Quality technician jobs in Fremont, CA

Job Title: Battery Manufacturing Technician Pay Rate: Up to $36.66/hr DOE Zip Code: 95134 Job Type: Contract As a Battery Manufacturing Technician, you will be in a hands-on role assembling our battery packs for our aircraft. The battery production line is a mixture of automated and semi-automated processes, so you will be interacting with dispense systems, robot cells, and laser welding equipment. JOB RESPONSIBILITIES: * Work closely with the engineering teams to support equipment bring-up and process validation * Use manual, semi-automated, and automated equipment to build battery packs * Troubleshoot equipment and processes * Debug battery pack issues * Build basic lab fixtures and tools * Perform routine maintenance on equipment * Perform inspections and measurements of product dimensions using basic metrology tools, (calipers, micrometer, depth gauges, measurement microscope, etc…) Battery Manufacturing Technician REQUIRED QUALIFICATIONS: * Associate's Degree, or 5+ years in manufacturing or battery industry * Direct hands-on build experience with mechanical and electronic assemblies using technical documentation * High workmanship standards * Ability to follow formal build instructions and document deviations * Excellent documentation and written communication; proficient using Microsoft Office * Basic knowledge of drafting standards (read and interpret mechanical and electrical drawings) to produce parts and assemblies * Experience using measurement and inspection (caliper, micrometer, height gage, CMM…) * Familiarity with 5S or similar workplace organization methods * Experience following all aspects of maintenance safety protocol (LOTO, 5S, Arc Flash, etc.). Bonus Qualifications: * Direct experience building and testing high voltage battery modules and / or packs * Experience with battery end of line testing and battery cyclers * Direct experience programming and troubleshooting industrial automation (PLC, robots, gantries, etc…) If you are interested in this role, please apply via the apply now link provided. Our overriding goal is to provide quality staffing solutions that help people, organizations, and communities succeed. Belcan is a leading provider of qualified personnel to many of the world's most respected enterprises. We offer excellent opportunities for contract, temporary, temp-to-hire, and direct assignments. We are the employer of choice for thousands worldwide. For more information, please visit our website at Belcan.com Belcan is an equal opportunity employer. Your application and candidacy will not be considered based on race, color, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws.

Day-to-Day We are looking for a driven individual who thrives in a fast-paced dynamic work environment, being hands on and interacting with innovative, new and exciting tech. We can offer the opportunity to grow Electromechanical skills plus long term career growth opportunities. The Manufacturing Technician I will work on site 5 days a week in Santa Clara, CA. This person is primarily responsible for providing updates to the line lead/ engineers of build/work status. In addition, identifies problems with recommendations for improvement or correction. They will assist in modifying procedures to improve equipment operation or processes. They record assignments and prepare documentation concerning materials, parts used, concepts, designs, drawings, and processes. This role reports into the Surgical Robotics Manufacturing organization. Do you use your technical and interpersonal communication skills to work in group settings and seek out diverse perspectives with multi-functional team members? Join our team to take part in this unique and exciting new product introduction! Desired Skill Sets Works well with a diverse team of different skills sets. Willingness to learn and grow. 2+ years of experience as an assembler, tester, or associate of a Type I, II or III medical device company or complex electromechanical capital equipment manufacturer Understanding of Good Documentation Practices (GDP) Proficient at multiple assembly and test tasks while meeting requirements for workmanship, safety, and productivity Relevant demonstrated experience with anti-static/ESD principles and controls. Vocational training Certificate, Technical or associate's degree Experience with using Learning Management Systems such as cornerstone, AGILE PLM, MES, ERP experience (SAP, QAD, Camstar) Electrical troubleshooting experience such as proper use of Loctite, multimeter, isolation, grounding, use oscilloscope to aid problem solving. Compensation: $25.00/hr to $30.00/hr. Exact compensation may vary based on several factors, including skills, experience, and education. Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.

Ultimate Staffing is looking to hire Manufacturing Technicians to work at our customer's site in San Jose CA. Temporary and Temporary to Hire positions available. Responsible for operating and maintaining equipment used in the production of goods, ensuring quality standards and safety protocols are met. Duties include assembling components, monitoring machinery, performing inspections, documenting production data, and supporting process improvements. Technicians work in cleanroom or lab environments and follow strict SOPs, GMP, and safety guidelines. Ideal candidates are detail-oriented, mechanically inclined, and capable of working in fast-paced, team-driven settings. If you can work in a clean room environment and can follow GMPs, SOPs and have good Data Entry skills apply. Shifts available: Day: 6:30AM to 3:00PM Day: 8:00 AM to 4:30PM Day: 8:30 AM to 5:00PM 2nd shift: 6% Differential pay. 1:00PM to 9:30PM 2:30PM to 11:00PM Pay rate ranges $25 to $30 per hour DOE. Experienced R&D Technicians will be compensated according to experience. Desired Skills and Experience Ultimate Staffing is hiring manufacturing technicians to work onsite at our customer located in San Jose CA. All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

