quality engineer

Gevin Oil and Gas Equipment Trading LLC

Looking for a (female) Quality engineer with 2&ndash;3 years of experience in the automotive sector.Requirements:Bachelor's in Mechanical, Automotive, Industrial, or related engineering fieldExperience in manufacturing, production, quality, or R&amp;D within the automotive industryJob Type: Full-timePay: Rs100,000.00 - Rs200,000.00 per monthWork Location: In person

Quality Engineer

Bluesurf Technologies

Job Description &ndash; Field Quality Engineer (ISO Certification)Position: Field Quality Engineer Department: Quality / ISO Consulting Location: Bhosari Pimpri Chinchwad Reports To: Project Manager / Quality LeadRole Overview:The Field Quality Engineer will be responsible for supporting ISO certification projects by conducting on-site quality assessments, implementing standard operating procedures (SOPs), auditing client processes, and ensuring compliance with ISO standards (e.g., ISO 9001, ISO 14001, ISO 45001, etc.). This role involves close interaction with client teams, documentation of findings, and assisting in the preparation of certification-ready systems.Key Responsibilities:<ul><li>On-Site Quality Assessment &amp; Auditing</li><li>Conduct field visits to client locations to evaluate processes against ISO requirements.</li><li>Perform gap analysis and prepare audit reports highlighting non-conformities.</li><li>Assist in internal audits before certification audits.</li><li>Documentation &amp; SOP Development</li><li>Collect client inputs and prepare standardized documentation (quality manuals, SOPs, checklists).</li><li>Maintain centralized records of client data, audit reports, and corrective actions.</li><li>Implementation Support</li><li>Guide client teams in implementing corrective and preventive actions (CAPA).</li><li>Support clients in adopting standardized processes, forms, and templates.</li><li>Monitor effectiveness of implementation through follow-ups and site checks.</li><li>Client Communication</li><li>Coordinate with client representatives to clarify requirements.</li><li>Assist in drafting professional emails, reports, and presentations for client updates.</li><li>Ensure timely communication of project milestones and issues.</li><li>Training &amp; Awareness</li><li>Conduct basic awareness sessions for client employees on ISO standards and best practices.</li><li>Provide hands-on guidance in quality control techniques.</li><li>Project Execution Support</li><li>Track progress of client certification projects and report delays or risks to Project Manager.</li><li>Ensure timelines are met for documentation, audits, and certification readiness.</li></ul>Qualifications &amp; Skills Required:<ul><li>Education:</li><li>Diploma/Degree in Mechanical/Industrial/Production Engineering or related field.</li><li>Experience:</li><li>1&ndash;3 years of experience in Quality Assurance/Quality Control/ISO implementation (freshers with ISO training may be considered).</li><li>Skills:</li><li>Knowledge of ISO standards (9001, 14001, 45001 preferred).</li><li>Strong documentation and report writing skills.</li><li>Ability to conduct on-site audits and interact with client teams.</li><li>Proficiency in MS Office</li><li>Good communication and interpersonal skills.</li><li>Other Requirements:</li><li>Willingness to travel to client sites.</li><li>Problem-solving mindset and attention to detail.</li></ul>Performance Indicators (KPIs):<ul><li>Timely completion of client audits and documentation.</li><li>Accuracy and quality of reports submitted.</li><li>Number of non-conformities resolved before certification audit.</li><li>Client satisfaction and feedback.</li><li>Contribution to project delivery within deadlines.</li></ul>Job Types: Full-time, PermanentPay: &#8377;20,000.00 - &#8377;35,000.00 per monthBenefits:<ul><li>Cell phone reimbursement</li><li>Health insurance</li><li>Paid sick time</li></ul>Experience:<ul><li>Microsoft Excel: 1 year (Required)</li><li>Microsoft Word: 1 year (Required)</li><li>Field service: 1 year (Required)</li><li>Auditing: 1 year (Required)</li></ul>Work Location: In person

