Looking to move to Carlsbad and want to connect with local employers? Fill out this form and we’ll help you get recruited.
Bachem is a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. With over 50 years of experience and expertise Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide and offers a comprehensive range of services. Bachem operates internationally with headquarters in Switzerland and locations in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange. For further information, see www.bachem.com. A brief overview The Manager / Sr. Manager, Quality Control fulfills a critical role in the active pharmaceutical ingredient (API) manufacturing operations. This individual is responsible for managing and coordinating stability testing, raw material qualification, testing and release, and validation projects. The Manager / Sr. Manager coordinates both in-house and contract laboratory testing activities. Additionally, this individual supports the Director, Quality Control in reviewing data and reports. This role also serves to advance analytical capabilities and contributes to the development of the Quality Control department. What you will do Manage and oversee execution of QC testing including IPC, API, raw material, validation, release, EM and microbial testing Supervise QC Scientists. Provide training, day-to-day scheduling, mentoring, and coaching for QC personnel Establish and revise specifications and sampling plans for IPC, raw materials and final product Develop and optimize new and existing analytical methods for qualification and release testing Coordinate stability program and the testing to meet stability endpoints, as needed Manage IPC release activities, raw material and API release activities to meet deadlines tied to manufacturing schedules Write, review, and approve QC Standard Operating procedures (SOP’s) as needed Evaluate, recommend, and implement new analytical technologies and instrumentation for raw material, final product, In process, microbial, environmental, and water testing Investigate Out-Of-Specification (OOS) test results, write reports and implement corrective and preventive actions (CAPA) to prevent recurrences Manage external test laboratories for contract testing of raw materials and other related testing Review test data for completeness and accuracy Provide timely responses to internal and external inquiries Stay abreast of new developments in analytical technologies Contribute to improvements in laboratory operations to increase efficiency and GMP compliance Qualifications Bachelor's degree in a relevant scientific field with a minimum of 8 years’ industry experience Master's degree in a relevant scientific field with a minimum of 5 years’ industry experience (preferred) PhD in a relevant scientific field with a minimum of 2 years’ industry experience (preferred) 1-3 years’ management experience (preferred) 1-3 years’ experience in managing projects (preferred) Extensive experience in GMP laboratory testing such as IPC, HPLC, GC, TLC, UV-VIS Spectrophotometer, Karl Fisher Titrator, FTIR, MS, LAL, bioburden, etc. Thorough knowledge and understanding of analytical chemistry, including USP materials testing Creativity to solve technical and compliance problems Comply with good housekeeping and safety practices Experience in writing standard operating procedures (SOP’s) and test methods Excellent written and oral communication skills Excellent computer knowledge, including Microsoft Word, Excel, Power Point and Access Ability to effectively organize, multitask, and work in a fast-paced, deadline driven work environment Ability to communicate in a proactive and solution-focused manner, including keeping management aware of potential issues Detail oriented with the ability to troubleshoot and resolve problems Ability to work independently and manage one’s time Ability to drive projects to success under time constraints Communicate effectively and ability to function well in a team environment Base salary range: Manager: $109,396 - $164,095 Sr. Manager: $133,304 - $183,293 Placement of new hires in these wage ranges is based on several factors including education, skill sets, experience, and training. Total Rewards We offer all Team Members a total rewards package including competitive pay, annual performance bonus, a generous benefit package with comprehensive Medical/Dental/Vision coverage, 401(k) plan with employer contribution, and paid vacation, personal and sick days. Corporate Social Responsibility Bachem takes responsibility for future generations by a careful handling of resources and avoiding environmental risks. We continually improve our ecological performance and develop and implement new approaches for enhancing employees’ environmental awareness. EcoVadis has awarded Bachem Gold Medal status in their assessment of Bachem. Bachem Americas is an Equal Opportunity Employer As an equal opportunity employer, we celebrate the diversity of our team and are committed to building an inclusive workplace where individuals are hired and advanced based on merit, skills, and qualifications. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or other legally protected status. Please note: unsolicited resumes from recruitment agencies will not be considered. Nearest Major Market: San Diego
