A leading biotechnology company is looking for a Technical
Writer for a 12 month contract. The ideal candidate must have
manufacturing experience and knowledge of current Good
Manufacturing Practices. They will be developing and revising
Standard Operating Procedures, Protocols, and technical
Essential Job Functions:
? Carries out responsibilities in accordance with the
organization?s policies, procedures, and state, federal and local
? Writes and revises Standard Operating Procedures (SOP's) for
technical, complex manufacturing equipment.
? Demonstrates strong technical writing ability.
? Prepares various documents and forms for pharmaceutical related
? Writes change control documentation to adequately describe and
justify process and/or equipment changes.
? Develops and executes test protocols to qualify and confirm
proper operation of technical manufacturing equipment.
? Demonstrates exceptional organization and ability to successfully
perform multiple projects simultaneously.
? Performs related duties as assigned.
Requirements Required Knowledge and Skills in:
? Current Good Manufacturing Practices (cGMP) and Food and Drug
Administration (FDA) requirements
? English usage, grammar, spelling and punctuation
? Technical writing principles and techniques
? Research practices and techniques in order to conduct technical
data and research
? Computer operations and software applications
? Communicating clearly and concisely, both orally and in
? Writing SOP's, revisions, change controls, and other pertinent
? Preparing and presenting information to management, co-workers
? Handling multiple projects, duties and tasks
We are an equal employment opportunity employer and will consider
all qualified candidates without regard to disability or protected