15 Food Industry jobs in San Jose

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team, you will join other outstanding scientists in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

The Opportunity:

Playing a project leading role and Subject Matter Expert (SME) of late phase and commercial Quality Control within in Quality Control within the CMC function, this position will be responsible for overseeing a team and individually contributing to the management of QC activities from process validation to commercial launch readiness supports of drug substance (DS), drug product (DP) and final product (FP) manufacturing. The candidate will also be responsible for post-approval QC related activities including lifecycle management regulatory submissions such as CBE, PAS, etc.

• Provide strategic and tactical ownership for QC activities of late phase and commercial programs, including but not limited to commercial launch readiness including establishment of CDMO and/or CTL.
• End to end process management for analytical purposes in support of manufacturing operations for release of commercial product.
• Oversee and manage outsourced commercial QC activities at CDMOs and/or contract testing labs (CTLs) for release and stability purposes.
• Manage quality events related to commercial QC testing such as lab investigation (e.g., OOS/OOT), deviations, change controls (e.g., CBE 30/CBE 0) and CAPAs.
• Support regulatory submissions and commercial life cycle management to maintain operational uniformity.
• Collaborate with cross functional teams including CMC RA, DS, DP, Supply Chain and Quality Assurance to achieve project goals per timelines.

• BS or MS in Chemistry, Pharmaceutical Science or related discipline.
• 10+ years of relevant industrial experience in analytical development/QC.
• Solid understanding of relevant compliance and regulatory requirements as applicable to data integrity, process validation, manufacture sampling and testing, stability study, method validation and transfer, etc.
• Effective written and verbal communication skills and interpersonal skills.
• Extensive knowledge and understanding of cGMP guidelines and practices, as well as related / best industry practices.
• Strong problem-solving skills with sound technically driven decision-making ability
• Excellent communication skills (verbal, written and technical), strong interpersonal/collaboration skills and planning skills.
• Ability to think critically and creatively and be able to work independently to determine appropriate resources for resolution of problems.
• Ability to multi-task and thrive in a fast-paced innovative environment.

• Experience in solid oral dosage including dissolution testing.
• Work experience and knowledge of global regulatory submissions (IND, IMPD, NDA and MAA, etc.) is preferred.
• Commercial QC experience.
• Chromatographic experience in development, optimization, and troubleshooting.

• Provide day-to-day supervision of all inspection and metrology activities, including incoming, in-process, final, and CMM inspection.
• Manage and develop a team of Quality Control Inspectors (QCIs), CMM Programmers, and metrology personnel through coaching, performance feedback, and skills cross-training to ensure a flexible and capable inspection function.
• Prioritize and coordinate daily inspection workload to support production flow, meet delivery commitments, and minimize delays or bottlenecks.
• Lead the implementation and continuous improvement of a modern, risk-based inspection strategy that aligns inspection methods with part criticality and manufacturing capabilities.
• Partner cross-functionally with CNC programming, engineering, and production to proactively identify quality risks, drive manufacturability improvements, and integrate inspection into upstream processes.
• Support new product introduction (NPI) and design-for-manufacturing (DFM) initiatives by developing right-sized inspection plans and ensuring readiness of inspection processes and resources.
• Maintain working knowledge of CMM programming (Calypso preferred) to provide technical oversight, while delegating routine programming tasks to support personnel where applicable.
• Monitor and improve inspection efficiency, accuracy, and data integrity; support metric tracking and corrective action efforts tied to internal and customer quality performance.
• Champion a culture of quality, accountability, and problem-solving within the inspection team.

• Deep knowledge of aerospace/defense industry quality standards (AS9100, GD&T, NADCAP experience is a plus).
• Strong understanding of risk-based quality inspection principles and PFMEA/Control Plan elements.
• Proficient in CMM programming (Calypso preferred), but capable of leading others rather than owning all programming responsibilities.
• Experience working in fast-paced, high-mix machining or manufacturing environments.
• Comfortable leading cross-functional efforts and influencing without direct authority.
• Strong communication, coaching, and problem-solving skills.

• Bachelor of Science in related field which can be substituted with commensurate experience.
• 7+ years in quality inspection or metrology, with 3+ years in a leadership or supervisory role.

• QCIs are cross-trained, agile, and engaged with production.
• Reduce overreliance on CMM as a default inspection solution-inspection methods should suit application-specific requirements.
• You are present and involved in daily operations, not isolated to a desk or programming booth.
• Inspection strategy is visibly improving throughput and quality performance.

