Description
Contract GMP Consultant/QA Specialist - Denmark - 5 Months +Leading Medical Devices company are urgently looking for a Contract Process Validation Consultant with expertise in GMP for 5 months to perform process validation of the client's antibody production at their site in Denmark.
Contract GMP Consultant/QA Specialist - Denmark - 5 Months +
Leading Medical Devices company are urgently looking for a Contract Process Validation Consultant with expertise in GMP for 5 months to perform process validation of the client's antibody production at their site in Denmark.
Tasks:-
* Review general biological prodction techniques and methods, especially protein purification (chromatopgraphic systems), protein conjugation and antibody fractioning
* Validate and review existing systems, documentation and SOPs
* Participate in quality audits and enhance quality management systems
* Lead the activities within the area
Experience:-
* 5 years or more experience within production for Pharmaceutical or Medical Devices companies in a GMP regulated environment
* Process validation of production methods in a regulated environment
* Process documentation for biological production techniques (GMP)
* Fluent English, knowledge of a Nordic language would be beneficial bot not essential
Rate: Negotiable (depending upon experience)
Location: Denmark
Duration: 5 Months (extensions possible)
For more information please contact Tim Heathcote at Real Staffing Group on for more information regarding this position