Quality control analyst jobs in Caldwell, ID - 107 jobs

Aircraft Quality Control Inspector - OR Area - 1601- Direct Hire Our Client is internationally known for creating the premier Passenger to Cargo aircraft conversion. We are seeking a dedicated Aircraft Quality Control Inspector to work in our Beaverton, OR location. This full time position reports to the Quality Manager and is an essential contributor to the team. Core Responsibilities: • Inspect aircraft assemblies and sub-assemblies for fastener installation, cable harness assembly installation, part location, riveting, sealing, etc. for acceptable workmanship, proper functioning, and completeness. • Use calibrated Our Client inspection equipment such as calipers, micrometers, height gages, radius gages, rivet gages, etc. to measure and evaluate characteristics of aircraft parts and assemblies. • Read and understand engineering drawings, blueprints, specifications, standards, and other instructions. • Perform in-process, first article, and final inspections in accordance with AS9102 standards and/or customer requirements. • Identify and document nonconformities for MRB and engineering review. • Assist with internal quality audits in preparation for FAA and vendor audits. • Help track, manage, and maintain list of calibrated shop inspection tools and equipment. • Assist with training and providing guidance to other team members. • Other tasks reasonably requested due to the nature of the position. Skills and Experience: • High school or equivalent; technical or vocational education a plus. • FAA Airframe and Powerplant (A&P) license highly preferred • Minimum three years of recent aircraft quality inspection experience, preferably in a manufacturing facility • Experience reading and interpreting engineering drawings and specifications • Basic understanding of Geometric Dimension and Tolerancing (GD&T) methods • Proficient in the use of inspection tools and procedures to accept/reject critical part dimensions • Working knowledge of Microsoft Office and SharePoint software applications TO APPLY: Please email your resume and a cover letter to hiring@Our Clientaircraft.com for consideration or apply for the position on Indeed. If interested, please send your updated resume in Word doc format to Jigar at *********************** with preferred pay requirements and availability and we will follow up immediately

Job DescriptionSerán BioScience is looking for a scientist with laboratory experience to support manufacturing of pharmaceutical drug products within our In-Process Control group. As a scientist within the Quality Control department you will work alongside a team of scientists and operators to ensure the highest quality product by testing raw materials and production equipment within GMP manufacturing and laboratory environments. Qualified candidates will demonstrate expertise in utilizing specialized laboratory equipment, techniques, and methodologies for technical assessments and data analysis purposes. Preference will be given to those with experience in GMP environments and technical data review specific to the pharmaceutical industry. Serán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.Duties and Responsibilities Adheres to Standard Operating Procedures, cGMPs, Quality Manual, and company policies Performs routine testing using analytical equipment including but not limited to HPLC, GC, KFC, Disso, etc. Conducts appearance testing, solution preparation, raw material sampling, and pH measurement Drafts stability tables, sets-up stability studies, logs-in samples and standards Cleans lab and glassware and disposes of analytical waste appropriately Participates in process improvement and other non-routine projects Enters clean spaces with appropriate PPE to collect various samples Is familiar with introductory analytical equipment (e.g., HPLC, GC-HS, TOC, FT-IR) Is familiar with raw materials testing requirements (compendial and client testing) Conducts peer review of routine testing at the discretion of the relevant supervisor Performs technical writing and reporting including but not limited to: incident reporting, laboratory investigations, CAPAs, SOPs, trend reports, risk assessments, etc. Performs hypothesis testing or investigative work for OOS results under management and SME guidance Demonstrates cross-functional support capabilities with other QC teams Responsibilities may increase in scope to align with company initiatives All other related duties as assigned Required Skills and Abilities Hands-on lab experience in HPLC, CG-HS, TOC, FT-IR Hands-on lab experience with raw materials testing Strong verbal and written communication skills Demonstrated ability to collaborate and work in cross-functional teams Strong organizational skills and attention to detail Follows detailed written and oral instructions Strong time management skills with a proven ability to meet variable and competing deadlines Strong analytical and problem-solving skills Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the Company Multitasks and adjusts priorities in a fast-paced environment, while maintaining focus and managing disruption and/or unexpected needs Accepts feedback from a variety of sources and constructively manages conflict Ability to prioritize tasks and to keep leadership apprised of performance to timelines Ability to function well in a high-paced and at times stressful environment Proficient with Microsoft Office Suite or related software Education and Experience Bachelor's degree in related scientific discipline 3 years of hands-on laboratory experience required, cGMP preferred Minimum of 2 years of GMP experience required to be considered for Scientist II Physical Requirements Prolonged periods of sitting or standing at a desk and working on a computer Prolonged periods of sitting or standing in laboratory environment Must be able to lift up to 25 pounds at times Adheres to predicable in-person attendance Motor skills required for basic laboratory operations Compensation correlates to skills and experience presented by selected candidate. Visit ******************************** to learn more about company culture and the community of Bend, Oregon. Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. Benefits Summary:Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees' wellbeing, along with access to pet insurance. The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701 We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Benefits: 401(k) Dental insurance Health insurance Paid time off Vision insurance The Quality Control Inspector performs visual inspection to verify conformance to AWS D1.1 Structural Welding Code Steel requirements and customer specification and other manufacturing processes related to steel fabrication. Essential Duties and Responsibilities: Perform Visual Inspection and dimensional inspections to verify product/component compliance for in-process and final QC inspections on manufactured/fabricated parts and assemblies. Identify and record any product quality problem(s) while communicating all quality issues to management in a timely manner, along with recommendations for any corrective actions that may be necessary. Witness testing of the welder test assemblies and/or welding operator qualification tests or supervise these activities when performed by third-party testing. Verify that the base materials and consumable welding materials conform to the specifications and that the welding filler metals used are as specified for each base material or combination of base materials. Verify documentation of performance qualification test results and ensure welders qualifications are current. Verify that the welding procedures are as specified and are qualified, and that the welding is performed in conformance with the applicable procedure. Ability to understand and use basic inspection tools, such as a tape measure. Able to read and interpret product drawings, specifications, visual work instructions and navigate codebooks. Ensures materials and products are in accordance with established tolerance levels for quality and performance. Perform duties in accordance with TRC's Quality Management System and Safety procedures. Recording inspection results by completing inspection reports, writing NCRs, reject defective parts, label, and segregate as necessary as well as inputting data into quality/production database. Able to perform basic math. Willingness to be trained and ability to learn in fast paced environments. Willing to work overtime on weekdays and weekends. Promote and actively embrace the concept of a collaborative environment, with an emphasis on customer service, respect, and candor. Safety is a cultural value, and it must be promoted and always enforced. Minimum Qualifications/Experience: High school diploma or general education degree (GED). Minimum of 3 (five) years of experience in an occupational function that has a direct relationship to welded assemblies fabricated to national or international standards and be directly involved in one or more of the following: Design, production, construction, examination, or repair. Knowledge of dimensional inspectional. Additional skills: Familiar with SMAW, FCAW, GMAW welding processes. Familiar with VT, UT, MT, and PT testing processes. Other Qualifications: CWI certification preferred but not required. Looking Night Shift employees Physical Demands While performing the duties of this Job, the employee is occasionally required to stand, handle steel, reach with hands and arms. The employee is occasionally required to walk; sit, kneel, crouch, or crawl. The employee must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 25 pounds, and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include ability to pass a visual acuity test. Work Environment While performing the duties of this Job, the employee is frequently exposed to moving mechanical parts. The employee is occasionally exposed to high noises. The employee is occasionally exposed to high, precarious places; fumes or airborne particles; risk of electrical shock and vibration. Compensation: $20.95 - $26.25 per hour SEAA is a not-for-profit organization dedicated to the advancement of steel industry professionals. SEAA assists our members in their employee recruitment, hiring and training processes and we provide on-going safety and training support in effort to nurture success.

