quality systems engineer

Revance Therapeutics

<div>Job Summary:

The Quality Computer Systems Engineer will create and execute Computer System Validation (CSV) protocols for key projects that impact quality systems. They will support the maintenance of the site Master Validation Plan and facilitate critical CSV planning. 

Reporting to: Quality Assurance Manager &ndash; Technical Services 
Location: Johnson City, TN - onsite 

Responsibilities/Essential Duties:
<ul>
<li>Assist URS creation and support of SRS and FRS testing and review.</li>
<li>Ability to create and/or manage VP, CS, IQ, OQ, PQ, RTM and applicable support controls to assure on-time completion of CSV projects, and meet all compliance requirements.</li>
<li>Aid with developing procedural controls to ensure continued system maintenance and compliance.</li>
<li>Assess critical, major, and minor changes to key quality systems to determine appropriate qualification requirements to support the Change Control System.</li>
<li>Create computerized systems Risk Assessment reports.</li>
<li>Conduct system audits, and as applicable, provide gap assessment planning.</li>
<li>Compile multiple forms of communications, describing the completed computerized system, simplifying and organizing the given information to create test planning, with justifications for how the system will be tested, writing test scripts for positively and negatively testing the system utilizing applicable user roles, and then documenting in cGDP format for each tested scenario.
<ul><li>Create an RTM for this testing to assure system control and compliance.</li>
<li>Summarize the collected testing data and including any deviation for required corrective action, review, and approval.</li></ul></li> 
</ul>
Basic Qualifications:
<ul><li>Bachelor's degree and 3+ years' directly related experience.</li></ul> 


Preferred Qualifications:
<ul>
<li>Bachelor's degree in computer science, scientific, or engineering discipline.</li>
<li>Progressive experience in a related role within a cGMP environment, with working knowledge of CFR 210, 211, 820, and 21 CFR Part 11.</li>
<li>Familiar with ISPE, GAMP, and system life cycle deliverables.</li>
<li>Ability to problem-solve and fully participate in diverse cross-functional teams to achieve business objectives.</li>
<li>Excellent written and verbal communication skills.</li>
<li>A service-centered, team-building attitude.</li>
<li>Ability to handle multiple tasks simultaneously, having good planning and organizational skills.</li>
<li>Strong proficiency in Microsoft Office suite of products, and having experience with application software, and equipment control systems hardware/software/firmware, with the ability to navigate and document varied human-machine interfaces.</li>
<li>Experiences with Serialization, LIMS, Agilent OpenLAB, eInfotree, LORENZ docuBridge, Reliance, Salesforce, and electronic Batch Records, and varied computer-assisted equipment, or similar.</li>
<li>Knowledge of networking principles, practices, and technologies, as well as cloud-based systems architecture, are helpful to support IT team members for interfaced software undergoing validation.</li>
<li>Candidates knowledgeable in advanced LIMS and ERP systems may possess suitable skill sets that can be adapted to support CSV.</li></ul> 
 
Company Summary:

Crown is a proud member of the Revance Portfolio of skincare offerings. Revance is a fast-growing global aesthetics and skincare company focused on providing innovative aesthetics and market-leading skincare offerings throughout every stage of life. With a differentiated portfolio of products spanning 60 countries, Revance meets the evolving needs of patients and consumers worldwide through continued innovation and commercialization of new products and treatments. 
 
What Revance invests in you:
<ul>
<li>Competitive Compensation including base salary and annual performance bonus.</li>
<li>Flexible PTO, holidays, and parental leave.</li>
<li>Generous healthcare benefits, HSA match, 401k match, employer paid life and disability insurance, pet insurance, wellness discounts and much more!</li>
</ul>
Work Environment &amp; Physical Requirements

This position requires extended periods of standing and walking on a manufacturing floor environment. Protective equipment (safety glasses, hearing protection, gowning) must be worn as required. The role operates in a temperature-controlled pharmaceutical manufacturing facility. Occasional lifting of up to 30 lbs may be required. Must be available to respond to critical shift issues outside of scheduled hours on an as-needed basis. 

