Quality Control Technician Salary in California, USA

Resource Label Group, LLC is a leading full-service provider of label and packaging solutions with a diverse product offering which includes pressure sensitive labels, shrink sleeves, RFID/NFC technology, sustainable product solutions, scent activation technology, pharmaceutical packaging and fulfillment services. Resource Label provides products and services for the food, beverage, chemical, household products, personal care, nutraceutical, pharmaceutical, medical device, and technology industries. With twenty-seven locations across the U.S. and Canada, Resource Label Group provides national leadership and scale to deliver capabilities, technologies, systems, and creative solutions that customers require. As Resource Label Group continues to grow, we are always looking for talented individuals to join our team! Every person in our company contributes to our success. We offer an employee centric, collaborative culture that is technology driven and focused on delivering valuable, creative solutions. Our core values embody the way we interact with each other just as it influences the way we interact with clients. We are currently recruiting for a Quality Assurance Technician Trainee to join our team! The Quality Assurance Technician will be responsible for inspecting raw materials and work in process with finished goods to ensure compliance with product specifications.Preparing and implementing quality assurance policies and procedures.Performing routine inspections and quality tests.Identifying and resolving workflow and production issues.Developing quality standards, conducting tests, and identifying issues in the production of our products or services.Ensure that standards and safety regulations are observed.Address and discuss issues and proposed solutions with superiors.Document quality assurance activities and create audit reports.Make recommendations for improvement.Create training materials and operating manuals.Exhibits thoroughness and consistency when conducting quality control, testing, and audits.Is proactive in non-conformance prevention and maintains a desire to help the organization to consistently achieve high quality and service expectations.The overall job performance meets the satisfaction of the Quality Control Supervisor/Management Representative.Assists with nonconformance Return Material Authorization (RMA) investigations and continuous improvement initiatives. Assists in updating RMAs in the ERP system when requested by a manager.Attends scheduled meetings and training sessions as needed to support quality control activities and employee development.Conducts customer-specific, routine quality control and testing as identified on production tickets and checklists.Conducts testing and collects production performance data as needed in support of non-routine quality control checks. Adaptability - Adapts to changes in the work environment; Manages competing demands; Changes approach or method to best fit the situation; Able to deal with frequent change, delays, or unexpected events.Computer - Is computer literate and can utilize Microsoft office software; Possesses office equipment knowledge.Cost Consciousness - Works within approved budget; Contributes to profits and revenue; Conserves organizational resources.Customer Service - Manages difficult or emotional customer situations; Responds promptly to customer needs; Solicits customer feedback to improve service; Responds to requests for service and assistance; Meets Commitments.Interpersonal - Focuses on solving conflict, not blaming; Listens to others without interrupting; Keeps emotions under control; Remains open to others' ideas and tries new things.Teamwork - Balances team and individual responsibilities; Exhibits objectivity and openness to others' views; Gives and welcomes feedback; Contributes to building a positive team spirit; Puts success of team above own interests; Supports everyone's efforts to succeed.Oral Communication - Speaks clearly and persuasively in positive or negative situations; Listens and gets clarification; Responds well to questions.Reasoning Ability - Ability to apply common sense understanding to carry out instructions furnished in written, oral or diagram form. Ability to deal with problems involving several concrete variables in standardized situations.Judgment - Displays willingness to make decisions; Exhibits sound and accurate judgment; Supports and explains reasoning for decisions; Includes appropriate people in decision-making process; Makes timely decisions.Problem Solving - Identifies and resolves problems in a timely manner; Gathers and analyzes information skillfully; Develops alternative solutions; Works well in group problem solving situations; Uses reason even when dealing with emotional topics.Professionalism - Approaches others in a tactful manner; Reacts well under pressure; Treats others with respect and consideration regardless of their status or position; Accepts responsibility for own actions; Follows through on commitments.Planning/Organizing - Prioritizes and plans work activities; Uses time efficiently; Plans for additional resources; Sets goals and objectives.Although no positions answer directly to the Quality Technician, it is incumbent upon this position to cultivate and ensure effective relationships and communications with all departments within Resource Label Group to ensure the highest level of technical service is achieved. The Ideal Candidate Will Have: Excellent data collection and analysis skills.Strong attention to detail.Demonstrates accuracy and thoroughness.Looks for ways to improve and promote quality.Applies feedback to improve performance.Monitors own work to ensure quality.Adapts to changes in the work environment & manages competing demands.Changes approach or method to best fit the situation - able to deal with frequent change, delays, or unexpected events.Supports and explains reasoning for decisions while including appropriate people in decision-making process.Understands business implications of decisions. Displays orientation to profitability. Aligns work with strategic goals. Why work with us? Take a look at all we have to offer!Paid Time Off and Paid HolidaysComprehensive and Competitive Medical, Dental and Vision coverageCompany Paid Short-Term Disability Insurance and Life InsuranceAdditional Benefits - Long-Term Disability, Supplemental Life, Accident and Critical Illness Coverage PlansExcellent 401(k) retirement plan with generous company contributionWe pride ourselves in investing in our employees by offering onsite training and the ability to have unlimited growth potential within our organizationWe believe in rewarding our employees with performance-based salary increasesCheck out this video to learn more about us! https://vimeo.com/553408937/659ab4290f

