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Sr. Quality Assurance Specialist Location: San Diego, CA | Employment Type: Full-Time Join a team dedicated to quality, innovation, and impact. PolyPeptide is a global leader in peptide manufacturing, supporting some of the most advanced therapies in the pharmaceutical and biotechnology industries. We are seeking a Senior Quality Assurance Specialist who is passionate about quality, compliance, and continuous improvement. In this role, you will play a critical part in ensuring that clinical and commercial products meet the highest regulatory and quality standards while contributing directly to PolyPeptide’s commitment to delivering exceptional quality and on-time delivery to our customers. This is an excellent opportunity for an experienced QA professional to work in a collaborative, science-driven environment and contribute to products that support life-changing therapies worldwide. Position Summary The Senior Quality Assurance Specialist ensures compliance with regulatory standards and internal procedures by overseeing key quality activities associated with cGMP manufacturing and testing. This role supports product release for clinical and commercial products, manages quality documentation, and participates in investigations, audits, and process improvements across the organization. Working closely with cross-functional teams including Manufacturing, Quality Control, Regulatory Affairs, and Corporate Quality, this position helps maintain PolyPeptide’s strong regulatory compliance record and commitment to operational excellence. Key Responsibilities Participate in core QA activities including deviation investigations, batch record review, annual product review, QC data review, and generation of Certificates of Analysis (CoA) for clinical and commercial product release. Update and maintain Standard Operating Procedures (SOPs) and Material Review Reports. Coordinate and interact with contract testing laboratories. Provide backup support for Quality Assurance Specialist (Compliance) activities including: Supplier audits Change control CAPA management Complaint handling Document control systems cGMP training support Provide backup support, as delegated, for lot release authority. Ensure site adherence to Quality System requirements, cGMP standards, and ICH guidelines. Support the annual review and continuous improvement of the Quality System, including operational efficiency improvements and regulatory updates. Collaborate with Regulatory Affairs, Manufacturing, Development, Marketing, and Corporate Quality on customer projects, regulatory submissions, and global quality standard harmonization. Contribute to maintaining PolyPeptide’s strong compliance record with FDA and other regulatory agencies. Perform additional responsibilities as assigned. Qualifications Education Required Bachelor’s degree in a scientific discipline such as Chemistry, Biology, or Pharmaceutical Sciences Preferred Lean Six Sigma certification Experience 5–7 years of Quality Assurance experience in a pharmaceutical, biotechnology, or CDMO environment Technical Knowledge Strong understanding of FDA, EMA, ICH, and cGMP regulations Experience with Active Pharmaceutical Ingredients (APIs) preferred Experience with peptides or oligonucleotides highly desirable Skills and Competencies Ability to make independent compliance decisions based on regulatory knowledge, risk evaluation, and available data Experience reviewing technical documentation and manufacturing records Strong analytical thinking and problem-solving skills Excellent written and verbal communication Ability to manage priorities and collaborate across departments Key competencies include: GMP compliance and regulatory knowledge Quality documentation and batch record review Attention to detail and accuracy Cross-functional communication and collaboration Deviation investigation and problem resolution Work Environment This role may be based in an office, laboratory, or GMP manufacturing environment depending on the specific assignment. Responsibilities may include: Working at a computer in a standard office setting Working in controlled environments requiring appropriate gowning and PPE Frequent movement between office, lab, and manufacturing areas Physical Requirements Prolonged sitting or standing depending on work activities Occasional lifting of up to 25 pounds Repetitive tasks such as pipetting, weighing, or data entry Use of laboratory or manufacturing equipment Potential exposure to chemicals, equipment noise, or temperature-controlled environments Occasional evening or weekend work to support operational timelines Reasonable accommodations will be provided where needed. Why PolyPeptide Laboratories At PolyPeptide Laboratories, you’ll work on highly technical, meaningful science that directly supports life-changing medicines. We offer real ownership, strong cross-functional collaboration, and the opportunity to influence how products are manufactured—not just execute them. If you are a quality professional who thrives in a regulated environment and wants to make an impact in the pharmaceutical industry, we encourage you to apply. Salary: $75k-$83k We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.
