Finden Sie Projekte und Festanstellungen in der Life Science Branche
search
reorder

Supply Chain Specialist - I m/w/d (EN)

[17137]
Supply Chain Management

Assoc. Supply Chain Specialist, Material Compliance works closely with above site supply chain team (Dunboyne), local quality, tech transfer, procurement, and manufacturing operations as well as other self-directed work teams in the site’s value stream. Project title: Supply Chain Specialist - I m/w/d Type of employment: Payroll Industry: Biotech Skills: Supply Chain Management Project start: 01.04.2026 Project duration: 12 months Location: Luzern, Schweiz Key Activities: ·Create and maintain supply chain records in our supplier qualification system. ·Assess all material related changes (vendor or site initiated) and drive quality change control where needed. ·Support supplier qualification activities, request supplier audits for new partners. ·Build an excellent relationship with suppliers of assigned categories in order to ensure value is created and delivered for the site. ·Create material specifications as part of the material qualification activities to support material releases. ·Ensure material is sourced/implemented with the required quality grades for clinical manufacturing. ·Collaborate with internal and external stakeholders (tech transfer, procurement, manufacturing) for material identification and supplier selection. Contribute to define a standardized material platform. ·Support supply chain team on quality and compliance related issues through investigations, change controls, quality risk assessments etc. ·Initiate and formulate proposals / business cases for quality improvement projects including deliverables and planning for the development and implementation of proposed improvements. Requirements: ·Bachelor’s or Master’s degree in engineering, pharmacy or science related field or a minimum of 3 years’ experience working in a relevant academic or industry field. ·Experience within quality operations/ compliance or supporting supply chain or operations role within a pharmaceutical company ·Excellent command of English, both written and verbal – ability to work within all levels of the organisation from shopfloor staff to site leadership team. ·Strong communication skills ·Good influencing / collaboration skills and teamwork mindset ·Strong analytical and priority management skills ·Experience in leading change management initiatives – building both people competence and introducing new processes ·Sense of initiative and overall coordination of projects and activities ·Excellent trouble shooting and problem-solving skills, ability to challenge the status quo with a continuous improvement mindset. ·Computer literate with advanced skills in MS Office, especially Excel ·SAP knowledge is an advantage ·Promoting a culture where diversity and inclusion is supported. ·Ability and willingness to keep learning

Assoc. Supply Chain Specialist, Material Compliance works closely with above site supply chain team (Dunboyne), local quality, tech transfer, procurement, and manufacturing operations as well as other self-directed work teams in the site’s value stream.


Project title: Supply Chain Specialist - I m/w/d
Type of employment: Payroll
Industry: Biotech
Skills: Supply Chain Management
Project start: 01.04.2026
Project duration: 12 months
Location: Luzern, Schweiz


Key Activities:

  • Create and maintain supply chain records in our supplier qualification system.
  • Assess all material related changes (vendor or site initiated) and drive quality change control where needed.
  • Support supplier qualification activities, request supplier audits for new partners.
  • Build an excellent relationship with suppliers of assigned categories in order to ensure value is created and delivered for the site.
  • Create material specifications as part of the material qualification activities to support material releases.
  • Ensure material is sourced/implemented with the required quality grades for clinical manufacturing.
  • Collaborate with internal and external stakeholders (tech transfer, procurement, manufacturing) for material identification and supplier selection. Contribute to define a standardized material platform.
  • Support supply chain team on quality and compliance related issues through investigations, change controls, quality risk assessments etc.
  • Initiate and formulate proposals / business cases for quality improvement projects including deliverables and planning for the development and implementation of proposed improvements.

Requirements:

  • Bachelor’s or Master’s degree in engineering, pharmacy or science related field or a minimum of 3 years’ experience working in a relevant academic or industry field.
  • Experience within quality operations/ compliance or supporting supply chain or operations role within a pharmaceutical company
  • Excellent command of English, both written and verbal – ability to work within all levels of the organisation from shopfloor staff to site leadership team.
  • Strong communication skills
  • Good influencing / collaboration skills and teamwork mindset
  • Strong analytical and priority management skills
  • Experience in leading change management initiatives – building both people competence and introducing new processes
  • Sense of initiative and overall coordination of projects and activities
  • Excellent trouble shooting and problem-solving skills, ability to challenge the status quo with a continuous improvement mindset.
  • Computer literate with advanced skills in MS Office, especially Excel
  • SAP knowledge is an advantage
  • Promoting a culture where diversity and inclusion is supported.
  • Ability and willingness to keep learning







map Luzern, Schweiz date_range 01.04.2026 update Temporary
Direkter Kontakt

Luca Furler

Senior Consultant
mail l.furler@aristo-group.ch
phone +41 44 27439 00


Nichts passendes dabei? Senden Sie uns eine Nachricht!

Sie sind nicht fündig geworden? Senden Sie uns einfach Ihre Kontaktdaten und ein kurzes Profil und wir melden uns umgehend bei Ihnen, um die nächsten Schritte gemeinsam mit Ihnen zu definieren.