***10 days of PTO + 6 paid holidays + Benefits*** APPLY TODAY!For immediate consideration, email your resume to ghermone @actalentservices.com Description:Write Standard Operating Procedures (SOPs) for Chemistry equipment calibration, cleaning, operation, and maintenance.Perform inventory for Chemistry chemicals and consumables. Creation of chemical hygiene plans.Collaborate with external vendors for equipment preventive maintenance and calibration.Review and approve investigations for determination of root cause, corrections, and corrective/preventative actions for deviations, excursions, and audit findings.Review of generated Chemistry raw data and approval of final reports.Develop staff to perform proper Root Cause Analysis and investigations.Additional Skills & Qualifications:3-5 years' experience in Quality Control Chemistry or Quality Assurance with a Chemistry focus - open to any CTL / CMO backgrounds, not industry specific, but pharma would be ideal, then non-sterile cosmetic, then food.Strong technical writing skills of procedures, policies, and work instructions.Ability to work independently.Experience Level:Intermediate LevelAbout ActalentActalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.Diversity, Equity & InclusionAt Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:Hiring diverse talentMaintaining an inclusive environment through persistent self-reflectionBuilding a culture of care, engagement, and recognition with clear outcomesEnsuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.

RESPONSIBILITIES:Kforce has a client in San Francisco, CA seeking a talented and highly motivated Quality Assurance Technician !! for a contract position. The ideal candidate has great communication skills,can remove roadblocks, detail oriented, and has a knack for breaking websites. Quality Assurance Technicians regularly work with Developers, Product Managers and other Quality Engineers to ensure the proper operation of the production environment. During the development cycle, the Quality Assurance Technician will identify use cases, create test cases, execute tests, and report results.REQUIREMENTS: BS in Computer Science or equivalent experience 2-4 years industry experience testing software, including website applications Strong verbal and written communication skills are essential Experience in building the test plans and test cases Experience running the manual regression for ongoing app releases Experience with QA process and Software Development Life Cycle Experience with Selenium highly desired The pay range is the lowest to highest compensation we reasonably in good faith believe we would pay at posting for this role. We may ultimately pay more or less than this range. Employee pay is based on factors like relevant education, qualifications, certifications, experience, skills, seniority, location, performance, union contract and business needs. This range may be modified in the future. We offer comprehensive benefits including medical/dental/vision insurance, HSA, FSA, 401(k), and life, disability & ADD insurance to eligible employees. Salaried personnel receive paid time off. Hourly employees are not eligible for paid time off unless required by law. Hourly employees on a Service Contract Act project are eligible for paid sick leave. Note: Pay is not considered compensation until it is earned, vested and determinable. The amount and availability of any compensation remains in Kforce's sole discretion unless and until paid and may be modified in its discretion consistent with the law. This job is not eligible for bonuses, incentives or commissions. Kforce is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.