Merint

We are seeking a detail-oriented and experienced Quality Engineer to ensure that all furniture and joinery products meet internal and external quality standards. The role involves developing quality control processes, inspecting finished goods, and working closely with production teams to maintain consistency, reduce defects, and continuously improve manufacturing practices.Key Responsibilities:Quality Control &amp; Inspection:<ul><li>Develop, implement, and maintain quality assurance standards and procedures for all joinery and furniture production processes.</li><li>Inspect incoming raw materials (e.g., veneers, laminates, hardware) to ensure they meet specified requirements.</li><li>Conduct in-process and final inspections of furniture and joinery items to identify defects and non-conformities.</li><li>Approve/reject finished products with respect to quality standards and customer specifications.</li><li>Analyze production and quality data to identify trends and root causes of defects or inefficiencies.</li><li>Work with production, design, and procurement teams to resolve quality issues and implement corrective/preventive actions.</li><li>Recommend and assist in the implementation of process improvements to reduce waste, increase consistency, and optimize performance.</li><li>Maintain accurate records of inspections, test results, and quality reports.</li></ul>Required Qualifications and Skills:<ul><li>Bachelor&rsquo;s degree in any Engineering discipline.</li><li>2+ years of experience in quality assurance or quality engineering in a manufacturing environment; furniture or joinery experience preferred.</li><li>Strong understanding of woodworking processes, finishes, adhesives, joinery techniques, and materials.</li><li>Proficiency in Microsoft Office and basic familiarity with ERP/MRP systems.</li><li>Good communication and interpersonal skills.</li></ul>Job Types: Full-time, PermanentPay: AED3,000.00 - AED4,000.00 per month

Danone

<div>About the job

At Danone, Manufacturing the best products and supplying them to meet demand is a key driver for our plant teams. We are currently looking to hire a Quality Engineer based in City of Industry, California! 


The Quality Engineer will support the implementation of the Danone North America Quality Assurance standards through technical guidance, analysis, and leadership to continuously improve quality performance. The Quality Engineer is accountable for capability assessment and improvement in the areas of food safety controls, product specification performance, as well as cleaning and sanitation validation. 

Responsibilities:
<ul>
<li>Provide Quality and Food Safety technical guidance, analysis, and leadership driving improvements in manufacturing processes, sanitation processes/systems, and quality systems.</li>
<li>Represent Quality and Food Safety as a leader of the plant&rsquo;s Quality Pillar within the company&rsquo;s IWS program for assigned business unit(s).</li>
<li>Ensure compliance to Danone Food Safety &amp; Quality standards, ODA, FDA, and FSSC 22000 standards, and adherence to specifications. Support internal and external audit requirements. Perform necessary audit tasks and support closure of action items.</li>
<li>Participate as a member of the Food Safety Team and assist in the development, revisions, and implementation of the Food Safety Plan.</li>
<li>Support the Quality Management System and participate in development &amp; review of quality and sanitation SOPs. Assist &amp; potentially lead implementation of QFS programs.</li>
<li>Develop, design, and conduct training and mentoring about food safety and quality topics to develop a strong quality culture.</li>
<li>Assess and work to improve process capability across key product platforms.</li>
<li>Compile and analyze KPIs indicative of production line health (quality performance, microbiological quality, preventive maintenance, sanitation effectiveness, etc.) and drive improvement actions.</li>
<li>Investigate, analyze, and assess consumer and customer complaints. Develop, train, and launch the process to engage the entire manufacturing team on the process to investigate and improve complaint processes. Ensure product non-conformances and process non conformances are tracked and logged for corrective action into the Quality system.</li>
<li>Develop expertise working within the various Danone ERP (SAP), WMS, LIMS, and Quality computer systems (Veeva).</li>
<li>Support the analysis of customer and consumer feedback to identify improvement
 
opportunities. Drive improvement by implementing corrective actions.</li>
<li>Provide training and mentoring to operations teams on food safety and quality related topics to develop a strong quality culture.</li>
<li>Support the validation of cleaning effectiveness via the sanitation (&ldquo;Neptune&rdquo;) program.</li>
<li>Support the development of quality and sanitation SOPs.</li>
<li>Manage and troubleshoot non-conformances (raw materials, packaging, product,
 
environmental monitoring, etc.) and drive root cause analysis. Assign corrective action, collaborate with supply-quality and other functions, and follow-up on completion. production processes, etc.</li>
<li>Support change management processes related to new products, packaging, equipment, and processes.</li></ul> 


Base compensation range for this position is $90K - $120K per year commensurate with experience.

