Manufacturing Quality Engineer

Arcmed
Boonton, NJ, United States
Full-time

The Quality Engineer is a working member of the Quality team whose primary responsibilities are listed below. They will report to the Quality Manager and ensure that Arcmed is compliant with its own standardized processes and procedures.

Promote quality across the entire company by raising awareness and driving improvements. October Start Date

Essential duties and responsibilities :

Oversee CAPA, work with Manufacturing, Operations and Engineering to assist with containment, root cause analysis, corrective action, and preventive action.

Conduct effectivity checks for CAPAs.

Return Material Authorizations, supports RMA requests from customers, tracks, and trends RMA data for Management Review, they will assist with RMA investigations as needed and provide feedback to the customer.

As well as complaint handling.

  • Monitor and measure Key Performance Indicators (KPIs) and present findings during Management Review
  • Conduct training to internal procedures.
  • Non conformances and Material Review Board (MRB), disposition non conformances, disposition discrepancy material reports, manage MRB process as needed, tracks and trends nonconformance and MRB data.
  • Represent Quality in product development teams / projects. Work with various Engineering groups or QA Manager to develop and execute plans including quality plan, risk management, Process Failure Mode and Effects Analysis (PFMEA), control plans, production part approval process (PPAP), part qualification checklist (PQC)
  • Design verification and process validation (IQ, OQ, PQ)
  • Process capability (cpk). Understand statistics and how it impacts statistical control over process.
  • Lead Supplier Corrective Actions Requests (SCARs) - containment, root cause analysis, corrective action, and preventive action.
  • Ability to interpret Geometric Dimensioning and Tolerancing (GD&T)
  • Work as directed by manager.

Qualifications :

  • Bachelor’s degree in an Engineering discipline.
  • Knowledge of ISO 9001, ISO 13485 and other recognized international quality system standards.
  • Read, analyze, and interpret technical procedures and regulations.
  • Write technical reports, business correspondence, technical procedures, as well as administrative procedures.
  • Interpret and inspect to GD&T
  • Present proposals, data, and issues to Arcmed personnel at all levels.
  • Independently determine and develop an approach to a wide range of issues and problems. Solutions must be thorough, practical, and consistent with organization objectives.
  • Represent the department in frequent cross-functional interactions and possible customer, subcontractor, or vendor contacts.
  • Provide solutions to difficult technical issues associated with specific projects.
  • Determine and develop technical solutions to a wide range of difficult problems.
  • Experience with Epicor a plus.
  • Microsoft : Word; Teams; Visio; OneNote, PowerPoint, Outlook
  • Ability to operate media equipment such as tablets, smartphones, and other electronic equipment.
  • Ability to work with general office equipment.
  • Ability to work with and understand databases a must and the ability to learn technical skills.

Physical requirements :

  • Shall have essential physical skills; be able to run, squat, stoop / bend, kneel, climb stairs, be able to lift at least 50 pounds (or ¼ own body weight).
  • Shall have adequate vision, reading, writing, and documentation skills, and hearing to perform the essential functions of the job.
  • Shall be able to visually differentiate colors.
  • Will be engaged in speaking, sitting, walking, driving, listening, and in communicating both orally and in writing while performing his or her duties.
  • Must be able to listen and respond to questions and instructions.

About Arcmed

  • Arcmed partners with the world’s top Diagnostic and Analytical OEMs, Engineers, and Scientists to improve human health.
  • We provide technology and supply chain solutions for the design and manufacture of precise fluid handling components for diagnostic and analytical instruments.
  • Our product portfolio offers configurable fluidic components and engineered systems used for precise reagent and sample handling in instrumentation for OEMs in the In-Vitro Diagnostic (IVD), Next Generation Sequencing (NGS), and analytical chemistry markets.
  • Arcmed offers labware and chromatography components to scientific laboratories in drug discovery and downstream biotech development workflows.
  • We are recognized as a leader in helping engineers, scientists, and doctors to solve the world’s toughest diagnostic and analytical challenges.

