Softworld QA Document Control Specialist in Lexington, Massachusetts

QA Document Control Specialist

Lexington, MA

| Contract

Post Date: 03/05/2018

2018-03-05 2018-04-20

Job ID: 225767

Industry: Life Sciences

Job Description

QA Document Control Specialist Cambridge, MA 6 month contract

The ideal candidate will have a manufacturing background with strong experience with GMP documentation such as Batch Records and SOPs.

Prior experience working in a Pharmaceutical industry

Prior experience working in a GMP environment and with GMP documentation

Prior experience working with paper based processes/ Experience working with an EDMS is a PLUS

Proficient in MS Word and Excel

Strong interpersonal and communications skills; written and oral

Solid understanding of applicable regulatory requirements