The Quality Control Laboratory Assistant (QC Lab) helps to provide support to the Quality Control Laboratory while focusing on processing and organizing incoming samples for receipt, preparing samples for client and contract lab shipments, communicating with internal and external partners, and supporting other processes within the Quality Control Laboratory and Quality Department. Duties and Responsibilities: Log and processes incoming samples for receipt Maintain sample tracking log Prepare samples for shipment to contract laboratories for analysis and to clients for approval Assist with ordering and inventory maintenance of QC laboratory supplies Work closely with internal/external partners and communicate sample disposition Communicate effectively with clients on sample shipments and provide tracking information Perform equipment calibration activities and shipping of equipment for calibrations Maintain product standards and prepare standards for use May assist with raw material, component, and finished goods inspection (ANSI Inspection) Participate in Lean initiates, GEMBA walks, and other process improvement activities May assist with data entry of batch records, OOS, and other information assigned Other duties as assigned Elevation Labs provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, or genetics. In addition to federal law requirements, Elevation Labs complies with applicable state and local laws governing nondiscrimination in employment at every location in which the Company has facilities. 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 essential duties listed are representative of the major duties required of this job; ability to perform the essential functions with or without reasonable accommodation is required. Elevation Labs may make reasonable accommodation to the known physical or mental limitation of otherwise-qualified individuals with disabilities unless the accommodation would impose an undue hardship on the operation of our business. This job description is not designed or intended to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required for this job. Specific duties and responsibilities may vary based upon departmental needs. Incumbent may be asked to perform other duties as assigned. Knowledge & Skills: Ideal Candidate Qualifications: High attention to detail and organization with effective time management skills Background in receiving and shipping packages using online platforms Able to communicate effectively in writing and verbally in English Able to operate a computer (i.e., Microsoft applications, ERP system, lab software) Perform essential duties and responsibilities efficiently and accurately with minimal supervision Education/Experience: High School Diploma or Equivalent Prefer experience with sample receipt in a laboratory setting Physical/Mental Demands: Regularly/Frequently required to sit, stand, walk, stoop, kneel, bend Regularly/Frequently use hands to keyboard or type, handle materials, manipulate tools, and reach with hands and arms Occasionally/Frequently lift and/or move up to 25 pounds and, infrequently, up to 50 pounds Perform tasks requiring manual dexterity and use of tools and equipment parts Must be able to move between facilities on our campus Specific vision abilities required by this classification include close vision, depth perception, color determination, and ability to adjust focus Must be able to communicate effectively in person, by telephone, and via messaging Requires composure and ability to prioritize and handle many urgent tasks and requests simultaneously with a high level of competence and accuracy Maintain confidentiality The physical demands identified above are representative of those that will be required to successfully perform the essential functions of this job. Work Environment: Office, Lab and Manufacturing settings Noise level is usually moderate Fast paced Regularly required to work in areas where chemical materials are encountered Regularly required to wear appropriate personal protective equipment May involve exposure to shop environment including variable noise levels Must customarily have a high consciousness for personnel and equipment safety

Quality Assurance Associate Department: Quality Assurance Unit JD-023 Reports To: Quality Assurance Manager FLSA Status: Non-Exempt OMIC USA, Inc. is an international Analytical Laboratory and is committed to global food health and safety through the analytical testing services we offer to our clients. MISSION OF THE ROLE: The Quality Assurance Associate position supports the Quality Assurance Manager in the tasks required to verify regulatory compliance of all operations associated with the laboratory (e.g. sample receipt, processing, analytical, reporting, sales and human resources, etc.) with accreditation standards. (e.g. ISO/IEC 17025:2017) and contributes to the on-going development of the laboratory's quality management system. Based on experience, the Associate can take self-directed ownership for some QA tasks and contribute to quality management system continuous improvement. Serves as QA Manager's backup as directed. RESPONSIBILITIES: Other duties may be assigned. Support the Quality Assurance Manager in maintenance and continuous improvement of the quality management system. This includes but is not limited to: Perform in-depth Internal Audits Continuous improvement, and implementation of systems for compliance Proactive document control to ensure all documents are within the system Proficiency Testing; scheduling, reporting & follow up Supplier qualification, and traceability Perform internal audits of the quality management system to ensure compliance to the appropriate standards and accreditation programs and identify areas of non-conformance and/or areas for improvement. Perform procedural audits of methods conducted in the laboratory against the appropriate SOPs and LABs to ensure accuracy of procedural documentation and adherence to laboratory procedures in the areas of analytical technique, QC and quality system compliance, including: reference material/solution tracking, reagents & solutions tracking, equip verification logs, instrument logbooks, training records, document control, and data package compliance. Report audit details (observations, findings, non-compliances and non-conformances) to the Quality Assurance Manager and assist with resolution as applicable. Supports the Quality Assurance Manager and assists in external audit activities as needed, including implementation of corrective action and improvements the Laboratory receives, as they relate to the quality management system. Promote QAU information and QA training to laboratory staff, in meetings and as needed. Periodically reconcile database records of Suppliers of externally provided products and services to the laboratory, to ensure qualification records are kept up to date; maintain supporting documentation and traceability in LIMS. Records new laboratory equipment information in LIMS for unique identification and tracking purposes. Work with laboratory staff to ensure routine maintenance documentation is in place before use. Coordinate and oversee internal & external calibration and verification of laboratory support equipment (pipette performance, temperature accuracy, etc.) The actual calibration/verification tasks may be performed by this position or other assigned laboratory personnel Coordinate external calibration and/or repair of equipment as needed. Communicate non-conformities to Quality Assurance Manager for course of action and/or data impact assessments. Maintain documentation of support equipment calibration both internal and external (hard copy, electronic and data base). Ensure training of new lab personnel on operation and best practices for pipette use and handling, when applicable. The actual training tasks may be performed by this position or other assigned laboratory personnel, however this position is responsible for being a back-up trainer. Assists the Quality Assurance Manager and laboratory staff by reviewing new or revised documentation for overall conformity with our internal policies and procedures as well as regulatory compliance, when applicable, prior to inclusion in the Document Control systems. Ensure that routine maintenance/consumable replacement for residue water purification systems and on-site technician visits are scheduled as needed. Audit electronic water quality/use logs and records to ensure they are being maintained as needed. Ensure new personnel are trained in operation and best practices; serve as back-up trainer. Periodically reconcile database records of reference materials and solutions to ensure that records are complete and accurate; maintain documentation of notification for corrections to be made by Chemists and traceability of completion. Ensure disposal of expired solutions (and neat as applicable). Periodically check physical neat standards and stock solutions for compliance (correct labeling, assigned physical locations, etc.) and maintain records of non-compliance. Supports the Quality Assurance Manager with maintaining quality records (hard copy, electronic, or data base) associated with the Quality Management System, including audit reports, training, schedules and document control. Performs annual quality record and data archival, including labelling and organizing new entries for ease of locating and retrieving. Schedules annual disposal of records, ensuring retention periods of regulatory and contractual timeframes are maintained. SUPERVISORY RESPONSIBILITIES: This role has no supervisory responsibilities. SKILLS AND EXPERIENCE: EDUCATION Bachelor's degree (B.S.) in Chemistry, Biology or related science from a four-year college or university and two years relevant QA experience working in a regulated laboratory; or equivalent combination of education and experience. CERTIFICATES, LICENSES, REGISTRATIONS None SKILLS & EXPERIENCE Working knowledge of common laboratory equipment types, test methods, and regulations/ standards (preferably ISO 17025 or similar) Improvement initiatives Learning initiatives Ability to handle multiple priorities and deadlines Analytical and problem-solving skills High emotional Intelligence Good cultural awareness and communication with people who have diverse backgrounds Experienced user of MS Office and Adobe Acrobat PERFORMANCE FACTORS Page Break Quality of Work Communication Adaptability Teamwork Time Management Knowledge and Skills Initiative Dependability Page Break LANGUAGE SKILLS Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations. Ability to write Standard Operating Procedures, analytical methods, reports, business correspondences, and additional laboratory documentation. Ability to perform standard quality assurance / quality control evaluation procedures, including audits. Technical writing for preparing manuals and documentation. MATHEMATICAL SKILLS Ability to apply advanced mathematical concepts such as exponents, logarithms, and quadratic equations. Ability to apply mathematical operations to tasks such as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis. REASONING ABILITY Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. SKILLS & EXPERIENCE Familiar with the laboratory business environment Experience working in international businesses OTHERS: TRAINING REQUIREMENTS OJT in understanding company operating systems, including the maintenance and operation of extraction and analytical equipment, and passing the Initial Demonstration of Capability (IDOC) for existing SOPs. PHYSICAL DEMANDS While performing the duties of this job, the employee is regularly required to be able to hear and understand instructions and handle items involving repetitive hand and wrist movement. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. WORK ENVIRONMENT Works in a laboratory using analytical equipment. Employee may have exposure to hazardous chemicals and solvents. The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Management reserves the right to add, modify, change, or remove work assignments. This job description is designed to outline primary duties, qualifications, and job scope, but not limit the employee nor the company to just the work identified. It is OMIC USA Inc.'s expectation that each employee will offer their services wherever and whenever necessary to ensure the success of the Company and that each employee is adhering to the Company's policy set up in the Company's Employee Handbook.

