Quality Engineer Salary at Heat-Flo Inc BETA

Quality Engineer – Manufacturing $80,000 - $100,000 + Company Vehicle + Excellent Benefits Smithfield, Rhode Island (Commutable from: Pawtucket, Providence, Woonsocket, Cumberland, Attleboro, Burrillville) Are you a Quality Engineer, looking to step up in to multisite role where you will be responsible for all Quality and will be fast tracked in to a Management position? This is an excellent opportunity to put your own stamp on this expanding organization and grow your own team in the future. This is a great time to join this well-established manufacturer as they continue to grow and dominate their industry. They have a great reputation for developing their engineers and always look to promote internally. On offer is a varied role where you will be responsible for implementing quality standards across 5 facilities. You will be working closely with Quality Inspectors on each site and ensuring all standards are adhered to. This role would suit a Quality Engineer, who wants to progress in

Summary: Initial 6-month contract; potential for Temp-to-Hire (long-term) Schedule: 8:30 am - 5 pm, M-F Location: On Site, Marlborough, MA Experience: 3-5 years, Bachelor's degree Performs inspections and sets quality assurance testing models for analysis of raw materials, materials in process, and finished products. Supports Test Method Validation Remediation Assists in the review and improvement of existing test method validation documentation Implements remediation plans to ensure test methods comply with current regulatory standards. Documentation and Compliance Ensures validation documents meet FDA, ISO 13485, and other relevant regulatory requirements. Maintains accurate and organized records of validation activities. Qualifications Requires a bachelor's degree and 0-2 years of experience in the field or in a related area. Has knowledge of commonly-used concepts, practices, and procedures within a particular field. Relies on instructions and pre-established guidelines to perform

Role Overview: The Software QA Engineer will be pivotal in improving the stability and reliability of the company’s software ecosystem, which spans mobile apps, web apps, cloud services, firmware, and Bluetooth connectivity. This role reports directly to the CTO. This individual will develop and execute comprehensive end-to-end test strategies that address critical stability concerns, including device connectivity, data integrity, and latency issues across the entire system. The role will also involve collaborating with the development team to ensure the smooth rollout of new features and accelerate product improvements, directly contributing to delivering a high-quality user experience. Join a passionate, QA-friendly culture where quality and customer happiness are at the core of what we do. Key Responsibilities:Test Planning & Strategy Develop and document comprehensive, end-to-end test strategies to address critical stability concerns, including: Bluetooth connectivity between weara

$30 -- $33 per hr max pay CONTRACT through the end of the year with high potential to extend or convert Chelmsford, MA - onsite Education / Experience Requirements B.A. or B.S. degree in a technical discipline, such as engineering or science (equivalent experience may be considered). 2 to 5 years of quality engineering or design assurance experience (preferably in the medical device industry). Specialized Skills / Other Requirements ASQ certification preferred (e.g. CQE, CQA, CMDA, CRE, CSSGB/CSSBB). Basic understanding of industry regulations such as ISO 13485, ISO 14971 and FDA 21CFR820. Proficient in MS Office, and Minitab or other statistical software's. Strong organizational and time management skills to meet deadlines while managing multiple projects. Strong analytical and critical thinking skills. Proficient in technical report writing and review. Strong verbal and written communication skills. Foster a positive culture of growth, collaboration, and achievement across the organi

Job description: Quality Engineer II Location – Marlborough, MA (ONSITE) Duration: 6+ months Contract (Conversion possible for the right candidate) INTAKE NOTES: • Shift Hours: 8:30-5pm • Required Education: Requires a bachelor's degree in Engineering, Quality Assurance, or a related field • Required # of years’ experience: 3-5 Manager Notes: Supports Test Method Validation Remediation: Assists in the review and improvement of existing test method validation documentation Implements remediation plans to ensure test methods comply with current regulatory standards. Documentation and Compliance: Ensures validation documents meet FDA, ISO 13485, and other relevant regulatory requirements. Maintains accurate and organized records of validation activities. Qualifications: Requires a bachelor's degree in Engineering, Quality Assurance, or a related field. 3-5 years of experience in test method validation or a related area. Knowledge and Skills: Familiar with commonly used concepts, practices

Exciting direct hire Opportunity available for an experienced Supplier Quality Engineer with a strong background in supplier performance monitoring, audits, and implementing a supplier scorecarding process. Please review the description below! Supplier Quality Engineer – Summary The Supplier Quality Engineer plays a vital role in ensuring supplier compliance, performance, and continuous improvement within manufacturing operations. This position serves as the primary contact for supplier-related quality concerns, conducting audits, driving corrective actions, and implementing performance scorecards. By collaborating with Operations, Supply Chain, and Engineering teams, the Supplier Quality Engineer helps refine processes, maintain quality standards, and support new supplier qualifications. Strong problem-solving, analytical, and organizational skills are key to success in this role.

Quality Engineer II 3 month contract Raynham, MA - onsite 5x a week Required Skills & Experience Industry: Minimum of 4 years of experience in medical device manufacturing or other highly regulated industries. Understanding of investment casting (foundry processing) is preferred but not required. Validation: Strong background in process validations (IQs, OQ/PQs, TMVs) is required. Quality & Compliance: Champions compliance to applicable Global Regulations and standards (e.g. QSRs, ISO, EN and Medical Device Directive (MDD) requirements). Raises Quality issues as appropriate. Proficiency in conducting non-conformance investigations and maintaining non-conformance records; strong investigation skills and ability to manage multiple investigations are essential. Experience in supporting Corrective and Preventive Actions (CAPA) preferred but not required; includes Action Plan (AP) and Effectivity Monitoring (EM) tasks. Change Control: Experience with change control processing via PLM system

The Senior Quality Engineer is responsible for coordinating quality activities within Spincraft. The Senior Quality Engineer is expected to exercise sound technical judgment using data gathered from internal monitoring to implement and sustain suitable processes that enable continual improvement to reach efficiency targets. The Senior Quality Engineer works closely with all levels of the Engineering, Finance, Production, Purchasing, Facilities, and EHS departments to ensure that systems and processes across the facility consider quality requirements to match strategy. The Senior Quality Engineer reports directly to the Quality Manager. What You'll Do Develop and implement quality documentation such as procedures, work instructions, single-point lessons, etc. Interpret complex drawings, documents, and specifications to facilitate product/process implementation. Monitor and analyze quality trends and performance, and reports to Quality Manager. Collaborate with Quality Manager and Operat