We use cookies to improve your experience on this website.

Document Control Specialist (cGMP – Pharmaceutical) JD819633

JD819633

DPS is looking for a proven Document Control Specialist to assist with a BioPharma client in the Greater Boston, MA area. The ideal candidate should have previous experience working within a GMP environment and have familiarity with Veeva and Microsoft Excel.

Category:
Administration
Location:
Massachusetts
Years of Experience Req.:
2+
Date Posted:
15/02/2019
Days Remaining:
13
Employment Type:
Full-time
Education Level Req.:
Bachelors Preferred

Document Control Specialist (cGMP – Pharmaceutical)    JD819633

Greater Boston, MA area

 

Summary:

 

DPS is looking for a proven Document Control Specialist to assist with a BioPharma client in the Greater Boston, MA area. The ideal candidate should have previous experience working within a GMP environment and have familiarity with Veeva and Microsoft Excel.

 

Responsibilities:

  • Ensure documentation is processed, formatted, issued, and made effective accurately.
  • Responsible for reviewing Document Change Controls to ensure proper revision control records.
  • Assist in the document periodic review process.
  • Maintain assigned document and part numbers within their respective processes.
  • Perform other projects related to improvement of quality systems as needed and required by management.

 

Qualifications:

  • Bachelor’s degree is desired but not required and replaceable by experience.
  • 1-2 years’ experience in document control in biotech or related regulated industry.
  • Experience with EDMS systems, preferably Veeva Vault Quality Docs.
  • Must have previous GMP experience.
  • Should have familiarity with Microsoft Office Suite, Adobe Pro, etc.
  • Requires excellent organiz698561.942794ational, interpersonal, and communications skills.
  • Must exhibit professional behavior and appearance and be aware of the importance of teamwork within the assigned department.
Back to top