The Staff Quality Engineer is responsible for leading and sustaining the Corrective and Preventive Action (CAPA) process to ensure timely, effective, and compliant resolution of quality issues. This role drives root cause analysis, risk-based decision-making, and continuous improvement initiatives while maintaining adherence to internal policies, procedures, and regulatory requirements. The individual will collaborate across functions and work independently to design, implement, and optimize quality system solutions that enhance product reliability and process performance. Responsibilities and Duties • Support company goals, objectives, policies, and procedures to ensure alignment with quality and regulatory standards. • Lead and manage the entire CAPA lifecycle, including initiation, investigation, action planning, implementation, and effectiveness verification. • Serve as Subject Matter Expert (SME) for root cause analysis; provide guidance and training on structured problem-solving tools such as 5 Whys, Fishbone (Ishikawa), and Fault Tree Analysis to eliminate systemic issues. • Perform and support risk assessments (e.g., FMEA) and integrate risk management principles into CAPA activities and sustaining engineering changes. • Identify, prioritize, and implement proactive quality improvements to prevent recurrence of issues and enhance process robustness. • Collect, analyze, and trend CAPA and quality system metrics to identify patterns, drive continuous improvement, and report findings to management. • Communicate CAPA findings, progress, and outcomes effectively across cross-functional teams, ensuring transparency and accountability. • Create, revise, and review Standard Operating Procedures (SOPs) and related documentation to maintain compliance with latest regulatory standards • Assist with internal audits and management reviews, ensuring readiness for external inspections and regulatory audits. Requirements • Bachelor's degree in an engineering or related technical discipline or equivalent • Minimum of 7 years in Quality Assurance/Quality Engineering role within the Medical Device Industry • Proven experience with FDA 21 CFR Part 820, ISO 13485, and ISO 14971 standards. • In depth knowledge of CAPA process, requirements and investigational techniques • Working knowledge of design controls, risk management, process validation, and statistical techniques. • Proficiency in root cause analysis tools such as Ishikawa (Fishbone) diagrams, Fault Tree Analysis, Contradiction Matrix, and 5 Whys. • Ability to collect, review, and interpret data for trend analysis and continuous improvement. • Self-motivated, able to work independently, and driven to achieve results with a sense of urgency. • Effective at dealing with change and ambiguity as business needs shift, demonstrating flexibility while ensuring compliance. • Strong written and verbal communication skills; comfortable presenting to small and large groups. • Proficient in Microsoft Office Suite with advanced skills in Excel, PowerPoint, Visio, and Word. Salary Range: $154,000 - $165,000

You will have an opportunity to identify and own high impact projects to life saving medical devices. In this opportunity, you will independently support Commercial Operations to ensure the high-quality manufacturing of Class II/III interventional medical devices. This position will provide work with problems of advanced scope where the analysis of situation or data requires a review of identifiable factors. Work with collaborative teams to exercise good judgment to determine appropriate quality actions, and communicate and implement quality objectives. Specific Duties and Responsibilities •Support Commercial Operations and Manufacturing activities such as Incoming/In-process/Final Inspections, NCRs, CAPAs, Engineering Change Orders, Control Chart Investigations, Deviation Authorizations, and Equipment sustaining activities. •Support assigned manufacturing product lines and perform failure analyses and defect investigations as appropriate. •Execute and collaborate on Continuous Improvement efforts. •Execute and support supplier activities such as Second Source Qualifications, Supplier Changes, and SCARs. • Interface with other engineering departments within the company, and suppliers on quality related issues. • Collaborate and/or help lead in the development of manufacturing documentation. • Design, improve and support Test Methods, Testing Equipment and TMVs. • Recommend revisions to specifications, acceptance criteria, and manufacturing documentation to improve quality of product and/or Manufacturing Operations. • Provide guidance to junior Quality Engineers in support of departmental functions. • Perform responsibilities required by the Quality System and other duties as assigned or requested. •Ensure other members of the department follow the QMS, regulations, standards, and procedures. • Perform other work-related duties as assigned. Position Qualifications Minimum education and experience: • Associate's or Bachelor's degree in Engineering, a Life Science or a related field with 3+ years of quality engineering or relevant experience, preferably in a medical devices environment, or equivalent combination of education and experience Additional qualifications: • Familiarity with QSR, ISO, and other applicable regulations and laws required • Excellent verbal, written, and interpersonal communication skills required • Leadership skills desired • Proficiency with MS Word, Excel, and PowerPoint required Working Conditions • General office, laboratory, and cleanroom environments • Requires some lifting and moving of up to 25 pounds • The employee is frequently required to stand, walk, sit, and reach with hands and arms, and to use a computer, sitting for extended periods. Specific vision abilities required by this job includes the ability to read, close vision, distance vision, color vision, peripheral vision, and depth perception. • Alameda, CA • Starting Base Salary is $109,000/year to $152,000/year The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. What We Offer •A collaborative teamwork environment where learning is constant, and performance is rewarded. •The opportunity to be part of the team that is revolutionizing the treatment of some of the world's most devastating diseases. •A generous benefits package for eligible employees that includes medical, dental, vision, life, AD&D, short and long-term disability insurance, 401(k) with employer match, an employee stock purchase plan, paid parental leave, eleven paid company holidays per year, a minimum of fifteen days of accrued vacation per year, which increases with tenure, and paid sick time in compliance with applicable law(s). Penumbra, Inc., headquartered in Alameda, California, is a global healthcare company focused on innovative therapies. Penumbra designs, develops, manufactures, and markets novel products and has a broad portfolio that addresses challenging medical conditions in markets with significant unmet need. Penumbra sells its products to hospitals and healthcare providers primarily through its direct sales organization in the United States, most of Europe, Canada, and Australia, and through distributors in select international markets. The Penumbra logo is a trademark of Penumbra, Inc. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, age, disability, military or veteran status, or any other characteristic protected by federal, state, or local laws. If you reside in the State of California, please also refer to Penumbra's Privacy Notice for California Residents. For additional information on Penumbra's commitment to being an equal opportunity employer, please see Penumbra's AAP Policy Statement.

