Supply Chain Manager for Clinical Trial medications
Qrios Minds AB / Biomedicinjobb / Göteborg
2023-11-14
Observera att sista ansökningsdag har passerat.
➡️ Klicka här för den senare publicerade platsannonsen "Supply Chain Manager for Clinical Trial medications" (publicerad 2024-04-22) ⬅️
Visa alla biomedicinjobb i Göteborg,
Mölndal,
Partille,
Kungälv,
Lerum eller i
hela Sverige Visa alla jobb hos Qrios Minds AB i Göteborg,
Mölndal,
Stenungsund,
Borås,
Varberg eller i
hela Sverige Would you like to utilise 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.
We have an exciting opportunity for talented Supply Chain Managers to join our Clinical Study Supply Chain team in Gothenburg, Sweden. This is a key role within our Clinical Manufacturing and Supply teams, and we make sure clinical trial medications are available at the right quality, in the right quantity at the right time for every patient taking part in AstraZeneca's trials all over the world. Our goal is to never miss a patient.
In Pharmaceutical Technology and Development (PT&D) we are the bridge which turns forward-thinking science into actual medicines that help millions of people around the world. We work across the entire value chain, crafting and delivering active ingredients, formulations and devices required to support new medicines - from supplies for use in early toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture.
About the position
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.
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.
Responsibilities
Your main responsibilities will 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.
Your profile
Essential for the role:
• Bachelor's Degree in Supply Chain, business or scientific subject area - equivalent experience within Supply Chain will be considered
• Experience within a Supply Chain Management environment with a holistic knowledge of end-to-end supply chain activities (minimum 2 years experience desirable)
• Proficient IT skills with an ability to adapt and operate in bespoke multiple systems
• Experience in running projects and in?uencing customer demands
• Experience of demand planning and forecasting and risk identification and management
• Excellent English written and verbal communication skills
Desirable for the role:
• 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)
• Knowledge of clinical development processes relevant to the supply of clinical materials
• Working in a leading role within a team
About the organisation
This is a consultant assignement at AstraZeneca in Göteborg for 1 year. During this time you will be hired by QRIOS Life Science. We work with Sweden's leading pharmaceutical and life science companies. So whether you're interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.
Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you're looking for a world of exciting assignments and new contacts, you'll like being a consultant.
About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world's leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.
Ersättning Fast lön
Så ansöker du Sista dag att ansöka är 2023-11-23
Arbetsgivarens referens Arbetsgivarens referens för detta jobb är "940".
Omfattning Detta är ett heltidsjobb.
Arbetsgivare Qrios Minds AB (org.nr 556599-5999),
http://www.qrios.se/ Arbetsplats Qrios Life Science & Engineering AB
Kontakt Alma Foric
alma.foric@qrios.se 073-850 49 73 Jobbnummer 8262402
Observera att sista ansökningsdag har passerat.