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THE POSITION Oceanside Operations (OCN) is a drug substance manufacturing organization dedicated to the reliable production of Roche’s commercial portfolio and pipeline products. Every year, OCN delivers millions of units of life-saving medicines to patients around the globe by leveraging its two integrated value streams: Stainless Steel and Single-Use production systems. As a Validation Engineer at OCN, you will play a critical role in ensuring that equipment, facilities, utilities, manufacturing processes, and cleaning/sanitization systems meet rigorous qualification and validation standards. Drawing from your expertise in qualification principles, engineering design fundamentals, manufacturing processes, and health authority expectations, you will review and approve validation documents, oversee tech transfers, and support Make-Assess-Release (MAR) activities. Beyond technical expertise, you will model Genentech’s values and core competencies, showcasing strong leadership, communication, and collaboration skills. In this role, you will work closely with cross-functional teams, including Engineering, MSAT, Quality Assurance, and Manufacturing, facilitating meetings and driving impactful projects. This is an opportunity to make a meaningful contribution to delivering essential therapies to patients worldwide. The Opportunity Manage and track the Validation program, including execution and assigned validation projects and ensure target timelines are met and/or issues are communicated / escalated effectively and consistently. Generate, review and approve a variety of Qualification Documents (IQs, OQs, IOQs, PQs, Engineering commissioning and turnover packages, Project Plans and Summary Reports) for equipment, facilities and utilities as well as support Cleaning and Process Validation. Strong understanding of commercial production environment and requirements. Proven ability to make suggestions for improvements as well as ensure programs are operating in a compliant and validated state. Perform role of subject matter expert and assess change control and discrepancy events for validated systems. Participate in cross-functional team meetings and where required, lead/facilitate meetings. Ensure the integration of environmental health, safety, and security into the business processes, systems and programs while reporting safety and environmental incidents including injuries, illnesses, and safety suggestions within one’s functional area. Foster a positive safety culture in which no one gets hurt. Who you are BS degree in Engineering or relevant scientific discipline. 4 - 6 years combined engineering/validation experience with a minimum of 3 years hands-on experience with equipment / utility / data review and analysis in a batch manufacturing environment within the pharmaceutical / biotechnology industry. Quality and Regulatory Knowledge: Must understand Quality standards, GMPs, Health Authority Regulations, cGMP regulations, Validation practices, and general compliance principles. Technical and System Expertise: Experience with CHO based manufacturing processes, Delta V automation system, Syncade and electronic Validation Execution. Hands-on experience commissioning/validating GMP equipment/utilities preferred. Communication Skills: Excellent verbal and written communication skills, and proven ability to manage multiple activities while maintaining organization. Teamwork and Initiative: Demonstrates initiative, problem anticipation, familiarity with project management principles, ability to work effectively in customer service/business partner roles, and strong collaboration skills with staff at all levels. Work Environment/Physical Demands/Safety Considerations Works in an office environment. Not a remote opportunity, expectation is to be onsite to support operations. On occasion my work in the clean room environment that requires gowning in the form of hospital scrubs, bunny suits, gloves and steel toe boots be worn. Also, no make-up or jewelry can be worn when working in the clean room environment. May be exposed to hazardous materials and chemicals. May be required to lift up to 30 lbs. Relocation benefits are available for this posting. The expected salary range for this position based on the primary location of California is $80,500 - $149,500. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Benefits Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants. JOB FACTS Job Sub Category Quality Schedule Full time Job Type Regular Posted Date Mar 18th 2026 Job ID 202603-105882
