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Quality Control Scientist I/II, In-Process Control
SerÁN Bioscience
Quality control analyst job in Bend, OR
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.
$51k-87k yearly est. 14d ago
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Quality Control Technician
Office 4.1
Quality control analyst job in Pocatello, ID
Job Title: Quality Control Canning Technician
Department: Canning Department
Reports To: Canning Supervisor
FLSA Status: Non-Exempt
Prepared By: Canning Business Unit Manager
Salary Level: 6A C
SUMMARY
This position is responsible to ensure product compliance with all Critical Control Points and Preventative Controls for the production of Low Acid Canned Foods (LACF) (21CFR113).
Completes quality checks for Canning activities to assure that WIPs (work-in-process) and finished products meet specified requirements. Assesses manufacturing and equipment conditions to assure they meet specified requirements.
Provision for coverage of these responsibilities during an absence includes substitution by Canning Op 1, QFS Canning Coordinator, or similar trained and qualified personnel.
ESSENTIAL DUTIES AND RESPONSIBILITIES may include the following. Other duties may be assigned.
Conducts monitoring tests on WIPs and/or finished products: weight, viscosity, pH, brix, moisture, strained weight, vacuums, etc.
Evaluates flavor, texture and odor of soups, sauces and finished products.
Monitors physical and numerical values on equipment such as temperature, time, pressure, metal rejection, etc.
Inspects and evaluates packaging including can seams, label placement, lid tightness, line clearance between products, etc.
Reviews and verifies canning paperwork and monitoring tests are completed in an accurate and timely manner with appropriate response to out of specification events
Immediately reports out-of-spec materials and operating conditions to the Manufacturing and QFS Supervisors.
Assists with solutions to problems encountered with products and procedures.
Immediately track and report (place on Hold) product when raw materials, WIPs, or finished product do not meet requirements.
Monitors Good Manufacturing Practices of all individuals in the plant and warehouse. Advises infractions to supervisor.
SUPERVISORY RESPONSIBILITIES
This job has no supervisory responsibilities.
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/or EXPERIENCE
High school diploma or general education degree (GED); or one to three months related experience and/or training; or equivalent combination of education and experience.
Preferred:
Previous experience with food products
SKILLS
Detail oriented
Works well with others
Basic math skills
Bilingual Spanish/English
Reliable/Dependable
LANGUAGE SKILLS
Ability to read and comprehend simple instructions, short correspondence, and memos.
Ability to write simple correspondence.
Ability to effectively present information in one-on-one and small group situations to customers, clients, and other employees of the organization.
MATHEMATICAL SKILLS
Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.
Ability to compute rate, ratio, and percent and to draw and interpret bar graphs.
REASONING ABILITY
Ability to understand and utilize a 24-hour clock.
Ability to apply common sense understanding to carry out detailed but uninvolved written or oral instructions.
Ability to deal with problems involving a few concrete variables in standardized situations.
CERTIFICATES, LICENSES, REGISTRATIONS
Successful completion of Better Process Control School certification
Canning Technician will require special training on can seam analysis
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. 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 sit. The employee is occasionally required to stand; walk; use hands to finger, handle, or feel; talk or hear; and taste or smell. The employee must occasionally lift and/or move up to 10 pounds. Specific vision abilities required by this job include close vision, and color vision.
WORK ENVIRONMENT
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.
While performing the duties of this job, the employee is occasionally exposed to wet and/or humid conditions and moving mechanical parts. The noise level in the work environment is usually loud.
$36k-48k yearly est. 5d ago
QA Associate
Omic USA Inc.
Quality control analyst job in Portland, OR
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.
$46k-71k yearly est. 12d ago
Sr. QC Analyst
Compass Consulting
Quality control analyst job in Hillsboro, OR
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.
$65k-87k yearly est. 43d ago
Quality Control Technician
Yellowstone Local 3.9
Quality control analyst job in Tigard, OR
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.
$70k-90k yearly 11d ago
ELID - QC Tech (A-Shift)
Elevation Labs 4.2
Quality control analyst job in Idaho Falls, ID
Inspects and oversees all production line inspections of all finished goods manufactured in the production area.
Duties and Responsibilities:
Review the Batch Ticket Checklist for the following: Clearing area of previous job materials; correct packing materials on the floor for the job; encoding devices are set correctly for lot code and/or expiration date; set-up fill weights are in spec; label height is correct and signed-off label placement standard is nearby; all retain samples have been collected and taken to the Q.C. lab.
