Quality control analyst jobs in Bellingham, WA

We are a fusion power company based in Everett, WA, with the mission to build the world's first fusion power plant, enabling a future with unlimited clean electricity. Our vision is a world with clean, reliable, and affordable energy for everyone. Since Helion's founding in 2013, we have raised over $1 billion from long-time investors such as Sam Altman, Mithril, and Capricorn Investment Group as well as new investors SoftBank and Lightspeed to propel us forward. Our last prototype, Trenta, completed 10,000 high-power pulses and reached plasma temperatures of 100 million degrees Celsius (9 keV). We are now operating Polaris, our next prototype on the path to the world's first fusion power plant. This is a pivotal time to join Helion. You will tackle real-world challenges with a team that prizes urgency, rigor, ownership, and a commitment to delivering hard truths - values essential to achieving what no one has before. Together, we will change the future of energy, because the world can't wait. What You Will Be Doing: You will lead and support a team of R&D technicians who contribute directly to Helion's scientific and engineering development efforts. In this role, you will manage daily operations, prioritize technician workloads, and ensure safe, high-quality execution of lab and testing activities. You will report to the R&D Manager, and this is an onsite role located at our Everett, WA office. This role will start out Monday-Friday but will eventually move to Friday - Sunday shift as the team grows. You Will: * Oversee and coordinate daily activities of the R&D technician team, including scheduling, task assignment, and performance monitoring * Provide mentorship and reinforce best practices to continuously raise team standards and technical capabilities * Independently install, troubleshoot, test, inspect, repair, and service lab systems including high-voltage power supplies, charging systems, pulse power capacitors, vacuum systems, and plasma systems * Perform preventative maintenance on lab and test equipment to ensure operational readiness * Ensure compliance with all safety regulations and protocols, including radiation protection and environmental standards * Maintain quality control procedures that exceed industry standards * Keep accurate records related to operations, inventory, and equipment maintenance Required Skills: * 5+ years of experience assigning tasks, monitoring performance, and ensuring adherence to operational and design standards * Availability to support a 1st shift schedule: Monday-Friday, 6:30 AM to 2:30 PM * Proven ability to motivate teams, collaborate across departments, and communicate effectively with stakeholders * Experience operating Mobile Elevating Work Platforms or other heavy equipment * Experience testing and troubleshooting electromechanical components and working in confined spaces * Ability to manage multiple priorities in a fast-paced environment * Hands-on experience assembling or installing hardware and equipment in an industrial or R&D setting #LI-Onsite #LI-TM1 Total Compensation and Benefits Helion's compensation package includes a competitively benchmarked base salary, meaningful equity grants, and comprehensive benefits. Final compensation is determined through a holistic evaluation of your experience, qualifications, and our commitment to internal equity - ensuring fairness and transparency across our teams. We are committed to fostering a fair and equitable environment in every aspect of our operations, including compensation. This is an exempt salaried role. Annual Base Pay $100,000-$130,000 USD Benefits Our total compensation package includes benefits, including but not limited to: * Medical, Dental, and Vision plans for employees and their families * 31 Days of PTO (21 vacation days and 10 sick days) * 10 Paid holidays, plus company-wide winter break * Up to 5% employer 401(k) match * Short term disability, long term disability, and life insurance * Paid parental leave and support (up to 16 weeks) * Annual wellness stipend Helion is an equal opportunity employer and value diversity at our company. We do not discriminate based on race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. If you need assistance or an accommodation during the interview process, please let us know.

