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Join Our Team and Keep Moving Forward with Breg! At Breg, we are dedicated to advancing orthopedic solutions that enhance the lives of patients and support healthcare professionals. As a leader in the orthopedic industry, we provide innovative products, consulting, technology, and services that help people move forward with confidence. We are currently seeking a Senior Industrial Engineer to join our team in Carlsbad, CA. If you thrive in a dynamic environment where innovation and impact go hand in hand, this is the opportunity for you. Who You Are You are a forward-thinking professional who values collaboration, innovation, and making a meaningful difference. You bring expertise in demonstrating ownership and accountability, plan, execute, control, deliver and communicate effectively and are eager to contribute to a team that is committed to delivering exceptional patient outcomes. What You’ll Do As a Senior Industrial Engineer, you will: Analyzes and improves distribution center processes including receiving, storage, picking, packing, and shipping. Designs and implements material flow systems that reduce handling time, improve throughput, and support operational flexibility. Leads facility layout redesigns to optimize space utilization and streamline logistics operations. Applies Lean Manufacturing and Six Sigma methodologies to drive continuous improvement in warehousing and supply chain performance. Collaborates with cross-functional teams including Logistics, Supply Chain, and Manufacturing to support operational changes and new product introductions. Conducts time studies, workflow analysis, and capacity planning to identify inefficiencies and recommend solutions. Develops and maintains Standard Operating Procedures (SOPs), visual management tools, and performance dashboards. Supports Design for Manufacturability (DFM) efforts with a focus on downstream material handling and distribution efficiency. Responsible for behaving in a professional manner both internally and externally in relationships that positively impact the company's reputation and comply with the company's policies and practices. Responsible for being accountable and committed to demonstrating Breg’s cultural beliefs and achieving the key results of the company. Responsible for promoting Breg's culture within the organization using established tools such as storytelling, providing focused feedback, and recognition. The performance of the position is aligned with the culture of commitment and accountability, following the steps of: See it, Own it, Solve it, and Do it. Collaborate with cross-functional teams to drive excellence in patient care and business solutions. What You Bring Bachelor’s degree in industrial engineering or related field is required. 5+ years of experience in industrial engineering with a strong focus on distribution center operations, material flow, and Lean practices is required. Experience working with Lean manufacturing and Six Sigma is required. Proven experience in warehouse layout design, process mapping, and logistics optimization is required. Proficiency in Computer Aided Design (CAD) tools and simulation software for layout and flow analysis is required. Excellent project management skills are required. Computer proficient to include web browser/internet search, MS Outlook, Word, and Power Point capabilities. Technical competence includes the ability to learn new software and systems and proficiency in Excel is required. Experience with Oracle, Customer Relations Management (CRM), and Power Business Intelligence (BI) is preferred. A passion for innovation and a commitment to Breg's mission to keep moving forward. Why Breg? At Breg, we invest in our people and culture. We offer: Comprehensive Benefits: Medical, dental, vision, disability, and life insurance, effective the first of the month after hire. Work-Life Balance: Paid Time Off (PTO) and company-paid holidays. Growth & Development: Opportunities for professional advancement within a company that values your contributions. Commitment to Diversity & Inclusion: Breg is proud to be an Equal Employment Opportunity employer, fostering a diverse and inclusive workplace. For more information regarding Company benefits, please see https://www.breg.com/benefits Compensation Salary Range: $125,500.00 - $140,000.00. Actual compensation is determined by factors such as experience, skills, and business needs. This range reflects the minimum and maximum target range for new hire base salary/pay across all US locations. Actual pay is based on many factors unique to each candidate, including but not limited to geographical location, work experience, skill set, relevant trainings and certifications, and business needs. The base pay range is subject to change and may be modified in the future. This role may also be eligible for [bonus/commission/equity]. Ready to Move Forward? If you’re ready to be part of a company that is redefining orthopedic care, apply today at www.breg.com/careers. Breg is an Equal Employment Opportunity Employer and dedicated to a diverse work force and Drug Free work environment. EOE/Minorities/Females/Vet/Disabled are encouraged to apply. Applicants must be currently authorized to work in the United States on a full-time basis. The Company will not sponsor applicants for work visas for this position. #LI-TK1 Education Required Bachelors or better in Engineering Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
