@Biocartis_

Production Support Engineer

Mechelen / 2016028
Contact

Biocartis NV / Email: HR@biocartis.com

Function Type
Full time
Experience Required

Experience in a manufacturing organisation producing medical devices, pharmaceuticals or in-vitro diagnostics working within an ISO13485 / GMP compliant environment is an asset.

Affinity with Gowning and cleaning activities and materials and event management

Education

Technical Bachelor degree or equivalent by experience.

Functional Area
Manufacturing
Travel Percentage
0-5

Purpose of the organization

To support the cartridge production activities and teams in a broad variety of tasks (see below).

Tasks/outcome domains

  • Maintain a safe and clean work environment
  • Giving general support to production personnel:
    • Training follow-up
    • Gowning and cleaning activities and materials
    • Ensure that all direct staff comply with the Biocartis policies on safety and quality.
    • Purchasing of small equipment / tools
  • Supporting the day to day business (in close collaboration with the shift supervisors) :
    • Follow-up output and daily KPIs and use of these data to grow
    • Stimulate flow (standard work / material flow / 5S / …)
    • Actively looking for / implementing of continuous improvement opportunities (including flows, processes, documents,…)
    • Reporting and follow-up of issues, non-conformities or complaints
    • Review of batch records and necessary documentation
    • Keeping records and working instructions up to date
    • Maintain compliance with policies and procedures
  • Representing production in different projects:
    • Production “voice” (as customer of projects): making sure the production needs are covered in the deliverables – follow-up during project roll-out
    • Contact person: communication from project team to production team and the other way around – collect and share information between different parties
    • Create buy-in of the production team 

 

Profile & competencies

  • You have a technical Bachelor background or equivalent by experience.
  • Standard schedule in day – flexibility required to come in shift if needed for specific task/period.
  • Experience in a manufacturing organisation producing medical devices, pharmaceuticals or in-vitro diagnostics working within an ISO13485 / GMP compliant environment is an asset.
  • Affinity with Gowning and cleaning activities and materials and event management
  • Good communications skills as well as observational skills.
  • Well-organized, pro-active, planner.
  • Team player;
  • Advanced knowledge, orally and in writing of Dutch, and English.

 

Our offering

We offer you a challenging job in an exciting environment, working for top entrepreneurs in the biotech industry. You can be part of a very dynamic, young and growing team in a highly innovative environment. You will have freedom to shape your work and shape your job. Your input is highly appreciated. Of course we offer you a fitting compensation package.

 

Interested?

Please apply by e-mail (CV and motivational letter) to HR@biocartis.com using the job ID 2016028 as a reference.

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