Quality control inspector jobs in San Rafael, CA - 196 jobs

Want to make an impact? As a Quality Technician reporting to the Quality Supervisor, you'll be a key player in ensuring every candy we make is safe, consistent, and top-quality. You'll monitor production processes, inspect materials and packaging, verify procedures, maintain documentation, calibrate equipment, and ensure our formulations, nutritional info, and ingredient statements are accurate. Your work helps keep our products delicious and compliant every day. ***Position requires the ability to work overtime. As a result, it may require working varying start times, end times, and weekends dependent on business needs. Ways you will make a difference Inspects supplies, raw materials, WIP, and finished products to verify quality standards. Reviews formulas to ensure all processing parameters and procedures are in compliance. Samples and documents process data to meet product specifications. Verifies processing data and makes recommendations if necessary. Evaluates and approves all work in progress and finished products. Performs basic computer skills including but not limited to Windows, Spreadsheets, and Word Processing. Implements statistical methodology to analysis processing. Calibrates testing equipment periodically. Provides and assists in designing forms for the manufacturing departments. Reports all discrepancies to Quality Assurance leadership. Coordinates with Operations staff the successful disposition of non-conforming product. Supports internal audit programs. Inherent in each position is a general duty to maintain each respective work area in a safe and sanitary condition. Regular, predictable, full-time attendance is required as an essential function of this position. The employee may be required to perform other such duties within the scope of their employment as may be assigned. The employee must also possess the ability to take direction, follow instructions, work with others, follow work rules and schedules, focus on details, and work flexible hours as needed (including weekends). Skills that will make you successful To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. LANGUAGE SKILLS Ability to read, analyze, and interpret general business periodicals, technical procedures, or governmental regulations. Ability to effectively present information and respond to questions from groups of managers, clients, and customers. MATHEMATICAL SKILLS Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, and percent. REASONING ABILITY Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. OTHER SKILLS AND ABILITIES Proficiency with MS Office, including Word, Excel, and Outlook; Redzone, database and ERP system experience preferred. Strong understanding and commitment to food safety and quality; knowledge of HACCP and FSMA standards preferred. Ability to manage time and multitask successfully. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is frequently required to stand, walk, and taste or smell work in progress and finished goods. The employee is occasionally required to sit; during product evaluations they are required to use hands to manipulate, handle, or feel objects, tools, or controls; and talk or hear. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision and color vision. The employee must ascend and descend stairs or climb on high platforms of up to 15 feet high, in order to perform essential functions and report to their respective workstation. The employee is occasionally required to reach with hands and arms, balance, stoop, kneel, crouch, or crawl. WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee frequently works near moving mechanical parts. The employee will be exposed to high heat (140F) for up to 10 minutes and low temperature (below 40F) to perform specific tasks. The employee occasionally works in outside weather conditions and is occasionally exposed to wet and/or humid conditions and toxic or caustic chemicals. The employee must have the ability to tolerate strong fruity, spicy, bold or pungent smells as part of routine QA checks. The noise level in the work environment is usually loud. Experiences that will support your success One year certificate from college or technical school; or two (2) to three (3) years related experience and/or training; or equivalent combination of education and experience. An equivalency of education could possibly fulfill formal degree requirements. At Ferrara, we're proud to support our employees by providing comprehensive benefits such as health insurance, dental insurance, a 401(k), and paid time off (PTO). Eligible employees may also receive an annual bonus based on company performance. Learn more about our benefits at *******************************************

The Quality Inspector performs quality inspections and ensures quality problem resolution for product manufacturing and packaging according to procedures, specifications and standards. This position also assists the Quality department with administrative aspects of quality maintenance and remediation. This is a 3 rd shift position, with working hours from 11:00pm - 7:30am, Monday through Friday. ESSENTIAL FUNCTIONS In-process quality checks - perform visual and physical verification of production logs, data and components; assist with documentation and segregation of nonconforming components; collect/document samples and deliver to QC In-process quality checks - perform visual and physical verification of data, products and procedures throughout packaging, labeling, etc. Alert production staff to stop production if quality problems are identified Problem solves with production staff to achieve prompt resolution of identified quality issues Equipment set up verifications - Verify information, paperwork, logs, blends and components are correct against work orders and properly staged and that samples are available at each machine prior to production Equipment changeover verifications - Verify that previous product is fully cleared from processing equipment and downstream production and that new product information is correctly entered GMP facility walks - Identify and correct GMP violations or inconsistencies in quality procedures Verify that documentation is complete for the production run after changeovers Batch Production Run review - perform final verification of hard copy and electronic BPR data Assist with investigative tasks in the Quality Department Assist in deviation report generation or development and implementation of corrective action plans Assist with report writing, compiling and reporting results, SOP revisions and work instructions Provide administrative support to the department Assist with accurate data collection and metrics reporting (Nonconforming material, First Run Quality and Quality Audits) Other duties as assigned SUPERVISORY/BUDGET N/A REQUIREMENTS Education/Experience: High school graduate or equivalent 1-2 years QA/QC experience in food, wine, pharma, or dietary supplements manufacturing facility preferred Previous 3 rd shift/graveyard experience strongly preferred Knowledge/Abilities/Skills: Intermediate mathematics skills including percentages Conversant with units of measure such as grams or pounds Able to solve problems and make decisions based on company and/or quality policy Ability to read, interpret and apply quality standards, SOP's, specifications and work instructions Strong analytical and problem solving skills Strong organization and detailed work Strong verbal and written communication skills Strong interpersonal skills Commitment to and ability to demonstrate TM's Company values: Find good intentions, Stay curious, Be real and open, Create together, Make a meaningful difference, Keep raising the bar Bilingual (English/Spanish) preferred Technical Skills: Intermediate MS Office skills Production Management Software (RedZone preferred), System Integration Software (Ignition) eQMS software (MasterControl) Measurement tools and software including force gauge, calipers, balances, vacuum chambers Travel Requirements: N/A Work Environment: Fast paced production environment working across all areas of production including finished product, blending, case packing, warehouse maintenance and quality control Simultaneous support for up to eight manufacturing lines along with all the ancillary equipment, tasks and processes Office Hours/Location: This position is based in Sebastopol, CA. Shift hours are from 11:00pm-7:30am, Monday through Friday, with occasional Saturday work. Remote candidates will not be considered for this role. Traditional Medicinals, Inc. and its subsidiaries are proud equal-opportunity employers. We wholeheartedly embrace authenticity, diversity, and people's differences. We acknowledge, celebrate, and support individuality to the great advantage of our consumers, our stakeholders, our products, and the planet. We are committed to building an inclusive workplace for all our people. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. Compensation range is $24.62 - $32.31 per hour, plus 15% shift differential. Compensation is determined based on non-discriminatory, business-related factors, including but not limited to, training, experience, education and/or professional certifications, geographic location, and market data.