TITLE: Production Radiochemist (TerraPower Isotopes) The TerraPower Isotopes (TPI) division has been established to pursue medical isotopes development: advancing nuclear science for significant human health benefits. We seek to support revolutionary radiotherapies for treatments of various cancers through the supply of radioisotopes, notably actinium-225. TerraPower currently has unique access to a supply of thorium for the long-term production of actinium-225 in the growing Targeted Alpha Therapy (TAT) market and may expand into other nuclear related medical treatments in the future. The TerraPower Isotopes program is an integral part of the Washington State based TerraPower team, a company working to raise living standards globally. In 2006, the company originated with Bill Gates and a group of like-minded visionaries who evaluated the fundamental challenges to raising living standards around the world. TerraPower's mission is to be a world leader in new nuclear technologies, while developing innovators and future leaders in the nuclear field. TerraPower is seeking to hire highly motivated and forward-thinking professionals who are interested in focusing on advanced radiopharmaceutical applications and influencing change within nuclear medicine. TerraPower is an Equal Opportunity Employer. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state, or local law. In addition, as a federal contractor, TerraPower has instituted an Affirmative Action Plan (AAP) to proactively recruit, hire, and promote women, minorities, disabled persons and veterans. Production Radiochemist TerraPower is seeking a Production Radiochemist to join us in developing and isolating unique radioisotopes intended for use in targeted therapy for cancer. The successful candidate will be a key contributor in building radiochemical generators and providing isotopes to the pharmaceutical industry. This role will entail a wide breadth including daily radiochemical process operation in hot cells and gloveboxes, batch production, and support quality control activities for the manufacture of radioisotopes. This position will also support basic maintenance, troubleshooting and process documentation. This position interfaces with a dynamic interdisciplinary environment in which effective communication, teamwork and collaboration is required, while maintaining composure to act safely, ensure quality of data, and enable timely decision-making. The position will require good judgement in ensuring regulatory compliance while delivering on commercial production needs. Responsibilities The Production Radiochemist's primary responsibilities include: * Support daily radioisotope production activities including preparation of materials, execution of hot cell and glovebox based radiochemical process operations, and dispensing and release of product batches. * Perform hands-on manufacturing of radioisotopes (in hot cells and gloveboxes), following standard operating procedures (SOPs) and batch records. * Lead preparation of documentation for product batch records. * Lead cleaning and maintenance of production equipment. * Lead preparation of materials and stock solutions to enable production. * Maintain documentation on process operations as directed by SOPs. * As needed, follow SOPs to prepare and analyze test samples as required for quality control of production processes. * Liaise and collaborate with TPI Quality Assurance (QA) and broader TerraPower Materials & Chemistry team to support production planning, issue-resolution, audits, inspection, sample QA, out-of-specification investigations, corrective action program reports resolution, etc. * Assist in hands-on training and transfer of institutional knowledge to new team-members and other members of TerraPower team. * Support maintenance of material and supply inventories required for process operations and procurement/replenishment as needed to ensure smooth operations. * Perform other general duties associated with the position as required. * Perform all work in compliance with site safety and radiation protection guidelines. Key Qualifications and Skills * Minimum of Bachelor's degree in chemistry or other relevant physical science with 1 2 years of experience working in a radiopharmaceutical or radioisotope production role. * Proficiency and experience in the handling of radioactive materials with an emphasis on alpha emitting isotopes. * Demonstrated knowledge and experience working according to safety procedures in a hazardous environment (chemical and radiological). * Proficiency and 1-2 years of experience conducting radiochemical operations in a hot cell and glovebox environment. Demonstrated proficiency executing telemanipulator-based process operations is strongly desirable. * Must be able to perform routine physical tasks with and without respiratory protection. * Experience working and communicating productively in a multidisciplinary team to meet production goals and commitments. * Flexibility to work periodic off-shift hours in support of routine production. * Commitment to maintaining integrity of operations and documentation through strict adherence to SOPs. * Ability to understand requirements (regulations, codes and standards, etc.), incorporate them into TerraPower documents, and provide associated guidance to TerraPower personnel. * Strong organizational, communication, and interpersonal skills with a desire to foster teamwork within a diverse team focused on achieving TerraPower mission. * The successful candidate will possess integrity and a high degree of respect and trust for their teammates. Job Functions Job Functions are physical actions and/or working conditions associated with the position. These functions may also constitute essential functions for the job which the employee must be able to fulfill, with or without accommodation. An applicant's ability to perform and/or tolerate the following actions and conditions will be discussed, and workplace accommodations may be made on a case-by-case basis following an individualized assessment of the applicant and other considerations, including but not limited to any governing safety standards: * Motor Abilities: Sitting and standing for extended periods, bending/stooping, grasping/gripping, fine motor control (hands) included extended operations with telemanipulators. * Physical exertion and/or requirements: Moderate, with ability to safely lift up to 20 pounds * Repetitive work: Prolonged * Special Senses: Visual and audio focused work * Work Conditions: Stairs, typing/keyboard, standard and/or sitting working environment of >8 hrs./day * Position is based in Everett, WA and work on-site in a radiochemical production laboratory is required * Travel required 0-15% TerraPower's technology is controlled for export by various agencies of the U.S. Government. TerraPower must evaluate applicants who are foreign nationals (other than asylees, refugees, or lawful permanent residents) in accordance with U.S. Government export control requirements. To facilitate TerraPower's export control reviews, you will be asked as part of the application process to identify whether you are a U.S. Citizen or national, asylee, refugee, or lawful permanent resident of the United States. Government export authorization approval times vary. Based on the business needs for a particular position, TerraPower may not consider a foreign national from a country if it is impracticable to obtain timely Government export approval. Job details Salary Range Level 9: $99,041 - $148,561 Salary Range Level 10: $113,605 - $170,408 * Typically, our employee salaries are within .90 - 1.0 of the mid-point of the posted salary bands. Any salary offered within the posted salary band is based on market data and commensurate with the selected candidate's qualifications and experience. This range is specific to Washington State. Benefits: * Competitive Compensation * Salary, eligible to participate in discretionary short-term incentive payments * Comprehensive Medical and Wellness Benefits Medical * Vision * Dental * Life * Life and Disability * Gender Affirmation Benefits * Parental Leave * 401k Plan * Generous Paid Time Off (PTO) * 21 days of annually accrued PTO * Generous Holiday Schedule * 10 paid holidays * Relocation Assistance * Professional and Educational Support Opportunities * Flexible Work Schedule TerraPower Career and Benefits information: **********************************************

