Supply Chain Manager – Clinical Trial Medications / Clinical Supply Study L at WeQuel

Gothenburg, Västra Götaland County, Sweden -

Full Time

Start Date

Immediate

Expiry Date

07 Jul, 26

Salary

0.0

Posted On

08 Apr, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Supply chain management, Clinical trial management, Demand planning, Forecasting, Risk mitigation, Inventory management, IRT systems, GMP compliance, Project management, Stakeholder management, GCP, Lean methodology, Change control, Deviation management

Industry

Business Consulting and Services

Description

Consulting assignment at AstraZeneca | Gothenburg WeQuel is now looking for two experienced Supply Chain Managers on behalf of a client within AstraZeneca’s Clinical Supply Chain organization in Gothenburg. This is a full-time consulting assignment where you will play a key role in ensuring that clinical trial medications reach patients worldwide with the right quality, quantity, and timing. About the assignment AstraZeneca is a global, science-led biopharmaceutical company committed to delivering life-changing medicines. Within Pharmaceutical Technology & Development (PT&D), you will be part of the organization that bridges research and commercial manufacturing. In this role, you will lead the end-to-end supply chain for global clinical studies, working cross-functionally in a fast-paced R&D environment. Your role As a Supply Chain Manager / Clinical Supply Study Lead, you will: Lead the design, planning, and setup of clinical supply chains Project manage delivery of clinical supplies across global studies Collaborate with cross-functional stakeholders and external partners Manage demand planning, forecasting, and risk mitigation Take ownership of inventory management, including rework, expiry handling, and recalls Operate and manage IRT systems for supply planning Ensure compliance within GMP quality systems (deviations, change controls, complaints) Requirements Bachelor’s degree in science, business, or equivalent experience Experience within supply chain and/or pharmaceutical industry Strong understanding of end-to-end supply chain processes Experience in demand planning, forecasting, and risk management Proven ability to lead projects and influence stakeholders Excellent communication skills in English Strong problem-solving, negotiation, and collaboration skills Ability to work in complex systems and adapt to change Meritorious Knowledge of GMP / GCP Understanding of clinical development and clinical supply processes Lean experience Experience handling quality events (deviations, change controls, complaints) Assignment details Start: June 1, 2026 End: May 31, 2027 Scope: Full-time (100%) Location: Gothenburg Number of roles: 2 About WeQuel WeQuel is a modern consulting company built on the philosophy “we are equal” and “people first.” We specialize in connecting top talent with leading companies within Life Science, industry, and technology. At WeQuel, you become part of a strong network of consultants, supported throughout your assignments from matching to delivery and beyond.

Responsibilities

The Supply Chain Manager will lead the end-to-end supply chain for global clinical studies, ensuring the timely and quality delivery of medications. Responsibilities include demand planning, inventory management, and ensuring compliance with GMP quality systems.