Quality Release Manager to AstraZeneca
Qrios AB / Apotekarjobb / Stockholm
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hela Sverige Are you ready to take the next step in your career and make a real impact on global health? QRIOS is now looking for a Quality Release Manager for an exciting consulting assignment at our client, AstraZeneca. Starting in August, this role offers a unique opportunity to be part of the External Quality team - a global function within AstraZeneca Operations that ensures product quality from external suppliers.
At AstraZeneca, you'll join a vibrant, inclusive environment where science, innovation, and collaboration drive everything we do. You'll be part of a purpose-driven team where every voice matters, and your work contributes directly to delivering life-changing medicines to patients around the world. From laboratory research to large-scale manufacturing, quality is at the heart of every step - and this is your chance to be part of it.
About the position
As a Quality Release Manager you will be accountable for product release for products manufactured by AZ external contract manufacturers, quality system element governance, change control, SOP management, and quality risk management. Additionally under your responsibility will be the maintenance of quality data and records in relevant quality management support systems. Your role will also involve facilitating process and system improvements and supporting audits and inspection requests for sites as well as handle deviation investigations and quality issue management. You will collaborate with colleagues and customers across many countries and interact cross-functionally with supply chain, technical, regulatory and project teams in AZ.
Your profile
Essentials for the role.
• Masters degree in a science / technical field such as Pharmacy, Biology, Chemistry or Engineering.
• Minimum 1 yrs experience in either the pharmaceutical operations environment or pharmaceutical Quality Assurance role
• Minimum 1 yrs demonstrated experience of release processes, the quality event process, change control process
• Strong demonstrated knowledge of cGMPs, Quality Systems and the pharmaceutical supply chain environment.
• Excellent oral and written communication skills [English and local language(s)]
• Strong problem solving skills
• Strong negotiating/influencing skills
• Ability to work independently under their own initiative
• Ability to be in the office in Gärtuna, minimum 3 days/week
Desirable for the role
• Experience working in a PCO/PET organization or Lean/Six Sigma training
• Multi-site / multi-functional experience
At AstraZeneca we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and fuel your entrepreneurial spirit. There's no better place to make a difference to medicine, patients, and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth, and development.
Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available and we hope it's yours.
Ersättning Fast l?n
Så ansöker du Sista dag att ansöka är 2025-06-12
Arbetsgivarens referens Arbetsgivarens referens för detta jobb är "1269".
Omfattning Detta är ett heltidsjobb.
Arbetsgivare Qrios AB (org.nr 556599-5999),
http://www.qrios.se/ Arbetsplats Qrios Life Science & Engineering AB
Kontakt Hanna Peterson
hanna.peterson@qrios.se 072-076 72 73 Jobbnummer 9373434
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