*SUMMARY: *Perform floral quality inspections. Ensure product meets company quality specifications. Hours - 5:00am - 1:30pm (Availability to work OT on weekdays and weekends) Work Schedule: Monday - Friday (Subject to Change) Approximate dates of Assignment: 04/15/2026 - 05/04/2026 (Subject to change) 04/20/2026 - 05/04/2026 (Subject to Change) *ESSENTIAL DUTIES AND RESPONSIBILITIES include*: Other duties may be assigned. * Verify bouquet/arrangement is made according to recipe specifications. * Ensure bouquet wrap and plant food are placed correctly. * Verify bouquets are being cut the same length. * Audit daily production table statistics for accuracy. * Ensure UPC labels contain the correct code, pricing and production date and pull date. * Ensure correct numbers of stems are being used. * Print daily PO arrivals * Being able to find and select boxes to check * Make inspections * UPC information * Standard compliance * Assortment * Make reports * Water testing * Critical age inventory * Check of temperatures and pH * Notify Quality Control Manager/Production Supervisor regarding any issues concerning quality. * *QUALIFICATIONS* * 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. * Ability to work on weekends and holidays (peak season's). * Ability to work in a refrigerated environment. * Ability to lift up to 50 lbs. (heavy lifting) * Ability to follow directions. * Ability to communicate effectively in English and Spanish. * Ability to work effectively and relate well with others. * Basic computer skills. *EDUCATION and/or EXPERIENCE* Minimum one -year experience in the floral industry training. High School or GED preferred. *LANGUAGE SKILLS* Ability to read and comprehend simple instructions, short correspondence, and memos. Ability to write simple correspondence. Ability to effectively present information in on-on-one and small group situations to customers, clients, and other employees of the organization. Ability to converse in English and Spanish. *MATHEMATICAL SKILLS* Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, and percent and to draw and interpret bar graphs. *REASONING ABILITY* Ability to apply common sense understanding to carry out detailed but uninvolved written or oral instructions. Ability to deal with problems involving a few concrete variables in standardized situations. *PHYSICAL DEMANDS* The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is required to frequently stand, walk, use hands to finger, handle, or feel and talk or hear, and to reach with hands and arms. The employee must frequently lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. *WORK ENVIRONMENT* The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly exposed to extreme cold, wet and humid conditions (non-weather). The noise level in the work environment is usually moderate. Copy and paste the link below and apply directly to our career center for the Quality Control position: https://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=3ca6dfee-a9c1-4e24-a942-a8e3179da5e4&ccId=9201070367831_2&lang=en_US Job Type: Temporary Pay: From $18.50 per hour Work Location: In person
At ACON labs, we are making a difference in medical care by offering medical devices for diagnosing a variety of conditions. In addition, we are able to streamline and reduce costs for the physician and/or patient directly. Come join us in developing the latest technologies that enhance human life and be a part of our growing, dynamic company. We are seeking a Senior Quality Assurance Engineer to join our team. As a Senior Quality Engineer, you will manage and lead operations and continuous improvements of the company’s CAPAs, NCMR/Deviations and Supplier Management programs to ensure the best practices and compliance with federal and global regulatory requirements. *Essential Duties and Responsibilities (includes but not limited to):* CAPA Program * Manage the company’s CAPA processes with focus on driving improvements in products and process performance. · Coordinates and support activities for root cause investigations, and implementation of corrections and corrective actions, as well as evaluation of effectiveness of implemented changes. · Facilitate cross functional team discussions in support of CAPA investigations and risk impact assessment report documents as per defined timelines. * Monitor CAPA KPIs, perform analysis, and interpret trends for process/product quality improvements. * Provide training and coaching to employees authoring, reviewing, and approving CAPAs. * Provide subject matter expertise on CAPA activities to the overall site. * Establish and maintain expert knowledge on quality system CAPA regulatory requirements in accordance with applicable FDA Regulations (21 CFR: Parts 820), and ICH Guidance, as well as other applicable regulatory requirements applicable to the organization. Manufacturing Deviations, NCMRs, and Variances: · Manage the process for issuing and evaluating Manufacturing Deviations and support resolution, as required. · Manage the process for issuing and evaluating Non-Conformance records (NCMR’s) and support resolution of Quality issues. · Manage the process for issuing and evaluating Variance reports for QMS processes and support resolution, as required. Other: · Participate in company’s Internal Audit program. · Act as SME for CAPAs, Manufacturing Deviations, NCMRs, and Variances during Regulatory and Customers audits. · Supports Management review by providing data and KPIs related to essential duties. · Maintains Lot number database and provides part numbers and lot numbers as requested. · Reviews/Scans upstream DHRs and creates COCs upon approval. · Other duties may be assigned *Supervisory Responsibilities* · May oversee and mentor junior staff *Education and/or Experience* · Bachelor’s degree in life science or engineering, or equivalent focus of study from an accredited university or college with 5-8 plus years relevant experience or master’s degree with 3-5 plus years of relevant experience. *Required Knowledge, Skills and Abilities* · Proficient knowledge of Quality Engineering policies, principles and best practices including quality standards: ISO 13485, 21CFR Part 820, ISO 14971, and other appropriate industry standards. · Strong team player. · Must be well organized, detail-oriented and able to maintain precise records. · Ability to multi-task, prioritize and manage time effectively, while maintaining quality. · Must have strong oral and written communication skills and computer skills. · Successful history of working independently with minimal supervision. · Strong interpersonal skills with reputation for collaboration with colleagues · Strong computer skills including MS Office (Word, Excel, PowerPoint, MS Project) The salary range for this