Logistics Lead (m/f/d) at CordenPharma
Muttenz, BL, Switzerland -
Full Time


Start Date

Immediate

Expiry Date

15 Jul, 25

Salary

0.0

Posted On

09 May, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Logistics/Procurement

Description

CordenPharma ist eine der führenden Contract Development and Manufacturing Organizations (CDMO) und entwickelt und produziert im Auftrag ihrer Kunden als „Full-Service“-Dienstleister pharmazeutische Wirkstoffe, Arzneimittel und damit verbundene Verpackungsdienstleistungen. Die Gruppe beschäftigt rund 3.000 Mitarbeiter.
Unser Netzwerk in Europa und den USA bietet flexible und spezialisierte Lösungen für sechs Technologieplattformen: Peptides, Lipids & Carbohydrates, Injectables, Highly Potent & Oncology, Small Molecules und Oligonucleotides. Wir streben nach Spitzenleistungen bei der Unterstützung dieses Netzwerks und engagieren uns für die Bereitstellung von Produkten höchster Qualität zum Wohle der Patienten.

WAS DICH ERWARTET

CordenPharma is making a bold move to expand its Peptide Platform, strengthening our position as a global leader in CDMO peptide manufacturing. A major milestone in this journey is the construction of a state-of-the-art peptide manufacturing facility in Muttenz, Switzerland – located just outside Basel, a major biotech and pharma hub.
As part of this exciting expansion, looking for a Logistics Lead. This is a fantastic opportunity for a professional passionate about materials management, logistics, and compliance in a GMP-regulated environment. You will oversee the entire materials management function, ensuring that all activities comply with GMP guidelines, internal policies, and legal requirements. You will be responsible for defining, implementing, and ensuring compliance with processes to drive operational excellence.

Your Tasks will include:

  • Lead and develop the materials management team to enhance performance and efficiency.
  • Identify areas for process improvement and implement changes.
  • Collaborate with internal teams to ensure smooth operations.
  • Ensure GMP compliance by creating, training, and implementing SOPs
  • Track and manage CAPAs, ensuring high-quality standards.
  • Support projects and audits related to materials management.
  • Oversee inventory, shipping, and waste disposal processes.
  • Ensure proper storage and handling of materials, including temperature-sensitive products.
  • Manage master data in the ERP system and generate relevant reports.
  • Supervise raw material, intermediate, and final product storage in line with GMP requirements.

UM DIESE ROLLE ERFOLGREICH ZU MEISTERN, SUCHEN WIR NACH FOLGENDEN QUALIFIKATIONEN:

  • Education in logistics or a related field, with several years of experience in a similar role, ideally within the chemical or pharmaceutical industry.
  • Proven leadership experience, with the ability to manage and motivate a team.
  • Strong communication skills and flexibility, with a team-oriented mindset.
  • Excellent problem-solving skills, attention to detail, and proactive approach.
  • Resilient, structured personality with a hands-on mindset.
  • Experience with ERP systems, MS Office tools, and EMS systems, including electronic batch records.
  • Previous experience in a GMP-regulated environment.
  • Fluent in both German and English (written and spoken).
Responsibilities
  • Lead and develop the materials management team to enhance performance and efficiency.
  • Identify areas for process improvement and implement changes.
  • Collaborate with internal teams to ensure smooth operations.
  • Ensure GMP compliance by creating, training, and implementing SOPs
  • Track and manage CAPAs, ensuring high-quality standards.
  • Support projects and audits related to materials management.
  • Oversee inventory, shipping, and waste disposal processes.
  • Ensure proper storage and handling of materials, including temperature-sensitive products.
  • Manage master data in the ERP system and generate relevant reports.
  • Supervise raw material, intermediate, and final product storage in line with GMP requirements
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