Arbetsbeskrivning

At Avaron, you get the security of permanent employment combined with the variety of working at different customers. We place specialists across everything from tech, IT and industry to project management and business support – and whatever the assignment, you have a consultant manager who is there for you and your development.

You will play a central role in making sure clinical trial medications reach patients across global studies with the right quality, quantity and timing. In this role, you work in a complex R&D environment where study requirements can change quickly and where supply chain decisions have a direct impact on clinical delivery.

You will project manage the design, planning and set-up of study supply chains, while leading cross-functional collaboration with internal teams and external partners. The role sits at the intersection of clinical development, manufacturing, quality and planning, giving you broad visibility across the end-to-end supply chain. It is a strong opportunity for you who enjoy combining operational ownership with project leadership in a field that contributes to new medicines.

• You will project manage the delivery of clinical supplies across a portfolio of studies.
• You will design, plan and set up study supply chains to support on-time delivery.
• You will lead cross-functional dialogue with internal teams and external partners on study design requirements and changes that affect supply.
• You will balance supply plans with cost considerations and potential risks to continuity.
• You will drive proactive risk management and mitigation for issues that may affect quality or delivery.
• You will take ownership of inventory management, including rework, recalls, shelf life extensions, expiry date management and stock destruction.
• You will manage the IRT system to support demand and supply planning.
• You will work within GMP Quality Management Systems and handle deviations, complaints and change controls.

• Bachelor’s Degree in a scientific or business subject area, or equivalent experience.
• Experience within a supply chain environment or the pharmaceutical industry.
• Holistic knowledge of end-to-end supply chain activities.
• Experience of demand planning, forecasting, and risk identification and management.
• Experience in running projects and influencing customer demands.
• Excellent English written and verbal communication skills.
• Proficient IT skills and the ability to adapt and work in multiple bespoke systems.
• You are able to learn continuously and adapt to new processes in a changing environment.

• Awareness of GMP (Good Manufacturing Practise) and GCP (Good Clinical Practice).
• Knowledge of clinical development processes relevant to the supply of clinical materials.
• Lean knowledge and understanding.
• Experience handling Quality Events such as Deviations, Change Controls, and Complaints.

• Permanent employment at Avaron AB
• Occupational pension
• Wellness allowance of SEK 5,000 per year

Selections are made on an ongoing basis – apply as soon as you can.