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<h3>Job Description</h3>
Job Description
We are actively seeking skilled Machinists, Tool Makers, CNC Operators, 4 &amp; 5-axis Mills, Lathes, Wire Machine, CMM, Tube Bending, Inspectors and Aerospace Quality Engineers to become part of our growing team.
Tube Specialties, Inc. in Tempe, Arizona is a small business that specializes in precision tube fabrication for the Aircraft/Aerospace and Defense industries. We are seeking experienced and highly skilled people. Founded in 1973, TSI is dedicated to delivering high-quality, intricate assemblies, including complex manifolds, bent assemblies, and critical components for fighter jets and anti-ballistic missiles. We pride ourselves on our commitment to excellence and innovation. TSI possesses most aerospace certifications (AS9100, NADCAP) as well as we are an E4B4 security company.
Company DescriptionManufacturing Aerospace parts 
<h3>Company Description</h3>
Manufacturing Aerospace parts

Machinist, Tool Maker, 4/5 Axis CNC Operator & Quality Engineer

<h3>Job Description</h3>
Job Description
Industrial Maintenance Technician – Pasteurization Equipment 
 SHIFT: Wednesday - Saturday; 6PM - 6AM Training is estimated to last at least 4 weeks and will be Monday - Friday from 6:30AM-2:30PM 
POSITION SUMMARY:
This position is responsible for the installation, troubleshooting, repairing and maintenance of industrial pasteurization equipment according to safety and productive maintenance systems to achieve customer satisfaction and departmental objectives.
 
OVERVIEW OF JOB DUTIES AND RESPONSIBILITIES:
<ul>
<li>Relevant experience as a maintenance technician working on industrial food processing equipment or similar. Pasteurization equipment desired. </li>
<li>Troubleshoots equipment problems to reduce productivity losses.</li>
<li>Implements long term corrective actions to avoid repeat issues.</li>
<li>Maintains spare parts inventory to support production and customer needs while maintaining budget and inventory objectives.</li>
<li>Documents and reports machine performance, corrective actions, maintenance activities, parts utilization, and inventory to achieve efficiency and regular operation of equipment. </li>
<li>Follows all standard work procedures, safety regulations, and policies to maintain a safe working environment.</li>
<li>Uses a C.M.M.S work order system to address work orders.</li>
<li>Maintain and repair shop equipment; clean and maintain assigned work area; dispose of hazardous materials according to established procedures.</li>
<li>Must be flexible to work overtime, weekends, and any shift to meet business demands.</li>
<li>Must be able to work at assigned customer plant and travel to other customer plants as needed to meet business demands.</li>
<li>May periodically travel domestically and internationally.</li>
<li>Follows proper safety procedures and safeguards others’ safety at all times, understanding the obligation to refuse to perform any tasks that are unsafe.</li>
<li>Complies with maintenance training according to schedule</li>
<li>Maintains work assigned area or normal working area so that it is clean and orderly.</li>
<li>Accept all other duties as assigned.</li>
</ul>
 
SUMMARY OF QUALIFICATIONS:
<ul>
<li>High School Diploma or equivalent</li>
<li>Relevant experience working as a maintenance technician or repairing equipment, specifically with industrial pasteurization equipment. </li>
<li>Experience working with hand tools</li>
<li>Ability to communicate effectively with team members and customers</li>
<li>Ability to work under pressure with a high degree of professionalism and customer service</li>
<li>Ability to work efficiently and with little to no direct supervision or alone</li>
<li>Basic knowledge of mechanical and electrical skills (sensors, PLCs, circuits, etc.)</li>
<li>Valid driver’s license and reliable transportation</li>
</ul>
 
PHYSICAL DEMANDS/WORKING CONDITIONS:
<ul>
<li>Wednesday to Saturday or Saturday to Wednesday: 6PM-6AM</li>
<li>Capable of pushing, pulling, and lifting up 50 pounds</li>
<li>Capable of standing and walking up to 12 hours a day</li>
<li>Capable of climbing, bending, squatting, kneeling, and reaching above shoulder height</li>
<li>Capable of working in hot or humid environment.</li>
</ul>
The compensation range for this role is $23.65/hr to $30/hr, there is a shift differential for 3rd shift. 
 