Who are we: Magnaflow is a leading manufacturer and supplier based in Oceanside, CA of premium products to the automotive aftermarket industry such as catalytic converters, performance exhaust and replacement exhaust. Through the Camburg division in Huntington Beach, CA. Magnaflow also supplies race-inspired performance suspension products and vehicle uplifting services, Magnaflow is focused on future growth through both new business development and new product introduction. our websites are www.magnaflow.com and www.camburg.com. Salary Range: $19.50 to $23.50 USD *Final agreed upon compensation will be based on a variety of factors including but not limited to an individual’s related experience, education, certifications, skills, and work location What you will be doing: A Manufacturing Production Associate is responsible for supporting the production process by operating machinery, assembling products, ensuring quality control, and maintaining a smooth workflow within the manufacturing environment. The role involves performing hands-on tasks to help meet production goals while adhering to safety and quality standards. Responsibilities: Assist in the setup, operation, and monitoring of production machinery and equipment to ensure smooth and efficient production. Assemble parts or products according to specifications, using tools or machines to complete tasks such as fitting, welding, or fastening. Inspect products during and after production to ensure they meet quality standards. Identify defects or issues and report them to supervisors for corrective action. Load and unload materials, parts, and finished goods for production processes. Ensure that the necessary materials are readily available for the production team. Operate manufacturing equipment, monitor performance, and troubleshoot minor issues to maintain production speed and quality. Follow all safety protocols and guidelines to ensure a safe working environment. Report unsafe conditions or practices to supervisors immediately. Maintain accurate production records, including time logs, inventory counts, quality checks, and report progress to team leaders or supervisors. Suggest ways to improve production efficiency, reduce waste, and optimize workflows to meet production targets. Work closely with other production team members, including engineers, quality control, and maintenance teams, to meet production goals and deadlines. 2nd Shift Schedule: 2:00PM-10:30PM M-F Skills & Qualifications: Familiarity with manufacturing processes, equipment, and tools. Ability to spot quality issues and ensure products meet specified standards. Basic skills in operating machinery or equipment used in production. Capability to stand for long periods, lift heavy objects, and perform repetitive tasks. Ability to troubleshoot minor machine or production issues to maintain workflow. Strong communication and collaboration skills to work effectively within a production team. Knowledge of safety practices and willingness to adhere to them. Education & Experience: High school diploma or equivalent. Previous experience in a manufacturing or production environment is typically preferred but not always required. On-the-job training may be provided for those with no prior experience.
Job Title: Validation Associate III Job Location (Short): San Diego, CA, USA, 92121 Posting Start Date: 8/28/25 Do you want to take responsibility and make a difference with your work? With your expertise, we can achieve great goals together. We are WACKER - Reliable. Determined. Ambitious. As one of the world's most research-intensive chemical companies, we've been making countless products that are an integral part of your everyday life possible for over 100 years. From vegan food to resource-efficient buildings to solar cells, we develop sustainable solutions that change the future. To strengthen our team in San Diego , we are looking for you as a(n) Validation Associate III . The Validation Associate III at Wacker Biotech will play a critical role in supporting the development, optimization, and execution of validation & engineering processes for the production of plasmid DNA (pDNA) and other biopharmaceutical products. This position requires a highly skilled and experienced professional who is familiar with a variety of validation & engineering concepts, practices, and procedures. The ideal candidate will rely on their expertise and judgment to plan and accomplish goals, while providing technical leadership, driving continuous improvement initiatives, and supporting Building Management Systems (BMS), automation systems and validation activities to ensure operational excellence. Essential Functions: Subject Matter Expert (SME) for Building Management System (BMS) and Automation Support to ensure proper monitoring and control of critical facility systems, including HVAC, utilities, and environmental conditions. Troubleshoot and resolve issues related to BMS and automation systems to minimize downtime and ensure operational stability. Collaborate with vendors and contractors to implement upgrades or modifications to BMS and automation systems. Process Improvement and Problem Solving, identify opportunities for process optimization and implement innovative solutions to improve manufacturing performance. Plan, execute, and oversee validation & engineering projects, ensuring they are completed on time, within scope, and on budget. Manage the process of required documentation, including project plans, validation protocols, and technical reports. Troubleshoot and resolve complex equipment and process issues to minimize downtime and ensure operational stability. Collaborate with vendors and contractors to ensure equipment and systems meet performance and compliance requirements. Stay up to date with industry trends and emerging technologies to drive innovation in biopharmaceutical manufacturing. Evaluate and implement new technologies to enhance production capabilities and efficiency. Work closely with cross-functional teams to ensure alignment on project goals and deliverables. Communicate project updates, risks, and outcomes to stakeholders and leadership. Foster a collaborative and innovative work environment that supports team success. Position Qualifications: Bachelor’s degree in validation or engineering (Chemical, Mechanical, or related field) 5-8 years of experience in a FDA and GMP regulated industry. ISO 7 & ISO 8 gowning experience is preferred. Familiarity with a variety of relevant validation & engineering concepts, practices, and procedures. Strong problem-solving and analytical skills, with the ability to develop creative solutions. Proven ability to manage multiple complex projects simultaneously. Experience with Building Management Systems (BMS) and automation technologies. Excellent written and verbal communication skills, with experience in technical writing and documentation. Proficiency in validation & engineering software and tools, as well as Microsoft Office Suite. Knowledge of regulatory requirements, including FDA, GMP, and ISO standards. Requires good written, verbal, and interpersonal communication skills and the ability to effectively interact with all levels. Ability to handle multiple assignments and changing priorities. Positive, proactive approach to drive assignments/tasks to completion. Proficiency with Microsoft Word, Excel, PowerPoint Ability or capable of lifting up to fifty (50) lbs. The anticipated salary range for candidates who will work in California is $76,500-$101,500. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Wacker is a multi-state employer, and this salary range may not reflect positions that work in other states. What do we offer? WACKER strives to reward its employees in a fair and equitable manner. Our Total Rewards Package considers employee wellbeing and is comprised of compensation, benefits, work-life balance, performance & recognition, and career development. Compensation and Incentive plans Medical, Dental, and Vision Insurance effective day 1 Paid Time Off in addition to personal days and holidays Paid parental leave Wellbeing fund Flexible hybrid work arrangements 401(k) with company match Education Assistance Program Career development and advancement opportunities Support for Community Involvement We are looking forward to your online application at www.wacker.com. Reference Code: 29926 LI-KM1 #IND123 The information contained herein is not intended to be an all-inclusive list of the duties and responsibilities of the job, nor are they intended to be an all-inclusive list of the skills and abilities required to do the job. A minimum requirement for this US-based position is the ability to work legally in the United States on a permanent unrestricted basis. Visa sponsorship is not available for this position, including any type of US permanent residency (e.g., for a green card). Wacker is an Equal Opportunity Employer. We actively promote the equality of opportunity for all who are qualified and bring the requisite experience, talent, skill and potential, without regard to age, disability, sex, race, religion or belief, marriage/civil partnership, pregnancy/maternity, sexual orientation, or any other protected characteristics. We welcome all applications from a wide range of candidates. Selection for roles will be based on individual merit alone.
*Job Summary* Quality Control Inspector with electrical, mechanical and electro-mechanical background is required. *Roles & Responsibilities* This position has responsibility for: The visual, mechanical, dimensional, functional, or electrical inspection of raw materials, parts, assemblies or final product in receiving inspection or production assembly process. This position works under general supervision. Parts will be inspected to engineering drawings, customer purchase orders, manufacturer specifications and industry standards. The inspections will be performed to engineering requirements specified per ANSI Y14.5 Geometric Dimensioning and Tolerance (GD&T) or equivalent standard. Must have the ability to read / interpret engineering drawings and Purchase Orders (POs). The inspector will be responsible for performing ERP system transaction including Returning material back to Supplier. Responsible to facility material review meeting with a cross functional team. Competency Requirements In order to perform the job successfully, an individual should demonstrate the following competencies: Problem Solving Decision Making Analytical Thinking Read Blueprints Oversight *Minimum Qualifications (Experience and Skills)* The candidate must have experience using various mechanical inspection tools, such as micrometers and calipers, and test equipment. Experience performing First Article Inspections (FAIs) and knowledge of applicable industry standards like IPC-A-610 or equivalent is highly desired. Quality Control Inspector candidate will have a minimum of five years’ experience performing inspections in electronics manufacturing with proficiency using Microsoft Word and Excel. Should read and understand engineering drawings The ideal candidate will have 5-10 years’ experience in testing and inspection in a manufacturing or production environment. Candidate should have experience in ERP system transactions, MRB (Material review board) Must have good communication skills, both written and verbal. Must be able to develop a good rapport with other departmental members. Skilful presentation of work issues to prevent negative reactions. Job Type: Contract Pay: $30.00 - $35.00 per hour Expected hours: 40 per week Education: * High school or equivalent (Preferred) Work Location: In person
Leading medical device components manufacturer has immediate openings for experienced CNC Swiss Machine Operators to join their team. Operates automated CNC machinery such as Swiss machines and related equipment to fabricate precision metal parts by performing the following duties. PRINCIPAL ACCOUNTABILITIES * Reads and interprets blueprints to maintain dimensions within tolerances of precision machined parts. * Able to troubleshoot and resolve most machine operation issues without assistance and able to perform basic machine set ups. * Reads and interprets Process Sheets to ensure parts are manufactured in accordance with standard processing requirements. * Maintains machine specific tools and consumables to ensure effective operation of equipment * Ensures high quality of parts by closely monitoring and adjusting operation of machine and/or tooling while regularly inspecting parts for conformance to requirements. * Ability to quickly detect and correct minor malfunctions or out-of-tolerance machining. * Performs secondary bench operations as required, which includes but is not limited to inspection, harperization, de-burring, and cleaning of parts. * Maintains lot traceability, work orders/travelers, and good