Job DescriptionSalary: 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 Visions 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.

The QC Inspector's main responsibility is to inspect, accept or reject work performed in a particular discipline in compliance with applicable Codes and specifications. Discipline can be civil, structural, mechanical or piping. This posting is to gather a qualified pool of candidates as the need arises to hire for various maintenance and turnaround projects. Once an opening occurs, we will reach out to qualified candidates. Essential Functions Actively support the Company's commitment to safety and its “Core Values.” Represent the Company at all times with high moral standards while adhering to the Company's “Code of Business Conduct and Ethics.” Responsible to observe and follow all safety procedures and regulations at the job-site. Perform inspections and witness tests as required. Prepare reports and quality records in compliance with procedures. Coordinate areas of QC work with other department's work, such as, start-up, engineering, process, etc. Perform receipt inspections of material for work area in conjunction with material control staff as required. Perform system verification on completed systems to assure correct installation per design specifications. Control measuring and test equipment, as required to insure accuracy. Perform additional assignments per supervisor's direction. Qualifications 2+ year's minimum experience. AWS CWI minimum required. API 653 certification preferred. Should be familiar with ASME Sec. VIII, Sec. IX, B31.1, B31.3, API ************* Codes Strong understanding of corporate and industry practices, processes and standards and their impact on project activities. Excellent oral and written communication skills; good computer skills including MS Word and Excel. Washington law requires pay information in job postings. The typical hiring range for this position in Washington is shown below. The pay rate will depend on the successful candidate's qualifications and prior experience, specific skill set, geographic location, internal equity, and other factors influencing pay. As such, an actual salary may fall closer to one or the other end of this range, and in certain circumstances, may fall outside the listed hiring range. Hiring range: $45.62 to $52.13 per hour Full range for this position, available over time: $45.62 to $52.13 per hour In addition, full-time employees are offered a comprehensive benefits package, including medical, dental and vision plans covering eligible employees and dependents, disability benefits, life and AD&D insurance, an employee assistance program (EAP), a 401(k) plan with company match, an employee stock purchase plan (ESPP), a robust wellness program and adoption assistance. At Matrix, we are dedicated to building a diverse, inclusive, and authentic workplace. We encourage all whose experience aligns with the listed qualifications to apply and explore joining our organization. EEO/M/F/Disability/Vets/Affirmative Action Employer We are an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, genetic information, marital status, disability, veteran status, or other legally protected characteristic or category.

ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers . If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post. Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. Your role is crucial in maintaining this commitment and driving forward our mission to improve patient outcomes. What You Will Achieve In this role, you will: Execute on defined and established procedures, work instructions and templates Process documents in electronic Document Management System Answer basic questions and send routine notifications Issue and reconcile batch records, forms, and logbooks Maintain and distribute documents to Controlled Document Locations Back-up the Records Management job function as required Responsible for receiving and logging GMP records, cataloging, physical or electronic filing, and retrieval as needed Works with GMP personnel submitting and retrieving records to ensure records are maintained and tracked in a compliant manner and are readily retrievable. Participates in cross-functional teams to implement, update, or upgrade systems or processes related to the management of GMP records. Supports GMP regulatory audits and inspections ensuring timely retrieval of both physical and electronic records. Scans and digitizes GMP records and verifies as true copies. Performed reconciliation of completed records issued for GMP activities. Collects and assists with reporting on relevant metrics. Works with off-site storage facilities to ensure compliant submission and retrieval of GMP records. Contribute to milestones related to specific projects. Participates in continual improvement activities within Document Control and GMP Records management. Additional Qualifications/Responsibilities Here Is What You Need (Minimum Requirements) Bachelor's degree with any years of experience, or an Associate's degree with 3 years of relevant experience, or a high school diploma (or equivalent) and 6 years of relevant experience Experience in the pharmaceutical industry and Quality administered systems Sound knowledge of current Good Manufacturing Practices (part of GxP) Ability to work effectively in a team environment, both within one's own team and interdepartmental teams Effective written and oral communication skills Bonus Points If You Have (Preferred Requirements) Experience at a manufacturing site. Managing and writing deviations, Change Control and CAPA Experience in production batch record issuance, reconciliation, investigation of non-conformance, root cause analysis and change control management Strong problem-solving skills Ability to work independently and as part of a team Excellent time management and multitasking abilities PHYSICAL/MENTAL REQUIREMENTS N/A NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS N/A Work Location Assignment: On Premise The annual base salary for this position ranges from $66,500.00 to $110,900.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.

Requirements Mechanical background and have worked with 12V electronics and hydraulics Familiar with general mechanical equipment and have a basic understanding of operating functions Experience in the safe use of hand or power tools such as drills, caulk gun or air gun Quality, accuracy, and the ability to work within a scheduled paced environment Must be 18 years of age or older High school diploma or GED required A clean driving record with a valid driver's license All applicants must be able to pass a pre-employment drug screen & background check Class B drivers license preferred Ability to work alone, unsupervised yet finish tasks on time Please visit ***************** to learn more about our company and our products and services. All applicants must be able to pass a pre-employment drug screen, background check, and any other pre-employment qualification processes that may apply. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. Veteran Friendly Employer: Shredfast & ShredSupply believe in hiring military veterans. We know your service trained you in many of the areas we value, such as; leadership, teamwork, performance, integrity, and safety. If your experience matches our requirements, we want you to apply. Salary Description $20.00 - $22.00

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-Wednesday E/O Thursday 6am-6pm 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 * Shift Differential pay is available for this position, and is determined by hours worked on selected shift. Weekday Days Shift 12HRS 2.5% * 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: ******************************

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

* Shift differentials for Weekend Shift Dogwood Industries - Who We Are Build your future with Dogwood Industries! Dogwood Industries is at the forefront of designing and manufacturing Pre-engineered Panelized Relocatable Metal Buildings, delivering industry leading solutions for mission-critical projects across industrial and DoD markets. Through a precise blend of manufacturing and construction, we build high-performance, rapidly deployable structures that keep critical missions moving forward. Our team provides leadership in the design process that transforms the way our clients work by delivering buildings as equipment solutions in harsh environments around the world. If you are motivated by innovation, thrive in a fast-paced setting, and want to be part of a team that is rapidly growing and revolutionizing the building industry, we'd love to speak with you! General Job Description Dogwood Industries LLC is seeking an experienced Quality Control Inspector (QCI) to join our team in Sedro-Woolley, WA. A successful candidate will be experienced in inspection procedures in an industrial setting and will demonstrate an understanding of quality control procedures and key elements of the inspection process and documentation thereof. Duties & Responsibilities The core responsibility of the QCI is to inspect and report non-conformances in accordance with drawings, inspection checklists or other specifications identified in the quality assurance plan. Daily, the QCI may be engaged in these activities: * Identify defective or non-conforming work * Issue reports and document resolution of non-conforming conditions * Execute and document specific test plans * Maintain and distribute accurate drawings and red line corrections * Maintain quality control records, documents, and logs * Perform incoming material inspections and vendor inspections when required * Perform first article, visual and dimensional checks at all stages of production * Other duties as assigned Requirements Requirements * Familiarity with AWS D1.1/AWS D1.2 weld inspection * Strong organizational and communication skills * Ability to manage change along with competing priorities * Fluency in English with excellent written and oral skills * Proficiency in standard Office computer applications * CWI certification is a plus Qualifications * 1+ years' experience in quality control * Minimum high school diploma or vocational degree * Experience in steel fabrication or general construction * Ability to read and understand engineering drawings and shop drawings Physical Requirements/Work Environment This position requires moderate physical activity in a manufacturing environment. While performing the duties of this job, the employee is regularly required to have full range of mobility in upper and lower body, able to reach overhead, able to work in various positions, including, but not limited to, stooping, standing, bending over, sitting, kneeling, squatting; use hands to handle, or feel objects, tools or controls; reach with hands and arms; climb stairs; balance for extended periods of time. Be able to lift 60 pounds of weight when required. The employee will be exposed to shop elements such as noise, dust, fumes, and odors. Compensation $28.00 - $38.00 hourly, depending on experience and qualifications. Shift differentials for Weekend Shift Benefits * Health Benefits, including medical, dental and vision * Company paid and supplemental life insurance * Short-term disability * Long-term disability * Additional voluntary benefits * Paid vacation, paid sick leave and paid holidays * 401(k) retirement plan, with employer match * Employee Referral Bonus Program Applicant Notes * Applicants must provide complete work history with employer references for last three to five years * All employees are subject to a pre-employment background check and pre-employment and random drug testing. Due to working in / being exposed to a safety sensitive environment, THC testing will occur as part of all drug screens. Application Assistance If you are an individual with a disability and need a reasonable accommodation in the application or hiring process, please contact Dogwood's HR department at ************** or ************************. Location This position is based out of the Dogwood Factory Office at 500 Metcalf st, Sedro-Woolley, WA 98284. There may be travel to the Dogwood Everett, WA Factory as needed. Equal Employment Opportunity: All qualified applicants will receive consideration for employment without regard to race/ethnicity, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, age, or any other status protected by law. For more information about our commitment to equal employment opportunity, please see this government poster: Know Your Rights: Workplace Discrimination is Illegal. Disclaimer: Although the Company has attempted to accurately and thoroughly describe this position, the Company reserves the right to change the same, including to change, add to or subtract from the duties outlined, within the sole discretion of the Company, at any time, with or without advance notice. In order to meet company deadlines, work in excess of 40 hours per week may be required from time to time. PM22