This section of the job description is required by the American with Disability Act (ADA). The ADA requires that job descriptions reflect the physical and mental demands required to effectively perform the essential duties of the job. The ADA prohibits employers from discriminating against a &quot;qualified individual with a disability&quot; in all aspects of the employment relationship. A &quot;qualified individual with a disability&quot; is &quot;an individual who meets the education, experience, skill, and other job-related requirements of a position held or desired, and who, with reasonable accommodation, can perform the essential functions of a specified job.&quot;

Revance is an Equal Opportunity employer. All qualified applicants will receive consideration for employment based on merit, without regard to race, color, religion, sex, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.</div>

Quality Computer Systems Engineer

MK Fluidic Systems

Quality Assurance EngineerFull-Time | On-Site | Las Vegas, NV 89144 | Reports to: Quality ManagerAbout MK Fluidic SystemsMK Fluidic Systems (MKFS) is a Las Vegas-based precision manufacturer specializing in custom fluidic systems for medical, industrial, and defense applications. With a team of approximately 70 employees, we combine advanced manufacturing capabilities with rigorous quality standards to deliver mission-critical components to our customers. We are ISO 9001 and ISO 13485 certified.Position SummaryThe Quality Assurance Engineer ensures compliance with established procedures, industry regulations, and customer requirements through document review, audits, and facilitation of risk, data, and root cause analysis. This role is hands-on and cross-functional, working closely with production, engineering, and supply chain teams to maintain and improve our quality management system.Key Responsibilities<ul><li>Develop, implement, and monitor quality control processes, equipment standards, and product quality for existing and new products in a manufacturing environment.</li><li>Create and refine methods to inspect, test, and evaluate the reliability of manufacturing processes, products, and production equipment.</li><li>Lead root cause analysis, testing, and verification activities in response to nonconformances; develop and implement corrective action plans.</li><li>Identify, document, and segregate nonconforming products; participate in Material Review Board (MRB) disposition decisions.</li><li>Manage supplier quality activities including onboarding, evaluation, and nonconformance resolution.</li><li>Collaborate with production personnel to analyze and verify the capability of production processes and vendor-supplied parts and services.</li><li>Conduct analysis of production data to identify trends and drive process improvement initiatives.</li><li>Assist with internal and external audits of the quality management system and company processes.</li><li>Develop and maintain quality documentation, including inspection procedures, work instructions, and process workflows.</li><li>Train and support production and administrative staff on quality processes and requirements.</li><li>Collaborate with cross-functional teams to resolve quality issues and support continuous improvement.</li></ul>Required Qualifications<ul><li>Bachelor&rsquo;s degree in Engineering, Quality, or a related field preferred; equivalent combination of education and hands-on manufacturing quality experience will be considered.</li><li>3&ndash;5 years of experience in a quality engineering or quality assurance role within a manufacturing environment.</li><li>Knowledge and hands-on experience with ISO quality system standards (ISO 9001 and/or ISO 13485).</li><li>Experience with NCRs, bills of materials, engineering blueprints/specifications, and inventory control systems.</li><li>Proficiency with ERP/MRP systems (experience with Infor VISUAL is a plus).</li><li>Strong Microsoft Office skills, particularly Excel and Word.</li><li>Ability to read and interpret engineering design drawings, technical plans, and reports.</li><li>Experience with the use and calibration of mechanical measuring tools including calipers, micrometers, indicators, gauge blocks, plug gauges, thread gauges, ring gauges, air gauges, and optical comparators.</li><li>Strong analytical skills with the ability to interpret data, identify trends, and apply statistical concepts.</li><li>Ability to define problems, collect data, establish facts, and draw valid conclusions.</li><li>Effective written and verbal communication skills; ability to prepare reports and present information clearly.</li><li>Ability to organize and prioritize tasks to meet deadlines in a fast-paced environment.</li></ul>Preferred Qualifications<ul><li>Experience with Keyence inspection systems.</li><li>Familiarity with project management techniques and tools.</li><li>ASQ certification (CQE, CQA, or similar).</li><li>Experience in medical device or aerospace manufacturing environments.</li><li>Lean Six Sigma training or certification.</li></ul>Physical Demands &amp; Work EnvironmentThis role involves frequent sitting and walking with occasional standing, reaching, and lifting. The work environment includes exposure to moving mechanical parts and moderate to loud noise levels. Personal protective equipment may be required in certain areas of the facility.Compensation &amp; Benefits<ul><li>Competitive salary commensurate with experience</li><li>Health, dental, and vision insurance</li><li>401(k) retirement plan</li><li>Paid time off</li><li>Monday through Friday day shift schedule</li></ul>LocationThis is an on-site position located in Las Vegas, NV 89144. Candidates must be able to commute to or relocate to the Las Vegas area prior to start date.Pay: $70,000.00 - $85,000.00 per yearBenefits:<ul><li>401(k)</li><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Work Location: In person