Overview: The Machine Operator at K-Tube Technologies will be Skilled in operating machinery in one or more departments of Weld, Plug, Sink, Straightening, Centerless Grind, Cutting, Cleaning, Packaging, Echo Tip, and Double Lumen. Capable under limited Supervision to perform set ups in accordance with established procedures. Proficient in inspection techniques of measuring OD, using laser micrometers, pin gauges for measuring ID, point micrometers for wall measurement, and able to utilize microscopic inspection techniques. Will also be responsible for the maintenance of all tooling used in manufacturing. Must be certified to operate multiple machines and sign off on production. Performs sampling procedure in accordance with appropriate Work Instruction. Responsibilities: • Responsible for producing material that meets or exceeds established quality and productivity standards. • Responsible for set up, run, and troubleshooting of production equipment on multiple work orders and machines simultaneously. • Inform Shift Supervisor of production and/or quality problems. • Record production results on process record and electronically. • Record labor hours against work orders electronically. • Measure samples and record results per the sample form. • Perform related duties as assigned by supervisors. • Detect and report defective materials or questionable conditions to the department supervisor. • Maintain the work area and equipment in clean orderly condition and follow prescribed safety regulations. • Must be familiar with the basic machine functions in order to perform the tasks stated above. • Must be willing to accept and receive frequent supervision and assistance with regard to machine set-up and workmanship standards. • Must be willing to be trained and work in multiple departments based on workload and business needs. • Must be willing to work mandatory overtime on Saturdays and or on any other days scheduled per business needs. • Must be familiar with the Company Policy Manual and adhere to behavior and attendance guidelines. May be required to train temporary employees, new hires, or other team members as requested by management. • Will be required to perform other duties as requested, directed or assigned. Qualifications: Education and Experience: • High School Diploma or equivalent years of relevant experience • Six months manufacturing experience Job Knowledge, Skills and Abilities: • Must have good communication skills, both written and spoken. • Must be able to read and interpret drawings, follow routers, use simple math, and use basic hand-held measuring tools • Must be able to use precision measuring instruments (pin gauges, calipers, lasermikes, etc.) to check parts for conformance to prescribed specifications Must be able to use a microscope to inspect parts samples for defects and conformance to prescribed specifications • Must be able to navigate a computer Physical Requirements • Must be able to lift up to 25 pounds • Moderate to heavy physical effort required • Ability to stand for long period of time • Regularly required to sit or stand, reach and move about the facility Work Environment • Work performed in a manufacturing environment • Exposure to metals, lubricants, solvents, electrolytes and other hazardous materials • May work in different departments or shifts as production needs require • Required to wear K-Tube t-shirt Personal Protective Equipment • ANSI Z87.1 compliant Safety glasses and ASTM F2413.18 (I/C) compliant safety shoes are required • Other personal safety equipment required as listed in SDS depending on task may include safety goggles, ear protection, full-face shield, apron, arm guards, rubber boots and gloves Status: Full Time/Non-Exempt Reports to: Production Supervisor
About us One team. Global challenges. Infinite opportunities. At Viasat, we’re on a mission to deliver connections with the capacity to change the world. For more than 35 years, Viasat has helped shape how consumers, businesses, governments and militaries around the globe communicate. We’re looking for people who think big, act fearlessly, and create an inclusive environment that drives positive impact to join our team. What you'll do We are thrilled to announce an exciting opportunity for an onsite Value Engineer to join our dynamic team in Carlsbad, CA, Tempe, AZ, Germantown, MD or Duluth,GA! You will be responsible for coordinating all Design-to-Cost aspects of a given product development, and continuous improvement. You will collaborate with many engineering teams such as Electrical, Mechanical, PWA Design & Fabrication, Assembly, New Product Introduction, Component, Industrial, Test, Cable and Qualification Engineering as well as Supply Chain to ensure cost and quality are optimized to deliver a robust and competitive product. The day-to-day Drive design decisions and changes with the Engineering Design and Reliability teams to reduce cost and complexity, while maintaining sufficient design margin Engage the various Manufacturing subject areas such as Mechanical/Assembly, Test and Industrial Engineering to optimize the Production processes for cost, efficiency and quality. Ensure qualification and regulatory compliance for each Viasat internally designed product Refine the Bill of Material (BOM), leveraging Supply Chain and Component Engineering, to minimize cost and maintain quality. Provide a vision for a strategic manufacturing approach that optimizes existing factory assets and processes to minimize production non-recurring engineering costs. Drive/participate on product make buy decisions. Understand the customer experience, including installation, operation, removal and repair and optimize the Viasat product lines for those activities. Manage the product lifecycle, identify and implement continuous improvement and engineering changes for all phases of the lifecycle from inception to End of Life Support After Market Services by monitoring field returns and proactively addressing reliability issues and championing continuous