position takes into account a wide range of factors including education, experience, knowledge, skills, geography, and abilities of the candidate, in addition to internal equity and alignment with market data. At ACON it is not typical for an individual to be hired at or near the top range for their role and compensation decisions are dependent on the facts and circumstances of each case. The salary range for this position is $81,000 -$95,000. ACON offers a comprehensive benefits package including medical, dental, vision, life, and disability insurance, along with a 401(k) plan, employee assistance program, paid time off (including sick time), and paid Holidays. All benefits are non-contractual, and ACON may amend, terminate, or enhance the benefits provided, as it deems appropriate. Job Type: Full-time Pay: $81,000.00 - $95,000.00 per year Benefits: * 401(k) * 401(k) matching * Dental insurance * Employee assistance program * Flexible spending account * Health insurance * Life insurance * Paid time off * Vision insurance Work Location: In person
We are currently recruiting for a Flexo Press Operator to join our Production Team! In this role, you will be responsible for setting up and operating the printing press to produce labels and related products. *_Responsibilities:_* · Reads job order and loads dies into press, installs print cylinder on shaft and installs print cylinder in press. · Fills ink pans, screens with prescribed inks. · Starts press, adjusting speed and alignment of stock to the print cylinder as necessary. · Engages print cylinders; adjusts printing impression as necessary, places print cylinders lead-to-lead and runs down approval strip. · Cuts sample of approval strip from printed roll, inspects for imperfections such as print to print out of register, print to die out of register, missing impression, making adjustments as necessary. · Cleans plates, print cylinders and dies as needed, performs daily, weekly and monthly maintenance as required. · Mixes inks to produce and maintain desired colors and viscosity. · Keeps work areas clear and organized; maintains housekeeping standards *_Qualifications:_* High school diploma or general education degree (GED); or one to three years related experience and/or training; or equivalent combination of education and experience A minimum of one year of flexographic printing press experience preferred Ability to add, subtract, multiply and divide in all units of measure, using whole numbers, common fractions and decimals Must be able to read and interpret ruler, scales and other measurement devices. While performing the duties of this job, the employee is regularly required to stand and frequently is required to walk The employee must frequently lift and/or move up to 50 pounds with or without mechanical assistance Specific vision abilities required by this job include close vision, color vision, depth perception and ability to adjust focus Excellent 401(k) retirement plan with generous company contribution Job Type: Full-time Pay: $28.00 - $38.00 per hour Education: * High school or equivalent (Preferred) Work Location: In person
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 Quality Control Senior Associate, Microbiology & Sample Management, is responsible for performing routine and non-routine Environmental Monitoring (EM), routine testing of incoming raw materials, product (in-process, release, and stability) in support of GMP manufacturing at Abzena. The Senior Associate will also be responsible for the receipt, control, and disposal of GMP samples submitted to the QC lab. Responsibilities Perform routine, non-routine environmental monitoring (EM) of the GMP manufacturing facilities for total particulates, air viables, and surface viables. Gown for and work in a cleanroom environment. Perform routine monitoring of pharmaceutical water systems. Perform routine monitoring of pharmaceutical gas systems. Perform bioburden and endotoxin testing. Initiate and participate in the investigations of EM excursions, deviations, and out of specifications. Assess any potential impact on product quality. Author and execute qualification/validation protocols. Author qualification/validation reports. Assist in trending EM data and generate quarterly reports and yearly reports. Performs stability set downs and pulls, Reference Standard pulls, and maintains documentation associated with stability pulls and Reference Standard/ sample traceability. Perform analysis of in-process samples, APIs, and stability samples using existing methods. Support assay transfer, qualification and validation activities for client’s specific methods. Receive, log, inventory, and transfer/distribute incoming Non-GMP (if applicable) and GMP samples into QC Sample Submission and appropriate laboratory. Maintain QC lab equipment and provide assistance, as needed, during equipment and facility qualification activities. Interact closely with other departments to ensure efficient, compliant and timely execution of project activities. Provide assistance as needed to maintain functioning QC Laboratory, including material ordering, inventory control, general housekeeping and other duties. Initiates purchase and shipment requests and outsource sample submission forms for outsource testing. Accurately and precisely document and record laboratory activities, results, and conclusions. Provides review of compendial testing data and associated documentation. Author and review Quality Control standard operating procedures (SOPs) Adhere to quality standards set by regulations and Abzena’s policies, procedures and mission. Communicate effectively with supervisors, colleagues and subordinates. Follow best practices related to the systems and processes that support the practices and documentation in the GMP facility for manufacturing clinical material Operate at a consistent and exemplary level of efficiency, producing high quality and accurate results with a customer driven focus. Qualifications Minimum of a B.S degree in Microbiology or related