Document Control Specialist GMP

20 May 2024

Vacancy expired!

Piper Companies is seeking a

Document Control Specialist for a CDMO in

Lansing, MI. The

Document Control Specialist will ensure proper archival of all data including electronic data generated from drug manufacturing. This includes storage and retrieval of all study data.

Responsibilities of the Document Control Specialist:

• Catalog and index vital study documentation in the correct order.

• Keep records of the study documents filed on site, archived offsite, or destroyed according to SOPs and federal regulations

• Input information onto databases as required by the offsite storage facility and for tracking purposes

• Secure all protocols, raw data, reports, and final documentation in accordance with any approved SOPs, protocols, and regulations

• Perform scanning, sorting, and filing of study documents and digital resources

• Discover information from file base per request

• Track materials removed from files to ensure that borrowed files are returned

• Handle the disposition of documents in accordance with company policy, contracts, SOP, and federal and state regulations

• Perform other duties as assigned

Qualifications of the Document Control Specialist:

• 1+ years of experience in GMP document control with veeva vault experience

• B.A. or B.S. in health sciences or any other related field

• Superior written, written, social, and organizational skills

Compensation for the Document Control Specialist:

•

Salary Range: $22 - $26/hr based on relevant years of experience

•

Comprehensive Benefits: Health, Dental, Vision, 401K

  • ID: #49971919
  • State: Michigan Lansing 48901 Lansing USA
  • City: Lansing
  • Salary: USD TBD TBD
  • Job type: Permanent
  • Showed: 2023-05-20
  • Deadline: 2023-07-18
  • Category: Admin/office