Build Your Career. Build America's Future. Vulcan Materials Company is the nation's largest producer of construction aggregates and a major producer of aggregates-based construction materials including asphalt and ready-mixed concrete. When you join Vulcan, it's more than starting an exciting career - you get to make a difference for millions of people every day across the country. When you join Vulcan, you join a dynamic culture in which career development is encouraged, excellence is rewarded, and diversity is valued. No matter the role or the location across the country, every member of the Vulcan team lives through the Vulcan Way: doing the right thing, the right way, at the right time. We're Coming Back Together To Be Together 100% In Office & Onsite At Vulcan Materials, we believe that the heart of our success lies in the strength of our engagement, our connection, and our commitment to developing our people. We are excited to restore the collaborative in-person environment that fuels our innovation and growth. This move is not just about being physically present; it's about reigniting the spirit that comes from face-to-face interactions, fostering a collaborative, inclusive culture where every voice is heard and everyone thrives. What You'll Do: Ensure Quality Control. Conduct routine testing of in-process materials, raw materials, environmental samples, and finished materials to ensure quality control of products at the point of production, shipping, and arrival upon the job site. Adhere to testing methods, including American Society for Testing and Materials (ASTM), American Association of State Highway and Transportation Officials (AASHTO) and Department of Transportation (DOT). Document and Report Information. Complete all required reports in a timely and accurate manner, interpreting, documenting, and storing the results. Communicate test results in a timely manner to the supervisor and properly document in a database. Maintain Lab Standards. Ensure housekeeping standards are maintained in and around the lab. Troubleshoot problems and review basic product specifications. Inspect, calibrate, and maintain testing equipment periodically. Monitor Stockpile. Inspect stockpiles, materials sources, and truckloads at plant sites. Monitor the daily construction of the stockpile to ensure that segregation and contamination is kept to a minimum or eliminated. Notify management immediately if contamination is identified. Inspect Equipment and Structures. Conduct routine inspections of the plant equipment in order to ensure safe, reliable, and compliant operations to maximize production and minimize interruptions. Additional Responsibilities. Other duties as assigned. Skills You'll Need: Experience. Prior training or experience in the materials testing field is preferred. Knowledge of general principles and practices of aggregate production is preferred. Safety Knowledge. Must display knowledge and awareness of construction and mining site hazards. Math Skills. Must possess good math skills and demonstrate the ability to perform simple to moderately complex arithmetic calculations. Technology Skills. Must have the ability to use computerized equipment and technology. Must be proficient in Microsoft Office Suite, Google, Oracle Business Environment, and other software packages relevant to the position. What You'll Like About Us: Great Company Culture. Our people share a competitive drive for excellence in an environment of trust, teamwork, open-mindedness and communication. Safe. Industry leader in health and safety standards. We are committed to creating a safe work environment and protecting all employees and customers. Meaningful Work. What sets up apart is the work we do impacts daily lives - and every employee contributes. Our aggregates produced are used to build roads, schools, hospitals, airports, and housing throughout the United States. Health Benefits. Medical, Dental, Vision programs, plus much more. Rest and Relaxation. Paid vacation, personal floating days, and paid holidays. Prepare for the Future. 401(k) with company match and contribution. Training and Development. We see our development programs and helping our employees meet their goals as a key part of our business. Salary Range: the base salary range for this role is between $30.00 to $36.00 per hour. This range is not inclusive of our discretionary bonus or equity package. When determining a candidate's compensation, we consider a number of factors, including skillset, experience, job scope, and current market data. Vulcan Materials Company is committed to employing a diverse workforce. You will receive consideration without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, gender expression, veteran status, or disability. You also have the right to be free from discrimination for medical needs arising from pregnancy, childbirth, or related medical conditions. NOTICE TO TEMPORARY STAFFING AGENCIES, PLACEMENT SERVICES AND PROFESSIONAL RECRUITERS Vulcan Materials Company has an internal recruiting department. Please review our policy as it relates to the use of temporary staffing agencies, placement services and professional recruiters.

