Clinical Supply Associate
Avaron AB
📍 Göteborg
⏰ Heltid
📋 Vanlig anställning
🗓 Ansök senast 6 maj 2026
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About the Company
Avaron helps you find assignments that match your skills and ambitions. As a permanently employed consultant with us, you get competitive terms – combined with the variety and growth that a consulting career offers.
About the Assignment
You will be part of a global pharmaceutical environment where innovative science is translated into clinical material that supports the development of new medicines. In this role, you will help make sure clinical supply and related information are coordinated, documented, and delivered with high quality to meet clinical demand.
The assignment sits close to both supply chain and quality, which means you will work in a process-driven setting with clear links to patient impact, compliance, and continuous improvement. You will also work with digital tools and structured ways of working in an agile environment where details matter just as much as the bigger picture.
This is an exciting opportunity for you if you want to build a career within Clinical Supply Management and gain broad exposure to supply chain, quality processes, and improvement work in a global organization.
Job DescriptionYou will support the coordination of purchasing and delivery of external commercial products used in clinical supply.
You will facilitate documentation activities to help maintain inspection readiness in line with international GMP standards.
You will work with electronic document archiving and quality control of documentation and related information.
You will participate in User Acceptance Testing of digital systems and help secure effective ways of working.
You will document and coordinate product quality complaints and GMP deviations.
You will use supply chain management systems to support agile and structured daily work.
You will contribute to continuous improvement of clinical supply chain processes through visual management, problem solving, global standardization, and process confirmation.
RequirementsHands-on experience of GMP, GCP, and GDP.
An academic scientific background and a clear interest in supply chain management.
A structured and organized way of working, with strong aptitude for digital systems.
You are comfortable in a process-oriented workplace and enjoy task-based activities with a clear customer and patient focus.
Strong communication skills.
A collaborative mindset, good problem-solving ability, and a strong focus on quality.
You thrive in a high-paced and agile environment.
You can balance attention to detail with the ability to see the bigger picture.
Nice to haveBachelor’s or master’s degree in a scientific discipline.
Degree in supply chain leadership.
What We OfferPermanent employment at Avaron AB
Occupational pension
Wellness allowance of SEK 5,000 per year
Application
Selections are made on an ongoing basis – apply as soon as you can.
Avaron helps you find assignments that match your skills and ambitions. As a permanently employed consultant with us, you get competitive terms – combined with the variety and growth that a consulting career offers.
About the Assignment
You will be part of a global pharmaceutical environment where innovative science is translated into clinical material that supports the development of new medicines. In this role, you will help make sure clinical supply and related information are coordinated, documented, and delivered with high quality to meet clinical demand.
The assignment sits close to both supply chain and quality, which means you will work in a process-driven setting with clear links to patient impact, compliance, and continuous improvement. You will also work with digital tools and structured ways of working in an agile environment where details matter just as much as the bigger picture.
This is an exciting opportunity for you if you want to build a career within Clinical Supply Management and gain broad exposure to supply chain, quality processes, and improvement work in a global organization.
Job DescriptionYou will support the coordination of purchasing and delivery of external commercial products used in clinical supply.
You will facilitate documentation activities to help maintain inspection readiness in line with international GMP standards.
You will work with electronic document archiving and quality control of documentation and related information.
You will participate in User Acceptance Testing of digital systems and help secure effective ways of working.
You will document and coordinate product quality complaints and GMP deviations.
You will use supply chain management systems to support agile and structured daily work.
You will contribute to continuous improvement of clinical supply chain processes through visual management, problem solving, global standardization, and process confirmation.
RequirementsHands-on experience of GMP, GCP, and GDP.
An academic scientific background and a clear interest in supply chain management.
A structured and organized way of working, with strong aptitude for digital systems.
You are comfortable in a process-oriented workplace and enjoy task-based activities with a clear customer and patient focus.
Strong communication skills.
A collaborative mindset, good problem-solving ability, and a strong focus on quality.
You thrive in a high-paced and agile environment.
You can balance attention to detail with the ability to see the bigger picture.
Nice to haveBachelor’s or master’s degree in a scientific discipline.
Degree in supply chain leadership.
What We OfferPermanent employment at Avaron AB
Occupational pension
Wellness allowance of SEK 5,000 per year
Application
Selections are made on an ongoing basis – apply as soon as you can.