improvement both for cost and performance. Explore new technologies that may offer cost savings or performance improvement for Viasat products. What you'll need 10 years or more of an engineering field that lends itself to Value Engineering role. A well-rounded Hardware engineering competence. Demonstrated success/examples of driving cost out of products. A fundamental understanding of Reliability concepts including MTBF, HALT, ALT, ect. Experience taking a product into Production and/or cost optimization of an existing product with proven collaboration with Operations. A detailed understanding of the different technical facets of Operations including Manufacturing, Test, Fabrication and Production. Experience working with supply chain to provide cost and technical recommendations on supplier selection, make vs buy trade, etc. Technical finance experience to support activities such as Return on Investment, etc. Experience developing supplier contractual language such as Statements of Work, Memorandum of Understanding, ect. Experience working with external contract manufacturers, custom semi-conductor foundries or other critical suppliers. Capable of providing technical support and recommendations across multiple and simultaneous product developments and sustaining activities. Leadership, communication and organizational skills are essential. Bachelor of Science or equivalent experience in Mechanical, Electrical, Manufacturing, Industrial, Aerospace Engineering, Physics, or other related field. Up to 25% domestic and international travel (averaged over time). What will help you on the job Master of Science or equivalent experience in Mechanical, Electrical, Manufacturing, Industrial, Aerospace Engineering, Physics or other related field. Mid to high volume product design experience. Demonstrated risk mitigation planning and execution. Experience with an Original Design Manufacturer (ODM) engagement. Experience with semiconductor technical management. Previous experience with 3GPP product designs. Understanding of the theory of satellite communications. Previous international contract manufacturing and supplier management experience. Comfortable with independent domestic and international travel. Salary range $167,000.00 - $264,000.00 / annually. For specific work locations within San Jose, the San Francisco Bay area and New York City metropolitan area, the base pay range for this role is $207,500.00- $311,500.00/ annually At Viasat, we consider many factors when it comes to compensation, including the scope of the position as well as your background and experience. Base pay may vary depending on job-related knowledge, skills, and experience. Additional cash or stock incentives may be provided as part of the compensation package, in addition to a range of medical, financial, and/or other benefits, dependent on the position offered. Learn more about Viasat’s comprehensive benefit offerings that are focused on your holistic health and wellness at https://careers.viasat.com/benefits. EEO Statement Viasat is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, ancestry, physical or mental disability, medical condition, marital status, genetics, age, or veteran status or any other applicable legally protected status or characteristic. If you would like to request an accommodation on the basis of disability for completing this on-line application, please click here.
GROW WITH US: Tandem Diabetes Care creates new possibilities for people living with diabetes, their loved ones, and their healthcare providers through a positively different experience. We’d love for you to team up with us to “innovate every day,” put “people first,” and take the “no-shortcuts” approach that has propelled us to become a leader in the diabetes technology industry. STAY AWESOME: Tandem Diabetes Care is proud to manufacture and sell the Tandem Mobi system and t:slim X2 insulin pump with Control-IQ+ technology — an advanced predictive algorithm that automates insulin delivery. But we’re so much more than that. Our company’s human-centered approach to design, development, and support delivers innovative products and services for people who use insulin. Because many of our own team members live with diabetes, or have a loved one impacted by diabetes, the work is personal, and we are committed to the cause. Learn more at tandemdiabetes.com A DAY IN THE LIFE: A team member contributing to the troubleshooting and testing for medical devices supporting insulin pump therapy. Performs all aspects of manufacturing engineering of electromechanical insulin pumps. Contributes to both sustaining and new development efforts, including aspects of new product introduction. Participates in manufacturing development planning and execution for prototype, pilot, and production design transfer. Participates in the implementation of product cost reduction programs throughout the life cycle of the product. Manufacturing Engineering Interns are also responsible for: Improve productivity by performing ergonomic evaluations, time studies, simulation, and line balancing Cost analysis Process documentation Capacity utilization analysis Optimize assembly flow and process to minimize people per machine per day Failure analysis Materials inspection Assists manufacturing personnel on procedure, process, and equipment changes. Supports R&D and Design Engineering to aid in the transition of new products and processes to manufacturing: Assists Operations, Manufacturing and Production leaders in Prototype Development Planning activities and pilot build activities. Other duties as assigned. WHEN & WHERE YOU’LL WORK: Onsite: This position is fully onsite and open to candidates located in San Diego, California. Equipment for the role will be provided and training will occur onsite. Schedule: This position will work Monday - Friday from 8:00 AM - 5:00 PM PST. WHAT YOU'LL NEED: Knowledge, skills & abilities: Experienced with MS Office Possess analytic and statistic skills, and have the ability to work independently. Good