Danone North America additionally offers a performance-based bonus and has a strong benefits package including Medical, Dental, Vision, Prescription Drug Coverage, 401k Plan, Wellness Program, Life Insurance, Tuition Reimbursement, Flexible Time Off, and Paid Parental Bonding Leave, among other benefit plan options.
About you

Education and Experience (Requirements): 

<ul>
<li>Bachelor&rsquo;s Degree in a science or engineering related field (Microbiology, Food Safety, Food Engineering, or similar) or other technical discipline.</li>
<li>5+ years of experience in the dairy/food/beverage manufacturing industry.</li>
<li>In lieu of a degree, 10+ years of experience in the dairy/food/beverage manufacturing industry will be considered</li>
<li>Supervisory experience preferred, not required</li></ul> 
 
Knowledge, Skills and Abilities: 

<ul>
<li>Proven ability to establish, optimize and maintain world-class quality system and team.</li>
<li>Prior experience using structured and data driven problem-solving techniques (RCPS, DMAIC, Six-sigma, LEAN, etc.).</li>
<li>Excellent communication, leadership and interpersonal skills.</li>
<li>The ability to influence others and be a team player.</li>
<li>The ability to develop/implement core work practices and standards that ensure
 
excellence in quality.</li>
<li>The ability to rapidly assess, analyze, and quickly resolve complicated quality problems with little initial information or direction and with varying degrees of ambiguity.</li>
<li>The ability to multitask and manage priorities while allocating time to long-term, quality continuous improvement projects.</li>
<li>Strong &ldquo;self-management&rdquo; skills and be comfortable working with minimal supervision.</li>
<li>Established project management skills.</li>
<li>Must bring leadership, interpersonal and communication skills required to interact with various levels of plant and corporate personnel and influence others.</li>
<li>Willingness to work flexible schedules as needed to support 7-day per week, 24-hour per day production facilities. Work schedules could include off-shift or weekend work.</li>
</ul>About us

Danone U.S. is part of Danone North America, a purpose-driven company and an industry leader in the food and beverage category. You&rsquo;ll work with some of the best-known food and beverage brands in the world. Our strong portfolio of brands includes: Activia&reg;, DanActive&reg;, Danimals&reg;, Dannon&reg;, evian&reg;, Follow Your Heart&reg;, Happy Family&reg; Organics, International Delight&reg;, Light + Fit&reg;, Nutricia &reg;, Oikos&reg;, Silk&reg;, So Delicious&reg; Dairy Free, ST&#333;K&reg; Cold Brew Coffee &reg;, Too Good &amp; Co&trade;, and YoCrunch&reg;. 
With approximately 5,000 employees and 13 production locations across the U.S., Danone North America's mission is to bring health through food to as many people as possible. 
You&rsquo;ll be part of one of the largest Certified B Corps&trade; in the world, working to make sure our company creates real value for people and the planet. Come join our movement for a healthier world: One Planet. One Health BY YOU. 
Danone North America is proud to be an Equal Opportunity employer. It is our policy to give equal employment opportunities to all qualified persons without regard to legally protected characteristics, or any other consideration made unlawful by applicable federal, state/provincial and/or local law. For our EEO policy statement and your EEO rights under law click here. 
#LI-NORAM; #LI-ON-SITE; #LI-KP1</div>

Amphenol

<div>Are you passionate about driving quality excellence and continuous improvement? Amphenol Pcd is seeking a Quality Engineer to join our team in Beverly, MA. The Quality Engineer is responsible for supporting Suppliers, Customers (Internal &amp; External), FAI, QWI and all other duties as assigned. This position is highly customer focused requiring excellent interpersonal and communication skills to manage quality assurance responsibilities and ensure compliance across all levels of the organization on major programs from design through production stages.

Essential Functions:
<ul>
<li>Drive Continuous Improvement activities throughout the business</li>
<li>Interface with programs, top management, functional organizations, customers, and suppliers</li>
<li>Prepare reports, corrective action statements, metrics, and other documents in support of product line</li>
<li>Perform routine self-assessment surveys of product line</li>
<li>Perform/oversee first article inspection efforts on product line</li>
<li>Review proposals, contracts, specifications, and other technical data to determine and implement requirements</li>
<li>Additional duties as assigned.</li>
</ul>
Required Skills / Qualifications:
<ul>
<li>Demonstrated understanding of quality engineering responsibilities, preferably with hands-on experience in Quality or Production Operations.</li>
<li>Familiarity with processes and procedures to ensure compliance with specifications, procedures, and industry standards such as ISO9001/AS9100.</li>
<li>Exceptional oral, written, and presentation skills, along with the ability to establish positive working relationships and effectively communicate with programs, lines of business, top management, functional organizations, peers, and production employees.</li>
<li>Proven ability to work in compliance to a Quality Management System.</li>
<li>Prior experience with analyzing and resolving process issues, ranging from basic to complex in nature.</li>
<li>Proficiency with Microsoft Office applications.</li>
<li>ASME Y14.5 Tolerance &amp; Dimensioning.</li>
<li>Inspection hand tools &amp; methods.</li>
</ul>
Desired Education:
<ul>
<li>Bachelor&rsquo;s degree in Engineering, Quality, or a related technical field preferred.
</li>
</ul>A Little Bit About Us:

Amphenol Pcd, a subsidiary of Amphenol Corporation, is one of the world's leading suppliers of interconnect products for Military, Commercial Aerospace, and Industrial applications. Located north of Boston in Beverly, Massachusetts, we design and manufacture a wide range of products &ndash; System Attachments, Junction Modules, Relay Sockets, Terminal Blocks, Rectangular &amp; Circular Connectors, and Cable Assemblies &amp; Adapters. With facilities in North America and Asia, Amphenol Pcd products are chosen by hundreds of OEMs around the world reliant on Amphenol's technical excellence, global network of distributors, and cost-effective solutions for custom systems.

Due to the nature of our business, the candidate must be able to legally work in the United States; we are unable to provide sponsorship. Position requires candidate to be a U.S. person as defined in ITAR, 22 CFR 120.15 (U.S. Citizenship or Resident Alien Status) and defined by 8 U.S.C. 1101(a) (20).

Amphenol Pcd is a proud Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran status or disability status.

This organization participates in E-Verify. 
Benefits
401k, Dental Insurance, Life Insurance, Medical Insurance, Vision 
 
 
 
 
Powered by ExactHire:6gkq1mdnvm4gxn5ovw0e</div>

R R pujara & co.

ndustry:Job Title: Quality EngineerReports to: Plant Head / ManagerLocation: Valsad &amp; Ahmedabad (Gujarat).Job Summary:We're seeking a highly skilled Quality Engineer to join our team in the insulation packaging material manufacturing industry. The successful candidate will be responsible for ensuring the quality of our products, implementing quality control processes, and driving continuous improvement initiatives.Key Responsibilities:1. Develop, implement, and maintain quality control processes and procedures to ensure compliance with industry standards and regulations.2. Conduct regular audits and inspections to identify areas for improvement and ensure compliance with quality standards.3. Collaborate with cross-functional teams, including production, research and development, and procurement, to resolve quality issues and implement corrective actions.4. Analyze data and trends to identify opportunities for quality improvement and implement initiatives to drive continuous improvement.5. Develop and maintain quality metrics and reports to track performance and provide insights for improvement.6. Ensure compliance with relevant industry standards, regulations, and customer requirements.7. Provide training and guidance to production staff on quality procedures and best practices.Requirements:1. Bachelor's degree in Engineering, Quality Management, or a related field.2. Minimum 3-5 years of experience in quality engineering or a related field, preferably in the insulation packaging material manufacturing industry.3. Strong knowledge of quality management principles, practices, and standards (e.g., ISO 9001).4. Excellent analytical, problem-solving, and communication skills.5. Ability to work effectively in a team environment and collaborate with cross-functional teams.Nice to Have:1. Certification in quality management (e.g., CQE, CQA).2. Experience with lean manufacturing principles and tools.3. Familiarity with industry-specific regulations and standards (e.g., ASTM, UL).If you're a motivated and detail-oriented quality professional looking to join a dynamic team, please submit your application.Job Type: Full-timePay: &#8377;18,517.62 - &#8377;36,527.52 per monthWork Location: In person