Job Title: QC Associate Scientist - Raw Materials Shifts: Days, Monday to Friday, 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.

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

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

BPI Medical is growing at a remarkable rate and offers a rewarding career for a proven leader interested in making a difference every day. We embrace our entrepreneurial culture and have created a workplace where collaboration is essential, courage is rewarded, speed is expected, and agility is the norm to meet our customer's needs. Our motto is "Its gotta be right. its gotta be fast. no exceptions." We live by our values of Integrity, Quality, On-time Delivery, Collaboration, Growth Mindset and Compassion. We have a relaxed work atmosphere with an exceptional staff. We understand that continuous improvement is more than a business philosophy. It's a personal contribution to making our customers, our business, and our team members better every day. This position will engage in quality control activities designed to inspect, measure, and verify the effectiveness, and adherence to medical industry quality standards. The position is expected to work independently with the ability to exercise sound judgment, following established processes and procedures that govern quality control inspection. Conducting inspections and tests on incoming raw materials, components, and finished products to ensure they meet established quality standards and specifications. Performing visual inspections, measurements, and functional tests on medical devices to verify their compliance with applicable regulations and standards, such as ISO 13485 and FDA guidelines. Documenting inspection results and maintaining accurate records of quality control activities in accordance with regulatory requirements. Proficient in the use of mechanical inspection equipment; including micrometers, calipers, fixed gauges, optical comparator, CMM and other inspection measuring tools. Identifying and reporting non-conformities or deviations to appropriate personnel for investigation and corrective action. Participating in investigations of quality issues and working with cross-functional teams to determine root cause and implement corrective and preventive actions. Ensuring that inspection equipment and tools are calibrated and maintained in accordance with regulatory requirements and company procedures. Developing and implementing quality control procedures and work instructions to ensure consistent product quality. Collaborating with production staff and other stakeholders to address quality issues and drive continuous improvement. Participating in internal and external quality audits to ensure compliance with applicable regulations and standards. Communicating effectively with customers, suppliers, and other stakeholders on quality-related matters, including product quality, regulatory compliance, and quality system requirements. We are proud to be an Equal Opportunity Employer. BPI Medical, also known as Ben's Precision Instruments, was founded by a machinist-craftsman from Holland. Ben Overmars Sr. is both an immigrant and a worker performing fully with a disability. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability. As a federal contractor, BPI Medical is required to participate in the federal government's E-Verify program. With E-Verify we are able to confirm the employment authorization of all newly hired employees and most existing employees through an electronic database maintained by the Social Security Administration and Department of Homeland Security.

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.

