Document Control Associate

19 Aug 2023

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 GMPelectronic documentation managementAdditional Skills & Qualifications:Needs strong experience with documentation, organization, and issuing reportsfiling/scanning/creating binders/organizing and tracking files Issuing batch records will be the most importantreview batch records for QA Previous QA experienceDiversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

Hiring diverse talent

Maintaining an inclusive environment through persistent self-reflection

Building a culture of care, engagement, and recognition with clear outcomes

Ensuring growth opportunities for our people

Actalent is an equal opportunity employer.About Actalent Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021.

  • ID: #50242842
  • State: New Jersey Ledgewood 07852 Ledgewood USA
  • City: Ledgewood
  • Salary: USD TBD TBD
  • Showed: 2023-08-19
  • Deadline: 2023-10-18
  • Category: Et cetera