GMP Documentation Specialist

Job details

GMP Documentation Specialist: We are looking to speak with an experienced GMP Documentation Specialist to join this leading organisation. The GMP Documentation Specialist will make a key contribution to the organisation from the outset, planning and executing a project to collate, index and transfer to a new building, critical documentation including pharmaceutical manufacturing records.

GMP Documentation Specialist - key responsibilities:

- Devising a system for identifying, collating and indexing a range of manufacturing, analytical and support documents currently located in various locations across the site
- Planning the transferral of documents under control, to be put into operation on completion of the new building

GMP Documentation Specialist - qualifications and experience:

• Proven experience of documentation and archiving systems to meet European and US GMP regulatory requirements
• Familiarity of working within a highly regulated environment
• Knowledge of the 'rules' associated with Pharmaceutical GMP, including the use of computerised databases for document tracking.

GMP Documentation Specialist: A great opportunity for a GMP Documentation Specialist to work on a contract basis for a highly regarded and well recognised company.