9 Quality Control jobs in Vancouver
Quality Control Lead
97240 Portland, Oregon
Southland Industries
Posted 11 days ago
Job Viewed
Job Description
**POSITION SUMMARY**
The Quality Control (QC) Lead is responsible for overseeing the overall implementation of the Quality Control Plan and coordinates all project testing, inspections, and reporting matters directly with the Project Commissioning Lead, Shop Managers & Project Team. Continuously improves the quality of the program through the full project life cycle.
**What you'll do:**
+ Manage and document inspections for jurisdictional, contract compliance and 3rd party requirements. document management of inspection set of drawings and individual tests leading up to final inspection coordinate jurisdictional visits with trade superintendents, include required and appropriate documentation in programs (such as Autodesk Construction Cloud (ACC)) for testing documentation.
+ Maintain certifications for qualified individuals and continuity logs verify work being done in accordance with qualified procedures and individuals.
+ Ensure that all materials and construction are in accordance with the requirements for the completeness, accuracy and constructability in accordance with applicable building codes and project specifications.
+ Participate in progress and QC meetings. Review contract drawings and identify areas/scopes where items need addressed to confirm install scope is in alignment with CD's. Verify RFI's and/or submittals cover any differences.
+ Document fabrications in accordance with Work Package's. Identify deficiencies in either quality or accuracy, document deficiencies via NCR and have corrected prior to shipment to site. Provide summary visit information and documentation to communicate with team status of WP's.
+ Verify equipment and systems installed comply with appropriate install details, requirements manufacture and/or contract drawings, completeness and quality. Develop list of items that need corrected with Trade Superintendents and/or Shop Managers. Track and oversee items on list to completion. Involved in L2 process and documentation for equipment receiving and set in place (ready for energization). Work through resolution of owner punch items relating to install scope quality with Trade Superintendents, Shop Managers, and other team members.
**What you'll need to be successful:**
+ Strong understanding and experience in Lean construction/manufacturing
+ Strong written and verbal communication skills
+ Strong analytical and project management skills
+ Ability to multi-task and prioritize projects
+ Advanced customer service skills
+ Strong presentation skills
+ Experience in progressive quality control roles preferred
+ People management preferred
+ Strong computer skills, including Microsoft Office Suite-Excel and Word and Bluebeam
+ Certified Weld Inspector (CWI) Certification is strongly preferred
+ Experience with Quality Control for Electrical Work is Preferred
**YOU Matter**
**PEOPLE FIRST: BUILDING TALENT BY DESIGN**
At Southland we aspire to build a workforce that's as diverse as the people who occupy the buildings we design, build and maintain. Building talent by design is our intentional approach to creating a truly safe, collaborative, and inclusive work environment that fosters growth, empowers professional achievement, and where people are treated with respect at all levels.
If you're someone with a true passion for our industry, a life-long learner, with high accountability and a drive for results we're looking for you! At Southland, we hire problem solvers that are focused on providing customer value through continuous improvement and will take ownership to create the best experiences that will have an impact wider than their own job. We thrive on creating a strong company and culture where you'll feel engaged, challenged, and valued.
If you're ready for the next big step in your career and want a career full of fun and excitement and to be a part of a fast-paced growing company, then **JOIN** our team and become a part of an organization that values **PEOPLE** , **SAFETY, INNOVATION, COLLABORATION, INTEGRITY, ACCOUNTABILITY & SUSTAINABILITY.**
**Benefits:**
As an employee-owned company, we offer a comprehensive benefits package that includes excellent benefits for you and your family:
+ 401(k) Plan with **50% Company Match** (no cap) and immediate 100% vesting
+ Annual incentive program based upon performance, profitability, and achievement
+ **Medical, Dental, Vision Insurance - 100% Paid for Employee**
+ Term Life, AD&D Insurance, and Voluntary Life Insurance
+ Disability Income Protection Insurance
+ Pre-tax Flexible Spending Plans (Health and Dependent Care)
+ Holidays/Vacation/Personal Time/Life Events Leave
+ Numerous training opportunities and company paid membership for professional associations and licenses
**For more information on Southland Industries, please visit our website: ** Southland Careers ( ** or on ** Facebook ( ** or ** LinkedIN ( ** **
To hear what our employees are saying about working at Southland Industries, check out our Culture site - **Explore Our Culture ( Industries and all its subsidiaries are an **Equal Opportunity Employer ** and prohibits discrimination and harassment of any kind. We are committed to the principle of equal employment opportunity for all employees and to providing our employees with a safe work environment free of discrimination and harassment. All employment decisions at Southland Industries are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, gender, gender identity, sex, national origin, ancestry, age, disability, medical condition, marital status, sexual orientation, family care or medical leave status, veteran status, or any other status protected by the laws or regulations in the locations where we operate. Southland Industries will not tolerate discrimination or harassment based on any of these characteristics.
