We're seeking a Computerized System Validation (CSV) Expert to join the team coordinating Commissioning & Qualification (C&Q) activities for a new pharmaceutical plant
Support C&Q planning and execution (plans, protocols, reviews).
Develop and maintain CSV documentation (VPP, SRA, FRP, DRA).
Collaborate with Engineering, Operations, and Quality teamsExpertise in MES (Siemens Opcenter), DCS (PCS7), OSI Pi, SCADA.
Real is a Life Sciences specialist, part of SThree, the global STEM workforce consultancy. With expertise in biotechnology, pharmaceutical and medical technology, Real advises businesses, builds expert teams and delivers project solutions.
Real is a Life Sciences specialist, part of SThree, the global STEM workforce consultancy. With expertise in biotechnology, pharmaceutical and medical technology, Real advises businesses, builds expert teams and delivers project solutions.
We have a current opportunity for a CSV Expert on a Contract basis. The position will be based in Wallonia. For further information about this position please apply.
The project is looking for validation expert to join the team.
This position will be part of the team coordinating and tracking the C&Q activities for the project.
Main responsibilities are the following:
* To be part of the commissioning and qualification team of the new plant to meet the Project requirements:
o follow and update as necessary, a Commissioning and Qualification Plan
o Create and update the CSV governing documents as necessary (including VPP, SRA, FRP, DRA)
o Deliver CSV documents for all activities being into the scope (Design review, design qualification, IOC protocols, IOQ protocols etc.).
o ensure that all Commissioning and Qualification issues, across all disciplines, are addressed through all phases of the Project life cycle.
* To report to the CQV lead of the project
* To work in close collaboration with the Engineering, Operations and Quality Representatives.
* Provides support for the use of KNEAT tool.
Specialty:
Minimum Requirements:
English is mandatory, French is mandatory.
5+ years experiences in pharmaceutical industry as CSV Engineer.
Driving and proactive mindset
Solution oriented
Use of KNEAT tool is advantage
Computerized system validation (MES (SIemens OPcenter), DCS (PCS7 siemens), OSI Pi systems, SCADA
Real is a Life Sciences specialist, part of SThree, the global STEM workforce consultancy. With expertise in biotechnology, pharmaceutical and medical technology, Real advises businesses, builds expert teams and delivers project solutions.
We have a current opportunity for a CSV Expert on a Contract basis. The position will be based in Wallonia. For further information about this position please apply.
Business Consulting, Protocols, Expertise, Pcs7, Pharmaceuticals, DRA, Solution Oriented, Project Management, Driving, Validation, Projects, Pharmaceuticals, Contracts, Design, DCS, Design review, Engineering, VOS, Consulting, OSI, Proactivity, Life Science, Project Lifecycle, Offering Support, Health Technology, Operations, IOC, Biotechnology, SCADA