CQV Engineer
Visp , Switzerland

The ultimate purpose of technology teams in GxP environments is to serve the evolving needs of the business. We are a specialist provider of consultancy and implementation services for IT infrastructure and data architectures within life science manufacturing. Our role is to be a companion on the road for technology teams to be able to use as a tool at times when decisions need to be made.

We now have an amazing opportunity for an experienced CQV Engineer to join our clients growing team and work on site in Switzerland. This role is a full-time permanent role based on our clients site in Switzerland.

Your responsibilities will include, but won’t be limited to –
  • Manage all CQV activities associated with execution from the initiation/concept phase through construction to handover of multiple projects thus ensuring that all CQV activities are delivered to meet client expectations to the highest safety, environmental, quality, and operational & performance standards.
  • Direct support for the project managers who are delivering the projects.
  • Communicate and troubleshoot any issues arising from doc prep and doc execution phase of projects.
  • Assess and manage change controls in conjunction with the project managers including change control generation, review and approval.
  • Identify the appropriate Commissioning and Qualification strategy (IC/IQ and OC/OQ) to apply on specific project and define the list of activities required.
  • Communicate scope, cost and schedule impact to project managers and Client as required.
  • Assess and manage the requirements for CQV execution support from vendors, contractors, etc.
  • Implementation and co-ordination of new hire on-boarding and mentoring program
  • Focussing on safety, schedule, and budget adherence while complying with good engineering practices, company policies, regulations, and codes
The Requirements:
  • A relevant 3rd level Engineering qualification.
  • Have at least 3 years of experience in equipment commissioning, qualification, and validation (IQ, OQ, PQ)
  • 2 – 3 years of previous experience in a data centre environment.
  • You must be competent with current FDA and EU regulations and best practices.
  • Fluent in English
About us:

Oleson is a technology strategy & transformation practice. We are uniquely focused on IT/OT systems in manufacturing operations with a particular strength in regulated life sciences manufacturing. You already have trusted control system and applications vendors. Our strength is in taking a full system view and understanding the complex relationships between

– Manufacturing operations
– Business continuity
– IT infrastructure
– Compliance & change control
– System lifecycle planning

We have developed our own knowledge and process to ensure your IT/OT systems directly drive your business needs. We are ready to provide strategic advice or specific implementation services. To deliver successful projects you can use our capabilities selectively to augment the capabilities of your own project delivery team. We have a vast amount of experience in complex capital projects IT/OT projects in manufacturing operations.- 

To find out more about what we do visit our website here – https://oleson.io/



Don’t worry if there isn’t a current opportunity that suits your own expertise and interests. Positions arise with us for experienced
professionals on an ongoing basis. To register your interest for future roles that arise within our team, please email recruitment@oleson.io

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