discipline with 5 years of experience in environmental monitoring of GMP facilities. Minimum of three (5) years of experience working within a GMP Microbiology Lab. Knowledge of theoretical and practical aspects of analytical methods utilized in microbiology labs, including Bioburden, TOC, Endotoxin, Conductivity, Gram staining, and Microscopy. Experience with the transfer and qualification/ validation of large molecule focused methods. Experience with preparing test reports, qualification/validation protocols, and SOPs. Ability to gown and gain access to the cleanroom and utilities areas. Ability to author excursion reports, trend reports, qualification/ validation protocols, qualification/validation reports, CAPAs, and SOPs as needed. Demonstrate understanding of USP, EP, and FDA microbiology testing requirements Strong written and oral communication skills, proficient with Microsoft Office software Support Microbiology staff members as needed 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. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
Predator Motorsports Inc. is the world leader in Hummer H1 Off-Road custom vehicle builds. We have been in business for over 21 years and are quickly expanding despite this dire economic environment. Predator Motorsports is considered an essential business and while adhering to the CDC’s Guidance pertaining to COVID-19 we have and will remain open during the California Stay at Home Orders. We have two locations, one in California and one in Florida. Our Vista, California location is looking for a Full-Time Fabricator to join our team. The ideal candidate for this position is a Welder/ Fabricator with a minimum of 3 years of fabrication experience in metal and automotive fixtures. They must be able to work both independently and as a team member to complete work assignments. *Basic knowledge of tube bending, Grinding ,Finishing & MIG welding proficiency is required.* *Job Description:* Fabricate off-road parts for hummer vehicles specializing in tig welding. Assemble and weld production parts *Duties include but are not limited to:* · Fabricator will be involved in metal handling, cleaning of parts, materials, and equipment. · Able to follow directions and tasks as specified by supervisor · Weld steel and aluminum components with welding equipment as specified by layouts, engineering drawings, work orders, or verbal instructions · Able to follow directions and tasks as specified by supervisor. · Weld steel and aluminum components with welding equipment as specified by layouts, engineering drawings, work orders, or verbal instructions. · Work includes set-up, laying out work using jigs/fixtures or hand layouts to fabricate parts and/or rework finished products. · Work with other employees to assist in the fabrication or welding of multi-component parts. · Operate hoists, hand power tools, grinders, cutting torch, and other hand tools related to the jobs needs. · Inspect and correct welds as necessary to meet product specifications. · Read, understand and follow job order specifications, engineering drawings, and/or work orders. *Desired Attributes:* · *Strong Attention to detail and a willingness to learn.* · Willingness to cross-train and perform the work of other job tasks in addition to the primary assigned position. · Reliability and a “team focused “attitude is a must. _*A Welding Test will be administered to determine experience level. If contacted for an interview, please bring your Welding Helmet and Gloves.*_ Due to the nature of our business, we have adopted a STRICT DRUG FREE policy. Candidates will be required to pass a drug test prior to employment. Please note that Full-Time benefits shall include, Medical (50% of Employee Cost paid by Employer),Dental, Vision and PTO. _****Schedule will be Four 10 Hr Days per week (6:30 AM-5:00 PM) Monday through Thursday.****_ If you feel that you meet the requirements, kindly reply with a cover letter and a copy of your resume. We are looking forward to hearing from you! _***** Please note that this position is direct hire only. No Recruiters, thank you.*****_' ' Work Location: * One location Work Remotely * No Job Type: Full-time Pay: $22.00 - $27.00 per hour Benefits: * Dental insurance * Health insurance * Life insurance * Paid time off * Vision insurance Experience: * Welding: 1 year (Required) Work Location: In person
*Location: San Clemente, CA* *Company: Modern Shelving* Modern Shelving, a growing small business specializing in modern storage and organization systems, is looking for a Production and Packaging Specialist to join our warehouse team in San Clemente, CA. About Modern Shelving We design and manufacture contemporary shelving and storage solutions for both residential and commercial customers. Our team is focused on quality, reliability, and excellent customer service, and we are expanding to meet increasing demand. Position Overview The Production and Packaging Specialist will support daily warehouse operations, including the preparation, assembly, and packaging of shelving components and related materials. Key Responsibilities * Assist with production and assembly of shelving unit components. * Perform light machining and cutting of aluminum components to specified measurements. * Inspect products to ensure quality and consistency. * Package finished products for shipment according to company standards. * Maintain a clean, safe, and organized work area. * Work with team members to meet production and shipping deadlines. Opportunities for Growth Modern Shelving supports employee development and internal advancement. As you gain experience, there may be opportunities to take on additional responsibilities in production, logistics, or warehouse coordination. Qualifications * Strong attention to detail. * Willingness to learn and work in a fast-paced environment. * Ability to follow written and verbal instructions. * Ability to work effectively as part of a team. * Previous warehouse, production, or manufacturing experience is helpful but not required. * Ability to regularly lift and move boxes or products weighing 50 pounds or more. * Reliable attendance and punctuality are essential. How to Apply Please email your resume and a brief cover letter describing your relevant skills and interest in the position to: *[email protected]* Modern Shelving is an equal opportunity employer. All qualified applicants are encouraged to apply. *Mandatory drug testing is required for all potential hires.* Versión en Español *Especialista en Producción y Empaque* Ubicación: San Clemente, CA Empresa: Modern Shelving Modern Shelving, un negocio pequeño en crecimiento especializado en sistemas modernos de almacenamiento y organización, busca un Especialista en Producción y Empaque para unirse a nuestro equipo de almacén en San Clemente, CA. Sobre Modern Shelving Diseñamos y fabricamos soluciones contemporáneas de estanterías y almacenamiento para clientes residenciales y comerciales. Nuestro equipo se enfoca en la calidad, la confiabilidad y el excelente servicio al cliente, y estamos ampliando nuestro equipo para cubrir la creciente demanda. Descripción del Puesto El Especialista en Producción y Empaque apoyará las operaciones diarias del almacén, incluyendo la preparación, ensamblaje y empaque de componentes de estanterías y materiales relacionados. Responsabilidades * Asistir en la producción y ensamblaje de componentes de unidades de estantería. * Realizar trabajos ligeros de maquinado y corte de componentes de aluminio según medidas especificadas. * Inspeccionar productos para asegurar su calidad y consistencia. * Empacar productos terminados para su envío conforme a los estándares de la empresa. * Mantener un área de trabajo limpia, segura y organizada. * Colaborar con los miembros del equipo para cumplir con los plazos de producción y envío. Oportunidades de Crecimiento Modern Shelving valora el desarrollo de sus empleados y ofrece oportunidades de crecimiento interno. A medida que adquieras experiencia, podrás asumir responsabilidades adicionales en producción, logística o coordinación de almacén. Calificaciones * Gran atención al detalle. * Disposición para aprender y trabajar en un entorno de ritmo rápido. * Capacidad para seguir instrucciones orales y escritas. * Capacidad para trabajar de manera efectiva en equipo. * Experiencia previa en almacén, producción o manufactura es un plus, pero no es indispensable. * Capacidad para levantar y mover cajas o productos de 50 libras (aprox. 23 kg) o más de forma regular. * Asistencia y puntualidad confiables. Cómo Aplicar Envía tu currículum y una breve carta de presentación describiendo tus habilidades relevantes y tu interés en el puesto a: *[email protected]* Modern Shelving es un empleador que ofrece igualdad de oportunidades. Animamos a candidatos de todos los orígenes a postularse. *Se requiere prueba de drogas obligatoria para todos los candidatos seleccionados.* نسخه به زبان فارسی *کارشناس تولید و بستهبندی* موقعیت: سن کلمنته، کالیفرنیا شرکت: Modern Shelving شرکت Modern Shelving، یک کسبوکار کوچک در حال رشد در زمینه طراحی و تولید سیستمهای مدرن قفسهبندی و نگهداری، به دنبال جذب یک کارشناس تولید و بستهبندی برای تیم انبار خود در سن کلمنته، کالیفرنیا است. درباره Modern Shelving ما راهحلهای مدرن قفسهبندی و ذخیرهسازی را برای خانهها و کسبوکارها طراحی و تولید میکنیم. تمرکز ما بر کیفیت، قابل اعتماد بودن محصولات و رضایت مشتری است و برای پاسخگویی به تقاضای رو به رشد، تیم خود را گسترش میدهیم. شرح موقعیت شغلی کارشناس تولید و بستهبندی از عملیات روزانه انبار پشتیبانی میکند، از جمله آمادهسازی، مونتاژ و بستهبندی قطعات قفسهها و سایر اجزا. مسئولیتها * کمک در تولید و مونتاژ قطعات واحدهای قفسهبندی. * انجام ماشینکاری سبک و برش قطعات آلومینیومی طبق اندازههای مشخص. * کنترل و اطمینان از کیفیت و یکنواختی محصولات. * بستهبندی محصولات نهایی برای ارسال مطابق با استانداردهای شرکت. * حفظ محیط کاری تمیز، ایمن و منظم. * همکاری با سایر اعضای تیم برای رسیدن به اهداف تولید و ارسال. فرصتهای رشد Modern Shelving از رشد شغلی کارکنان حمایت میکند و فرصت ارتقای داخلی را فراهم میسازد. با کسب تجربه، میتوانید مسئولیتهای بیشتری در بخش تولید، لجستیک یا هماهنگی انبار بر عهده بگیرید. شرایط مورد نیاز * دقت و توجه بالا به جزئیات. * تمایل به یادگیری و کار در محیط پرسرعت. * توانایی پیروی از دستورالعملهای شفاهی و کتبی. * توانایی کار گروهی مؤثر. * تجربه قبلی در انبار، تولید یا ساخت مزیت محسوب میشود، اما الزامی نیست. * توانایی بلند کردن و جابهجایی منظم جعبهها یا محصولاتی با وزن ۵۰ پوند (حدود ۲۳ کیلوگرم) یا بیشتر. * تعهد به حضور منظم و وقتشناسی. نحوه ارسال درخواست لطفاً رزومه خود و یک نامه کوتاه انگیزشی که مهارتهای مرتبط و علاقه شما به این موقعیت را توضیح میدهد، به آدرس زیر ایمیل کنید: *[email protected]* Modern Shelving یک کارفرمای دارای فرصت برابر برای همه متقاضیان است و از افراد با هر پیشینهای برای ارسال درخواست استقبال میکند. *انجام آزمایش مواد مخدر برای تمامی استخدامهای احتمالی الزامی است* Job Type: Full-time Pay: $17.00 - $22.00 per hour Benefits: * Paid time off * Professional development assistance Experience: * manufacturing: 1 year (Preferred) Language: * Spanish (Preferred) Location: * San Clemente, CA (Preferred) Work Location: In person
General Atomics Aeronautical Systems, Inc. (GA-ASI), an affiliate of General Atomics, is a world leader in proven, reliable remotely piloted aircraft and tactical reconnaissance radars, as well as advanced high-resolution surveillance systems. We have an exciting opportunity for a Second Shift Quality Inspector to join our Poway, CA team. This position is responsible for performing precise detailed inspections of aircraft, aircraft sub-assemblies, and systems using established inspection procedures, techniques and methods. Performs inspections on Line Replaceable Units (LRU’s), electrical/mechanical installations, composite assemblies, aircraft, and all additional duties needed to inspect, witness test, and maintain current configuration of units and tests. Ensures all measuring devices and test equipment are within calibration dates that conform to required standards. Responsible for tracking and ensuring that all items submitted for inspection or testing are at their