Company: Jensen Specialty Welding Location: Vista, CA Job Type: Full-Time ⸻ About Us Jensen Specialty Welding is a small, fast-paced welding shop specializing in stainless steel pipe and structural fabrication. We take pride in quality work, a strong team environment, and getting the job done right. ⸻ Position Overview We are looking for a reliable, hardworking Shop Helper to assist our welders and fitters with day-to-day shop operations. This is a great opportunity for someone looking to get into the welding trade and grow with a company. ⸻ Responsibilities * Assist welders and pipe fitters with fabrication and assembly * Cut, grind, prep, and clean materials * Measure and organize materials for jobs * Maintain a clean and safe work environment * Load/unload materials and deliveries * Operate basic shop tools and equipment * Run errands or pick up materials as needed ⸻ Requirements * Strong work ethic and willingness to learn * Ability to lift 50+ lbs and work on your feet * Basic mechanical aptitude * Reliable transportation and punctuality * Ability to follow directions and work as part of a team * Construction or shop experience is a plus (not required) ⸻ Preferred (Not Required) * Experience with grinders, saws, or hand tools * Interest in welding or pipe fitting as a career * Forklift experience ⸻ Pay & Benefits * $18–$24/hour (depending on experience) * Opportunity for growth into welding or pipe fitting roles * Overtime opportunities ⸻ Why Work With Us * Small team, no corporate BS * Opportunity to learn a skilled trade * Steady work with room to grow * Hands-on training from experienced welders ⸻ How to Apply Send your resume and a brief description of your experience to: [email protected] Or apply in person at: 934 S. Andreasen Dr. Escondido, Ca 92029 Pay: $18.00 - $24.00 per hour Benefits: * 401(k) Work Location: In person
HME has been creating innovative products for the drive-thru and pro-audio industries since 1971. From the very beginning, we've known these solutions would never have happened without the customer-focused people who make up our company. HME has a team environment with a culture of collaboration, learning, and growth. With subsidiaries located in California, Missouri, Canada, UK, India, and China, companies around the world depend on HME for clear, reliable communication solutions. From setting the standard for drive-thru headsets and timer systems in the quick service restaurant (QSR) industry to developing professional audio equipment used in the Olympic Games, HME strives to create the newest, most innovative products on the market while providing quality care and attention to its customers. Come join our team! Come write your chapter of the HME story. Are you good with your hands? Do assembly instructions make sense to you? Are you looking to start a new career and not just another job? HME is actively recruiting candidates with great Attitudes and Aptitude for an Assembler Tester I, 2nd shift, Temp to Hire. In this position, with training and under direct supervision, performs various electro-mechanical assembly, test and inspection procedures to ensure that production schedules and quality standards are met. May use automated test equipment, handheld tools, soldering iron, assembly drawings, bills of materials, schematics, written instructions, and/or other applicable documents. This is a 2nd shift position working 2:30 - 11:00pm Monday-Friday. What you will do in the position: Assembles, reworks, and/or reassembles product as specified on applicable documentation. Verifies accuracy of instruction documents (e.g. schematics, assembly drawings, bills of material). Checks work for accuracy, quality, and conformance to specifications. Uses a computer for data entry and inputs serial numbers into the mainframe. Packages parts into kits for shipping. Labels and packages product including manuals and accessories. Informs supervisor or lead of work-related problems. Record test data and results What you will need to succeed in this position: Up to 6 months electronics assembly experience Ability to perform basic assembly operations. Ability to read and interpret manufacturing drawings and assembly aides. Ability to complete assignments within specific time parameters under direct supervision. Good verbal, reading, writing, and comprehension skills. Basic computer skills. Good manual dexterity. Basic computer skills GED required The starting rate is $18.00/hr plus a 10% shift differential. This may vary depending on experience and other factors. Our benefits package includes tuition reimbursement; 3 weeks paid vacation your first year, paid holidays, medical, vision, and dental coverage, pet insurance, life insurance, and 401K contributions. The physical demands and work environment 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. The employee will occasionally lift and move up to 50 pounds with assistance.