• Is not a United States citizen
• Is not lawfully admitted for permanent residence in the U.S.
• Does not have politically protected status (embassy, refugee, or asylum)
• Has dual U.S. / foreign citizenship

Sanmina Corporation (Nasdaq: SANM) is a leading integrated manufacturing solutions provider serving the fastest growing segments of the global Electronics Manufacturing Services (EMS) market. Recognized as a technology leader, Sanmina Corporation provides end-to-end manufacturing solutions, delivering superior quality and support to Original Equipment Manufacturers (OEMs) primarily in the communications networks, defense and aerospace, industrial and semiconductor systems, medical, multimedia, computing and storage, automotive and clean technology sectors. Sanmina Corporation has facilities strategically located in key regions throughout the world.

Job Purpose :

Performs product inspection and/or audits of quality control programs. Performs packaging line and manufacturing inspections, and sampling and testing of incoming components and raw materials. Ensures raw materials, in-process and finished products meet company standards. May apply approval or rejection labels to bulk raw materials once analytical data is evaluated.

Nature of Duties/Responsibilities:

• Responsible for providing immediate quality feedback to SMT operators while running the line.
• Responsible for scanning findings in quality tool
• Responsible to perform FA (First Articles)
• Responsible to read and interpret work instructions, Deviations, BOM's, Travelers etc.
• Able to help other areas such as TLA inspection, Final QC, Final Kit Audit Verification.

Education and Experience:

• Minimum of 2-4years of experience in SMT Quality Assurance Control/Inspection process per IPC-610 class 2,3 (PCBA and Mechanical components)
• Experience in feeder verification on and off line
• Minimum knowledge in component ID, polarity verification, workmanship inspection, part value verification using digital meter.
• Experience using microscopes, Ohm meters, manual and stationary magnifying glass
• Good written and verbal communication
• Computer literate

Sanmina is an Equal Opportunity Employer

Salary Range(annual):$42,000 - $3,000 ( 20 - 25 / hourly)

Actual base pay within this range (determined at the offer stage) will be based on a candidate's years of relevant work experience, education, certifications, and skills, and is just one element of our total rewards package. The total rewards package also includes a variety of benefits, including health insurance coverage, life and disability insurance, savings plan, Company paid holidays and paid time off (PTO) for vacation and/or personal business and, depending on the role, may include eligibility for restricted stock unit awards and participation in a discretionary bonus program.