IEH Laboratories, a Leader in Food Safety, is now accepting applications for a Laboratory Analyst position at its facility in Seattle, 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 $21.00 - $23.00 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 laboratory operates weekends, so candidates must be willing to work occasional weekends and off-schedule hours when necessary. Due to exposure to various food allergens in the laboratory environment, applicants with moderate-to-severe food allergies are discouraged from

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. **

OFM classification title: Instruction & Classroom Support Tech 2 Walla Walla Community College is accepting applications to fill the part-time role of Lab Tech for our Chemistry department on the Walla Walla Campus. At Walla Walla Community College, we inspire all students to discover their potential and achieve their goals by providing relevant, equitable, and innovative learning opportunities and services. As an organization, we value learning opportunities, a sense of community, diversity, health and humor, excellence, integrity, teamwork, innovation, personal and professional growth, and sustainability. General Responsibilities: The Chemistry Laboratory Support Technician will fill an educational support position at the Walla Walla campus. This technician will provide direct support to science instruction through management of the Chemistry laboratories and prep areas. Chemistry Lab Support: * Collaborate with supervisor and science faculty to determine equipment and reagent needs for pending lab sessions. * Anticipate and communicate needs to supervisor with respect to lab materials, supplies, and equipment to ensure continuity of instructional labs. * Assist students in learning the safe use of specific lab equipment and appropriately handling materials to be used during the lab exercise. * Maintain a safe, secure, well-organized and adequately stocked storage space for instruments, equipment, glassware, chemicals. * Familiar with, and comfortable with using solutions with extreme pH's and organic solvents * Communicate the need for regular preventative maintenance and repair on scientific instruments and devices, * Familiarity of Vernier instruments and probes. * Notify supervisor, or chemistry instructor when equipment needs repairs or adjustments. * Follow safe laboratory standards and practices including the handling, storage, and disposal of hazardous chemicals and bring safety concerns forward to the supervisor. * Understand when and how to use PPE effectively Essential Functions: Reagent Preparation * Prepare chemistry reagent solutions using precision balances and laboratory glassware * Maintain chemical inventory * Maintain and control proper reagent waste stream * Properly store reagents * Maintain a safe working environment by following EH&S, OSHA, federal, and state regulations and standards Laboratory Environment Maintenance * Maintain clean work areas and lab benches * Maintain proper lab hygiene in prep room and lab room during and in between lab sessions * Wash glassware and maintain glassware supply * Maintain clean refrigerators and storage cabinets General Lab Maintenance * Assemble and dismantle lab equipment and materials * Organize storage, prep room, and lab spaces * Maintain equipment, Vernier instruments, and supply drawers * Notify supervisor or science faculty for repair needs General Laboratory Support * Participate in regular meetings to outline weekly assignments and ensure standards are being met to the satisfaction of the team * Assist students and support instructors during lab * Effectively communicate needs and concerns of supervisor or faculty as they arise * Ability to recognize the value of cultural, ethnic, gender and other individual differences in people. * Ability to build constructive working relationships characterized by a high level of acceptance, cooperation and mutual respect. Required Qualifications: Equivalent combination of education and experience may be considered at the discretion of the college. * AA in science or equivalent work experience * Demonstrate strong understanding of precision lab techniques, and handling hazardous reagents. * Be able to communicate well orally and relate meaningfully with instructors of diverse experiences, and abilities. Preferred/Desired Qualifications: * Previous related work history in chemistry or analytical laboratory setting * Previous experience in laboratory science education * Bilingual English/Spanish This part-time temporary position (up to 17-hours per week) is located at the Walla Walla Campus. Work is performed almost exclusively in a lab classroom and prep room. Lab techs will work with hazardous materials and reagents. Tools and equipment will include computers, lab balances, auto pipettors, fume hoods, and DI water system. In-person interactions will occur with students, staff, and faculty. Academic schedule changes by the year and quarter, therefore there may be some flexibility to hours worked. Vacation, sick leave and personal leave benefits are available on a pro-rated basis. Persons hired must be able to provide acceptable documentation of lawful authorization to work in the United States within three (3) days of employment. WWCC participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Candidates may be subject to a criminal history background check as a condition of employment. Information from the background check may not necessarily preclude employment but will be considered in determining the applicant's suitability and competence to perform in the position. WWCC requires all employees to participate in direct deposit for payment of salary. WWCC is a tobacco free campus.This position is posted as open until filled. Applications are screened as received. To qualify for consideration, applicants must meet required qualifications and submit a complete application packet that includes the following: * Online application * Resume * Names and contact information for three professional references. * Unofficial Transcripts (if applicable)

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