Erika Cavallin Email & Phone Number | I have extensive experience in developing and validating new bioanalytical methods to be able to determine drug substances in biological matrices with LC-MS/MS and sample analysis. I have worked more than 10 years according to GLP and this experience has provided me with excellent sense of quality. I am skilled in report writing in GEL and QC-check. I have always delivered requested validated methods and GLP-results on time during my time at Astra Zeneca, despite on multiple occasions being faced with challenging tasks and short timelines. I have expertise in programming and developing liquid classes as well as performing maintenance and writing operating instructions and control instructions for liquid handling robots. I have also been supporting users and educated new users. I am thorough and systematic in the way I work, with a strong sense of quality. I am good at working independently and perform well under pressure. I am flexible, positive and enthusiastic and a team player, cooperating well with others.

Erika Cavallin

I have extensive experience in developing and validating new bioanalytical methods to be able to det...
Greater Gothenburg Metropolitan Area, Greater Gothenburg Metropolitan Area, Sweden

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Erika Cavallin’s Email erika.cavallin@astrazeneca.com

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Erika Cavallin’s Location Greater Gothenburg Metropolitan Area, Greater Gothenburg Metropolitan Area, Sweden

Erika Cavallin’s Current Industry Astrazeneca

Erika Cavallin’s Prior Industry Molndal Global Dmpk Im | Molndal Astrazeneca R And D Molndal

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Work Experience

Astrazeneca

Senior Research Scientist

2012-07-01 00:00:00 - Present

Molndal Global Dmpk Im

Senior Research Scientist, Regulatory Bioanalysis

2009-05-01 00:00:00 - 2012-06-01 00:00:00

Molndal Astrazeneca R And D Molndal

Research Scientist

2000-03-01 00:00:00 - 2009-04-01 00:00:00

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FAQ About Erika Cavallin

Erika Cavallin is located at
Greater Gothenburg Metropolitan Area, Greater Gothenburg Metropolitan Area, Sweden

Erika Cavallin is a I have extensive experience in developing and validating new bioanalytical methods to be able to determine drug substances in biological matrices with LC-MS/MS and sample analysis. I have worked more than 10 years according to GLP and this experience has provided me with excellent sense of quality. I am skilled in report writing in GEL and QC-check. I have always delivered requested validated methods and GLP-results on time during my time at Astra Zeneca, despite on multiple occasions being faced with challenging tasks and short timelines. I have expertise in programming and developing liquid classes as well as performing maintenance and writing operating instructions and control instructions for liquid handling robots. I have also been supporting users and educated new users. I am thorough and systematic in the way I work, with a strong sense of quality. I am good at working independently and perform well under pressure. I am flexible, positive and enthusiastic and a team player, cooperating well with others.