Join our mission-driven Quality team as the Quality Control Inspector at Endologix! WHO WE ARE: Endologix LLC is a California-based global medical device company dedicated to improving patients' lives through innovative therapies for the interventional treatment of vascular disease. Our therapeutic portfolio addresses clinically relevant unmet needs, spanning from abdominal aortic aneurysms to lower limb peripheral vascular disease. We are committed to delivering excellent clinical outcomes through precision in product design, advanced manufacturing, and comprehensive physician training-supported by industry-leading clinical evidence. At Endologix, we're driven by purpose, innovation, and the opportunity to make a lasting impact in vascular health. What sets us apart is not just our technology, but our culture. At Endologix, we foster a forward-thinking, mission-driven environment where every team member plays a vital role in advancing patient care. Our values guide how we operate: we prioritize patient outcomes, act with integrity, stay curious and innovative, move boldly in pursuit of excellence, and collaborate across teams and with physicians to achieve exceptional results. As for our people? We empower them with the tools, trust, and continuous learning they need to grow. If you're passionate about making a meaningful difference in healthcare, you'll find purpose and belonging here. ABOUT THE ROLE: We're looking for a Quality Control Inspector to join our mission-driven Quality team. In this role, you'll be responsible for performing inspections of components, subassemblies, and finished medical devices to ensure compliance with quality standards and regulatory requirements. This includes conducting quality checks, performance tests, reviewing documentation, and verifying Device History Records (DHR) for product release in accordance with the medical device Quality Management System (QMS). Responsibilities WHAT YOU'LL DO: * Perform audits, inspections, configuration checks, and functional testing to ensure product quality and compliance with established procedures. * Review and verify lot history records for completeness, accuracy, and adherence to SOPs; investigate records related to customer experience reports. * Inspect subassemblies, finished products, purchased components, and tools using defined criteria and standard mechanical, and/or electrical measurements. * Conduct product rework on subassemblies or finished goods as required. * Accurately document inspection and testing results in compliance with Good Documentation Practices (GDP). * Review Device History Records (DHR) for compliance with established procedures and GDP requirements. * Identify issues and provide initial recommendations for corrective actions or process improvements to supervisors. * Perform product testing to ensure conformance to quality standards. * Work within a cleanroom environment, following all applicable protocols and safety requirements. * Perform temperature and particle count monitoring; manage ERP (QAD) and MES application transactions; handle multiple tasks efficiently in a fast-paced manufacturing environment. * Perform other duties as assigned by the supervisor. * Demonstrate punctuality, reliability, and a strong work ethic. Qualifications WHAT YOU'LL BRING: Education: * High School Diploma or equivalent required. Experience: * 1-5 years of Quality Control experience, preferably in the medical device industry. Skills/Competencies: * Ability to understand and follow technical procedures, work instructions, and basic specifications related to the inspection of products and components. * Skill in identifying relevant information in technical drawings and documents and reporting any discrepancies to the supervisor. * Familiarity with applicable quality standards and willingness to learn about specific regulations under supervision * Mechanical aptitude and working knowledge of measurement instruments. * Strong written and verbal communication skills for reports, correspondence, and presentations. * Mathematical proficiency in fractions, percentages, ratios, and proportions. * Problem-solving skills with the ability to work in a cross-functional environment and manage multiple priorities. WHAT WE OFFER: At Endologix, we know that great work starts with great people - and people do their best when they feel valued and supported. That's why we offer competitive pay, solid benefits, career growth, a culture that genuinely cares, and the flexibility you need to thrive both at work and at home. But more than that, we offer purpose. You'll be part of a team that's making a real impact on patients' lives. When you join us, you're not just taking a job, you're building a meaningful career with a team that's invested in your success. The compensation package includes: * Hourly rate of $24.03/hr-$29.44/hr * Discretionary bonus * Equity participation as approved by Board of Directors (4-year vesting schedule) * Comprehensive health, dental, and vision insurance plans * Generous PTO and holiday schedule * 401(k) retirement plan with company match Plus: * Employee wellness initiatives and mental health support * Collaborative and inclusive company culture focused on impact and innovation * Opportunities for career growth and internal mobility HOW WE LEAD WITH OUR CORE VALUES: * Patient Outcomes Drive Us: We improve lives with every advancement we deliver. * Integrity Defines Us: We do what's right, stay transparent, prioritize quality, and own our actions. * Innovation Advances Us: We stay curious, adaptable, and push boundaries. * Boldness Propels Us: We take smart risks and are unafraid in our pursuit of excellence. * Collaboration Unites Us: We partner across teams and with physicians to drive exceptional results. OUR COMMITMENT TO EQUAL OPPORTUNITY & VETERAN INCLUSION: Endologix LLC is an Equal Opportunity and Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, or any other characteristic protected by applicable federal, state, or local law. As a federal contractor, Endologix LLC is committed to taking affirmative action to recruit, employ, and advance in employment qualified individuals with disabilities and protected veterans.