***All employment offers are contingent upon successful, drug tests, background checks and professional reference checks. ***
***We are not able to offer sponsorship of employment at this time***
If you don't feel this position is a match for you, we encourage you to share it with others. Feel free to share throughout your social networks and follow us on Facebook, Twitter, LinkedIn, and Instagram to keep up to date on what we're doing as a company.
Required Skills
Required Experience
The Quality Control (QC) Lead is responsible for overseeing the overall implementation of the Quality Control Plan and coordinates all project testing, inspections, and reporting matters directly with the Project Commissioning Lead, Shop Managers & Project Team. Continuously improves the quality of the program through the full project life cycle.
**What you'll do:**
+ Manage and document inspections for jurisdictional, contract compliance and 3rd party requirements. document management of inspection set of drawings and individual tests leading up to final inspection coordinate jurisdictional visits with trade superintendents, include required and appropriate documentation in programs (such as Autodesk Construction Cloud (ACC)) for testing documentation.
+ Maintain certifications for qualified individuals and continuity logs verify work being done in accordance with qualified procedures and individuals.
+ Ensure that all materials and construction are in accordance with the requirements for the completeness, accuracy and constructability in accordance with applicable building codes and project specifications.
+ Participate in progress and QC meetings. Review contract drawings and identify areas/scopes where items need addressed to confirm install scope is in alignment with CD's. Verify RFI's and/or submittals cover any differences.
+ Document fabrications in accordance with Work Package's. Identify deficiencies in either quality or accuracy, document deficiencies via NCR and have corrected prior to shipment to site. Provide summary visit information and documentation to communicate with team status of WP's.
+ Verify equipment and systems installed comply with appropriate install details, requirements manufacture and/or contract drawings, completeness and quality. Develop list of items that need corrected with Trade Superintendents and/or Shop Managers. Track and oversee items on list to completion. Involved in L2 process and documentation for equipment receiving and set in place (ready for energization). Work through resolution of owner punch items relating to install scope quality with Trade Superintendents, Shop Managers, and other team members.
**What you'll need to be successful:**
+ Strong understanding and experience in Lean construction/manufacturing
+ Strong written and verbal communication skills
+ Strong analytical and project management skills
+ Ability to multi-task and prioritize projects
+ Advanced customer service skills
+ Strong presentation skills
+ Experience in progressive quality control roles preferred
+ People management preferred
+ Strong computer skills, including Microsoft Office Suite-Excel and Word and Bluebeam
+ Certified Weld Inspector (CWI) Certification is strongly preferred
+ Experience with Quality Control for Electrical Work is Preferred
**YOU Matter**
**PEOPLE FIRST: BUILDING TALENT BY DESIGN**
At Southland we aspire to build a workforce that's as diverse as the people who occupy the buildings we design, build and maintain. Building talent by design is our intentional approach to creating a truly safe, collaborative, and inclusive work environment that fosters growth, empowers professional achievement, and where people are treated with respect at all levels.
If you're someone with a true passion for our industry, a life-long learner, with high accountability and a drive for results we're looking for you! At Southland, we hire problem solvers that are focused on providing customer value through continuous improvement and will take ownership to create the best experiences that will have an impact wider than their own job. We thrive on creating a strong company and culture where you'll feel engaged, challenged, and valued.
