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Application Engineer - Sales

Tomz CorporationUnited States🇺🇸United StatesPosted Oct 6, 2026

Quick Overview

Seniority
Mid Senior
Work mode
Hybrid
Location
United States
Posted
8 hours ago
Microsoft Office

Job Description

Job Description
TOMZ Corporation is looking for a highly motivated Quality Engineer to join our team in Berlin, CT!! Reporting to the Quality Engineering Manager, this position will be responsible for the activities associated with Quality Design & Development (QD&D) Control and Assurance during Product Development Process (PDP) activities as well as continuation design & development support for sustaining manufacturing and product distribution. Develop and execute Quality Plans for Quality Product Design and Development projects.

Collaborate with engineering teams to initiate and support the development and updates of Risk Management documentation in accordance with project requirements. Establish severity and risk-based Process Master Validation Plan strategies with appropriate V&V rationales. Support operational and process qualifications for customer manufacturing processes in collaboration with engineering teams. Represent Quality Engineering in design reviews. Support initial qualification audit activities for Customer and Regulatory Agencies.

Support qualification activities related to supplier and vendor design characterization requirements for projects, including conducting audits and assessments. Support Quality Best Practices and contribute to continuous improvement in GDP/GMP. Apply sound, systematic problem-solving methods in identifying, prioritizing, communicating, and resolving quality issues. Ensure that all site personnel comply with the site-level Quality Management System and training requirements. Support the development of Quality Agreements for external customers. Adhere to the TOMZ Quality Management System.

Advanced Post-Secondary Education, Training or Certification coursework. Quality certification(s) (e.g., Skilled in First Article Inspections and Component Qualifications. ISO 900/9001, ISO 13485, and 21CFR 820, EU MDR, pertaining to product development, design controls, good manufacturing practices, supplier qualification, auditing, quality control (GD&T, Nonconforming Materials, MRB), Corrective and Preventive Actions, and customer complaints). Experience in effectively supporting audits by customers and external regulatory agencies.

Strong verbal and written English language communication skills. Successfully meet TOMZ-specific positional and functional on-the-job training requirements. Proficiency with Microsoft Office. Minimum 4-Year degree or equivalent of directly transferrable industry work experience (Engineering or Quality discipline preferred). Experience in Class I, II, and/or III medical device manufacturing within a regulated environment (e.g., Aerospace, Defense, Pharmaceutical, etc.). Team lift or mechanical assistance required for objects over 50 pounds.

Exposure to oil, grease, occupational noise, cleaning solvents, dust, metal particles, sparks, coolant, and sharp-edged materials. Personal protective equipment (PPE) such as safety glasses, dust masks, ear plugs, cut-resistant or chemical-resistant gloves, and engineering controls may be required. Perform keyboard entries with frequent operation of a computer.

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