“This Company requires all staff, staff augmentation external workers, and certain other external workers, in the United States and Puerto Rico vaccinated from COVID 19 as a condition of assignment at this company. In accordance with applicable law, this company will provide reasonable accommodations staff augmentation external workers qualify on the basis of a medical reason or a sincerely held religious belief, practice, or observance. Such accommodation may not pose an undue hardship this company, its operations, or its staff.”
    
Top 3 Must Have Skill Sets:    

• project management (managing multiple projects to completion)
• critical thinking
• document creation/revision specific to pharmaceutical and/or biotech industry preferred

Day to Day Responsibilities:    

Day to day responsibilities will vary by project and day and will include a combination of the following:

• work independently to edit, format and/or write SOPs or Work Instructions or other supporting documents within a controlled document system
• QC/revise existing documentation according to template/style guide
• act as “scribe” writing documents according to template/style guide during meetings with subject matter experts
• lead team of subject matter experts to facilitate discussion and review of process and documentation with time, experience, and demonstrated ability,
• role may serve as a project manager to lead “sub-projects” representing R&D Quality processes from beginning to end including strategy for process documentation and oversight of documentation

"This posting is for Contingent Worker, not an FTE"