Our Values

  • We always act with intention and drive to achieve our purpose.
  • Teamwork, collaboration, and diverse opinions make us stronger.
  • We are unafraid to make timely decisions, and we empower our people to make decisions, execute them and move forward.
  • We value people that take the initiative and hold themselves accountable.
  • Challenging the status quo helps us grow. Look for and call out improvements.

The qualifications, physical demands, and work environment described herein are representative of those an employee will encounter and must meet to successfully perform the essential functions of this job.

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The requirements listed in this document are the minimum levels of knowledge, skills, or abilities.

Arcmed is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.

This document does not create an employment contract, implied or otherwise, other than an "at will" relationship .

The above noted job description is not intended to describe, in detail, the variety of tasks that may be assigned but rather to give the incumbent a general sense of the responsibilities and expectations of his / her position.

As the nature of business demands change, so, too, may the essential functions of this position.

11 days ago
Related jobs
Jobot
East Hanover, New Jersey

They are in the market to add a Quality Engineer to their team to help support and implement the quality program. Interface with customers, sales, and engineering to resolve quality issues and analyze customer complaints as part of the 8D team. Implement and maintain our quality system in line with ...

Arcmed
Boonton, New Jersey

The Quality Engineer is a working member of the Quality team whose primary responsibilities are listed below. Oversee CAPA, work with Manufacturing, Operations and Engineering to assist with containment, root cause analysis, corrective action, and preventive action. Work with various Engineering gro...

Promoted
GCR Professional Services
Boonton, New Jersey

Senior Test Engineer – ATE/EE. Client seeks an Electrical Engineer to support ATE development in the Power & Control Actuation Systems (PAS) / Space. ...

Promoted
KLA
Totowa, New Jersey

Our expert teams of physicists, engineers, data scientists and problem-solvers work together with the world's leading technology providers to accelerate the delivery of tomorrow's electronic devices. ...

Promoted
PMI (Project Management Institute)
Newark, New Jersey

JobPosting","title":"QA & Automation Engineer III","datePosted":"2024-09-04T00:00:00","validThrough":null,"description":"QA Automation Engineer (Multiple Openings), Project Management Institute, Inc. QA Automation Engineer (Multiple Openings), Project Management Institute, Inc. Newtown Square, PA: P...

Promoted
OLI Systems
Parsippany-Troy Hills, New Jersey

We are seeking a Process Systems Engineer to join a multidisciplinary, entrepreneurial team to contribute to the ongoing development and innovation of OLI’s unique computational modeling platform with a specific focus on multiphase, multicomponent electrolyte systems. Development of our next g...

Promoted
HEPCO, Inc.
Hanover, New Jersey

Our client is seeking an experienced Senior Mechanical Engineer with at least 12 years of expertise to lead a team of 8 engineers in designing and overseeing complex mechanical systems for vertical structures such as buildings, towers, and cooling towers. Key Responsibilities:Mechanical System Desig...

Promoted
Regeneron Pharmaceuticals, Inc.
Bernards, New Jersey

The Regeneron GVP Quality Management Lead (QML) is a key position that we believe will guide and lead all aspects of quality and compliance within global pharmacovigilance (PV) system. Manager to build strategic partnerships and direct risk-based quality management activities with key partners impac...

Promoted
Getinge
Wayne, New Jersey

ASQ Certified Quality Engineer, ASQ Certified Reliability Engineer, ASQ Certified Software Quality Engineer, and Six Sigma Green Belt certification is preferred. Quality Product Engineer is part of the QE - Product Development team is responsible for ensuring the product software (embedded and featu...

Promoted
Breeze Eastern
Hanover, New Jersey

Miniumum of 5 years professional experience in mechanical engineering, preferably mechanical systems/ rotating machinery (transmissions, mechanisms, clutches, gears, drum s, cabling involved in hoisting and winching equipment in an aerospace environment). Independently evaluates, selects and applies...