Strong History. New Vision. Yellowstone Local is proud to represent Fought and Company, an industry leader in structural steel fabrication. You're a seasoned Quality Control Technician who takes pride in doing things by the book, and making sure everyone else does too. You're not here to babysit sloppy work. You're here to protect the integrity of every weld and structure that leaves the shop. What's in it for You? Competitive pay: $70,000-$90,000 annually, based on experience and certifications Full-time schedule: 4x10s, Monday-Thursday Overtime paid at time and a half, frequently available on Fridays and Saturdays, with occasional Sundays Medical, dental, and vision insurance 401(k) and pension plan Free prescription safety glasses Yearly performance bonus based on company performance On-site work in Tigard, OR, minimal travel required Why You'll Love It Here Safety is the top priority. This team lives and breathes a safety-first mindset You'll work for a legacy company with a bold new vision We're building a world-class QC team to take control in-house and raise the industry standard Your standards matter. We don't cut corners, ever Your voice counts. We want proactive problem solvers, not silent box-checkers You'll inspect structural components and bridge parts that shape the infrastructure of the Pacific Northwest Your New Role Perform magnetic particle testing (MT) and ultrasonic testing (UT) to Level II standards Inspect bridge and structural components using AWS D1.1, D1.5, and D1.8 codes Maintain detailed and accurate inspection and testing records Execute assigned tasks from the QC Supervisor and QC Manager Collaborate with fabrication teams to solve quality issues in real time Support AISC certification standards and ensure all work meets or exceeds specs Based in Tigard, Oregon Hiring Expectations: Apply today, complete a quick phone screening, and get ready for an interview with our team to discuss your goals and experience. AWS Certified Welding Inspector (CWI) Level II certification in Magnetic Particle Testing (MT) Level II certification in Ultrasonic Testing (UT) 3 to 5 years of quality control or inspection experience Experience with AWS D1.1 Structural, D1.5 Bridge, and D1.8 Seismic standards Detail-oriented with strong communication and reporting skills High school diploma or equivalent Must be able to work full-time onsite in Tigard, OR with availability for overtime Fought and Company is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment regardless of race, color, religion, gender, gender identity, sexual orientation, national origin, genetics, disability, age, or veteran status.

Temp The Quality Control Technician will be primarily responsible for ensuring compliance with cGMP's, raw material and component receiving, releasing outbound finished goods, maintaining the Environmental Monitoring Program, and keeping quality records organized and neat.

Temp Food Production Quality Control Pay: Day Shift $23.60/hour (+ $2.50 night shift differential for hours worked between 5pm - 5am) Schedule: 3 - 4 day work weeks with set shifts 8pm - 8am Shift 4 - Thursday - Saturday every other Wednesday Night Shift Location: Mcminnville, OR GLISS General Labor & Industrial Staffing Solutions is hiring for Food Production Quality Control Technicians. In this role you are responsible for testing materials and finished products to ensure they conform to all applicable laws and company standards. Quality control technicians test products across the three stages of production (before, in-process, and final) to ensure quality levels are met. If you have QC/QA experience and looking for a temp-to hire position APPLY TODAY Responsibilities: Coach and train employees on GMP's. Enforce GMP's to maintain a quality product manufactured in a safe environment and meeting all targeted requirements. Maintain, and enforce company quality standards. Ensure plant operations staff delivers quality products within specification. Provide regular and timely feedback to production operations and Supervision as to critical process analytical measurements. Conduct routine testing and quality checks per schedule. Conduct allergen verification testing and gluten testing in accordance with certifying bodies and internal procedures. Assess product quality and accept or reject from processing. Ensure date codes are changed on containers to reflect proper identification of product being processed. The ability to work with individuals at all levels of the organization, including appropriate confrontation as needed when any individual or department is not compliant with quality expectations. Audit and analyze food contact equipment for cleanliness. Perform sanitation inspection of production workstations prior to startup, changeover or shift relief and communicate deficiencies to supervisor. Reject unsanitary production equipment. Calibrate or replace malfunctioning equipment. Properly and timely complete all shift documentation. Routine housekeeping of assigned workstation and adjacent areas. Manage any and all HOLDS from assigned shift and ensure product, material disposition is following Food Safety requirements. Perform required line checks. Examples are metal detection, weight checks, lot checks, etc. Inspect raw materials upon arrival, ensure proper paperwork accompanies the raw materials and pull raw material retains as required. Inspect packaging materials upon arrival, ensure proper paperwork accompanies the packaging material and pull packaging material retains as required. Communicate any non-conformance issues to the Quality Supervisor or Director of Quality. Ensure team members follow all appropriate SOPs, GMPs and safety requirements. Verify equipment is calibrated as required and documented accordingly. Provide proper paperwork to the operations and warehouse teams. Qualifications: Quality Control/Assurance experience in a manufacturing or food production facility 6 months+ Knowledge of HACCP with HACCP training Must work well in a team environment and have strong communication skills. Work independently, set priorities to meet deadlines, handle multiple tasks, and make decisions under pressure. Excellent analytical and problem-solving skills with heightened attention to detail Required: - Ability to commit to a 12-hour workday & standing/walking the entirety of the shift - Working overtime weekly & working weekend days - Speak, read & write fluent English as orientation is required and material available at this time is only in English - Ability to lift up to 50lbs - Resume & longevity of past jobs is important to this position BENEFITS OFFERED TO ELIGIBLE EMPLOYEES: Medical Insurance Dental Insurance Vision Insurance 401(k) retirement plan Referral bonuses HOW TO APPLY: 1. Online Application: Start the first part of your application online at WWW.GENERAL-LBR.COM 2. Call to Schedule: Once your application is complete, call us at ************ to schedule an interview. Applications are accepted by appointment only, Office Hours: Monday-Thursday, 8:00 AM-5:00 PM 3070 Lancaster Dr NE Salem, OR 97305