The Position 2026 Summer Intern - Genentech Summer Program - Manufacturing We are now accepting applications for the Summer 2026 Genentech Summer Internship Program. This post is for manufacturing-based roles in Oceanside, CA. There are separate posts for laboratory, informatics, and operations based roles in Oceanside, CA. The Opportunity As an intern, you will perform various tasks under the guidance and mentorship of your manager. You will be expected to attend meetings, read independently on relevant topics, follow a training schedule set by your supervisor, and perform tasks independently as appropriate. You will also be expected to summarize the purpose of your work and any findings, and you will present future recommendations in the form of an oral and poster presentation. Program Highlights Intensive 12-weeks, full-time (40 hours per week) paid internship. Program start dates are in May/June (Summer). A stipend, based on location, will be provided to help alleviate costs associated with the internship. Ownership of challenging and impactful business-critical projects. Work with some of the most talented people in the biotechnology industry. Who You Are (Required) Required Education: You meet one of the following criteria: Must be pursuing or have attained an Associate's Degree. Must be pursuing a Bachelor's Degree (enrolled student). Must have attained a Bachelor's Degree (not currently enrolled in a graduate program). Must be pursuing a Master's Degree (enrolled student). Required Majors: STEM major with coursework in Biomanufacturing, Biotechnology, Biology, Chemistry, Bioengineering, or similar. Required Skills: Familiarity with spreadsheets like Microsoft Excel with a basic understanding of how to organize data and use them to do calculations. Experience with presentations using programs like Google Slides or PowerPoint. Time management: organizing to-do lists, setting priorities, and following through to meet goals and deadlines. Experience with organizational software: Google calendar or others. Preferred Knowledge, Skills, and Qualifications: Excellent communication, collaboration, and interpersonal skills. Complements our culture and the standards that guide our daily behavior & decisions: Integrity, Courage, and Passion. Outstanding communication, collaboration, interpersonal, and problem-solving skills. Integrity, Courage, and Passion that complements our company culture. Interest in a STEM career, preferably in biotech/pharma. Careful, detail-oriented working style. Commitment to being trained in a new area and asking questions to support learning. Adaptive learner who can adjust to change easily. Please note: The goal of the internship will be to train you. The following skills will give you an idea of different opportunities. You do NOT need to have all of these skills in order to apply. Not all internships will use all these skills. Pipetting and wet lab measurements: how to use a scale, volumetric flasks, or graduated cylinders. Understanding of chemistry calculations: determine molarity, % Volume, or how to calculate for dilutions. Familiarity with mammalian cell culture and aseptic techniques. Familiarity with bioreactors. Familiarity with spreadsheets like Microsoft Excel with a basic understanding of how to organize data and use them to do calculations. Relocation benefits are not available for this job posting. The expected salary range for this position based on the primary location of California is $23.00-$35.00 per hour. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. This position also qualifies for paid holiday time off benefits. Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.
The Position Oceanside Operations (OCN) is a drug substance manufacturing organization dedicated to the reliable production of Roche’s commercial portfolio and pipeline products. Every year, OCN delivers millions of units of life-saving medicines to patients around the globe by leveraging its two integrated value streams: Stainless Steel and Single-Use production systems. As a Validation Engineer at OCN, you will play a critical role in ensuring that equipment, facilities, utilities, manufacturing processes, and cleaning/sanitization systems meet rigorous qualification and validation standards. Drawing from your expertise in qualification principles, engineering design fundamentals, manufacturing processes, and health authority expectations, you will review and approve validation documents, oversee tech transfers, and support Make-Assess-Release (MAR) activities. Beyond technical expertise, you will model Genentech’s values and core competencies, showcasing strong leadership, communication, and collaboration skills. In this role, you will work closely with cross-functional teams, including Engineering, MSAT, Quality Assurance, and Manufacturing, facilitating meetings and driving impactful projects. This is an opportunity to make a meaningful contribution to delivering essential therapies to patients worldwide. The Opportunity Manage and track the Validation program, including execution and assigned validation projects and ensure target timelines are met and/or issues are communicated / escalated effectively and consistently. Generate, review and approve a variety of Qualification Documents (IQs, OQs, IOQs, PQs, Engineering commissioning and turnover packages, Project Plans and Summary Reports) for equipment, facilities and utilities as well as support Cleaning and Process Validation. Strong understanding of commercial production environment and requirements. Proven ability to make suggestions for improvements as well as ensure programs are operating in a compliant and validated state. Perform role of subject matter expert and assess change control and discrepancy events for validated systems. Participate in cross-functional team meetings and where required, lead/facilitate meetings. Ensure the integration of environmental health, safety, and security into the business processes, systems and programs while reporting safety and environmental incidents including injuries, illnesses, and safety suggestions within one’s functional area. Foster a positive safety culture in which no one gets hurt. Who you are BS degree in Engineering or relevant scientific discipline. 