Ipsen USA is the industry leader for versatile heat treatment systems and advanced process technology. Our advanced equipment is developed for Aerospace, Automotive, Energy, Medical, Tool & Die, and other various industries across the globe.Ipsen International IncDescription: Ipsen is a drug free workplaceAre you a maintenance mechanic with electrical experience looking for a change? Are you looking to move from repairing equipment to troubleshooting? We have the position for you! Come grow with Ipsen.SummaryThe Quality Control Technician troubleshoots and verifies new equipment performs properly, safely, and meets all contractual specifications. They accurately document all ISO paperwork used in furnace builds per prints and schematics. Ensures equipment is working effectively prior to shipping equipment to customers or Factory Acceptance Testing (FAT).Essential Duties and ResponsibilitiesSafely inspects large two door control cabinets while power is on utilizing electrical prints. Read and provide timely replies to supplier and intercompany emails.Compile data, create job folders and use the collected data to process orders accurately.Maintain all required ISO forms pertaining to Quality ControlEnsure proper cross-reference sales orders and spec sheets while processing orders.Perform inspection of new parts, program new parts, assure matching quantities based off bill of material and create packing slip.Work with engineering, production control, project management, and production to resolve issues.Adheres to company policies and procedures in regard to safety, attendance and tardiness. Up to 10% travel to customer sites for troubleshooting.Requirements: Knowledge, Skills and AbilitiesPossess strong attention to detail, accurately maintaining records and files.Ability to read, understand, and use electrical prints for equipment repair.Ability to read mechanical blueprints.Ability to use a voltmeter.Ability to use program VFD's and connect to PLC's using a laptop.Ability to troubleshoot industrial equipment in a broke-down environment.Possess strong math skills including ability to add, subtract, multiply, and divide in all units of measure. Possess strong analytical and problem-solving skills. Ability to safely and confidently work with 480/120-volt AC & 24-volt DC.Possess strong computer skills including MS OfficeEducation and ExperienceHigh School Diploma or equivalent required. Advanced education or related technical training beyond high school is strongly preferred. Prior experience working with and troubleshooting electrical systems is required. Prior experience working in industrial maintenance capacity strongly desired. Physical/Visual/Mental/ Environmental FactorsThe demands described 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. 1. Regularly required to sit and use hands and finger dexterity. 2. Occasionally required to stand, walk, stoop, kneel, crouch and reach with hands and arms.3. Required to climb ladders as well as climb on top of machinery with use of a harness.4. Occasionally required to lift up to 25 pounds.5. Regularly requires close vision, hearing and talking.6. Regularly exposed to loud noise level 7. Frequently exposed to moving mechanical parts All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. PI239586059

Innova Solutions is immediately hiring for a Quality Control Research Associate - II. Position type: Fulltime - Contract Duration: 13 Months Location: Santa Monica, California As a Quality Control Research Associate - II, you will: Job Description: All previous level plus: Conduct non-routine analysis of raw materials, intermediates, and finished product samples. Troubleshoot instrumentation and test methods. Assists in the training of QC staff as needed. Applies knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Working knowledge and proficiency with Microsoft Office software. Writes and executes protocols and reports. Evaluates equipment for purchase and performs installations and qualifications of the new instruments. Thank you! Deeksha Gupta Team Lead - Recruitment (+1) 213-788-7669 [email protected] RANGE AND BENEFITS: Pay Range*: $33-$35/Hour. *Pay range offered to a successful candidate will be based on several factors, including the candidate's education, work experience, work location, specific job duties, certifications, etc. Benefits: Innova Solutions offers benefits( based on eligibility) that include the following: Medical & pharmacy coverage, Dental/vision insurance, 401(k), Health saving account (HSA) and Flexible spending account (FSA), Life Insurance, Pet Insurance, Short term and Long term Disability, Accident & Critical illness coverage, Pre-paid legal & ID theft protection, Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP). ABOUT INNOVA SOLUTIONS: Founded in 1998 and headquartered in Atlanta, Georgia, Innova Solutions employs approximately 50,000 professionals worldwide and reports an annual revenue approaching $3 Billion. Through our global delivery centers across North America, Asia, and Europe, we deliver strategic technology and business transformation solutions to our clients, enabling them to operate as leaders within their fields. Recent Recognitions: One of Largest IT Consulting Staffing firms in the USA - Recognized as #4 by Staffing Industry Analysts (SIA 2022) ClearlyRated® Client Diamond Award Winner (2020) One of the Largest Certified MBE Companies in the NMSDC Network (2022) Advanced Tier Services partner with AWS and Gold with MS Website: https://www.innovasolutions.com/ Innova Solutions is an Equal Opportunity Employer and prohibits any kind of unlawful discrimination and harassment. Innova Solutions is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment on the basis of race, color, religion or belief, national origin, citizenship, social or ethnic origin, sex, age, physical or mental disability, veteran status, marital status, domestic partner status, sexual orientation, or any other status protected by the statutes, rules, and regulations in the locations where it operates. If you are an individual with a disability and need a reasonable accommodation to assist with your job search or application for employment, please contact us at [email protected] or (770) 493-5588. Please indicate the specifics of the assistance needed. Innova Solutions encourages all interested and qualified candidates to apply for employment opportunities. Innova Solutions (HireGenics/Volt) does not discriminate against applicants based on citizenship status, immigration status, or national origin, in accordance with 8 U.S.C. § 1324b. The company will consider for employment qualified applicants with arrest and conviction records in a manner that complies with the San Francisco Fair Chance Ordinance, the Los Angeles Fair Chance Initiative for Hiring Ordinance, and other applicable laws.