Immediate Quality Control Associate Opportunity QC - Days (5:00am to 1:30pm) Salary Compensation: $17 base pay $500 Sign on Bonus* The Quality Control Technician position is responsible for a variety of different production duties. He or she will be responsible for operating various testing stations to record product data and monitor food quality status. He or she will enter data into software for quality records as well as monitor food safety in the work area. Quality Control Technicians must have high attention to detail and work at a fast pace in order to meet their key performance indicators safely and accurately. He or she also supports functions in production, sanitation and daily cleaning. Roles and Responsibilities: Monitor all production Critical Control Points (CCP's) and record data. Maintain clear and legible documentation and manually perform accurate data entry in a timely manner. Ensure that all evaluation equipment is clean and functioning properly. Responsible for placing non-conforming product on hold. Communicate any problem, product spec issue or changes in production quality to supervisor or lead personnel. Collect all samples required during production operation. Perform ATP swabbing and additional types of swabbing as needed. Operate moisture analysis, bulk density, and rotap sampling equipment. Verify pre-op documentation and periodically perform QC checks in working areas. Verify product labeling at production start-up. Verify and inspect ingredients and lot traceability on production paperwork. Monitor internal pre-requisite programs. Responsible for clear and accurate shift pass downs. Follow Standard Operating Procedures (SOP's) for line equipment and complete cleaning as needed. Follow Good Manufacturing Practices (GMP's) while in all production areas. Maintain a safe, clean, and organized work area. Participate in continuous improvement process. Complete all other duties and responsibilities as assigned or required. Knowledge, Skills, and Abilities: Must be hard working and able to work in a fast-paced, goal-oriented environment. Must be punctual and self-motivated. Ability to work individually and with a team. Must be able to perform physical requirements of the position including walking, standing, stooping and climbing. Ability to lift up to 35 pounds without restriction, using proper safety methods. Must have excellent communication skills. Computer literacy required; must be proficient in MS Word, Excel, and the Internet. Proven ability to accurately perform data entry. Demonstrated ability in basic mathematics. Must be extremely detail oriented. Must be able to work in a facility that handles allergens including, but not limited to: wheat, soy, egg, milk, celery and mustard. Ability to work in open environments, exposed to pungent odors and varying climates. Education and Experience: High School Diploma or GED preferred. Minimum of 6 months prior experience in quality control or a related field preferred. Benefits: Medical Insurance. Voluntary Dental and Vision Insurance. 80 Vacation Hours Annually. 40 Sick Time Hours Annually. Flexible Benefits Plan. Matching 401(k) Plan. BBQ's and Picnics. HB's Vision: To positively impact the lives of our families, partners, and communities for future generations by leading innovation in the food chain. HB's Mission: To develop and deliver the best food solutions for people and planet. Values: The values by which HB Specialty Foods operates its business are based upon the Company's own, unique “BLENDS” concept: COLLABORATION QUALITY INTEGRITY APPRECIATION KINDNESS SAFETY HB Specialty Foods is committed to equal opportunity for all, without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. HB Specialty Foods will make reasonable accommodations for known physical or mental limitations of otherwise qualified employees and applicants with disabilities unless the accommodation would impose an undue hardship on the operation of our business. If you are interested in applying for an employment opportunity and feel you need a reasonable accommodation pursuant to the ADA, please contact us at ************.

Nova Analytic Labs is seeking a highly motivated and qualified scientist to join our cannabis testing laboratory startup, located in Portland, ME. The testing Nova Analytic Labs will perform is critical to the health and safety of recreational and medicinal cannabis and hemp products. Nova Analytic Labs will provide the highest quality and safety in testing to the community by combining advanced technology and innovative scientific methods. As a startup, we are particularly interested in individuals with well\-rounded capabilities and an eager appetite to grow and build a successful enterprise. The ideal candidate will possess sound scientific knowledge, management skills, and an eye for continuous improvement. Flexibility and dedication are a must. The Lab Analyst I works directly under Lab Manager and ensures all samples are received, extracted, analyzed and reported in compliance with company policies and procedures. Other duties may be assigned as necessary. Duties and Responsibilities Responsible for day to day receipt and analysis of samples Responsible for solution prep and tracking Responsible for maintaining equipment logs and maintenance Perform extractions and prepare samples for analysis on LC\/MS, GC\/MS and ICP\/MS Responsible for data entry of samples in the lab Responsible for understanding and following all necessary SOPs Produce quality, mistake\-free work in the lab Ensures resolution of errors before results are released to clients Continuously seeks out new and better ideas, driving best practices Ensure samples are received, requisitioned and extracted in a manner that is compliant with SOPs Other duties as assigned by management Requirements Bachelor degree in a science related field or one year experience in a high complexity laboratory, food testing, or environmental testing laboratory High school diploma with at least 2 years experience in a high complexity laboratory, food testing, or environmental testing laboratory Some experience in a high complexity laboratory preferred Some experience with LC\/MS, GC\/MS and ICP\/MS Benefits Health care, Employee bonus\/profit sharing "}}],"is Mobile":false,"iframe":"true","job Type":"Full time","apply Name":"Apply Now","zsoid":"658476418","FontFamily":"Verdana, Geneva, sans\-serif","job OtherDetails":[{"field Label":"Industry","uitype":2,"value":"Cannabis Testing"},{"field Label":"Work Experience","uitype":2,"value":"1\-3 years"},{"field Label":"Salary","uitype":1,"value":"50k\-60k annually"},{"field Label":"City","uitype":1,"value":"Portland"},{"field Label":"State\/Province","uitype":1,"value":"Maine"},{"field Label":"Zip\/Postal Code","uitype":1,"value":"04103"}],"header Name":"Lab Analyst I","widget Id":"**********00072311","is JobBoard":"false","user Id":"**********00217001","attach Arr":[],"custom Template":"3","is CandidateLoginEnabled":false,"job Id":"**********00944085","FontSize":"12","google IndexUrl":"https:\/\/nova\-analyticlabs.zohorecruit.com\/recruit\/ViewJob.na?digest=hy RQVBoMJAbuDRSyhPCH4wc6IBmI3C5h5aYJJV25G8I\-&embedsource=Google","location":"Portland","embedsource":"CareerSite","indeed CallBackUrl":"https:\/\/recruit.zoho.com\/recruit\/JBApplyAuth.do","logo Id":"keztafeaadcb89cb34a278aa494453c4c0a8d"}