Benefits
<ul>
<li>Medical (PPO &amp; HSA), dental, and vision insurance </li>
<li>Paid time off including vacation, sick leave, and holidays </li>
<li>Employee assistance program (EAP) </li>
<li>401k with Company Match</li>
<li>Profit sharing </li>
<li>Free Life Insurance</li>
<li>Free Accidental Death and Dismemberment Insurance</li>
<li>Free Short-term &amp; Long-term Disability Insurance </li>
</ul>
 
*Salary information is a general guideline only. Actual compensation considers factors such as (but not limited to) the scope and responsibilities of the position, location, work experience, education, and key skills. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
*Our Company is dedicated to the principles of equal employment opportunity in any term, condition, or privilege of employment. We do not discriminate against applicants or employees on the basis of age, ancestry, race, sex (including pregnancy and sexual orientation/gender identity), color, religion, national origin, parental status, marital status, political affiliation, family medical history or genetic information, military or veteran status, disability, medical condition, or any other non-merit based factor or status protected by federal, state or local law
The above statements are intended to describe the general nature and level of work being performed by most people assigned to this job. They are not intended to be an exhaustive list of all responsibilities, duties, and requirements. Scheduling flexibility is required to accommodate changing business needs
 Wednesday to Saturday 6PM - 6AM Training (At least 4 weeks): Monday to Friday 6:30AM - 2PM

INDUSTRIAL MAINTENANCE TECH - PASTEURIZATION EQUIPMENT (6PM-6AM)

<h3>Job Description</h3>
Job Description
Job Title: Quality Control Inspector 
Job Location: Simi Valley, CA (This role is 100% onsite)
Business Unit: Space Vector
Schedule:9/80: Employees work 9 out of every14 days – totaling 80 hours worked – and have every other Friday off.
About Fisica Inc.
Fisica, Inc. is a premier manufacturer of advanced defense products, specializing in the design and production of airborne and ground-based antennas, as well as cutting-edge electromagnetic systems and simulators. Headquartered in San Leandro, California, with additional operations in Simi Valley, Fisica plays a vital role as a trusted partner to leading defense primes and the U.S. Department of Defense.
Our company operates as - ATI, Randtron, Datron and Space Vector—each bringing deep expertise and innovation to the defense sector. Led by a seasoned management team, Fisica is committed to excellence in engineering, manufacturing, and mission-critical solutions that enhance national security.
At Fisica, we foster a strong, collaborative work culture that values individual contributions and empowers our employees. Our commitment to innovation, integrity, and teamwork makes us a leader in the defense industry and an exceptional place to build a career.
 
Primary Function:
Responsible for performing inspections, tests and/or audits of purchased parts, units, materials, equipment, panel/module level assemblies and quality control programs to specifications. Interprets manufacturing drawings, diagrams, specifications and lists to approve or reject units, test setups, or systems for in process or final assemblies. Inspects and may perform minor rework on defective or malfunctioning units or systems. Maintains support documentation and performs sampling and testing of incoming components, raw materials, and build of assemblies. Reviews and reports performance data. Ensure raw materials, in-process and finished products meet company and test standards. Determines or assists in determining methods and procedures necessary for inspection. May interface with customer quality representatives or suppliers.
Overall Summary
Fully proficient support individual contributor. Works under limited supervision. May be a resource to other employees in areas of expertise. Assignments are moderately difficult requiring some judgment.
Nature of Supervision
Works under limited supervision. Less detailed instructions are provided and minimal peer review is required.
Communication &amp; Influence
Communicates with contacts typically within and outside the department on matters that involve obtaining or providing information requiring explanation or interpretation to understand and reach agreement. May be a resource to other employees in areas of proficiency.
Innovation &amp; Complexity
Work may be structured within identified boundaries and procedures. Follows established processes to complete tasks. Identifies problems and issues in straightforward situations. Resolves most issues.
Organization Impact
Works to achieve operational targets within job area which has moderate impact on the overall achievement of results for the team. Work is of moderate scope, typically on larger, task-related activities.
Education &amp; Experience
Requires fully proficient job knowledge/skills. Requires a High School Diploma or equivalent and a minimum of 6 years of prior relevant experience or 2 years post-Secondary/Associates Degree with a minimum of 2 years of prior related experience.
 
In compliance with pay transparency requirements, the salary range for this role $51,000 - $94,500. This is not a guarantee of compensation or salary, as the final offer amount may vary based on factors including but not limited to experience and geographic location. Fisica Inc also offers a variety of benefits, including health and disability insurance, 401(k) match, flexible spending accounts, EAP, education assistance, parental leave, paid time off, and company-paid holidays. The specific programs and options available to an employee may vary depending on the date of hire, and schedule type.
EEO Statement Fisica is proud to be an Equal Opportunity Employer. Fisica is committed to treating all employees and applicants for employment with respect and dignity and maintaining a workplace that is free from unlawful discrimination. All applicants will be considered for employment without regard to race, color, religion, age, national origin, ancestry, ethnicity, gender (including pregnancy, childbirth, breastfeeding or other related medical conditions), gender identity, gender expression, sexual orientation, marital status, military and veteran status, disability, genetic information, citizenship status, characteristic or membership in any other group protected by federal, state or local laws. Fisica maintains a drug-free workplace and performs pre-employment substance abuse testing and background checks, where permitted by law. Fisica is an E-Verify Employer. Please click here for the E-Verify Poster in English or Spanish. For information regarding your Right To Work, please click here for English or Spanish.
 
