Vitalograph is the world’s leading manufacturer of medical respiratory diagnostic devices and software, used in the diagnosis of respiratory disorders, and advanced high-reliability equipment and software systems used in respiratory end-point clinical drug trials. We design and manufacture respiratory diagnostic devices, software, and consumables for healthcare professionals, for almost 60 years, and serve customers in over 100 countries. Headquartered in the UK, Vitalograph has operations in Ireland, Germany and the USA.

REQUIRED SKILLS AND EXPERIENCE:

• 3rd level qualification, or equivalent including experience, in a science or engineering discipline.
• At least 3 years experience in medical device manufacturing within a QC or QA role, using ISO 13485, CE Marking and FDA QSRs.
• Good project planning and organizational abilities.
• Assertive, with strong interpersonal and communications skills.
• Pro-active with proven ability to work under own initiative, while being a strong team player.
• Excellent skills with word, excel and other MS suite packages.
• Good command of written English needed for record closure.
• Willingness to travel to other Vitalograph sites as necessary.
  Job Types: Full-time, Permanent
  Work Location: In perso

THE ROLE:

Reporting to the Quality Manager, the Quality Technician provides Quality Assurance support and direction to
Operations and the QMS.

KEY RESPONSIBILITIES:

• Documentation Control – release of Documents, updating Bills of Materials, archiving
• Assist with Quality Engineering support for Operations and R&D teams
• Support with the drafting of SOPs and associated documentation for QMS
• Completion of timely record and metric related transactions
• Support NC, CAPA & Complaint assessment, use of root cause tools, and trending analysis
• Contribute to Continuous Improvement initiatives
• Support Vendor Quality Engineer & Quality Engineering activities as needed.
• Perform other duties as may be assigned in support of compliance or QMS activities.
• Flexibility is a requirement of this position, and the successful candidate must be prepared to undertake such other duties as assigned by the Quality Manager. Such duties can be outside the normal area (and hours) of work.