Job DescriptionCertified Group is committed to delivering expert solutions and quality testing our customers can feel confident in - on time, every time - so the world can trust in what it consumes. As a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services, Certified Group includes Food Safety Net Services (FSNS), FSNS Certification & Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc. Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, nicotine, cannabis, and hemp industries. We have embarked on an important journey to unify and strengthen our culture by living these core values: Start with the Customer, Drive to Deliver, Commit to Safety and Quality, and Believe in the Team - including believing in you. We are currently looking for a Pathogen Lab Analyst to join our growing team! $1000 HIRING BONUS!!! Job Summary: Perform analytical and microbiological testing of food products, ingredients, and environmentals. The position performs the application and evaluation of approved microbiological techniques and methodologies. Essential Responsibilities: Accurately perform and read test results and notify Laboratory Management of deviations Prepare and analyze samples for indicator organisms, pathogens, and chemistries Apply aseptic/microbiological techniques in daily workload Report inventory and expendable supplies/materials needed for testing requirements Provide routine preventive maintenance by daily cleaning, sanitizing, trash disposal, and equipment quality control Assist in quality duties to by taking incubator temperatures, inoculating control organisms, running media controls, etc. Pursue an assigned series of processes, procedures, or techniques in accordance with FSNS policies/procedures and customer requirements Maintain a high degree of technical competence by reading scientific journals, attending professional workshops, and being aware of food industry issues and trends Perform all activities in a neat, safe, hygienic, and efficient manner Share information in an open and timely manner Assisting with managing priorities and schedule such that individual goals as well as team goals are achieved with encouraged participation in the Food Safety Net Services Team Responsible for the safety of oneself and others working within their area Supervision: This job does has no supervisory responsibilities. Education & Experience: Associate degree in Life Science or related field with two or more years of laboratory experience, preferred Two or more years of experience in a commercial food-testing or analytical laboratory Or equivalent combination of education and experience Working knowledge of aseptic sampling technique, automated lab equipment, and acceptable methods and procedures Familiarity with GLP, OSHA guidelines, FDA, BAM, APHA, ISO, and USP methods and procedures Broad knowledge of concepts, practices, and procedures of a food testing laboratory Ability to travel when necessary Physical Demands/Work Environment: Dexterity of hands and fingers to operate a computer keyboard, mouse and to handle other communications/computer components Potential exposure to odors, fumes, airborne particles, hazardous chemicals, and microbiological pathogens Noise level varies from quiet to loud Temperature varies from hot to cold Interactive and fast-paced team oriented tasks Overnight Travel is required at the discretion of management Occasionally lift and/or move up to 25 pounds Color vision and depth perception Benefits: Progressive 401k Retirement Savings Plan Employer Paid Short- Term and Long-Term Disability, and Life Insurance Group Medical Tuition Reimbursement Flexible Spending Accounts Dental Paid Holidays and Time Off Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status.

The metal fabrication Quality Control Technician is responsible for verifying all fabricated metal parts meet established quality standards. The technician will work closely with the Quality Engineer to complete inspections throughout the production process. This involves using measuring tools and techniques to identify defects, ensuring compliance with blueprints and specifications, and reporting any issues to production teams to maintain product quality and prevent further problems. Responsibilities + Inspect fabricated parts by visually and physically examining metal components at various stages of production, such as raw materials, cut pieces, welded joints, and finished products, to check for dimensional accuracy, surface defects, and compliance with design specifications. + Utilize measuring tools such as tape measures, levels, calipers, micrometers, gauges, and other measuring instruments to ensure tolerances are met. + Read blueprints and specifications to thoroughly understand engineering drawings and technical specifications and verify that each fabricated part adheres to the intended design. + Identify potential quality issues such as misalignment, warping, scratches, dents, improper welding, and other imperfections during inspection. + Document inspection findings on quality control forms, noting any non-conforming parts and documenting corrective actions taken. + Communicate with production teams by reporting identified issues to production personnel and providing feedback to improve manufacturing processes and prevent future quality problems. + Implement corrective actions by working with operators to address quality issues by adjusting machining parameters, re-working defective parts, or implementing process improvements. + Maintain quality standards by ensuring adherence to established quality control procedures and industry standards, including safety regulations. Essential Skills + Strong understanding of metal fabrication processes, including cutting, welding, and bending. + Proficiency in reading and interpreting blueprints and technical drawings. + Attention to detail with the ability to check large quantities of documents to ensure they meet code specifications. + Expertise in using both standard and precision measuring tools, such as tape measures, levels, calipers, micrometers, and gauges. + Excellent communication and problem-solving skills. + Familiarity with quality control methodologies and documentation practices. + Proficiency in working with computers, including Word, Excel, Adobe, and Outlook. Work Environment The role involves splitting time between the office and the shop floor, looking at parts, reviewing documentation specific to each build, and interacting with machine operators, welders, and inspectors. Flexible start and finish times for scheduling are offered, and the company supports obtaining a CWI certification if not already held. Upon conversion, 100% of medical benefits are paid for the employee and all family members, and the 401k employer contribution is based on profitability, not dropping below 15% in the past five years. Job Type & Location This is a Contract to Hire position based out of Portland, OR. Pay and Benefits The pay range for this position is $23.00 - $30.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Portland,OR. Application Deadline This position is anticipated to close on Jan 29, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Location: 255 N Steelhead Way, Boise, ID 83704 Hire type: Full-Time Shift: 1st Shift Pay Range: $20 - $22 /hr Schedule: Monday to Friday Ability to commute/relocate: Boise, ID 83704: Reliably commute or planning to relocate before starting work (Required) JOB description Position Summary: The QA Inspector is responsible for inspecting parts, manufactured both internally and externally and providing information relative to the compliance of the parts relative to released documentation. This position will also include Final Weapons inspection as well as lasering of finished parts. PWS has a vast portfolio of weapons systems in production as well as in development. Candidates need to have understanding of basic weapons function and be willingness to learn internal process that we use. Essential Duties and Responsibilities: Inspect parts daily using appropriate measurement devices Maintain Quality Assurance paperwork Work with shop/vendor to resolve parts issues Maintain clean workspace with some shared tools Competencies: To perform the job successfully, an individual should demonstrate the following: Communications - Exhibits good listening and comprehension. Expresses ideas and thoughts in written form. Expresses ideas and thoughts verbally. Keeps others adequately informed. Selects and uses appropriate communication methods. Verbal communication skills are paramount. Must be able to deal with different personalities while effectively communicating the discrepancy to the team. Customer Service - Displays courtesy and sensitivity. Manages difficult or emotional customer situations. Meets commitments. Responds promptly to customer needs. Solicits customer feedback to improve service. Dependability - Commits to doing the best job possible. Follows instruction. Keeps commitments. Meets attendance and punctuality guidelines. Responds to requests for service and assistance. Takes responsibility for own actions. Planning & Organization - Integrates changes smoothly. Plans for additional resources. Prioritizes and plans work activities. Sets goals and objectives. Uses time efficiently. Works in an organized manner. Must be detail oriented. Quality - Fosters quality focus in others. Improves processes. Measures key outcomes. Sets clear quality requirements. Solicits and applies customer feedback. Use of Technology - Adapts to new technologies. Demonstrates required skills. Keeps technical skills up to date. Troubleshoots technological problems. Uses technology to increase productivity. Flexibility - The ability to quickly adapt to new challenges that arise in a manufacturing environment. Ability to work with people on a team Lean Manufacturing - Exercises a commitment to driving value and eliminating waste. 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 may be made to enable individuals with disabilities to perform the essential functions: Education/Experience: Degree from academic or trade school preferred but not required. Should have experience with GD&T, MCOSMOS, MeasurLink 8 and above. Experience using and setting ring gages, using thread wires, and knowledge of thread classes. Experience using different types of dial gages, basic hand tool measurement equipment including measuring coating thickness. Experience using Mahr and Mitutoyo equipment. Knowledge of basic calibration schedule and requirements. Prior machine shop experience. Language Ability: Read, analyze and interpret typical manufacturing documents. Ability to read and interpret technical drawings as well as identify non-conformances on physical parts. Effectively present information and respond to questions from managers. Mathematical Ability: Must be able to conduct many types of mathematical problems including the ability to calculate figures and amounts such as proportions, percentages, area, circumference and volume. Ability to apply concepts of basic algebra and geometry. Reasoning Ability: Solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Interpret a variety of instructions furnished in written, oral, diagram, or schedule form. Critical Thinking/Problem Solving a must. Integrity is a high priority in this department of PWS. Computer Skills: To perform this job successfully, individuals must have basic computer related skills including familiarization with word processing, spreadsheet, and MRP/ERP software. Certificates and Licenses: Lean/Six Sigma and QA certification desirable but not required. Past machining experience a plus. Supervisory Responsibilities: none required Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. The noise level in the work environment is usually moderate. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to sit. The employee is frequently required to talk or hear. The employee is occasionally required to stand; walk; use hands to finger, handle, or feel and reach with hands and arms. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision and ability to adjust focus. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Qualifications other: Cannot have Felony conviction-weapons will be handled daily throughout the facility. Job will start immediately upon hire. Benefits: 401(k) Dental insurance Health insurance Paid time off Vision insurance