Quality Engineer

Pentax Medical

<div><div><div>About PENTAX Medical</div>
</div>
<div><div>Our mission is to improve the standard of patient care and quality of healthcare delivery by providing the best endoscopic products and services with a focus on QUALITY, CLINICALLY RELEVANT INNOVATION, and SIMPLICITY. Through leading edge R&amp;D and manufacturing, PENTAX Medical provides endoscopic imaging devices and solutions to the global medical community.</div></div> 
<div>
</div><div></div><div><div>Position Opening: Senior Quality Engineer</div></div> 
<div>
</div><div></div><div><div>Why JOIN Us?</div>
</div>
<div><div>We are an established medical device leader that is preparing for high growth. This means that PENTAX is looking to invest in its team and provide a collaborative and encouraging work environment.</div></div> 
<div>
</div><div></div><div><div>PENTAX Medical is proud of its comprehensive benefits program and generous Paid Time Off and Holiday policy.</div></div> 
<div>
</div><div></div><div><div>Want More INFO?</div>
</div>
<div>The Sr. Quality Engineer, QMS will lead and implement quality improvement, remediation initiatives, and facilitate the change management process within the PENTAX Medical Montvale, NJ facility. Partner with cross functional departments related to quality initiative and to ensure timely CAPA evaluation/investigation, root cause(s) determination, action plan development, and effective implementation. 
 
The Sr. Quality Engineer QMS will also prepare periodic metrics to ensure the effectiveness of the Quality System, CAPA and Change Management processes. Lastly, the incumbent is responsible for ensuring the CAPA and Change Management processes meet all applicable global regulatory standards and that comprehensive records of all required activities are maintained.
</div>
<div>Responsibilities of Senior Quality Engineer
<div><div><ul><li>Utilizing cross functional teams, facilitate the investigation of CAPA and identify action plans</li>
<li>Maintaining thorough, well documented records of all CAPA activities</li>
<li>Monitoring and facilitating the timely completion of all CAPA activities including, but not limited to, evaluation, investigation, action completion, and verification of effectiveness</li>
<li>Facilitate the effective implementation of Product and Process changes by leading the site Change Management process</li>
<li>Manage the CAPA and Change Management review board agenda(s), facilitate periodic meetings, and generate minutes</li>
<li>Monitor and facilitate the timely completion and closure of Product and Process changes in the Change Management program.</li>
<li>Prepare periodic metrics to ensure the effectiveness of the Quality System, CAPA and Change Management processes</li>
<li>Develop strong working relationships with domestic and global partners to ensure consistent, effective Quality System, CAPA and Change Management processes</li>
<li>Develop CAPA and Change Management training programs and conduct training for new/existing employees</li>
<li>Support &amp; Lead Management Review</li>
<li>Support &amp; Lead Document Control and Training processes</li>
<li>Participate in the Internal &amp; External Audit team</li>
<li>Interact with regulatory bodies during inspections/audits</li>
<li>Manage site-wide initiatives/projects as needed</li>
</ul>
</div></div></div><div></div><div>Requirements of Senior Quality Engineer
<div><ul><li>Bachelor&rsquo;s degree in Engineering, Life Sciences or a related field (Masters preferred)</li>
<li>Minimum of 5 years&rsquo; Quality System experience in an FDA, MDR, and/or ISO regulated environment</li>
<li>Thorough understanding of CAPA processes, Product and Process Change Management, and Quality Systems in general</li>
<li>Six sigma certified or demonstrated proficiency in quality investigations</li>
<li>Strong ability to manage critical projects as part of an interdisciplinary team</li>
<li>Excellent problem solving, technical writing, and communication skills</li>
<li>Must be self-motivated and detailed oriented</li>
<li>ASQ Certified Quality Engineer (CQE) certification and/or ASQ Certified Quality Auditor and/or ISO 13485 or MDSAP lead auditor a plus</li>
</ul></div><div><div>It is the ongoing policy and practice of PENTAX Medical to provide equal opportunity in employment to all employees and applicants. No person shall be discriminated against in any condition of employment because of age 40 and over, color, disability, gender identity, genetic information, military or veteran status, national origin, race, religion, sex, sexual orientation or any other applicable status protected by state or local law.</div></div></div></div>