latest release level. Maintains neat and legible inspection and test records as required. May perform duties as required in the assembly/disassembly inspection of components, assemblies or sub-assemblies. DUTIES AND RESPONSIBILITIES: Visually inspects aircraft and aircraft installation sub-assemblies. Performs in-process and final inspection or tests of aircraft, major components, subsystems and systems. Records test equipment calibration information and test data during system tests. Maintains proper records of these tests and inspections and configuration of systems under tests. Interfaces with customer representatives during inspections and tests of company products. Presents written inspection results, including configuration data when requested by the customer. Coordinates regularly with supervisory and engineering personnel. Notifies engineering of nonconforming characteristics and initiates written and verbal reports. Executes internal surveillance inspection and follow up. May assemble components, assemblies or sub-assemblies and perform other duties required in the assembly of equipment or units. May disassemble, modify, rework, reassemble and test experimental/prototype assemblies or assemblies according to specifications. May provide direction and guidance to less experienced staff. Maintains the strict confidentiality of sensitive information. Performs other duties as assigned. Responsible for observing all laws, regulations, and other applicable obligations wherever and whenever business is conducted on behalf of the Company. Expected to work in a safe manner in accordance with established operating procedures and practices. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. Job Qualifications Typically requires an associate's degree, trade school certificate, military training or equivalent in quality inspections or certification by a professional group such as ASQ or AWS, and one or more years of progressive experience in electrical, mechanical, electromechanical or metrology inspection and calibration. May substitute additional experience in lieu of formal education and training. Requires an extensive knowledge of inspection procedures, processes, devices and aids in a manufacturing environment as well as a wide and comprehensive knowledge of inspection concepts and principles including the ability to read and understand complex engineering drawings, specifications, procedures and manuals. Must possess: The ability to identify, analyze and interpret data. Strong interpersonal, verbal and written communication skills to explain detailed information effectively with all levels of employees including management and outside customers and vendors. Organization skills to maintain flow of work within the unit. The ability to establish priorities and maintain the confidentiality of sensitive information. Detailed knowledge of computer operations and applications and word processing and spreadsheets. The ability to work both independently and in a team environment is essential as is the ability to work extended hours required. FAA Airframe or Powerplant Certification, Inspection Authorization, past FAA designee experience or Military equivalent is preferred. Ability to obtain and maintain DoD Security clearance is required. Job Category Quality Experience Level Entry-Level (0-2 years) Workstyle Onsite Full-Time/Part-Time Full-Time Hourly Pay Range Low 52,020 Pay Range High 77,325 Travel Percentage Required 0% - 25% Relocation Assistance Provided? No US Citizenship Required? Yes Clearance Required? Desired Clearance Level Secret
What if the work you did every day could impact the lives of people you know? Or all of humanity? At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients. Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible. Job Summary: This role is responsible for performing quality control activities that support the release, characterization, and ongoing evaluation of purchased raw materials, intermediates, and finished goods. The position combines hands‑on laboratory testing with data analysis, documentation, and cross‑functional collaboration to ensure materials meet established specifications. Responsibilities: Inspect of purchased raw materials, intermediates, and finished goods, according to established procedures. May perform routine and non-routine analytical, biochemical, and molecular biology assays to support release, characterization and testing of purchased raw materials, production intermediates, and finished goods. Analysis of data generated by functional assays. Assist with or may lead projects around QC process improvements and qualification of changes using project management tools to achieve timelines on multiple projects with a high level of independence. May participate in developing and validating analytical and functional testing methodology, revising and updating work instructions and supporting documentation. Work with test method development, MTT, and QA in the transfer of new QC test methods. May participate in lab execution of experiments for technical support of production testing including OOS (out of specification) and NC investigations, root cause analysis and CAPA activities. Requirements: Ability to work effectively in warehouse environments, including exposure to cold and freezer temperatures. Proficiency with Microsoft Office tools (Excel, Word, and PowerPoint) essential. Excellent cross-functional collaboration, soft influence, written and verbal communication skills Molecular biology laboratory skills such as multichannel pipetting, etc. required. Ability to author and revise work instructions and perform assays with little guidance. Ability to respond quickly to shifting priorities and meet deadlines. Works on assignments requiring considerable judgment and initiative. Understands implications of work and makes recommendations for solutions. Determines methods and procedures on new assignments, typically has team leader responsibility. Listed responsibilities are an essential, but not exhaustive