Document Control Specialist


Framingham, MA

Industry: Biotech/Pharma


Less than 5 years

Posted 189 days ago

  by    Jitendra Kushwah

This job is no longer available.

  • Process and control documentation in compliance with current Good Manufacturing Practices (cGMP) and local policies and procedures.
  • Ensure documentation is written, edited, reviewed and approved in a timely manner to meet established deadlines.
  • Compile document status reports, transition plans, file technical documentation, reports and master SOPs and associated records.
  • Writes departmental procedures and documentation.
  • Updates and maintains document tracking worksheets.
  • Assists with cGMP documentation and training as required. 
  • Application of skills to perform identified tasks and additional work with knowledge acquired through experience to perform work.
  • Able to work with limited instruction on routine assignments while under little to no supervision. 
  • Receives general instructions on new work and able to follow through to completion.

Required Education & Skills:

  • Education: AssociateDegree with 3-5years experience.
  • Experience with word processing, MS Office, Adobe acrobat, and document management systems such as livelink and documentum. 
  • Good Attention to detail is required and ability to shift priorities to work on urgent projects when needed.
$50K - $60K
$50K - $60K base, TBD bonus