Perform QA audits internally and at investigator sites of clinical trial data & records to assure compliance with SOPs, study protocols. Good Clinical Practice Guidelines and relevant regulations.
Looking for a proactive individual, keen to take on the integral role of Medical Information Specialist within our expanding operation in the UK, working with some of the biggest names in the pharmaceutical industry.
M.Pharm / M.Sc ; 3-5 years of relevant experience in Quality Control department, Analytical Development Lab. Good communication, technical report writing skills and E- Mail etiquette.
Experience in Tablet and Liquid Packing & Manufacturing (Primary & Secondary, Good understanding of Track & Trace and Serialization Systems, Operational knowledge of Liquid Oral Formulations in the Packing Section
Sciences or Pharmacy Graduates (B.Sc./M.Sc./B. Pharm./M. Pharm.) with 0 to 5 years Experiences in parenteral manufacturing (vial / ampoules / bottles of glass or Plastic through, BFS technology).
Responsible for Formulation Development of Nasals Formulations. Responsible for conducting Formulation Development Trials and documenting the details in LNB.