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:
Bachelors 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 . We conduct interviews on an ongoing basis so please submit your application as soon as possible.
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 contribut...
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:
Bachelors 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 . We conduct interviews on an ongoing basis so please submit your application as soon as possible.
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