housekeeping practices at all times. * Quickly raises any machining or quality issues with appropriate supervision or engineering support. * Ability to learn and work on a wide variety of part numbers and/or departments. * Participates in local programs and initiatives to improve EHS performance. * Accurately records daily production and provides detailed handover. * May suggest areas for improvement to the production process e.g. complete kaizen suggestions and participate in 5 Why investigation problem solving analysis. QUALIFICATIONS/ KNOWLEDGE/ EXPERIENCE (TECHNICAL/ PROFESSIONAL KNOWLEDGE & SKILLS COMPETENCY) * High school diploma or equivalent and/or vocational training preferred * Minimum of 1-3 years of CNC type machining work experience with demonstrated ability or related technical certificate program. * Ability to operate CNC type machines at a high level of precision, and utilize micrometers, optical comparator, and other related equipment with optimal accuracy. * Ability to operate machinery such as: bench grinder, mill, lathe, laser or other related manufacturing machinery. * Ability to use in process inspection tools. * Ability to occasionally lift 10 – 20 pounds. * Employee stands, sits and walks frequently. * Frequently required to reach with both hands and arms and occasionally stoop, kneel, or crouch. * Specific vision abilities required by this job include close vision, peripheral vision, depth perception, and the ability to adjust focus * Direct experience with Swiss manufacturing is highly preferred Shifts available: 2nd shift: 2:00 pm - 10:30 pm (1 opening) - Pay: $22/hr + 10% shift diff = *$24.20/hr* Join our team today and contribute your expertise as we continue to deliver exceptional products in the medical device industry through precision machining! Job Type: Full-time Pay: $24.20 per hour Benefits: * Health insurance Work Location: In person
Digital Force Technologies (DFT) Position: Senior CNC Programmer What We Do: Digital Force Technologies (DFT) is a defense technology provider with a 25-year history of developing and fielding advanced sensor systems, force protection solutions, and tactical surveillance products. DFT’s extensive history of innovation, in-house expertise, and robust network of technology partners allows DFT to rapidly addresses critical Department of Defense (DoD) and Federal Agency requirements. DFT’s engineering team is a diverse and skilled group, determined to develop advanced technical solutions. DFT offers a unique chance to develop and work with modern technologies while delivering impact and seeing products grow from concept to reality. DFT is a results driven culture focused on innovation, creativity, and growth. If you have a passion for solving complex problems, making an immediate impact on a dynamic, and fast moving, product development team, we’d love to hear from you! What We Need: Reporting to a Senior Engineering Manager, the Senior CNC Programmer will be responsible for running the internal prototype CNC Machine shop. This includes programing, setting up, and running 3 and 5 Axis CNC mills, saws, drill presses, and other machining equipment to support a fast-paced product development environment. This person will devise and manage complex CNC set-ups independently to ensure a quality product is produced. What You’ll Do: Program, setup and run Hass 3 and 5 Axis CNC mills daily to produce small run prototype parts. Work directly with the engineering design team on critical parts and the fixtures required for machining them. Oversee the maintenance schedule of the machine shop and work with external vendors as needed for preventative maintenance and repairs. Work with external vendors to order the material and tooling needed to complete parts. Measure parts to ensure critical features meet required specifications. Required Skills/Qualifications BS in Mechanical or Manufacturing Engineering & 5+yrs exp in CNC Programming and operation, OR HS Diploma and Vocational Training & 10+yrs exp in CNC Programming and operation. Strong skills in CNC programming and machine operation. Proficiency in CAD/CAM software, particularly in MasterCAM and a familiarity with G-Code. Experience with 4-axis and 5-axis machining operations. Knowledge of manufacturing processes and quality control standards. Excellent problem-solving skills and attention to detail. Ability to work collaboratively in a team environment and communicate effectively. Knowledge of proper use of measuring tools / gauges and cutting tools. Ability to read blueprint dimensions and tolerances. Ability to determine cutter speeds and feeds for basic materials. Able to properly use inserts, fixtures, and tooling. Good communication and basic math skills. Strong organizational, problem-solving, and analytical skills. Ability to work on complex projects with general direction and minimal guidance. Preferred Qualifications Familiarity with Solidworks. Direct experience with 5-Axis HAAS UMC machines. PHYSICAL DEMANDS AND WORK ENVIRONMENT: Frequently lift to 50 lbs. Stand up to 5 hours at a time. What We Offer: DFT offers a comprehensive benefit package including medical, dental, vision, 401K w/ 5% company match, life insurance, short term disability, 3 weeks PTO, 13 company holidays, and much more. In addition, DFT provides a company culture that encourages: Collaboration Innovation Employee engagement Motivation Salary Range - $95,000 - $115,000 (Based on experience) - The salary range for this role is an estimate based on a wide range of compensation factors, inclusive of base salary only. Actual salary offer may vary based on (but not limited to) work experience, education and/or training, critical skills, and/or business considerations. If you are looking for a dynamic place to work where your contribution makes a difference in supporting the mission, DFT is the right company for you. EEOC Statement - DFT is an equal-opportunity employer, and we encourage candidates from all backgrounds to apply. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability or protected veteran status. Day Shift