4 - 6 years combined engineering/validation experience with a minimum of 3 years hands-on experience with equipment / utility / data review and analysis in a batch manufacturing environment within the pharmaceutical / biotechnology industry. Quality and Regulatory Knowledge: Must understand Quality standards, GMPs, Health Authority Regulations, cGMP regulations, Validation practices, and general compliance principles. Technical and System Expertise: Experience with CHO based manufacturing processes, Delta V automation system, Syncade and electronic Validation Execution. Hands-on experience commissioning/validating GMP equipment/utilities preferred. Communication Skills: Excellent verbal and written communication skills, and proven ability to manage multiple activities while maintaining organization. Teamwork and Initiative: Demonstrates initiative, problem anticipation, familiarity with project management principles, ability to work effectively in customer service/business partner roles, and strong collaboration skills with staff at all levels. Work Environment/Physical Demands/Safety Considerations Works in an office environment. Not a remote opportunity, expectation is to be onsite to support operations. On occasion my work in the clean room environment that requires gowning in the form of hospital scrubs, bunny suits, gloves and steel toe boots be worn. Also, no make-up or jewelry can be worn when working in the clean room environment. May be exposed to hazardous materials and chemicals. May be required to lift up to 30 lbs. Relocation benefits are available for this posting. The expected salary range for this position based on the primary location of California is $80,500 - $149,500. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Benefits Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.
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 Quality Engineer (QE) / Validation fulfills a critical role in GMP operations, supporting cleaning validation activities for API and PMO manufacturing, and the qualification of equipment, facilities, utilities. This position will work in close cooperation with Manufacturing, Engineering, and other functional areas to plan and perform validation activities under the Quality Engineering scope of work. This individual must also monitor facility / utility validated systems, plan, write and execute validation/ qualification protocols, reports, and other technical documents, as well as conduct related investigations What you will do Develop strategy, establish acceptance criteria, generate, execute cleaning validation protocols and reports Perform, coordinate, execute and analyze cleaning recovery studies. Lead cross-functional project teams to address issues and ensure on-time completion of all qualification / validation deliverables. Provide qualification / validation guidance and strategy during project planning and development phases. Train, coach and mentor team members. Write validation protocols and final reports, test methods, standard operating procedures, and technical reports. Planning, writing, and executing qualification protocols (DQ, IQ, OQ, PQ) and reports. Independently conduct and document investigations related to validation studies. Based on validation studies, evaluate and make recommendations for improvements to operations, processes and methods. Accountable for the accuracy and validity of testing results Support and assist with inspections and audits. Plan and perform required periodic re-validation / re-qualification activities Work and communicate with different associates within the company to ensure timely completion of assigned tasks and projects. Adherence to cGMP and safety procedures and contribute to GMP systems improvements. Perform other related duties as assigned. Qualifications Bachelor’s degree in science discipline (chemistry, biochemistry, biology or equivalent) Master's degree (preferred) 5+ years of Commissioning, Qualification & Validation (CQV) / cleaning validation experience in a GMP/GDP environment Experience with planning, writing and executing qualification protocols (IQ, OQ, PQ) and reports Experience with validation / monitoring of critical pharmaceutical utility systems, including purified water, nitrogen systems and cold storage units Experience with planning and execution of cleaning validation of production lab glassware and equipment including performance of validation studies, writing validation protocols and reports and other technical documents, as well as conducting validation related investigations Experience with developing coupon spike and recovery studies for cleaning validation Experience with Lean Six Sigma methods: root cause analysis, failure mode analysis and analyzing / organizing complex technical problems Understanding of cleaning validation requirements for pharmaceutical industry Knowledge of and ability to perform MAC calculation for APIs Understanding of GMP for Active Pharmaceutical Ingredients per ICH Q7. Knowledge of the chemical composition, structure, and properties of substances and of the chemical processes and transformations they undergo, including use of chemicals and their interactions, danger signs, production techniques, and disposal methods. Mid or large-size CapEx project experience General lab instrumentation knowledge and operation experience. Capable of working methodically and adhering to rules and regulations. Base salary range: Engineer II: $84,274 - $115,877 Sr Engineer: $103,939 - $142,916 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