If you're ready for the next big step in your career and want a career full of fun and excitement and to be a part of a fast-paced growing company, then **JOIN** our team and become a part of an organization that values **PEOPLE** , **SAFETY, INNOVATION, COLLABORATION, INTEGRITY, ACCOUNTABILITY & SUSTAINABILITY.**
**Benefits:**
As an employee-owned company, we offer a comprehensive benefits package that includes excellent benefits for you and your family:
+ 401(k) Plan with **50% Company Match** (no cap) and immediate 100% vesting
+ Annual incentive program based upon performance, profitability, and achievement
+ **Medical, Dental, Vision Insurance - 100% Paid for Employee**
+ Term Life, AD&D Insurance, and Voluntary Life Insurance
+ Disability Income Protection Insurance
+ Pre-tax Flexible Spending Plans (Health and Dependent Care)
+ Holidays/Vacation/Personal Time/Life Events Leave
+ Numerous training opportunities and company paid membership for professional associations and licenses
**For more information on Southland Industries, please visit our website: ** Southland Careers ( ** or on ** Facebook ( ** or ** LinkedIN ( ** **
To hear what our employees are saying about working at Southland Industries, check out our Culture site - **Explore Our Culture ( Industries and all its subsidiaries are an **Equal Opportunity Employer ** and prohibits discrimination and harassment of any kind. We are committed to the principle of equal employment opportunity for all employees and to providing our employees with a safe work environment free of discrimination and harassment. All employment decisions at Southland Industries are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, gender, gender identity, sex, national origin, ancestry, age, disability, medical condition, marital status, sexual orientation, family care or medical leave status, veteran status, or any other status protected by the laws or regulations in the locations where we operate. Southland Industries will not tolerate discrimination or harassment based on any of these characteristics.
***All employment offers are contingent upon successful, drug tests, background checks and professional reference checks. ***
***We are not able to offer sponsorship of employment at this time***
If you don't feel this position is a match for you, we encourage you to share it with others. Feel free to share throughout your social networks and follow us on Facebook, Twitter, LinkedIn, and Instagram to keep up to date on what we're doing as a company.
Required Skills
Required Experience
View Now
0
Quality Control Technician
97240 Portland, Oregon
Primo Brands
Posted 15 days ago
Job Viewed
Job Description
Overview
Primo Brands is a leading branded beverage company in North America with a focus on healthy hydration. We are proud to offer an extensive and iconic portfolio of highly recognizable, sustainably sourced, and conveniently packaged branded beverages distributed across more than 150,000 retail outlets.
**If you are a current associate of Primo Brands, please apply via myADP or Success Factors.**
**Pay: $23 - $24 / hour**
**Portland, OR**
**Monday to Friday 12:00 PM start time**
Responsibilities
+ This position is responsible for quality control testing of raw source water, water processing and finished bottled water products to ensure regulatory compliance with the applicable Food and Drug Administration (FDA), State, Local, International Bottled Water Association (IBWA), and Primo Water North America (PWNA) bottled water and beverage safety and quality standards.
+ Perform microbiological and wet chemistry testing on source water, process and finished product samples in accordance with Standard Methods and PWNA requirements (standard operating procedures and policies).
+ Maintain detailed and accurate documentation of all analyses and inspections concerning incoming raw materials, water processing treatment equipment and production processes.
+ Monitor and maintain manufacturing plant quality assurance programs to ensure adherence to established FDA, State, local, IBWA and PWNA standards.
+ Contribute as a member of the Food Safety team to ensure compliance with all applicable bottled water and beverage safety and quality standards.
+ Work with production and maintenance departments on various projects as necessary and appropriate.
+ Assist with cleaning and sanitization (Clean-In-Place (CIP) duties for the water processing equipment and production areas as necessary and appropriate, according to regulatory standards.
+ Manage multiple tasks and priorities while maintaining detailed and accurate records, quality and safety standards.
+ Understand and use water processing and mineral batching computer controls to effectively changeover production lines for different bottled water type production runs ensuring all quality control testing is within Primo Water North America specification (s).
+ Maintain an organized and clean work environment.
+ Perform other tasks as directed.
Qualifications
+ Microbiology, Food Science, Biology, Chemistry or related field experience.
+ Excellent analytical and problem-solving skills with strong written and oral communication skills.
+ Ability to make quality decisions independently and works well with limited supervision, both individually and as a team.
+ Understanding Food Safety principles and Current Good Manufacturing Practices (cGMP).
+ Understanding of Good Laboratory Practices (GLPs) and aseptic sampling and handling techniques to collect samples for microbiological analysis including: E. coli, Total Coliform and Heterotrophic Plate count (HPC).
+ Ability to pass the International Bottled Water Association (IBWA) Certified Plant Operator (CPO) exam and maintain the certification.
+ Ability to become a Preventive Controls Qualified Individual (PCQI) as part of the FDA Food Safety Modernization Act (FSMA) requirements.
+ Ability to become a Safe Quality Food (SQF) Practitioner (Only required in MV & CAN).