Duties and Responsibilities: Perform inspections of purchased parts according to acceptance criteria using standard sampling plan. Able to perform First Article Inspection (FAI) of manufactured parts, electromechanical assemblies and final assemblies. Physical, mechanical and/or electrical measurements in compliance with the company Quality System. Accurately document results of inspection / testing and maintain controlled document files, logs and test records. Inspect cables per wiring configuration. Initiate non-conformance process and assist in resolving non-conformances. Monitor receiving inspection backlog. Able to be flexible with the work schedule. Process SAP transactions to segregate and disposition non-conforming product. Other duties and responsibilities in the Quality Department as assigned. Ability to conduct basic troubleshooting and problem resolution. Education and Experience: High School Diploma or Equivalent. Preferred one year of experience in an FDA regulated environment and/or ISO 13485 standards in the medical device industry and/or in-vitro diagnostics preferred. Technical and physical position requirements: Familiar with measuring equipment such as micrometer, caliper height gauges, plug gauges. Able to lift at least 35 lbs. Strong attention to details and ability to understand and follow complex procedures. Working knowledge and experience in basic computer applications such as Microsoft Word, Excel and Outlook. Effective and clear written and verbal communication skills in English language. The US base salary range for this full-time position is $20.60 - $31.60. Our salary ranges are determined by role, level, and location. The range displayed on each job posting reflects the base pay target range for new hire salaries for the position. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. In addition to compensation, Zoetis offers a comprehensive benefits package that supports the physical, emotional and financial wellbeing of our colleagues and their families including healthcare and insurance benefits beginning on day one, a 401K plan with a match and profit-sharing contribution from Zoetis, and 4 weeks of vacation. Visit zoetisbenefits.com to learn more. Full time RegularColleague Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search. Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at ********************************** to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at ********************** site, or (2) via email to/from addresses using only the Zoetis domain of “@zoetis.com”. In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.

The Bed Control Coordinator insures the effective and efficient utilization of acute and long-term care beds, and hospital resources as well as insuring proper registration procedures are followed. This position acts as a liaison between physician, department managers, patients and external agencies concerning the admitting process and is responsible for maintaining the confidentiality of all patient information. Responsibilities POSITION SPECIFIC DUTIES (other duties may be assigned) Assumes responsibility for position responsibilities outlined in the Registrar job description. Maintains the hospital census and reconciliation with nursing units. Calculate observation hours and enter on the account. Reports direct admissions to the nursing supervisor who determines medical necessity and appropriate level of care; coordinates effective patient flow to insure internal and external customer satisfaction; informs physicians of patient arrival times; coordinates admissions with nursing units, ambulances and external entities. Evaluates patient financial status at admission and/or referring to the Patient Financial Advisor as appropriate. Secures and releases patient valuables at admission and discharge. Prepares all surgery and/or GI packets for the following day securing patient orders, insurance verifications and patient notification of possible out of pockets. Completes additional projects as requested by Supervisor or Director. Takes initiative and performs as self-starter in daily activities. Qualifications QUALIFICATIONS/JOB REQUIREMENTS: EXPERIENCE: One year of patient registration experience in an acute facility. More years of experience may be required if hired in a registration area that demands more experience. Work in a physician's office may be substituted for an acute hospital setting if duties are similar. OTHER SKILLS, ABILITIES & KNOWLEDGE: Understands the registration process, managed care/capitation, Medi‑Cal, Medicare regulations, Medical Terminology, HIPAA, ABN, and EMTALA regulations Works effectively with the public, physicians, and staff Provides quality customer service including enhancing patient satisfaction while possessing the ability to work in a high volume production‑oriented and structured environment

Akkodis is seeking an Inspector, Quality Control for a Contract with a client in Pleasanton, CA. Candidate will perform visual inspection of incoming and in‑process components to ensure conformance with quality standards. Rate Range: $25/hour to $27/hour; The rate may be negotiable based on experience, education, geographic location, and other factors. Inspector, Quality Control job responsibilities include: * Perform routine visual inspection of electronic, mechanical, and electro‑mechanical components to verify conformance with quality standards. * Review and accurately follow written instructions, drawings, and inspection criteria to ensure proper evaluation of materials. * Document inspection results using multiple computer applications and maintain accurate records within internal systems. * Identify, segregate, and report non‑conforming materials, escalating issues when necessary. * Support in‑process inspection activities to ensure product quality throughout the manufacturing workflow. * Collaborate with team members and communicate clearly to resolve basic inspection‑related questions or discrepancies. Required Qualifications: * High school diploma or equivalent. * Minimum 1 year of experience in visual inspection or related quality roles. * Strong English reading comprehension and communication skills. * Ability to navigate multiple computer applications for documentation and inspection tasks. If you are interested in this role, then please click APPLY NOW. For other opportunities available at Akkodis, or any questions, feel free to contact me at ******************************. Pay Details: $25.00 to $27.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to ****************************************************** The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: * The California Fair Chance Act * Los Angeles City Fair Chance Ordinance * Los Angeles County Fair Chance Ordinance for Employers * San Francisco Fair Chance Ordinance Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

The Quality Control Inspector is responsible for verifying that products manufactured by Sierra Circuits, Inc. meet the requirements of our customers using various inspection tools and inspection methods. KEY RESPONSIBILITIES: QC Inspector Visual inspection under magnification on printed circuit boards. Identify quality defects to conformance specs and complete reject report (NCMR). Obtain FAI report and packaging requirements before moving the order to shipping. Maintain clean and orderly workspace. Perform final count of acceptable parts and sign the traveler. Complete first article report / or AS91002 report. Other duties as assigned. QUALIFICATIONS - KNOWLEDGE/SKILLS- EXPERIENCE: Excellent oral and written communication skills. Exceptional multi-tasking, organizational skills, strong attention to detail and accuracy. Strong interpersonal skills and ability to work with all levels of management Self-motivator and a sense of ownership and urgency. Must be able to maintain confidentiality & professionalism at all times. Proficient in Microsoft Office, using Excel, PowerPoint, and Word required. Read, write and communicate in English. Basic arithmetic in reference to instructions where interpretations are required. Ability to visually verify fine detail work. Ability to understand and follow directions when inspecting printed circuit boards. Basic understanding of prints and specifications, ability to complete FAI reports and communicate via email with customer inquiries. Moderate physical lifting of up to 20-Ibs Some out-of-department in-process inspection. SUPERVISES: None PHYSICAL DEMANDS: The physical demands described here represent those that an employee must meet to perform the essential functions of this job successfully. While performing the duties of this job, the employee is regularly required to talk or hear. The employee must frequently stand, walk, and reach with hands and arms. The ability to lift 20-40 lbs., open filing cabinets, and bend, stand, or climb on step ladders as necessary. ENVIRONMENT: Office and Manufacturing - Comply with safety and protective equipment as required. California Hourly Salary range from $20.00 - $26.00 with Benefits and Perks. Day Shift and Night Shift

