Quality control analyst jobs in Corvallis, OR

R&D Partners is seeking to hire a Quality Control Technician I in Hillsboro, OR. Your main responsibilities as a Quality Control Technician I: Impacts quality of own work and the work of others on the team; works within guidelines and policies. Maintain a state of inspection readiness. Works autonomously with guidance only on complex new assignments. Uses ability as a technical/functional expert to contribute in development of concepts and techniques, and to complete complex assignments in creative and effective ways. Perform environmental monitoring and water sampling. What we are looking for in a Quality Control Technician I: B.A. or B.S. degree (preferably in Life Science) and at minimum 3 years experience in a cGMP pharmaceutical, biopharmaceutical industry Hands-on industrial laboratory experience with aseptic sampling and testing techniques. Demonstrated ability to apply knowledge of scientific theories, principles, and techniques used in analytical or biological test procedures. Routinely exercises sound judgment, reasoning and problem solving. Capable of working under moderate supervision and determining own short-term priorities. Why Choose R&D Partners? As an employee, you have access to a comprehensive benefits package including: Medical insurance PPO, HMO & Dental & Vision insurance 401k plan Employee Assistance Program Long-term disability Weekly payroll Expense reimbursement Online timecard approval Pay Scale: $70,188 $87,736 Dependent on Experience) R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies. R&D Partners is an equal-opportunity employer.

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.

Our client is a leading biotechnology company that discovers, develops, manufactures and commercializes medicines to treat patients with serious or life-threatening medical conditions. They are among the world's leading biotech companies, with multiple products on the market and a promising development pipeline. Role Overview: Responsibilities include Implementing, modifying, and enforcing Quality Control policies, procedures, specifications and testing methods consistent with cGMP, regulations, appropriate compendium, and company standards, policies, plans, objectives and procedures. Routine sampling, performing, and reviewing a variety of assays in the Quality Control organization in support of In-process, drug product, finished product, raw materials and incoming inspection, and environmental monitoring testing in a cGMP environment. The QC Analyst must be able to Interpret data, troubleshoots, assay failures and equipment issues while adhering to strict guidelines on cGMP documentation. Supports method validation activities, performance qualifications, method transfers, discrepancy/out-of-specification investigations and collaborates with stakeholders to identify improvement opportunities in technology and business processes. Ensure maintenance and calibration of laboratory equipment and systems. Support during cGMP audits and Health Authority inspections as needed, and follow up on any corrective measures as required. Duties: Impacts quality of own work and the work of others on the team; works within guidelines and policies. Maintain a state of inspection readiness. Works autonomously with guidance only on complex new assignments. Uses ability as a technical/functional expert to contribute in development of concepts and techniques, and to complete complex assignments in creative and effective ways. Perform environmental monitoring and water sampling. Has interaction at the Supervisor and Manager levels on matters pertaining to the immediate area of work. Interactions require tact and effective communication skills as they often involve complex and sensitive information. Participate in the design and implementation of department and cross-functional initiatives. Apply basic theory and technical principles to address moderately complex problems. Troubleshoot and initiate the resolution of Quality issues by fostering effective interdepartmental and cross functional partnerships. Serve as a technical subject matter expert (SME) in support of department functions.

Serán BioScience is searching for an experienced Quality Assurance Associate to aid in regulatory compliance for the manufacturing of oral solid dosage drug products. The primary responsibilities of this role will be to support the daily activities of Serán's Quality Assurance department by ensuring GMP regulations and internal SOPs are followed throughout the clinical manufacturing process. Essential task include reviewing and approving production records, analytical data, and internal QA documentation. Additional responsibilities include conducting risk analyses and investigations and participating in audits and inspections. Quality experience in a GMP Pharmaceutical Manufacturing setting is a requirement for this position with the ability for the title and compensation to commensurate with experience. 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 Documents authorships, reviews, and approves of SOPs, batch production and quality control (QC) records, certificates of analysis, method validations, and equipment qualifications Applies working knowledge of best practices in GMP and understands how Quality integrates with other business areas Initiates and oversees investigations Manages corrective and preventive actions (CAPA) Supports internal audits, client audits and regulatory inspections, with the potential to host Manages controlled document issuance and archival Performs quality reviews with minimal oversight Communicates quality-related information to internal teams with minimal guidance Responsibilities may increase in scope to align with company initiatives Performs all other related duties as assigned Required Skills and Abilities Knowledge of GMP and FDA regulations for clinical trial materials; commercial knowledge is desirable but not required Confident understanding of change control procedures, CAPA program, investigation and root cause analysis, and good documentation practices Excellent organizational skills and attention to detail Excellent time management skills with a proven ability to meet deadlines Strong analytical and problem-solving skills Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the company Demonstrates the ability to collaborate and work in cross-functional teams Accepts feedback from a variety of sources and constructively manages conflict Ability to prioritize tasks and to delegate them when appropriate Excellent verbal and written communication skills Ability to function well in a high-paced and at times stressful environment Proficient with Microsoft Office Suite or related software Ability to solve complex problems, take a new perspective on existing solutions, and exercise sound judgment based on the analysis of multiple sources of information to make independent decisions Education and Experience Bachelor's degree, preferably in a scientific discipline 3 years of GMP experience within a QC or QA role to meet the minimum qualifications for an Associate II 6 years of GMP experience within a QC or QA role to meet the minimum qualifications for an Associate III Pharmaceutical Manufacturing experience required, Oral Solid Dosage preferred Physical Requirements Prolonged periods of sitting or standing at a desk and working on a computer Must be able to lift up to 15 pounds at times Ability to wear required personal protective equipment (PPE), including safety glasses, hearing protection, hard hat, and safety shoes Adheres to consistent and predictable in-person attendance 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