+ Ability to support regulatory and internal audits.
+ Ability to stoop, bend, lift and twist on a regular basis.
+ Ability to work overtime as needed.
+ Ability to stand for long periods of time.
+ Ability to repeatedly lift 50 pounds.
+ Working knowledge of MS Word, Excel and PowerPoint.
Primo Brands' established portfolio includes billion-dollar brands Poland Spring® and Pure Life®, premium brands like Saratoga® and Mountain Valley®, regional leaders such as Arrowhead®, Deer Park®, Ice Mountain® Ozarka®, and Zephyrhills®, purified brands, Primo Water® and Sparkletts®, and flavored and enhanced brands like Splash® and AC+ION®. Our extensive direct-to-consumer offerings and industry-leading line-up of innovative water dispensers create consumer connectivity through recurring water purchases across Water Direct, Water Exchange, and Water Refill. At Primo Brands, our more than 11,000 associates are at the heart of what we do and deliver on our mission to provide healthy hydration to consumers wherever, however and whenever they want it. We believe in fostering a respectful culture, which values our associates who are deeply invested in quality hydration, our communities, and the sustainability of our packaging and water sources for generations to come.
Primo Brands is proud to be an Equal Opportunity and Affirmative Action employer, seeking to create a welcoming and diverse environment. We do not discriminate based on race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state, and local law.
Primo Brands is a leading branded beverage company in North America with a focus on healthy hydration. We are proud to offer an extensive and iconic portfolio of highly recognizable, sustainably sourced, and conveniently packaged branded beverages distributed across more than 150,000 retail outlets.
**If you are a current associate of Primo Brands, please apply via myADP or Success Factors.**
**Pay: $23 - $24 / hour**
**Portland, OR**
**Monday to Friday 12:00 PM start time**
Responsibilities
+ This position is responsible for quality control testing of raw source water, water processing and finished bottled water products to ensure regulatory compliance with the applicable Food and Drug Administration (FDA), State, Local, International Bottled Water Association (IBWA), and Primo Water North America (PWNA) bottled water and beverage safety and quality standards.
+ Perform microbiological and wet chemistry testing on source water, process and finished product samples in accordance with Standard Methods and PWNA requirements (standard operating procedures and policies).
+ Maintain detailed and accurate documentation of all analyses and inspections concerning incoming raw materials, water processing treatment equipment and production processes.
+ Monitor and maintain manufacturing plant quality assurance programs to ensure adherence to established FDA, State, local, IBWA and PWNA standards.
+ Contribute as a member of the Food Safety team to ensure compliance with all applicable bottled water and beverage safety and quality standards.
+ Work with production and maintenance departments on various projects as necessary and appropriate.
+ Assist with cleaning and sanitization (Clean-In-Place (CIP) duties for the water processing equipment and production areas as necessary and appropriate, according to regulatory standards.
+ Manage multiple tasks and priorities while maintaining detailed and accurate records, quality and safety standards.
+ Understand and use water processing and mineral batching computer controls to effectively changeover production lines for different bottled water type production runs ensuring all quality control testing is within Primo Water North America specification (s).
+ Maintain an organized and clean work environment.
+ Perform other tasks as directed.
Qualifications
+ Microbiology, Food Science, Biology, Chemistry or related field experience.
+ Excellent analytical and problem-solving skills with strong written and oral communication skills.
+ Ability to make quality decisions independently and works well with limited supervision, both individually and as a team.
+ Understanding Food Safety principles and Current Good Manufacturing Practices (cGMP).
+ Understanding of Good Laboratory Practices (GLPs) and aseptic sampling and handling techniques to collect samples for microbiological analysis including: E. coli, Total Coliform and Heterotrophic Plate count (HPC).
+ Ability to pass the International Bottled Water Association (IBWA) Certified Plant Operator (CPO) exam and maintain the certification.
+ Ability to become a Preventive Controls Qualified Individual (PCQI) as part of the FDA Food Safety Modernization Act (FSMA) requirements.
+ Ability to become a Safe Quality Food (SQF) Practitioner (Only required in MV & CAN).
+ Ability to support regulatory and internal audits.
+ Ability to stoop, bend, lift and twist on a regular basis.
+ Ability to work overtime as needed.
+ Ability to stand for long periods of time.
+ Ability to repeatedly lift 50 pounds.
+ Working knowledge of MS Word, Excel and PowerPoint.