Alvah Contracting, LLC. Is owned by MasTec Inc. and is primarily located in the Bay Area of California. The principal office location is in South San Francisco, CA. The field operations are in Boulder Creek, Salinas, Benicia, Calistoga, Richmond, San Francisco, and Lincoln. An additional smaller operation is in the Midwest with offices in Wisconsin. Alvah Contracting has the primary Distribution Electric Contract for PG&E in the bay area and has been working in the area since 2007. We maintain PG&E's Overhead and Underground Electrical distribution system along with performing civil construction and providing traffic control services. Position Summary Due to rapid growth in our work with PG&E, we need a Document Quality Specialist to support our electric construction work by ensuring proper documentation of all work and timely resolution of any go-backs. The Quality Assurance Specialist reports to the Program Manager and supports both the Project Management and Field Operations team across the system. Job Responsibilities Accurately and effectively review as-built documentation Correct, combine, and sort all required documentation to be sent to Customer Communicate and dispatch go-backs to Field Operations team Ensure adherence to internal and external deadlines and documentation standards Track closeout and quality data in company's work management systems Send out weekly quality metrics to required stakeholders Create, understand, and improve documentation standards Work with team to identify and eliminate quality roadblocks to improve metrics Support Project Management and Field Operation teams with closeout and quality needs Qualifications Minimum: Data entry capabilities with speed and accuracy Attention to detail and ability to multi-task Prioritize and plan work activities and use time efficiently Competency in Microsoft applications including Word, Excel and Outlook Excellent organizational, verbal and written communication skills required Desired: Experience with similar duties a plus Track record of continuous process improvement

- Sr. Quality Engineer Full time About the Role: The Sr. Quality Engineer will implement and maintain FDA QSR (21 CFR 820) and ISO 13485 quality systems for the CellFX System and related medical devices, supporting R&D, manufacturing, regulatory, and clinical teams. Key Responsibilities: Provide quality and compliance guidance for product design and manufacturing. Develop and maintain quality systems, risk management (ISO 14971), and traceability documentation. Manage biocompatibility (ISO 10993) and sterilization (ISO 11135/11137) testing. Implement process controls, conduct statistical analyses, and support MRB activities. Review quality performance data and assist in labeling, UDI, and regulatory submissions. Support audits (FDA, Notified Body, MDSAP) and management reviews. Qualifications: BS in Engineering, Science, or related field; 5+ years of quality experience in Class II/III medical devices (cardiovascular preferred). Deep knowledge of FDA QSR, ISO 13485, MDR, ISO 14971, ISO 10993, and related standards. Experience from product development to commercialization. Strong analytical, communication, and problem-solving skills. Proficient in Microsoft Office; able to travel up to 10%.

About the Company At Presidio Medical, we are transforming the way neuromodulation balances the human nervous system and are striving to end the cycle of unnecessary pain and help patients live their best lives. Presidio's Ultra Low Frequency (ULF™) Neuromodulation System blends innovative circuit design, computational modeling, material science advancements and expertise in neuroscience and electrochemistry. Our therapy is designed to target localized pain by reducing neuronal responses.3 Suppression of these signals may ease pain for some patients suffering from nociceptive pain. Our focus is to break the cycle of constrained thinking about chronic nociceptive pain. Our goal is to create a world with less suffering - one that may offer relief to patients who have had limited therapeutic options. Position Summary: We are seeking an experienced and driven Senior/Staff Quality Engineer (Design Assurance) to play a key role in maintaining and enhancing our Quality Management System. This position is open to both Senior and Staff level candidates, offering a clear path for professional growth based on experience, technical depth, and leadership capabilities. You will ensure product quality and regulatory compliance by managing key processes from design through manufacturing. Key Responsibilities: Design & Development Support: Partner with R&D to establish quality requirements and support design verification & validation (V&V), including testing for sterilization, packaging, and shelf-life. Risk Management: Maintain the Risk Management File in accordance with ISO 14971. Staff-level candidates will be expected to lead this process for assigned projects. Product & Process Control: Oversee quality activities for production, including incoming inspection, in-process testing, and final product release. Manage non-conforming product and lead investigations. Supplier Management: Qualify new suppliers, maintain the Approved Supplier List (ASL), and manage the Supplier Corrective Action Request (SCAR) program. Corrective Action: Lead the CAPA process from initiation through investigation, implementation, and verification of effectiveness. QMS & Audits: Support internal and external audits. Staff-level candidates will act as a Subject Matter Expert (SME) during audits and help lead continuous improvement initiatives for the QMS. Mentorship: Staff-level candidates will provide guidance and mentorship to junior quality engineers. Comply with Presidio Medical's quality system requirements as well as any applicable regulatory requirements. Comply with all health and safety regulations, policies, and work practices. Other duties as assigned. Role Leveling: At the Senior Level, you are a proven, hands-on engineer who reliably executes and manages core quality subsystems with minimal supervision. At the Staff Level, you are a technical leader and subject matter expert who tackles more complex projects, leads risk management activities, mentors others, and represents the quality function as an audit SME. Qualifications & Experience: Bachelor's degree in Engineering or a related scientific field. 5+ years of quality engineering experience in the medical device industry for Senior level. 8+ years of progressive quality engineering experience for Staff level. Required for All Levels: Proven hands-on experience with design controls and a strong working knowledge of FDA 21 CFR 820, ISO 13485, and ISO 14971. ISO 13485 Lead Auditor certification is a plus. Strongly Preferred for Staff Level: Demonstrated expertise in developing and maintaining Risk Management Files. Experience with software V&V (SaMD experience is a plus). Proven experience as a subject matter expert during external regulatory audits. The final salary offered will be determined based on the candidate's professional experience, qualifications, and geographic location. Physical Demands: Varied sitting, standing, and walking. Ability to lift and carry 50lbs. or less. Range: $125,000 - $165,000.00 Note: This role is not sponsorship eligible. This role is based in San Mateo, CA ***Presidio Medical is not engaging with staffing agencies at this time***