Senior Quality Engineer

Aptyx

<div>The Quality Engineer is responsible for supporting and maintaining the Quality Management System (QMS) within a regulated medical device manufacturing environment. This role leads and supports validation activities, internal audits, nonconformance investigations, environmental monitoring review, and risk management activities. The Quality Engineer partners closely with Engineering, Manufacturing, and Quality teams to ensure compliance, drive continuous improvement, and support successful product development and transfer to production.
Performance is evaluated based on quality of work, timeliness, productivity, adherence to procedures, regulatory compliance, safety performance, and contribution to continuous improvement initiatives.
ESSENTIAL DUTIES AND RESPONSIBILITIES
SafetyCompliance<ul><li>
Promote and maintain a strong safety culture, ensuring adherence to all site safety policies and procedures
</li><li>Comply with applicable regulatory requirements including FDA QSR, ISO 13485, ISO 14971, OSHA, EPA, and internal quality system requirements
</li><li>Maintain compliance with Good Manufacturing Practices (cGMP) and ensure regulatory readiness in all assigned activities
</li></ul>Quality SystemsRegulatory Compliance<ul><li>
Support maintenance and continuous improvement of the Quality Management System (QMS)
</li><li>Ensure timely and compliant execution of quality system processes and documentation control
</li><li>Evaluate compliance trends and recommend improvements to strengthen system effectiveness
</li></ul>ValidationProcess Development Support<ul><li>
Develop, review, and approve validation protocols and final reports (IQ/OQ/PQ as applicable)
</li><li>Review experimental and process development documentation for completeness and compliance
</li><li>Support transfer of new products from development into manufacturing, ensuring alignment with specifications and quality requirements
</li><li>Participate in process improvement and validation lifecycle activities
</li></ul>Nonconformance, CAPADisposition Activities<ul><li>
Review and approve nonconformance investigations and material dispositions (MRB activities)
</li><li>Approve rework plans and ensure compliance with defined quality requirements
</li><li>Support root cause analysis and corrective/preventive action (CAPA) investigations
</li><li>Review defect threshold investigations and associated data analysis
</li><li>Ensure timely closure and effectiveness verification of assigned CAPAs
</li></ul>Risk Management (PFMEA)<ul><li>
Develop, maintain, and update Process Failure Mode and Effects Analyses (PFMEAs)
</li><li>Collaborate with Engineering and Manufacturing to identify risks and implement mitigation strategies
</li><li>Ensure risk management documentation aligns with ISO 14971 principles and product lifecycle requirements
</li></ul>Internal AuditingQuality Monitoring<ul><li>
Plan, conduct, and document internal audits across manufacturing and support functions
</li><li>Track audit findings and ensure timely closure of corrective actions
</li><li>Generate audit reports and support regulatory and customer audits as needed
</li><li>Review environmental monitoring data and investigate excursions beyond established limits
</li></ul>CustomerManufacturing Support<ul><li>
Assist with customer complaint investigations and technical response activities