Primo Brands' established portfolio includes billion-dollar brands Poland Spring® and Pure Life®, premium brands like Saratoga® and Mountain Valley®, regional leaders such as Arrowhead®, Deer Park®, Ice Mountain® Ozarka®, and Zephyrhills®, purified brands, Primo Water® and Sparkletts®, and flavored and enhanced brands like Splash® and AC+ION®. Our extensive direct-to-consumer offerings and industry-leading line-up of innovative water dispensers create consumer connectivity through recurring water purchases across Water Direct, Water Exchange, and Water Refill. At Primo Brands, our more than 11,000 associates are at the heart of what we do and deliver on our mission to provide healthy hydration to consumers wherever, however and whenever they want it. We believe in fostering a respectful culture, which values our associates who are deeply invested in quality hydration, our communities, and the sustainability of our packaging and water sources for generations to come.
Primo Brands is proud to be an Equal Opportunity and Affirmative Action employer, seeking to create a welcoming and diverse environment. We do not discriminate based on race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state, and local law.
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1
Quality Control Manager
97201 Portland, Oregon
$95000 Annually
WhatJobs
Posted 7 days ago
Job Viewed
Job Description
Our client is seeking a highly experienced and detail-oriented Quality Control Manager to oversee operations from a remote capacity, supporting their manufacturing facility in Portland, Oregon, US . This role is fully remote, requiring strong organizational and communication skills to effectively manage quality assurance processes from a distance. You will be responsible for establishing and maintaining a robust quality management system, ensuring all products meet stringent industry standards and customer specifications. This includes developing and implementing quality control procedures, conducting regular audits, analyzing quality data, and driving continuous improvement initiatives. You will work closely with on-site production teams, engineering, and supply chain departments to identify and resolve quality issues, implement corrective actions, and prevent future defects. The ideal candidate will possess extensive experience in quality assurance, preferably within a manufacturing environment, with a strong understanding of ISO 9001 or similar quality management systems. Proficiency in statistical process control (SPC), root cause analysis, and quality documentation is essential. Strong leadership, problem-solving, and analytical skills are required, along with the ability to effectively manage and motivate teams remotely. Responsibilities include: Developing, implementing, and maintaining the quality management system; Establishing quality control standards and procedures; Conducting internal audits and inspections; Analyzing production data to identify trends and areas for improvement; Leading root cause analysis for quality deviations and implementing corrective/preventive actions; Collaborating with production and engineering teams to resolve quality issues; Ensuring compliance with all relevant regulatory requirements; Managing quality documentation and records; Training and mentoring quality control personnel. This is a crucial role in ensuring product excellence and customer satisfaction, offering the opportunity to significantly impact our client's commitment to quality from a flexible remote setting.
Apply Now
2
Quality Control Technician
97123 Hillsboro, Oregon
Paradigm Information Services, Inc.
Posted 4 days ago
Job Viewed
Job Description
Paradigm in searching for a Quality Control Technician to play a key role in supporting manufacturing operations by performing quality inspections to ensure products meet required standards and specifications. Type: 6-month contract to hireLocation: On-site, Hillsboro, ORBenefits: Medical, dental, vision, life, 401K, PTO, and sick leaveAs a Quality Control Technician, you will: Follow the weekly production and shipping schedule as directed by the supervisor or team leadVerify all required documentation is received before beginning workReview and interpret assembly drawings, Bills of Materials (BOMs), and work instructionsInspect SMT and through-hole assemblies in accordance with IPC-610 Class II & III standardsOperate and program Automatic Optical Inspection (AOI) and X-ray machinesConduct first article inspectionsLog inspection results and quality data into the company databaseIdentify and communicate documentation discrepanciesRequirements Our skills and experience wish list includes: High school diploma or GED; college coursework preferred Experience in manufacturing or electronics requiredFamiliarity with IPC-610 standardsExperience operating and programming AOI and X-ray machinesAbility to read blueprints and use basic measuring toolsStrong attention to detail and communication skillsAbility to identify electronic components and part numbersFamiliarity with ISO 9000 processes and LEAN methodologiesBasic computer skills; proficiency in MS Office (Word, Excel, PowerPoint) preferred BenefitsParadigm offers a competitive benefits package that includes medical, dental, vision, life, 401K, PTO, and sick days. About Us, Paradigm Want to love Mondays? It's possible when you love what you do. Paradigm is a staffing solutions firm dedicated to finding the perfect job for candidates. We're connected with some of the most innovative tech companies around, giving our employees that competitive edge needed in today's job market. Paradigm Information Services does not discriminate on the basis of race, sex, color, religion, age, national origin, marital status, disability, veteran status, genetic information, sexual orientation, gender identity or any other reason prohibited by law in provision of employment opportunities and benefits.