22 hours ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. This range is provided by FM Industries. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $80,000.00/yr - $0,000.00/yr Salary Range: 80,000.00 To 90,000.00 Annually FM Industries is recognized as a premier manufacturing solutions provider of manufacturing services for the semiconductor capital equipment market. We specialize in build to print, precision machined components, anodization and engineered thermal spray coatings. FM Industries promotes an environment that not only encourages your best, but also rewards it with plenty of room to grow. FM industries is a premier manufacturing solutions provider. We have locations in Northern California and Phoenix, Arizona. Since 2002, the business has been part of NGK Insulators , based in Nagoya, Japan. Our partnership with NGK is highly collaborative and complimentary. SUMMARY OF POSITION: The primary responsibility of this position is to plan, analyze, administer, and coordinate the Quality Assurance functions of Quality Control. Supervise and program CMM’s and inspect parts as needed to maintain the production schedule and on-time deliveries. ESSENTIAL DUTIES: Plan and administer the Quality Control function of the department. Create and execute inspection methods and techniques that will assure quality is achieved and maintained. Coordinate quality activity with entire quality control staff to enhance teamwork and continuous improvement throughout the plant. Analyze the performance of our quality control system and work with people at all levels to meet customer’s requirements for Total Quality performance. Supervise inspectors to accomplish first piece/first article inspections, in-process inspection, final inspections, Certificate of Conformance (CoC) and outside process receiving inspection tasks as required. Manage all assigned labor (time and attendance) and fixed cost for the inspection department. Maintain a calibration system which includes employee owned measuring tools as well as company owned measuring equipment. Assure current print revisions and current process instructions are readily available for inspection of assigned parts. Inspection records shall be maintained which show pertinent information for each production run of assigned parts. Measure and analyze key quality performance data. Make recommendations to management on specific opportunities to improve quality. Develop training and procedures to support and audit operator in-process inspections and required documentation. Develop and implement quality plans on an ongoing basis. The quality plan should specify the requirements for people, equipment and systems to be used for continuous improvement of quality. Recommend changes to documentation which supports quality improvement, (i.e., Engineering Change Requests, process instructions, raw material requirements). Leads and applies the principles of “Total Quality” to the workplace, to include 5S and safety standards. Participate and maintain assigned responsibility for ISO 9001:2008 documented quality systems. Be responsible for insuring that inspectors know and comply with all ISO 9001:2008 requirements within their area of responsibility. Provide quality inspection support of a value stream in a back-up support role as needed. Monitor all tooling / inspection equipment inventory, purchase new equipment and supervise the repair of inspection equipment. Supervise 6-10 hourly inspectors Executes necessary precautions to ensure safety and compliance with Company, OSHA, and other standards and regulations Comply with applicable environmental, health and safety laws and regulations, Company policy and accepted safe work practices. EDUCATION AND/OR EXPERIENCE REQUIRED: High school graduate or equivalent. Degree in Business Administration, Quality Management, Logistics, Supply Chain Management. 3 to 5 years experience of quality control and machining in manufacturing environment. Experience in supervising and leading a manufacturing team. This position will supervise 6-10 hourly inspectors. Experience and knowledge reading drawings (prints) is required. Experience and knowledge working with GD&T Experience supervising and working on shop floor environment Inspection lab and processing experience Experience in semi-conductor, medical device, automotive, aerospace or precision machining manufacturing Thorough understanding and utilization of the root cause/corrective action process onsite and within supply base Detail orientated and organized, with ability to work at a high level of accuracy Ability to interact with fellow employees in a professional manner Strong problem-solving and analytical abilities Independent, can work with limited supervision and direction CULTURE: At FM Industries our success is powered by people and technology. Our culture is what makes FM a fun and rewarding place to work. We champion diversity and we are always seeking new ways to amaze our customers. Success is celebrated and integrity is the core of who we are at FM Industries. WHAT CAN BE OFFER YOU FOR ALL YOUR HARD WORK? PTO Program Medical, Dental, Vision and Life Insurance Short and Long-Term Disability Coverage Tuition Assistance Pet Insurance Flexible Spending Plans Health Spending Plans 401(k) Retirement Savings - with a generous company match! Give us your best and we'll give you ours! Seniority level Seniority level Associate Employment type Employment type Full-time Job function Job function Engineering and Quality Assurance Industries Semiconductors Referrals increase your chances of interviewing at FM Industries by 2x Inferred from the description for this job Medical insurance Vision insurance Disability insurance Tuition assistance Get notified about new Quality Control Supervisor jobs in Fremont, CA . Newark, CA $82,000. 0- 114,000.00 1 month ago Union City, CA 66,129.00- 120,817.00 3 weeks ago Newark, CA 80,000.00- 95,000.00 6 days ago Fremont, CA 72,000.00- 120,000.00 2 weeks ago Hayward, CA 65,000.00- 75,000.00 2 months ago Newark, CA 80,000.00- 90,000.00 1 week ago Hayward, CA 95,000.00- 120,000.00 22 hours ago San Jose, CA 77,000.00- 91,000.00 2 months ago San Jose, CA 77,000.00- 91,000.00 1 week ago Assembly Solutions Production Supervisor Santa Clara, CA 80,300.00- 100,400.00 1 month ago Assembly Solutions Production Supervisor Food Safety and Quality Assurance Senior Supervisor South San Francisco, CA 75,200.00- 101,600.00 2 weeks ago SBC Clinical Laboratory Scientist I - Night Shift (10 or 11pm start) SBC Clinical Laboratory Scientist I - Technical Services - Evening Shift (2pm Start) SBC Clinical Laboratory Scientist I - Night Shift (10 or 11pm start) SBC Clinical Laboratory Scientist I - Technical Services - Evening Shift (2pm Start) Clinical Lab Scientist - Histocompatibility & Immunogenetics /HLA Lab - Overnight Shift Social Science Research Professional 1, General Surgery (Hybrid Opportunity) We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr

Join to apply for the Quality Control Laboratory Manager role at SCN BestCo

1 month ago Be among the first 25 applicants

Join to apply for the Quality Control Laboratory Manager role at SCN BestCo

Get AI-powered advice on this job and more exclusive features.