Check the Batch Ticket Bill of Materials/Component Sheet to be sure all parts are accounted for and that they are correct. This includes comparing Item Numbers and Item Description to carton labeling and the individual packaging components.
Check the filling equipment cleaning log to be sure it was updated when the last product was removed and cleaned.
Inspect at the first finished goods produced to be sure they look perfect. If the finished goods represent an item that we have not produced before it needs to be approved.
Q.C. Inspection Records. All out of specification results or defects should be circled and adequate notes of all follow-up action noted in the Job History Notes.
Q.C. Inspections should be completed four times an hour of run time. Run time includes additional packing, lot coding or labeling operations completed after off -line filling operations.
Look at finished goods for any/all defects as noted on the A.C. Inspection Records.
Report any/all problems to the Shift Lead immediately.
If there is a problem, ask the Machine Operator and/or Line Coordinator to stop the process immediately so the problem can be evaluated and corrected. This also prevents unnecessary or excessive rework.
Follow-up on defect problems by examining finished foods to be sure the problem has truly been corrected.
Must be able to perform the essential job functions with or without reasonable accommodation without posing a direct threat to the individual or others.
Always maintain a safe and clean work environment.
Additional Responsibilities:
Performs clerical tasks in the laboratories.
Performs assigned tasks in the Production area.
Performs other duties as assigned or needed.
Read and understand English paperwork.
Write and communicate in English.
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:
Perform quick and accurate count verifications.
Perform basic mathematical calculations (addition, subtraction, multiplication, division, percentages).
Perform work using good organizational skills and attention to detail.
Write legibly.
Communicate by written and/or verbally the nature of discrepancies and defects of the inspected materials.
Basic knowledge of personal computers.
Work with minimum supervision.
Perform tasks requiring manual dexterity and use of tools and/or machines (pallet jack, tape gun, hand tools).
Perform essential duties and responsibilities efficiently, accurately, and safely.
Education/Experience:
High school diploma or equivalent.
Ability to read, write, and speak English
Experience with Pallet Jacks, tape guns, tape machines, heat guns, labelers.
Previous experience with Liquid filling Machines, cappers, conveyors, lot coders & shrink tunnels preferred.
Physical/Mental Demands:
Regularly/Frequently required to sit, stand, walk, stoop, kneel, bend.
Regularly/Frequently use hands to keyboard or type, handle materials, or manipulate tools.
Regularly reach with hands and arms.
Climb stairs.
Occasionally/Frequently lift and/or move up to 50 pounds.
Specific vision abilities required by this classification include close vision, depth perception and ability to adjust focus.
Sufficient clarity of speech and hearing abilities required by this classification includes those which permit the employee to discern verbal instructions and communicate effectively in person and by telephone.
Requires composure and ability to prioritize and manage 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:
Regularly required to work in areas where chemical materials are encountered.
Manufacturing setting with moving machinery.
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.
$37k-48k yearly est. 3d ago
Quality Control Technician
Pinnacle Recruitment Services
Quality control analyst job in Idaho City, ID
Job Description
About Our Partner:
Our partner is a high-capacity frozen potato processing facility specializing in the production of frozen French fry products. The operation is driven by a strong commitment to food safety, product consistency, and regulatory compliance. Located in Idaho, the plant plays a critical role in delivering high-quality frozen potato products to customers nationwide while maintaining strict USDA, FDA, and HACCP standards.
What Our Partner Offers:
Comprehensive Benefits: Competitive salary, medical, dental, and vision insurance, paid time off and holidays, and a 401(k) with company match.
Stable Manufacturing Environment: Join a well-established frozen food operation with consistent production demand and long-term stability.
Quality-Focused Culture: Work in an environment where food safety, product integrity, and continuous improvement are core priorities.
Hands-On Impact: Play a key role in ensuring product quality and food safety from raw potatoes through finished frozen French fry products.
How You'll Contribute to Our Partner's Success:
As the Quality Control Technician, you will be responsible for monitoring, testing, and verifying product quality throughout the manufacturing process. You will support food safety systems, ensure compliance with regulatory and customer requirements, and work closely with production teams to identify and resolve quality issues. Your role will directly impact product consistency, safety, and customer satisfaction.