Apply Now
3
Quality Control Coordinator
Wilsonville, Oregon
Employee Magnets
Posted 9 days ago
Job Viewed
Job Description
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
Apply Now
4
Remote Quality Control Manager
97204 Portland, Oregon
$115000 Annually
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client is seeking an experienced and meticulous Quality Control Manager to lead our remote quality assurance efforts within the manufacturing sector. This pivotal role will be responsible for developing, implementing, and maintaining comprehensive quality management systems to ensure our products consistently meet the highest industry standards and customer expectations. You will manage a team of quality professionals, provide strategic direction for quality initiatives, and drive continuous improvement across all production processes. This is a fully remote position, offering the flexibility to work from anywhere in the US while overseeing critical quality functions. The ideal candidate possesses a deep understanding of quality control methodologies, statistical process control (SPC), regulatory compliance, and quality auditing. Your leadership will be instrumental in fostering a culture of quality excellence throughout the organization. Responsibilities include establishing and enforcing quality control standards and procedures, developing and implementing quality training programs for staff, conducting internal audits to ensure compliance with standards and regulations, analyzing quality data and identifying trends to implement corrective and preventive actions (CAPA), managing customer complaints and feedback to drive product improvements, collaborating with R&D, production, and engineering teams to integrate quality considerations into product design and development, and overseeing the certification and accreditation processes. You will also be responsible for reporting on quality performance metrics to senior management and ensuring that all manufacturing processes adhere to relevant quality management systems (e.g., ISO 9001). The ability to lead and motivate a remote team effectively, coupled with strong problem-solving and decision-making skills, is essential for success in this role. Our client is committed to empowering remote talent to drive operational excellence.
Qualifications:
Qualifications:
- Bachelor's degree in Engineering, Science, or a related technical field. Master's degree preferred.
- 7+ years of experience in quality assurance or quality control within a manufacturing environment.
- Proven experience in developing and implementing quality management systems (e.g., ISO 9001, Six Sigma, Lean Manufacturing).
- Strong knowledge of statistical process control (SPC), root cause analysis, and CAPA methodologies.
- Demonstrated leadership and team management skills, with experience managing remote teams.
- Excellent analytical, problem-solving, and decision-making abilities.
- Proficiency in quality management software and data analysis tools.
- Strong understanding of regulatory compliance requirements for the manufacturing industry.
- Exceptional communication, interpersonal, and reporting skills.
- Ability to work independently, prioritize tasks, and manage projects effectively in a remote setting.
- Relevant certifications (e.g., ASQ Certified Quality Manager) are highly desirable.
- Must be authorized to work in the US.
Apply Now
5
Aviation Quality Control Inspector
97239 Portland, Oregon
$88000 Annually
WhatJobs
Posted 7 days ago
Job Viewed
Job Description
Our client, a leader in aviation manufacturing and maintenance, is seeking a meticulous and experienced Aviation Quality Control Inspector to join their team, operating remotely with potential travel to Portland, Oregon, US . This critical role ensures that all aircraft components and manufactured parts meet the highest standards of quality, safety, and regulatory compliance. You will be responsible for conducting comprehensive inspections, verifying documentation, and implementing quality assurance procedures throughout the production and maintenance processes. This position requires a deep understanding of aviation standards, precision measurement techniques, and a strong commitment to upholding aviation safety. Your ability to identify deviations and recommend corrective actions will be vital.
Responsibilities:
Qualifications:
Join our client in upholding the highest standards of quality and safety in the aerospace sector.
Responsibilities:
- Perform thorough inspections of aircraft components, assemblies, and finished products using various precision measuring instruments and testing equipment.
- Verify that all work performed complies with relevant FAA regulations, company standards, and customer specifications.
- Review and approve maintenance records, production logs, and other quality-related documentation.
- Identify non-conformities and defects, document findings accurately, and initiate corrective action reports.
- Conduct audits of workshops, processes, and documentation to ensure adherence to quality standards.
- Collaborate with engineering, production, and maintenance teams to resolve quality issues.
- Participate in root cause analysis of quality problems and implement effective preventive measures.