Description: Albina Co. is seeking a detail-oriented Quality Control Technician to perform inspections, verify product conformity, and support our quality assurance processes. This role ensures our customers receive products that meet strict specifications and industry standards. The ideal candidate is self-motivated, skilled in measurement and documentation, and preferably a Certified Weld Inspector (CWI).Key Responsibilities Perform First Article, In-Process, and Final inspections. Conduct Ultrasonic Testing and Dye Penetrant Testing per specifications. Review shop orders, drawings, and customer requirements before production release. Maintain accurate QC paperwork, inspection reports, and calibrated measurement tools. Inspect welds, review welding documentation, and monitor welding processes. Support creation and review of process instructions and quality documentation. Communicate effectively with production teams and customers as needed. Why Albina Co.? Opportunity to work with advanced tools and technology (CMM, HoloLens, Fab Station). Supportive team environment with opportunities to grow your QC and inspection skill set. Competitive wages and benefits. Requirements: Qualifications CWI certification preferred. Ability to read blueprints/drawings and perform precise measurements. Experience with Microsoft Office; familiarity with Bluebeam, AutoCAD, BendPro, or CMM equipment a plus. Strong problem-solving, critical-thinking, and communication skills. Ability to work independently in a fast-paced environment. Physical Requirements Ability to stand for extended periods and lift up to 50 lbs. Work in both shop and office environments. PI62544e6c4856-31181-39207458

Job Description Stay comfortable at Northern Gold Foods! We are a climate-controlled facility. Northern Gold Foods (USA) is actively recruiting Quality Control Technicians to join our team here at our Junction City, Oregon location. Great products begin with great people, and we're always looking for the best. We produce a variety of breakfast and granola products for some the world's most iconic brands and retailers. With state-of-the-art facilities, and unmatched experience, we solve challenges that others can't. That's why many consider us the best in the world at what we do. SUMMARY: Quality Control Technicians are responsible for monitoring, sampling, and testing food products to ensure they comply with quality standardcs and customer specifications. SHIFT TIMES: Our Weekend Nights Quality Control Technicians are scheduled to work three 12-hour shifts, Friday through Sunday 6:00 PM - 6:30 AM. ESSENTIAL JOB FUNCTIONS: Monitoring, sampling, and testing food products to ensure they comply with quality standards and customer specifications Verification of sanitation activities, including preoperational inspections, swabbing, and communicating corrective actions to production personnel Liaising with production personnel and supervisors on day-to-day activities Work with customers and consumers to resolve complaints; trend and report complaints to senior management with root cause analysis and continuous improvement recommendations Investigate, trend, analyze and report complaints quarterly ESSENTIAL QUALIFICATIONS: Strong computer and organizational skills; working knowledge of MS Office. Excellent interpersonal, written, and oral communication skills. PHYSICAL DEMANDS: Activities include walking, kneeling, lifting, climbing ladders and stairs, bending, stacking, twisting, pulling, pushing, inserting, sitting, squatting, standing, accumulating, and collating motions. Be able to handle 50lbs of material with assistance occasionally. WORK CONDITIONS: Must be available to work overtime hours if needed Shifts are 12 hours, 3 days a week BENEFITS: A la carte health, dental, and vision plans 401k 8 Paid holidays AD&D & Life insurance Retention bonus program Merit raises Competitive PTO policy Employee referral program And more Northern Gold Foods is an Equal Opportunity Employer. We are committed to creating an inclusive environment where all qualified applicants receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other legally protected characteristic.

EMPWR is Growing - Join Our Team! We make healthy, delicious snack bars and are expanding fast. With over 1,300 employees across modern facilities, we focus on teamwork, safety, and growth. Be part of our journey to shape the future of healthy snacking in our state-of-the-art production facilities. Shifts available: Shift 4: 8pm - 8am every other Wednesday to Saturday Position Overview Quality control technicians 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. 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. Requirements Knowledge of HACCP with HACCP training preferred. 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. Weekend and overtime work may be required. Excellent analytical and problem-solving skills with heightened attention to detail We offer you: · Competitive Salary: Starting at $23.60 per hour (+ $2.50 night shift differential for hours worked between 5pm - 5am) with opportunities for overtime. · Continuous Learning and Development: Benefit from our training programs designed to help you grow your skills and advance in your career. · Health and Wellness: Comprehensive health insurance (medical, dental, and vision) starting on your first day of employment. · Paid Time Off: Enjoy 2-weeks paid time off (PTO) and 7 paid holidays, so you can rest and recharge, spend time with family, or pursue personal interests. · Retirement Plans: Plan for the future with our 401(k) retirement plan options, including an automatic 3% company matching to help you save for retirement. · Work-Life Balance: We understand the importance of balance. Our fixed work schedules make it so you know your time off, allowing you to plan fun activities. · Modern, Safe Work Environment: Work in a facility that is modern, clean, with comfortable temperature and adheres to the highest standards of safety and quality. Download attachment(s) This job as a PDF file

