Quality control analyst jobs in East Wenatchee, WA

About Us: BlackSky is a real-time intelligence company. We own and operate the world's most advanced space-based intelligence platform and provide customers satellite imagery, automated analytics and high-frequency monitoring of strategic locations, economic assets and events from around the globe. BlackSky is trusted by the most demanding allied military and intelligence organizations and commercial companies to deliver foresight into critical matters that affect national security and the economy. BlackSky's data enables governments and businesses to see, understand and anticipate change as it happens, giving them the ultimate strategic advantage so they can act quickly. Our global team works with cutting-edge technology to make a difference around the world and prides itself on being people-first, customer-focused and fun. BlackSky is looking for a talented and creative Senior Image Annotation/Quality Control Analyst to support the development, operation, and capability evolution of Spectra AI, BlackSky's cutting edge AI/ML Platform. As part of the machine learning team, you are instrumental in shaping our computer vision products by managing the quality of data that trains AI/ML models. You will help manage and grow the entire labeling process that trains Spectra AI, overseeing remote data labeling teams and actively assessing the quality of trained models, which create critical timely insights for our customers. While the locations listed in the job posting are ideal, we would love candidates near either our Herndon, VA or Seattle, WA offices. We may also consider remote candidates in certain states. Responsibilities: Lead and manage data labeling teams, providing oversight for labeling campaigns. Research for AI product development, identifying geographic areas where objects exist, developing object ontologies, building annotation instructions, and identifying imagery for annotation. Collaborate with machine learning and product teams to define metrics, assess, and report on the quality of machine learning models in development and production using statistical and quality assurance approaches. Work with the machine learning and product teams to define and measure the performance of machine learning models against SLAs. Identify customer requirements and liaise with computer vision team to codify specifications for training datasets. Create processes, tools, and scripts to manage and track data quality and labeling performance. Take part in the entire project lifecycle from requirements development to deployment. Innovate and streamline data annotation processes. Other job-related duties as assigned. Required Qualifications: Minimum of five (5) years of hands-on experience as a data quality engineer, imagery analyst, GIS analyst, or quality assurance engineer in the space of satellites, computer vision, or machine learning. Bachelor's Degree or higher in one of the following fields: computer science, GIS, data science, mathematics, physics, statistics, or another scientific field. Experience interpreting satellite imagery to identify objects, behaviors, or activities and working with GIS datasets. Hands on experience with annotation platforms such as LabelBox, SuperAnnotate, AWS Sagemaker, or CVAT. Experience managing remote annotation workforces such as CloudFactory, Hive, or iMerit. Collaborates well with others and able to communicate ideas to those with other backgrounds. Experience with quality assurance practices, model testing & evaluation, and computing metrics & statistics from data. Attention to detail and ability to define, enforce, and follow rigorous process controls for managing data. The program this role will support requires Us-born citizenship. Preferred Qualifications: Experience with AI advancements in image annotation such as the Segment Anything Model (SAM). Embeddings and other AI Assistance tools. Experience writing code and scripts, especially for processing and evaluating large amounts of data. Proficiency with Python for automation and data manipulation tasks. Knowledge and experience working in an AWS Cloud environment. Demonstrated ability to lead and manage small teams. Ability to obtain and maintain a US security clearance. Life at BlackSky for full-time US benefits eligible employees includes: Medical, dental, vision, disability, group term life and AD&D, voluntary life and AD&D insurance BlackSky pays 100% of employee-only premiums for medical, dental and vision and contributes $100/month for out-of-pocket expenses! 15 days of PTO, 11 Company holidays, four Floating Holidays (pro-rated based on hire date), one day of paid volunteerism leave per year, parental leave and more 401(k) pre-tax and Roth deferral options with employer match Flexible Spending Accounts Employee Stock Purchase Program Employee Assistance and Travel Assistance Programs Employer matching donations Professional development Mac or PC? Your choice! Awesome swag The anticipated base salary range for candidates in Seattle, WA is $100,000-115,000 per year. The final compensation package offered to a successful candidate will be dependent on specific background and education. BlackSky is a multi-state employer, and this pay scale may not reflect salary ranges in other states or locations outside of Seattle, WA. BlackSky is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action Employer All Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, sexual orientation, gender identity, disability, protected veteran status or any other characteristic protected by law. To conform to U.S. Government space technology export regulations, including the International Traffic in Arms Regulations (ITAR) you must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. Department of State. #LI-Remote EEO/AAP/ Pay Transparency Statements: ***************************************************************** ************************************************************************************************

Jubilant HollisterStier LLC, Spokane's Largest Manufacturing Company, and well-established member of the business community, provides a complete range of services to support the pharmaceutical and biopharmaceutical industries. Jubilant HollisterStier is a nationally recognized contract manufacturer of sterile injectable vials, and lyophilized products. The Allergy business is a worldwide leader in the manufacture of allergenic extracts, targeted primarily at treating allergies and asthma. Jubilant HollisterStier is a proud member of the Jubilant Pharma family. Our Promise: Caring, Sharing, Growing We will, with the utmost care for the environment and society, continue to enhance value for our customers and stakeholders by providing innovative products and economically efficient solutions' through growth, cost effectiveness and wise investment of resources. Job Description: The QA Compliance Associate provides support to the company Deviations, Corrective and Preventive Action (CAPA) program through a complete assessment of Root Cause Analysis (RCA) of Deviations and vendor complaints/issues. Assure product compliance and product safety. Ensure accurate and timely data entry and oversight of the company Quality Systems related to Deviations, CAPA and vendor complaint activities. * Review Deviations, investigations and CAPAs to ensure accuracy, consistency and compliance with applicable SOPs/Policies, Specifications and related guidelines/regulations. * Accountable for facilitating Deviations investigation/resolution, assessing product impact and for completing/writing final assessment/lot disposition for QA Management and Client review and approval. * Enters data into database in support of the corporate RCA and CAPA activities. * Provide oversight of investigational RCA group activities including preparation of meeting agenda, providing necessary information to meeting participants, publishing of meeting minutes, and follow-up on agreed upon activities and tasks. * Interface with management and responsible individuals to assure task completion on or before established due dates. * Responsible for supporting quality systems, processes and procedures (e.g. Deviations, CAPA, Vendor complaint, etc…) to assure compliance and product quality and safety. * Accountable for assisting the QA and applicable Department Management to ensure and follow up on implementation of corrective actions that stem from deviations, audit or regulatory inspections. * Provide Deviations and CAPA metrics as needed in support of management review of system data. * Work extensively with appropriate department(s) to gain an understanding of the production/analytical testing process and other applicable process to ensure capture of appropriate details and conclusions in the investigation or corrective action documents. Qualifications: * Associates Degree in Biology, Chemistry or related field required. * 5 years of experience may be used in a lieu of an Associate's degree required * Bachelor's Degree in a science field desired. * Sologic Certificate desired * Minimum 2 years of experience required. Bachelor's degree can be used in lieu of experience. * Pharmaceutical and FDA regulated industry experience desired. * Experience with technical writing, investigations, CAPA systems, building & manufacturing processes/systems, and QC analysis is highly desired. * Direct or supporting aseptic manufacturing experience in bio/pharma industry desired. * Microsoft Word & Excel experience required. * Knowledge of cGMPs desired. Shift: Weekday Days, Monday - Friday Compensation & Benefits: This is an on-site, full-time position located in Spokane, WA. * Hiring Wage: $30.99 - $41.93 hr. depending on experience, with opportunity for growth, promotion and annual raises. Midpoint and above is reserved for employees who have longevity with Jubilant HollisterStier and consistently exhibit outstanding performance over a period of time in the role * Medical, Dental, Vision, Flexible Spending and Health Savings Accounts * Life, AD&D, Short and Long Term Disability * 401(k) with company match * Generous paid time off plan * Employee Assistance Program Unlock your potential with Jubilant HollisterStier! If you're seeking a dynamic and rewarding career, we welcome your application today! ******************************** * Please click on the Spokane, Wa. Link* Jubilant HollisterStier is an EEO/AA Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If you require assistance applying for a position, please contact our HR Department at: ******************************