#LI-KW1

Quality Inspector

<h3>Job Description</h3>
Job Description
Calyxo, Inc. is a medical device company headquartered in Pleasanton, California, USA. The company was founded in 2016 to address the profound need for improved kidney stone treatment. Kidney stone disease is a common, painful condition that consumes vast amounts of healthcare resources each year. Our team is led by executives and investors with a proven track record of commercializing paradigm-shifting devices to meet unmet needs within urology.
Are you ready to change the future of kidney stone treatment? We are seeking high achievers who want to be part of a dynamic team working in a fun, diverse atmosphere.
Summary:
We are seeking a skilled and detail-oriented Staff Quality Engineer to join our New Product Development (NPD) team. This role is responsible for ensuring that our Class-II new products meet the highest quality standards throughout the development process, from concept to commercialization. The ideal candidate will have experience in the medical device industry and a strong understanding of quality engineering principles, design controls, project management, and regulatory requirements.
This role will focus on ensuring that quality is embedded in the design, development, and manufacturing of new medical devices. The ideal candidate will have a strong background in quality engineering within the medical device industry, with experience supporting Class-II or Class-III product development lifecycle and software development, from concept through commercialization.
In This Role, You Will:
<ul>
<li>Ensure design controls for new product development and improvement project activities, including risk management, design V&amp;V, product software validation, design reviews, tagging/tracing, non-product tools validation, test method validation, and design transfer are in compliance with Calyxo Quality System, FDA 21 CFR Part 820, ISO 13485, ISO 14971, IEC 62304, IEC 60601, and relevant global regulations.</li>
<li>Drive risk management activities per ISO 14971, including risk management plan, hazard analysis, FMEAs (design, software, user), risk-benefit analysis, and risk management report.</li>
<li>Own and maintain design control documentation in compliance with ISO 13485 and 21 CFR Part 820.</li>
<li>Collaborate with R&amp;D, PMO, Regulatory Affairs, and Manufacturing to ensure robust design inputs, outputs, traceability and quality considerations are integrated into all phases of the product development lifecycle.</li>
<li>Maintain accurate and up-to-date quality records, including test reports, validation reports, and risk management documentation. Prepare and present quality-related reports to management and project teams.</li>
<li>Promote a structured software development process in compliance with IEC 62304, assuring that a state of control is maintained with robust software risk management.</li>
<li>Support regulatory submissions (e.g., 510(k), CE Mark) by providing design assurance documentation and justifications.</li>
<li>Support sterilization assessments as per ISO 11135 EO and ISO 11137 radiation requirements.</li>
<li>Support biocompatibility assessments as per ISO 10993 requirements.</li>
<li>Lead root cause investigations and corrective actions related to design-related issues.</li>
<li>Mentor junior engineers and promote a culture of quality and continuous improvement.</li>
<li>Stay current with evolving regulatory standards and industry best practices.</li>
<li>Collarborate with R&amp;D to acheive electrical safety and EMC certification.</li>
<li>Partner with supplier quality team and new suppliers to ensure that components and materials meet specified quality standards. Participate in supplier qualification and audit processes as needed.</li>
<li>Support complaints investigations, NCs and/or CAPA related to NPI complaints post-launch.</li>
<li>Conduct DHF audits at each phase to ensure phase deliverables are complete.</li>
<li>Review and approve engineering documentation, test protocols, and reports to ensure compliance and technical integrity.</li>
<li>Identify opportunities for continuous improvement in product design and manufacturing processes. Lead or participate in initiatives to enhance product quality, reduce costs, and improve overall efficiency.</li>
</ul>
Who You Will Report To:
<ul>
<li> Director, Design Quality Assurance</li>
</ul>
Requirements:
<ul>
<li>Bachelor's degree in Engineering, Biomedical Engineering, Mechanical Engineering, Systems Engineering or a related technical field.</li>