We’re looking for an experienced plant operator to run day-to-day operations at our Poway, CA crushing plant. *Responsibilities include:* * Operating plant controls and oversee plant operations * Loading haul trucks efficiently and safely * Performing daily maintenance and basic inspections * Keeping the worksite clean, safe, and organized * Collaborate with team members to optimize production processes and improve efficiency *Requirements:* * Proven experience operating heavy equipment * Familiarity with crushing plants, screen plants, or similar aggregate/recycling operations preferred * Strong work ethic and reliability * Ability to perform routine equipment maintenance and safety checks * Comfortable working outdoors in a hands-on environment Job Type: Full-time Pay: $28.00 - $35.00 per hour Work Location: In person
Additional Location(s): N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions. About: Boston Scientific was recognized by Forbes as one of the Best Workplaces for Engineers in 2026, reflecting a culture where engineers do meaningful work. Boston Scientific was recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, reflecting the culture our employees experience every day. Apply your engineering expertise to ensure patient safety and product excellence by joining the Design Assurance team within our Structural Heart Valves division. As a Senior Design Assurance Engineer, you will support new product development and commercialized products that improve the delivery of care for patients around the world. In this highly visible role, you will influence design strategy, risk management, and lifecycle quality activities while partnering with cross-functional leaders in R&D, manufacturing, regulatory, and clinical. You will thrive in a high-performance culture that values diversity, innovation, global collaboration and a winning spirit — where continuous learning and meaningful impact are part of every project. Work model, sponsorship, relocation: This role is on-site in Carlsbad, California, to support hands-on collaboration and cross-functional partnership. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Relocation assistance is available for qualified candidates. Your responsibilities will include: Lead and apply advanced, systematic problem-solving methodologies to resolve complex product and process quality issues across the product lifecycle. Provide senior-level quality engineering leadership on cross-functional new product development teams, ensuring robust design inputs, verification and validation strategies and regulatory compliance. Drive the implementation and continuous improvement of risk management activities, including hazard analysis, fault tree analysis and FMEAs, ensuring alignment with ISO 14971 and internal standards. Develop and approve verification and validation protocols and reports, applying advanced statistical techniques and ensuring compliance with global regulatory requirements. Establish, review and maintain Design History File documentation, including design requirements, specifications and design outputs, ensuring inspection readiness. Lead design change control activities, assessing product and process impacts while ensuring compliance and patient safety. Monitor field performance of new and established medical devices, analyze trends against risk assessments and drive corrective and preventive actions as needed. Mentor junior engineers and contribute to the development of best practices that elevate team capability and performance. Qualifications: Required qualifications: Bachelor of Science degree in Engineering or a related technical field. Minimum of 7 years' experience in quality engineering or design assurance within the medical device industry. Demonstrated expertise in risk management, design controls and product verification and validation. Strong knowledge of global quality system regulations and standards, including ISO 13485 and ISO 14971. Proven ability to lead cross-functional initiatives and influence stakeholders at multiple organizational levels. Strong written and verbal communication skills. Ability to manage multiple priorities and navigate ambiguity in a fast-paced environment. Preferred qualifications: Degree in biomedical or mechanical engineering. Experience supporting cardiovascular implantable medical devices. Certification in quality engineering (e.g., CQE) or related credential. Demonstrated use of advanced quality tools and statistical methodologies. Passion for continuous improvement, talent development and building high-performing teams. Requisition ID: 625287 Minimum Salary: $ 89200 Maximum Salary: $ 169500 The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see www.bscbenefitsconnect.com—will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above. Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements). Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements). For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability. Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn. Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class. Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination. Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.