</li><li>Partner with Manufacturing and Engineering to resolve quality issues and improve process capability
</li><li>Support daily production activities through participation in meetings and real-time issue resolution
</li></ul>TrainingContinuous Improvement<ul><li>
Support employee training related to quality systems and compliance requirements
</li><li>Participate in continuous improvement initiatives and cross-functional projects
</li><li>Lead or support assigned quality and operational improvement projects
</li></ul>DocumentationReporting<ul><li>
Create and maintain controlled quality system documentation, including validation records and risk assessments
</li><li>Generate and track special handling documentation and quality records as required
</li><li>Maintain accurate and complete records in compliance with regulatory requirements
</li></ul>SUPERVISORY RESPONSIBILITIES<ul><li>
None
</li></ul>QUALIFICATIONS REQUIREMENTS
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable accommodations may be made.
EducationExperience<ul><li>
High school diploma or GED required
</li><li>Associate or Bachelor's degree in Engineering, Science, or related technical field preferred
</li><li>5&ndash;7 years of experience in medical device manufacturing or regulated manufacturing environment required
</li><li>Strong knowledge of cGMP and ISO 13485 requirements required
</li><li>Working knowledge of ISO 14971 risk management principles required
</li></ul>Technical Skills<ul><li>
Proficient in Microsoft Office (Word, Excel, PowerPoint, Project)
</li><li>Experience with statistical tools and data analysis techniques preferred
</li><li>Familiarity with ERP and quality systems preferred
</li><li>Strong technical writing and documentation skills
</li></ul>Communication Skills<ul><li>
Strong verbal and written communication skills across all organizational levels
</li><li>Ability to present technical information clearly and effectively
</li><li>Ability to facilitate cross-functional discussions and training sessions
</li><li>Strong collaboration skills with Engineering, Manufacturing, and Quality teams
</li></ul>MathematicalAnalytical Skills<ul><li>
Ability to work with basic mathematical concepts including addition, subtraction, multiplication, division, fractions, and decimals
</li><li>Ability to analyze data trends using spreadsheets and statistical tools
</li><li>Ability to interpret quality data and identify process variation
</li></ul>Reasoning Ability<ul><li>
Ability to apply logical thinking to solve problems and interpret technical instructions
</li><li>Ability to make sound, data-driven decisions in a regulated environment
</li><li>Ability to manage multiple priorities and independently execute tasks
</li></ul>PHYSICAL DEMANDS<ul><li>
Must be able to analyze data in multiple formats and systems
</li><li>Must be able to make independent decisions related to quality and compliance
</li><li>May be required to lift and/or move up to 50 pounds
</li><li>Ability to work in both office and controlled manufacturing environments
</li></ul>WORK ENVIRONMENT<ul><li>
Primarily office-based with periodic exposure to manufacturing environments
</li><li>Manufacturing areas may require PPE such as hairnets, smocks, gloves, and safety glasses
</li><li>Exposure to controlled environments and low-level chemical or solvent odors may occur
</li><li>Work environment is generally well-lit and temperature controlled</li></ul></div>