QuidelOrtho Corporation

<div><h2 class="jobSectionHeader">The Opportunity 
</h2>QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most &ndash; home to hospital, lab to clinic.
Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all.
<h2 class="jobSectionHeader">The Role
</h2>As we continue to THRIVE we are seeking a Quality Engineer to work in our Carlsbad, location. The Quality Engineer is responsible for owning and coordinating all Quality Engineering functions and activities for the defined processes. This individual is also responsible for supporting the Production, Quality Control, Engineering and Quality Assurance departments and the associated activities, which include receiving inspection, in-process inspection, and finished goods inspection in achieving and exceeding company goals and objectives. In addition, this individual is responsible for supporting the administration, implementation, and continuous improvement of the quality systems associated with non-conforming materials (This involves seeing the product as soon as it is qualified, observing flow, interacting with personnel etc.), inspection control plans (assessing existing control plans by witnessing product qualifications, evaluating qualification equipment, troubleshooting qualification equipment etc.), and corrective/preventive action (witnessing product performance, understanding causes and support corrective action implementation). This individual also supports corporate strategic goals and objectives through internal audits, support of manufacturing operations, quality support for manufacturing processes for new product development/ product improvement projects, and support of manufacturing process improvement projects.
This position is in Carlsbad, CA.
<h2 class="jobSectionHeader">The Responsibilities
</h2><ul><li>Process Flow Diagrams and Control Plans.
</li><li>Review, revision, and maintenance of FMEA/ Risk Analyses.
</li><li>Validations.
</li><li>Generation of protocols and support for creating validation protocols.
</li><li>Generation of master validation plans for manufacturing processes and product improvements.
</li><li>Work with Engineering to validate process components.
</li><li>Work with Engineering to develop test methods.
</li><li>Sampling plans.
</li><li>Factory/Quality Standards to support customer complaints.
</li><li>Provides technical support for departmental activities in significantly reducing product rejection, scrap, and variances, and improving both the quality and business systems inefficiencies. Collects data for development of corrective actions. Works with Manufacturing and Engineering groups to write and execute validations of process and system improvements.
</li><li>Provides technical support for the non-conforming materials function through effective technical root cause failure analysis, material dispositioning and corrective action implementation. Actively supports closed loop corrective actions through effective technical root cause failure analysis and troubleshooting investigations in resolving and precluding product, service and system failures and inefficiencies.
</li><li>Reviews procedural deviations for compliance with internal quality and external regulatory requirements. Ensure deviation proposals are appropriate, results support dispositions, and documentation is complete. Performs adequate risk assessments for deviation proposals. Maintains &ldquo;Deviations&rdquo; database for tracking and identification of potential Corrective Actions.
</li><li>Implements quality control support activities, such as the validation of material and process specifications, development of statistical based quality inspection control plans, support of product/process validations, and assurance of quality related deliverables within product development regulations.
</li><li>Ensures compliance of the validation system to quality and regulatory standards &ndash; supports the Validation Review Committee, reviews validation protocols and reports for completeness and compliance, provides statistical analysis of validation data, provides statistically based sampling plans.
</li><li>Contributes to the corporate efforts in support of the internal quality audit program and external supplier assessment.
</li><li>Assists in the development, implementation, and monitoring of the corporate quality system functions and culture in support of and in compliance with the Quality Policy, corporate/department goals, and external regulations.
</li><li>Performs duties in compliance with established business policies.
</li><li>Perform other work-related duties as assigned.
</li></ul><h2 class="jobSectionHeader">The Individual
</h2>Required:
<ul><li>B.S. in Engineering/Chemistry/Biology/Technical Discipline preferred or equivalent combination of certification and work experience.
</li><li>2-5 years&rsquo; experience in Quality and Manufacturing Systems in Medical Device or other highly regulated industries and high-volume manufacturing environments.
</li><li>Quality Tools &ndash; Problem Solving / Statistical Process Control / Process Capability / ISO 9001 / ISO 13485 / Design of Experiments / Sampling Plans.
</li><li>Communication Skills &ndash; Ability to communicate effectively with all levels of employees throughout the organization. Able to develop and maintain strong working relationships with internal and external customers.
</li><li>Computer skills &ndash; proficient in Microsoft Office, statistical software programs, operating systems, voice, and email (not exhaustive).
</li><li>Project management, multiple tasking, and excellent prioritization skills.
</li><li>Knowledge of quality systems and regulations for the medical device industry.