Kenvue is currently recruiting for a: QA Associate I-Investigations What we do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we're the house of iconic brands - including NEUTROGENA , AVEENO , TYLENOL , LISTERINE , JOHNSON'S and BAND-AID that you already know and love. Science is our passion; care is our talent. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage - and have brilliant opportunities waiting for you! Join us in shaping our future-and yours. For more information, click here. Role reports to: Supervisor 1, Quality Assurance Location: North America, United States, Pennsylvania, Fort Washington Work Location: Fully Onsite What you will do The QA Associate I - Investigations is accountable to supporting the investigation and CAPA process that pertains to the QC laboratories, facilities, manufacturing and packaging operations in addition to guidance on compliance and Good Manufacturing Practice (GMP) to meet company procedures, standards and regulatory expectations. This position assures that non-conformance investigations, laboratory investigations and quality systems are in compliance with the good manufacturing practices and good laboratory practices as established in the code of local government regulations and company procedures. Supports multiple functions in providing sound and timely decision making by utilizing root cause analysis, statistical, and problem-solving tools. Through the investigation process, this position will identify significant compliance issues and prioritize for action. Responsible for supporting the monitoring of investigation and CAPA systems, effectiveness, and continuous improvement of the Investigation /CAPA system at the Fort Washington site and Network / Global levels, as required. Ensures Investigation / CAPA Corrective and preventative Quality System compliance as established in 21 Code of Federal Regulations (CFR) 210 and 211 Current Good Manufacturing Practices (cGMP) regarding quality methods and manufacturing and packaging processes and procedures. Ensures that the process meets all internal and regulatory quality standards. Key Responsibilities Initiates deviations, performs root cause analysis, conduct investigations to assess impact on products and process, recommends product disposition and recommends change controls and CAPA's as needed. Investigate process deviations through discussion with all applicable parties, such as: Manufacturing Ops, Tech Ops, Packaging Ops, and Maintenance. Draft reports to summarize the details surrounding the deviations for input into the EtQ Symphony system. Prepare draft investigations and investigational protocols as required. Ensure all investigations are drafted to meet site specified timelines and are completed prior to release of associated product(s). Make recommendations for corrective and/or preventative actions and discuss with applicable parties, such as: Manufacturing Ops, Tech Ops, Packaging Ops, and Maintenance. Participate in cross functional meetings related to investigations, CAPAs and product disposition as applicable to assist in identifying and eliminating daily challenges on compliance that affect the quality of the product. Assist in monitoring corrective/preventative measures to confirm effectiveness. Assist QA Release group and Operations to determine/understand their needs in order to support investigations. Participate in other projects/initiatives as assigned. What we are looking for Required Qualifications Bachelor's degree in a relevant field or equivalent. Requires 0-2 Years Work Experience Prior experience in liquid manufacturing in an OTC or Pharmaceutical facility. (Plant QA experience preferred) Experience with working effectively in a team-based environment. Good problem-solving skills, willing to dig deep to understand underlying issues. Excellent written and verbal communication skills. Self-directed to manage priorities and adhere to deadlines Clear and effective communication skills Strong experience using the Microsoft Office suite of applications (Word, Excel, PowerPoint) Desired Qualifications Familiarity with quality systems, regulations, and business impact. Understanding of quality frameworks and processes. Experience with audits, inspections, and corrective action plans. Experience with LIMS, SAP, and EtQ is preferred. What's in it for you Annual base salary for new hires in this position ranges: $61,880.00 - $87,360.00 This takes into account a number of factors including work location, the candidate's skills, experience, education level & other job-related factors. Competitive Benefit Package* Paid Company Holidays, Paid Vacation, Volunteer Time & More! Learning & Development Opportunities Kenvuer Impact Networks This list could vary based on location/region *Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process. Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on merit without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.

Our Bank Operations team is seeking a bank operations quality control specialist to fill a temporary assignment on-site in Tacoma, Washington . This position is responsible for completing deposit account quality control reviews in a timely and accurate manner, while providing quality customer service to internal/external customers. This assignment is a Full -Time on-site role, Monday through Friday 8:00 a.m. to 5:00 p.m. for approximately 180 days (December 2025 through May 2026). As a temporary employee, you will be eligible to participate in a 401(k) plan with company match, accrue sick time, and will have access to the Employee Assistance Program. Salary Range: $23.00 - $28.00 hourly The Role at a Glance: Performs quality control review for all new deposit accounts, maintenance of deposit accounts, and safe deposit boxes to ensure compliance with internal procedures and regulatory requirements. May assist with second review of bank operations high risk maintenance activities to ensure accuracy and adherence to procedure and controls. May assist with the review of department/branch general ledger reconciliations and transaction processing. May participate in the quality control review of high-risk areas including dormant account processing, negotiable instrument certifications, SOX controls and regulatory customer communications. May assist with the review of critical maintenance reports for monetary and non-monetary transactions to ensure all transactions are appropriate and supported by applicable documentation. Understands and maintains working knowledge of, and ensures bank activities are performed in compliance with, all state and federal banking laws and regulations applicable to assigned area. Understands and comply with all policies, procedures, standards and guidance relevant to assigned job responsibilities. Core Skills and Qualifications: 3+ years of recent experience in a branch and/or bank operations support role required. Working knowledge of applicable rules and regulations, report review functions and current working knowledge across various functional bank operations areas i.e., deposit operations, item processing, dormant account review, compliance strongly preferred. High School Diploma or equivalent required. Associate's degree or higher in Accounting of Finance preferred. Equivalent combination of education, experience, and training in a relevant role may be considered. Provides an exceptional level of quality service for internal and external customers and responds to customers' needs, questions and concerns in an accurate, effective, and timely manner. Effective listening verbal, written and telephone etiquette business communication skills, with the ability to read, write, speak and understand English well. Working knowledge and understanding of banking policies, procedures, and terminology related to banking laws and regulatory requirements applicable to various deposit accounts and operations. Working knowledge of deposit documentation, with the ability read/interpret documents or authorizations, ensuring accurate data input and/or approvals have been attained. Working knowledge of bank accounting practices including the understanding of debit/credit relationships; math skills to calculate interest, balance accounts and locate routine mathematical errors. Detail oriented with strong organizational and time management skills; with the ability to manage multiple assignments, ensuring that priorities are set and commitments and deadlines are met, with direct and/or moderate oversight. Excellent analytical ability, data review and processing skills, with the ability to identify and resolve exceptions and interpret data. Unquestionable integrity in handling sensitive and confidential information required. Proficient knowledge and use of MS Office products (Word, Excel, Outlook) and retrieval of data, with the ability to adapt to and learn new products and technologies quickly. Recent working knowledge of financial services systems and experience utilizing digital servicing and client file management applications, i.e., FISERV / DNA - required. Working Environment/Conditions: Climate controlled office environment. Work involves being able to concentrate on the matter at hand, under sometimes distracting work conditions and frequent employee and/or customer contacts and interruptions during the day. Work requires regular attendance, punctuality and adherence to agreed-upon schedule with willingness to work a flexible and/or rotating schedule and or extended hours, and assist at other locations or remotely, as needed. Physical Demands/Effort: Work may involve the constant use of computer screens, reading of reports, and sitting throughout the day. Ability to operate a computer keyboard, multi-line telephone, photocopier, scanner and facsimile which often requires dexterity of hands and fingers with repetitive wrist and hand motion. Typically sitting at a desk or table; intermittently standing, stooping, bending at the waist, kneeling or crouching to file materials. Occasional lifting and/or moving up to 10 lbs. (files, boxes, etc.). The above statements are intended to describe the general nature and level of work being performed and are not an exclusive list of all qualifications for this position. Heritage Bank is an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran status, disability, or any other basis protected by applicable law. Job applicants have certain legal rights. Please click here for information regarding these rights. If you need assistance completing the online application, please email: ******************************* Salary Range Disclaimer The base salary range represents Heritage Bank's current salary range for the position / assignment. Actual salaries will vary depending on factors including, but not limited to, qualifications, experience, and job performance. ##JobCategory:Bank Operations## ##Street:3615 Pacific Ave## ##City:Tacoma## ##State:WA## ##ZipCode:98418## ##Internal:false## *mon

A successful biotech company is looking for an experienced and detail-oriented Associate to join our Quality Assurance team on site in Bothell, WA. Unfortunately at this time no relocation or visa sponsorship provided. At ELITechGroup, we are committed to supporting health systems globally. We take pride in our team and strive to maintain a work environment that is both professionally challenging and personally fulfilling. As a valued member of our team, you would contribute to the manufacturing and distribution of in vitro diagnostic products to clients in over 100 countries. You will have the opportunity to work alongside some of the brightest minds in the industry, as our team is dedicated to solving problems and delivering excellent products. This position is ideal for someone with some experience in the biotech industry and audits, who takes pride in learning all aspects of the job and adhering to procedures and standards. You will receive guidance from a supportive team that will ensure you are trained and capable of performing your responsibilities effectively. The primary focus of the QA Associate role is to support commercial production to ensure consistent compliance with regulatory and industry expectations. Assist the QA department in maintaining the Quality focused culture by ensuring documentation is complete, accurate and that Batch records are executed in accordance with approved and effective standard operating procedures and specifications. Summary With direction, has part of the responsibility for ELITechGroup MDx Quality Assurance activities. Essential Duties and Responsibilities * Performs review of manufacturing batch records, enter information in Disposition Log, filing of batch records, and ensure the records are complete and stored in a manner where they are readily retrievable. * Performs finished product inspection. * Performs review and approval of labels. * Reviews SPEC sheets, enter information in Disposition Log, file. * Assists QA with the tracking and/or completion of CAPAs and Customer Complaints. * Assists QA with the tracking and/or completion of NCRs, OOSs, TMPs. * Assigns part numbers. * Reviews, tracks, and files training forms. Ensures the training log is updated. * Reviews calibration/maintenance records, update tracking log, file. * Ensure the records are complete and stored in a manner where they are readily retrievable. * Participates during audits (FDA, ISO, vendor) * Assists Document Control, (assign CC and document numbers, assist in obtaining approvals, auditing external documents, etc.) when necessary. * Other duties and task as assigned. Competencies To perform the job successfully, an individual should demonstrate the following competencies: Organizational Support - follows policies and procedures; completes administrative tasks correctly and on time; supports organization's goals and values. Quality - Demonstrates accuracy and thoroughness; monitors own work to ensure quality. Written Communication - writes clearly and informatively; able to read and interpret written information. Qualifications The requirements listed below are representative of the knowledge, skill, and/or ability required. * Bachelor's degree (B.A. or B.S.), or equivalent combination of education and experience. * Minimum of 2 years' experience in working in an FDA or ISO regulated environment or equivalent training. * Knowledge of ISO 13485, ISO 9001, and FDA QSR preferred

Job Title: QC Associate Scientist - Raw Materials Shifts: Days, Friday to Monday, 8:00am/8:30am till 5:00pm/5:30pm, Some flexibility required for business needs. About Us: this is who we are At Just Evotec Biologics, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, learning from each other, and pushing the boundaries of what's possible. We're on a mission to create a place where curiosity isn't just encouraged-it's celebrated. Are you someone who asks questions, seeks answers, and isn't afraid to go deeper? #BeCureious with us and see where your curiosity can take you! The Role: / your challenge, …in our journey We're looking for a passionate and curious QC Associate Scientist - Raw Materials to join our team. If you're excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you'll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories. As a QC Associate Scientist - Raw Materials at Just Evotec Biologics, you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It's a role where your curiosity will fuel both your personal growth and the success of the team. Position The role provides the inspection, sampling, and QC analysis of raw materials and supplies in support of our GMP manufacturing operations. What You'll Do: * Perform routine/non-routine QC testing using by techniques such as cell-based assays, ELISA, and qPCR. * Ensure timely and accurate completion of GMP documentation. * Collaborate with Supply Chain, Supplier Quality, Materials Management, and external contract laboratories to qualify and release raw materials. * Conduct laboratory investigations, deviations, OOS, change controls and CAPAs * Support equipment qualification (IQ, OQ, PQ). * Create, maintain, and revise SOPs, methods and associated documents. * Support all operations of the QC labs including the ordering supplies and maintaining laboratory equipment and lab spaces. * Support client audit/inspection readiness plans and interact with regulatory agencies during inspections on analytical related matters. * Participate in daily and weekly operation meetings. Who You Are: * Bachelor's degree in chemistry or related science with 0-3 years experience in related field (GMP experience preferred). * Knowledge of current instrumentation and procedures used in an analytical laboratory. * High attention to detail and organized. * Experience with Microsoft Office apps (Word, Excel, PowerPoint). Why Join Us: * Growth Opportunities: We're a company that believes in continuous learning and development. Whether it's professional courses, mentorship, or new projects, we'll help you grow. * Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life. Site based Redmond. * Inclusive Culture: We're committed to building a diverse and inclusive environment where everyone's voice is valued, and curiosity is encouraged. * Innovative Projects: You'll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success. * A Place for Big Ideas: We don't just talk about thinking outside the box-we throw the box away. If you've got ideas, we want to hear them. Are You Still Curious? If you've read this far, then chances are you've got a curious mind-just like us. So, what are you waiting for? Take the leap and apply today. We can't wait to see where your curiosity leads you-and how it will shape the future of Just Evotec Biologics. Let your curiosity guide your career-#BeCurious and explore the endless possibilities at Just Evotec Biologics! The base pay range for this position at commencement of employment is expected to be $78,000 to $83,000; Base salary offered may vary depending on the individual's skills, experience and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, flexible work, generous paid time off and paid holiday, wellness and transportation benefits. Evotec (US) Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.