Why work for PCI Pharma Services? At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don’t say no, we figure out how. Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. Job Details: We are looking for a Drug Product Manufacturing Associate II who is responsible for executing GMP production of injectable pharmaceuticals by following all applicable SOP's. Manufacturing associates are responsible for preparing equipment and materials for GMP aseptic production and operating equipment such from glasswashers, autoclaves, depyrogenation ovens and automated filling machines. Responsibilities: Participate in one or more areas of the aseptic manufacturing injectable pharmaceuticals using GMP's in FDA regulated facility. Assists technical personnel with troubleshooting mechanical issues that arise with manufacturing equipment. Performs various semi-routine manufacturing tasks under the guidelines of established SOP’s and cGMP regulations. Troubleshoots manufacturing processes that are semi-complex in level under cGMP guidelines and under the supervision of management. Assists in the research and implementation of new methods and technologies to enhance operations. Prepares components, media, buffers, and other solutions as needed. Accurately documents data and writes/reviews batch records under cGMP guidelines. Prepares material components for production. Regular and reliable attendance on a full time basis [or in accordance with posted schedule]. Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices. Embodies PCI Pharma Service’s cultural values and aligns daily actions with department goals and company culture. Requirements: High school diploma required. Bachelors in a science or engineering discipline preferred. Minimum of two (2) years of relevant experience in manufacturing, laboratory, mechanical or engineering positions. Ability to work with cross functional teams. Detail oriented with strong written and verbal communication skills. Ability to work independently, within prescribed guidelines, or as a team member. Demonstrated ability to follow detailed directions in a manufacturing GMP environment. Familiarity with cGMP, manufacturing, machine operations, and data entry. Must be familiar with Microsoft Office applications. The base hourly range for this position is $21.69 to $24.40 plus annual performance bonus eligibility. Final offer amounts are determined by multiple factors including and not limited to specific and relevant experience, credentials, geography and subject matter expertise. Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future Equal Employment Opportunity (EEO) Statement: PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture. #LI-KC1 Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
We are seeking a highly skilled and creative Automation Design Engineer to join our Automation Practice. This role is responsible for designing end-to-end automation solutions that align with business goals, technical architecture, and standards. The ideal candidate will combine strong technical expertise with process design thinking to deliver scalable, secure, and innovative automation systems. Requirements: Key Responsibilities: • Solution Design • Analyze business processes and design automation solutions that optimize performance and reduce manual effort. • Create detailed design documents, process maps, and technical specifications. • Collaborate with RPA developers, software engineers, and business analysts to ensure seamless implementation. • Architecture Alignment • Ensure automation designs align with enterprise architecture and data models. • Contribute to the development of reusable design patterns and frameworks. • Integrate automation solutions with existing systems and platforms. • Innovation & Prototyping • Support the Innovation Hub by designing and testing prototypes that demonstrate new automation capabilities. • Evaluate emerging technologies and recommend design enhancements. • Governance & Standards • Adhere to CoE standards for documentation, metadata management, coding, and testing. • Participate in design reviews and contribute to the continuous improvement of design practices. • Security & Compliance • Incorporate security and compliance requirements into automation designs. • Collaborate with security teams to ensure secure architecture and data handling. • Change Management & Communication • Support change management efforts by documenting design rationale and communicating with stakeholders. • Assist in training and onboarding teams to understand and adopt automation designs. Qualifications: • Bachelor’s degree in Engineering, Computer Science, Information Systems, or related field (Preferred). • 3+ years of experience in automation design, process engineering, or solution architecture. • Strong understanding of automation technologies (RPA, workflow automation, scripting). • Experience with process modeling tools (e.g., BPMN, Visio) and design documentation. • Familiarity with enterprise architecture, data integration, and system interoperability. Preferred Skills: • Experience working in a Center of Excellence or enterprise automation environment. • Knowledge of metadata management and technical documentation standards. • Exposure to AI/ML, low-code platforms, and cloud-based automation tools. • Strong communication and stakeholder engagement skills. Benefits: Since 1993, ITP has been providing reliable, cost-effective solutions to meet our customers’ goals and objectives in the commercial and public marketplace. We are Women Owned Small Business Certified with a GSA IT 70 Schedule and a Navy SeaPort-e contract. We offer a full range of benefits, Health, 401K, Life, Disability, Student Loan Help, Bonuses...etc. Smart? Motivated? Ready to roll? You'll feel right at home at ITP. Where creativity is encouraged, initiative is rewarded, and reputations are made. A career here translates into continual opportunities to grow and expand on what you can do as we help clients become high-performance organizations. There's no better place to grow your career! If you wish to be part of this dynamic opportunity, please apply to this job posting.