Job DescriptionDescription: Ascentec Engineering is hiring! We offer an exciting environment where you can carve your own path to success. The QC Documentation Specialist will work with the Quality Control inspection department to create and submit First Article/ Dimensional Inspection reports to Semiconductor and Aerospace customers. This position is on-site (not hybrid/not remote) at our Tualatin, Oregon headquarters and is not eligible for Visa sponsorship. Requirements: JOB RESPONSIBILITIES: Prepare, submit for approval and file First Article Inspection Report (FAIR) and Dimensional Inspection Report (DIR) documentation Review customer PO's and PO's to suppliers for requirements and Specification compliance Provide FAIR/DIR approval to release product for shipment Edit FAIR/DIR drawings with bubble numbers on all drawing requirements and features Create FAIR/DIR spreadsheets for inspectors input Photograph product, packaging and labeling for FAIR documentation Work with Customer Source Inspectors reviewing completed FAIR/DIR's Schedule Customer and Supplier Source Inspections Other duties as assigned JOB QUALIFICATIONS / EXPERIENCE AND TECHNICAL SKILLS: Able to read mechanical drawings/blueprints for machined parts and assemblies Experience with Visual IPI, DISCUS, or Net Inspect FAIR software Associate degree in English or Communications preferred. Minimum 2 years' experience with manufacturing document control or First Article documentation preferred. Proficient in Microsoft Outlook, Word and Excel PERSONAL QUALIFICATIONS: Self-Starter / Self-Motivated / Flexible / Detail Oriented Reliable and dependable Positive customer focused attitude Enjoys fast pace and rapidly changing environment Honest with stellar integrity Professional demeanor and respectful to people in all situations Flexible and willing to help others as needs and tasks change often Team player Exceptional attention to detail with excellent writing and communication skills in English. Self-directed with the ability to work independently and prioritize responsibilities. WORKING CONDITIONS: Bend and lift up to 50 lbs. The noise level in the work environment is usually low. Must be flexible to work varying schedules and hours as needed. The employee must be able to perform the essential functions of the position satisfactorily and, if requested, reasonable accommodations will be made to enable employees with disabilities to perform the essential functions of the job, absent undue hardship. The employer retains the right to change or assign other duties to this position. COMPENSATION / BENEFITS: $20 to $27 per hour DOE Medical / Dental / Vision 401k with company match up to 4% Tiered Quarterly Bonus Program Short-term and Long-term Disability Tuition Assistance or Reimbursement Life Insurance Paid time off / paid holidays Employee Assistance Programs Applicant must be able to pass a drug screen and criminal background check prior to employment. ITAR REQUIREMENTS: 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. Learn more about the ITAR here. Ascentec Engineering is an Equal Opportunity Employer; employment with Ascentec Engineering is governed on the basis of merit, competence and qualifications and will not be influenced in any manner by race, color, religion, gender, national origin/ethnicity, veteran status, disability status, age, sexual orientation, gender identity, marital status, mental or physical disability or any other legally protected status.

The Quality Associate reviews heat treat work for compliance to specification requirements. They interface with customers to communicate issues, status updates, and works to resolve those issues. They own the quality withhold area where they coordinate rework with internal and external stakeholders. They work on improvement projects to support their coworkers. Essential Duties and Responsibilities include the following. Other duties may be assigned. Perform final quality review of customer orders to ensure compliance with specifications, documentation completeness, and accuracy prior to shipment. Compile and prepare special process certification packets, including all required customer documentation, certifications, and test reports. Communicate quality-related issues, testing delays, or documentation requirements with customers in a clear and timely manner. Prepare purchase orders for external testing services; coordinate logistics and scheduling with outside labs; ensure timely delivery of test results. Provide outside testing schedules and updates to customer service and production teams to support accurate planning and delivery timelines. Collaborate with production personnel to identify, investigate, and resolve internal quality concerns; support process improvement initiatives and maintain alignment with quality standards. Own the nonconformance and rework process; ensure resolution and documentation. Participates in continuous improvement efforts. Assists with write up of commercial orders. Supports corrective action program to address deficiencies. Maintains punctual, regular, and predictable attendance. EDUCATION and/or EXPERIENCE One-year certificate from college or technical school; or three to six months related experience and/or training; or equivalent combination of education and experience. Stack Metallurgical Services, LLC offers a full range of benefits which include: Medical/Dental/Vision Flexible Spending Account Health Savings Account Short term and long-term disability Basic Life and AD&D Insurance 401(k) with match Employee Assistance Program Paid Holidays Paid Time Off Tri-Met Bus Pass Subsidy Stack Metallurgical is an equal opportunity employer, and all qualified applicants will receive consideration for employment 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.