Job Title: QC Associate Scientist - Raw Materials Shifts: Days, Friday to Monday, 8:00am/8:30am till 5:00pm/5:30pm, Some flexibility required for business needs. About Us: this is who we are At Just Evotec Biologics, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, learning from each other, and pushing the boundaries of what's possible. We're on a mission to create a place where curiosity isn't just encouraged-it's celebrated. Are you someone who asks questions, seeks answers, and isn't afraid to go deeper? #BeCureious with us and see where your curiosity can take you! The Role: / your challenge, …in our journey We're looking for a passionate and curious QC Associate Scientist - Raw Materials to join our team. If you're excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you'll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories. As a QC Associate Scientist - Raw Materials at Just Evotec Biologics, you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It's a role where your curiosity will fuel both your personal growth and the success of the team. Position The role provides the inspection, sampling, and QC analysis of raw materials and supplies in support of our GMP manufacturing operations. What You'll Do: Perform routine/non-routine QC testing using by techniques such as cell-based assays, ELISA, and qPCR. Ensure timely and accurate completion of GMP documentation. Collaborate with Supply Chain, Supplier Quality, Materials Management, and external contract laboratories to qualify and release raw materials. Conduct laboratory investigations, deviations, OOS, change controls and CAPAs Support equipment qualification (IQ, OQ, PQ). Create, maintain, and revise SOPs, methods and associated documents. Support all operations of the QC labs including the ordering supplies and maintaining laboratory equipment and lab spaces. Support client audit/inspection readiness plans and interact with regulatory agencies during inspections on analytical related matters. Participate in daily and weekly operation meetings. Who You Are: Bachelor's degree in chemistry or related science with 0-3 years experience in related field (GMP experience preferred). Knowledge of current instrumentation and procedures used in an analytical laboratory. High attention to detail and organized. Experience with Microsoft Office apps (Word, Excel, PowerPoint). Why Join Us: Growth Opportunities: We're a company that believes in continuous learning and development. Whether it's professional courses, mentorship, or new projects, we'll help you grow. Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life. Site based Redmond. Inclusive Culture: We're committed to building a diverse and inclusive environment where everyone's voice is valued, and curiosity is encouraged. Innovative Projects: You'll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success. A Place for Big Ideas: We don't just talk about thinking outside the box-we throw the box away. If you've got ideas, we want to hear them. Are You Still Curious? If you've read this far, then chances are you've got a curious mind-just like us. So, what are you waiting for? Take the leap and apply today. We can't wait to see where your curiosity leads you-and how it will shape the future of Just Evotec Biologics. Let your curiosity guide your career-#BeCurious and explore the endless possibilities at Just Evotec Biologics! The base pay range for this position at commencement of employment is expected to be $78,000 to $83,000; Base salary offered may vary depending on the individual's skills, experience and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, flexible work, generous paid time off and paid holiday, wellness and transportation benefits. Evotec (US) Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.

JOB TITLE: Research Chemist REPORTS TO: Senior Chemist STATUS: Full-time, exempt SALARY RANGE: $85,000-$95,000/year based on experience and qualifications BENEFITS: Medical, dental, and vision insurance, optional FSA/HSA, 401k with 6% employer match, life and AD&D insurance, Employee Assistance Program, short & long term disability, tuition reimbursement, 21.67 days of paid time off + 10 holidays About Tidal Vision: We believe that sustainability should not require customers to compromise on price, convenience, or performance. Our mission is to create positive and systemic environmental impact by making our biopolymer solutions cost competitive, more convenient, and better performing than the synthetic chemicals we displace. We value innovation and take pride in challenging the status-quo; we choose to view obstacles as opportunities. We value new ideas and encourage the team to apply creativity and invent new solutions to meet challenging demands. We foster open, direct communication, and a collaborative working environment through our unique approach to work culture. We value our employees and demonstrate that through our compensation and benefits programs and opportunities for growth and development. About Tidal Vision's Unique Work Culture: Tidal Vision strives to build and invest in the highest performing and most innovative team. We put our people and customers above process, avoid company-wide rules as much as possible, and have the courage to take unusual approaches to advance our mission. With this approach, we believe we can create a more flexible, fun, stimulating, creative, collaborative, and innovative organization. Our commitment to developing, practicing and promoting direct and open communication, responsibility and freedom, and leading with and seeking context is a responsibility for every role at Tidal Vision. JOB SUMMARY: The Research Chemist will directly assist a Senior Chemist with research projects, focusing on chitin and chitosan biopolymer chemistry, and including polymer synthesis and modification. The Research Chemist will be responsible for preparing experimental recipes and following experimental strategies as directed by the Senior Chemist, as well as performing chemical analysis. The position will also participate in experimental strategy sessions, project reviews, and directed and self-directed literature reviews. ESSENTIAL JOB FUNCTIONS: Prepare experimental recipes as directed by the Senior Chemist Follow experimental strategies and designs as directed by the Senior Chemist Perform chemical analysis at the direction of the Senior Chemist or the analytical chemistry team Participate in experimental strategy sessions and project reviews Conduct directed and self-directed literature reviews focusing on topics of industrial interest Maintain laboratory equipment and ensure proper functioning Maintain accurate records of experimental procedures and results Collaborate with other members of the research team to achieve research goals Communicate research findings to the Senior Chemist and other members of the research team Prioritize laboratory safety, green chemistry, and sustainable industrial practices Provide vocal feedback throughout the research process BASIC QUALIFICATIONS: Graduate degree in Chemistry, Biochemistry, or related field and/or 2+ years demonstrable experience in chemical synthesis/functionalization projects Laboratory experience involving biochemistry and/or biopolymers Strong organizational skills and attention to detail Strong written and verbal communication skills specific to a laboratory setting Positive attitude towards sustainable and green practices Ability to work independently and creatively in a scientific environment Licensing & Special Requirements Incumbent is subject to a criminal background check WORKING CONDITIONS & PHYSICAL REQUIREMENTS Most of the work is performed in a laboratory environment. Sitting or standing for long periods may be required. The ability to hear, smell, and move freely is critical to the safety for this role. Proper PPE is required. Tidal Vision provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. The statements contained herein reflect general details as necessary to describe the principal functions of this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements. Individuals may perform other duties as assigned including work in other functional areas to cover absences or relief, to equalize peak work periods, or otherwise to balance the workload. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of the employer.