Company Description Who is Steico Industries? STEICO has made its name manufacturing precision tube and duct assemblies to the world's major airframe manufacturers. We manufacture tube and duct assemblies. We work with a wide variety of materials including aluminum, steel, titanium, and other alloys and produce parts of all complexities. STEICO holds accreditations with NADCAP and is certified to AS9100 and ISO14001. Our focus on responsiveness and continuous improvement regularly creates manufacturing innovation. STEICO is an integral part of our customers supply chains that include Boeing, Lockheed Martin, BAE, Northrop Grumman, Honeywell, Honda Aviation, and many others. About our parent company: Senior is an FTSE UK based international manufacturing Group with 26 operations in 12 countries. Senior designs, manufactures and markets high-technology components and systems for the principal original equipment producers in the worldwide aerospace, defense, and land vehicle and power & energy markets. We have a long history of well-respected brands and an excellent reputation in our key market sectors. Senior delivers value to its customers and shareholders via operational excellence that is underpinned by its people and processes. Senior’s experienced manpower support, effective use of raw material, and high technology enable it to deliver optimized components within a short development time and at most competitive prices. The Group is split into two divisions, Aerospace and Flexonics, servicing five key sectors. Our global values underpin what we do, and how we do it … Job Description AM Shift: Monday - Friday 7:00AM - 3:30PM Pay: $17.00 - $19.00 an hour depending on experience Safety – Integrity – Customer Focus – Respect & Trust – Accountability – Excellence As an Assembly Tool Tech you will: Utilizing a combination of machined fixture components and components built in SLA machines, clean and assemble tooling for use in manufacturing. Will operate the SLA machines by adding raw materials as needed, starting build files and removing completed builds. Assists as needed with tool coordination on the manufacturing floor in order to efficiently link tooling with work orders at time of need to eliminate tooling constraints. What will my responsibilities include? Operate SLA (Stereolithography) machines, starting builds and removing completed builds. Perform cleaning and maintenance of SLA machines. Clean SLA components after build completion. Operate waterjet to create needed fixture components. Assemble SLA and machined components in order to produce assembly tool for inspectionand use. Perform visual inspection of purchased machined components. Assist with tool coordination in shop in order to link jobs with work orders as needed. Operate shop equipment such as bandsaw, manual lathe, sander. Other reasonable duties as business and operational needs dictate. Using required PPE for the department Qualifications What key skills and experience do I need? Blueprint/drawing interpretation, fabrication and assembly experience. Previous experience in manufacturing environment Ability to communicate respectfully and knowledgably with co-workers and customers both verbally and written. Requires English verbal and written skills Requires basic math skills sufficient to perform basic calculations Working knowledge of MS word and excel Education: High School diploma or equivalent. Additional Information Why Join Steico Industries, Inc.? Joining Steico Industries, Inc. a company of Senior Plc. means not only a rewarding career with a tight-knit and collaborative team, but you will also enjoy a competitive compensation package that includes a market-led base salary and a comprehensive benefits package along with wellness benefits, employee recognition program, matching 401k plan, paid vacation, flexible hours, employee wellness activities, tuition reimbursement, and community involvement initiatives. Please understand that you will only be considered an applicant if you apply for a posted position directly through our Company website and meet the qualifications of the job. If you need a reasonable accommodation to apply, please contact the Steico Industries at 760-438-8015. Prior to an offer of employment, applicant employment references maybe requested. Trade Compliance Statement Access to our facilities is restricted under the International Traffic in Arms Regulations (ITAR) and/or the Export Administration Regulations (EAR) to U.S. Persons (U.S. Citizens, lawful permanent residents, U.S. Nationals, U.S. refugees, asylees, or temporary residents under amnesty provisions ), and to properly licensed foreign persons. Applicants receiving a conditional offer of employment will be required to provide information to determine whether they are subject to these regulations and, if so, to assess their country of chargeability for export control purposes. Additionally, potential employee names will be screened against the Consolidated Screening List (maintained by the United States government) to determine eligibility to receive controlled technical data. To ensure there is no unexpected delay to your start date with our Company and due to the potential need to obtain an export license, we would like to promptly assess whether such a license is needed to access our facility and/or systems. Such licenses can take several weeks/months to obtain from the U.S. Government. Our Trade Compliance department may reach out to you with a Licensing Assessment form, which we request you kindly complete and return as soon as possible. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. EOE M/F/D/V/VEVRAA Federal Contractor