Pacific Recycling, Inc. is a family-owned scrap metal recycling facility that values honesty and hard work. We have been recycling metal in Lane County for over 25 years and are proud to be an equal-opportunity employer. We are looking for a friendly, reliable, and hard-working person to join our team immediately. Job Summary: Quality Control is responsible for greeting, directing, and assisting customers. Grading materials, identifying prohibited items, and coordinating with scale and equipment operators. General Responsibilities: Inspect inbound and outbound loads Material grading - ensure products meet specifications and sort/separate accordingly Prohibited materials (sealed containers, hazardous materials, explosives, etc.) Direct and assist customers with material unloading Direct traffic effectively Communicate clearly and efficiently via radio to scale and equipment operators Use forklifts for unloading assistance Physical Demands: Frequently required to reach with hands and arms Able to talk and hear Standing, sitting, walking, squatting, bending, lifting, reaching, and grasping Dexterity of hands and fingers Lift up to 50 pounds from the floor to waist level and carry such objects for at least 30 feet Exposed to moving mechanical parts Frequently exposed to wet and/or humid conditions, heat, and outside weather conditions The noise level in the work environment varies from loud to very loud Experience & Qualifications Must be able to communicate effectively in English to understand instructions and emergency communications 18 years of age Must be able to pass a drug test Experience in scrapyard preferred but not required Self-motivated and eager to learn Reliable with the ability to adhere to a work schedule Forklift certification (Preferred) What We Offer: Competitive pay and bonus plan PTO starts at 2 weeks per year and increases with years of service 8 paid holidays Company-sponsored medical, vision, and dental insurance Annual safety boot reimbursement 401k Free gym membership Starting pay 18-19/hr DOE Full time position at 40 hours per week

Proven to Perform. From the edges of space to the bottoms of ocean, our materials are proven to perform -- and so is our team. We're hiring high performers as proven as our products. Join us. ATI is seeking a Lab Analyst to join our Millersburg, Oregon team. This is a night shift position and works a 12 hour Fixed Pitman Schedule, 2 days working, 2 days off, 3 days working from 7:00pm - 7:00am. This schedule offers a predictable 12 hour shift, a 3 day weekend every other week, and built in daily overtime. Schedule example: Week 1: Work Monday & Tuesday, off Wednesday & Thursday, work Friday, Saturday, Sunday Week 2: Off Monday & Tuesday, work Wednesday & Thursday, off Friday, Saturday, Sunday The person in this role reports to a Sr. Leader and will work in conjunction with other laboratory leaders to facilitate various laboratory needs. As a Lab Analyst, you are instrumental in preparing and analyzing a variety of samples by multiple analytical techniques, including ICP-OES and ICP-MS. In addition, you will put samples into solution using routine dissolution techniques, perform various wet and gravimetric chemical analyses, and practice continuous improvement on existing and new processes. In order to be successful and provide immediate impact, you will have to quickly learn ATI's processes and work with cross-functional teams within the Analytical Laboratory. You will have strong interpersonal and communication skills, be driven to meet deadlines, and have exceptional attention to detail. Additional Responsibilities Contributes to Daily Management Board communication and information-sharing activities Demonstrates Safety as a value with routine safety contacts and hazard abatements Evaluates and prioritizes incoming samples Performs routine preventive maintenance activities on instruments Works with laboratory purchasing representatives to maintain minimum inventory of critical items Performs basic problem-solving on a daily basis and as a team member during formal root cause analysis events Processes analytical data for entry into LIMS database Participates in continuous improvement activities

Proven to Perform. From the edges of space to the bottoms of ocean, our materials are proven to perform -- and so is our team. We're hiring high performers as proven as our products. Join us. ATI is seeking a Lab Analyst to join our Millersburg, Oregon team. This is a night shift position and works a 12 hour Fixed Pitman Schedule, 2 days working, 2 days off, 3 days working from 7:00pm - 7:00am. This schedule offers a predictable 12 hour shift, a 3 day weekend every other week, and built in daily overtime. Schedule example: Week 1: Work Monday & Tuesday, off Wednesday & Thursday, work Friday, Saturday, Sunday Week 2: Off Monday & Tuesday, work Wednesday & Thursday, off Friday, Saturday, Sunday The person in this role reports to a Sr. Leader and will work in conjunction with other laboratory leaders to facilitate various laboratory needs. As a Lab Analyst, you are instrumental in preparing and analyzing a variety of samples by multiple analytical techniques, including ICP-OES and ICP-MS. In addition, you will put samples into solution using routine dissolution techniques, perform various wet and gravimetric chemical analyses, and practice continuous improvement on existing and new processes. In order to be successful and provide immediate impact, you will have to quickly learn ATI's processes and work with cross-functional teams within the Analytical Laboratory. You will have strong interpersonal and communication skills, be driven to meet deadlines, and have exceptional attention to detail. Additional Responsibilities Contributes to Daily Management Board communication and information-sharing activities Demonstrates Safety as a value with routine safety contacts and hazard abatements Evaluates and prioritizes incoming samples Performs routine preventive maintenance activities on instruments Works with laboratory purchasing representatives to maintain minimum inventory of critical items Performs basic problem-solving on a daily basis and as a team member during formal root cause analysis events Processes analytical data for entry into LIMS database Participates in continuous improvement activities