</li><li>Quality Engineer should have a results-oriented commitment to the continuing evolution of the quality control system within defined regulatory and corporate requirements.
</li><li>This requires a practical, common sense knowledge base and approach in developing, implementing, and administrating the quality control system, especially as it relates to technical problem solving, implementation of corrective actions, development of statistical-based inspection control plans and supplier management and direct material control.
</li><li>The individual must be technically knowledgeable with respect to quality systems, regulatory standards, supplier/subcontractor management, manufacturing systems, product development, project management, material flows, and general production principles.
</li><li>The individual is responsible for supporting the implementation and administration of departmental procedures that will affect the long-term quality and manufacturing strategies within the organization.
</li></ul>Preferred:
<ul><li>Auditing experience and certification strongly.
</li></ul><h2 class="jobSectionHeader">Internal Customers:
</h2><ul><li>Manufacturing &ndash; interacts with all levels of manufacturing on a regular basis on such activities as conducting product and system failure analysis, non-conforming material dispositioning, releasing product, reviewing/closing documentation, planning/implementing goals and objectives, conducting system training, implementing corrective and preventive action, performing systems assessment/feedback and supporting product/process validations.
</li><li>Engineering &ndash; interacts with the engineering staff and management on conducting technical failure analysis to resolve and preclude quality issues, developing of material and manufacturing specifications, supporting product and process validations, and supporting departmental/corporate goals and process improvements.
</li><li>R&amp;D &ndash; provides Quality Engineering support for product development and product improvement projects by such activities as validation of material and process specifications and implementation of supplier, material, and inspection control plans.
</li><li>Materials &ndash; interacts with all levels in providing technical guidance and support for material control and compliance issues, resolving non-conforming materials, and supporting departmental/corporate goals and objectives and process improvements.
</li><li>Quality Department Management &amp; Personnel &ndash; assists the development and improvement of department functions and personnel by providing technical support to ensure department success, increase morale and productivity to create/improve an environment that fosters continuous improvement and teamwork.
</li></ul><h2 class="jobSectionHeader">External Customers:
</h2><ul><li>N/A
</li></ul><h2 class="jobSectionHeader">How we Work:
</h2>At QuidelOrtho, our culture is shaped by four core behaviors that guide how we collaborate, make decisions, and support each other and those we serve.
The ideal candidate will exhibit these behaviors, as we believe they&rsquo;re essential to how we thrive as a team and achieve meaningful impact:
<ul><li>Thrive Together &ndash; Collaborate intentionally, grow as a team.
</li><li>Make It Happen &ndash; Focus on priorities, embrace continuous improvement.
</li><li>Commit to Service &ndash; Cultivate a service mindset.
</li><li>Embrace Inclusion &ndash; Be open and authentic, welcome diverse perspectives
</li></ul><h2 class="jobSectionHeader">The Work Environment
</h2><ul><li>The work environment characteristics are representative of an office, laboratory, and manufacturing environment.
</li><li>Flexible work hours to meet project deadlines.
</li></ul><h2 class="jobSectionHeader">The Physical Demands
</h2><ul><li>Requires ability to lift up to 20 lbs. on occasion.
</li><li>Up to 75% at desk, on manufacturing floor, walking, standing, and sitting for extended periods of time are routine to accomplish tasks in this role.
</li><li>Specific vision abilities required by this job include close and distance vision and the ability to adjust focus.
</li><li>Must have the ability to operate lab equipment.
</li><li>Requires use of Personal Protective Equipment as posted.
</li></ul><h2 class="jobSectionHeader">Salary Transparency
</h2>T he salary range for this position takes into account a wide range of factors including: education, experience, knowledge, skills, geography, and abilities of the candidate, in addition to internal equity and alignment with market data. At QuidelOrtho, its is not typical for an individual to be hired at or near the top range for their role and compensation decisions are dependent on that facts and circumstances of each case. The salary range for this position is $79,000 to $154,000 and is bonus eligible. QuidelOrtho offers a comprehensive benefits package including medical, dental, vision, life, and disability insurance, along with a 401(k) plan, employee assistance program, Employee Stock Purchase Plan, paid time off (including sick time) and paid Holidays. All benefits are non-contractual, and QuidelOrtho may amend, terminate, or enhance the benefits provided, as it deems appropriate.
<h2 class="jobSectionHeader">Equal Employment Opportunity
</h2>QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform the duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability, please contact us at r ecruiting@quidelortho.com .
#LI-SP1</div>

Search 10000+ Quality engineer jobs near you this September. New roles added regularly across leading industries. Apply today.

10000 quality engineer jobs NEAR_ME

Quality Engineer

Quality Engineer

Quality Engineer

Quality Engineer

Quality Engineer

Quality Engineer

Quality Engineer