Now Hiring: Senior Quality Engineer - Class II/III Medical Devices No Sponsorship Available SF Bay Area | Onsite $120K-$150K Base + Bonus + Stock Options I'm partnering with a cutting-edge Bay Area medical device innovator! They're looking for a well-rounded Senior Quality Engineer experienced in: Sterilization (EO, Radiation, Packaging Validation) Biocompatibility (ISO 10993) Risk Management (ISO 14971) Design Assurance, Design Controls, and 21 CFR 820 / ISO 13485 Compliance This is an exciting opportunity to work on Class II/III devices from concept through commercialization in a collaborative, innovation-driven environment. If you're a local Bay Area professional with a strong Quality background in medical devices, and you're open to an onsite opportunity, I'd love to connect and share more details. DM me! #QualityEngineering #MedicalDevices #BayAreaJobs #Biotech #MedTech #Hiring #Engineering #NoSponsorship

The Sr. Development Quality Engineer will serve as a technical representative providing design quality expertise to a product development team. Responsible for maintaining a strong collaborative partnership with cross-functional team members to achieve patient/user safety, customer satisfaction, and organizational success. RESPONSIBILITIES • Lead and/or support on-time completion of Design Control deliverables • Support the establishment of objective, measurable, and verifiable product requirements • Support Design Verification and Validation planning & execution, including any cross-functional investigation & resolution activities • Lead Risk Management activities from product concept through commercialization • Support test method development and lead test method validation activities • Support manufacturing process development & qualification for new product and design changes • Support the establishment of component specification definitions, supplied component sampling plan development, and vendor qualifications • Support biocompatibility and sterilization qualifications • Support audits and quality system improvement activities • Support Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and regulatory requirements. • Comply with Client, U.S. FDA, EUMDR and other requirements, as applicable. • Maintain positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and suppliers. Basic Qualifications: • Bachelor's degree in Engineering or Technical Field. • Minimum of 5 years of experience in R&D, Process/Manufacturing Engineering, and/or Quality with at least 2 years supporting product development. • Experience in medical devices and associated regulations/standards. • Experience in test method development and validation • Experience in preparing risk assessments, FMEA and other risk documents. Preferred Qualifications: • Advanced Degree in Engineering/Technical Field • Experience in active implantable medical devices. • Knowledge of requirements management tools (e.g., DOORS) and use of problem reporting systems (e.g., JIRA). • Working knowledge of statistics and its application to verification and validation? “Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.” If you are inclined, I would be happy to set up some time to chat more about your background and career interests to see if there could be a possible match. Please feel free to call me on ************ or send me email on ******************** Regards Niraj kumar

Job Title: Formulation Technician Duration: 12 Months Shifts: M-F from 6pm-2.30pm, $23.00/hr W2 M-F from 2pm-10.30pm, $25.30/hr W2 A Day in the Life: Testing of resin products on specialized instruments to meet customer demand. Responsible for the staging and compounding of raw materials within weight tolerances (e.g. micrograms to kilograms), milling, blending, aseptic liquid filling. Performs cleaning, inspection, calibration and assists in the maintenance of equipment. Maintains related logs and records. Performs equipment troubleshooting. Handles raw materials per GMP and Safety requirements. Uses equipment such as pipettors, balances, osmometer, turbidmeter and pH meters. QUALIFICATION REQUIREMENTS: Minimum of High School Diploma or equivalent. Minimum of 6 months experience in a high-paced laboratory environment or manufacturing facility. Must be able to read, write, and follow testing and inspection procedures. Able to follow batch record instructions and will be expected to weigh microgram to kilograms quantities of individual raw materials, calibrate equipment. Follow safety policies and procedures, operate milling equipment, perform sterile filtration and any other tasks required to complete cell culture media manufacturing. Standard product testing, such as osmolality, pH and turbidity, will also be performed in this job.