Do you want to change the world? Zipline uses drones to deliver critical and lifesaving medicine to thousands of hospitals serving millions of people in multiple countries. Our mission is to provide every human on Earth with instant access to vital medical supplies. Join Zipline and help us make this a reality for billions of people. About the Role As the Quality Inspector Supervisor at Zipline, you will lead our team of inspectors who safeguard the quality of all incoming parts and components that make our aircraft safe and reliable. You will be responsible for training, developing, and managing a team of inspectors, ensuring inspection best practices are upheld, and driving continuous improvements in how we assess hardware quality. You will collaborate closely with the material planning team to align inspection priorities with production needs and with Quality Engineering to support root-cause analysis and corrective actions. This role requires a strong technical background in GD&T and inspection tooling, as well as excellent communication and task management skills to ensure the team's success. This position is ideal for someone who enjoys coaching others, thrives in a fast-moving environment, and takes pride in building inspection processes that scale. What You'll Do Team Leadership & Development Supervise and develop a team of quality inspectors, upholding best practices and providing training in inspection methods, GD&T interpretation, and use of tooling/fixtures. Set clear expectations for performance, hold the team accountable to quality standards, and create growth opportunities for individuals. Foster a culture of ownership, precision, and continuous improvement within the inspection team. Inspection Planning & Prioritization Partner with the material planning team to determine daily/weekly inspection priorities and allocate resources accordingly. Balance workloads across the team by understanding work scope, inspection complexity, and inspector capabilities. Ensure timely inspections that support production schedules without compromising quality. Technical Expertise Act as the subject-matter expert on GD&T, metrology, and inspection tooling/fixtures. Review and critique inspection plans, drawings, and fixture designs, providing feedback on feasibility and tolerance stack-ups. Guide the team in using the right tools for each inspection and identifying tricky or non-obvious issues. Process Improvement & Communication Develop and refine inspection processes that scale with increased production rates. Ensure accurate documentation and traceability of inspection results in the quality-management system. Drive clear communication of inspection results, nonconformances, and priorities across teams. Collaborate with Quality Engineering to support root-cause investigations and corrective actions. What You'll Bring 5+ years of hands-on quality inspection experience in manufacturing, aerospace, or related fields, including at least 2 years in a leadership or supervisory role. Deep technical literacy: proven expertise in GD&T, engineering drawings, schematics, and inspection plans. Strong knowledge of inspection tooling, fixtures, and metrology methods. Demonstrated ability to train, mentor, and coach others in inspection best practices. Experience prioritizing workloads and balancing resources across a team. Excellent communication and organizational skills; able to clearly assign work, track progress, and communicate status. Experience collaborating with planning, engineering, and production teams to align quality and schedule goals. Proficiency with quality documentation software (e.g., 1Factory), task tracking tools (e.g., Jira), and general computer literacy. Strong attention to detail with a disciplined, process-driven mindset. Experience inspecting composites (carbon fiber or similar) strongly preferred. Other Requirements Ability to lift up to 20 lbs and perform hands-on work throughout the day Comfort working with tools, chemicals, and hardware in a lab/manufacturing environment (including respirator use when required) What Else You Need To Know Zipline is an equal opportunity employer and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws or our own sensibilities. We value diversity at Zipline and welcome applications from those who are traditionally underrepresented in tech. If you like the sound of this position but are not sure if you are the perfect fit, please apply!

Title: Quality Technician Schedule: Monday Friday Pay Range: $30-$36/hr on w2 The Quality Technician will report to the Receiving Quality team lead and will have the goal to support the development of business processes to ensure that products and services provide a high level of quality that meets defined standards and specifications. This role will be helping in establishing high quality standards and ensuring product quality standards are met through inspection, documentation, and process improvement activities across receiving quality operations. The role will support quality management systems by conducting audits, performing root cause analysis, and implementing corrective actions while collaborating with cross-functional teams to maintain high-quality standards in manufacturing and services. In this role you will: Perform part level quality inspection to ensure the product is meeting specifications. Process incoming material and validate conformance to established quality standards Document various procedures and work instructions Support creating and reporting metrics to demonstrate quality status Enter test result data into SAP and JIRA systems Help in Root Cause Analysis activities, Corrective Action implementation and validation Support process improvement activities Work with cross-functional teams as needed Create inspection plans to conduct visual, functional, and mechanical measurements, & tests across multitudes of parts ranging from injection molding, castings, 3D printing parts to PCBAs, and electrical sub-assemblies Perform Metrology tasks using CMM as needed Previous mechanical, electrical, and electronics equipment inspection background with ability to use precision measurement tools Experience in defining and executing quality inspection criteria for the injection molding, castings, 3D printing parts to PCBAs, and electrical sub-assemblies is required Qualifications Minimum 2 years experience in the manufacturing environment (automotive, semiconductor, or aerospace fields are preferred). Experience in performing Quality inspections based on control plan Familiarity with Google suite (Google Docs, Google Sheets, Google Slides) Strong planning, organizational, analytical, interpersonal, decision-making, oral and written communication skills Bonus Qualifications Previous experience in SAP and/or JIRA system Industry background and/or experience in;automotive, software, contract manufacturing, customer management