<li>Minimum 10 to 12+ years of experience in quality engineering within the medical device industry, with strong record of being a vital part of NPD launch.</li>
<li>Strong knowledge, applications, and subject matter expertise of ISO 13485, ISO 14971, IEC 62304 and FDA 21 CFR Part 820.</li>
<li>Excellent presentation skills and proactive leading mindset. Effective communication, collaborative attitude, and strong accountability mindset.</li>
<li>Detailed understanding of design controls, risk management, and process validation in the context of medical device development from concept to feasibility to V&amp;V to design transfer to launch.</li>
<li>Experience with systems design verification and validation (V&amp;V) activities, including support for development of test protocols and reports.</li>
<li>Hands-on experience working with FMEA tools (design, software, user).</li>
<li>Excellent problem-solving skills, with the ability to analyze complex technical issues and develop effective solutions. Proficient in statistical tools applications such as Minitab, Jump etc.</li>
<li>Detail-oriented, with a commitment to producing high-quality work and maintaining rigorous documentation.</li>
<li>Certifications such as ASQ CQE (Americal Society for Quality Certified Quality Engineer), ASQ CSQE (Certified Software Quality Engineer), Six Sigma Black Belth or similar are a plus.</li>
<li>Work location: Pleasanton, CA.</li>
<li>Travel: 5-10% domestic travel may be required.</li>
<li>Full time employment.</li>
<li>Must be able to lift 10-15 pounds and sit for up to 8 hours/day.</li>
<li>Compliance with relevant county, state, and Federal rules regarding vaccinations.</li>
<li>Hybrid 4 days/week onsite, 1 day remote.</li>
</ul>
What We Offer:
At Calyxo, you will be part of a knowledgeable, high-achieving, experienced and fun team. You will work in a diverse work environment with experienced, proven leaders and have an opportunity to shape our company culture. You will experience constant learning and dynamic challenges to help you grow and be the best version of yourself. 
We also offer a compensation plan as follows:
<ul>
<li>A competitive base salary of $165,000 - $195,000 and variable incentive plan</li>
<li>Stock options – ownership and a stake in growing a mission-driven company</li>
<li>Employee benefits package that includes 401(k), healthcare insurance and paid time off</li>
</ul>
Calyxo is deeply committed to fostering an environment where diversity and inclusion are not only valued but also prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways. Diverse viewpoints bring diverse capabilities, which strengthen our focus and fuel our growth. Calyxo is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status or any other applicable legally protected characteristics
Legal authorization to work in the United States is required. In compliance with federal law, all persons hired will be required to verify their identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire. 
Disclaimer:
At Calyxo, we prioritize a transparent and structured interview process to ensure the best fit for both our candidates and our team. Please be aware of the following:
<ul>
<li>Structured Interview Process: Our hiring process includes multiple stages of interviews where you will have the opportunity to communicate directly with Calyxo employees. This ensures that you gain a comprehensive understanding of the role and our company culture.</li>
<li>Verification of Identity: We do not extend job offers without first meeting candidates, either virtually or in person. This step is crucial to maintain the integrity of our hiring process and to ensure mutual alignment.</li>
<li>Beware of Scams: Calyxo will never request sensitive personal information, such as your full name, address, phone number, or identification documents, via email or online forms before an official interview. Calyxo representatives will always contact you using an email format of <a href="mailto:firstname.lastname@calyxoinc.com" target="_blank">firstname.lastname@calyxoinc.com</a>. If you receive a request for information from any other domain, please contact us directly at <a href="mailto:info@calyxoinc.comto" target="_blank">info@calyxoinc.comto</a> verify the legitimacy of the communication.</li>
</ul>
We appreciate your interest in joining Calyxo and look forward to getting to know you through our official channels.

