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Sr Associate Regulatory Affairs – CMC

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 Skill Sets:
• 1-2 years work experience in Regulatory Affairs, or Pharmaceutical Industry
• Can-do Attitude – Ideal candidate does not easily give up. The candidate will be provided direction and support but will need to be methodical and analytical when completing tasks while exhibiting a positive attitude (Amgen is a very large organization and there will be many parties the candidate will need to engage with for project success).
• Attention to Detail – Ideal candidate will be thorough and deliver a polished work product.

Day to Day Responsibilities:                
Daily responsibilities will be focused on providing submission execution support to products across modalities, regions and phases of development

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

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