Quality Assurance Associate at Lumen Bioscience - . Join Lumen as a QA Associate for Qualification Support in this temporary position. In this role, you'll support our Quality Assurance team in commissioning, qualification, and validation (CQV) activities that ensure compliance with pharmaceutical cGxP quality system processes. You'll contribute to equipment qualification workflows, maintenance management, and documentation that enable Lumen's commitment to quality excellence. You'll perform tasks including document management, record review, preventative maintenance coordination, and SOP authoring. You'll work within 21 CFR part 210/211 standards, manage qualification documentation in our electronic quality management system (eQMS), and collaborate across manufacturing and quality control teams to maintain equipment readiness and regulatory compliance. Duties and Responsibilities: Support QA Associate and QA Specialist in commissioning, qualification, and validation (CQV) related tasks. Perform scanning and archival of CQV documents and records. Review maintenance and calibration related records for accuracy and completeness. Work with manufacturing and quality control to ensure timely completion of preventative maintenance and calibration activities. Assist with writing or reviewing qualification and validation standard operating procedures (SOPs). Assist with writing or reviewing operation and maintenance procedures. Determining equipment qualification gaps for manufacturing and quality control. May assist in the preparation of CQV metrics reports. May assist with the investigation and triage of CQV related deviations, CAPAs, or other quality events. Qualifications & Requirements: Educational Background: Bachelor's degree in a relevant scientific field, and/or experience in a cGXP or other regulated environment. Technical Knowledge: Knowledge of relevant cGMP, ISO 9001, and ICH requirements as it relates to equipment and qualification. Technical Skills: High proficiency in Microsoft Word, Excel, and SharePoint. Personal Attributes: Well-organized, detail-oriented, strong technical skills, excellent written and verbal communication skills. Strong interpersonal skills and the ability to effectively collaborate with others in a dynamic team environment. Physical Requirements: Ability to sit and stand for extended periods (2+ hours each). Occasionally lift or carry items up to 20 kg. Benefits at Lumen Bioscience: Free onsite parking or public transportation subsidies. At Lumen Bioscience, we foster a collaborative and innovative work environment where your contributions directly impact biotechnology and global health solutions. Join us and play a vital role in maintaining exceptional quality standards and regulatory compliance. Compensation Range $27 - $30 USD

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Measures, records, analyzes and interprets testing data of product for quality attributes in a production setting. Actively participates, supports and performs training on the requirements of SQF, GMP and HACCP programs. Applying computer skills including but not limited to Microsoft Office: Excel, Word, etc. Follows & participates in plant housekeeping guidelines designed to ensure a safe work environment. Assists in the planning, implementation, documentation and reporting results of routine sampling, trial runs, environmental testing, and prepares test samples. Prepares routine and special reports- including gathering, summarizing and interpreting data. See lists of tasks. Applies basic understanding of equipment and processes in resolving & preventing Quality problems. Advises production personnel of quality problems & works together with Supervision to develop and implement corrective and preventive action plans. Assist in investigating customer complaints. Maintain laboratory and equipment. Performs other related duties and tasks as needed. QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions.

Job Description Number of openings: 1 Fulltime, Year Round and 1 Fulltime Temporary Working Shift: Day Shift Hours & Work Days: 11:00 am - 8:00 pm, Monday - Friday; May vary depending on production. Current Stemilt employees if interested may apply in the Human Resource Department. Qualifications: Must be able to lift at least 40 lbs. Must be flexible with working schedule. Must have knowledge of Stemilt grades and standards. Must have the ability to use a calculator and perform basic math functions. Must have the ability to read and write English. Must have excellent communication skills. Duties: Will take fruit samples and evaluate them for bruising and defects. Will also be driving to different Stemilt locations. Additional duties may be assigned based on department needs.

