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Cheryl Wilding Location
Cambridge, GB
Cheryl Wilding Work
Group Head of QA @ (June 2021 - Present)
Head of Quality, DNA Services @ (April 2019 - June 2021)
Managing Director @ (August 2015 - Present)
QA Officer @ (July 2014 - August 2015)
Pharmaceutical Microbiology and Sterile Manufacture Validation @ (June 2008 - November 2013)
Microbiologist @ (October 2004 - February 2006)
Medical Laboratory Technician @ Addenbrookes Hospital Microbiology (August 1999 - September 2000)
Cheryl Wilding Education
Anglia Ruskin University
BSc (Hons) (Forensic Science)
2000-2004
Cheryl Wilding Skills
Microbiology
GMP
GLP
Lifesciences
Biotechnology
Pharmacueticals
Disinfection
Clean Rooms
Sterilization
Standardized Testing
Quality Assurance
Auditing
Medical Devices
Aseptic Technique
ELISA
Laboratory
Validation
CAPA
Environmental Monitoring
Pharmaceutical Industry
Life Sciences
FDA
Pharmaceutics
Quality System
Regulatory Affairs
Quality Control
Change Control
V&V
Technology Transfer
Management
HPLC
Cleaning Validation
LIMS
21 CFR Part 11
SOP
U.S. Food and Drug Administration (FDA)
Standard Operating Procedure (SOP)
Good Laboratory Practice (GLP)
Good Manufacturing Practice (GMP)
Cheryl Wilding Summary
Cheryl Wilding, based in Cambridge, GB, is currently a Group Head of QA at Touchlight. Cheryl Wilding brings experience from previous roles at Touchlight, Croxon Consulting Ltd, Intertek Melbourn and Tristel plc. Cheryl Wilding holds a 2000 - 2004 BSc (Hons) in Forensic Science @ Anglia Ruskin University. With a robust skill set that includes Microbiology, GMP, GLP, Lifesciences, Biotechnology and more. Cheryl Wilding has 3 emails and 1 mobile phone numbers on RocketReach.
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