Company Description Who is Steico Industries? STEICO has made its name manufacturing precision tube and duct assemblies to the world's major airframe manufacturers. We manufacture tube and duct assemblies. We work with a wide variety of materials including aluminum, steel, titanium, and other alloys and produce parts of all complexities. STEICO holds accreditations with NADCAP and is certified to AS9100 and ISO14001. Our focus on responsiveness and continuous improvement regularly creates manufacturing innovation. STEICO is an integral part of our customers supply chains that include Boeing, Lockheed Martin, BAE, Northrop Grumman, Honeywell, Honda Aviation, and many others. About our parent company: Senior is an FTSE UK based international manufacturing Group with 26 operations in 12 countries. Senior designs, manufactures and markets high-technology components and systems for the principal original equipment producers in the worldwide aerospace, defense, and land vehicle and power & energy markets. We have a long history of well-respected brands and an excellent reputation in our key market sectors. Senior delivers value to its customers and shareholders via operational excellence that is underpinned by its people and processes. Senior’s experienced manpower support, effective use of raw material, and high technology enable it to deliver optimized components within a short development time and at most competitive prices. The Group is split into two divisions, Aerospace and Flexonics, servicing five key sectors. Our global values underpin what we do, and how we do it … Job Description AM Shift: Monday - Friday 7:00AM - 3:30PM Pay: $25.00 - $29.00 an hour depending on experience Safety – Integrity – Customer Focus – Respect & Trust – Accountability – Excellence As an NDT level II Penetrant you will: Responsible for testing tube and duct assemblies and detailed components. Uses automated and manual techniques including digital radiography (DR) and fluorescent penetrant inspection (FPI) to perform non-destructive tests (NDT) to identify errors or defects. What will my responsibilities include? Set up and standardize equipment, process parts, interpret/evaluate acceptance rejection, and document results. Perform all NDT level I & II responsibilities using industry standards. Conduct system performance checks in accordance industry standards. Training of Trainee/level I and level II Technicians to Industry standards Follow written practices such as procedures and work instructions. Knowledge of relevant product manufacturing and inspection technology. Set up and operate Digital X-ray equipment following procedure, Including interpretation of images. Capable of processing with existing FPI procedure, Including interpretation of assemblies. Perform preventative maintenance on equipment in the department. Maintaining 5s and safety requirements for the area. Read and understand blueprints and customer data. Other reasonable duties as business and operational needs dictate. Qualifications What key skills and experience do I need? Three years’ experience in the NDT Methods(s) and manufacturing processes as a certified Level II Candidate for NDT certification. Must have the skills and formal training needed to become certified to NAS 410, level II in the applicable test method, and be able to pass an annual eye examination per the requirements of NAS 410. Education, training, and experience to be qualified for certification. OJT (on the job training) hours must meet the minimum requirement in order to be certified for NDT Level II per NAS 410. Education: High School Diploma, GED or equivalent work experience. Experience: North Star Imaging (NSI) equipment (preferred) Fuji Film, computed radiography (CR) experience is a plus. Experience with Film Radiography (RT) is a plus. Experience with inspecting tools such as microscopes, loop, blacklight and pin gauges. Additional Information Why Join Steico Industries, Inc.? Joining Steico Industries, Inc. a company of Senior Plc. means not only a rewarding career with a tight-knit and collaborative team, but you will also enjoy a competitive compensation package that includes a market-led base salary and a comprehensive benefits package along with wellness benefits, employee recognition program, matching 401k plan, paid vacation, flexible hours, employee wellness activities, tuition reimbursement, and community involvement initiatives. Please understand that you will only be considered an applicant if you apply for a posted position directly through our Company website and meet the qualifications of the job. If you need a reasonable accommodation to apply, please contact the Steico Industries at 760-438-8015. Prior to an offer of employment, applicant employment references maybe requested. Trade Compliance Statement Access to our facilities is restricted under the International Traffic in Arms Regulations (ITAR) and/or the Export Administration Regulations (EAR) to U.S. Persons (U.S. Citizens, lawful permanent residents, U.S. Nationals, U.S. refugees, asylees, or temporary residents under amnesty provisions ), and to properly licensed foreign persons. Applicants receiving a conditional offer of employment will be required to provide information to determine whether they are subject to these regulations and, if so, to assess their country of chargeability for export control purposes. Additionally, potential employee names will be screened against the Consolidated Screening List (maintained by the United States government) to determine eligibility to receive controlled technical data. To ensure there is no unexpected delay to your start date with our Company and due to the potential need to obtain an export license, we would like to promptly assess whether such a license is needed to access our facility and/or systems. Such licenses can take several weeks/months to obtain from the U.S. Government. Our Trade Compliance department may reach out to you with a Licensing Assessment form, which we request you kindly complete and return as soon as possible. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. EOE M/F/D/V/VEVRAA Federal Contractor