Are you interested in joining IDEXX as a R&D Product Support & Enhancement Laboratory Technician? This is an opportunity to be a member of the Assay R&D organization. Your role will be critical to lab and instrument maintenance as well as managing and testing new product prior to release. What you will do: Performs laboratory testing of various pet assay and other animal illnesses, injuries and diseases; processes specimens, manages assay results, and assists in assay research Performs testing across multiple platforms that require a strong level of technical ability, including proper pipetting technique Maintains and communicates schedules and changes in schedules Manages lab inventory, procures supplies and stocks shelves Responsible for general lab maintenance and overall cleanliness of lab and lab equipment Supports and maintains various processes, systems and databases Performs record keeping, data collection, analysis, and electronic notebook Receives and aliquots biological samples as well as maintains sample tracking database Performs instrument calibration and QC Potential to handle sterile or biohazardous materials Prepare and dilute reagents What you need to succeed: High School degree with 0-3 years of experience or science related associates degree with no experience Vet technicians are encouraged to apply Ability to properly pipette is required Ability to read and interpret documents such as safety rules, standard operating procedures (SOPs), material safety data sheets (MSDSs), operating and maintenance instructions, instrument and software manuals, government rules and technical procedures Good computer skills: Microsoft Office Suite preferred, Strong Excel skills required Ability to prioritize and multi-task Strong initiative and follow through as well as self-motivation Attention to detail Strong verbal and written communication skills in order to collaborate across the organization working with different scientists Must be reliable - attendance is an essential function of the position Ability to work independently and as a team contributor Willingness to learn new skills What you can expect from us: Hourly Pay Range: $21.50/hour Opportunity for annual cash bonus Health / Dental / Vision Benefits Day-One 5% matching 401k Additional benefits including but not limited to financial support, pet insurance, mental health resources, volunteer paid days off, employee stock program, foundation donation matching, and much more If you're looking for a role that'll challenge you, offer a variety of work and learning, while helping an amazing industry, we'd love to hear from you! Why IDEXX: We're proud of the work we do because our work matters. An innovation leader in every industry we serve, we follow our Purpose and Guiding Principles to help pet owners worldwide keep their companion animals healthy and happy, to ensure safe drinking water for billions, and to help farmers protect livestock and poultry from disease. We have customers in over 175 countries and a global workforce of over 10,000 talented people. So, what does that mean for you? We enrich the livelihoods of our employees with a positive and respectful work culture that embraces challenges and encourages learning and discovery. At IDEXX, you will be supported by competitive compensation, incentives, and benefits while enjoying purposeful work that drives improvement. Let's pursue what matters together. IDEXX values a diverse workforce and workplace and strongly encourages women, people of color, LGBTQ+ individuals, people with disabilities, members of ethnic minorities, foreign-born residents, and veterans to apply. IDEXX is an equal opportunity employer. Applicants will not be discriminated against because of race, color, creed, sex, sexual orientation, gender identity or expression, age, religion, national origin, citizenship status, disability, ancestry, marital status, veteran status, medical condition, or any protected category prohibited by local, state, or federal laws. While we appreciate our staffing partners, we are unable to accept unsolicited agency resumes. #LI-CAG

