Engineering lead coordinator

placeBraine-l'Alleud calendar_month 

Join a dynamic team committed to managing large-scale projects in the pharmaceutical sector, with a strong emphasis on innovation, international collaboration and technical rigour!

As a Engineering lead coordinator, you will play a key role in the management of industrial investment projects (CAPEX), ensuring the feasibility, implementation and commissioning of equipment and processes within a GMP-compliant pharmaceutical environment.

You will also be responsible for transferring technical knowledge to the operational teams and will play an active role in the continuous improvement of processes and equipment.

  • key responsibilities

Main tasks:

  • Assess the feasibility and risks associated with capital expenditure projects (CAPEX);
  • Represent the customer's expectations and use your expertise to define requirements (URS) and design solutions;
  • Manage suppliers through to completion of the FAT, SAT and equipment commissioning stages;
  • Support the qualification of equipment in accordance with internal SOPs and ICH guidelines;
  • Organise, where appropriate, the technical transfer of processes, including:
  • Drawing up the transfer strategy and preparing or reviewing test protocols;
  • Coordination of support departments (RA, QC, QA, Qualification/Validation, Development, IT, Supply Chain, HSE, Metrology, Purchasing, Facilities, Finance, Utilities, etc.);
  • Preparing and programming equipment (manufacturing recipes);
  • Managing experimental tests and checking that equipment is operating correctly;
  • Passing on the technical know-how acquired during commissioning and qualification ;
  • Support for the drafting of production documentation (SOPs, manufacturing instructions) ;
  • Participation in training, validation protocols and reports ;
  • Formalised sharing of knowledge on internal platforms (House of Knowledge type) ;
  • Support customer teams during pre-approval inspections of new equipment or processes;
  • Identify, propose and implement technical solutions to increase production capacity, reduce costs (COGS), improve efficiency and enhance quality compliance;
  • Overseeing the strict application of health and safety rules and contributing to the continuous improvement of practices;
  • Being in the front line for the handling of technical problems, investigations and deviations related to delivered equipment;
  • Applying best engineering practices in terms of cost estimation, schedule management, levels of definition (LOD), project management, commissioning, etc.
  • qualifications

Specific skills required:

  • Bachelor's or Master's level;
  • Technical expertise in automation, packaging technologies and medical devices;
  • Solid project management experience, with the ability to prioritise effectively and manage several tasks in parallel;
  • Team spirit: ability to work in a collaborative, multi-disciplinary and multi-site environment;
  • Excellent communication skills: ability to express yourself clearly, concisely and in a way that is appropriate to the audience; ability to communicate reactively and effectively in the event of problems;
  • Technical writing: ability to write or contribute to internal documentation (protocols, reports, instructions, etc.);
  • Knowledge sharing: ability to gather, synthesise and structure information to make it accessible and useful to project stakeholders;
  • Good knowledge of Good Manufacturing Practice (GMP).

Problem-solving skills:

  • Ability to solve problems independently, using a pragmatic and structured approach ;
  • Observe processes, collect and analyse relevant data, identify root causes, assess potential impacts and propose concrete, sustainable solutions ;
  • Applying an iterative approach to continuous improvement, combining analytical rigour and practical sense.

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