Staff Quality Engineer, Design Quality - Pleasanton, CA

<h3>Job Description</h3>
Job Description
Crusoe's mission is to accelerate the abundance of energy and intelligence. We’re crafting the engine that powers a world where people can create ambitiously with AI — without sacrificing scale, speed, or sustainability.
Be a part of the AI revolution with sustainable technology at Crusoe. Here, you'll drive meaningful innovation, make a tangible impact, and join a team that’s setting the pace for responsible, transformative cloud infrastructure.
About This Role:
Join Crusoe Energy as a Capacity Planning Manager, a pivotal role providing critical leadership to our Capacity Planning &amp; Efficiency team. You will drive the effective forecasting, allocation, and optimization of resources essential for our AI cloud and data center expansion. This position uniquely balances service, infrastructure, financial, and business constraints to scalably manage exceptions and achieve company-level impact. You will collaborate across diverse engineering and business teams, directly shaping Crusoe’s ability to efficiently plan, optimize, and expand its cloud capabilities while upholding our unwavering commitment to sustainability and operational excellence. This is a full-time position.
What You'll Be Working On:
<ul>
<li>
Scale Infrastructure Resources: Own and manage services and plans to efficiently scale compute, network, and storage infrastructure.
</li>
<li>
Drive Executive Decision-Making: Develop and analyze business and technical data and scenarios to inform high-level executive decisions regarding infrastructure and Crusoe products.
</li>
<li>
Execute Capacity Planning: Implement end-to-end capacity planning processes, methodologies, and data to deliver optimized and executable capacity plans.
</li>
<li>
Proactively Address Issues: Identify and build solutions for capacity-related challenges, ensuring timely resolution.
</li>
<li>
Forecast and Manage Deployment: Understand demand sources and trends to generate accurate forecasts, analyze changes, and develop strategic deployment plans.
</li>
<li>
Partner for Optimal Scaling: Collaborate with product and Go-To-Market/Sales teams to align on demand signals and requirements, ensuring optimal infrastructure scaling and service placement.
</li>
<li>
Optimize Across Engineering: Partner across the engineering landscape to optimize at the intersection of hardware, infrastructure, and software, working closely with service owners, SRE, and hardware teams.
</li>
<li>
Balance Cost and Product: Work with the Finance team to balance cost efficiency with technical and product considerations.
</li>
<li>
Drive Strategic Change: Define problem statements, collect data, build analytical models, and recommend changes to drive strategic optimization.
</li>
<li>
Improve Planning Efficiency: Define and implement improvements to planning efficiency and quality, partnering with software engineers for development.
</li>
<li>
Monitor Capacity: Drive the requirements and development of capacity dashboards to monitor and proactively manage capacity shifts.
</li>
<li>
Analyze Financial Data: Analyze customer usage, revenue trends, and financial reports, contributing to budget planning and assessing capacity impact.
</li>
<li>
Model Capital Efficiencies: Gather data from functional groups, mine large volumes of information, and create models to drive capital and operational efficiencies.
</li>
</ul>
What You'll Bring to the Team:
<ul>
<li>
Educational Foundation: Possess a Bachelor’s or Master’s degree in Mathematics, Computer Engineering, Computer Science, Operations Research, Data Science, or equivalent professional experience.
</li>
<li>
Capacity Planning Expertise: Bring 3+ years of experience in Capacity Planning or Demand Planning within a related field.
</li>
<li>
Dynamic Environment Adaptability: Thrive in fast-paced environments, effectively collaborating with multidisciplinary teams.
</li>
<li>
Exceptional Problem-Solving: Demonstrate exceptional problem-solving skills and a data-driven approach to decision-making.
</li>
<li>
Strong Communication &amp; Collaboration: Exhibit excellent communication, presentation, and collaboration abilities to work effectively with internal and external stakeholders.
</li>
</ul>
Bonus Points:
<ul>
<li>
Advanced Degree: A Master's degree in Mathematics, Data Science, Operations Research, or another technical field.
</li>
</ul>
Benefits:
<ul>
<li>
Industry competitive pay
</li>
<li>
Restricted Stock Units in a fast growing, well-funded technology company
</li>
<li>
Health insurance package options that include HDHP and PPO, vision, and dental for you and your dependents
</li>
<li>
Employer contributions to HSA accounts
</li>
<li>
Paid Parental Leave
</li>
<li>
Paid life insurance, short-term and long-term disability
</li>
<li>
Teladoc
</li>
<li>
401(k) with a 100% match up to 4% of salary
</li>
<li>
Generous paid time off and holiday schedule
</li>
<li>
Cell phone reimbursement
</li>
<li>
Tuition reimbursement
</li>
<li>
Subscription to the Calm app
</li>
<li>
MetLife Legal
</li>
<li>
Company paid commuter benefit; $300/month
</li>
</ul>
Compensation Range
Compensation will be paid in the range of up to $128,000 - $150,000. Restricted Stock Units are included in all offers. Compensation to be determined by the applicants knowledge, education, and abilities, as well as internal equity and alignment with market data.
Crusoe is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, disability, genetic information, pregnancy, citizenship, marital status, sex/gender, sexual preference/ orientation, gender identity, age, veteran status, national origin, or any other status protected by law or regulation.

TPM / Capacity Planning Manager

<h3>Job Description</h3>
Job DescriptionSalary: $67,000 - $75,000/annual 
An exciting opportunity to join the Transportation &amp; Planning Program at City Heights Community Development Corporation is now available. City Heights CDC is a 501(C)3 non-profit organization in San Diego with a mission to enhance the quality of life in City Heights by working with our community to create and sustain quality affordable housing, livable neighborhoods, and foster economic self-sufficiency.
The Transportation &amp; Planning Program works with City Heights residents to envision the community they want to live in, works to have that vision represented in plans and policies, and then utilizes organizing and advocacy to implement those plans and policies. In doing so, we popularize urban planning and policymaking and facilitate the implementation of policy/systems/environmental change to achieve livable neighborhoods and mobility justice.
City Heights CDC is seeking a Transportation &amp; Planning Program Manager that will engage directly with residents, grassroots partners, and public agencies to co-create neighborhood visions, influence local and regional planning processes, and implement people-centered policy, infrastructure solutions, and capital improvement projects. This position blends community organizing, planning, project management, and policy advocacy
 
Major Responsibilities/Duties:
<ul>
<li>Support day-to-day operational and administrative aspects of grant-funded projects</li>
</ul>
<ul>
<li>Work with funders from the California Air Resources Board (CARB), The California Endowment, MTS, and San Diego Association of Governments (SANDAG) to provide timely reporting on program activities</li>
<li>Coordinate and support the planning, design, and implementation of capital improvement projects in partnership with residents, consultants, and public agencies</li>
<li>Oversee project scopes, timelines, and budgets related to capital improvements, ensuring alignment with community-identified priorities</li>
<li>Research transportation projects, planning issues, and policy/systems/environmental change</li>
<li>Work with residents, community partners, and City Heights CDC staff to popularize planning and facilitate the implementation of policy/systems/environmental change to achieve livable neighborhoods</li>
</ul>
 
