Immediate Document Control associate opportunity within a leading pharmaceutical company that is looking for someone to join their team and help with their QA documentation. This position is first shift and is looking for anyone with previous experience working with Batch records within a diagnostic or pharmaceutical setting.

Description:

• Filing, scanning, organizing all of QA documentation and records

• Hard copy/paper documents

• Some issuance of controlled documents

• All within the QA department

• BRs- issuing- Master copy and looking at the schedule. 25% will be issuing batch records.

• Another GMP coming from would be great- she is more focused on the clerk functions and organizations

• Can train on GMP electronic documentation management

Additional Skills & Qualifications:

Needs strong experience with documentation, organization, and issuing reports

filing/scanning/creating binders/organizing and tracking files

Issuing batch records will be the most important

review batch records for QA

Previous QA experience

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

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At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

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