Dr. Rita Martins Olofsson

Angestellt, Team Leader, QC BioAssay Department, CMC Biologics A/S (CMO - Biopharmaceuticals Manufacture), Copenhagen, Denmark

Soeborg, Dänemark

Fähigkeiten und Kenntnisse

Biochemist with broad experience within biochemist
Enzyme assay development
Analytical methods development/transfer/ validatio
GMP/GDP-compliance work within Biotechnology/Pharm
protein stability and protein chemistry.

Werdegang

Berufserfahrung von Rita Martins Olofsson

  • Bis heute 12 Jahre und 6 Monate, seit Jan. 2012

    Team Leader, QC BioAssay Department

    CMC Biologics A/S (CMO - Biopharmaceuticals Manufacture), Copenhagen, Denmark

  • 5 Jahre und 7 Monate, Juni 2006 - Dez. 2011

    Scientist (Analytical Services/QC - Biochemistry Department)

    CMC Biologics A/S (CMO - Biopharmaceuticals Manufacture), Copenhagen, Denmark

    - GMP documentation - Analytical methods: electrophoresis, Endotoxin test (LAL), pH, OD measurements, osmolality, ELISA, qPCR for residual DNA, HCP and other residual analysis, potency assays, bioassays - QC Project coordinator in project teams - Transfer/development of analytical methods - Validation of analytical methods according to ICH guidelines - Reference Material establishment - Qualification of laboratory equipment - Training of new employees/cross-training colleagues -LEAN work

  • 2 Jahre und 7 Monate, Nov. 2003 - Mai 2006

    Post Doc Researcher (Biochemist)

    Carlsberg Research Center (Copenhagen, Denmark)

    - Method development CE-fluorescence for carbohydrate, glycolipid and protein analysis - Development of novel fluorescence-based methods for carbohydrate, glycoconjugate and protein analysis and detection (microplate, gel, membrane blots and solid-phase approaches) - Protein and solid-phase derivatization via amino- and thiol-reactive probes and linkers - Discovery of new glycosyltransferases involved in bacterial LPS biosynthesis - Enzyme assay development (glycosidases and glycosyltransferases)

  • 2 Monate, Okt. 1999 - Nov. 1999

    Course-lab assistant (Bioseparation master course)

    Lund University, Sweden

    - Design/supervision of a pilot-scale purification of yeast ADH using homogenization, micro- and ultra-filtration, phase-partitioning and IEC - Purification of a recombinant LDH-(His)6 by IMAC

  • 1 Jahr, Jan. 1998 - Dez. 1998

    Chemical Engineer (Quality Control Laboratory)

    OM-Portuguesa (Pharmaceutical industry), Lisbon, Portugal

    - QC of raw materials, intermediates, final products (tablets, capsules, gels, liquid preparations) - Analytical chemistry (HPLC, TLC, Karl Fischer titration, dissolution and other specific analysis) - Analytical methods validation and company certification procedures (GLP)

  • 2 Monate, Juli 1996 - Aug. 1996

    Quality Control Laboratory Trainee

    Laboratórios Normal (Pharmaceutical industry), Lisbon, Portugal

    QC with tasks within analytical chemistry and microbiology.

Ausbildung von Rita Martins Olofsson

  • Instituto Superior Técnico (Lisboa, Portugal) - M.Sc. Chemical Engineering

    (Biotechnology branch) Lunds University (Sweden) - Ph.D. in Biotechnology

Sprachen

  • Englisch

    -

  • Spanisch

    -

  • Portugiesisch

    -

  • Französisch

    -

  • Schwedisch

    -

  • Norwegisch

    -

  • Dänisch

    -

Interessen

photography
cooking
traveling
badminton
guitarr

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