Qualifications/Skills, the ideal candidate will have:
<ul>
<li>Bachelors degree or higher: Desired fields include Urban Studies &amp; Planning, Sociology, Political Science, Law, Public Policy, Public Affairs, Public Administration, or related fields 2 - 4 years of experience conducting community engagement, urban planning, policy analysis, or coordination of grant-funded activities</li>
<li>Experience managing or supporting capital improvement projects or infrastructure planning</li>
<li>Familiarity with design-build processes, city capital improvement programs (CIP), or public works project delivery</li>
<li>Experience working with under-resourced and multi-cultural communities</li>
<li>Bilingual in Spanish, Somali, Vietnamese, or Khmer (Cambodian)</li>
<li>Strong organizational communication and interpersonal skills, verbal and written</li>
<li>Knowledge of and/or experience working with community-based nonprofits or grassroots campaigns Grant writing and administration experience</li>
<li>High attention to detail and ability to carry out assignments independently</li>
<li>Ability to facilitate group discussions and work with a dynamic team</li>
</ul>
 
Benefits: Medical, dental, and vision insurance; a 401K retirement plan that includes an employer match; generous paid time off and holidays; every other Friday our offices are closed; City Heights CDC is committed to the professional growth of all employees and provides training opportunities accordingly.
 
City Heights residents and individuals who ride transit, walk, bike, or skate as primary modes of transportation are encouraged to apply.

Transportation & Planning Program Manager

<h3>Job Description</h3>
Job Description
NO EXTERNAL RECRUITERS PLEASE
**No Sponsorship/Transfer Available**
 
Company Summary:

For over 60 years, MeriCal has been at the forefront of innovation in the dietary supplement industry, delivering custom manufacturing and packaging solutions with passion and precision. With state-of-the-art facilities in Southern California and Ogden, UT, we transform ideas into high-quality products—from research and development to the finished products. Our team, with over 30 years of combined experience, is dedicated to crafting exceptional gummies, probiotics, tablets, capsules, chewables, and powders using clinically backed ingredients. At MeriCal, we don’t just meet expectations—we exceed them, every time. Join us and be part of a dynamic, forward-thinking team shaping the future of nutrition!
The Opportunity:
A Quality Inspector is responsible for ensuring all dietary supplement products comply with the specifications established by Merical and cGMPs. The Quality Inspector is responsible for conducting objective &amp; subjective measures and making determinations if any non-conformance occurred. The Quality Inspector works to guarantee high quality output through random sampling and testing on anything from receiving, in process manufacturing and finished packaging product for release. Items that do not meet specifications are investigated and written documented corrective actions taken to ensure the issue does not occur again.

What You’ll Do:
<ul>
<li>Ensuring Good Manufacturing Practices [21 CFR Part 111,117 &amp; 211) are adhered. Independently perform inspection across multiple production stages proficiently and ensure compliance with quality</li>
<li>standards.</li>
<li>Ability to follow instructions to comprehend the quality expectations for the materials, components or products.</li>
<li>Conducts sampling (Analytical, Microbial, Customer and Retains] and ensures testing against appropriate methods. Sampling must be conducted appropriately using good technique and verifying</li>
<li>against dimensional and functional specifications. Maintain records of testing, information, and various metrics such as quantity of defective products per batch.</li>
<li>Collect samples for Analytical, Microbial, Customer and Retains as applicable and document within the appropriate quality record (batch record, specification, unipoint, etc.}.</li>
<li>Communicate to next level leader prior to rejecting raw materials, in process manufacturing or finished product with respect to quality standards.</li>
<li>Performs in process testing [such as allergen, ATP, Water Activity, Brix, Hardness, Thickness, Friability, etc.]. Provides guidance to manufacturing team on corrective actions for out-of-specification results.</li>
<li>Verifies Bill of Materials [bulk &amp; packaging components} and ensures proper 10 tagging and organization of raw materials, components, staged bulk and finished goods on the production floor including reconciliation and pallet counts.</li>
<li>Ability to enter quality data &amp; verify expiration dates into ERP system prior to Finished Goods release.</li>
<li>Verifies batch record matches items staged within manufacturing and packaging lines.</li>
<li>Verifies monitoring equipment [scales, metal detectors, torque meter etc.] is functioning correctly per our established SOPs.</li>
<li>Conduct bulk and final product acceptable quality limit (AQL} inspections per established SOPs. Understands varying sampling schemes based on sample size and AQL parameters.</li>
<li>Responsible for reviewing the cleaning Logs and provide verification authorization signature to release lines.</li>
<li>Ensure proper hold procedures and communication or alert management of any unusual occurrence and any pertinent issues that affect raw materials, production and/or packaging.</li>
<li>Inspects and maintains working environment routinely and ensures adherence to company safety policies and procedures.</li>
<li>May be required to operate forklift, pallet jacks, etc. if needed.</li>
<li>Performs other duties as assigned.</li>
</ul>
What You’ll Bring:
<ul>
<li>Must have 3+ experience working in a quality related environment.</li>
<li>Should be able to lift a maximum of 25-30 lbs. of material when needed.</li>
<li>Food Safety or Dietary Supplement Experience a plus.</li>
</ul>

