Equipement Implementation Manager

10-10-2020 braine-l'alleud

Our client is a global biopharmaceutical company focusing on creating value for people living with neurology and immunology.


You have at least 5 years experience in a pharmaceutical/chemical industry in a laboratory or manufacturing environment? You have experience in equipment implementation?

Don't hesitate to contact me : aurelia.sautiere@cx.ausy.be

  • Coordinates, plans, tracks and monitors all pilot plant activities especially regarding equipment implementation in alignment with the Pilot Plant Management
  • Ensures good collaboration with all customers and stakeholders of the pilot plant and warehouse and provides active scientific and technical guidance/support to them 
  • Develops and maintains fit-for-purpose equipment that are compliant with all relevant regulatory guidelines and SOPs
  • Provides and defines efficient workflows and business processes especially regarding equipment in alignment with Pilot Plant Management

Mission responsibilities:

  • To lead the benchmarking, purchasing and qualification/validation activities for new equipment for the pilot plant
  • To communicate the planning, activities, due-dates, attention points to all stakeholders of a project
  • To support all co-workers and stakeholders (QA, metrology, qualification, maintenance and site facilities) of the Prod Dev Pilot plant and warehouse area with technical assistance and coordination of technical activities
  • To provide appropriate documentation for all quality related activities
  • To support the development and maintenance of an overall process to ensure that all equipment are in an appropriate condition ready for pharmaceutical use
  • To train co-workers in the field of quality/safety related technical operations
  • To ensure cGMP compliance of premises, equipment and procedures within the pilot plant and warehouse area as determines by the manager
  • To ensure quality assurance activities are carried out in time
  •  To apply all relevant regulations, guidelines and operating procedures (regulatory, quality and safety)

jouw aanbod

  • Min 5-7 years’ experience in a laboratory or manufacturing environment, preferably in pharmaceutical or chemical industry
  • Experience in a GMP regulated environment
  • Experience in both R&D and commercial manufacturing of the pharmaceutical industry is an asset
  • Very good administrative, organizational and documentation skills are mandatory
  • Good knowledge in English is mandatory
  • Ability to communicate and collaborate within the team, Product Development department 
  • To be observant, identify or prevent from problems or issues and to raise them with supervisor when necessary
  • Consistently will to improve processes: SOP, business processes ...
  • Ability to prioritize activities in alignment with supervisor
  • Ability to delivery in a changing development environment
  • Working with Trackwise, Source, SAP is a huge asset

wat bieden wij?

We offer an attractive salary with extra-legal advantages : 

  • Group insurance
  • Hospitalisation insurance
  • Meal vouchers of 7 euros gross per working day
  • Reimbursement km or company car 
  • Monthly allowance (50 euros net per month)
  • A 13th month
  • Training
  • Etc

A rate as freelance is also possible.

ingenieur (m/v)
voltijds, freelance
onmiddellijke vaste indienstname
contact informatie
Aurélia Sautière
aurelia.sautiere@cx.ausy.be 02 474 60 16
02 474 60 16