organizational skills with the ability to prioritize workload. Able to effectively convey information related to work product in one on one conversation or in a group. Able to work effectively in a team environment. Able to alter behavior and opinions considering new information. Minimum certifications/educational level: Completion of Junior year in Science or Engineering or a related field, preferred. COMPENSATION: The starting base pay range for this position is $30.00 - $37.80 per hour. Base pay will vary based on job-related knowledge, skills, experience and may also fluctuate depending on candidate’s location and the overall job market. Please note that is a temporary position. As a temporary employee you will be employed through a staff agency partner. Benefits during your temporary assignment may be provided by the staffing agency. Access to Tandem sponsored benefits is contingent upon conversion from temporary to regular full-time status. Conversion is determined based upon business need and job performance. YOU SHOULD KNOW: Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable state and local Fair Chance laws and regulations. A conditional offer of employment from Tandem is contingent upon successful completion of a pre-employment screening process comprised of a drug test (excluding marijuana) and background check, which includes a review of criminal history information. Tandem has good cause to conduct a review of criminal history information of candidates for this position, as this role may involve access to proprietary, sensitive and/or confidential information, including customer protected health information. This review is required to ensure that individuals in such roles uphold high standards of trust and integrity so as to protect the interests of our customers, employees, and stakeholders. SPONSORSHIP: Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. WHY YOU’LL LOVE WORKING HERE: At Tandem, we believe joy fuels excellence. That's why we've built a workplace that celebrates your achievements and supports your well-being. Our team thrives on pushing boundaries and fostering growth, all while maintaining a spirit of fun and camaraderie. This is just one of the ways we stay awesome! Explore the benefits and reasons to love Tandem at https://www.tandemdiabetes.com/careers. BE YOU, WITH US! We embrace the value that every single one of us brings to the table. But sometimes we forget that when we don’t meet 100% of a job description’s criteria – maybe you’re feeling that way right now? We encourage you to apply anyway. Because we want you to be you, with us. Tandem is firmly committed to being an equal opportunity employer and does not discriminate on the basis of age, disability, sex, race, religion or belief, gender identity or expression, marriage/civil partnership, pregnancy/maternity, or sexual orientation. We are an inclusive organization, and we welcome applications from a wide range of candidates. Selection for roles will be based on individual merit alone. REFERRALS: We love a good referral! If you know someone who would be a great fit for this position, please share! APPLICATION DEADLINE: The position will be posted until a final candidate is selected for the requisition or the requisition has a sufficient number of applications. Make a move that matters. Join Tandem Diabetes Care, where we're turning challenges into triumphs every day and where your talents will help shape a healthier, happier tomorrow. #LI-HJ1 #LI-Onsite
Primarch Manufacturing is a leading nutritional supplement manufacturer employing over 50 full-time employees. We are currently seeking qualified candidates to join our growing production team. Primarch is looking for responsible, motivated, and self-directed individuals seeking full-time employment in a fast-paced, team-oriented environment. Schedule Monday – Friday, 7:30 AM – 4:00 PM Position Summary Clean Room Manufacturing Production Associates are responsible for weighing, blending, packaging, and boxing nutritional supplement products as part of a production team operating within a clean room manufacturing environment. Employees will work in teams of two to four and rotate throughout the shift to gain experience in all aspects of the production process. Essential Job Duties Weighing and measuring raw materials Labeling and packaging finished products Mixing dry powder formulations Performing basic documentation and batch record completion Following Good Manufacturing Practices (GMP) Maintaining a clean and sanitized clean room environment Assisting with order preparation and packaging Employees will rotate between responsibilities throughout the shift to support team production goals. Physical Requirements Ability to stand for the duration of the shift Ability to lift up to 50 lbs of raw materials as needed Ability to work in a clean room manufacturing environment Preferred Experience Experience in the following equipment or systems is a plus: Industrial mixers Capsule filling machines Form-Fill-Seal machines Auger fillers Wrap labeling machines ERP/SRP batching systems Batch record documentation Compensation Hourly pay for this position ranges from $20.00 to $25.00 per hour, depending on experience. Employees who demonstrate strong performance, reliability, and consistent attendance may have opportunities for advancement and increased responsibilities as they grow within the company. Benefits Primarch offers a competitive benefits package including: Medical insurance Dental insurance Vision insurance Paid vacation (eligible after one year of service) Application Requirements Please attach a resume when submitting your application. Applications submitted without a resume will not be considered. Candidates must be able to reliably report to the Vista, California facility (Business Park Drive and Liberty Way) for scheduled shifts as this is an onsite role. Qualified candidates will be contacted via email to schedule an interview. Primarch Manufacturing is an Equal Opportunity Employer.