Description:RIX Industries is a technology-focused company specializing in the design, development and manufacturing of gas generation systems, precision compressor solutions, and cryogenic cooling technologies for critical applications in Marine, Aerospace, Land, Energy, Industrial, Medical, and Critical Infrastructure markets. Founded in 1878, the company is headquartered in Benicia, CA, and operates additional facilities in Sparks, NV and Rockville, CA.Position SummaryThe Quality Control Technician is primarily responsible for development and maintenance of the Quality System at RIX Industries.ResponsibilitiesReceive in process and final inspections as necessary to support company goals and schedule performance. Inspections and supporting actions and duties are described in the RIX Quality Control Manual.Determine the acceptability of parts, processes, repairs, and corrective actions taken to resolve deficiencies.Maintain inspection and other records as necessary to document and support the quality system requirements of the company. These records must be clear, concise and consistent with company requirements.Maintaining calibration and Government Property records. Document and implement necessary changes to assigned sections of the Quality Manual and System.Supplemental tasks and duties may from time to time be assigned inside and outside the area of Quality Control. These tasks and duties will be defined and assigned by the Quality Control Supervisor.All Other Duties as AssignedRequirements:Minimum QualificationsHigh School Diploma or equivalent.Ability to read and interpret complex blueprints. Proficiency in the use of precision measuring instruments and complex measuring equipment. Technical competence including knowledge of casting, machining, welding and assembly of complex mechanical equipment. Ability to read and understanding of corporate structure and how Quality Control affects corporate operations. General computer skills including knowledge of Microsoft Word, Excel and basic typing skills. Training or education in MIL I 45208A, MIL Q 9859A, and ISO 9000.Practical math skills, up to and including Geometry and Trigonometry.Undergraduate studies/AA.Ability to communicate with others to exchange information both orally and in writing.Citizenship: U.S. Citizen or qualified U.S. Person in accordance with ALU 22CFR 120.15. May require the ability to obtain DOD security clearance.Preferred QualificationsProficient in the use and programming of a Zeiss CMM, using Zeiss Calypso software highly desired.Three years' experience in visual, dimensional and mechanical inspection of precision parts. This includes castings, machined parts, process control and testing.Weld inspection experience as a certified Visual Weld Inspector, or certified Visible Dye Penetrant Inspector (for example, ASNT or AWS).Experience in heavy manufacturing and assembly operations.Physical Requirements & Work EnvironmentThis position is regularly exposed to the following conditions:Manufacturing, warehouse and office environmentsWhile working near moving equipment, mechanical parts and lift trucks; must have the ability to follow safe operating procedures.May be exposed to loud noise, fumes and/or toxic chemicals.Must have the following physical abilities:Ability to stoop, kneel, crouch, bend, stretch, reach, and lift.Ability to lift up to 50 pounds regularly.Ability to sit or stand for extended periods at a desk or table as well as machine tools or printers.Equal OpportunityRIX Industries is committed to a continuing program of equal employment opportunity. All persons have equal employment opportunities with RIX Industries, regardless of their sex, race, color, age, religion, creed, sexual orientation, national origin, ancestry, physical or mental disability, medical condition (cancer or genetic characteristics), marital status, gender (including gender identity or gender expression), familial status, military or veteran status, genetic information, pregnancy, childbirth, breastfeeding, or related conditions (or any other group or category within the framework of the applicable discrimination laws and regulations).PI239706458