Education Requirements:
<ul>
<li>High School Diploma/Certificate; one-year related experience and/or training; or equivalent combination of education and experience.</li>
</ul>

The Perks:
<ul>
<li>No-cost vision insurance (yes, you read that right!), employer-paid life insurance, paid company holidays, generous paid time off, sick leave, employee assistance program, and a comprehensive wellness program. </li>
<li>Affordable medical and dental insurance plans are tailored for you and your dependents.</li>
<li>Exceptional supplemental benefits, including Accident, Critical Illness, Hospitalization indemnity plans, and pet insurance.</li>
<li>401(k) matching plan and more!</li>
</ul>

A reasonable estimate of the current base pay range for this position is $22.00 - $24.00 The compensation offered may vary depending on the candidate’s geographic region, job-related knowledge, skills, and/or education.

MeriCal uses E-Verify to confirm authorization to work in the United States. For more information on E-Verify, please visit the following website: <a href="https://www.e-verify.gov/employees" target="_blank">https://www.e-verify.gov/employees</a>

MeriCal is an equal opportunity employer and is committed to providing a workplace that is inclusive and free of discrimination and harassment. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. We encourage individuals of all backgrounds to apply. We believe in creating a diverse and inclusive workplace where all employees feel valued and respected, and where differences are embraced as strengths. We are dedicated to fostering an environment that promotes equality and celebrates diversity.

Quality Inspector II

<h3>Job Description</h3>
Job DescriptionAbout Us&nbsp; Fluxergy is a rapidly growing in vitro diagnostics company innovating on the cutting-edge of laboratory testing. We’re developing the first and only multi-modal point-of-care platform that enables molecular, clinical chemistry, immunoassay, and hematology testing on the same system.&nbsp;&nbsp; Our platform spans many markets including the clinical, veterinary, and food safety industries. We are seeking self-motivated problem solvers who are excited to help decentralize traditional laboratory infrastructure.&nbsp;&nbsp; At the core of our company’s identity is a strong foundation in engineering. We take great pride in our commitment to critical thinking and pragmatic problem-solving through a modular and systemic perspective. We hold the conviction that transparent communication, coupled with the flexibility to adjust to evolving scenarios and the willingness to venture beyond familiar territories, is crucial to both our success and yours.&nbsp;&nbsp; Our product: <a href="https://vimeo.com/176673475&amp;nbsp" target="_blank">https://vimeo.com/176673475&amp;nbsp</a>; About the RoleFluxergy is seeking two experienced Assembly Technicians to support the build of our next-generation in vitro diagnostic (IVD) instrumentation. In this temporary, onsite role, you will assemble complex electro-mechanical and electro-optical systems, perform in-process testing, and complete required documentation in accordance with medical device quality standards. This position is ideal for technicians who thrive in regulated environments and enjoy working on sophisticated, high-impact products.What You Will Do
<ul>
<li>Assemble complex subassemblies and integrate them into final IVD diagnostic systems</li>
<li>Build electro-mechanical and electro-optical assemblies with a high level of precision</li>
<li>Perform soldering of fine connections and program PCBAs using established procedures</li>
<li>Conduct in-process inspections and testing using tools such as multimeters, oscilloscopes, and calipers</li>
<li>Handle ESD-sensitive components in accordance with best practices</li>
<li>Read, interpret, and follow detailed work instructions and assembly documentation</li>
<li>Complete accurate build records and documentation in compliance with medical device and company quality standards</li>
<li>Collaborate with manufacturing, quality, and R&amp;D teams to address build issues, non-conformances, or unusual assembly scenarios</li>
<li>Support continuous improvement efforts related to assembly processes and documentation</li>
</ul>
What You Will Need to Have
<ul>
<li>5+ years of hands-on experience assembling complex products made up of multiple subsystems</li>
<li>Experience working in a regulated manufacturing environment (medical device, diagnostics, aerospace, or similar)</li>
<li>Prior experience in an ISO-certified manufacturing environment</li>
<li>Proficiency assembling electro-mechanical and electro-optical components</li>
<li>Strong soldering skills, including fine-pitch or delicate connections</li>
<li>Experience programming PCBAs using a defined, documented process</li>
<li>Familiarity with ESD-sensitive components and proper handling procedures</li>
<li>Experience using test and measurement equipment such as multimeters, oscilloscopes, and calipers</li>
<li>Ability to read, understand, and strictly follow complex work instructions and procedures</li>
<li>High attention to detail and commitment to quality and documentation accuracy</li>
<li>Ability to work 1st shift schedule (06:30AM - 03:00PM), Monday through Friday</li>
</ul>
Strong Plus Qualifications:
<ul>
<li>Experience working on FDA-regulated products</li>
<li>Experience partnering with R&amp;D teams to finalize work instructions or resolve non-conformances</li>
</ul>
Interview Process&nbsp;&nbsp;Our interview processes my differ slightly from role-to-role; however, most of our interviews will follow a similar pattern:&nbsp; - Recruiter Interview &nbsp;- On-site Interview- Decision&nbsp; &nbsp;&nbsp; We are an early-stage company and may change our interview process from time-to-time, but our hope is everyone who interviews with us has a positive experience, even if an offer isn’t presented.&nbsp;&nbsp; Salary Range: $20.00 - $25.00/hr Additional InformationFluxergy is an equal opportunity employer. We do not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, marital status, age, disability, national or ethnic origin, military service status, citizenship, or other protected characteristic. Fluxergy participates in the E-Verify program. Please click&nbsp;here,&nbsp;here, here for more information. Fluxergy is committed to protecting your personal data. Please review our Privacy Policy. 
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Production Technician II (Temporary)