Vulcan Wireless Inc.

<div>
 
 
 Company Description
 
 
 
 Vulcan Wireless specializes in providing advanced digital communication solutions for both terrestrial and space applications. Catering to domestic and international clients, the company offers turnkey communication systems for military and commercial customers. With expertise in embedded software, digital signal processing, and digital radio design, Vulcan Wireless ensures seamless transition from concept to production. Our innovative solutions drive reliable, cutting-edge communication technologies.
 
 
 
 
 
 
 Position Summary
 
 
 
 QA Engineers will support the Quality Assurance team in maintaining quality systems, ensuring compliance, and supporting audit readiness. This role provides hands-on experience with
 
 ISO 9001 and AS9100 Quality Management Systems (QMS)
 
 , ITAR compliance, and aerospace/defense quality processes.
 
 
 
 
 
 
 Key Responsibilities
 
 
 <ul>
 <li>
 Support and maintain the
 
 ISO 9001 and AS9100 Quality Management Systems (QMS)
 
 </li>
 <li>
 Prepare for, support, and follow up on
 
 internal and external audits
 
 </li>
 <li>
 Maintain
 
 audit-ready documentation
 
 for ISO 9001 and AS9100 compliance
 </li>
 <li>
 Ensure
 
 configuration control
 
 of hardware and software (versions, revisions, traceability)
 </li>
 <li>
 Support
 
 Supplier Corrective Action Requests (SCARs)
 
 , including tracking and follow-up
 </li>
 <li>
 Assist in
 
 supplier quality compliance
 
 and supplier audits
 </li>
 <li>
 Assist in providing
 
 training on quality standards and processes
 
 </li>
 <li>
 Record and maintain
 
 quality records, reports, and inspection data
 
 </li>
 <li>
 Support
 
 ITAR compliance processes
 
 within QA procedures
 </li>
 </ul>
 
 
 
 
 
 Required Qualifications
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in
 
 Engineering, Computer Science, or related technical field
 
 </li>
 <li>
 
 Junior QA Engineer:
 
 1&ndash;2 years of QA, manufacturing, or engineering experience
 </li>
 <li>
 
 Mid-level QA Engineer:
 
 3&ndash;4 years of QA, manufacturing, or engineering experience
 </li>
 <li>
 Hands-on experience supporting
 
 ISO 9001 QMS implementation and maintenance
 
 </li>
 <li>
 Experience participating in or preparing for
 
 AS9100 audits
 
 </li>
 <li>
 Experience supporting or conducting
 
 internal audits
 
 </li>
 </ul>
 
 
 
 
 
 Preferred Qualifications
 
 
 <ul>
 <li>
 Direct experience in the
 
 aerospace or defense industry
 
 </li>
 <li>
 AS9100
 
 internal auditor or lead auditor certification
 
 </li>
 <li>
 Familiarity with
 
 risk-based thinking
 
 and
 
 product safety requirements
 
 </li>
 <li>
 Experience with
 
 supplier quality and SCAR processes
 
 </li>
 <li>
 Exposure to
 
 ITAR compliance requirements
 
 </li>
 </ul>
 
 
 
 
 
 Key Skills
 
 
 <ul>
 <li>
 Strong
 
 analytical and problem-solving skills
 
 </li>
 <li>
 Excellent
 
 documentation and communication skills
 
 </li>
 <li>
 Detail-oriented with strong
 
 organizational skills
 
 </li>
 <li>
 Ability to manage multiple priorities in a fast-paced environment
 </li>
 </ul>
 
 
 
 
 
 Salary Range (Carlsbad, CA)
 
 
 
 
 Experience Level&nbsp;Salary Range
 
 
 
 
 Junior (1&ndash;2 years)
 
 
 
 &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;$65,000 &ndash; $85,000
 
 
 
 Mid-level (3&ndash;4 years)
 
 
 
 &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;$85,000 &ndash; $105,000
 
 
 
 
 
 
 Work Environment &amp; Physical Requirements
 
 
 <ul>
 <li>
 Primarily sedentary with extended computer use
 </li>
 <li>
 Occasional standing, walking, and light lifting (up to 25 lbs)
 </li>
 <li>
 Onsite, full-time position
 </li>
 </ul>
 
 
 
 
 
 Benefits
 
 
 <ul>
 <li>
 100% Company-paid medical, dental, and vision for employee
 </li>
 <li>
 401(k) with company match
 </li>
 <li>
 Paid holidays, vacation, and sick leave
 </li>
 <li>
 Life Insurance, AD&amp;D, and LTD
 </li>
 <li>
 Employee Assistance Program (EAP)
 </li>
 <li>
 Tuition reimbursement
 </li>
 <li>
 Referral bonuses
 </li>
 <li>
 Bonus opportunities
 </li>
 </ul>
 <li>
 
 </li>
 
 
 Other Duties
 
 
 
 This job description is not intended to be a comprehensive list of all responsibilities. Duties may change based on business needs.
 
 
 
 
 
 
 Why Join Vulcan Wireless?
 
 
 
 Join a
 
 fast-growing team building innovative communication systems for satellite applications
 
 and gain experience in ISO 9001/AS9100 compliance within the aerospace and defense industry.
 
 
 
 
 
 
 EEOC
 
 
 
 
 Vulcan Wireless, Inc. is an equal-opportunity employer regarding race, color, religion, sex, national origin, age, disability, marital status, veteran status, sexual orientation, genetic information or any other protected characteristic under applicable law.
 