*About Our Company* MDI Advanced Systems USA Inc. was established in February 2024 as the U.S. branch of MDI (Mitsuboshi Diamond Industrial Co., Ltd., Osaka, Japan) MDI is a leading equipment manufacturer specializing in precision processing technologies, including scribing, breaking, drilling, and patterning. We provide proprietary cutting tools, laser systems, and automated equipment designed to achieve high productivity. Since 1935, we have applied patented cutting technologies to glass and other hard and brittle materials. Our equipment and tools also support multi-layered structures, including metal and organic materials. *Position Overview* * Job Title: Process Engineer * Job Type: Full-time * Classification: Exempt (Managerial/Professional) * Visa Sponsorship: Not Available * Location: San Diego, CA92121- Onsite * Work Schedule: Monday-Friday (Saturday, Sunday and holidays off) * Relocation: This role is an onsite position located in San Diego, CA. Candidates applying from outside the area must be willing to relocate at their own expense prior to the start date, as the company does not provide relocation assistance * Travel: Domestic and international travel required (including Japan); travel allowance provided *Preferred Qualification* * Japanese language skills are not required but preferred * Japanese language skills and/or an understanding of Japanese culture would be highly beneficial for this role *Job Description* As a Process Engineer, you will * Test and evaluate customer samples using our singulation (cutting/dividing) equipment * Interact closely with customers and collaborate with headquarters in Japan * Prepare detailed technical reports * Analyze and interpret test results * Travel as needed for business purposes * Bachelor's degree in engineering or a related field * Entry-level candidates encouraged to apply * Ability to work onsite and travel internationally * References required after interview *Compensation* * Salary: $66,560-$80,000 per year (DOE) *Benefits* * Simple IRA Plan with Matching * Health, Dental, and Vision insurance * Paid Time Off (PTO) and Sick Leave * Travel allowance for business trips We provide a competitive compensation and benefits package along with a flexible work schedule that supports work-life balance. Equal Employment Opportunity & Background check MDI Advanced Systems USA Inc. is an Equal Opportunity Employer Employment is contingent upon successful completion of a background check in accordance with applicable law. At-Will Employment Employment with MDI Advanced Systems USA Inc. is on at-will basis. This means that either the employee or the company may terminate employment at any time, with or without cause or notice, in accordance with applicable law. Pay: $66,560.00 - $80,000.00 per year Benefits: * Dental insurance * Flexible schedule * Health insurance * Paid time off * Retirement plan * Vision insurance Application Question(s): * Do you have Japanese language skills or interest in learning Japanese? Education: * Bachelor's (Required) Ability to Commute: * San Diego, CA 92121 (Required) Ability to Relocate: * San Diego, CA 92121: Relocate before starting work (Required) Willingness to travel: * 25% (Required) Work Location: In person
Are you looking to power the next leap in the exciting world of advanced electronics?Do you want to help solve problems that drive success in the rapidly evolving technology and connectivity landscape? Then bring your problem-solving, passion, and creativity to help us power the next leap in electronics. AtQnity, we’re more than a global leader in materials and solutions for advanced electronics and high-tech industries – we’re a tight-knit team that is motivated by new possibilities, and always up for a challenge. All our dedicated teams contribute to making cutting-edge technology possible. We value forward-thinking challengers, boundary-pushers, and diverse perspectives across all our departments, because we know we play a critical role in the world enabling faster progress for all. Learn how you can start or jumpstart your career with us. PRIMARY RESPONSIBILITIES, CORE DUTIES& KEY AREAS OF ACCOUNTABILITY: • Applies engineering principles and techniques to develop engineering solutions using a variety of tools. • Lead the development, implementation, and optimization of manufacturing processes to ensure efficiency, quality, and cost-effectiveness. • Collaborate with