Key Responsibilities:
Conduct routine quality checks on raw materials, in-process products, and finished frozen French fries
Monitor Critical Control Points (CCPs) in accordance with HACCP plans
Perform sensory evaluations including color, texture, taste, odor, and appearance
Verify product specifications such as cut size, moisture, oil content, and defect levels
Collect, retain, and document samples for laboratory testing
Calibrate and verify accuracy of quality testing equipment (thermometers, scales, metal detectors, etc.)
Inspect packaging for correct labeling, coding, seals, and case integrity
Monitor sanitation practices and GMP compliance in production and packaging areas
Identify and report non-conforming products and assist with corrective and preventive actions
Complete quality records, logs, and reports accurately and in a timely manner
Communicate quality concerns to production supervisors and QA management
Participate in internal audits, customer audits, and regulatory inspections
Support continuous improvement initiatives related to quality and food safety
Follow all food safety, workplace safety, and company policies
Qualifications:
High school diploma or GED required; associate degree in Food Science or related field preferred
2-5 years of quality control or food manufacturing experience (frozen foods or potato processing preferred)
Working knowledge of HACCP, GMPs, food safety, and sanitation standards
Ability to read and interpret product specifications and quality standards
Strong attention to detail with accurate documentation skills
Familiarity with Microsoft Excel, Word, and QA systems
$37k-50k yearly est. 13d ago
QA Associate
Actalent
Quality control analyst job in Portland, OR
Job Title: QA AssociateJob Description The Quality Assurance Associate plays a crucial role in supporting the Quality Assurance Manager to ensure regulatory compliance across all laboratory operations. This position focuses on maintaining and continuously improving the laboratory's quality management system, in alignment with accreditation standards such as ISO/IEC:2017. Based on experience, the QA Associate may take ownership of specific QA tasks and serve as a backup for the QA Manager.
Responsibilities
* Support the Quality Assurance Manager in maintaining and improving the quality management system.
* Conduct in-depth internal audits and procedural audits against SOPs and LABs to ensure compliance.
* Report audit findings and assist in their resolution.
* Assist in external audit activities and implement corrective actions.
* Promote QA training and manage database records of external suppliers.
* Record and track new laboratory equipment information in LIMS.
* Coordinate internal and external calibration and verification of laboratory equipment.
* Review new or revised documentation for conformity with internal policies and regulatory compliance.
* Ensure routine maintenance and consumable replacement for water purification systems.
* Reconcile records of reference materials and solutions and ensure proper disposal of expired items.
* Maintain quality records and perform annual quality record and data archival.
Essential Skills
* Proficiency in quality assurance and regulatory compliance.
* Experience with quality management systems, GLP, ISO standards, and chemistry.
* Bachelor's degree in Chemistry, Biology, or related science from a four-year college or university and two years of relevant QA experience in a regulated laboratory.
* Working knowledge of laboratory equipment, test methods, and regulations.
* Strong analytical and problem-solving skills.
* Proficient in MS Office and Adobe Acrobat.
Additional Skills & Qualifications
* Experience with improvement and learning initiatives.
* Ability to handle multiple priorities and deadlines.
Work Environment
The position is based in a fast-paced analytical laboratory operating from 9:00 am to 5:30 pm. The team comprises six chemists, and the QA Associate reports to the Lab Manager. The work involves regular use of analytical equipment with possible exposure to hazardous chemicals. Employees must be able to understand instructions and perform repetitive hand and wrist movements. Reasonable accommodations are available for qualified individuals with disabilities. The laboratory offers designated free parking downtown, medical and dental insurance, a 401(k) plan, paid time off, and other benefits. The company organizes monthly food events, summer BBQs, and a 'Kids to Work Day'.
Job Type & Location
This is a Permanent position based out of Portland, OR.
Pay and Benefits
The pay range for this position is $52000.00 - $52000.00/yr.
Medical/vision insurance (company covers 100% of EE premium and 90% of dependent and HSA- company covers 100% of premium and contributes to HSA every month), dental insurance, LTD, FSA, supplemental insurance, LegalShield/IDShield, 401(k), PTO
Workplace Type
This is a fully onsite position in Portland,OR.
Application Deadline
This position is anticipated to close on Jan 24, 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 for other accommodation options.
$52k-52k yearly 4d ago
Quality Control
Capital Employment Group
Quality control analyst job in Boise, ID
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.
