“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 Skills
Day to Day Responsibilities:
- At least 2 year industry experience (non academia) in QC
- Bachelors Degree in Science or Engineering
- GMP experience
Under general supervision, this position will perform routine administrative, documentation and execution processes relating to templating testing procedures into Amgen electronic systems in support of the data acquisition integration. This position will be responsible for one or more of the following activities: - Performing templating, routing supporting documents, performing quality checks of templated information to confirm accuracy, running scenarios to identify errors, documenting outcomes of qualification activities, gathering feedback on requirements, supporting administrative execution of qualification, document management.
Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures.
"This posting is for Contingent Worker, not an FTE"