Helping an on-demand, autonomous ride-hailing company find Engineering Technicians to support operations and ensure the smooth flow of materials across product development and manufacturing. In this role, you'll work with a motivated, high-energy team to ensure timely project completion within the engineering lab. You'll support cross-functional teams developing next-generation products where success is measured by quality, precision, and adherence to schedule. The ideal candidate is enthusiastic, innovative, and self-motivated, with a strong commitment to craftsmanship and continuous improvement. You're comfortable working independently on routine tasks, following detailed processes, and maintaining a high standard of work with minimal supervision. As an Engineering Technician, you'll: Assist engineers during new product development to optimize manufacturing processes. Support engineers in developing solutions and alternative assembly techniques to resolve technical issues. Accurately assemble and test a range of electronic hardware, from engineering prototypes through short-run production. Act as a quality delegate by inspecting work from other technicians in the engineering lab. Perform final product testing in accordance with written procedures. Maintain a clean, organized, and safe work area. Communicate clearly and effectively to ensure accurate and complete information sharing. Demonstrate reliability through consistent attendance and punctuality. Roles and Responsibilities: Must be able to follow directions while closely adhering to process detail for each assignment. Assist engineers during the development of new products to optimize the manufacturing process. Assist Engineers in the development of solutions and alternative assembly techniques to resolve issues. Accurately assemble and test a variety of electronic hardware from engineering prototypes through short run production. Perform as a Quality Delegate, inspecting work from other technicians in the Engineering Lab Carry out assignments in a safe and efficient manner. Be informative and communicate in a way that is complete, accurate and clear. Maintain a consistent track-record of attendance and prompt arrival at work. Perform final product testing in accordance with written procedures. Ensure your work area and equipment is kept neat, clean, and well organized. Required Skills: Bachelor's Degree with 4 to 6 years' experience in electro-mechanical assembly. Technical training, such as soldering, trade school, or OJT classes (preferred). Ability to read technical documents and drawings. Working knowledge of Google Suit including Docs, Sheets, and Slides, experience using a computer for entering data, and using the internet Ability to communicate effectively in English Proficient using standard assembly tools: cutters, crimpers, soldering irons, pin insertion/removal tools, and torque tools Hands-on lab experience such as soldering, power supplies, signal generators, oscilloscopes. Proficient verbal and written English language skills and prior experience working with product development teams in a low volume manufacturing setting. IPC-610, IPC-620, or JSTD-10

Join Yorke Engineering, LLC, an Environmental Consulting leader in California that implements Environmental Engineering and Compliance solutions for our clients throughout California. Our mission is to solve environmental compliance problems for industrial and governmental/infrastructure facilities. We are a growing and dynamic organization of highly respected professionals. Yorke Engineering, LLC has assisted over 1,400 client organizations with their Air Quality and Environmental Compliance, Engineering, and Permitting needs. Our philosophy is to efficiently help government and industrial customers with the complex array of environmental laws and regulations. From simple permits to complex agency negotiations, from small companies to the largest of California's organizations, Yorke successfully solves our clients' Air Quality and Environmental challenges. Our team has over 1,000 years of combined environmental experience and consists of engineers and scientists that specialize in Air Quality, Waste, Water, CEQA, Safety, and Industrial Hygiene. We are looking for a sharp Mid to Senior level Air Quality Engineer/Scientist (Environmental Permitting and Compliance) to join our team in Northern CA. This is a full-time position at 40 hours per week from one of our Northern CA offices (Berkeley, San Francisco, or San Jose) during our normal business hours. We offer competitive salaries, a full benefits package including Paid Time Off, Holidays, Full Medical/Dental/Vision, along with a 401k program with a generous company match. Position Summary: The Mid to Senior level Air Quality Engineer/Scientist (Environmental Permitting and Compliance) performs professional engineering work, leading and executing the compliance and permitting functions in relation to Air Quality Regulations and Compliance. This candidate will be reviewing processes and equipment, analyzing permit-related technical and regulatory issues, and communicating those analyses within Yorke, the client organization, with government agencies and with the public at large. The work is challenging, broad in scope, and variable from project to project. The position involves effective communication, decision-making, and time management. The candidate performs other duties as required or assigned. The candidate's experience and qualifications we are seeking include: 5-15+ years of work experience in the Air Quality and/or Environmental industry in an engineering role (preferably in a consulting environment); Experience in the environmental services industry focusing on Air Quality services: Process and equipment review; Air quality permitting under BAAQMD, SCAQMD, SJVAPCD and other Air Districts, including Title V Permitting; RECLAIM implementation and reporting; Annual Emissions Reporting; Air Dispersion Modeling; Air Quality Assessments including Data Analysis and Emission Inventories; General Air Quality Compliance for facilities in CA. Ability to be an active team member on project teams towards project completion within project scope, budget and schedule and ensure quality work product and deliverables; Ability to work with clients, staff, and regulators through effective communication and expertise by fostering a collaborative environment without losing focus of quality; Proven track record or desire to engage in successful regulatory work in dealing with the SCAQMD, BAAQMD, SJVAPCD, EPA, CARB and/or other similar regulatory agencies; Experience or desire to work on-site at client facilities; Prepare reports and submissions in timely manner; Experience with handling highly technical data and technical data interpretation; Highly motivated to continue working in Air Quality environmental field and expand their knowledge and experience; CA Regulatory/Compliance experience is required. Job Requirements: B.S or M.S. degree in Chemical Engineering, Environmental Engineering, or Mechanical Engineering, or other relevant technical degrees from an accredited college (minimum GPA of 3.0); Ability to work collaboratively in a team fashion, handle several projects at once, prioritize work, and work efficiently; Desire to learn or developing technical expertise in environmental rules and regulations; Excellent oral and written communications skills; Experience in conflict resolution and crisis management; Track record of successful analysis, interpretation, and application of rules and regulations towards practical solutions; Ability to think critically and develop solutions; Software Knowledge: Strong Microsoft Excel, Word, Outlook, and Powerpoint skills (required); Microsoft 365 Applications, including Sharepoint (a plus) EIT, CPP or P.E. Certification (a plus).

