Job Description

Job Description

Quality Engineer – Galway

My client, a start up medical device company in Galway is seeking a Quality Engineer to join their team. Ideally the candidate would have experience in sterilisation and have a minimum of 2 years’ experience as a Quality Engineer or similar role in a medical device manufacturing environment.

Job Responsibilities

  • Experienced in process validation techniques including risk management, statistical techniques in compliance with regulatory requirements.
  • Lead process risk management process in compliance with EN ISO 14971 and preparation of risk management files and FMEAs.
  • Responsible for the compilation and execution of Process Validation Protocols in conjunction with manufacturing.
  • Supports Supplier Qualification, Assessment and Audit process at key Suppliers.
  • Establish and maintain incoming, in-process & final inspections requirements and support design and validation test requirements as required.
  • Generates NCRs and CAPAs for product defects and non-conformities observed and follows up to ensure effective closure.
  • Manages sterilization activities, responsible for sterilization evaluation documentation and product release.
  • Supports the management of all calibration and maintenance programs for all equipment.
  • Manages validation and monitoring activities associated with particulate and biocontamination control.
  • Manages change requests in a timely manner and ensures effective closure.
  • Supports the training program and manages records for staff.
  • Drives changes in procedures and standards to facilitate Drives the metrics system / trending for all quality system measurable.
  • Interfaces with all departments (including Production, Design & Regulatory) on product development, transfer and improvement projects as required.
  • Supports the design verification process including reviewing protocols, reports, design and quality documentation supporting product development.
  • Support various Quality Management System activities including internal audits.

Candidate Overview

  • Degree in Biomedical engineering/science discipline or Quality Management together with experience in an engineering function, preferably within a medical device or related industry.
  • Minimum 2 years’ experience as Quality Engineer or similar role in a medical device manufacturing environment.
  • Must be a solutions provider.
  • Strong technical skills and analytical problem-solving ability combined with attention to detail to achieve project deliverables.
  • Knowledge of Medical Device Quality Management System Requirements ISO 13485, MDD 93/42 EEC, 21 CFR Part 820, CMDR.
  • Excellent interpersonal and communication skills.
  • Proven ability to work well as part of a team and on own initiative in a face paced environment.
  • Advanced PC skills such as Excel, Word, PowerPoint.

Desirable:

  • Experience or training in one or more of the following; Biocompatibility, Ethylene Oxide sterilization validation or microbiology.
  • Previous neurovascular medical device Design or Quality Assurance experience.
  • Prior experience in computer systems validation or Gamp 5.

For more information please forward CV’s to Megan.warr@cpl.ie or call 091 507 515.

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