 
 
 
 
 
 
 ITAR REQUIREMENTS
 
 
 
 
 To conform to the U.S. Government space technology export regulations, including the International Traffic in Arms (ITAR) you must be a U.S. citizen as defined by 8 U.S.C. 1324b(a)(3).
 
 
 
 
 
 
 
 
 
 
 
 
 
 
</div>

Entry to Mid-Level Quality Assurance (QA) Engineer

Executive Alliance

<div>
 
 Our client is seeking a highly detail-oriented and technically capable
 
 Quality Assurance Engineer
 
 to support, maintain, and continuously improve the company&rsquo;s Quality Management System (QMS). This role ensures that products, processes, and systems comply with applicable ISO standards, customer requirements, contractual obligations, and internal procedures.
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 Job Function:
 
 
 <ul>
 <li>
 Maintain, implement, and continuously improve the Quality Management System in accordance with ISO 9001 or equivalent standards.
 </li>
 <li>
 Ensure compliance with:
 </li>
 </ul>
 
 - Customer and contract requirements
 
 
 - Engineering drawings and technical data packages
 
 
 - Internal procedures and work instructions
 
 
 - Applicable regulatory and industry standards
 
 <ul>
 <li>
 Support internal, customer, and external audits and manage audit findings and corrective actions.
 </li>
 <li>
 Maintain quality records, objective evidence, and traceability documentation in accordance with QMS requirements.
 </li>
 <li>
 Support management reviews and quality performance reporting.
 </li>
 </ul>
 
 Review and interpret engineering drawings, specifications, and contractual requirements.
 
 <ul>
 <li>
 Develop and maintain:
 </li>
 </ul>
 
 - Inspection and test plans
 
 
 - Quality control procedures
 
 
 - Process control documentation
 
 <ul>
 <li>
 Support and perform:
 </li>
 </ul>
 
 - Incoming inspection
 
 
 - In-process inspection
 
 
 - Final inspection
 
 
 - First Article Inspections (FAI) where applicable
 
 <ul>
 <li>
 Ensure measurement and test equipment is used in accordance with calibration and control procedures.
 </li>
 </ul>
 
 
 
 
 
 
 
 
 Job Requirement:
 
 
 
 
 Required Qualifications
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Engineering, Quality, Manufacturing, or related technical field (or equivalent experience).
 </li>
 <li>
 3+ years of experience in quality engineering, quality assurance, or manufacturing quality.
 </li>
 <li>
 Strong ability to read and interpret engineering drawings and technical specifications.
 </li>
 <li>
 Working knowledge of ISO 9001 or similar quality management systems.
 </li>
 <li>
 Experience with root cause analysis, corrective action systems, and quality documentation.
 </li>
 <li>
 Strong written and verbal communication skills.
 </li>
 <li>
 Proficient in Microsoft Office and quality documentation systems.
 </li>
 </ul>
 
 
 
 
 
 Preferred Qualifications
 
 
 <ul>
 <li>
 Experience in defense, aerospace, or regulated manufacturing environments.
 </li>
 <li>
 Experience with First Article Inspection (FAI) and government or military contracts.
 </li>
 <li>
 Experience with supplier quality management.
 </li>
 <li>
 ASQ, ISO, or other quality-related certifications are a plus.
 </li>
 </ul>
 
 
</div>

Quality Assurance Engineer

Parsons

<div>In a world of possibilities, pursue one with endless opportunities. Imagine Next! 

