Technical Support Engineer Salary at Azenta Inc BETA

Type of Requisition: Regular Clearance Level Must Currently Possess: Top Secret/SCI Clearance Level Must Be Able to Obtain: Top Secret SCI + Polygraph Public Trust/Other Required: None Job Family: Information Security Job Qualifications: Skills: Information Assurance, Information Security, Information Systems Certifications: None Experience: 15 + years of related experience US Citizenship Required: Yes Job Description: Transform technology into opportunity as an Information Assurance System Security Engineer (ISSE) III with GDIT. A career in enterprise IT means connecting and enhancing the systems that matter most. At GDIT you’ll be at the forefront of innovation and play a meaningful part in improving how agencies operate. At GDIT, people are our differentiator. As an ISSE III you will help ensure today is safe and tomorrow is smarter. The ISSE III is primarily responsible for conducting information system security engineering activities with a focus on lifecycle of current systems an

Wollaston Alloys/CPP Boston is a stainless steel and high alloy sand casting foundry that has been based in Braintree, MA for over 60 years! We manufacture components for the defense market as well for commercial markets such as power generation industries. Wollaston Alloys/CPP Boston is a fast-paced company that has continued to grow over its long history! Wollaston Alloys/CPP Boston is seeking a driven individual to join our team as a Quality Engineer! The Quality Engineer is a crucial position within our facility. This is an excellent opportunity for to join a fast-paced company that has continued to grow over the past 60 years! CPP offers a competitive compensation and benefits package, which includes a bonus program, medical/dental/vision/life/disability insurance, 401K with match, paid vacation and holidays, paid training, and a great team culture! Major Responsibilities Coordinate with our customer’s Engineering, Quality, and Purchasing representatives, suppliers, and all depart

JETCOOL Technologies is seeking an experienced Quality Engineer to provide the analytics and guidance to effectively manage product and process quality for all JetCool products. Strong preference will be given to those with a proven history. JETCOOL Technologies is a fast-moving technology company spun out of MIT and now a member of the Flex family. Our technology provides game-changing cooling solutions for aerospace, electric vehicles, and data centers. Join us to be part of one of today’s fastest growing industries, while having a positive impact on society sustainability through innovative technologies. Duties/Responsibilities: Establish statistical process control measurement methods to gather product and process quality performance. Work with Development Engineering and Manufacturing Engineering to set up the proper quality control metrics for all JetCool products. Work with external suppliers, domestically and internationally to validate in-factory quality management tools, cont

This candidate will be responsible quality and first article inspection and plans. PC Demis programming would be a huge plus, develop and analyzing quality initiatives. Responsibilities Strong First Article Inspection and Inspection plans PC Demis programming Develop, execute, and analyze quality reporting measures Calibration management NDT (non destructive testing) a plus Qualifications 4+ years' of industry experience Aerospace/As9100/Defense OR CNC machinery Strong knowledge of quality tools used in the industry Analytical and quantitative approach to problem solving

Quality Engineer - Wakefield, MA - $100k - $120k US Citizen or GC holders only No C2C This role ensures that design changes for new and existing catheter and console products meet regulatory and quality standards throughout the design, development, and manufacturing transfer processes. Achieving this will involve close collaboration with cross-functional teams. The Quality Engineer will be involved in all product development phases, including design, reliability testing, design controls, feasibility assessments, verification and validation, process development, risk management, and delivery. Responsibilities: Focus on sterile disposable and electrical hardware product design. Participate in design control, project planning, and quality reviews. Review and provide feedback on requirements, specifications, and design documents. Draft and review design control deliverables for product and design changes. Contribute to risk analysis (FMEAs, hazard analysis, etc.) and manage risk requiremen

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

Pay: $32-$33 per hour Location: Chelmsford, MA (100% 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 softwares. 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 organization.

This position will play a critical role in developing, maintaining, and managing products and processes in accordance with ISO9001:2015 & AS9100: 2016 D standards. You will also be responsible for managing records, creating document packages, performing pre-production reviews, and ensuring that the company complies with its Quality Management System (QMS). Responsibilities • Maintain and adhere to ISO 9001/AS9100 Quality Management System documentation • Represent the company during audits of Quality System, procedures, products and processes • Manage calibration activities and recall • Coordinate and support product and process approvals with customers, source inspectors and auditors. • Assist in continuous development and refinement of our Quality Management System • Assist in developing Quality control policies • Develop and implement methods and procedures for inspecting, testing and evaluation of products for compliance • Supports manufacturing process development & qualification