The Company: Pacific Aerospace & Electronics (PacAero) is seeking an entry-level Diode Technician I to join our team. A successful candidate is committed to pushing the boundaries of technology, performance, and innovation. Join us and connect your career to the future! PacAero's core businesses include an array of electronic connectors and housings for the world's most extreme environments. PacAero is primarily located in Wenatchee, WA with a remote manufacturing site, Bonded Metals, located in Sequim, WA. Working together, we employ proprietary technologies, best practices engineering, and specialized manufacturing techniques to produce hermetic connectors and electronic packaging that perform in the world's most extreme environments. PacAero's products are hard at work in medical components, such as cardiac-function devices, on key aerospace & defense programs, in space and deep below the earth's surface. The Position: The QC Inspector I is responsible for performing in-process and final inspections of product to verify conformance with internal quality standards and customer requirements. Schedule: Monday through Friday, 6am to 2:30pm Primary Responsibilities Work cooperatively with all employees. Willingness to adapt work schedule to company needs. Consistently at work and on time. Perform other miscellaneous duties as assigned. Observe safety regulations and follow protective equipment requirements. Report hazardous observations to your lead or supervisor. Comprehend and follow all parts handling requirements. QC Inspector I responsibilities Demonstrate a basic ability to read and comprehend drawings and applicable inspection documentation. Perform the following inspection tests for First Article, In Process and / or Final Inspection. Initiate Nonconformance Reports as required. Perform product identification and traceability activities as required (Material and Process certification retrieval). Review shipping paperwork for completeness and accuracy. Follow daily clean up and housekeeping procedures. Comply with all quality, safety, and work related rules and regulations. Benefits: At PacAero, we strive to create an inclusive and supportive work environment, and our benefits package is a reflection of this commitment. Our benefit offerings include: Insurance Benefits: We provide our employees with access to a comprehensive benefits package that includes medical, dental, and vision insurance, critical illness, hospital indemnity, and long-term care to ensure they can prioritize their health and well-being. Paid Time Off (PTO): We believe in the importance of work-life balance, so we offer generous PTO allowances that accrue with each pay period so that our employees can rest and recharge, spend time with family and friends, or pursue personal interests. Paid Holidays: We recognize the importance of spending time with loved ones during holidays, so our employees receive paid holidays to celebrate and enjoy these moments. Growth Participation Units (GPUs): We provide growth participation units (GPUs) to our employees, which represent a share of the company's growth and success. Our GPUs are issued to all employees and as we increase the value of our business, they grow in value as well. When our current private equity firms sells the company, GPUs will be paid out, with all employees sharing in the profits from the sale. 401(k) w/ Matching: We offer a 100% match, up to 4%, to help our employees save for their future. Short-Term & Long-Term Disability Insurances: We want to ensure that our employees are protected in case of unexpected circumstances, and provide short-term & long-term disability insurances, entirely employer paid. Tuition Reimbursement: We believe in continuous learning and development and offer tuition reimbursement to support our employees' educational goals. Additional Perks: Our employees enjoy a range of additional benefits such as dependable work schedules, overtime opportunities, term life & AD&D insurance, corporate gym membership discounts, and more. Due to ITAR Requirements, all PacAero employees must be classified as US Persons and are required to show proof upon hire. *U.S. Person as defined by 22 C.F.R. 120.15 of the ITAR: U.S. Person means a person who is a lawful permanent resident as defined by 8 U.S.C. 1101(a)(20) or who is a protected individual as defined by 8 U.S.C. 1324b(a)(3). It also means any corporation, business association, partnership, society, trust, or any other entity, organization or group that is incorporated to do business in the United States. PacAero provides equal employment opportunity to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, veteran status, or any other characteristic protected by federal or state law. Requirements Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and / or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essentials functions. Essential: Read, write, speak and comprehend the English language. Good computer skills. Must be able to retain information. Must have legible handwriting. Dependability: Follows instructions, responds to management direction. Takes responsibility for own actions. Identify process improvements. Requires minimal supervision to perform everyday tasks. Demonstrates strong independent thinking with problem solving skills. Effectively give completion dates. Support company/management decisions. Offers help when needed. Understanding of the effects of process deviation. Able to advise management of policy violations. Basic math skills. Seeks out duties to ensure you are consistently productive. Consistently meets company minimum labor efficiency rates. Education/Previous Experience Requirements High School graduate or equivalent. Work Environment Contaminants: Works with hazardous chemicals. Protective gear: Personal protective equipment (PPE) is a requirement for safety. Shift work: Must be flexible to work any of the following shifts: Mon-Fri 6am-2:30pm and Mon-Fri 2:30pm-11pm. Physical Requirements: Standing/Sitting: Able to sit and/or stand for extended periods of time. Manual dexterity: Fine motor skills and hand-eye coordination are necessary for manipulating tools and performing precise measurements with a Microscope. Precision and vision: Specific vision ability to have natural or corrected near distance acuity in at least one eye. Capable of passing the Jaeger Number 2 test and a color vision test. In addition, all employees of PA&E are expected to: · Promote teamwork and cooperative effort · Maintain a clean, safe, and unobstructed work area · Understand and apply appropriate quality improvement processes Salary Description $19/hr

Full-time Description : Redi-Bag is a leading manufacturer in the plastic bag industry, committed to delivering high-quality and sustainable packaging solutions. We are seeking a dedicated and detail-oriented Quality Technician to join our team at the plastic extrusion plant. Job Description: We are looking for a Quality Technician to play a critical role in ensuring the quality and consistency of our plastic bag production. The ideal candidate will have a strong understanding of quality control processes, attention to detail, and a commitment to upholding the highest standards of product integrity. Requirements Key Responsibilities: · Conduct quality inspections and checks on plastic bags at various stages of the production process. · Document and report any quality issues, defects, or deviations from specifications to the Quality Manager. · Perform measurements, tests, and visual inspections to verify product conformance to quality standards. · Collaborate with production and maintenance teams to address and resolve quality-related issues. · Assist in the development and implementation of quality control procedures and guidelines. · Read and interpret quality specifications, work instructions, and testing procedures to ensure compliance. · Participate in root cause analysis and continuous improvement initiatives to enhance product quality and consistency. Qualifications: · High school diploma or equivalent; relevant technical certifications or experience in quality control is a plus. · Strong attention to detail and the ability to conduct thorough and accurate quality inspections. · Good communication skills and the ability to work collaboratively with cross-functional teams. · Basic understanding of measurement tools, testing equipment, and quality control techniques. · Ability to read and interpret quality specifications, work instructions, and testing procedures. · Familiarity with quality management systems and a commitment to continuous improvement. Benefits: · Competitive salary and benefits package · Opportunities for career development and advancement within the organization · A positive and collaborative work environment focused on quality and innovation Application Process: To apply for the Quality Technician position, please submit your resume and a cover letter outlining your relevant experience and qualifications. Pay: $22.00 to $26.00

Temp Understand/interpret order sheets and product descriptions to ensure accuracy Coordinate various products to load on trailers (up to 20 trailers per day) Responsible for accurate counts and product quality Work in a team REQUIREMENTS Excellent math skills Excellent communication skills, must be able to read, write and comprehend information, reports, instruction and correspondence Excellent reasoning ability, be able to apply common sense and understand detailed or oral instructions, problem solving skills Forklift experience Be able to push, pull, bend, twist and grip heavy packaged product by hand as well as by forklift Positive attitude Pay starts at 10.60 1205 Prudential Blvd , Cowlitz, WA 98632, United States of America

We are SGS - the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 98,000 employees operate a network of 2,650 offices and laboratories, working together to enable a better, safer and more interconnected world. * Prepare and analyze samples according to SGS' analytical SOPs using instrumentation specific to the department and analytical methodologies. * Perform analytical measurements that are both accurate and precise. * Work independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. * Understand and apply basic analytical chemistry principles. * Make standards and reagents as required and document work appropriately. * Use and update LIMS to track and manage workload. * Follow safe practices and maintain a safe working environment. * Work with the Senior Analysist to manage workload. * Apply technical judgment to determine potential problems for samples. * Calibrate instrumentation * Process and report analytical results. * Update and load work into LIMS. Use LIMS for appropriate background information. * Use technical judgment to determine the appropriate analytical approach for various sample matrices. * Appropriately use lab applications. * Track instrument quality control. * Appropriately follow safety, operational integrity and quality control requirements for the work that is done. Qualifications * BS degree with relevant lab classes or equivalent experience - Required * Environmental laboratory experience - Preferred Additional Information The hourly rate for this position is $21.63-$24.97. This position is eligible for overtime pay. In addition, your compensation package includes the following benefits: * Participation in the Company's benefit programs coincident or following the first of the month in which you are hired. * Immediate eligibility to participate in the Company's 401K Retirement Plan * Paid vacation * Four (4) floating holidays annually * Seven (7) company observed holidays paid * Sick time accrual SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required. This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time. If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call ************ for assistance and leave a message. You will receive a call back. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.