MWH is a leading water and wastewater treatment focused general contractor in the US with a rich history dating back to the 19th century Fueled by the mission of Building a Better World our teams are rapidly growing across the nation As a company committed to our teams well being and growth we offer a supportive work environment opportunities for advancement and the chance to contribute to a mission that shapes the future Your expertise and ambition are valued here The work we do matters The critical systems infrastructure we build changes lives betters communities and improves ecosystems If youre passionate about this we want to hear from you About the Role MWH is currently seeking an experienced Quality Control Inspector to support project work in Gresham OR The Tunnel & Piping QC Inspector is responsible for performing quality inspections and documentation for tunneling and pipeline construction activities on public agency infrastructure projects This role ensures work is performed in compliance with approved plans specifications quality requirements and regulatory standards and supports the project Quality Control program through proactive field inspections and reporting Primary Responsibilities Perform field inspections of tunneling and piping construction activities to verify compliance with contract documents and quality standards Inspect installation of pipe materials joints coatings linings supports and appurtenances Monitor tunneling operations including excavation ground support lining installation and restoration Verify compliance with approved means and methods inspection and test plans and quality procedures Document inspection results test data and non conforming work; track corrective actions Coordinate with field crews superintendents and Owner inspectors to resolve quality issues Verify materials certifications and test reports meet project and Owner requirements Support preparation of quality records inspection logs and as built documentation Required Qualifications 9 years of experience in construction inspection or quality control for tunneling and pipeline projects Proven experience inspecting large diameter piping installations and tunnel related work Strong knowledge of construction drawings specifications and inspection standards Familiarity with public agency construction and quality requirements Strong attention to detail documentation and communication skills Ability to work independently in active construction environments Preferred Qualifications Experience on municipal water or wastewater infrastructure projects Familiarity with tunneling methods OSHA 30 Confined Space and First AidCPR certifications Compensation Anticipated yearly salary for this role is 130000 150000 based on experience Benefits Group health & welfare benefits including options for medical dental and vision100 Company Paid Benefits Employee Life Insurance & Accidental Death & Dismemberment AD&D Spouse and Dependent Life & AD&D Short Term Disability STD Long Term Disability LTD Employee Assistance Program and Health AdvocateVoluntary benefits at discounted group rates for accidents critical illness and hospital indemnity Flexible Time Off Program includes vacation and personal time Paid Sick and Safe LeavePaid Parental Leave Program10 Paid Holidays 401k Plan company matching contributions up to 4Employee Referral Program MWH Constructors is a global project delivery company in heavy civil construction with a focus on water and wastewater treatment infrastructure With the ultimate goal of delivering maximum value to clients and their local communities MWH Constructors provides single source integrated design and construction services through a full range of project delivery methods Incorporating industry leading preconstruction and construction services the Companys multi disciplined team of engineering and construction professionals delivers a wide range of projects including new facilities infrastructure improvement and expansion and capital construction services Equal Opportunity Employer including disabled and veterans Please note that all positions require pre employment screening including drug and background check as a condition of employment LI JB1

We are Nightforce OpticsRUGGED. RELIABLE. REPEATABLE.™ Nightforce Optics is a leading manufacturer and marketer of premium sport optics products, including riflescopes, spotting scopes and accessories. Known for its rugged products designed for use in punishing conditions, Nightforce is the industry benchmark for high-quality, high-performance products. Nightforce Optics, Inc., was established in 1992 with one goal in mind: to build the finest riflescopes on the market. The same qualities that have made Nightforce the choice of professionals have now created a dedicated following among hunters and serious shooters. We want you to become part of our story! Nightforce Optics is seeking a dedicated Quality Control Inspector to join our team. The Quality Control Inspector plays a critical role in ensuring products meet established quality standards and specifications throughout all stages of the manufacturing process. This position is responsible for performing advanced inspections and testing, identifying and resolving quality issues, and supporting continuous improvement initiatives. The position works closely with production and engineering teams to drive consistent product quality and support the company's overall quality assurance objectives. What You Will Be Doing: Essential Job Duties Perform visual, dimensional, and functional inspections of raw materials, in-process components, and finished products to ensure compliance with engineering drawings and quality specifications. Use precision measuring tools such as micrometers, calipers, height gauges, CMMs, and optical/vision systems to determine product conformance. Develop and execute inspection plans, selecting appropriate methods, tools, and techniques to meet product and process requirements. Operate CMM and vision systems; assist with developing, programming, and optimizing inspection programs for new and existing components. Diagnose and troubleshoot standard inspection and measurement system issues, providing actionable recommendations for resolution. Identify quality issues, support root cause analysis, and assist with corrective and preventive actions to improve product quality. Maintain accurate inspection records, quality logs, and nonconformance documentation; communicate results and concerns to appropriate teams. Ensure inspection activities comply with company procedures, safety requirements, and applicable industry standards. Verify proper calibration, maintenance, and functionality of inspection tools and equipment; report and resolve equipment issues as needed. Collaborate closely with production, engineering, and other departments to resolve quality concerns and support efficient manufacturing workflows. Requirements What we need to see: Required Qualifications High school diploma or equivalent 3+ years in quality control, machining, or a related manufacturing role, including familiarity with quality inspection tools and techniques Solid understanding of interpreting technical drawings Strong understanding of quality control principles, methods, and tools Experience with advanced measuring instruments including but not limited to micrometers, calipers, CMM, etc. Ability to analyze data and generate detailed reports Proficiency with basic computer programs Excellent problem-solving skills, with the ability to identify issues and implement corrective actions Strong organizational and time-management skills Good communication and interpersonal skills for working with different departments and team members Physical Requirements: Required to LIFT/CARRY: 25 pounds up and occasionally up to 50 pounds with or without accommodation Required to PULL/PUSH Frequently: up to 25 pounds Bend: Frequently Twist: Occasionally Squat: Occasionally Climb: Occasionally Kneel/Crawl: Occasionally Reach/Reach Overhead: Frequently Finger Dexterity/Fine Manipulation: Continuously Sit: Frequently Stand: Frequently Computer/Mouse Use: Continuously Drive: Occasionally Repetitive Motion: Substantial movements of the wrist, hands, and/or fingers What Sets Us Apart? 100% paid benefits for the employee including: medical, dental, vision, short term disability, long term disability, and life insurance Paid Time Off Package - 60 hours your first year and increases year after year 10-13 paid holidays per year Matching 401k after one year of employment 4-day work week, who doesn't like 3-day weekends? Pride in our product Employee discount on scopes and Nightforce apparel Nightforce Optics is an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race/ethnicity, color, religion, gender, sex, national origin, age, sexual orientation, gender identity, protected veteran status, disability or any other category protected by law. Note: All job offers are contingent on passing pre-employment requirements, including a drug screen and criminal background check. Applicants must also be a "US Person" as defined by the International Traffic in Arms Regulations (ITAR). Application Deadline: February 1, 2026 @11:59pm

Serán BioScience is looking for a scientist with laboratory experience to support manufacturing of pharmaceutical drug products within our In-Process Control group. As a scientist within the Quality Control department you will work alongside a team of scientists and operators to ensure the highest quality product by testing raw materials and production equipment within GMP manufacturing and laboratory environments. Qualified candidates will demonstrate expertise in utilizing specialized laboratory equipment, techniques, and methodologies for technical assessments and data analysis purposes. Preference will be given to those with experience in GMP environments and technical data review specific to the pharmaceutical industry. Serán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.Duties and Responsibilities Adheres to Standard Operating Procedures, cGMPs, Quality Manual, and company policies Performs routine testing using analytical equipment including but not limited to HPLC, GC, KFC, Disso, etc. Conducts appearance testing, solution preparation, raw material sampling, and pH measurement Drafts stability tables, sets-up stability studies, logs-in samples and standards Cleans lab and glassware and disposes of analytical waste appropriately Participates in process improvement and other non-routine projects Enters clean spaces with appropriate PPE to collect various samples Is familiar with introductory analytical equipment (e.g., HPLC, GC-HS, TOC, FT-IR) Is familiar with raw materials testing requirements (compendial and client testing) Conducts peer review of routine testing at the discretion of the relevant supervisor Performs technical writing and reporting including but not limited to: incident reporting, laboratory investigations, CAPAs, SOPs, trend reports, risk assessments, etc. Performs hypothesis testing or investigative work for OOS results under management and SME guidance Demonstrates cross-functional support capabilities with other QC teams Responsibilities may increase in scope to align with company initiatives All other related duties as assigned Required Skills and Abilities Hands-on lab experience in HPLC, CG-HS, TOC, FT-IR Hands-on lab experience with raw materials testing Strong verbal and written communication skills Demonstrated ability to collaborate and work in cross-functional teams Strong organizational skills and attention to detail Follows detailed written and oral instructions Strong time management skills with a proven ability to meet variable and competing deadlines Strong analytical and problem-solving skills Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the Company Multitasks and adjusts priorities in a fast-paced environment, while maintaining focus and managing disruption and/or unexpected needs Accepts feedback from a variety of sources and constructively manages conflict Ability to prioritize tasks and to keep leadership apprised of performance to timelines Ability to function well in a high-paced and at times stressful environment Proficient with Microsoft Office Suite or related software Education and Experience Bachelor's degree in related scientific discipline 3 years of hands-on laboratory experience required, cGMP preferred Minimum of 2 years of GMP experience required to be considered for Scientist II Physical Requirements Prolonged periods of sitting or standing at a desk and working on a computer Prolonged periods of sitting or standing in laboratory environment Must be able to lift up to 25 pounds at times Adheres to predicable in-person attendance Motor skills required for basic laboratory operations Compensation correlates to skills and experience presented by selected candidate. Visit ******************************** to learn more about company culture and the community of Bend, Oregon. Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. Benefits Summary:Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees' wellbeing, along with access to pet insurance. The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701