*Sol-ti strives as a team to promote a passion for healthy living and sustainability. We are committed to helping our partners and customers through our liquids of vitality - preserving our planet with the use of premium and consumer preferred, glass packaging. Our innovative glass packaging is not only for purity and taste but aligns with our company wide mission.* *Sol-ti, meaning “of the sun”, encourages our partners worldwide to let their inner light shine bright. Sol-ti is employee owned, growing rapidly, and expanding through promotions from within as quickly as our talent pool allows, but we need experienced new partners.* *Sol-ti is currently the Highest Velocity Refrigerated Beverage Company in the United States. We sell more product per store per week on average in all stores that Sol-ti sells in.* _*Position Summary:*_ As a Packaging Technician you will be responsible for the operation, maintenance, and supporting processes of packaging equipment in making high quality and safe products. _*Job Responsivities:*_ * Strong communication with your team to deliver daily goals * Equipment operation (startups, shutdowns, changeovers, maintenance, cleaning, inspection, troubleshooting, training, material handling) * Increase equipment uptime, decrease downtime * Implement improvements on equipment and processes * Partner with Technical, Maintenance, and Operations team to problem solve and make improvements * Proactively escalate issues as required to address problems * Model integrity and support our mission, vision, and values * Great attendance and strong work ethic * Follow all Safety and Quality / Good Manufacturing policies and complete all training * 1st and 2nd shift positions available (3 x 12 hour shifts) _*Job Requirements:*_ * Food or Beverage manufacturing and packaging experience a must * Mechanical aptitude * Problem solver * Ability to adapt to change and shifting priorities * Self-directed and self-motivated * Works well with a team and open to new ideas * Comfortable with ambiguity as company scales and grows quickly Job Type: Full-time Pay: $20.00 - $21.00 per hour Benefits: * Dental insurance * Health insurance * Paid time off * Vision insurance Work Location: In person
*Production Technician* *Sol-ti strives as a team to promote a passion for healthy living and sustainability. We are committed to helping our* *partners and customers through our liquids of vitality - preserving our planet with the use of premium and consumer preferred, glass packaging. Our innovative glass packaging is not only for purity and taste but aligns with our company* *wide mission.* *Sol-ti, meaning “of the sun”, encourages our partners worldwide to let their inner light shine bright. Sol-ti is employee owned, growing rapidly, and expanding through promotions from within as quickly as our talent pool allows, but we* *need experienced new partners.* *Sol-ti is currently the Highest Velocity Refrigerated Beverage Company in the United States. We sell more product per store per week on average in all stores that Sol-ti sells in.* _*Position Summary:*_ As a Production Technician you will be responsible for the operation, maintenance, and supporting processes of packaging equipment in making high quality and safe products. _*Job Responsivities:*_ * Strong communication with your team to deliver daily goals * Equipment operation (startups, shutdowns, changeovers, maintenance, cleaning, inspection, troubleshooting, training, material handling) * Equipment includes juice presses, fruit grinders, citrus juicers, tanks, pumps, piping * Remove and clean change parts on juicer and grinder, and CIP tanks, hoses, pumps, and equipment in the batching area * Required to batch recipe, test analyticals, perform Quality assurance checks and complete documentation * Increase equipment uptime, decrease downtime, and perform simple repairs * Implement improvements on equipment and processes * Partner with Technical, Maintenance, and Operations team to problem solve and make improvements * Proactively escalate issues as required to address problems * Model integrity and support our mission, vision, and values * Great attendance and strong work ethic * Follow all Safety and Quality / Good Manufacturing policies and complete all training * All other responsibilities as required by the team _*Job Requirements:*_ * Food or Beverage manufacturing and production batching experience a must * Mechanical aptitude a must * Problem solver * Ability to adapt to change and shifting priorities * Self-directed and self-motivated * Works well with a team and open to new ideas * Comfortable with ambiguity as company scales and grows quickly * 1st and 2nd shift positions available (3 x 12 hour shifts) _*Sol-ti Benefits:*_ * Sol-ti contributes $200 towards the cost your medical premiums. $100 for your spouse and $50 for each of your dependents. * All you can drink Sol-ti while at HQ and the warehouse. * Keeps you hydrated at work without spending money. * High quality boots, socks, gloves and necessary gear. * Saves you time and money. * Sol-ti organic fruit offered daily. * Healthy fruit provided daily to keep you energized and save money. * Growth Opportunities. * Sol-ti is growing over 150% year over year. * Interested in career growth? The opportunities at Sol-ti are immense! * Employee Equity Plan. * Sol-ti is employee owned. * All full time employees are eligible to participate in our Employee Equity Plan. * Equity has a 1 year cliff (you much be at Sol-ti for a 1 year minimum). * Equity has a 4 year vesting schedule (full ownership occurs after 4 years). * Discretionary bonuses. * Monthly bonuses based on production metrics. * Perfect attendance awards. * Referral program. * Refer a friend or acquaintance to come to work at Sol-ti. * Up to $1,000 bonus based on length of employment (3 installments). Job Type: Full-time Pay: $20.00 - $21.00 per hour Benefits: * Dental insurance * Health insurance * Paid time off * Vision insurance Work Location: In person