The J.R. Simplot Company is a diverse, privately held global food and agriculture company headquartered in Boise, Idaho. We are a true farm-to-table company with an integrated portfolio including food processing and food brands, phosphate mining, fertilizer manufacturing, farming, ranching and cattle production, and other enterprises related to agriculture. Summary The Microbiology Laboratory Technician position is based at the Moses Lake Campus and operates within the Columbia Basin Factory. Reporting directly to the onsite Microbiology Lead, this role supports microbiological laboratory operations as part of Simplot's Global Food Safety and Quality program. Key responsibilities include sample collection, preparation, testing, result interpretation, and data entry for a variety of sample types-finished food products, in-process materials, water, environmental surfaces, and swabs. The technician will play a vital role in supporting microbiological testing across three factory locations: Moses Lake, Othello, and Columbia Basin. Key Responsibilities This position follows a 4-day, 10-hour shift schedule with alternating workdays to support continuous 7 day a week lab coverage. Operate independently within a small, fast-paced factory microbiology laboratory, consistently completing assigned tasks with minimal supervision. Conduct microbiological testing on finished food products, in-process materials, water samples, environmental swabs, surface swabs, and allergen testing when applicable. Responsibilities include sample collection, preparation, testing, result interpretation, and accurate data entry. Travel daily to Othello and Moses Lake factory locations using a company-provided vehicle to collect samples of finished products, in-process materials, and environmental swabs. Perform core laboratory duties such as media preparation, biohazard waste containment and disposal, scheduled cleaning, and basic equipment maintenance. Communicate effectively with Microbiology Lead, Global Food Corporate Microbiology, Quality Assurance, and factory personnel to ensure alignment and clarity. Maintain and report real-time test results and records in accordance with Global Food Laboratory corporate standards, including timely data entry into the Laboratory Information Management System (MMS). Responsible for gaining proficiency in the Enviromap environmental monitoring system across all three factory sites, including a thorough understanding of designated sampling locations at each facility. Adhere strictly to all corporate procedures and protocols established by the Global Food Laboratory. Participate in accredited laboratory proficiency testing programs and maintain satisfactory z-scores to uphold testing accuracy and reliability. Comply with all corporate Good Laboratory Practices (GLP) required for Biosafety Level II laboratory operations. Execute routine lab functions including inventory management, equipment and supply cleaning, media preparation, and biohazard waste handling. Demonstrate foundational knowledge of food microbiology principles and practices. Support Microbiology Lead in: Managing inventory of media and chemicals. Addressing internal customer inquiries related to sampling schedules, test results, corrective actions, and product release decisions. Perform additional duties as assigned to support laboratory operations and team objectives. Typical Education High school diploma or general education degree (GED) Relevant Experience Knowledge of laboratory audit standards and QA/QC programs. Knowledge of food microbiology and food processing. LIMS (Laboratory Information Systems) experience and/or knowledge. Other Information Must meet eligibility requirements to operate a company-provided vehicle for work-related travel. One year of related scientific coursework and/or experience. Basic math skills Good knowledge of computer and Microsoft products. Ability to sit and stand for long periods Ability to work independently with minimal supervision Detail-oriented, independent worker. Skilled in basic laboratory procedures. Knowledge of Good Laboratory Practices. Knowledge of Microsoft Office Suite software, specifically Excel and Word. Ability to lift up to 50 lbs., climb steep stairs and work in hot/cold environments Job Requisition ID: 24076 Travel Required: None Location(s): GF Plant - Moses Lake Country: United States Rate of Pay: $26.76/hr Attractive total rewards package that includes: Medical, dental, vision coverage 401(k) savings plan 10 Paid Holidays Vacation Time Details available in Collective Bargaining Agreement Paid Family Building Leave Education Assistance Benefits details available at simplotbenefits.com **The J.R. Simplot Company is proud to be an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, national origin, ancestry, age, sex, gender, gender identity, gender expression, genetic information, physical or mental disability, medical condition, sexual orientation, military or veteran status, marital status, or any other protected status. **

The J.R. Simplot Company is a diverse, privately held global food and agriculture company headquartered in Boise, Idaho. We are a true farm-to-table company with an integrated portfolio including food processing and food brands, phosphate mining, fertilizer manufacturing, farming, ranching and cattle production, and other enterprises related to agriculture. Summary The Microbiology Laboratory Technician position is based at the Moses Lake Campus and operates within the Columbia Basin Factory. Reporting directly to the onsite Microbiology Lead, this role supports microbiological laboratory operations as part of Simplot's Global Food Safety and Quality program. Key responsibilities include sample collection, preparation, testing, result interpretation, and data entry for a variety of sample types-finished food products, in-process materials, water, environmental surfaces, and swabs. The technician will play a vital role in supporting microbiological testing across three factory locations: Moses Lake, Othello, and Columbia Basin. Key Responsibilities * This position follows a 4-day, 10-hour shift schedule with alternating workdays to support continuous 7 day a week lab coverage. * Operate independently within a small, fast-paced factory microbiology laboratory, consistently completing assigned tasks with minimal supervision. * Conduct microbiological testing on finished food products, in-process materials, water samples, environmental swabs, surface swabs, and allergen testing when applicable. Responsibilities include sample collection, preparation, testing, result interpretation, and accurate data entry. * Travel daily to Othello and Moses Lake factory locations using a company-provided vehicle to collect samples of finished products, in-process materials, and environmental swabs. * Perform core laboratory duties such as media preparation, biohazard waste containment and disposal, scheduled cleaning, and basic equipment maintenance. * Communicate effectively with Microbiology Lead, Global Food Corporate Microbiology, Quality Assurance, and factory personnel to ensure alignment and clarity. * Maintain and report real-time test results and records in accordance with Global Food Laboratory corporate standards, including timely data entry into the Laboratory Information Management System (MMS). * Responsible for gaining proficiency in the Enviromap environmental monitoring system across all three factory sites, including a thorough understanding of designated sampling locations at each facility. * Adhere strictly to all corporate procedures and protocols established by the Global Food Laboratory. * Participate in accredited laboratory proficiency testing programs and maintain satisfactory z-scores to uphold testing accuracy and reliability. * Comply with all corporate Good Laboratory Practices (GLP) required for Biosafety Level II laboratory operations. * Execute routine lab functions including inventory management, equipment and supply cleaning, media preparation, and biohazard waste handling. * Demonstrate foundational knowledge of food microbiology principles and practices. * Support Microbiology Lead in: * Managing inventory of media and chemicals. * Addressing internal customer inquiries related to sampling schedules, test results, corrective actions, and product release decisions. * Perform additional duties as assigned to support laboratory operations and team objectives. Typical Education High school diploma or general education degree (GED) Relevant Experience * Knowledge of laboratory audit standards and QA/QC programs. * Knowledge of food microbiology and food processing. * LIMS (Laboratory Information Systems) experience and/or knowledge. Other Information * Must meet eligibility requirements to operate a company-provided vehicle for work-related travel. * One year of related scientific coursework and/or experience. * Basic math skills * Good knowledge of computer and Microsoft products. * Ability to sit and stand for long periods * Ability to work independently with minimal supervision * Detail-oriented, independent worker. * Skilled in basic laboratory procedures. * Knowledge of Good Laboratory Practices. * Knowledge of Microsoft Office Suite software, specifically Excel and Word. * Ability to lift up to 50 lbs., climb steep stairs and work in hot/cold environments Job Requisition ID: 24076 Travel Required: None Location(s): GF Plant - Moses Lake Country: United States Rate of Pay: $26.76/hr Attractive total rewards package that includes: * Medical, dental, vision coverage * 401(k) savings plan * 10 Paid Holidays * Vacation Time * Details available in Collective Bargaining Agreement * Paid Family Building Leave * Education Assistance * Benefits details available at simplotbenefits.com The J.R. Simplot Company is proud to be an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, national origin, ancestry, age, sex, gender, gender identity, gender expression, genetic information, physical or mental disability, medical condition, sexual orientation, military or veteran status, marital status, or any other protected status.

