Analytical Scientist, Advanced Drug Delivery
AstraZeneca AB / Biomedicinjobb / Göteborg
2020-01-17
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hela Sverige At AstraZeneca we turn ideas into life changing medicines and strive to continuously meet the unmet needs of patients worldwide. Working here means being entrepreneurial, thinking big, and working together to make the impossible a reality. 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.
Pharmaceutical Sciences at AstraZeneca delivers the therapies of the future through scientific leadership in drug delivery, design of synthetic routes, and manufacturing of Active Pharmaceutical Ingredients (API) and drug products. Our portfolio of projects spans traditional small molecules, peptides, oligonucleotides to RNA based therapeutics across AstraZeneca's therapy areas. Advanced Drug Delivery (ADD) resides within Pharmaceutical Sciences with a mission to provide novel products to AstraZeneca's clinical pipeline.
We are now recruiting a talented and motivated Analytical Scientist to join our New Modality GMP Analytics team within the ADD function in Gothenburg, Sweden.
As a Scientist working in the clinical development phase within ADD you will support drug projects from an analytical perspective, from candidate drug nomination over Phase II clinical trials. You will focus on advanced analytical characterization of biomolecules, primarily peptides, but also oligonucleotides, mRNA and other molecules of high complexity as well as drug delivery systems. The role covers development and validation of analytical methods, stability studies, release analysis, contribution to regulatory submissions as well as exploratory science work. Part of the work is performed according to Good Manufacturing Practice (GMP). You will work as a member of cross-functional pharmaceutical project teams and in close collaboration with other analysts, formulators, chemists and biologists at AstraZeneca in Sweden, UK and US.
Main Duties and Responsibilities
* Develop and validate analytical methodologies and specifications for biomolecules, with a focus on peptides.
* Plan and perform stability studies, release analysis and other supportive characterization experiments in clinical drug development projects.
* Generate, evaluate and report data clearly and reliably. Interpret findings and draw conclusions to make recommendations to project teams and other stakeholders.
* Prepare documentation and formal reports in accordance with current standard procedures and where appropriate, according to GMP standards. Generate data and give input to Chemistry, Manufacturing and Control (CMC) documents for regulatory submissions or enquiries.
* Give analytical support to scientific initiatives on new technologies/processes together with specialists and/or technology networks.
* Working as a member of cross-functional drug development project teams, representing your own group or science area.
* Ensure that your own work and the work of others are performed in accordance with appropriate Safety, Health and Environment (SHE), quality and compliance standards.
Essential Requirements
* MSc degree in a relevant scientific discipline (e.g., Analytical Chemistry, Biochemistry or Biotechnology).
* In-depth knowledge of analytical methodologies for peptide/protein characterization, such as chromatography, mass spectrometry and other biophysical/chemical characterization techniques.
* Experience of analytical work with peptides/proteins in pharmaceutical development.
* Thorough understanding of principles and applications of GMP.
* Ability to communicate in English both orally and in writing.
Desirable Requirements
* 3+ years of industrial experience of analytical work with peptides/biomolecules in clinical drug development phase.
* Expertise in analysis of peptide therapeutics for parenteral and oral administration routes.
* Experience of different formulation/delivery systems that may require different sample preparation techniques.
* Qualified to execute analytical work according to GMP.
* An interest in exploratory analytical work related to complex molecules, delivery systems and new technologies.
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.
For more information please contact Sara Richardson, Team Leader, +46 725821650,
We will screen candidates on a continuous basis. Welcome with your application no later than February 16, 2020.
Additional information
Our Gothenburg site:
https://www.astrazeneca.com/our-science/gothenburg.htmlLife in Gothenburg:
https://www.movetogothenburg.com/Culture and atmosphere of the Gothenburg site:
https://www.linkedin.com/feed/update/urn:li:activity:6496327311678410752/Varaktighet, arbetstid
Heltid Permanent
Publiceringsdatum2020-01-17ErsättningNot Specified
Så ansöker duSista dag att ansöka är 2020-01-31
Klicka på denna länk för att göra din ansökanFöretagAstrazeneca AB
Arbetsgivarens referens Arbetsgivarens referens för detta jobb är "R-071790".
Omfattning Detta är ett heltidsjobb.
Arbetsgivare Astrazeneca AB (org.nr 556011-7482)
Arbetsplats AstraZeneca
Jobbnummer 5047228
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