At Parsons, you can imagine a career where you thrive, work with exceptional people, and be yourself. Guided by our leadership vision of valuing people, embracing agility, and fostering growth, we cultivate an innovative culture that empowers you to achieve your full potential. Unleash your talent and redefine what&rsquo;s possible. 
Job Description:
Parsons is seeking a Quality Engineer to perform high-level quality activities on complex projects and functional programs. You will ensure that all products and services delivered are in strict accordance with customer requirements and Parsons&rsquo; global quality standards. This role requires regular interaction with project management, design, procurement, and construction teams to drive operational excellence.
What You Will Be Doing<ul><li>
System Support &amp; Optimization: Provide Quality Systems support using ISO 9001 as the foundation for process development, data reporting, and training.</li><li>
Audit Management: Plan and execute internal quality audits across offices and job sites. You will document findings to ensure compliance with contract requirements, codes, and specifications (Design, Procurement, Construction, etc.).</li><li>
Corrective Actions: Effectively document, follow up on, and close internal and external corrective actions. Analyze non-conformance trends to identify program-wide performance issues.</li><li>
Technical Reviews: Conduct quality engineering reviews of design documentation, vendor manuals, and technical deliverables to verify compliance with industry codes and regulatory commitments.</li><li>
Supply Chain Quality: Assist in qualification audits of suppliers and subcontractors to ensure they meet Parsons&rsquo; and the Client&rsquo;s rigorous quality expectations.</li><li>
Safety Integration: Promote safety awareness and participate in safety field audits and assessments to ensure a holistic approach to project risk.</li></ul>
Education &amp; Experience<ul><li>
Degree: Bachelor&rsquo;s Degree in Engineering, Business, Quality, or a related field.</li><li>
Experience: Typically 6+ years of related experience in the field of Quality.</li><li>
Certifications (Required/Preferred): * Lead Auditor certification (ISO 9001 or equivalent).<ul><li>
ASQ Certification (CMQ/OE, CQA, or CQE) is highly preferred.</li><li>
Specialized certifications (NQA-1, AWS Welding Inspector, NDT) are a plus.</li></ul></li><li>
Industry Knowledge: Working knowledge of infrastructure, aviation, or large-scale transportation projects</li></ul>
Skills &amp; Competencies<ul><li>
Systems Expertise: Deep knowledge of ISO 9000, ASME, ANSI, and ASTM standards.</li><li>
Analytical Skills: Proficiency in analyzing business metrics (ROI, cost per unit) and performing statistical process control.</li><li>
Communication: Ability to conduct management-level presentations and interface effectively with diverse professional groups.</li><li>
Software Proficiency: Expert knowledge of Microsoft Office (Word, Excel, PowerPoint, Access) and Visio.</li><li>
Attention to Detail: Strong risk assessment, problem-solving, and project planning skills are essential.</li></ul>
Parsons equally employs representation at all job levels no matter the race, color, religion, sex (including pregnancy), national origin, age, disability or genetic information.
We truly invest and care about our employee&rsquo;s wellbeing and provide endless growth opportunities as the sky is the limit, so aim for the stars! Imagine next and join the Parsons quest&mdash;APPLY TODAY!<div>
Parsons is aware of fraudulent recruitment practices. To learn more about recruitment fraud and how to report it, please refer to https://www.parsons.com/fraudulent-recruitment/.</div></div>
 <div><div><div>COMPETITIVE BENEFIT OFFERINGS</div></div><div><div><div> 
Financial Wellness</div><div> 
We care about your financial wellbeing. Parsons offers competitive pay and retirement plans to help you build wealth for the future while giving you the flexibility to diversify your investments.</div></div><div><div>
Work Life Harmony</div><div> 
Balance in life is important and time away from the office is imperative to allow you to refresh and focus your attention on the things that matter to you. Parsons supports your time away by providing paid time off and paid flexible holidays.</div></div><div><div>
Career Development</div><div> 
We are committed to fostering the personal and professional growth of our employees. Develop and advance yourself though our comprehensive training, educational and mentorship programs.</div></div><div><div> 
Veteran Support</div><div> 
We provide Industry leading benefits to support veterans and active-duty members to provide security for you and your family by offering robust leave and benefits; including paid active-duty military leave and paid time off when transitioning back to civilian life.</div></div><div><div>
Mind &amp; Body</div><div> 
At Parsons we inspire healthier habits, heathier minds, and a healthier you through our wellness program. Participate in our weekly Meditation Mondays and Wellness Wednesdays. Wellness, at Parsons, is more than just your annual checkup.</div></div><div><div>
Health</div><div> 
Health is not a one size fits all. At Parsons, we offer a robust Employee Assistance Program as well as comprehensive medical, dental and vision plans through large, national carriers with the choice of regional PPO, HDHP, or HMO networks.</div></div></div></div>

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