Quality Engineer Salary at Jetboil BETA

Job Description: Participate in the New Product Development (NPI) and design changes, Design History File (DHF) and Device Master Record (DMR) reviews meetings and fully understand the design control process and Quality Engineering. Utilize technical training and compliance experience to ensure that company design control projects comply with internal design control procedures in accordance with FDA and ISO requirements. ESSENTIAL JOB RESPONSIBILITIES AND DUTIES INCLUDE: Responsible for overall Design Quality process to ensure that company design control projects comply with internal design control procedures in accordance with FDA, ISO and other applicable requirements. Act as a subject matter expert on design control process and risk management process. Lead Risk Management activities from Product Concept through Commercialization. Provide guidance to internal and external stakeholders and ensure that design control requirements are being met in an effective manner in order to achiev

Third Pole is on a mission to expand the lifesaving benefits of Nitric Oxide inhalation therapy, making it accessible to millions of respiratory challenged newborns and adults around the world. This is a rare opportunity to be part of a rapidly growing team, making a huge social impact, touching the lives of those we love and care about most. We are a fast-paced startup developing a game-changing technology that generates Nitric Oxide on demand, at the patient location, from the air we breathe. Our Third Pole community is grounded in the values of collaboration, embracing diverse ideas, commitment, and transparency without the politics found in most companies. Our motto is we are only successful if we all cross the finish line together! Sound like you? In this role, you will apply your medical device design assurance expertise to ensure our medical devices are safe, effective, and delivered to our customers on time As a member of the QA/RA team, you will: - Own the Design Assurance fun

InnoTECH Staffing is looking to hire a fulltime / permanent (Senior) Quality Engineer for a Class II / III medical device company located in Waltham, MA. This role requires being onsite around 4 days a week and there is NO SPONSORSHIP available. This person must thrive in a fast-paced environment, be able to work on multiple product development and quality projects simultaneously, and be motivated by the opportunity to learn and make an impact in the organization. HUGE opportunity for someone who wants to learn and pick up new areas and be hands-on!!!! This is a unique role combining engineering design assurance and quality skills. The key someone who has done QA maintenance and has developed Quality systems along with QE Design and Mfg. roles with exposure to test method validation. Key Areas of Responsibility: Quality Assurance • Represent all aspects of Quality to ensure programs meet quality standards, as well as design control and regulatory requirements • Develop, implement, and

The ideal candidate is a critical thinker who will proactively improve the quality systems of the company through internal audits, participation in process improvement programs, and interaction with key partners to obtain constructive feedback. Responsibilities Develop standardized production, quality, and customer-service standards Identify potential risks before they become a problem, focusing on root cause analysis and preventive action Perform internal and external quality audits and compile detailed reports of findings Build a strong team through coaching, mentoring, specific training and performance evaluations Qualifications Bachelor's degree or equivalent experience in Engineering 5+ years' relevant work experience Highly organized with excellent attention to detail

Our client is a leading global provider of precision instruments, laboratory equipment, consumables, software and services to the research and cell Biology markets. They remain committed to bringing passion, industry knowledge and dedication to the range of products and services that are customer focused, bringing innovations to life. We are presently supporting their search for a Quality Engineer Manager based in Greater Boston MA. The Quality Engineer Manager, as part of the Quality Assurance Organization, will ensure products are designed, developed, and made to meet/exceed customer requirements. They will ensure all projects, programs and products as well as Quality- Assurance initiatives meet quality, reliability, and compliance requirements to deliver the highest quality products. JOB RESPONSIBILITIES Proactively implements best-in-class Quality Engineering practices. Responsible for Product/process assurance plans, master validation plans, validation protocols, inspection plans.

ResponsibilitiesPerform receiving inspections of raw materials, BOM items, and work-in-progress parts returning from outside processing (e.g., anodizing)Identify non-conformances through detailed visual and dimensional inspectionsDocument inspection results and any issues in the MES (ProShop)Conduct mechanical inspections of in-progress and finished goodsPerform visual inspections for surface defects like nicks and scratchesMeasure parts with hand tools (calipers, height gauges, thread gauges, etc.)Operate advanced metrology equipment (CMM, FARO laser scanning arms, microscopes, optical comparators, etc.) and related softwareSupport quality planning for new and repeat projectsPrepare internal 'dim-tagged' drawings and document inspection plansDetermine appropriate metrology equipment for each characteristic using best practices (e.g., 4:1 or 10:1 rules)Collaborate with manufacturing team members to optimize inspection timing and mitigate risk of non-conformancesDocument and help invest

We are looking for a skilled and proactive Quality Engineer to join our team in the semiconductor manufacturing sector. In this role, you will be key to ensuring the highest quality standards are maintained throughout the entire production process, from raw materials to final products. You'll collaborate with cross-functional teams to optimize processes, drive continuous improvements, and ensure that our products consistently meet industry requirements and customer expectations. Key Responsibilities: Develop and implement quality control processes to ensure our semiconductor products adhere to customer specifications and industry standards. Conduct inspections, audits, and testing to verify product quality and compliance. Investigate defects, non-conformance's, and failures, collaborating with the production team to resolve issues and apply corrective actions. Identify areas for improvement and lead initiatives to enhance the efficiency and quality of manufacturing processes. Collabora

Senior Manufacturing Quality Engineer - $100k-$135k Burlington, MA US Citizen or Green Card Holders only Our client is looking for an experienced Quality Engineer to join their team and support Manufacturing Engineering and Production Sustaining efforts in a dynamic medical device manufacturing environment. In this collaborative role, you'll work closely with Operations, R&D, and other teams to ensure compliance with the Quality Management System (QMS). Are you a seasoned Quality Engineer who thrives at the Operations end of Design Transfer? Do you excel at handling daily manufacturing challenges, leading yield improvement initiatives, and driving successful scale-up projects? Key Responsibilities: Ensure quality system implementation and oversight within manufacturing processes. Provide Design Assurance Engineering and support during Product Development or post-market changes. Collaborate cross-functionally to drive process improvements using Quality Systems. Ensure product specificat