<h3>Job Description</h3>
Job DescriptionSuperintendent - West Coast Leading Sheet Metal Manufacturer - Pomona, Ca This Jobot Job is hosted by: Jamal Elkhateib Are you a fit? Easy Apply now by clicking the "Apply Now" buttonand sending us your resume. Salary: $70 - $71.77 per hour 
A bit about us:
 Join a leading HVAC sheet-metal manufacturer based in Southern California, producing top-quality ductwork and components for major commercial and industrial projects across the West. With state-of-the-art equipment from CNC lasers to robotic welding, with a reputation for speed, precision, and reliability, we support contractors with quick-turn fabrication and 24/7 delivery. If you’re ready to bring your skills to a modern, high-performance shop where quality and teamwork drive everything we do, we’d love to have you on the team. 
Why join us?
 Accelerated Growth Options 401k with Match 100% paid benefits PTO Collaborative Leadership Life Dental Vision 
Job Details
 About the Role We’re seeking an experienced Shop Superintendent to lead our high-volume sheet metal fabrication operation in Pomona, CA. This is a hands-on leadership role overseeing approximately 200 skilled tradespeople producing HVAC sheet metal products and custom components that support major commercial and industrial projects across the region. As a key leader reporting to the VP of Operations, you’ll drive performance across quality, production, safety, and workforce development, ensuring our shop delivers best-in-class craftsmanship, efficiency, and union leadership. If you’re a proven fabrication or manufacturing leader who thrives in fast-paced environments and knows how to motivate large teams, we want to hear from you. What You’ll Do Lead Production Operations – Oversee all aspects of shop production, including scheduling, resource allocation, and workflow optimization for multiple concurrent projects. Ensure Quality &amp; Compliance – Implement and enforce QA standards; drive continuous improvement and resolve issues through root-cause analysis and corrective action. Champion Safety &amp; Cleanliness – Partner with Safety leadership to maintain a safe, compliant, and efficient work environment; enforce training and eliminate hazards proactively. Optimize Efficiency – Analyze productivity data to identify waste, improve throughput, and ensure on-time, under-budget delivery of projects. Develop &amp; Lead People – Coach, train, and mentor foremen and team leads; foster accountability, skill development, and high morale among the workforce. Strategic Execution – Align shop goals with company-wide initiatives; implement systems to monitor KPIs, resource planning, and labor utilization. What You Bring 5–10 years of experience managing a large fabrication or manufacturing shop (HVAC or sheet metal preferred). Demonstrated success leading 100+ employees in a union or high-volume production environment. Proven ability to drive operational excellence, safety, and workforce engagement. Strong organizational, communication, and problem-solving skills. Computer proficiency with Microsoft Office Suite and familiarity with Autodesk Fabrication or similar software. Bilingual English/Spanish is highly preferred. High school diploma or equivalent required. Interested in hearing more? Easy Apply now by clicking the "Apply Now" button. Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, age (40 and over), disability, military status, genetic information or any other basis protected by applicable federal, state, or local laws. Jobot also prohibits harassment of applicants or employees based on any of these protected categories. It is Jobot’s policy to comply with all applicable federal, state and local laws respecting consideration of unemployment status in making hiring decisions. Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance. Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from Jobot, and/or its agents and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here: jobot.com/privacy-policyCompany DescriptionJobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values. Founded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA). Ready to find a good job? Create your profile today at Jobot.com. 
<h3>Company Description</h3>
Jobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values.\r\n\r\nFounded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA).\r\n\r\nReady to find a good job? Create your profile today at Jobot.com.

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