Education and Professional Membership
- BSc (Hons) Microbiology
- Pg Dip Environmental Monitoring and Control
- Pg Dip Quality Assurance
- Member of the Royal Society of Biology
With over 20 years experience working in the Pharmaceutical Industry and 17 years experience as a QP, Christine has been working as an independent consultant QP since April 2009. Christine started her career in QC moving through to the QA Department and QP training as her career progressed, finally working as Head of Quality before leaving to pursue an independent career. She has experience of working in both ethical and generic pharmaceutical companies and with a wide range of dosage forms (sterile, non-sterile, tablets (solid and effervescent), liquids, creams, ointments, powders). Her particular areas of interest lie with the management of complex supply chains, the release of products imported from third countries and project management for new product development and/or site transfers.
She has a great deal of experience working with UK based companies to manage manufacture in third countries such as India and then subsequent retest and release in the UK. She works with companies (both IMP and Finished Product) to offer technical and regulatory assistance to them in the transfer of products from one site to another either inter-company or to a third party. In addition to her involvement in QP release and product transfers, she works as a GMP auditor, assists sites with remediation activities following Regulatory Body Inspections and/or preparation for Inspections, performs documentation system reviews and manages Technical Agreement and Product Quality Review systems for clients.
In all areas she can either review existing systems, and offer advice on how to move things forward or join a client and take responsibility for the work that is required. Christine is also willing to offer training services to assist with implementation and management of GMP compliance systems.
Email Christine Morris