Russell Sigler Inc. is a leading independent distributor in the HVAC industry, specializing in Carrier products for over 50 years. Our mission is to deliver exceptional service and products while fostering a supportive work environment for our employees. Position Summary: The Technical Engineer provides design, systems application, and proposal preparation. Works with outside sales engineers, territory managers, and customer contracting and engineering accounts. Responsible for a variety of tasks including equipment selection, job pricing, creation of bid projects, producing submittals, placing orders, and other key job responsibilities including but not limited to the following: Key Duties and Responsibilities: Provide high-level independent ownership of projects of varying size at the different stages of execution, sometimes from start to finish including design, vetting, bidding, submittals, and final release of order Read, interpret, and make pricing and technical equipment selections, and decisions based on contract documents, including but not limited to engineering specifications, engineered equipment schedules, and architectural/engineering plans Review of engineering design and contractual documents to identify areas of risk and compliance Utilize mechanical engineering to verify mechanical equipment is being applied and implemented within the intended and acceptable range of operation Estimating and proposal writing of complex commercial engineered equipment and automation projects Technical specification writing and review Design and application support of external consulting engineering firms for commercial and industrial construction projects Project site visits for engineering and application support of commercial equipment and automation. Offsite project and opportunity meetings with contractors, engineers, owners, and complementary trades Management of multiple time-sensitive deadlines simultaneously Coordinate between the contracting sales department and engineering sales department on design changes and strategy Interact and work closely on a daily basis with outside sales engineers, territory managers, engineering firms, contractors, owners, project coordinators, central bid desk, credit department, order entry department, customer assurance department, warehouse employees, and manufacturers Provide independent high-level direct support for certain contractors, engineers, and outside sales engineers Coordination and verification of multiple external vendors and internal departments to create complex single-package equipment and automation solutions Work among a team to complete a large array of projects in varying phases, delegating work among each other, and independently completing Participate in the development and maintenance of standard operating procedures Attend and participate in job meetings, sales meetings, and trainings Participate in the training of others within and outside of the department Self and group leadership of technical development training and education Critical Knowledge and Skills: Accuracy, analytical skills, and attention to detail are required Exceptional communication and customer service skills Detail oriented Multitasking and organizational skills Good judgment and planning skills Work independently with minimal supervision in a fast-paced work environment Research using systems, software and product guides, catalogs, and manufacturing literature Review, evaluate, and make suggestions and product recommendations to customers as well as provide technical support when needed Knowledge of HVAC Carrier Products is preferred Knowledge of Carrier software (Quote Builder, Sage, HVAC Partners, ECAT, vendor websites) is preferred Work in a constant state of alertness and a safe manner Education and Experience: BS in Engineering is required, a Mechanical Engineering degree is preferred Must have a minimum 3-5 years of HVAC industry and sales experience Pay Range: Starting at $70,000.00 annum. ** Russell Sigler, Inc. (Sigler) is an equal opportunity employer. All applicants will be considered for employment based on merit, qualifications, and business need **

Job Details Dynatect Ro-Lab - Tracy, CA Dynatect Ro-Lab - Tracy, CA Full Time High School $25.00 - $25.00 Hourly QA - Quality ControlDescription INFORMATION Department: Quality Reports to: Quality Manager Work Hours: Full-Time (approx. 40-hour workweek, Shift 1 or 2) FLSA Status NON-EXEMPT DESCRIPTION: The Quality Technician is responsible for performing required inspections of vendor supplied and Dynatect manufactured parts. These inspections are performed using criteria from applicable drawings, standards, specifications, and any other internal or external specified requirements. The Quality Technician is responsible for communicating with respective departments, vendors and individual employees to troubleshoot quality and process related issues. Additionally, the Quality Technician will be responsible for assisting and finding solutions to assigned internal and external complaints and corrective actions, and for assistance with identifying material and process non-conformances. The Quality Technician will also assist with continuous improvement projects that mitigate risk and ensure a quality product is delivered to the customer. PRIMARY RESPONSIBILITIES: Work in a safe and courteous manner. Perform product inspections. Perform calibration activities. Assist with resolving material and process non-conformities. Assist with continuous improvement activities. Promote and encourage a quality mindset in other employees. Attend Quality team meetings as scheduled. SECONDARY RESPONSIBILITIES: Perform other duties as assigned. SUPERVISORY RESPONSIBILITIES: None. Qualifications SKILLS AND ABILITIES Ability to keep accurate records. Be able to multi-task in a fast-paced environment. KNOWLEDGE AND EXPERIENCE Minimum of 3 years' experience in a manufacturing environment. Familiar with quality control and data analysis. Ability to follow documented procedures and standards. Proficient in Microsoft Office. Familiar with measurement equipment and its functionality.