The Quality Control Laboratory Assistant (QC Lab) helps to provide support to the Quality Control Laboratory while focusing on processing and organizing incoming samples for receipt, preparing samples for client and contract lab shipments, communicating with internal and external partners, and supporting other processes within the Quality Control Laboratory and Quality Department. Duties and Responsibilities: Log and processes incoming samples for receipt Maintain sample tracking log Prepare samples for shipment to contract laboratories for analysis and to clients for approval Assist with ordering and inventory maintenance of QC laboratory supplies Work closely with internal/external partners and communicate sample disposition Communicate effectively with clients on sample shipments and provide tracking information Perform equipment calibration activities and shipping of equipment for calibrations Maintain product standards and prepare standards for use May assist with raw material, component, and finished goods inspection (ANSI Inspection) Participate in Lean initiates, GEMBA walks, and other process improvement activities May assist with data entry of batch records, OOS, and other information assigned Other duties as assigned Elevation Labs provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, or genetics. In addition to federal law requirements, Elevation Labs complies with applicable state and local laws governing nondiscrimination in employment at every location in which the Company has facilities. 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 essential duties listed are representative of the major duties required of this job; ability to perform the essential functions with or without reasonable accommodation is required. Elevation Labs may make reasonable accommodation to the known physical or mental limitation of otherwise-qualified individuals with disabilities unless the accommodation would impose an undue hardship on the operation of our business. This job description is not designed or intended to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required for this job. Specific duties and responsibilities may vary based upon departmental needs. Incumbent may be asked to perform other duties as assigned. Knowledge & Skills: Ideal Candidate Qualifications: High attention to detail and organization with effective time management skills Background in receiving and shipping packages using online platforms Able to communicate effectively in writing and verbally in English Able to operate a computer (i.e., Microsoft applications, ERP system, lab software) Perform essential duties and responsibilities efficiently and accurately with minimal supervision Education/Experience: High School Diploma or Equivalent Prefer experience with sample receipt in a laboratory setting Physical/Mental Demands: Regularly/Frequently required to sit, stand, walk, stoop, kneel, bend Regularly/Frequently use hands to keyboard or type, handle materials, manipulate tools, and reach with hands and arms Occasionally/Frequently lift and/or move up to 25 pounds and, infrequently, up to 50 pounds Perform tasks requiring manual dexterity and use of tools and equipment parts Must be able to move between facilities on our campus Specific vision abilities required by this classification include close vision, depth perception, color determination, and ability to adjust focus Must be able to communicate effectively in person, by telephone, and via messaging Requires composure and ability to prioritize and handle many urgent tasks and requests simultaneously with a high level of competence and accuracy Maintain confidentiality The physical demands identified above are representative of those that will be required to successfully perform the essential functions of this job. Work Environment: Office, Lab and Manufacturing settings Noise level is usually moderate Fast paced Regularly required to work in areas where chemical materials are encountered Regularly required to wear appropriate personal protective equipment May involve exposure to shop environment including variable noise levels Must customarily have a high consciousness for personnel and equipment safety Job Posted by ApplicantPro

Certified Group is committed to delivering expert solutions and quality testing our customers can feel confident in - on time, every time - so the world can trust in what it consumes. As a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services, Certified Group includes Food Safety Net Services (FSNS), FSNS Certification & Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc. Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, nicotine, cannabis, and hemp industries. We have embarked on an important journey to unify and strengthen our culture by living these core values: Start with the Customer, Drive to Deliver, Commit to Safety and Quality, and Believe in the Team - including believing in you. We are currently looking for a Pathogen Lab Analyst to join our growing team! Job Summary: Perform analytical and microbiological testing of food products, ingredients, and environmentals. The position performs the application and evaluation of approved microbiological techniques and methodologies. Essential Responsibilities: * Accurately perform and read test results and notify Laboratory Management of deviations * Prepare and analyze samples for indicator organisms, pathogens, and chemistries * Apply aseptic/microbiological techniques in daily workload * Report inventory and expendable supplies/materials needed for testing requirements * Provide routine preventive maintenance by daily cleaning, sanitizing, trash disposal, and equipment quality control * Assist in quality duties to by taking incubator temperatures, inoculating control organisms, running media controls, etc. * Pursue an assigned series of processes, procedures, or techniques in accordance with FSNS policies/procedures and customer requirements * Maintain a high degree of technical competence by reading scientific journals, attending professional workshops, and being aware of food industry issues and trends * Perform all activities in a neat, safe, hygienic, and efficient manner * Share information in an open and timely manner * Assisting with managing priorities and schedule such that individual goals as well as team goals are achieved with encouraged participation in the Food Safety Net Services Team * Responsible for the safety of oneself and others working within their area Supervision: * This job does has no supervisory responsibilities. Education & Experience: * Associate degree in Life Science or related field with two or more years of laboratory experience, preferred * Two or more years of experience in a commercial food-testing or analytical laboratory * Or equivalent combination of education and experience * Working knowledge of aseptic sampling technique, automated lab equipment, and acceptable methods and procedures * Familiarity with GLP, OSHA guidelines, FDA, BAM, APHA, ISO, and USP methods and procedures * Broad knowledge of concepts, practices, and procedures of a food testing laboratory * Ability to travel when necessary Physical Demands/Work Environment: * Dexterity of hands and fingers to operate a computer keyboard, mouse and to handle other communications/computer components * Potential exposure to odors, fumes, airborne particles, hazardous chemicals, and microbiological pathogens * Noise level varies from quiet to loud * Temperature varies from hot to cold * Interactive and fast-paced team oriented tasks * Overnight Travel is required at the discretion of management * Occasionally lift and/or move up to 25 pounds * Color vision and depth perception Benefits: * Progressive 401k Retirement Savings Plan * Employer Paid Short- Term and Long-Term Disability, and Life Insurance * Group Medical * Tuition Reimbursement * Flexible Spending Accounts * Dental * Paid Holidays and Time Off Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status. Sunday-Thursday 12pm-9pm