- Stay updated on aviation quality standards, regulations, and best practices.
- Contribute to the continuous improvement of quality management systems.
- Maintain a safe and organized work environment, adhering to all safety protocols.
- Provide training and guidance to personnel on quality procedures and standards.
- Conduct final inspections and approve aircraft for release to service or shipment.
Qualifications:
- High school diploma or equivalent; technical certification or degree in a related field is a plus.
- FAA Airframe & Powerplant (A&P) certification is highly preferred.
- Minimum of 5 years of experience in quality control or assurance within the aviation industry.
- Demonstrated knowledge of aviation manufacturing processes, materials, and standards (e.g., AS9100).
- Proficiency in using inspection tools, gauges, and testing equipment.
- Strong understanding of FAA regulations (14 CFR Parts 21, 43, 91, 121, 135).
- Excellent attention to detail, accuracy, and analytical skills.
- Effective problem-solving and decision-making abilities.
- Strong written and verbal communication skills.
- Ability to interpret technical drawings, blueprints, and specifications.
- Willingness to travel as needed for inspections and audits.
Join our client in upholding the highest standards of quality and safety in the aerospace sector.
Apply Now
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6
Senior Quality Control Manager - Aerospace Components
97204 Portland, Oregon
$115000 Annually
WhatJobs
Posted 7 days ago
Job Viewed
Job Description
Our client, a leading manufacturer of high-precision aerospace components, is seeking a highly skilled Senior Quality Control Manager to lead their quality assurance initiatives at their facility in Portland, Oregon, US . This senior leadership position is responsible for ensuring that all manufactured products meet the stringent quality standards and regulatory requirements of the aerospace industry. The Senior Quality Control Manager will develop, implement, and maintain the company's quality management system (QMS), oversee inspection and testing processes, manage quality documentation, and lead the quality team. Key responsibilities include conducting internal audits, managing external audits from regulatory bodies and customers, investigating non-conformances, implementing corrective and preventive actions (CAPAs), and driving continuous improvement in quality processes. You will also be responsible for supplier quality management and ensuring that all incoming materials meet specifications. The ideal candidate will possess a Bachelor's degree in Engineering, Manufacturing Technology, or a related technical field, with a minimum of 8 years of experience in quality control or quality assurance within the aerospace manufacturing sector. Strong knowledge of AS9100 standards, FAA regulations, and other relevant quality systems is essential. Experience with various inspection and testing methodologies, including CMM programming, NDT, and visual inspection, is required. Excellent leadership, problem-solving, and communication skills are critical. This is a vital role for ensuring the safety and reliability of critical aerospace components produced in Portland, Oregon, US . If you are dedicated to upholding the highest standards of quality, we invite you to apply.
Apply Now
7
Quality Assurance Specialist (Document Control)
97124 Hillsboro, Oregon
Genentech
Posted 2 days ago
Job Viewed
Job Description
**The Position**
The QA Specialist position is an integral part of Genentech's Pharma Technical - Hillsboro Innovative Therapies (HIT) Compliance and Document Control team dedicated to ensuring the highest standards of document management and control for innovative cell therapies. As an integral member of the team, you will collaborate with various inter-site and intra-site departments to maintain compliance with Roche/Genentech policies and Health Authority regulations.
In this role, you will play a crucial part in ensuring compliance with regulatory requirements and maintaining a state of inspection readiness. You will be responsible for a broad range of topics including, but not limited to, Quality, Safety, Health and Environmental Services (SHE), training, metrics, documenting systems and processes, the Quality Management System, audit support, and system administration.
**The Opportunity:**
+ You will coordinate document lifecycle management activities including editing, printing, routing, retrieving, and archiving through use of the Electronic Document Management System (EDMS) and other business support tools
+ Issue GMP-controlled documents to relevant departments as needed
+ Maintain oversight of the Periodic Review Process for released documents and ensure compliance with Document and Records Management policies
+ Coordinate and execute the Print for Reconciliation (PfR) process to ensure the proper printing, retrieval and archival of GMP documents
+ Represent Quality on cross-functional and multi-site teams, ensuring efficient execution of document control activities
+ Provide training to internal customers on policies and procedures for the Document Control
+ You will foster an engaging work environment, promote a continuous improvement mindset, and ensure compliance with safety, health, and environmental requirements.
