Labelling Coordinator.

Job Details

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Job Details

For our client, a pharmaceutical company based in canton Lucerne, we are looking for a Labelling Coordinator.

 

General Information:
 

  • Start Date: ASAP
  • Duration: 1 year
  • Extension: possible
  • Workload: 100%
  • Workplace: canton Lucerne
  • Home office: up to 2 days/week, but mainly onsite

 

The primary activities include, but are not limited to:
 

  • Creation of label text translations using a translation database and approval of the translations regarding study-specific, company-internal, and country-specific regulatory requirements.
  • Create and monitor project schedule and coordinate projects from translation of label text to delivery of labels to packaging department.
  • Work proficiently within schedule driven and accountable to inform stakeholders if necessary.
  • Advising the responsible project manager on the determination of the label text in compliance with international regulatory requirements and internal company standards.
  • Ensuring that GMP quality and safety standards are met in Label Translation in accordance with internal and regulatory requirements.
     
 

Your profile:
 

  • Minimum a bachelor’s degree and/or at least 2 years’ experience in the clinical supplies space (packaging/ labeling operations).
  • Excellent communication, organizational and time management skills
  • Fluent in German and English
  • Able to work independently
  • Analytical thinking
  • Eye for detail
  • Able to work in the GMP environment
  • Very good in Microsoft Office (preferably proficient in Excel, Power BI and similar)
  • Supply planning oriented 
  • Result oriented
  • Team player

For our client, a pharmaceutical company based in canton Lucerne, we are looking for a Labelling Coordinator.

 

General Information:
 

  • Start Date: ASAP
  • Duration: 1 year
  • Extension: possible
  • Workload: 100%
  • Workplace: canton Lucerne
  • Home office: up to 2 days/week, but mainly onsite

 

The primary activities include, but are not limited to:
 

  • Creation of label text translations using a translation database and approval of the translations regarding study-specific, company-internal, and country-specific regulatory requirements.
  • Create and monitor project schedule and coordinate projects from translation of label text to delivery of labels to packaging department.
  • Work proficiently within schedule driven and accountable to inform stakeholders if necessary.
  • Advising the responsible project manager on the determination of the label text in compliance with international regulatory requirements and internal company standards.
  • Ensuring that GMP quality and safety standards are met in Label Translation in accordance with internal and regulatory requirements.
     
 

Your profile:
 

  • Minimum a bachelor’s degree and/or at least 2 years’ experience in the clinical supplies space (packaging/ labeling operations).
  • Excellent communication, organizational and time management skills
  • Fluent in German and English
  • Able to work independently
  • Analytical thinking
  • Eye for detail
  • Able to work in the GMP environment
  • Very good in Microsoft Office (preferably proficient in Excel, Power BI and similar)
  • Supply planning oriented 
  • Result oriented
  • Team player

kontaktiere uns.

wir sind da um deine Fragen zu beantworten.

MT

Marta Tomczyk

Danke für die Anmeldung zu persönlichen Job-Benachrichtigungen.