Qc Inspector Iii Jobs

Overview

Werfen

Werfen, founded in 1966, is a worldwide developer, manufacturer and distributor of specialized diagnostic instruments, related reagents, automation workcells, and data management solutions for use primarily in hospitals and independent clinical laboratories. The Company’s business lines include Hemostasis, Acute Care, and Autoimmunity diagnostics, as well as Original Equipment Manufacturing. Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We’re passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care.

Our North American Commercial Operations, as well as our Headquarters and Technology Center for Hemostasis and Acute Care Diagnostics, are based in Bedford, MA. Our Headquarters and Technology Center for Autoimmunity Diagnostics is based in San Diego, CA. Additionally, our Technology Center for Hemostasis and Blood Gas Reagents is in Orangeburg, NY, and our Technology Center for Whole Blood Hemostasis is in San Diego, CA.

Job Summary:

The QC Inspector III is responsible for the inspection of components, assemblies and finished goods at incoming, in-process and final inspection process steps.

Responsibilities

Key Accountabilities

Essential Functions:

• Maintain compliance with the company’s quality management system through training and adherence to policies, procedures and work instructions.
• Review device history records to ensure they are complete and accurate
• Perform first article and validations/verification inspections as required
• Issue non-conformance reports
• Perform in-process inspections
• Support special projects as assigned by management
• Ensure materials meet specifications/requirements.
• Perform inspections of packaged product to ensure completion and accuracy
• Perform mechanical, electrical, and visual inspections

Networking/Key Relationships:

• Quality Assurance and Regulatory Affairs management (special projects)
• Research and Development (R&D)
• Quality Engineering
• Operations
• Manufacturing Engineering

Qualifications

Minimum Knowledge & Experience Required for the Position:

• Minimum of five (5) years previous Quality Control (QC) and/or Quality Assurance (QA)experience required.
• High school diploma; additional technical training or schooling strongly preferred.
• Experience with electronic soldering techniques and visual printed circuit board inspection
• Experience performing First Article Inspection
• Experience with non-conformance reporting
• Previous experience/accountability recording inspection results
• Experience with current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP)
• Working knowledge of Microsoft Office
• Previous experience working in a regulated medical device manufacturing plant

Skills & Capabilities:

• Ability to read mechanical detail drawings, printed circuit board drawings, and parts list
• Ability to work with gages for mechanical inspection including but not limited to micrometer, caliper, depth gage, force gage, gage blocks, dial-indicator, multi-meter, digital thermometer, optical comparator, and vision inspection system.
• Strong understanding of IPC 610 (Acceptability of Electronic Assemblies)
• Knowledge of statistical acceptance sampling plans
• Understanding of Certificate of Conformance (C of C) and Certificate of Analysis (C of A) principles
• Knowledge of large Enterprise Resources Planning (ERP) system.

Compentencies:

• Problem Solving: Promptly and effectively handles issues and problems
• Independence: self-motivated-works under minimal supervision
• Collaboration: Ability to actively develop a network to bring best solutions to the team or customer
• Takes Initiative: Serves as a role model for “Quality First” by continuously improving on what matters most to customers
• Discretion: Acts Honest, Loyal, trustworthy
• Attention to Detail: Ability to pay close attention to detail is required
• Outstanding Performance Standards: Demonstrated ability to meet department goals
• Multi-Tasking: Ability to Juggle Priorities, and support changing business needs
• Professionalism: Must demonstrate professionalism during all interactions within company, customer and third parties
• Communication: Good written and verbal communication skills
• Accuracy: Work is accurate and completeness of record

Travel Requirements:

• Limited Travel.

The pay rate range for this role is $26.00 - $33.00 per hour Final compensation will ultimately depend on factors including education, relevant experience, skillset, knowledge, and business needs.

If you are interested in constantly learning and being challenged on a daily basis, we encourage you to submit your resume or CV.

Werfen appreciates and values diversity. We are an Equal Opportunity/Affirmative Action Employer M/F/D/V.

We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 5,000 employees around the world comprise our Werfen team.

www.werfen.com