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16 часов Π½Π°Π·Π°Π΄

Pharmaceutical Supply Chain Coordinator (Life Sciences)

Π€ΠΎΡ€ΠΌΠ°Ρ‚ Ρ€Π°Π±ΠΎΡ‚Ρ‹
remote (Ρ‚ΠΎΠ»ΡŒΠΊΠΎ Europe)
Π’ΠΈΠΏ Ρ€Π°Π±ΠΎΡ‚Ρ‹
fulltime
Π“Ρ€Π΅ΠΉΠ΄
junior
Английский
c1
Вакансия ΠΈΠ· списка Hirify.GlobalВакансия ΠΈΠ· Hirify Global, списка ΠΌΠ΅ΠΆΠ΄ΡƒΠ½Π°Ρ€ΠΎΠ΄Π½Ρ‹Ρ… tech-ΠΊΠΎΠΌΠΏΠ°Π½ΠΈΠΉ
Для мэтча ΠΈ ΠΎΡ‚ΠΊΠ»ΠΈΠΊΠ° Π½ΡƒΠΆΠ΅Π½ Plus

ΠœΡΡ‚Ρ‡ & Π‘ΠΎΠΏΡ€ΠΎΠ²ΠΎΠ΄

Для мэтча с этой вакансиСй Π½ΡƒΠΆΠ΅Π½ Plus

ОписаниС вакансии

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TL;DR

Pharmaceutical Supply Chain Coordinator (Life Sciences): Coordinating patient-material logistics, planning, forecasting, and compliant flows across the EMEA supply chain with an accent on Chain of Custody, Chain of Identity, and regulated pharmaceutical operations. Focus on resolving non-conformances, scheduling cryopreservation and manufacturing capacity, improving procedures, and rolling out supply chain systems.

Location: Remote work supporting patient-material operations across EMEA.

Company

Independent technology consulting firm delivering solutions across information systems, telecommunications, life sciences, and engineering through an international workforce.

What you will do

  • Act as the primary supply chain contact for treatment sites and commercial teams within an assigned country or region.
  • Coordinate inbound and outbound patient-material logistics across the EMEA V2V supply chain, including carrier communication, forecasting, and warehouse coordination.
  • Manage issues and non-conformances while ensuring Chain of Custody and Chain of Identity compliance in manual and automated processes.
  • Plan operational capacity by scheduling cryopreservation and manufacturing slots.
  • Support treatment-site certification through training and logistics test runs.
  • Develop SOPs, work instructions, performance metrics, and system improvements.

Requirements

  • 1–3 years of experience in the pharmaceutical industry or another highly regulated environment, ideally in supply chain, logistics, or operations.
  • Knowledge of quality systems, cGMP, and FDA regulations.
  • Ability to analyze process, system, technical, and regulatory information in a GMP environment.
  • Independent working style with strong attention to detail, accuracy, and operational judgment.
  • Strong stakeholder communication and collaboration skills in a global, evolving environment.
  • Fluent English required.

Nice to have

  • Experience with SAP or other ERP systems.
  • Continuous improvement and innovation mindset.

Culture & Benefits

  • Remote work, health insurance, meal vouchers, and a time savings account.
  • Long-term projects with major enterprise clients and support from internal Centers of Excellence.
  • Structured management support, regular project check-ins, and direct HR communication.
  • Functional and geographic mobility across multiple areas of expertise and countries.
  • Funded Microsoft certifications, extensive training, and access to in-house AI initiatives.
  • Referral bonuses and an active corporate social responsibility program.

Hiring process

  • Brief virtual or phone call.
  • Approximately three interviews with the hiring manager and relevant stakeholders.
  • Case study or technical, role-play, or problem-solving assessment depending on the role.

Π‘ΡƒΠ΄ΡŒΡ‚Π΅ остороТны: Ссли Ρ€Π°Π±ΠΎΡ‚ΠΎΠ΄Π°Ρ‚Π΅Π»ΡŒ просит Π²ΠΎΠΉΡ‚ΠΈ Π² ΠΈΡ… систСму, ΠΈΡΠΏΠΎΠ»ΡŒΠ·ΡƒΡ iCloud/Google, ΠΏΡ€ΠΈΡΠ»Π°Ρ‚ΡŒ ΠΊΠΎΠ΄/ΠΏΠ°Ρ€ΠΎΠ»ΡŒ, Π·Π°ΠΏΡƒΡΡ‚ΠΈΡ‚ΡŒ ΠΊΠΎΠ΄/ПО, Π½Π΅ Π΄Π΅Π»Π°ΠΉΡ‚Π΅ этого - это мошСнники. ΠžΠ±ΡΠ·Π°Ρ‚Π΅Π»ΡŒΠ½ΠΎ ΠΆΠΌΠΈΡ‚Π΅ "ΠŸΠΎΠΆΠ°Π»ΠΎΠ²Π°Ρ‚ΡŒΡΡ" ΠΈΠ»ΠΈ ΠΏΠΈΡˆΠΈΡ‚Π΅ Π² ΠΏΠΎΠ΄Π΄Π΅Ρ€ΠΆΠΊΡƒ. ΠŸΠΎΠ΄Ρ€ΠΎΠ±Π½Π΅Π΅ Π² Π³Π°ΠΉΠ΄Π΅ β†’