cross-functional teams to design, implement, and validate process improvements, ensuring adherence to industry standards and regulatory requirements. • Utilize lean and root cause methodologies and tools to analyze processes, identify areas for improvement, and drive continuous process enhancements. • Develop and maintain standardized work procedures, process documentation, and guidelines to ensure consistency and quality in manufacturing operations. • Assess the feasibility and soundness of proposed engineering tasks, build a resource plan for completion of these tasks, and track progress. • Monitors and analyzes process parameters to enhance product quality and yield. • Provide technical expertise and guidance to resolve complex manufacturing issues, troubleshoot problems, and optimize production throughput. • Identify, coordinate and/or participate in appropriate Management of Change processes. • Collaborate with suppliers and vendors to qualify alternative materials, optimize processes, drive quality improvements, and ensure compliance with specifications and standards. • Prepare and maintain process documentation, including process flow diagrams, operating procedures, and specifications. • Conduct risk assessments and implement process safety measures. • Collaborate with R teams to scale up laboratory processes to full production. • Work with the Quality team to establish acceptance criteria for materials and products. • Receives minimal supervision and guidance related to overall objectives, critical issues, new concepts, and policy matters. • Drive initiatives to enhance operational excellence, reduce waste, and increase overall productivity within the manufacturing environment. • Stay current with industry trends, technological advancements, and regulatory requirements. JOB QUALIFICATIONS Requirements: • Bachelor’s degree in mechanical, Chemical, Process, Manufacturing, Industrial Engineering, or a related field from an accredited university or an equivalent experience of 7+ years’ in an Engineering environment. • Process and continuous improvement experience are highly desirable (Six Sigma Green or Black belt is desirable) • Silicone and elastomer material knowledge is desired. • Experience with tool/mold qualification process is desired. • Mixing, calendaring, pressing, and extrusion processes knowledge is desired. • Experience working on a manufacturing site with robust quality management systems (ISO 9001 and AS9100 Aerospace Standards preferred). • Proven track record of successfully implementing process improvement initiatives and driving tangible results in a manufacturing environment. • Strong knowledge of lean manufacturing principles, standard work methodologies, and quality management systems. • Must be self-motivated and able to work independently with minimal supervision. • Good written and oral communication skills. • Interpersonal, people development, and training skills. • Ability to work as a team member in a respectful manner in a diverse work environment. • An active/inactive secret clearance or can obtain a clearance if requested. Key reasons for you to apply: • On-going learning and personal development opportunities in a rewarding work environment. • Start or continue on a career journey that can span different businesses, projects and functions with opportunities for personal and professional growth. Additionally, diversity, equity and inclusion are central to our high-performing culture Join ourTalent Community to stay connected with us! Qnity is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information. Qnity offers a comprehensive pay and benefits package. To learn more visit theCompensation and Benefits page. We use Artificial Intelligence (AI) to enhance our recruitment process. The Pay range for this role is $78,960.00 - $124,080.00 Annual How Base Pay is Determined: Qnity has job leveling frameworks that help organize roles based on progressive levels of responsibility, proficiency and qualifications. Each role has an associated pay range (or an established pay rate for some roles) based on the competitive market in each country where we operate. Each individual’s pay is based on a variety of factors, including their role and the associated pay range for that role, their geographic location (i.e., country, state, metropolitan area), as well as their skills, experience, education and certifications, and performance.