Job DescriptionDescription:Albina Co. is seeking a detail-oriented Quality Control Technician to perform inspections, verify product conformity, and support our quality assurance processes. This role ensures our customers receive products that meet strict specifications and industry standards. The ideal candidate is self-motivated, skilled in measurement and documentation, and preferably a Certified Weld Inspector (CWI).Key Responsibilities Perform First Article, In-Process, and Final inspections. Conduct Ultrasonic Testing and Dye Penetrant Testing per specifications. Review shop orders, drawings, and customer requirements before production release. Maintain accurate QC paperwork, inspection reports, and calibrated measurement tools. Inspect welds, review welding documentation, and monitor welding processes. Support creation and review of process instructions and quality documentation. Communicate effectively with production teams and customers as needed. Why Albina Co.? Opportunity to work with advanced tools and technology (CMM, HoloLens, Fab Station). Supportive team environment with opportunities to grow your QC and inspection skill set. Competitive wages and benefits. Requirements:Qualifications CWI certification preferred. Ability to read blueprints/drawings and perform precise measurements. Experience with Microsoft Office; familiarity with Bluebeam, AutoCAD, BendPro, or CMM equipment a plus. Strong problem-solving, critical-thinking, and communication skills. Ability to work independently in a fast-paced environment. Physical Requirements Ability to stand for extended periods and lift up to 50 lbs. Work in both shop and office environments.

Job Description Do you have an eye for detail? Are you great at noticing things that other's might miss? Are you looking for an excellent career in the semiconductor industry? Then this is the opportunity for you! Jireh Semiconductor in Hillsboro, OR is looking for someone to join their growing team in Quality Control. This is a night shift position with a compressed schedule, working Wednesday through Friday, every other Saturday. More days off each week, plus built in overtime pay and a 15% shift differential! This is a temp-to-hire position through an existing staffing partner, conversion depends on performance and business need. Every wafer produced must meet the basic electrical and visual criteria before shipping to packaging house or our customers. Inline QC inspection consists of performing visual inspection in Macro and Micro at various steps throughout the wafer manufacturing process. Since QC technicians are our wafer quality guard, they must demonstrate not only careful working attitude with attention to detail but also good understanding of processes. DUTIES & RESPONSIBILITIES Demonstrate good understanding of the importance of safety rules Understand and follow the clean room rules and wafer handling procedures; Able to work alone and in teams. Understand and follow the Inline QC Photo Develop Inspection and Post-Etch Inspection specifications. Understand and perform the basic requirements of Inline QC inspection; Proficient with image capture of defects, microscope operation, Microsoft Excel, Microsoft Word. Successfully catch wafers with misalignment, photo defects, etch defects and other defects at all levels. Successfully catch missing or extra layers. Put wafers on hold for rework or engineering evaluation as required by the specifications. Must understand the difference between random and systematic process issues/defects. Properly calculate the yield impact rate based on the visual inspection; Understand and follow the basic QC disposition rules. Generate CEDAs correctly. Hold lots for the correct module Process Engineer as needed. Must understand the film stacks, and basic Lithography, Etch, CMP and Thin-Film deposition processes. Flexibility to cover off-shifts as needed for vacations and sick time. PHYSICAL DEMANDS / WORK ENVIRONMENT Regularly required to sit or stand and move about the facility. Exposure to cleanroom elements such as noise, fumes and odors. Required to use a microscope for prolonged periods of time. REQUIRED EDUCATION & EXPERIENCE High School Diploma and above Good eyesight without color blindness. COMPANY INFORMATION: Alpha and Omega Semiconductor (AOS) is committed to excellence in design, manufacturing, and responsiveness to our customers through the continued development of new technologies, products and innovative solutions. We bring to the market devices designed to benefit our customers by meeting their product specific needs. Our mission is to bring value to our customers, shareholders and employees. AOS differentiates itself by integrating its Discrete and IC semiconductor process technology, product design, and advanced packaging know-how to develop high performance power management solutions. AOS's portfolio of products targets high-volume applications, including but not limited to portable computers, flat panel TVs, LED lighting, smart phones, battery packs, consumer and industrial motor controls and power supplies for TVs, computers, servers and telecommunications equipment. EEO Statement: Jireh Semiconductor prohibits discrimination based on race, color, religion, gender, national origin, age, disability, veteran status, marital status, pregnancy, gender expression or identity, sexual orientation or any other legally protected status. Jireh Semiconductor, Inc., a wholly owned subsidiary of Alpha and Omega Semiconductor Ltd., is the in-house wafer fab for AOS and is located in Hillsboro, Oregon. Job Posted by ApplicantPro

The Quality Control & Assembly Technician is responsible for assembling, testing, and inspecting misting systems, water filtration units, and related components to ensure all products meet company quality and performance standards. This position plays a critical role in maintaining product reliability, safety, and compliance through precise assembly, thorough inspection, and consistent documentation. This person will be working out of our office in Hillsboro, OR. Responsibilities Assemble misting systems, water filtration units, and related components according to work orders, blueprints, and schematics. Cut, fit, and connect tubing, fittings, pumps, filters, and nozzles using hand and power tools. Prepare and install electrical connections, motors, and control components as required. Verify proper assembly of water flow components to ensure leak-free and efficient performance. Perform pressure testing and system checks to confirm product functionality and compliance with specifications. Maintain accurate production and test records in accordance with company standards. Operate equipment such as tube cutters, crimpers, threaders, drills, and test benches safely and efficiently. Assist in machine setup, part alignment, and changeovers for different product runs. Monitor production line operations to ensure consistent output and quality. Identify and troubleshoot assembly or component issues during production. Inspect incoming materials (filters, fittings, pumps, housings) for defects or inconsistencies. Conduct in-process and final quality checks, including flow rate, pressure, and leak tests. Record and report defective materials or assembly issues to the supervisor or quality team. Follow company ISO and quality assurance standards and procedures. Maintain a clean, safe, and organized work area following 5S principles. Perform basic maintenance on tools and equipment; report any malfunctions. Follow all company safety protocols, including proper use of PPE and safe handling of pressurized or electrical components. Participate in safety meetings and training sessions. Collaborate with engineering, production, and warehouse teams to resolve issues and improve processes. Suggest improvements in assembly methods, materials, or workflow for greater efficiency and quality. Assist in training new team members or temporary workers as needed. 1-3 years of experience in mechanical assembly, production, or quality control preferred. Ability to read and interpret technical drawings, blueprints, and schematics. Basic knowledge of mechanical, electrical, and fluid systems. Strong attention to detail and commitment to quality workmanship. Proficiency in using hand and power tools, measuring instruments, and testing equipment. Ability to maintain accurate records and follow written and verbal instructions. Team-oriented attitude with a proactive approach to problem-solving. Standing, bending, and repetitive motion for extended periods. Manual dexterity for assembly and precision testing tasks. While performing the duties of this job, this position may require the individual to work rotating shifts assignments, weekends, holidays, and overtime as needed. Standby and on-call duty is required, and the individual must be able to respond to the facility within one hour. Some shifts will require working alone Manual dexterity for assembly and precision testing tasks. Sitting for long periods of time (3-4 hours) Ability to climb stairs, ladders and work from heights Must Have the ability to lift 50-60 pounds using company provided equipment Education Requirements High School Diploma or GED required. Safety/Drug Screening Capability to pass background checks and initial drug screening Valid driver's license About Smart Care Smart Care is a national repair and service provider for commercial foodservice, refrigeration, and cold storage equipment. Our offering of comprehensive mechanical services includes hot side cooking equipment, stand-alone refrigeration, specialty coffee and beverage, complex rack refrigeration and HVAC. Smart Care is an Equal Employment Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other protected class status. All qualified individuals are encouraged to apply. If you need a reasonable accommodation with respect to Smart Care's application or hiring process due to a disability, please contact the Human Resources department at *************************.