At Cepheid, we are passionate about improving health care through fast, accurate, diagnostic testing. Our mission drives us, every moment of every day, as we develop scalable, groundbreaking solutions to solve the world's most complex health challenges. Our associates are involved in every stage of molecular diagnostics, from ideation to development and delivery of testing advancements that improve patient outcomes across a range of settings. As a member of our team, you can make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development.Cepheid is proud to work alongside a community of six fellow Danaher Diagnostics companies. Together, we're working at the pace of change on diagnostic tools that address the world's biggest health challenges, driven by knowing that behind every test there is a patient waiting.Learn about the Danaher Business System which makes everything possible.The Quality Control Analyst I is responsible for finished product testing activities in accordance with GMP standards and FDA/ISO regulations. In this role, an associate will have the opportunity to learn new laboratory skills, participate in efficiency projects, and pursue growth opportunities within the quality control department.This position is part of the Quality Organization and will be located in Lodi, California. At Cepheid, our vision is to be the leading provider of seamlessly connected diagnostic solutions.In this role, you will have the opportunity to:Perform and document laboratory testing of finished product per procedures.Conduct data analysis according to established methods and product specifications.Support continuous improvement of QC processes, laboratories, and overall work environmentThe essential requirements of the job include:High School Degree (or equivalent) with at least 1 year of related work experience, or an AA / Technical Trade Degree.Must be able to work in a high-throughput, fast-paced environment.It would be a plus if you also possess previous experience in:Handling biological and chemical materials in a lab environment and working with pipettes.Working in a GMP compliance environment.Cepheid, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at danaherbenefitsinfo.com.The hourly range for this role is $22.00 - $30.00. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. We may ultimately pay more or less than the posted range. This range may be modified in the future.This job is also eligible for bonus/incentive pay.We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what's next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.The EEO posters are available here.We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at [email protected] to request accommodation.

Job Title: Quality Control Research Associate - IILocation: Santa Monica, CADuration: 12+ MonthsDescription: All previous level plus: Conduct non-routine analysis of raw materials, intermediates, and finished product samples. Troubleshoot instrumentation and test methods.Assists in the training of QC staff as needed. Applies knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Working knowledge and proficiency with Microsoft Office software. Writes and executes protocols and reports. Evaluates equipment for purchase and performs installations and qualifications of the new instruments

Location: Commerce, CaJob Overview: Position responsible for verification of product quality through inspection of in-process product and observation of finished product for conformance to internal specifications, customer specifications as documented in the Quality Policy, within the mandates of the Quality Management System and supporting of the Quality Objectives.Responsibilities & DutiesPerform "First Article" inspection at initiation of manufacturing. Collect and inspect all samples to assure that required dimensional, physical and visual requirements are being verified and data is accurately recorded. Perform required testing to verify conformance of product to requirements.Record data as hard copy, electronically and in specified log books as required.Initiate Non-Conformance reports as required.Obtain and record retain and pre-shipment sample results as required.Support activities for CAPA, NCR, and customer complaint investigations.Proficient in the use of computers.RequirementsMust be able to speak, write, and understand English Minimum requirement of Associates degree.Excellent verbal and written communication skills.Proficient in the use of computers.Experienced in an ISO or FDA regulated industry a plus.Must be able to work in a team environmentExperience working with testing equipment (calipers, micrometers, etc) requiredAbility to speak, read, and comprehend the English language as determined through appropriate testing and/or the interview process.Mathematics and reasoning skills as determined through applicable aptitude and achievement tests.Shift:Thursday- Saturday 6 am-6 pm with alternating Wednesday's 6 am- 6pm.

Quality Control Chemist5 days on-siteSupport a well-established CDMO in Irvine, CA, while expanding on your analytical experience in a cGMP environment. Day to day:Analytical testing of raw materials, in-process samples, and final products Predominately utilize HPLC, as well as other analytical instrumentation Adhere to all SOPs and cGMP regulationsProvide peer review for other technician's dataMaintain and troubleshoot HPLC and other analytical instrumentationSupport equipment calibrationsAdditional relevant tasks as neededExperience:Bachelor of Science in Chemistry or related fieldExperience in pharmaceutical/biotech environmentExposure to working with small moleculesExperience working with HPLC