Label Design Specialist (a)

Michael Page

Michael Page

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Key information

  • Publication date:

    15 April 2024
  • Workload:

    80 – 100%
  • Contract type:

    Temporary
  • Language:

    German (Intermediate)
  • Place of work:

    Lucerne
For our client, a leading international pharmaceutical company with modern offices in the canton of Lucerne, we are currently looking for a Label Design Specialist (a) for a temporary assignment of 1 year, with the high possibility of extension.

For our client, a leading international pharmaceutical company with modern offices in the canton of Lucerne, we are currently looking for a Label Design Specialist (a) for a temporary assignment of 1 year, with the high possibility of extension.

Description

In this role, the selected candidate will be responsible for the following tasks:

  • Proposing label sizes and study designs based on country specific label text.
  • Serving as SME for various questions on clinical labels from other teams.
  • Coordinating/advising Operations Planner on label strategy for a clinical packaging job.
  • Reviewing county-specific label text on accuracy and regulatory requirements.
  • Handling of randomization schedules for clinical studies.
  • Reviewing and release of label batch record documents.
  • Ensuring activities are completed within given timelines and timely escalation when issues arise.
  • Designing of Clinical Labels for primary and secondary packaging jobs.
  • Working according to GMP standards and internal guidelines.

Profile

To qualify for this position, the selected candidate must meet the following requirements:

  • Completed apprenticeship as a laboratory technician, chemist or business administrator.
  • Preferably with 2 years of experience in the clinical field for packaging and label production.
  • Experience with GMP requirements, quality processes, and SOP execution.
  • Experience in the field of clinical studies and their planning, preparation, coordination, production (labels), etc., is an advantage.
  • Proficiency in Microsoft applications (Word, Excel, PowerPoint).
  • Proficiency in both German and English (oral and written).
  • SAP knowledge is a plus.

Job Offer

Step into a renowned pharmaceutical industry company and contribute to the quality and compliance with regulatory GMP requirements.

Contact

  • Michael Page

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