Senior Quality System Engineer (m/f)

Job type:
on-site
Start date:
asap
Duration:
3 MM
From:
Hays AG
Location:
Baden-Wurttemberg
Published at:
10/10/2018
Country:
flag_no Austria
Contact person:
Kerstin Werner
Project ID:
1645959

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Senior Quality System Engineer (m/f)

Reference: 387833/1-en
Start: asap
Duration: 3 MM

Main tasks:
  • Assist with the running of the CAPA system including creating summaries, minuting meetings and contributing to root cause analysis determination
  • Perform Internal Audit, assist in the management of audit scheduling and updates on all related actions
  • Assist and where appropriate lead in the compilation and execution of validation protocols for new product/processes and software
  • Ensure correct implementation as per standard validation procedures
  • Re-validate as required due to engineering change, deviation analysis or upgrade in systems and materiel
  • Manage QA related change control for specific projects as directed
  • Be responsible for the introduction and correct use of statistical QA methods into the production environment, and provide technical resource for production team on relevant IQ/OQ/PQ protocol issues
  • Assist with the maintenance of the Master Validation Plan and Critical System Changes for validated systems
  • Review and identify potential improvements with the Leeds Quality System and products to better meet regulatory requirements
  • Document and maintain in good order all relevant Quality assurance sections of Device Development History File and DMR as directed
  • Co-ordinate product/technology transfer between facilities from a QA perspective
  • Develop and utilize DFMEA/PFMEA and other QA risk analysis techniques in order to minimize potential risk during development/implementation activity
  • Ensure compliance with all Documented Quality system, FDA QSR’s and ISO 9001 requirements during day to day and assigned audit/CAPA activities


Main qualifications
  • Must have an engineering background in manufacturing, with a proven ability to interpret and create engineering specifications and procedures
  • Must be PC literate, and familiar with MS Office applications
  • Must have a good understanding of engineering drawings and geometric Tolerating
  • Well developed organizational skills, with ability to work on own initiative
  • Good communication and presentation skills in order to effectively communicate technical and QA requirements to all functional departments and external facilities
  • Determined approach to problem solving, and ability to make appropriate decisions concerning product/process disposition and general Quality assurance procedural suitability
  • Ability to deal with flexible workload and type is essential, and also an ability to work productively within a project focused team environment
  • Self-motivated and self-disciplined, must be able to work unsupervised and equally well as part of a team
  • Very good German spoken and good in written and Fluent English (spoken and written)


Main advantages:
  • Continuous support during the assignment
  • Dynamic and innovative market environment
  • Fascinating, innovative environment in an international atmosphere



About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.

My contact at Hays:

My contact person:
Sabine Velandia Medina

Referencenumber:
387833/1

Make contact:
Email: