-time, Contract Pay: $20.00 - $21.00 per hour Work Location: In person
Looking to be part of a team where craftsmanship, teamwork, and innovation come together? Welcome to Caseman GPC—where we don’t just build cases, we build solutions that work in the real world. Our production team plays a critical role in bringing custom-designed cases and packaging solutions to life, here in Poway, California. *Our mission is simple but powerful:* To deliver packaging solutions that go beyond storage, providing the perfect balance of presentation value, protection, and usability. Every case we create helps our customers protect what matters, and you will play a key role in making that happen. At our core, we believe in: Integrity, Quality, and Customer Focus! The vibe? Warm, welcoming, and full of possibility. People stick around not just for the work, but for the team. If you're looking for a place where you can grow your skills and genuinely make a difference, you’ll feel right at home here. *How You Will Make an Impact:* * Apply adhesives and gluing techniques to assemble foam inserts and case components. * Assemble and finish custom cases and packaging solutions according to specifications. * Operate power tools and production machinery to support efficient workflows. * Review and follow production instructions, ensuring accuracy and consistency. * Inspect finished products to ensure they meet quality standards. * Collaborate with team members and supervisors to meet daily production goals. * Maintain a clean, organized, and safe workspace. *To Be Successful in This Role, You Must:* * Work with attention to detail to ensure every product meets Caseman GPC’s standards. * Communicate effectively with team members to support a smooth production flow. * Adapt quickly to a changing work environment and manage competing demands. * Be reliable, proactive, and committed to working safely. * Be willing to learn and grow with new tools, processes, or responsibilities. * Ensure deadlines are met without compromising quality. *To Qualify for This Role, You Must Have:* * Ability to work in a fast-paced, team-oriented environment. * Strong work ethic and reliability. * Attention to detail to ensure product meets quality standards. * Physical ability to lift, move, and handle materials as needed. *Preferred:* * Prior experience in production, assembly, or manufacturing. * Familiar with case assembly. * Experience using (Windows, Office, ClickUp, and Bandsaw) *Pay, Perks & Benefits:* * Medical, dental, and vision insurance * Paid vacation, holidays, and sick time * 401(k) with 4% match * Growth opportunities in a creative, forward-thinking environment Ready to Apply? If you're ready to take your skills to the next level in a company where thoughtful design and meaningful work come together, we’d love to meet you. Job Type: Full-time Pay: From $21.00 per hour Expected hours: 40 per week Benefits: * 401(k) matching * Dental insurance * Health insurance * Paid time off * Vision insurance People with a criminal record are encouraged to apply Application Question(s): * How many years of experience do you have working in a production environment? * What is your level of experience with computers? * What is your level of experience with Excel and/or Google Sheets? * If something’s slowing down your work, what would you do? * How would you make sure you can keep working when supplies are low? * What does being a good team member mean to you? * There is a hole in a foam insert that is currently 7-1/8’ deep, but the print calls for it to be 4-3/8” deep. How thick should the material we add be to bring the cavity to the correct height? Work Location: In person
*Quality Control Specialist* *Job Title: *Quality Control Specialist *Department: *Operations Department *Reports To: VP of Ops and MFG Ops Manger* *Salary/Pay Range:* $20.00-28.00 DOE As required by company need job hours may fall in one of the following: Full time: 30 - 40 hours /week (overtime may be required) JOB SUMMARY: Responsible for the organization, communication, and utilization of resources to efficiently complete the quality task assigned. Maintains quality standards by approving incoming materials, in process production, finished products, and recording quality results. Oversees and leads quality initiatives and trains other quality team members on all quality related procedures. RESPONSIBILITIES/ DAILY TASKS: Inspects incoming materials by confirming specifications, conducts visual and measurement tests, and inputs corresponding data into the system when required. * Participates in-process production by confirming specifications, conducting visual and measurement tests, and communicates any adjustments if necessary. * Inspects and approves finished goods by confirming specifications, performs a visual inspection, returns products for re-work, and confirms rework. * Documents and inputs all inspection results by inputting data into the Quality System. * Data entry on the ECO/ECR log and communicates with appropriate parties regarding current status and responsibilities. * Maintains measurement equipment and schedules calibration when necessary. * Maintains a safe working environment by following company standards and procedures, and complies with legal regulations. * Participates in maintaining the quality and organization of the company and reports any quality related issues in a timely manner. * Document quality activities/procedures as requested. * Trains and leads other quality team members in all quality related procedures and activities. * Other related tasks may be assigned such as counting, packaging, labeling or bagging the produced parts or the raw material in preparation for kitting. * Ability to work individually and / or within a team. QUALIFICATIONS: *Education/Experience* 12 months of quality related working experience. * ISO 9001 background/training preferred. *Knowledge, Skills and Other Abilities* * Adequate Math, Reading & Reasoning Ability – Ability to add, subtract, multiply, and divide. Ability to read and understand assembly instructions and interpret product drawings. Ability to understand to carry out instructions provided in written, oral, or diagram form. * Adequate understand in PC operations. * Knowledge of MS Office. * Strong Attention to Detail. * Individual is expected to have good verbal and written communications skills. * Able to train others and work in a team. * Organizational skills; Planning skills; Time Management skills. * Manual dexterity with the ability to maintain daily / weekly quota by working quickly and accurately. * Positive Attitude. * Ability to work overtime. _Physical Demands and Work Environment – The following physical demands and work environment characteristics are representative of those that must be met to successfully perform the essential functions of this job:_ Employee is regularly required to stand; walk; sit; use hands; reach with hands and arms; climb or balance; stoop, kneel, crouch or crawl; and talk or hear. The employee may be required to lift/and or more up to 20 pounds. Specific vision abilities required by this job include close vision, distance vision, peripheral vision, depth perception, ability to adjust focus and the ability to see color. While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts, work near ventilated and exhaust equipped soldering stations and some solvents and chemicals. The noise level in the work environment is usually moderate. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Job Type: Full-time Pay: $41,000.00 - $58,000.00 per year Benefits: * 401(k) * 401(k) matching * Dental insurance * Flexible spending account * Health insurance * Paid time off * Referral program * Vision insurance Schedule: * 8 hour shift * Day shift * Monday to Friday Work Location: In person
*Come join our team! C&H Machine in Escondido* We are seeking experienced full-time CNC Setup Mill Machinists. We are a medium-sized, fast-paced Job-Shop with consistent work and a strong supportive management team. We are looking for team players who are always willing to learn more. We have a dozen 3-Axis Machining Centers along with several Five-Axis and Horizontals to go with numerous Turning and EDM centers. We pride ourselves on our teamwork among our various departments providing exceptional quality parts for our customers. We encourage open communication and participation on the shop floor as a vital part of our quest for excellence. We look forward to meeting you! *Requirements:* * 5+ years of experience as a setup machinist on CNC Mills * Ability to use plan and use CAM system to program part for shop floor. * Hypermill experience a plus * Ability to read blueprints and GD&T symbols and develop appropriate machining methods. * Ability to use inspection tools to verify part conformance. * Knowledge of Fanuc, Haas, Fadal, and Okuma controls is a plus. * Able to communicate effectively both orally and written. *Benefits we offer (after 90 days of employment): * * Medical, dental, and vision insurance * 401K * 80 hours paid vacation. * 40 hours sick leave Job Type: Full-time Pay: $30.00 - $45.00 per hour Expected hours: 40 per week Benefits: * 401(k) * Dental insurance * Health insurance * On-the-job training * Paid time off * Vision insurance People with a criminal record are encouraged to apply Work Location: In person