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Automation Pharmaceutical Engineer M-F - Belgium  

CVO Europe (company)

Posted on : 19 October 2017

Project Description

Automation Pharmaceutical Engineer M-F



A Life Sciences specialist for over 20 years, CVO-EUROPE offers consulting, audit, and training services that are compliant with the regulatory requirements of the Chemical, Pharmaceutical, Biotechnology, Cosmetics, Food & Beverage, and Medical Devices industries.
With more than 350 consultants, CVO-EUROPE provides expertise in every activity that may affect patient health, product quality or data integrity.
CVO-EUROPE is an international group with business divisions in France, Belgium, Switzerland, and the USA.

To support our development, we are looking for :

Automation Pharmaceutical Engineer M-F

Permanent contract

• Individuallly or as part of a project team responsible for solution design and process layouts for site automation equipment including the following installations: PLC, DCS, Supervision & Monitoring Systems, Data Mgmt Systems (EMS/ABMS/MPMS), alarm systems and fire protection equipment.
• Responsible for the execution, coordination and follow-up of solution designs and technical matters related to Process Control to ensure construction, transformation, commissioning and qualification of the solution meets agreed cost, timing, technology and quality standards in line with the Global Technical Services standards.
• Key activities include:
- Define functional, technical and quality requirements.
- Realise process studies, P&ID’s and process layouts whilst considering the operating and EHS characteristics at all design steps.
- Ensure preparation and update of the project qualification and coordinate qualification activities of the installations.
- Ensure work inspections are issued in line with quality standards.
- Ensure systems legal conformity.
- Coordinate technicians during execution to secure contracts and connection of services (water, chemicals, gases) and electricity.

• Industrial or Civil Engineer with 10 years experience post graduation in its discipline with an experience in the Pharmaceutical industry
• You demonstrates deep knowledge in design and implementation of engineering projects.
• You have good project management skills: organisation, cost, time, schedule, contracting, procurement, qualification, validation, technologies Practical experience in project supervision and people management Perform his/her work in a cGMP consistent manner.

INTERRESTED ? Please, send your CV by E-mail :

publication date : 17/07/2017