*Production Technician* *Sol-ti strives as a team to promote a passion for healthy living and sustainability. We are committed to helping our* *partners and customers through our liquids of vitality - preserving our planet with the use of premium and consumer preferred, glass packaging. Our innovative glass packaging is not only for purity and taste but aligns with our company* *wide mission.* *Sol-ti, meaning “of the sun”, encourages our partners worldwide to let their inner light shine bright. Sol-ti is employee owned, growing rapidly, and expanding through promotions from within as quickly as our talent pool allows, but we* *need experienced new partners.* *Sol-ti is currently the Highest Velocity Refrigerated Beverage Company in the United States. We sell more product per store per week on average in all stores that Sol-ti sells in.* _*Position Summary:*_ As a Production Technician you will be responsible for the operation, maintenance, and supporting processes of packaging equipment in making high quality and safe products. _*Job Responsivities:*_ * Strong communication with your team to deliver daily goals * Equipment operation (startups, shutdowns, changeovers, maintenance, cleaning, inspection, troubleshooting, training, material handling) * Equipment includes juice presses, fruit grinders, citrus juicers, tanks, pumps, piping * Remove and clean change parts on juicer and grinder, and CIP tanks, hoses, pumps, and equipment in the batching area * Required to batch recipe, test analyticals, perform Quality assurance checks and complete documentation * Increase equipment uptime, decrease downtime, and perform simple repairs * Implement improvements on equipment and processes * Partner with Technical, Maintenance, and Operations team to problem solve and make improvements * Proactively escalate issues as required to address problems * Model integrity and support our mission, vision, and values * Great attendance and strong work ethic * Follow all Safety and Quality / Good Manufacturing policies and complete all training * All other responsibilities as required by the team _*Job Requirements:*_ * Food or Beverage manufacturing and production batching experience a must * Mechanical aptitude a must * Problem solver * Ability to adapt to change and shifting priorities * Self-directed and self-motivated * Works well with a team and open to new ideas * Comfortable with ambiguity as company scales and grows quickly * 1st and 2nd shift positions available (3 x 12 hour shifts) _*Sol-ti Benefits:*_ * Sol-ti contributes $200 towards the cost your medical premiums. $100 for your spouse and $50 for each of your dependents. * All you can drink Sol-ti while at HQ and the warehouse. * Keeps you hydrated at work without spending money. * High quality boots, socks, gloves and necessary gear. * Saves you time and money. * Sol-ti organic fruit offered daily. * Healthy fruit provided daily to keep you energized and save money. * Growth Opportunities. * Sol-ti is growing over 150% year over year. * Interested in career growth? The opportunities at Sol-ti are immense! * Employee Equity Plan. * Sol-ti is employee owned. * All full time employees are eligible to participate in our Employee Equity Plan. * Equity has a 1 year cliff (you much be at Sol-ti for a 1 year minimum). * Equity has a 4 year vesting schedule (full ownership occurs after 4 years). * Discretionary bonuses. * Monthly bonuses based on production metrics. * Perfect attendance awards. * Referral program. * Refer a friend or acquaintance to come to work at Sol-ti. * Up to $1,000 bonus based on length of employment (3 installments). Job Type: Full-time Pay: $20.00 - $21.00 per hour Benefits: * Dental insurance * Health insurance * Paid time off * Vision insurance Work Location: In person
About Nucleus Biologics At Nucleus Biologics, we are passionate about supporting the development of groundbreaking discoveries and improving the quality of life for patients. Our cell culture products and services fuel today’s therapies and tomorrow’s innovations. Cell culture media is a critical raw material used in the development of cell-based projects. As the Cell Performance Company™, we are the leading provider of custom cell growth media, tools, and technologies that support every stage of development from research through commercialization. We are committed to delivering premium products and services through a transparent, consistent, and proven supply chain that eliminates variability. About the role The Manufacturing Technician I will assist the Manufacturing team and report into the Associate Manufacturing Manager. This individual will work onsite at our San Diego, California location. What you'll do: Materials and Asset Management: · Assist in the management of inventory including raw materials, consumables, and finished products. · Oversee upkeep of equipment, including cleaning, preventative maintenance, and calibration. Production Support: · Execute manufacturing processes as outlined by the production schedule. · Ensure training records are up-to-date before batch record execution. · Perform essential cleanroom maintenance including cleaning, stocking materials, and maintaining accurate usage documentation. · Prepare materials for production through manufacturing tubing assemblies and conducting autoclave sterilization to ensure compliance with quality and safety standards. · Assist in supporting tasks including but not limited to preparation, cleans, critical monitoring, GDP documentation, and step execution. Compliance: · Maintain a solid understanding of and comply with cGMP (current Good Manufacturing Practices) and GDP (Good Documentation Practices). · Ensure proper tagging, maintenance, and calibration of assets and equipment is up to date prior to production. REQUIREMENTS: EDUCATION: · Associate Degree Required, Bachelor’s Degree is a plus · Preferred BS/BA in Biology/Immunology REQUIRED EXPERIENCE: · Requires 1+ years of experience in biologics or cell manufacturing · Prior experience working in cGMP environment is a plus. SKILLS & ABILITIES: · Strong attention to detail and organizational skills. · Experience in cGMP manufacturing environment is a plus. · Experience in formulation or media manufacturing is a plus. · Cell culture experience is a plus. · Effective verbal and written communication skills · Ability to exercise independent judgment consistent with Company guidelines · Strong process mindset PHYSICAL REQUIREMENTS: · Ability to hear and speak to employees and external associates on the phone and in person. · Ability to see the letters and numbers on a personal computer screen and on memos, reports and other documents (near vision) · Ability to walk and/or drive between buildings on campus, up to .3 miles for San Diego based positions · Ability to lift at 25 lbs. to a height of 3-4 feet on a regular basis. TRAVEL REQUIREMENTS: · May require travel to and from Nucleus Biologics offices or customer/vendor locations based on position. NOTE: The above statements are intended to describe the general nature and level of work being performed by incumbents. They are not intended to be an exhaustive list of all responsibilities, duties and skills required by all incumbents. Incumbents may perform other duties as assigned. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Management retains the right to add to or change the duties of the position at any time. The pay range for this role is: 25 - 26.50 USD per hour(San Diego, CA)
Kit Cut Operator — Light Composites Location: On-siteDepartment: Kit CutEmployment Type: Full-Time About Light Composites Light Composites is a precision composite manufacturer serving the defense, aerospace, medical, and industrial markets. We produce carbon fiber and composite components to exacting standards under our AS9100D / ISO 9001:2015 certified quality management system. Position Summary We are looking for a reliable, detail-oriented Kit Cut Operator to join our Kit Cut department. This role is responsible for stacking composite panels, monitoring material inventory, and supporting day-to-day kit cutting operations. The ideal candidate takes pride in doing quality work, follows procedures carefully, and communicates well with their team. Responsibilities Stack composite panels and materials according to work instructions and layup specifications Operate and monitor kit cutting equipment under supervision Track and report material inventory levels; notify leads when stock is low or discrepancies are found Stage kits and materials for downstream production operations Inspect materials for defects, damage, or non-conformance prior to use Maintain a clean, organized, and safe work area Follow all quality procedures, work instructions, and safety protocols Assist with general Kit Cut department tasks as directed by the department lead Document work performed accurately on travelers and production records Qualifications Required: High school diploma or equivalent Ability to stand for extended periods and lift up to 50 lbs Strong attention to detail and ability to follow written instructions Dependable attendance and punctuality Willingness to learn and take direction Preferred: Prior experience in composites, manufacturing, or warehouse environment Familiarity with inventory tracking or material handling Experience reading work orders or production travelers Basic computer skills What We Offer Competitive hourly wage Benefits package Opportunity to grow within a skilled manufacturing team Work on products used in aerospace, defense, and medical applications Light Composites is an equal opportunity employer.