Scope/Responsibilities of Role: Helping design AI systems that write regulatory documents. Deconstructing authoring/review/QC heuristics for engineers. Evaluating AI-generated content quality and identifying edge cases. Bridging the gap between domain expertise (medical writing) and technical product development. Must Have Skills for Role: 3+ years of medical writing experience in regulatory affairs. Direct experience with CTD documents (non-clinical and CMC). Knowledge of FDA, EMA, and ICH guidelines. Ability to extract and document rules/logic for technical teams. Strong QC capabilities. Nice to Have Skills for Role: Familiarity with structured content formats like XML or JSON. Experience working with life sciences software tools.

Full-time Description Perform finished product inspections by confirming specifications, conducting visual and measurement tests and rejecting and documenting unacceptable products. Maintain quality standards by performing in-process and finished products. Visually inspect products to ensure they are meeting requirements and specifications. Perform incoming inspection of components in accordance with company standards. Perform product testing/inspection. Complete final inspection of products prior to shipment. Fulfill customer component order inspection. Document all inspection results and any re-work that must be completed. Thrives in a fast-paced work environment, managing multiple priorities with speed, adaptability, and attention to detail. Additional projects/ roles/ responsibilities assigned by management. Requirements High school diploma or equivalent 3+ years of QC experience in cable and wire harnesses Must be able to use gauges, calipers, micrometers, rulers Basic math and computer skills Must be able to read blueprints Experience working in an engineering/manufacturing environment and/or Quality Management System experience, a plus. Salary Description $23.25 - $27.75

We offer market competitive compensation. Potential salary range for this role is $23.00-$27.00 Per Hour. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law MAIN PURPOSE OF JOB: This position is responsible for in-process and final visual inspection of parts. This position is on the production floor collecting samples and performing visual inspections. This is a highly responsible position requiring attention to detail and the ability to work with minimal amounts of supervision. This position requires the use and understanding of special quality inspection tools and equipment. MAIN JOB RESPONSIBILITIES: Collects samples at scheduled intervals from each machine. Perform the necessary visual Quality/SPC testing procedures on samples. Utilize tools, gauges and other inspection equipment to obtain product specification data. Accurately record information consistent with the department format. Communicate with Machine Technicians, Operators and Production Supervisors to run a consistent quality product. Follow all departmental procedures with respect to routine daily assignments. All workstation areas will be maintained in a neat and orderly manner. Inspect and document in-bound raw materials for conformance. Place non-conforming products on hold and create non-conforming records. Conduct quality inspection on rework product. Work on validation projects as needed. Manage production and validation projects. Update Quality Inspection requirements. Create Job Packets and manage device history records. Participate in Material Review Board activities. POSITION QUALIFICATIONS: Education: High School Diploma or GED (preferred) Ability to read and write in English. Experience with ANSI Sampling Plans Knowledge of measurement instrumentation (Caliper, Micrometer, Ruler, Gage Blocks, etc.) Experience with ISO 13485 processes Ability to read prints. Knowledge of Microsoft Word and Excel.

GENERAL INFORMATION Quality Inspector (II, III, or Senior) Department: Quality Assurance Reports to: Quality Engineering Purpose of the Job This Quality Inspector position will report to Quality Engineering. Main responsibilities include performing incoming inspections of materials/parts/products and reviewing and approval of manufacturing batch records and inspection records. This position will require to perform disposition of materials/parts/products. As a Quality Inspector, you will also support Quality Engineering with other Quality Management System (QMS) activities, such as assisting with environmental monitoring and quality metrics. Major Duties and Responsibilities Interpret drawings and specification documents. Perform incoming inspection of materials/components/subassemblies/finished products following standard operating procedures and using standard inspection tools, including the MicroVu and Keyence. Determine inspection sample size based on procedures, specifications, and standards. Help develop inspection methods, including automated inspection programs using the MicroVu and Keyence. Review/approve executed batch records for manufacturing and inspection records in accordance to QMS procedures and Good Documentation Practices. Approve/perform final disposition of materials/components/subassemblies/finished products. Assign and apply expiration dating labels to materials/parts/products, as per specifications/quality procedures. Initiate Non-Conformance Material Reports (NCMRs) and deviations when discrepancies are observed during inspections and record review process. Report discrepancies and issues to QA Engineering and affected function(s). Maintain materials in Quarantine (pending disposition) and MRB (under NCMR and deviations) in order. Maintain accurate records as per Document Control procedures. Support training of IQC personnel. Assist with performing environmental monitoring of Controlled Environment Rooms (CERs), as needed. Support Quality in the collection of quality metrics data. Interact closely with different functions of the organization. Education and/or Job Experience 2-5 years of experience performing inspections and reviews/approvals of manufacturing batch records/inspection records Government Regulated Environment experience such as FDA and ISO 13485 Must have adequate computer experience (knowledge of Microsoft Word, Excel) Experience working in a cGMP environment Skills and Specifications Attention to detail and organizational skills Good interpersonal and communication skills Ability to work as a part of a team and promote a team environment

