Quality Control Specialist Biochemistry to AstraZeneca

Poolia Sverige AB / Kemistjobb / Stockholm
Observera att sista ansökningsdag har passerat.


Visa alla kemistjobb i Stockholm, Solna, Lidingö, Sundbyberg, Danderyd eller i hela Sverige
Visa alla jobb hos Poolia Sverige AB i Stockholm, Solna, Lidingö, Sundbyberg, Danderyd eller i hela Sverige

We are now looking for a specialist within biochemistry to a consultant assignment as a subject matter expert at Sweden Biologics AstraZeneca in Södertälje.

Do you have expertise in, and passion for, Bioanalytical and Bioassay? Do you like to lead projects within a pharmaceutical setting and use your expertise in a company that follows the science and turns ideas into life changing medicines for patients? Then Sweden Biologics might be interesting for you! Please, don't hesitate and submit your application today!


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.

Sweden Biologics Quality Control:
At Sweden Biologics Quality control (QC) department is divided in to three functional groups, Bioassay, Biochemistry and Microbiology. Each group consists of approximately 6-8 persons. At the department QC immunologists, QC analytical biochemists, QC microbiologists work alongside QC specialists and QC information system specialists. All staff collaborate closely on general QC responsibilities whilst achieving group specific deliverables.
In order to further support the QC department, we are now recruiting an additional QC specialist within Biochemistry. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person.

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.

Varaktighet, arbetstid
Heltid Visstid, mer än 6 månader

Publiceringsdatum
2019-11-06

Ersättning
Fast lön

Så ansöker du
Sista dag att ansöka är 2019-11-13
Klicka på denna länk för att göra din ansökan

Företag
Poolia Sverige AB

Arbetsgivarens referens
Arbetsgivarens referens för detta jobb är "55173".

Omfattning
Detta är ett heltidsjobb.

Arbetsgivare
Poolia Sverige AB (org.nr 556426-7655), http://www.poolia.se

Arbetsplats
Poolia Life Science & Engineering AB

Jobbnummer
4943701

Observera att sista ansökningsdag har passerat.

Prenumerera på jobb från Poolia Sverige AB

Fyll i din e-postadress för att få e-postnotifiering när det dyker upp fler lediga jobb hos Poolia Sverige AB: