Senior Lab Equipment SME
- Belgium, Brussels
- Contract
- Life Sciences
This vacancy has now expired
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.
- 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
#LI-CB1
I have always received a highly professional & personable service from the team at QCS Staffing. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing's speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
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Chris
I manage this role.