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Project Management Senior Associate

Thousand Oaks, CA
“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
1) Change Control experience in Product Lifecycle Management, with Trackwise other
Quality System experience
2) Knowledge of GMPs and Biotech/Pharmaceutical Industry
3) Supply Chain and/or Quality background/experience, especially in Product Lifecycle
Management

Day to Day Responsibilities:
Train and gain access to systems required quickly.
Work independently, absorbing knowledge and experience through participating in various strategy and execution forums/meetings for all products, following SOPs, and learning from Supply Chain PMs, translating requirements into Change Control records = Customer Facing SKU Change Record (CFSCR) or Global Distribution Change Record (GDCR) that meets required regulations, compliance, and GMP standards.
Ensure timeliness of activities by partnering with Assessors and Task owners to ensure their activities are completed on time, supporting Launch or Variations of Amgen products.

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

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