Application Engineer in Berlin

Energy Jobline ZR; Berlin; On-site; EUR 80,000 - 98,000; Full time

Job summary

TOMZ Corporation is seeking a Quality Engineer in Berlin, CT to drive QD&D control within the PDP and to support sustaining manufacturing. You will develop quality plans, collaborate on risk management, and implement validation strategies while ensuring compliance with the QMS and regulatory requirements.

The role requires experience in audits, ISO/CE standards, and strong English communication. A 4-year degree and proficiency with MS Office are essential for success; team collaboration across

Qualifications

• Advanced post-secondary education or certification coursework.
• Knowledge of statistical techniques to analyze process capability.
• Quality certification(s) (e.g., ASQ CQE, QCI).
• Skilled in First Article Inspections and Component Qualifications.
• Knowledge of external standards: ISO 900/9001, ISO 13485, 21CFR 820, EU MDR.
• Experience supporting audits by customers and regulatory agencies.
• Strong verbal and written English communication skills.
• Proficiency with Microsoft Office.

Responsibilities

• Develop and execute Quality Plans for Quality Product Design and Development projects.
• Collaborate with engineering teams to support Risk Management documentation.
• Establish severity and risk-based Process Master Validation Plan strategies with V&V rationales.
• Support qualification audits for Customer and Regulatory Agencies.
• Represent Quality Engineering in design reviews.
• Apply systematic problem-solving to identify and resolve quality issues.
• Ensure site personnel comply with the Quality Management System.

Skills

Statistical techniques

Quality certifications

First Article Inspections

Regulated industry knowledge

English communication

Independent work / cross-functional

Problem-solving

Auditing support

MS Office

Education

4-year degree or equivalent

Tools

MS Office

Job description

Job DescriptionJob Description

TOMZ Corporation is looking for a highly motivated Quality Engineer to join our team in Berlin, CT!!

Summary of Position

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.

Essential Functions

• 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.
• Drive Test Method development with Operational and Business considerations and execution of Test Method Validations to measure effectiveness.
• Implement inspection plans for Incoming, In-Process and Final Product.
• Develop and justify appropriate sampling plans with characterization of test and inspection methods.
• 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.
• Perform other duties as assigned.

Qualifications

• Advanced Post-Secondary Education, Training or Certification coursework.
• Knowledge of statistical techniques to analyze process capability.
• Quality certification(s) (e.g., ASQ CQE, QCI, etc.).
• Skilled in First Article Inspections and Component Qualifications.
• Knowledge and experience with external standards: 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 communication skills.
• Successfully meet TOMZ-specific positional and functional on-the-job training requirements.
• Proficiency with Microsoft Office.
• A self-starter capable of working independently and as part of a team, with the ability to collaborate across various functional areas, including R&D, Manufacturing, and QA, to achieve results.

Education

• Minimum 4-Year degree or equivalent of directly transferrable industry work experience (Engineering or Quality discipline ).

Experience

• Minimum of 2-5 years’ experience in a regulated manufacturing environment.
• Experience in Class I, II, and/or III medical device manufacturing within a regulated environment(e.g., Aerospace, Defense, Pharmaceutical, etc.).

Physical Requirements

• Ability to bend, stoop, squat, kneel, and lift up to 50 pounds. Team lift or mechanical assistance required for objects over 50 pounds.
• Ability to sit for prolonged periods.
• 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.