We believe being healthy should not require tradeoffs. SCN BestCo is a leading innovator, developer and manufacturer of Vitamin, Mineral & Supplement (VMS), Over-the-Counter (OTC) and prebiotics/probiotics in enjoyable forms such as gummies, lozenges and chews. With over 50 years of excellence, our team leads the way in changing how consumers make healthier choices. With unique food science expertise and proprietary processes, weve pioneered many firsts. The fire in our belly to create new to the world products has guided and continues to be core to our mission of making health and wellness more enjoyable. Come join us and become a part of our winning formula!

The Quality Control (QC) Laboratory Manager dynamically leads staff and function related to all aspects of laboratory management internally and externally, including raw material, in-progress material, and finished product testing. This position manages skilled laboratory personnel, aligns testing priorities with production goals, drives analytical excellence, collaborates with the other Company sites, ensures compliance to regulatory and company policies and procedures, and implements continuous improvement initiatives.

Estimated starting annual base salary is $126,550.56 - $89,825.85 per year less applicable withholdings and deductions, paid on a bi-weekly basis. Please note that the actual compensation offered may vary based on relevant factors as determined by the Company, which may include, but is not limited to, location, experience, qualifications, education, skillset, and market conditions. The target base compensation for this role is in the low to middle of the range, with the top of the range reserved for only exceptional circumstances. In addition, this role is eligible for a discretionary, variable annual incentive, paid based on Company performance factors. SCN BestCo offers a competitive benefits package to eligible full-time employees, which currently includes medical, dental, and vision plans, 401(k) with employer matching contributions, life insurance, paid time off, tuition reimbursement, and more, as well as paid sick leave in accordance with applicable law. Each benefit is subject to eligibility requirements as specified in plan documents, and the Company reserves the right to modify the benefits it offers from time to time.

Essential Duties And Responsibilities

• Manage all laboratory operations by proactively prioritizing and assigning laboratory work.
• Plan, promote, and organize training activities related to quality and reliability to improve laboratory and manufacturing.
• Review and approve documentation related to the technical transfer of new line introductions, customer specification, requirements, memos, and all other laboratory and operations related documents.
• Oversee raw material, in-process material, and final product testing through data results reporting and review.
• Manage laboratory budget and resources effectively.
• Review and approve sample testing activities including leading Laboratory Out of Specification (OOS) investigations and driving OOS reductions.
• Implement continuous improvement initiatives for laboratory efficiencies, compliance, and effectiveness.
• Manage vendor relationships for laboratory supplies and services in collaboration with Supplier Quality and Operational Logistics teams.
• Author, review, revise, and maintain laboratory standard operating procedures (SOPs) and Work Instructions (WI).
• Analyze, track, and report laboratory data and documents and identify opportunities to improve accuracy and precision of testing protocols to support and maintain the Quality Management System (QMS).
• Maintain laboratory equipment performance by establishing quality standards; developing operations, quality, and troubleshooting procedures; annual qualification and instrument performance; arranging equipment replacement, service, and repair.
• Participate in internal audits of QC labs and external customer, certification, and regulatory inspections/audits including timely responses, action plans, and resolution to prevent recurrence.
  
  

• Recommend personnel actions (pay adjustments, promotions, transfers, terminations).
• Conduct performance reviews and manage individual performance.
• Communicate personnel actions following Human Resources (HR) and Department Head approval.
• Ensure safety and quality standards are enforced and met.
• Partner with HR to interview/screen potential new hires.
• Organize training and development opportunities for direct reports.
  
  

• Bachelors degree in food science, chemistry, biology, or related field.
• 8 years professional laboratory experience including quality control.
• 5 years experience in leadership, supervision and/or management.
  
  

• Advanced knowledge of laboratory practices, procedures, and systems.
• Strong understanding of laboratory analytical techniques (HPLC, UPLC, GC, UV-Vis, ICP-MS, others).
• Strong interpersonal, organizational, analytical, planning, communication, and leadership skills.
• Ability to analyze, troubleshoot, investigate, and document laboratory OOS results and provide resolution.
• Proficiency in Microsoft Office including Excel, Word, and Outlook.
• Ability to work with mathematical concepts such as probability and statistical inference, and fundamentals of plane and solid geometry and trigonometry. Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations.
• Must have the ability to communicate effectively, verbally and in writing, with internal staff and management. Ability to respond professionally and scientifically to cross-functional partners, customers, regulatory agencies, certifying bodies or members of the business community. Ability to effectively present information to top management, public groups, and/or boards of directors.
• Must be able to demonstrate practical problem solving and trouble shooting skills. Must be able to demonstrate practical problem solving and trouble shooting skills. Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.
  