At Niagara, we're looking for Team Members who want to be part of achieving our mission to provide our customers the highest quality most affordable bottled water. Consider applying here, if you want to: Work in an entrepreneurial and dynamic environment with a chance to make an impact. Develop lasting relationships with great people. Have the opportunity to build a satisfying career. We offer competitive compensation and benefits packages for our Team Members. Plant Quality TechnicianResponsible for executing corporate and plant specific Food Safety, Quality and Laboratory requirements. The QA Technician reports to QA Manager. In the absence of the Quality Assurance Technician, the QA Manager or designate will assume the job duties. Essential Functions Ensure all parameters of food safety and quality are being adhered to and maintained throughout the facility. Assist with batching chemicals/ingredients for production. Calibrate lab and line equipment for accurate results. Collect in-process and finished product samples. Conduct standardized qualitative and quantitative testing to ensure it meets specifications. Perform aseptic testing for microbial contamination. Follow protocols for documenting testing results. Recognize deficiencies and initiate proper follow-up. Identify and isolate product that does not meet standards. Aid in troubleshooting deficiencies and non-conformances. Review food safety and quality records. Actively participate in plant teams (HACCP, Safety, etc.) Conduct other duties as assigned by management. Please note this job description is not designed to contain a comprehensive list of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without prior notice. Qualifications Minimum Qualifications: 0 Years - Experience in Field or similar manufacturing environment 0 Years - Experience in Position 0 Years - Experience managing people/projects *experience may include a combination of work experience and education Must read, write and communicate in English. Must be able to work 12 hour shift (days or nights) on a rotating schedule Must follow GMP Policy - wear company issued shirt, hat, safety glasses, earplugs and hairnet in production areas. Able to lift up to 50 lbs. Able to work under pressure in a very fast paced environment Preferred Qualifications: 2 Years- Experience in Field or similar manufacturing environment 2 Years - Experience working in Position 2 Years - Experience managing people/projects *experience may include a combination of work experience and education Competencies This position embodies the values of Niagara's LIFE competency model, focusing on the following key drivers of success: Lead Like an Owner Makes safety the number one priority Keeps alert for safety issues and escalates immediately Effectively prioritizes tasks based on department goals Shows respect to others and confronts interpersonal issues directly Prioritizes resolution of customer issues effectively Responds promptly and honors commitments to internal and external customers InnovACT Makes recommendations to continuously improve policies, methods, procedures, and/or products Demonstrates adaptability by reacting appropriately to unexpected changes in situations or circumstances Increases performance through greater efficiency Find a Way Seeks to develop technical knowledge through learning from other experts Understands interdepartmental impact of individual decisions and actions Seeks solutions rather than placing blame Empowered to be Great Consistently looks for ways to improve one's self through growth and development opportunities Communicates clearly and promptly up, down, and across Communicates effectively to manage expectations Education Minimum Required: High School Diploma Preferred: Associate's Degree Certification/License: Required: N/A Preferred: HACCP Foreign Language Required: Full Professional Proficiency Preferred: None Required Typical Compensation Range Pay Rate Type: Hourly$23.52 - $31.16 / Hourly Benefits *********************************************** * *Los Angeles County applicants only** Qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers, the California Fair Chance Act, and any other applicable local and state laws. Any employment agency, person or entity that submits a résumé into this career site or to a hiring manager does so with the understanding that the applicant's résumé will become the property of Niagara Bottling, LLC. Niagara Bottling, LLC will have the right to hire that applicant at its discretion without any fee owed to the submitting employment agency, person or entity. Employment agencies that have fee agreements with Niagara Bottling, LLC and have been engaged on a search shall submit résumé to the designated Niagara Bottling, LLC recruiter or, upon authorization, submit résumé into this career site to be eligible for placement fees.

You will have an opportunity to identify and own high impact projects to life saving medical devices. In this opportunity, you will independently support Commercial Operations to ensure the high-quality manufacturing of Class II/III interventional medical devices. This position will provide work with problems of advanced scope where the analysis of situation or data requires a review of identifiable factors. Work with collaborative teams to exercise good judgment to determine appropriate quality actions, and communicate and implement quality objectives. Specific Duties and Responsibilities •Support Commercial Operations and Manufacturing activities such as Incoming/In-process/Final Inspections, NCRs, CAPAs, Engineering Change Orders, Control Chart Investigations, Deviation Authorizations, and Equipment sustaining activities. •Support assigned manufacturing product lines and perform failure analyses and defect investigations as appropriate. •Execute and collaborate on Continuous Improvement efforts. •Execute and support supplier activities such as Second Source Qualifications, Supplier Changes, and SCARs. • Interface with other engineering departments within the company, and suppliers on quality related issues. • Collaborate and/or help lead in the development of manufacturing documentation. • Design, improve and support Test Methods, Testing Equipment and TMVs. • Recommend revisions to specifications, acceptance criteria, and manufacturing documentation to improve quality of product and/or Manufacturing Operations. • Provide guidance to junior Quality Engineers in support of departmental functions. • Perform responsibilities required by the Quality System and other duties as assigned or requested. •Ensure other members of the department follow the QMS, regulations, standards, and procedures. • Perform other work-related duties as assigned. Position Qualifications Minimum education and experience: • Associate's or Bachelor's degree in Engineering, a Life Science or a related field with 3+ years of quality engineering or relevant experience, preferably in a medical devices environment, or equivalent combination of education and experience Additional qualifications: • Familiarity with QSR, ISO, and other applicable regulations and laws required • Excellent verbal, written, and interpersonal communication skills required • Leadership skills desired • Proficiency with MS Word, Excel, and PowerPoint required Working Conditions • General office, laboratory, and cleanroom environments • Requires some lifting and moving of up to 25 pounds • The employee is frequently required to stand, walk, sit, and reach with hands and arms, and to use a computer, sitting for extended periods. Specific vision abilities required by this job includes the ability to read, close vision, distance vision, color vision, peripheral vision, and depth perception. • Alameda, CA • Starting Base Salary is $109,000/year to $152,000/year The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. What We Offer •A collaborative teamwork environment where learning is constant, and performance is rewarded. •The opportunity to be part of the team that is revolutionizing the treatment of some of the world's most devastating diseases. •A generous benefits package for eligible employees that includes medical, dental, vision, life, AD&D, short and long-term disability insurance, 401(k) with employer match, an employee stock purchase plan, paid parental leave, eleven paid company holidays per year, a minimum of fifteen days of accrued vacation per year, which increases with tenure, and paid sick time in compliance with applicable law(s). Penumbra, Inc., headquartered in Alameda, California, is a global healthcare company focused on innovative therapies. Penumbra designs, develops, manufactures, and markets novel products and has a broad portfolio that addresses challenging medical conditions in markets with significant unmet need. Penumbra sells its products to hospitals and healthcare providers primarily through its direct sales organization in the United States, most of Europe, Canada, and Australia, and through distributors in select international markets. The Penumbra logo is a trademark of Penumbra, Inc. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, age, disability, military or veteran status, or any other characteristic protected by federal, state, or local laws. If you reside in the State of California, please also refer to Penumbra's Privacy Notice for California Residents. For additional information on Penumbra's commitment to being an equal opportunity employer, please see Penumbra's AAP Policy Statement.

