Quality Control Specialist to AstraZeneca Stockholm
Alten Sverige AB / Biomedicinjobb / Stockholm
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hela Sverige About AstraZeneca
AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. At AstraZeneca, we're proud to have a unique workplace 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.
We have an exciting opportunity for you to join our new biologics manufacturing plant at Gärtuna, Södertälje. The purpose-built facility will supply the next generation of biological drugs from the AstraZeneca pipeline; supporting the acceleration of the biologics portfolio. The new manufacturing plant will focus on the filling and packaging of protein therapeutics for late stage clinical and commercial products.
Main Duties and Responsibilities
In this position you will act as the Subject Matter Expert in a Quality Control Scientific discipline. You will provides expert technical and analytical support to the Quality Control function and site including instrumentation and methodology troubleshooting, non-routine analysis, and the evaluation and exploitation of new technology. Leading significant Quality Control investigations and change programs including introduction of new methods and technology transfer. You have expert knowledge and understanding of the functional area and laboratory instrumentation, as well as Good Manufacturing Practice/Good Laboratory Practice.
You will be driving and supporting change management within the QC function, and introduces and embeds new technology/systems into the QC function ensuring that the QC function remains contemporary and competitive. You will lead and Support method validation activities and the analytical technology transfer of QC methodology into and out of Operations, including the design of transfer protocols and strategies.
This position is at a high level of complexity, working on multiple priorities and at multiple levels within and outside the organisation. The role is critical to the organisation as this individual is responsible for QC of the company's commercial and clinical products.
Essential Requirements:
• Degree level/or equivalent in scientific discipline.
• Technical SME in a QC discipline.
• Sound knowledge and understanding of the principles and concepts of compliance management and Good Manufacturing Practice / Good Laboratory Practice.
• Language level: Fluent in both Swedish and English.
Desirable Requirements:
• Lead investigator expertise required.
• Effective problem solving skills.
• Biopharmaceutical industry experience.
• Project management and influencing skills.
What we offer you at ALTEN
Every employee is equally valuable in the success of ALTEN! We are driven by making people grow and develop, which is why we offer you the opportunity to work with what you are truly passionate about. At ALTEN, we have a broad range of assignments at most of the leading companies in Sweden in several different sectors, to make it possible for your wishes to come true. We offer both national and international opportunities and together with your coaching manager, you build your career path so you constantly are able to develop and achieve your goals and dreams!
As a consultant at ALTEN, you will get the genuine team feeling at your assignment but also a wonderful togetherness at ALTEN. Through our different internal networks, such as ALTEN Sports, Women@ALTEN and ALTEN Innovation you will get the opportunity to drive topics and activities that are close to your heart, together with your colleagues. All activities are of course optional. Work life balance is our top priority. We also have a collective agreement and other benefits like Pension, Insurances and Wellness grants.
We believe in growing together!
Varaktighet, arbetstid
Heltid Tillsvidareanställning
Publiceringsdatum2019-11-06ErsättningEnligt överenskommelse
Så ansöker duSista dag att ansöka är 2019-11-15
Klicka på denna länk för att göra din ansökanFöretagAlten Sverige AB
Omfattning Detta är ett heltidsjobb.
Arbetsgivare Alten Sverige AB (org.nr 556420-7453)
Jobbnummer 4942241
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