$34k-48k yearly est. 60d+ ago
Food Production Quality Control
Gliss
Quality control analyst job in McMinnville, OR
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
$23.6 hourly 3d ago
Lab Analyst I
Nova Analytic Labs 3.6
Quality control analyst job in Portland, OR
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
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$36k-49k yearly est. 60d+ ago
Lab Analyst 1
Certified Laboratories Inc. 4.2
Quality control analyst job in Boise, ID
Job Description
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
$33k-43k yearly est. 11d ago
Quality Control Tech
Boise Cascade Company 4.6
Quality control analyst job in Homedale, ID
Job Description
Boise Cascade Homedale has an exciting opening for a Quality Control Technician on Swing Shift.
Responsibilities:
The Quality Control Technician position requires a high level of self-motivation, accountability, and responsibility. This position will work swing shift (4:00 p.m. - 2:30 a.m.) following a training period. Daily tasks may include raw material evaluation, process monitoring and product testing, data collection, data entry, and report preparation. This person will participate in plant committees, safety programs, and the BIC process. This position can be seen as a good opportunity for advancement into a Supervisor position.
Leads the quality function for Homedale Beams swing shift.
Learns as much as possible about the entire glulam manufacturing process.
Communicates findings both orally and in writing to department leaders.
Perform all quality checks as required.
Maintains records as required.
Measures the effectiveness of the graders, and work with APA to train graders as required, improving grading accuracy.
Responds to directives/suggestions from APA inspectors, as required. Communicates such suggestions to the leaders in all cases.
Provides training to operations personnel on variety of topics related to his/her job responsibilities.
Performs beam quality audits and storage audits.
Monitors finishing for grading, matching accuracy, and proper warehousing.
Performs warehouse proper load identification and cleanliness.
Performs other quality checks and tasks as assigned.
Basic Qualifications:
High school diploma or general education degree (GED); Excellent communication skills and basic computer skills; must have competence in mathematics and basic statistics; effective communication and coordination within the department and with production supervisors is required.
Preferred Qualifications:
1+ years experience in quality control in the wood products industry
Bachelor's degree in Wood Science or Forestry
$40k-48k yearly est. 11d ago
QC Inspector
Primary Weapons
Quality control analyst job in Boise, ID
Location: 255 N Steelhead Way, Boise, ID 83704Hire type: Full-TimeShift: 1st ShiftPay 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
$20-22 hourly 28d ago
WX Auditor & Quality Control Inspector
Capeco Community Action Program of East Central Oregon
Quality control analyst job in Pendleton, OR
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.
$4.7k monthly 7d ago
Quality Control Inspector
Pacific Recycling Inc. 3.9
Quality control analyst job in Eugene, OR
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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
$40k-52k yearly est. Auto-Apply 60d+ ago
Aircraft QC Inspector-Oct 2022
Keltia Design, Inc.
Quality control analyst job in Beaverton, OR
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.
$37k-51k yearly est. 2d ago
Gas and Chemical Technician
Insight Global
Quality control analyst job in Tualatin, OR
The Gas and Chemical Technician will be responsible for supporting the technical demands of the site gas and/or chemical equipment. * Perform cylinder and drum changes on all chemical and gas systems and perform complex troubleshooting for all equipment.
* Ensure compliance in operation and maintenance procedures, safety.
* Be involved in Basic Safety Process, quality management, preventative maintenance, and training.
*Support installation, decommissioning, troubleshooting and repair of all Electronics Gas Systems, precursor delivery systems, & Bulk Chemical Distribution systems.
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to ********************.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: ****************************************************
Skills and Requirements
* High School Diploma or GED equivalent
* 1+ years of experience in maintenance or equipment technician
* ability to perform cylinder and drum changes on all chemical and gas systems. * Experience with chemical and gas distribution equipment
* Navy Nuclear power school or Military mechanic trained
$32k-45k yearly est. 6d ago
Quality Control Inspector
Nightforce Optics 4.1
Quality control analyst job in Orofino, ID
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
$38k-49k yearly est. 2d ago
Quality Control Scientist I/II, In-Process Control
SerN Bioscience
Quality control analyst job in Bend, OR
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
How much does a quality control analyst earn in Nampa, ID?
The average quality control analyst in Nampa, ID earns between $38,000 and $105,000 annually. This compares to the national average quality control analyst range of $40,000 to $86,000.
Average quality control analyst salary in Nampa, ID