Reports to: : Operations Manager (Everett) Type: : Full-Time, Non-Exempt (hourly) Schedule: : 1st Shift Compensation Range: : $20.24 to $ 25.00 per hour (DOE) Valence Surface Technologies production is open 24 hours per day. All shifts are as follows: 1st shift (Monday - Friday, 6:00 a.m. - 2:30 p.m.), 2nd shift (Monday - Friday, 2:00 p.m. - 10:30 p.m.), 3rd shift (Sunday - Friday, 12:00 a.m. - 8:30 a.m.) Essential Functions: : Monitor the performance of all equipment, gauges, and charts in the treatment plant and pump stations; Replace equipment when necessary Operate, maintain and repair malfunctions at the wastewater treatment plant Maintain, modify or repair instrumentation and control equipment including recorders, flow meters, and other water quality monitoring equipment Calibrate, clean, and ensure proper function of pH and ORP probes and controllers Operate and maintain rise pump stations Clean wet wells and operate pumps and valves to control and adjust flow and treatment process Setup hazardous waste cubic yard storage containers with proper labeling Operate sludge pump and filter press Collect, segregate, and transport hazardous waste from generation points to the hazardous waste storage area Label and sign appropriate hazardous and chemical reactants Inspect facility where hazardous waste is stored and evaluate compliance; track accumulation start dates of satellite storage container Compile and maintain a list of hazardous waste needing disposal and organize the waste for transport and disposal Review hazardous waste manifests and accompanying land disposal restriction notification forms for compliance Respond to hazardous waste spills in emergency situations Responsible for chemical process tank additions, make-ups, and remakes Assist in other duties as needed to ensure environmental compliance throughout the chemical processing facility Qualifications: Accountability -Ability to accept responsibility and account for his/her actions. Accuracy -Ability to perform work accurately and thoroughly. Applied Learning -Ability to participate in needed learning activities in a way that makes the most of the learning experience. Communication, Oral -Ability to communicate effectively with others using the spoken word. Conflict Resolution -Ability to deal with others in an antagonistic situation. Customer Oriented -Ability to take care of the customers' needs while following company procedures. Decision Making -Ability to make critical decisions while following company procedures.• Ethical -Ability to demonstrate conduct conforming to a set of values and accepted standards. Honesty / Integrity -Ability to be truthful and be seen as credible in the workplace. Initiative -Ability to make decisions or take actions to solve a problem or reach a goal. Judgment -The ability to formulate a sound decision using the available information. Problem Solving -Ability to find a solution for or to deal proactively with work-related problems. Technical Aptitude -Ability to comprehend complex technical topics and specialized information. Time Management -Ability to utilize the available time to organize and complete work within given deadlines. Tactful -Ability to show consideration for and maintain good relations with others. Self Motivated -Ability to be internally inspired to perform a task to the best of one's ability using his or her own drive or initiative. Safety Awareness -Ability to identify and correct conditions that affect employee safety. Resilient -Ability to recover from, or adjust to, misfortune or setbacks. Research Skills -Ability to design and conduct a systematic, objective, and critical investigation. Physical Demands: N (Not Applicable) Activity is not applicable to this position O (Occasionally) Position requires this activity up to 33% of the time (0 -2.5+ hrs/day) F (Frequently) Position requires this activity from 33% -66% ofthe time (2.5 -5.5+ hrs/day) C (Constantly) Position requires this activity more than 66% of the time (5.5+ hrs/day) Stand C Walk C Sit N Manually Manipulate O Reach Outward F Reach Above Shoulder O Climb F Crawl O Squat or Kneel O Bend O Grasp F Speak O Lift/Carry: 10 lbs or less C 11-20 lbs F 21-50 lbs F 51-100 lbs O Over 100 lbs N Push/Pull: 12 lbs or less C 13-25 lbs F 26-40 lbs F Work Environment Temperatures in the work environment can fluctuate with outside weather conditions. Due to the manufacturing environment, Personal Protection Equipment may be required including safety glasses, goggles, aprons, rubber boots, gloves, and a respirator (provided by Company). Application Process: Please apply at Aerospace Metal Finishing Careers | Aerospace Jobs (valencesurfacetech.com) with up-to-date work history and contact information. If you are a qualified candidate, one of our recruiters will reach out to you to learn more about your experience and tell you more about the job, compensation, and benefits. --------------------------------------------------------------------------------------------------------------------------------------------- Valence Surface Technologies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Additionally, Valence Surface Technologies participates in the E-Verify program to ensure employment eligibility of newly hired employees where required.

IEH Laboratories, a Leader in Food Safety, is now accepting applications for a Laboratory Analyst position at its facility in Cashmere, WA. Ideal candidates will possess the following: - A BS or BA in the biological sciences or related field (required) - Strong attention to detail - Proficiency with data entry and computer applications - Ability to multitask and work in a fast-paced environment - Strong written and verbal communication skills - Strong understanding of aseptic technique in the laboratory Laboratory Analyst duties include: analysis of food samples for pathogens via PCR and immunoassay; various microbe enumerations; data entry; pipet calibration; laboratory reporting; quality control; media preparation; and other duties as assigned. The pay for this position is $19.00 - $21.00 hourly. This is a full-time position and is eligible for the following benefits after a brief waiting period: medical, dental, vision, life/AD&D insurance, long- and short-term disability insurance, health and dependent care FSA plans, employee assistance program, 15 days of paid time off per year for sick leave and/or vacation, 6 paid holidays per year, 3 days paid bereavement leave, and 401(k) (with up to 3% employer match after eligibility criteria are met). The schedule for this position is Wednesday through Sunday, from 9:00am to 5:30pm. Due to exposure to various food allergens in the laboratory environment, applicants with moderate-to-severe food allergies are discouraged from