Are you a skilled cabinetry professional looking for your next big opportunity? We have an exciting contract position waiting for you! Join our team as a full-time Cabinet Installer and bring your expertise to a variety of residential projects, where you'll deliver quality craftsmanship and exceptional service. As a 1099 subcontractor, you'll enjoy the type of freedom and flexibility that typically comes with running your own independent business-setting your schedule, managing your workflow, and taking on projects that align with your availability. Pay Structure This role is paid per completed project, not hourly or salaried. Typical earnings range from $3,000–$5,000 per job Installers generally complete 1–3 jobs per month, depending on availability and project volume Payments are issued upon successful project completion This structure allows you to maximize your income while maintaining full control of your schedule. What You Can Expect Independence and autonomy as a 1099 subcontractor Flexible project scheduling Consistent communication and support from our team A steady pipeline of installation opportunities You will work on a project-by-project basis, coordinating directly with homeowners and our internal team to ensure high-quality installations. Professionalism, craftsmanship, and reliability are essential to success in this role. YOUR DAY-TO-DAY AS OUR CABINET INSTALLER In this cabinetry role, you will start your day by preparing your tools and gathering all necessary components for your upcoming installation. You will travel to job sites, armed with detailed designs from the initial meetings with the homeowners and designers. Upon arrival, you will provide in-home measurements, ensuring the installation will be accurate and tailored to the client's vision. Throughout your day, you will work efficiently to install pre-manufactured cabinetry, coordinating closely with homeowners and retail partners to ensure clear communication and quality service. As you finalize each installation, you will verify that every detail aligns with the design specifications, leaving clients delighted with their newly updated spaces. Here's what we need from you: 1+ year(s) of experience in cabinet installation or a related carpentry field Proficiency in installing pre-manufactured cabinetry and related woodwork with precision Your own required tools (saws, drills, levelers, etc.) and reliable transportation Ability to lift heavy components and work in various physical environments License or insurance and an EPA Renovator for Lead Safe Practices Certificate Strong ability to interpret blueprints and floor plans Excellent customer service skills and a professional demeanor Ability to work independently and with minimal supervision JOIN US Are you ready to take the next step in your career as a Cabinet Installer? We invite you to apply through our mobile-friendly application process.
HME has been creating innovative products for the drive-thru and pro-audio industries since 1971. From the very beginning, we've known these solutions would never have happened without the customer-focused people who make up our company. HME has a team environment with a culture of collaboration, learning, and growth. With subsidiaries located in California, Missouri, Canada, UK, India, and China, companies around the world depend on HME for clear, reliable communication solutions. From setting the standard for drive-thru headsets and timer systems in the quick service restaurant (QSR) industry to developing professional audio equipment used in the Olympic Games, HME strives to create the newest, most innovative products on the market while providing quality care and attention to its customers. Come join our team! Come write your chapter of the HME story. Are you good with your hands? Do assembly instructions make sense to you? Are you looking to start a new career and not just another job? HME is actively recruiting candidates with great Attitudes and Aptitude for an Assembler Tester I, 1st shift, Temp to Hire. In this position, with training and under direct supervision, performs various electro-mechanical assembly, test and inspection procedures to ensure that production schedules and quality standards are met. May use automated test equipment, handheld tools, soldering iron, assembly drawings, bills of materials, schematics, written instructions, and/or other applicable documents. This is a 1st shift position working 5:30 am - 2:00 pm Monday-Friday. What you will do in the position: Assembles, reworks, and/or reassembles product as specified on applicable documentation. Verifies accuracy of instruction documents (e.g. schematics, assembly drawings, bills of material). Checks work for accuracy, quality, and conformance to specifications. Uses a computer for data entry and inputs serial numbers into the mainframe. Packages parts into kits for shipping. Labels and packages product including manuals and accessories. Informs supervisor or lead of work-related problems.Record test data and results What you will need to succeed in this position: Up to 6 months electronics assembly experience Ability to perform basic assembly operations. Ability to read and interpret manufacturing drawings and assembly aides. Ability to complete assignments within specific time parameters under direct supervision. Good verbal, reading, writing, and comprehension skills. Basic computer skills. Good manual dexterity. Basic computer skills GED required The starting rate is $18.00/hr. Our benefits package includes tuition reimbursement; 3 weeks paid vacation your first year, paid holidays, medical, vision, and dental coverage, pet insurance, life insurance, and 401K contributions. The physical demands and work environment 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. The employee will occasionally lift and move up to 50 pounds with assistance.