Posição: Mid-Senior level

Tipo de empregos: Full-time

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Conteúdo do emprego

The Shift Supervisor is responsible for the organization and supervision of all activities related to cartridge production in order to guarantee high quality and on-time delivery.

Accountabilities

Maintaining a clean, GMP-compliant and safe working environment:

  • Ensure all rooms used by production teams are kept tidy and clean.
  • Ensure all cleaning activities are performed and documented according to the related procedures.
  • Ensure behavior of production personnel according to Good Manufacturing Practices (GMP) rules & regulations and the Biocartis policies on safety & quality.
  • Report and follow-up of safety issues.

Daily management of production team:

  • Make firm decisions that guarantee output, safety, quality and efficiency.
  • Completes production plan by scheduling and assigning personnel; monitoring progress; revising schedules; resolving problems; reporting on shift production summaries.
  • Ensure operation of equipment by calling for repairs.
  • Coaching, counseling and disciplining employees.
  • Coordinate and follow-up of training production personnel (completion, needs, documentation, assure knowledge transfer in production team).
  • Initiate and foster a spirit of cooperation within and between production shifts and lines.
  • Ensure knowledge / information transfer over different shifts.

Ownership for processes related to cartridge production:

  • Ensure cartridge production and related processes (e.g. IPC testing or spot solution preparation) are performed according to approved procedures and work instructions.
  • Ensure that the finished goods satisfy the Biocartis standards in terms of quality, cost, timeliness of delivery and the applicable compliance and legal standards.
  • Maintain and make use of visual management of manufacturing performance indicators.

Supporting tasks to production team:

Quality related:

  • Report and follow-up of issues, non-conformities or complaints.
  • Review and completion of necessary documentation (e.g. batch records,…).
  • Responsible for keeping production records and work instructions up to date.
  • Ensure any failed material is correctly quarantined.

Efficiency related:

  • Follow-up output and daily KPIs and use these data to grow.
  • Stimulate flow (standard work / material flow / 5S / …
  • Actively contribute to continuous improvement of processes, process flows, process efficiencies, lead times, cost of goods, etc.

Contact person for production team to internal and external partners:

  • Contact to teams for production planning of cartridge orders.
  • Contact to teams for planning and organization of technical interventions.
  • Support the start-up of new products and manufacturing processes.
  • Support internal and external visitors (including audits).
  • Act as production representative in multidisciplinary teams.

Profile requirements

  • Technical High school / Bachelor background or equivalent by experience.
  • Min. 2 years of experience as shift supervisor required or equivalent by relevant experience.
  • Min. five years’ experience in a manufacturing organization producing medical devices, pharmaceuticals or in-vitro diagnostics. Working within an ISO13485 / GMP compliant environment is a must.
  • Experience working in a controlled environment.
  • Team leader with well-developed interpersonal skills
  • Motivator and enthusiastic coach
  • Analytical mindset and problem solver
  • Very good communicational and organizational skills
  • Result oriented and driven
  • Willing to work in 2 shifts (early/late), fixed night or on weekends
  • Knowledge of lean principles is an asset
  • Planning and Organization: Time & priority management: plans activities effectively with respect for priorities and deadlines.
  • Communicating & Influencing: Communicates with persuasion: presents, explains and defends a complex message in a clear and concise way and persuades different stakeholders.
  • Adaptability to change: Supporting & facilitating change: enables and shapes change, helps others to understand the need for change and adapt to it.
  • Resilience: Maintains self-control, direction and effectiveness in high pressure situations.
  • Coaching & Development: Provides ongoing feedback, creates development opportunities and plans to meet employees’ needs and aspirations.
  • PC skills: MS Office
  • Languages: Advanced knowledge, orally and in writing of Dutch, preferably also English

Our offering

We offer you an exciting job in a fast growing international and innovative environment where you can work with top entrepreneurs in the biotech industry. You can be part of a very dynamic, young and growing team. You will have freedom to shape your work and shape your job where you deem it necessary: we value your input. Of course we offer you an appropriate compensation package.

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Data limite: 31-12-2025

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