Analytical Biochemist

We are now looking for Analytical Biochemists to future assignments at our client, a leading global pharmaceutical company south of Stockholm.
Do you have expertise in, and passion for, Bioanalytical and Bioassay? Would you like to apply your expertise in brand new laboratories with the highest technology, in a company that follows the science and turns ideas into life changing medicines? Please don´t hesitate and submit your application today!



Your role:

The QC Analytical Biochemist performs laboratory tests in accordance with the appropriate cGXP to produce reliable and precise data to support product release and scientific investigations.
Analytical testing could include:
• HPLC
• Gas Chromatography
• Electophoresis - CE and iCEF
• Protein concentration UV/Vis
• Device testing
• Compedial analysis such as sub.visibleparticulate, Appearance, visible paricles.
• pH, Osmolality, extractable volume

The Analytical Biochemist also
• Prepares specimens and samples for analysis
• Writes and execution of SOP and reports
• Keeps up to date with technical developments
• Performs routine tasks accurately and following written procedures to carry out analyses. Performs data review/approval and data retention activities. Input data for trending purposes
• You will also perform a variety of non-routine testing including analytical method transfer and validation, experimental/validation work and analytical support to production
• Maintains and operates standard laboratory equipment
• Evaluate generated result with Empower
• Provides support to functional and cross functional investigations when needed
• Ensures the compliance with Health & Safety Guidelines, SHE policy
• Leads by example and acts as a role model according AstraZeneca values and behaviors


Essential Requirements:

• Degree level/or equivalent in chemistry/biochemistry or a related discipline
• Experience in chromatography/electrophoresis
• Fluent in both Swedish and English


Desirable Requirements:

• Experience in a Good Manufacturing Practice (GMP) environment / Good Laboratory Practice (GLP)
• Understanding of Quality Control testing techniques
• Previous Biopharmaceutical Industry experience