Job Description CAPECO is a diverse group of people who are committed to creating a thriving community by providing education, resources, and services dedicated to eliminating poverty and contributing to the success of our community members. We hire people from all walks of life not because we must, but because we know it makes us stronger. If you share our passion for community, then we would love to meet you! Position: WEATHERIZATION AUDITOR & QUALITY CONTROL INSPECTOR Supervised by: Program Manager Department: Weatherization Classification: Regular Full Time Position Status: Non-Exempt Location: Pendleton Main Office Salary: $4,684 per month Benefits: Health, Dental, RX, Vision, FSA, Life Insurance, 401K Plan, Vacation, Sick, and Holidays POSITION OVERVIEW: Deliver weatherization auditing and inspection services in accordance with federal, state, local and utility standards. Perform occasional work involving installation of weatherization measures. Conduct training in proper installation of weatherization measures. Perform administrative work in an office setting. Assist in the development and delivery of Energy Education workshops. ESSENTIAL FUNCTIONS: An employee in this position may be called upon to do any or all of the following essential functions. This list is not all-inclusive; other duties, responsibilities and activities may change or be assigned at any time with or without notice. To perform this job successfully, an individual must be able to perform each essential function satisfactorily with or without reasonable accommodation. Conduct detailed energy audits on residential structures. Enter collected data into home energy performance analysis software to determine cost/benefit analysis. Administer diagnostic testing on all audited homes, including building and duct air leakage, static pressures, air handler performance, combustion appliance exhaust and draft testing, lead paint testing, and carbon monoxide testing. Collect samples when asbestos is suspected and submit them for testing. Identify health and safety issues. Make recommendations to management regarding selection of weatherization measures. Submit applications and reports to the state and other partner entities. Assist with administrative file work when needed. Perform brief pre-audit home inspections. Oversee contractor work through periodic inspections while jobs are in progress. Serve as primary point of contact for contractors with technical needs or questions. Support contractor work by offering hands-on or document-based training in areas where contractor knowledge or skill deficiencies are present. Provide customer service to clients regarding matters such as job progress, feedback or questions regarding contractors, and education about weatherization measures. Perform 6-month follow-up visits with clients to hear and address any concerns with completed work. Collaborate with administrative staff in matters such as contractor scheduling and bid and work order issuance. Abide by all compliance principles issued by Federal, State and Local rules and regulations relevant to client eligibility, file maintenance, audit and inspection standards, performance codes, and installation of acceptable weatherization measures and products. Maintain tools and diagnostic equipment. Ensure periodic maintenance schedules are met and perform safety checks for departmental vehicles. Serve on agency safety committee. Attend trainings to obtain certification requirements, learn new innovative technology, and incorporate new methods in our delivery of weatherization services. Assist with the development and delivery of energy conservation training courses including the proper installation of self-help materials. Read, analyze and interpret general business periodicals, professional journals, technical procedures, building codes, blueprints, and weatherization specifications. Performs other duties as assigned by the Weatherization Manager. REQUIRED KNOWLEDGE, SKILLS, ABILITIES AND MINIMUM QUALIFICATIONS: The requirements listed below are representative of the knowledge, skills, abilities, and minimum qualifications necessary to perform the essential functions of the position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Associate degree in related field, or three years of comparable experience and/or training, or equivalent combination of education and experience. Must have or obtain Oregon Lead Safe Renovator Certification, within 90 days from date of hire. Must have or obtain the following certifications within two years from date of hire: Oregon Residential Energy Analyst, Building Performance Institute residential energy auditor and quality control inspector, REM Design user, and all other certifications as deemed necessary to meet program requirements. Ability to work in a team environment. Must interact with the public, staff, contractors, peers and state program representatives in an informative and professional manner. Professionalism and workplace etiquette is expected when in the office and when conducting inspections/audits. Must present a clean, neat, and tasteful appearance during business hours or when representing CAPECO. Have a general knowledge of building techniques and weatherization materials. Ability to abide by regulations. Ability to travel out of area to attend training or deliver weatherization services. Working knowledge of office equipment (i.e. copier, fax, etc.) Strong computer skills in excel, word and outlook. Technical knowledge and ability to operate mechanical tools. Ability to communicate in a clear and concise manner; both orally and written with State officials, contractors, professional peers, clients and staff. Operate diagnostic equipment (blower door, duct blaster, infrared camera, pressure diagnostics, moisture meters, gas detection equipment, combustion analyzer, etc.) as required to meet program guidelines. Experience preferred. WORK ENVIRONMENT AND PHYSICAL DEMANDS: The physical demand and work environment characteristics described here are representative of those an employee encounters while performing the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is frequently required to stand; walk; sit; use hands to finger, handle or feel; climb or balance; stoop, kneel, crouch, or crawl; twist; bend; reach with hands and arms; talk and hear; use hands to manipulate. All audits require the employee to be in confined spaces such as crawl spaces under homes or in attics. The employee must occasionally lift and/or move objects of light to moderate weight (up to 50 pounds). Specific vision abilities required by this job include close vision and distance vision. While performing the duties of this job, the employee is frequently exposed to outside weather conditions (extreme heat and cold); moving mechanical parts; fumes or airborne particles; or risk of electrical shock. The noise level in the work environment is usually moderate. SPECIAL REQUIREMENTS: Must pass a criminal history background investigation; however, a conviction of a crime may not necessarily disqualify an individual from this position. CAPECO is a drug free workplace and pre-employment drug screening will be required. Due to federal funding, our drug screenings include the use of marijuana. Possession of, or ability to obtain, a valid Driver's License and insurable driving record is required. Travel may be required within the service area, including occasional out-of-town or overnight travel. Travel may require the use of a personal vehicle. Mileage for the business-related use of a personal vehicle will be reimbursed at the standard mileage rate as published per IRS guidelines. EQUAL OPPORTUNITY EMPLOYER CAPECO does not discriminate in employment opportunities or practices based on race, color, national origin, religion, sex, sexual orientation, gender identity/transgender status, age, disability, veteran or marital status, genetic information or any other characteristic protected by applicable law.

We are always looking forward to receiving resumes from candidates with skills and technical experience in the aerospace sector. We are very happy to receive speculative resumes if you are looking for a career change within the aerospace industry. Our flexible recruitment services will provide you with the following employment options: * Contract * Contract to Direct * Direct Our experienced consultants are experts in their field and are well placed to advise you on all aspects of aerospace recruitment opportunities, and employment trends.

QA Coordinator - Direct Hire - Wilsonville, OR Immediate opening for a Quality Control Specialist with RECENT experience working at a CNC machine shop / Fabrication Shop. Will have oversight of the Quality Control inspections of fabricated parts, inspections of produced parts, creation and review of non-conformance reports, creation and implementation of corrective and preventative action reports, interaction with product supplier quality teams, and identify areas for improvement. Must be able to read and understand engineering drawings and understand the application of symbols and tolerances. General Duties: Identification of product non-conformances, their root cause and appropriate CAPA Document and keep up to date register of all non-conformances, ensuring they are reported Document inward goods inspection, component and assembly in-process and out-going goods criteria & procedures Receive and process all customer queries and complaints Process warranty RMA parts, verify acceptability of returning parts, ensure part is return to original supplier for credit and investigation Ability and authority to cease production and customer shipments, and quarantine any defective part within the manufacturing process Day to day accountability and responsibility for the quality of the components being received from suppliers plus the final product being shipped out of the factory Inspect each & every piece of equipment to ensure non-conformances, investigate any cause and implement CAPAs within the specified limits Document product issues so that all affected parties (both internal and external) are aware of the problems and the CAPA. Process and log daily, all customer complaints received. Analyze individual complaints for appropriate CAPA and communicate with all people involved, including the person who raised the issue. Collect data pertaining to non-conforming products and customer complaints; prepare reports showing trends and other factors. Qualifications/Work Experience Minimum of 2 years of RECENT quality assurance experience in a CNC or Fabrication shop. Batch Processing involving complex engineering products will be a significant advantage Able to read and understand engineering drawing including and understanding the application of symbols and tolerances. Lean Manufacturing experience is a big plus Solid knowledge of MRP & ERP based inventory management procedures and enterprise systems for inwards goods handling and stock control activities Good understanding of mf material supply and distribution chains Methodical, organized, multi tasks, flexible and able to work under pressure Self-motivated, driven, work unsupervised, team player, passionate, professional, committed, honest and treating people with dignity and respect Able to solve problems & make decisions in line with organizational philosophies and practices High level of written, verbal and numeracy skills Demonstrates a willingness & ability to deliver information using different methods and ensures that messages have been received and understood. Good computer skills and English language proficiency, written and verbal is required

The position is responsible for ensuring that all products manufactured meet or exceed quality standards as well as all safety, environmental and ISO requirements. Implement continuous improvement initiatives in the manufacturing and QC environment. ESSENTIAL DUTIES AND RESPONSIBILITIES - Additional duties and responsibilities may be assigned as necessary. 1. QC Lab and Process Management (80%): Knowledge of work instructions, procedures, and calibration of QC instrumentation referenced in the LATICRETE Quality Control Manual. Ensures all lab testing results are filed all the Quality Control test data and enter pertinent information (CofAs) into the computer database (JDE). Ensure QC testing samples are obtained according to the Quality Requirements testing Level (Work Instruction 9.1.36) and maintain a storage system for retained samples. Monitors the execution of (G)ood (L)aboratory (P)ractices. Responsible for the entry of test results in the QC tracking system and the crosscheck of records. Has basic knowledge of 5S and can assist in training new employees Orders supplies for the QC lab and ensures the QC data-up system is maintained and updated daily. Assists in communications with production personnel to provide a smooth, efficient production flow of quality products, as needed. Ensures all QC instruments meet calibration requirements listed in the calibration work instructions. Works with team members to identify improved methods of QC analysis and/or new QC lab equipment to improve lab efficiencies. Ensure that all CoA's, MSDS, Calibration/Verification, meet ISO 9001 traceability. Complete and distribute all forms in accordance with the work instructions in the Q.C. Manual. Write a daily report of all QC testing performed on products received in the QC lab using the appropriate communication database or electronic format. Supports the root cause analysis investigation of nonconforming product Test and report on all Field Test complaints filed by technical services. Has the ability to provide improvements for QC lab workflow, testing, and other QC related activities Compare all C of A's against the Master C of A to determine acceptance or rejection and enter all pertinent data into the computer system Data Collection and Data Analysis (20%): Demonstrates problem solver abilities, while communicating with superiors with appropriate solutions in a timely and efficient manner. Computer Skills: Strong knowledge of Microsoft Office (Word, Excel) and Outlook; and ability to present technical data to QC team, business leaders and others as needed. Team Cooperation - lead the LATICRETE core values by maintaining a positive, cooperative, and professional attitude with all LATICRETE Employees and all customers. Provide and ensure batch adjustments are meeting expectations; based on QC lab batches performed. Has a strong technical knowledge of chemistry in the following area(s): cementitious chemistry, epoxy liquids, latex, and/or any LATICRETE product lines. Provide data to Quality Control Champion and Regional QC Managers for monthly KPI reports Quality Control Ways Of Working - QC WOW (Daily): Prioritize and allocate work: Delegate and allocate tasks to lab personnel to support company priorities and drive results. Set clear priorities for team and individuals, including appropriate allocation of resources (time, money and people). Build Team Culture: Consistently hold lab personnel accountable for upholding the organizations values. Properly and timely escalation of unhealthy conflict among peers and lab personnel. Foster an open environment where peers feel able to provide constructive feedback and suggestions for improvement. Communicate and Motivate: Communicate regular business updates. Convey information in a clear and timely manner. Listen carefully to the views and opinions of peers, lab personnel, and internal customers. REQUIRED SKILLS & 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 and Experience: Associates Degree in science or engineering or 3-5 years of QC laboratory experience Specialized Skills and Experience: Computer Skills: Strong knowledge of Microsoft Office (Word, Excel) and Outlook; and ability to present technical data to QC team, business leaders and others as needed. Excellent organization skills, ability to manage multiple projects with competing priorities. Good verbal, written, and math skills. Strong analytical and problem solving skill. Organized and meticulous. Possess the ability to roll-up the sleeves and execute daily QC responsibilities as required. May have strong technical knowledge or ability to leverage knowledge of chemistry in the following area(s): cementitious chemistry, epoxy liquids, latex, and/or any LATICRETE product lines. Demonstrated ability to provide improvements for QC lab workflow, testing, and other QC related activities - provide evidence of projects led Compare all C of A's against the Master C of A to determine acceptance or rejection and enter all pertinent data into the computer system. Ensures all QA requirements are met by the QC lab. Travel Requirement: Must be able to travel 0-5%. Physical Requirements: Must pass pre-employment physical. Lift: Must be able to lift and/or carry a minimum of 50 pounds. Push/Pull: Must be able to push/pull __50__ pounds. Stand: Must be able to stand __75__% of the day. Sitting: Must be able to sit __25__% of the day. Twisting/Bending: Must be able to twist/bend _25__% of the day. Squatting, Climbing and/or Crawling: Must be able to squat/climb/crawl __25_% of the day.