list, of the usual duties associated with the position. Changes to individual responsibilities may occur due to business needs. Experience/Education: Typically requires a Bachelor’s degree and at least 1-2 years of previous related experience, 4 to 6 years of appropriate lab/industry experience may substitute for a degree. The estimated base hourly range for the QC Associate 4 role based in the United States of America is: $27.50 - $41.25. Should the level or location of the role change during the hiring process, the applicable base pay range may be updated accordingly. Compensation decisions are dependent on several factors including, but not limited to, an individual’s qualifications, location where the role is to be performed, internal equity, and alignment with market data. Additionally, all employees are eligible for one of our variable cash programs (bonus or commission) and eligible roles may receive equity as part of the compensation package. We offer a wide range of benefits as innovative as our work, including access to genomics sequencing, family planning, health/dental/vision, retirement benefits, and paid time off. We are a company deeply rooted in belonging, promoting an inclusive environment where employees feel valued and empowered to contribute to our mission. Built on a strong foundation, Illumina has always prioritized openness, collaboration, and seeking alternative perspectives to propel innovation in genomics. We are proud to confirm a zero-net gap in pay, regardless of gender, ethnicity, or race. We also have several Employee Resource Groups (ERG) that deliver career development experiences, increase cultural awareness, and offer opportunities to engage in social responsibility. We are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information. Illumina conducts background checks on applicants for whom a conditional offer of employment has been made. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable local, state, and federal laws. Background check results may potentially result in the withdrawal of a conditional offer of employment. The background check process and any decisions made as a result shall be made in accordance with all applicable local, state, and federal laws. Illumina prohibits the use of generative artificial intelligence (AI) in the application and interview process. If you require accommodation to complete the application or interview process, please contact [email protected]. To learn more, visit: https://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf. The position will be posted until a final candidate is selected or the requisition has a sufficient number of qualified applicants. This role is not eligible for visa sponsorship.
What if the work you did every day could impact the lives of people you know? Or all of humanity? At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients. Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible. As a Process Development Engineer on Illumina’s Flow Cell Technical Operations team, you will own and sustain laser‑based, automated fabrication processes critical to Flow Cell Mechanical Operations. You will maintain process capability, improve tool performance, and support day‑to‑day manufacturing execution while enabling the introduction and scale‑up of new products, processes, and technologies. This role will collaborate closely with Manufacturing, Quality, and cross‑functional engineering teams. You will solve complex technical problems, drive continuous improvement, and ensure laser systems reliably support a growing and increasingly complex product pipeline. Responsibilities Sustain, troubleshoot, and improve automated, laser‑based manufacturing systems supporting high‑volume production Own day‑to‑day manufacturing performance, including yield, utilization, and efficiency Apply materials, optical, mechanical, and systems‑level knowledge to improve process performance and manufacturability Develop and execute experimental plans, DOEs, SPC responses, and risk assessments for on‑market support and new product transfers Drive continuous improvement initiatives focused on automation reliability, throughput, and process control Develop and maintain Camstar MES models to support automation workflows Create and execute test plans for equipment and software with defined requirements and acceptance criteria Troubleshoot mechanical, optical, laser, and instrumentation issues across integrated automation platforms Champion a strong safety culture through participation in safety risk assessments and mitigation activities Support cross‑functional and cross‑site efforts, including site transfers and remote troubleshooting Document system changes, investigations, and improvements in compliance with regulated manufacturing requirements Requirements Experience in biotech, pharmaceutical, chemical, or high‑tech manufacturing environments preferred Experience in sustaining or developing automated manufacturing equipment; laser‑based or opto‑mechanical systems preferred Experience supporting high‑volume manufacturing in regulated or quality‑driven environments preferred Experience with SPC, DOEs, and data‑driven process improvement is a plus Strong computer skills, including data analysis and manufacturing systems Experience with product or process development lifecycles and basic project management is a plus Strong written and verbal communication skills and ability to work effectively across departments Hands‑on experience troubleshooting complex mechanical, electrical, optical, or instrumentation systems Camstar MES experience a plus Experience supporting multiple manufacturing sites in a global environment is a plus Experience / Education 0-4 years of relevant experience with a bachelor’s degree, or equivalent work experience The estimated base salary range for the Process Engineer 1 or 2 - Laser Systems role based in the United States of America is: $82,500 - $123,700. Should the level or location of the role change during the hiring process, the applicable base