As the Sr. Quality Engineer, you will participate in the implementation and maintenance of QSR (21 CFR 820) and ISO 13485 quality systems and qualification activities of CellFX System, surgical disposable and reusable medical devices in support of the Company's research and development, manufacturing, regulatory, and clinical affairs efforts. In addition, this individual will support the development and implementation of quality systems and compliance activities. To Make An Impact, You Will: Provide expertise and guidance to product development and manufacturing teams in the areas of design assurance, design controls and compliance. Develop, establish, and maintain quality engineering methodologies, systems and practices that our' customer and regulatory requirements. Lead the risk management process in establishing risk management plan, conducting risk evaluation and analysis, and creating risk management report. Lead the process in establishing product traceability matrices, conducting requirement trace verification and analysis, and creating trace matrix reports. Manage all aspects of biocompatibility testing and sterilization including creating of test protocols and executing of testing. Proactively investigate, identify, and implement best-in-class quality engineering practices. Identify and implement effective process control systems to support the development, qualification, and on-going manufacturing of products to meet or exceed internal and external requirements. Develop and validate measurement methods, monitor design control standards, facilitate, and perform statistical analysis, and participate in MRB as appropriate. Lead the review of process and product quality performance, working in concert with various departments. Assist with development of product labeling, UDI compliance, translation, and investigator brochures for commercial and clinical studies. Design and implement methods and procedures for inspecting, testing, and evaluating components, sub-assemblies, and final assemblies. Support management review activities, regulatory audits including Notified Body audit (MDSAP) and assist with preparation of regulatory submissions. Carry out responsibilities in accordance with the organization's policies and applicable laws. Support the Quality Policy and Quality System. To Excel, You Will Bring: BS degree in Engineering, Science or a related field. 5 years of progressive quality engineering experience with Class II/III products in the medical device industry. Cardiovascular device experience is strongly preferred. Must have extensive work experience with FDA QSR (21 CFR Part 820 & Part 11) and ISO 13485/MDR requirements are required. Must have extensive knowledge and experience in Risk Assessment (ISO 14971) practices and implementation. Knowledge and experience in ISO 10993 standard series (Biocompatibility), AAMI/ISO 11135 & 11137 (EO & Irradiation sterilization), ISO 11607 & ASTM D4169 (Sterile Packaging & Performance Testing). Hands-on experience with medical devices from development through commercialization is highly desirable. Experience working in a start-up environment a plus. Mastered the use of quality disciplines, tools, and methodologies. Proficient knowledge and skill in Microsoft Office Suite applications. Excellent oral written communication skills and critical thinking skills. Ability to work conscientiously and with minimal direction, using good judgement, taking initiative to accomplish short and long-range projects, and recommend actions with minimal direction. Ability to work as a team member, multi-task and be very flexible to adapt to the ever-changing work priorities and requirements of a dynamic, fast-growing company. Ability to travel up to 10% of the time. Overnight and/or international travel may be required. Ability to lift 10-15 pounds.

Now Hiring: Senior Quality Engineer - Class II/III Medical Devices No Sponsorship Available SF Bay Area | Onsite $120K-$150K Base + Bonus + Stock Options I'm partnering with a cutting-edge Bay Area medical device innovator! They're looking for a well-rounded Senior Quality Engineer experienced in: Sterilization (EO, Radiation, Packaging Validation) Biocompatibility (ISO 10993) Risk Management (ISO 14971) Design Assurance, Design Controls, and 21 CFR 820 / ISO 13485 Compliance This is an exciting opportunity to work on Class II/III devices from concept through commercialization in a collaborative, innovation-driven environment. If you're a local Bay Area professional with a strong Quality background in medical devices, and you're open to an onsite opportunity, I'd love to connect and share more details. DM me! #QualityEngineering #MedicalDevices #BayAreaJobs #Biotech #MedTech #Hiring #Engineering #NoSponsorship