Hourly Rate: Not Sure
| Duration: 7-9 months
| Posted: Mar 01, 2015 | Ends: 13d, 9h |
Our company is requesting the service of an expert that develops, generates cGMP documentations (SOPs, Forms, Troubleshooting Guidelines, Work Instructions and Skills Qualification Checklists) for different types of oral solid dosage process and technologies. You will be responsible for the preparation of the documentation requested following current SOP development guidelines, including testing of the processing steps in the manufacturing areas; get information from equipment manufacturer manuals; assuring the procedures describes manufacturing process steps. Estimated time to complete this project is Dec 2015. ASSUMPTIONS: ? Prior to the start project activities, a per hour fee will be agreed upon. RESOURCES PROVIDED BY THE COMPANY MUST MEET THE FOLLOWING MINIMUM REQUIREMENTS IN ORDER TO BE CONSIDERED: ? Expertise in the generation of standard operating procedures for pharmaceutical companies ? Bachelor in Science; Industrial Engineering, Science, Industrial and Organizationa...
Category: Other - Engineering &...