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Pharmaceuticals located in San Carlos is seeking a Quality Assurance Batch Record Reviewer / Person-In-Plant to support Quality oversight of manufacturing operations for the NIGHT SHIFT. This is a temporary assignment. Responsible for on-the-floor, timely and effective GMP review and production close-out of batch record documentation in order to maintain a continuous flow of batch records Single point of contact in the plant during the assigned Manufacturing shift for the Batch Record Review Process and Quality matters. Operates on a 8-hour shift (10:00pm-6:30am) to support 24x5 Operations. • Responsibilities include approval and issuance of batch records, approving records; issue resolution; batch record review. • Reviews batch documentation for accuracy and completeness according to cGMP's to ensure timely release. • Supports/performs scanning of records for uploading into share folders • Conducts QA Person-In-Plant activities including, Area Approval, Line Clearance Approval, Batch Record Review, Deviation triage and preliminary investigation, etc. • Assists with Deviation investigations, Compliance investigations, and Customer complaint investigations. • Supports implementation of CAPAs, SOP revisions, Quality improvement initiatives, Operational Excellence projects, etc. • Adheres to internal/external Guidelines, Specifications and Regulatory requirements while reviewing batch documentation. • Ensures all GMP's, SOP's and protocols are followed. • Positively interacts with internal associates to quickly and effectively resolve issues. • Addresses deficiencies and ensures completion of follow-up actions, specifically those that target process fixes to maintain consistent resolutions to batch review issues according to GMP standards and Novartis objectives. Skills: • Minimum Requirements: MUST BE ABLE TO WORK NIGHT SHIFT 10:00pm-6:30am. First couple weeks of training will be day shift. • 2-5 years related manufacturing or quality experience. BS degree in science in preferred. • Demonstrated cGMP knowledge and experience. • Strong interpersonal, written, communication, and problem solving skills. • Must be well organized, flexible and able work with minimal supervision. • Prior experience with Quality Assurance Batch Record Review and/or Person-In-Plant is preferred. • Strong background and skills in Quality, Manufacturing, communication and computer related systems are preferred. • Experience with Deviation Investigations and Root Cause Analysis is a plus. • Experience with Microsoft Word / Excel, SAP and TrackWise is a plus. Qualifications • BS degree in science is preferred. Additional Information For more information, please contact Akriti Gupta ************** Morristown, NJ 07960

We are seeking a Server product system level inspection and testing in San Jose to join our production team by working efficiently in a fast paced environment and help with system level testing and troubleshooting. Essential Duties and Responsibilities: Includes the following essential duties and responsibilities (other duties may also be assigned): • Assist Server system level inspection & quality report related paperwork. • Assist server system level incoming quality control • Assist Server system level testing & troubleshooting • Perform other production quality related duties as directed by supervisor Qualifications: • High school diploma required • At least 1 years in the field of QC/QA function is preferred • Language Skills: English is required; Mandarin is a plus • Be able to comply with overtime requirements • Excellent troubleshooting skills • Actively promotes production, quality and safety standards • Motivated individual with the willingness to be a good team player Pay: $22-$24 #EmploynetJobsFremont

Qualifications: High School Diploma or equivalent; Associate's degree or technical certification in Optics or Manufacturing Technology preferred 2+ years of experience in Quality Inspection within precision manufacturing environment, preferably in optics or photonics Proven proficiency using precision measurement tools (calipers, micrometers, optical comparator, microscope, interferometers, radius benches) Ability to read and interpret engineering blueprints and apply GD&T principles Exceptional visual acuity and attention to detail for cosmetic inspection of delicate optical components Strong verbal and written communication skills and computer literacy for documentation Prior experience with optical inspection equipment (interferometers, autocollimators, specialized optical test benches) Experience with ERP or Quality Management System (QMS) software Knowledge of optical glass materials, properties, and ISO 9001 quality management systems Certified Quality Inspector (CQI) certification preferred Responsibilities: Perform incoming, in-process, and final inspections of optical components (lenses, mirrors, prisms, windows) and opto-mechanical assemblies Conduct visual inspection of optics for cosmetic defects (scratches, digs, bubbles, coating issues) according to established standards (MIL-PRF-13830B or custom specifications) Document inspection results accurately, generate inspection reports, and maintain meticulous records for traceability Identify and quarantine non-conforming materials or products, and collaborate with Manufacturing and Engineering teams to investigate root causes and support CAPA Assist in calibration and maintenance of inspection tools and equipment, and contribute to continuous improvement of quality processes