+ You will utilize your expertise and technical knowledge to implement and sustain Document Control systems in a simplified manner, ensuring efficiency and effectiveness
+ Support health authority inspections and internal audits, including acting as a Subject Matter Expert (SME)/presenter for Document Control
**Who You Are:**
+ You hold a Bachelor's degree or equivalent with at least 3 years of experience in a related scientific discipline and have experience working in the pharmaceutical or biopharmaceutical industry, with knowledge of cGMP, SOPs, and compliance requirements in a manufacturing environment
+ You possess technical proficiency in Quality systems and strong knowledge of cGMPs or equivalent regulations to ensure compliance
+ You possess excellent communication skills with the ability to influence stakeholders at all levels
+ Ability to prioritize multiple tasks and projects simultaneously while maintaining a high level of accuracy and attention to detail
+ Proven capability for systems thinking, with strong social skills and an emphasis on understanding and addressing the needs of various stakeholders
**Preferred Qualifications/Requirements:**
+ Previous experience with Cell and/or Gene therapies
+ Experience working in electronic document management systems such as Veeva
+ Strong technical writing ability
**Physical Requirements:**
+ Work in an office environment
+ Lift up to 25 lbs may be required
+ Ability to sit, stand, and move within work space for extended periods
+ May be required to sit at a computer terminal for extended periods
**Relocation benefits are not approved for this posting.**
**This is an on-site role; remote options are not available.**
The expected salary range for this position based on the primary location of Oregon is $67,500 - $125,300. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.
Benefits ( is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants ( .
The QA Specialist position is an integral part of Genentech's Pharma Technical - Hillsboro Innovative Therapies (HIT) Compliance and Document Control team dedicated to ensuring the highest standards of document management and control for innovative cell therapies. As an integral member of the team, you will collaborate with various inter-site and intra-site departments to maintain compliance with Roche/Genentech policies and Health Authority regulations.
In this role, you will play a crucial part in ensuring compliance with regulatory requirements and maintaining a state of inspection readiness. You will be responsible for a broad range of topics including, but not limited to, Quality, Safety, Health and Environmental Services (SHE), training, metrics, documenting systems and processes, the Quality Management System, audit support, and system administration.
**The Opportunity:**
+ You will coordinate document lifecycle management activities including editing, printing, routing, retrieving, and archiving through use of the Electronic Document Management System (EDMS) and other business support tools
+ Issue GMP-controlled documents to relevant departments as needed
+ Maintain oversight of the Periodic Review Process for released documents and ensure compliance with Document and Records Management policies
+ Coordinate and execute the Print for Reconciliation (PfR) process to ensure the proper printing, retrieval and archival of GMP documents
+ Represent Quality on cross-functional and multi-site teams, ensuring efficient execution of document control activities
+ Provide training to internal customers on policies and procedures for the Document Control
+ You will foster an engaging work environment, promote a continuous improvement mindset, and ensure compliance with safety, health, and environmental requirements.
+ You will utilize your expertise and technical knowledge to implement and sustain Document Control systems in a simplified manner, ensuring efficiency and effectiveness
+ Support health authority inspections and internal audits, including acting as a Subject Matter Expert (SME)/presenter for Document Control
**Who You Are:**
+ You hold a Bachelor's degree or equivalent with at least 3 years of experience in a related scientific discipline and have experience working in the pharmaceutical or biopharmaceutical industry, with knowledge of cGMP, SOPs, and compliance requirements in a manufacturing environment
+ You possess technical proficiency in Quality systems and strong knowledge of cGMPs or equivalent regulations to ensure compliance
+ You possess excellent communication skills with the ability to influence stakeholders at all levels
+ Ability to prioritize multiple tasks and projects simultaneously while maintaining a high level of accuracy and attention to detail
+ Proven capability for systems thinking, with strong social skills and an emphasis on understanding and addressing the needs of various stakeholders
**Preferred Qualifications/Requirements:**
+ Previous experience with Cell and/or Gene therapies
+ Experience working in electronic document management systems such as Veeva
+ Strong technical writing ability
**Physical Requirements:**
+ Work in an office environment
+ Lift up to 25 lbs may be required
+ Ability to sit, stand, and move within work space for extended periods
+ May be required to sit at a computer terminal for extended periods
**Relocation benefits are not approved for this posting.**
**This is an on-site role; remote options are not available.**
The expected salary range for this position based on the primary location of Oregon is $67,500 - $125,300. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.
Benefits ( is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants ( .
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