kim de Ruiter
Validation Technician at Byondis- Claim this Profile
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Nederlands Native or bilingual proficiency
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Engels -
Topline Score
Bio
Experience
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Byondis
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Netherlands
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Pharmaceutical Manufacturing
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200 - 300 Employee
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Validation Technician
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Apr 2020 - Present
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Synthon
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Netherlands
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Pharmaceutical Manufacturing
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700 & Above Employee
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Maintenance & validation technician
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Jun 2016 - Apr 2020
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MSD
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United States
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Pharmaceutical Manufacturing
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700 & Above Employee
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scientist , preclinical Development
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2011 - Jan 2015
- Analytical support (performing, reporting and verification of analytical methods). - Writing and reviewing analytical protocols and reports. - Development and validation of HPLC methods. - Manager HPLC systems (Troubleshooting, maintenance and qualification) - Manager GMP reference standards - Deviations ( equipment related issues) - Analytical support (performing, reporting and verification of analytical methods). - Writing and reviewing analytical protocols and reports. - Development and validation of HPLC methods. - Manager HPLC systems (Troubleshooting, maintenance and qualification) - Manager GMP reference standards - Deviations ( equipment related issues)
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Schering Plough
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oss
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Validation Engineer / Lab. support technician
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2009 - 2011
- Managing investments for the purchase of new equipment (writing VP,URS, GQP and VR documents) - Managing en coordinating equipment projects (IQ/OQ/PQ) - Validation, calibrating and control of analytical equipment - Troubleshooting and performing repairs on HPLC equipment - Verification of GMP documentation - Manager of lab consumables (HPLC colums, GMP reference standards, chemicals) - Managing investments for the purchase of new equipment (writing VP,URS, GQP and VR documents) - Managing en coordinating equipment projects (IQ/OQ/PQ) - Validation, calibrating and control of analytical equipment - Troubleshooting and performing repairs on HPLC equipment - Verification of GMP documentation - Manager of lab consumables (HPLC colums, GMP reference standards, chemicals)
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Organon
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United States
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Pharmaceutical Manufacturing
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700 & Above Employee
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Pharmaceutical laboratory assistent
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2007 - 2009
-Stability research of new pharmaceutical formulations in GMP environment -Analytical method development and validation (HPLC) -Data verification -Stability research of new pharmaceutical formulations in GMP environment -Analytical method development and validation (HPLC) -Data verification
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Organon
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United States
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Pharmaceutical Manufacturing
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700 & Above Employee
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Quality Control laboratory assistent
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2000 - 2006
- Quality control analyses in a GMP environment (HPLC, GC, Dissolution) - Stability analysis - Verification of analysis - Quality control analyses in a GMP environment (HPLC, GC, Dissolution) - Stability analysis - Verification of analysis
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Education
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Hogeschool van Arnhem en Nijmegen
Bachelor of Science (B.S.), Analytische chemie -
Nijmegen west
HAVO