  

• Masters degree or Ph. D. in related field.
• Prior experience with implementation and maintenance of Laboratory Information Management Systems (LIMS).
• Manufacturing, Consumer Packaged Goods, ISO, and/or GMP experience in dietary supplement or food manufacturing.
• Knowledge of USP methods and requirements.
• Experience with lean laboratory practices.
• Six Sigma certification.
• Professional certification (CQE, CQA, or similar).
  
  

• Seniority level Mid-Senior level

• Employment type Full-time

• Job function Research, Analyst, and Information Technology
• Industries Manufacturing

Referrals increase your chances of interviewing at SCN BestCo by 2x

Santa Cruz, CA 125,000.00- 172,000.00 2 hours ago

Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

We believe being healthy should not require tradeoffs. SCN BestCo is a leading innovator, developer and manufacturer of Vitamin, Mineral & Supplement (VMS), Over-the-Counter (OTC) and prebiotics/probiotics in enjoyable forms such as gummies, lozenges and chews. With over 50 years of excellence, our team leads the way in changing how consumers make healthier choices. With unique food science expertise and proprietary processes, we've pioneered many firsts. The fire in our belly to create new to the world products has guided and continues to be core to our mission of making health and wellness more enjoyable. Come join us and become a part of our winning formula!The Quality Control (QC) Laboratory Manager dynamically leads staff and function related to all aspects of laboratory management internally and externally, including raw material, in-progress material, and finished product testing. This position manages skilled laboratory personnel, aligns testing priorities with production goals, drives analytical excellence, collaborates with the other Company sites, ensures compliance to regulatory and company policies and procedures, and implements continuous improvement initiatives.Estimated starting annual base salary is $126,550.56 - $189,825.85 per year less applicable withholdings and deductions, paid on a bi-weekly basis. Please note that the actual compensation offered may vary based on relevant factors as determined by the Company, which may include, but is not limited to, location, experience, qualifications, education, skillset, and market conditions. The target base compensation for this role is in the low to middle of the range, with the top of the range reserved for only exceptional circumstances. In addition, this role is eligible for a discretionary, variable annual incentive, paid based on Company performance factors. SCN BestCo offers a competitive benefits package to eligible full-time employees, which currently includes medical, dental, and vision plans, 401(k) with employer matching contributions, life insurance, paid time off, tuition reimbursement, and more, as well as paid sick leave in accordance with applicable law. Each benefit is subject to eligibility requirements as specified in plan documents, and the Company reserves the right to modify the benefits it offers from time to time.Essential Duties and ResponsibilitiesManage all laboratory operations by proactively prioritizing and assigning laboratory work.Plan, promote, and organize training activities related to quality and reliability to improve laboratory and manufacturing.Review and approve documentation related to the technical transfer of new line introductions, customer specification, requirements, memos, and all other laboratory and operations related documents.Oversee raw material, in-process material, and final product testing through data results reporting and review.Manage laboratory budget and resources effectively.Review and approve sample testing activities including leading Laboratory Out of Specification (OOS) investigations and driving OOS reductions.Implement continuous improvement initiatives for laboratory efficiencies, compliance, and effectiveness.Manage vendor relationships for laboratory supplies and services in collaboration with Supplier Quality and Operational Logistics teams.Author, review, revise, and maintain laboratory standard operating procedures (SOPs) and Work Instructions (WI).Analyze, track, and report laboratory data and documents and identify opportunities to improve accuracy and precision of testing protocols to support and maintain the Quality Management System (QMS).Maintain laboratory equipment performance by establishing quality standards; developing operations, quality, and troubleshooting procedures; annual qualification and instrument performance; arranging equipment replacement, service, and repair.Participate in internal audits of QC labs and external customer, certification, and regulatory inspections/audits including timely responses, action plans, and resolution to prevent recurrence.People Leader ResponsibilitiesThis position carries out People Leader responsibilities in accordance with the Company's policies and applicable laws. Responsibilities include:Recommend personnel actions (pay adjustments, promotions, transfers, terminations).Conduct performance reviews and manage individual performance.Communicate personnel actions following Human Resources (HR) and Department Head approval.Ensure safety and quality standards are enforced and met.Partner with HR to interview/screen potential new hires.Organize training and development opportunities for direct reports.Required QualificationsEducation & Experience:Bachelor's degree in food science, chemistry, biology, or related field.8 years' professional laboratory experience including quality control.5 years' experience in leadership, supervision and/or management.Knowledge, Skills, & Abilities (KSAs):Advanced knowledge of laboratory practices, procedures, and systems.Strong understanding of laboratory analytical techniques (HPLC, UPLC, GC, UV-Vis, ICP-MS, others).Strong interpersonal, organizational, analytical, planning, communication, and leadership skills.Ability to analyze, troubleshoot, investigate, and document laboratory OOS results and provide resolution.Proficiency in Microsoft Office including Excel, Word, and Outlook.Ability to work with mathematical concepts such as probability and statistical inference, and fundamentals of plane and solid geometry and trigonometry. Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations. Must have the ability to communicate effectively, verbally and in writing, with internal staff and management. Ability to respond professionally and scientifically to cross-functional partners, customers, regulatory agencies, certifying bodies or members of the business community. Ability to effectively present information to top management, public groups, and/or boards of directors. Must be able to demonstrate practical problem solving and trouble shooting skills. Must be able to demonstrate practical problem solving and trouble shooting skills. Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.Preferred QualificationsMaster's degree or Ph. D. in related field.Prior experience with implementation and maintenance of Laboratory Information Management Systems (LIMS).Manufacturing, Consumer Packaged Goods, ISO, and/or GMP experience in dietary supplement or food manufacturing.Knowledge of USP methods and requirements.Experience with lean laboratory practices.Six Sigma certification.Professional certification (CQE, CQA, or similar).Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

1. Inspect in-process or finished production assemblies and sub-assemblies for conformance to quality assurance standards
2. Working from blueprint, engineering change notices, or established operating procedures determine acceptance or rejection or rework requirements of a part
3. May evaluate new procedures for non-standard rest and perform special set-up on new equipment
4. Assist others in correcting or preventing deficiencies in quality or workmanship
5. Give work direction to other inspectors
6. Know your customers' expectations and drive action to meet them
7. Perform first article process
8. Identify component
9. Perform related work as assigned

1. PCBA Experienced
2. Able to use measurement equipment.
3. Must be able to read ECO/Dev instruction/build drawer and BOM.
4. Familiar with SMT and identify component, IPC 610 Knowledge and preferred IPC Cert. Familiar w/ First Piece and First Article process.

1. Attention to detail
2. Communication skills - verbal and written
3. Organized and good critical thinking skills
4. Data collection, management and analysis
5. Team work
6. Ability to interpret complex customer rules and regulations
7. Demonstrated skills in project management and ability to train others to lead projects
8. Works well independently
9. Excellent interpersonal and communication skills
10. Ability to manage time and prioritize multiple task in a fast paced environment
11. Proficient in use of MS Office applications
12. Knowledge of Lean manufacturing fundamentals

Quality Control Supervisor (Fremont, Austin)

Responsibilities:

1. Follow warehouse safety guidelines and all the policies.
2. Train inspectors on proper time/data completion.
3. Ensure inspectors follow safety guidelines, all the policies, and quality standards.
4. Conduct opening and closing briefing daily.
5. Allocate manpower based on clients' build plan and sort list.
6. Conduct sort and cycle time study.
7. Conduct quality audit and internal audit.
8. Audit lineside and warehouse inventory to ensure no un-certified stock is in shelf locations and order inventory in a timely manner.
9. KPI monitoring.
10. Manage timesheet, inspection report, and supervising inspectors' work and documentation.
11. Recommend any necessary adjustments and changes to production processes.
12. Communicate any issues to direct supervisor immediately.
13. Be punctual, competent, attentive, and responsible.

Requirements:

1. High School Diploma or equivalent required, College or above preferred.
2. Language: Fluent in English.
3. Proficient in Excel and Google Forms.
4. Ability to organize and plan ahead to maximize job efficiency and work safely.
5. Excellent communication skills.
6. Ability to travel between locations.
7. Able to work in warehouse and factory settings.
8. Can frequently and repetitively lift, push, and carry up to 50 lbs and climb a 10" step and back down.