Supply Chain Manager - Clinical Trial medications | AstraZeneca | Gothenburg

Would you like to utilize your planning and supply chain knowledge to lead clinical supplies for your portfolio of global clinical studies? With constant new products and launches, there has never been a better time to join Global Clinical Supply Chain and shape our future with a significant contribution to life-changing medicines.

Brief information about the assignment:

Location: Gothenburg (Mölndal)
Type of employment: Consultant assignment
Assignment duration: 1 year, with the possibility of extension

About the role

In this role you will project manage the design, plan, and set-up of the study supply chain to ensure on time delivery of clinical supplies. You will also lead a cross-functional team enabling continuous dialogue with both internal and external partners on study design requirements and associated changes which may impact the supply chain elements of the study.

Key responsibilities include:

• Project manage the delivery of clinical supplies effectively and consistently, and input to the balance of costs and any risks to supply.
• Ensure effective communication with project teams and key partners across a global network.
• Support risk management of individual studies with proactive mitigation of risks that potentially impact the quality or delivery of supplies.
• Take ownership for Inventory management including any rework and recalls, extensions of shelf life and expiry date management, or stock destruction.
• Manage the Interactive Response Technology (IRT) system to execute demand and supply planning.
• Work within GMP Quality Management Systems ensuring that you actively handle any deviations, complaints and change controls.

Soft skills:
• Strong influencing, negotiating and problem-solving skills, across geographical and cultural boundaries
• Ability to adapt and operate in bespoke multiple systems.

About you

To be successful in this role you need to be a fast learner, self-driven and comfortable working in a high pace R&D environment. You need to be a collaborative team player, flexible and have strong communication, planning and problem-solving skills.

Essential:

• Bachelor’s Degree in a scientific or business subject area – equivalent experience will be considered
• Experience within a supply chain environment or pharmaceutical industry
• Holistic knowledge of end-to-end supply chain activities
• Excellent English written and verbal communication skills
• Proficient IT skills with an ability to adapt and operate in bespoke multiple systems

Desirable:

• 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
• Experienced in handling Quality Events (Deviations, Change Controls, Complaints)

As one of us

As an employed staffing consultant at Lernia, you will always receive a competitive salary, vacation benefits, pension contributions, insurance coverage, and be part of our collective agreement. We care about your well-being, which is why we offer all our consultants wellness allowances and access to occupational health services. During your employment, you will have a dedicated consultant manager responsible for your assignment, ensuring you thrive at your workplace while supporting and developing you in your professional role.

How to Apply

To apply for this position, click on the "Apply" link above and fill out the form. For any questions or inquiries, please contact hampus.svensson@lernia.se. We conduct interviews on an ongoing basis, so please submit your application as soon as possible.