In Process Document Specialist - Pharmaceuticals Not right for you? We've got others

Salary:
Confidential
Location:
Lancaster, SC
Posted:
February 18th 2021
Minimum Degree:
Associate
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We are looking for an In-Process Document Specialist I to be responsible for the review and of batch records during production and correcting cGMP errors in real time at primary assigned building.

Roles and Responsibilities:

 

Minimum Requirements:  Must possess good written and oral communication skills.  Must be proficient in MS Office Suite, strong mathematical background, and ability to coordinate multiple tasks efficiently.  Strong interpersonal skills and the ability to work well in a team environment is a must.

Education and Experience:  Position requires an Associate Degree or a minimum of three years' experience in QA related to a government regulated industry.

 


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