QMS Engineer in Neuchatel

veröffentlicht
Kontakt
Mayank Chaubey, Basel Professionals IT & Life Sciences
Jobtyp
Temporär
jetzt bewerben

job details

veröffentlicht
Ort
Neuchatel, Neuenburg
Sektor
Life Sciences
Jobtyp
Temporär
Referenznummer
9136
Kontakt
Mayank Chaubey, Basel Professionals IT & Life Sciences
Telefon
058 201 55 50
jetzt bewerben

Stellenbeschreibung

Our client, a leading international tobacco company, with seven of world’s top 15 brands, including  the world’s number one brand is looking for a      

 

QMS Engineer

 

Location: Neuchatel, Switzerland

Contract: Open Ended 100%

Start date: ASAP

Responsibilities:

  • Participate to the development of the Reduced Risk Products (RRP) Quality Management System (QMS).
  • Actively implement the QMS documentation with the different functions of the organization.
  • Ensure that the quality requirements of the RRP QMS are integrated into and addressed within RRP organization whereas on the other side that all newly defined and developed elements including IT systems for quality management are integrated and introduced into the new QMS.
  • Write, update, review Quality documentation (Standards, SOPs, WKIs) of Quality Management Systems in order to ensure compliance to GxPs and to other requirements defined by Regulatory department in order to build one RRP QMS.
  • Support RRP organization; actively participate to the implementation of QMS documents in eDMS (electronic Document Management System).
  • Serve as key contributor for assurance of implementation and training of processes, IT systems related (Doc management, Training management) & quality documents owned, written and used by the RRP organization.

Background:

  • Substantial years (5-8 years) of experience in environment with quality systems (ISO, GxP standards, FDA guidance, ICH guidelines) and preferably in the area of life sciences.
  • Very good knowledge of Quality Management Systems and standards (FDA, GxP, ISO). Knowledge of tobacco and reduced risk products including the regulatory environment surrounding these is an asset.
  • Excellent expertise in writing Quality Documentations (Standards, SOPs, WKIs).
  • Excellent expertise in IT systems used for QMS documents Management and for Training Management. Knowledge and expertise in IT systems for Non-Conformity & CAPA and Audit Management is an asset.
  • Excellent ability to work in X-functional teams.
  • Excellent communication and written skills in English. 

If this has raised your interest then

We are looking forward to receiving within your application:

  • Your CV in English

  • Latest Work Certificates

  • Your Motivation Letter  

  • The date of your availability

Apply now to be considered – Good to know you!

For more information and your application, please contact:

Mayank Chaubey
Consultant Professionals Life Sciences & Healthcare

Randstad (Suisse) SA

mayank.chaubey@ch.randstad.com