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Senior Lab Equipment SME

  1. Belgium, Brussels
Brussels
  1. Contract
Competitive
  1. Life Sciences
36236
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Senior Lab Equipment SME - Brussels, Belgium - 23 Months Contract

We are looking for an experienced Senior Lab Equipment SME for a fantastic 23 months contract based in Brussels, Belgium.

You will be working with our client who are a global biopharmaceutical organisation committed to improving the lives of people afflicted with neurological and immunological disease.

This is a superb opportunity if you are looking to advance your career in the field with a supportive and innovative company that will put you first. 

Responsibilities:
  • Define, track and finalise the list of equipment with all user’s needs.
  • Provide and ensure the day-to-day project coordination during the design and execution phases in accordance with safety, cost, schedule, quality, whilst ensuring compliance with local rules and regulations.
  • Chair, run and contribute to regular project team meetings, prepare, and issue meeting agendas and minutes, maintain action/decision log, owner of small equipment governance for the BBOC+ Project.
  • Owner of the overall equipment list, accountable to report on budget, ETC, commitment for the end-to-end delivery.
  • Maintain and optimise the workload and the overall plan for both project (analytical labs & small equipment)
  • Issue, communicate and update the project plan for both analytical labs and small equipment’s Plan. Provide input to other key stakeholders and strategic project documents, incl. KPI and progress reports.
  • Provide routine and ad hoc project status and performance information, including monthly project status updates and presentations to senior management and the wider organisation.
  • Ability to provide guidance and work with project stakeholders and suppliers to deliver all activities required to get equipment and analytical equipment installed and running.
  • Responsible for the planning, tracking and reporting of analytical labs and small equipment progress, status and risks/issues for the selected system(s). Take appropriate corrective actions as required to ensure deadlines and milestones are achieved.
  • Deep understanding and experience of all C&Q strategies, testing and activities.
  • Knowledge of safety, GMP and environmental regulatory requirements.
  • Strong coordination skill, structured, good communicator, organised, results oriented, committed, seek for team coordination and priority, leader.
  • High attention to helicopter view to prevent and prepare all activities in advance, ability to multi-task and take initiative to accurately complete assigned tasks by established deadlines.
Requirements:
  • Extensive experience within pharmaceutical companies and working with Engineering offices
  • Good knowledge in data integrity and IT requirements for lab equipment.
  • Excellent coordination skills to adapt to several customer’ requirements.
  • Fluent in English is mandatory. French is highly desirable (French speaking team).
  • Good Knowledge of cGxP requirements
  • Manage a fluent communication between different stakeholders (supplier, User and others)
  • Team player, Rigorous, Accountable, Involved, Proactive.
  • Pragmatic to solve issues
  • Autonomous, fully acting at own's initiative
If this role is of interest to you, please apply now!
 #LI-CB1
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