Gannet Dive Company is looking for part and full-time employees. We are expanding our inventory with new products, all of which are designed, fabricated, and assembled, locally in Encinitas. If you have experience with tying knots, woodwork, metalwork, and light industrial consider working for a great local company.. Looking to hire individuals who have: Minimum 2 years light manufacturing experience * Integrity * Attention to detail * Procedural memory * Their own vehicle * Minimum of a High School Diploma/GED * Must be willing to sign an NDA We offer flexibility schedules. time off for diving/spearfishing/surfing. Company dive trips. compensation is based on a 6 week probationary/training period at $16 per hour. After which there will be a performance review and increase in compensation for full employment. GANNET DIVE CO is regarded as one of the top manufacturers and innovators in the spearfishing / freediving community and is looking for motivated members to join the team. Apply by emailing your resume to the provided address. Job Types: Full-time, Part-time Pay: $18.00 - $35.00 per hour Benefits: * Flexible schedule * On-the-job training * Professional development assistance Work Location: In person
*Job Summary* We are seeking a highly skilled and detail-oriented CNC Lathe Programmer to join our dynamic manufacturing team. We have a small lathe department of 3 machines. 2, 2 axis lathes and 1, 2 spindle lathe with y axis and milling capabilities. In this role, you will be responsible for developing, testing, and optimizing CNC lathe programs to produce precision components efficiently and accurately. Your expertise in CNC programming, tooling, and measurement will ensure that production meets the highest quality standards. CNC MFG is an AS9100 aerospace supplier. *Duties* * Develop, write, and modify CNC lathe programs using Fanuc controls to produce complex parts with precision. * Interpret technical drawings, schematics, and blueprints to ensure accurate machining processes aligned with GD&T (Geometric Dimensioning & Tolerancing) standards. * Work in compliance with the AS9100 standard of manufacturing. * Utilize CAD (Computer-Aided Design) software such as MasterCam to create or review part models and tooling layouts. * Implement lean manufacturing principles to optimize machining workflows, reduce waste, and improve efficiency. * Set up CNC lathes by selecting appropriate tooling, fixtures, and cutting parameters; perform machine calibration using bore gauges, calipers, micrometers, and other precision measuring instruments. * Ensure all machining operations adhere to safety protocols while maintaining high standards of quality control through precise measurement and inspection techniques. *Requirements* * Proven experience programming CNC lathes with Fanuc controls as well as Haas in a manufacturing environment. * Strong proficiency in CAD/CAM software such as MasterCam for designing parts and tooling. * Knowledge of GD&T principles for interpreting blueprints and schematics accurately. * Mechanical knowledge of tooling setups, machining processes, and machine maintenance. * Familiarity with bore gauges, calipers, micrometers, and other precision measuring instruments. * Ability to read schematics, schematics diagrams, and technical drawings confidently. * Understanding of lean manufacturing practices to streamline production workflows. * Excellent math skills related to geometry, measurements, and machining calculations. Join us as a CNC Lathe Programmer where your expertise will drive precision manufacturing excellence! We value innovation, safety, and continuous improvement—help us shape the future of manufacturing through your skills! Pay: $28.00 - $35.00 per hour Benefits: * Paid time off Work Location: In person
* *We are a commercial construction company that does various trades but looking for *_Metal framers, Drywallers, T-bar guys_ *to join a family of workers that work all over Los Angeles, we build walls Using Metal studs and also Wood framing components, we hang drywall, we Tape and finish walls with topping sand finish ready for paint. We also Install Acoustical Ceilings T-Bar. If you can do any of these trades and have tools please contact me, Only serious applicants and will need you to start ASAP, Payroll only transportation, experience, and tool are a requirement. * Job Type: Full-time Pay: $26.00 - $30.00 per hour Benefits: * Employee assistance program * Employee discount Work Location: In person
Hydranautics is a part of the Nitto Group of companies and a global leader in the field of integrated membrane solutions which includes reverse osmosis, nanofiltration, ultrafiltration and microfiltration for water, wastewater and process treatment and applications. Currently used on seven continents throughout the world for diverse applications such as seawater desalination, industrial high-purity water, surface water treatment, wastewater treatment and specialty process applications. Here at Hydranautics, we believe that diversity is key to our competitive advantage. All qualified applicants will receive consideration for employment without regard to their race, color, religion, national origin, ancestry, sex, sexual orientation, age, disability, marital status, domestic partner status or medical condition. We are proud to be a Drug-free, E-Verify and EEO employer. We are proud to offer a generous compensation and robust benefits package to include medical, dental, vision, life insurance plans, F.S.A. and H.S.A plans, Retirement plans (401k and ROTH), (12) Paid company holidays, generous PTO, tuition reimbursement and career development, Employee Assistance Plan, and more. This is an onsite position in our Oceanside, CA facility. Job Description Under direct supervision, operate pre-treatment equipment for preparation of testing of elements. Set-up and shut down and prepare material for production loading and unloading onto testing equipment. Maintain a required level of output. Keep accurate records and logs associated with production, quality, quantity, and any other necessary record-keeping activities. Work with seawater and non-seawater products. Ensure all documentation accompanies product to final test stage. Work with pounds per square inch up to 200 (PSI). ESSENTIAL DUTIES and/or RESPONSIBILITIES: 1. Performs one or more functions within the Pre-Treat area such as vacuum rinsing, flushing, chlorine treatment, pressure testing and processing product through other various pressurized procedures. 2. Loads/unloads product from manufacturing transport equipment onto appropriate machine or production equipment. 3. Maintains daily, weekly, and monthly productivity goals set by production management, including clean-up, rework, core tube preparation or other production activities. 4. Documents product data information such as serial number, defects, rejects, scrap etc. on production logs, reports, or summaries as well as any other record keeping activities as they pertain to products throughout shift. 5. Follows all safety, quality, and lean manufacturing policies, processes or procedures including sustaining workstation and area in cleanliness in accordance with 5S standards. 6. Informs Production Supervisor and/or Production Lead of increased pattern of defects in products. 7. Other duties as assigned. KNOWLEDGE, SKILLS and/or ABILITIES: 1. Basic to intermediate language skills, including verbal and written proficiency in English; ability to read work instructions in English. 2. Work independently and foster a cooperative spirit within a large and/or small team while maintaining flexibility to changing priorities. 3. Must be detail-oriented and able to work in a fast-paced manufacturing environment with accurate record-keeping abilities. Outstanding follow-through to meet production requirements. 4. Recognize numbers and millimeters and perform basic mathematical calculations with the aid of a basic hand-held calculator. 5. Deal with standard and basic non-complex issues; basic problem-solving ability; carry out simple verbal work instructions. PHYSICAL DEMANDS and/or WORK ENVIRONMENT: (Typical physical demands and the work environment characteristics an employee must meet and encounter while performing the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.) 1. Must be able stand/walk constantly up to 8 hours a day. 2. Ability to frequently lift and carry items up to 45 pounds. Lifting requirement is approximately 30-40% of the shift at waist to shoulder height to lift elements onto inspection apparatus. 3. Ability to occasionally lift and carry items up to 50 pounds. 4. Ability to frequently lift items overhead up to 45 pounds. 5. Ability to twist and bend at the waist, squat, and climb stairs frequently up to 6 hours a day. 6. Ability to push/pull mechanical lifting devices and pallet jacks with elements frequently up to 6 hours a day. 7. Ability to grasp objects with a force up to 50 pounds. 8. Ability to reach frequently up to 6 hours a day when packaging elements. 9. Wrist deviation, and hand/wrist repetition is frequently required, up to 6 hours a day, when cleaning elements. 10. Gross hand manipulation of light-moderate strength is required to grab elements. 11. Fine hand manipulation of light-moderate strength is required to operate buttons on machines. 12. Gross foot manipulation of light-moderate strength is required to operate foot pedals. 13. Must be able to see/focus for close eye work (small figures), discriminate colors, perceive depths. 14. Must be able to speak/hear to fulfill verbal communications and respond to machine alarms/buzzers. 15. Subject to periodic exposures to varying temperatures, occasional exposure to noise levels above 85 decibels, gas/fumes/mists, and chemicals or hazardous materials while using personal protective equipment when required. 16. Must wear safety shoes in required areas. 17. Participation in daily exercise activities is expected. 18. Must be able to work extended hours per the demands of the business Qualifications MINIMUM EDUCATION and/or EXPERIENCE: 1. High school diploma or GED; and 6 months manufacturing experience; or equivalent combination of education and experience. 2. 6 months of experience in a manufacturing position within the organization, desirable.