pay range may be updated accordingly. Compensation decisions are dependent on several factors including, but not limited to, an individual’s qualifications, location where the role is to be performed, internal equity, and alignment with market data. Additionally, all employees are eligible for one of our variable cash programs (bonus or commission) and eligible roles may receive equity as part of the compensation package. We offer a wide range of benefits as innovative as our work, including access to genomics sequencing, family planning, health/dental/vision, retirement benefits, and paid time off. We are a company deeply rooted in belonging, promoting an inclusive environment where employees feel valued and empowered to contribute to our mission. Built on a strong foundation, Illumina has always prioritized openness, collaboration, and seeking alternative perspectives to propel innovation in genomics. We are proud to confirm a zero-net gap in pay, regardless of gender, ethnicity, or race. We also have several Employee Resource Groups (ERG) that deliver career development experiences, increase cultural awareness, and offer opportunities to engage in social responsibility. We are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information. Illumina conducts background checks on applicants for whom a conditional offer of employment has been made. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable local, state, and federal laws. Background check results may potentially result in the withdrawal of a conditional offer of employment. The background check process and any decisions made as a result shall be made in accordance with all applicable local, state, and federal laws. Illumina prohibits the use of generative artificial intelligence (AI) in the application and interview process. If you require accommodation to complete the application or interview process, please contact [email protected]. To learn more, visit: https://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf. The position will be posted until a final candidate is selected or the requisition has a sufficient number of qualified applicants. This role is not eligible for visa sponsorship.
*Job Overview* We are seeking a highly motivated and detail-oriented Quality Control Specialist – E‑Commerce (Amazon) to join our dynamic team. In this role, Quality is at the heart of everything we do—from product selection and handling to fulfillment and customer satisfaction. We are seeking a detail-driven *Quality Control Specialist* who will take ownership of quality standards for our Amazon and e‑business operations.. you will be responsible for ensuring the highest standards of product quality and compliance across our Amazon marketplace operations. Your expertise will help maintain rigorous quality systems, conduct thorough inspections, and uphold regulatory standards. This position offers an exciting opportunity to impact product excellence and customer satisfaction in a fast-paced e-commerce environment. *Duties* * Inspect floral products for freshness, damage, accuracy, and presentation prior to shipment * Enforce quality standards specific to Amazon and e‑commerce requirements * Monitor packing, labeling, and box integrity for e‑commerce orders * Identify quality issues and work with warehouse leadership to implement corrective actions * Document defects, trends, and root causes; provide clear reporting * Assist in reducing returns, refunds, negative feedback, and Amazon A‑to‑Z claims * Ensure compliance with Amazon seller performance metrics and customer expectations * Communicate quality standards clearly to packers and fulfillment staff * Participate in continuous improvement initiatives related to quality and efficiency Qualifications * 1–3 years of quality control, warehouse, or e‑commerce experience (Amazon experience strongly preferred) * Experience with perishable goods (produce, floral, or food) is a plus * Strong attention to detail and ability to spot defects quickly * Basic computer skills; familiarity with Amazon Seller Central is a plus * Ability to stand, walk, and inspect product for extended periods * Able to work in a fast-paced warehouse environment * Strong communication and problem-solving skills Pay: $19.00 - $24.00 per hour Expected hours: 40.0 per week Benefits: * 401(k) * Dental insurance * Health insurance * Paid time off * Vision insurance Work Location: In person
Pipeline/Piping Service Technician (Full-Time) Job location: San Marcos, CA *Job description:* Tap Master specializes in small to large pipeline specialty services including: Hot Tapping, Line Stopping, Pipe Freezing, Valve Insertions and more. We help the customer eliminate shutdowns and draining the system. Tap Master is looking for a reliable, hard working, self-motivated individual who is open to taking direction for this on-the-job training position with opportunity for growth. Most work is performed on a job-site in Southern California. Time not spent on jobsites will be spent preparing for jobs in our San Marcos, CA warehouse. We will provide training. Pay Range: $28-$32/hr base rate (this figure does not include benefits, bonuses, overtime or doubletime) *Qualifications*: *Physical ability to climb ladders, work from height (scissor lifts), reach equipment, lift and move heavy equipment *Available to work days/nights and weekends as needed. (Traveling out of state is sometimes required) *Experience and knowledge using hand & power tools *Ability to use and read a measuring tape *Ability to troubleshoot in fast paced environment *Excellent written & verbal communication skills *Must pass a pre-employment drug test, background check *Must have a valid California State driver's license *Must have a clean driving record * OSHA 30 card preferred (Tap Master can provide training for certification) * Bilingual a plus Job Type: Full-time Pay: $28.00 - $32.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Health insurance * Life insurance * Paid time off * Vision insurance Work Location: In person