Quality Inspector The Quality Inspector is responsible for performing detailed inspections and tests on incoming materials, in\-process components, and finished optical assemblies to guarantee compliance with engineering drawings, specifications, and internal quality standards. This role is crucial in upholding our commitment to precision manufacturing and a zero\-defect guarantee. Key Responsibilities: Perform Incoming, In\-Process, and Final Inspections of optical components (lenses, mirrors, prisms, windows) and opto\-mechanical assemblies. Utilize a variety of precision measuring instruments, including micrometers, calipers, height gauges, optical comparators, microscopes, interferometers, and radius benches to verify dimensions, tolerances, and cosmetic specifications. Conduct visual inspection of optics for cosmetic defects such as scratches, digs, bubbles, and coating issues according to established standards (e.g., MIL\-PRF\-13830B or custom customer specifications). Read and accurately interpret complex engineering drawings, specifications, and technical documents, including Geometric Dimensioning and Tolerancing (GD&T). Document inspection results accurately, generate inspection reports, and maintain meticulous records for traceability. Identify and quarantine non\-conforming materials or products, and collaborate with the Manufacturing and Engineering teams to investigate root causes and support Corrective and Preventative Actions (CAPA). Ensure all inspection activities adhere to company Standard Operating Procedures (SOPs) and quality management systems (e.g., ISO 9001). Assist in the calibration and maintenance of inspection tools and equipment to ensure accuracy. Contribute to the continuous improvement of quality processes and manufacturing efficiency. Adhere to all company safety protocols and maintain a clean and organized work environment, which may include a cleanroom environment. Requirements Minimum Qualifications: High School Diploma or equivalent. 2+ years of experience in Quality Inspection within a precision manufacturing environment, preferably in optics, photonics, or a related field. Proven proficiency in using precision measurement tools (calipers, micrometers, optical comparator, microscope). Ability to read and interpret engineering blueprints and apply GD&T principles. Exceptional visual acuity and attention to detail for cosmetic inspection of delicate components. Strong verbal and written communication skills and computer literacy for documentation. Ability to work independently, manage time effectively, and prioritize tasks in a fast\-paced environment. Preferred Qualifications: Associate's degree or technical certification in a related field (e.g., Optics, Manufacturing Technology). Prior experience with optical inspection equipment such as interferometers, autocollimators, or specialized optical test benches. Experience with an Enterprise Resource Planning (ERP) or Quality Management System (QMS) software. Knowledge of the principles of optical glass materials and their properties. Certified Quality Inspector (CQI) certification. Physical Requirements: Ability to sit or stand for extended periods. Manual dexterity and fine motor control for handling small, delicate optical components and using precision instruments. Sufficient visual acuity for magnified inspection under a microscope. Ability to lift and move up to 25 pounds occasionally. Benefits "}}],"is Mobile":false,"iframe":"true","job Type":"Full time","apply Name":"Apply Now","zsoid":"687062720","FontFamily":"PuviRegular","job OtherDetails":[{"field Label":"Industry","uitype":2,"value":"Manufacturing"},{"field Label":"City","uitype":1,"value":"Pleasant Hill"},{"field Label":"State\/Province","uitype":1,"value":"California"},{"field Label":"Zip\/Postal Code","uitype":1,"value":"94523"}],"header Name":"Quality Inspector\- Applied Optics","widget Id":"**********00072311","is JobBoard":"false","user Id":"**********02449001","attach Arr":[],"custom Template":"5","is CandidateLoginEnabled":true,"job Id":"**********03224003","FontSize":"15","location":"Pleasant Hill","embedsource":"CareerSite","indeed CallBackUrl":"https:\/\/recruit.zoho.com\/recruit\/JBApplyAuth.do","logo Id":"dk1on2d2aef**********9e772831fe0f3140"}

Here at Westfall Technik, we pride ourselves on being the fastest-growing Plastic Injection Manufacturing Company in the USA and soon globally. While many companies outsource their work, we believe in keeping our jobs in the US. We currently support over 1,500 Team Members across 15 facilities in the US, and we are still growing. At our Union City site, we invest in our people. Our overall success is largely attributed to our Team Members skills and talents, which have been impactful and essential to the growth of our business. Here, you ll get the opportunity to test your knowledge and skills and become a critical player within Westfall. We want you to view your time at Westfall as an investment in your future. We are currently seeking a Quality Inspector. Pay Rate/Shift: $22/hr +$2/hr Shift Differential for the 9pm-5:15am shift. Job Overview The Quality Inspector is responsible for inspecting materials, components, and finished products to ensure they meet specified standards and customer requirements. This role involves performing visual, dimensional, and functional inspections using measuring tools and testing equipment. The Quality Inspector documents findings, identifies defects or deviations, and works closely with production and quality teams to resolve issues. This position plays a critical role in maintaining product quality, reducing rework, and supporting compliance with internal and external quality standards. Key Responsibilities Perform First Article, In-Process, and Final Inspections Monitor and Document Quality Conduct CMM Testing Perform Dimensional and Functional Testing Report and Document Nonconformances Ensure Compliance with QMS and cGMP Assist in Audits Perform Sorting and Rework Assist in Training Inspector/Packers Ensure Safety Devices are Intact Follow Safety Procedures Job Requirements A high school diploma or equivalent is required. 2-3 years of plastic injection molding experience Excellent time management, organization, and planning skills. Advanced problem-solving and analytical skills. Must be detail-oriented Ability to multitask. Must possess good interpersonal and communication skills. Ability to promote a team atmosphere in the department and in other production-based areas. Must be able to work with minimal supervision, self-starter, and have high initiative. Computer skills. WORK ENVIRONMENT The work environment is usually in an office within a manufacturing facility with low to moderate noise level. The work environment characteristics described here are representative of those a Team Member encounters while performing the essential functions of this job. Westfall -Technik is an Equal Opportunity Employer that does not discriminate on the basis of actual or perceived race, color, national origin, ancestry, sex, gender, gender identity, gender expression, pregnancy, childbirth or related medical conditions, religious creed, physical disability, mental disability, age for individuals age 40 and over, medical condition (as defined by state law (for example, cancer or genetic characteristics or HIV/AIDS), marital status, military and veteran status, sexual orientation, genetic information, citizenship status or any other characteristic protected by federal, state or local law. Our management team is dedicated to this policy with respect to recruitment, hiring, placement, promotion, transfer, training, compensation, benefits, Team Member activities and general treatment during employment