Document Management Specialist, GXP

GForce Life Sciences

Princeton (NJ)

Hybrid

USD 60,000 - 80,000

Full time

14 days+
Application generator

A complete application in a minute — tailored resume and cover letter, ready to send.

Get past ATS filters

Benefits offered by this job

Medical insurance
Vision insurance

Job summary

A prominent life sciences company is seeking an Executive Recruiter for a 12-month contract primarily remote, based in Princeton, NJ. The role involves supporting GxP document management initiatives, facilitating project plans, and providing audit support. Ideal candidates will have a bachelor’s degree in a life science-related field and 4+ years of experience in document management systems. Familiarity with tools like Visio and SharePoint is advantageous. This position includes benefits such as medical and vision insurance.

Qualifications

  • Minimum of a bachelor’s degree, preferably in a life science-related field.
  • 4+ years of experience in the use of an electronic document management system, preferably in a GxP environment.
  • Experience with Visio, SharePoint, or Veeva (or similar EDMS) is a plus.

Responsibilities

  • Support the management of GDM initiatives and team meetings.
  • Ensure project plans are implemented in accordance with timelines.
  • Facilitate review, approval and tracking of documents.
  • Create procedural document templates with standardized formatting.
  • Use Electronic Document Management System.
  • Liaise with Training department on deployment of training.
  • Provide documentation support for audits/inspections.
  • Support any projects/process improvement initiatives.

Skills

Experience in electronic document management systems
GxP knowledge
Team management in MS Teams
Process improvement initiatives

Education

Bachelor's degree in a life science-related field

Tools

Visio
SharePoint
Veeva

Job description

Executive Recruiter at GForce Life Sciences

12-month contract

Primarily remote - Princeton, NJ (will need to be onsite for occasional meetings)

About the Role

The GxP Document Management Coordinator will perform delegated tasks, specifically as a backup for the LSOP Administrator, related to GxP procedural and governance document management as defined in the LSOP covering this activity.

Responsibilities
  • Support the management of GDM initiatives and team meetings, and manage teams and channels in MS Teams.
  • Ensure project plans are implemented in accordance with timelines, and any issues, challenges, or deviations are escalated for resolution in a timely manner.
  • Facilitate review, approval and tracking of documents.
  • Create procedural document templates with standardized formatting and styles.
  • Use Electronic Document Management System.
  • Liaise with Training department on deployment of training.
  • Provide documentation support for audits/inspections.
  • Complete all assigned Training.
  • Support any projects/process improvement initiatives.
Qualifications
  • Minimum of a bachelor’s degree, preferably in a life science‑related field.
  • 4+ years of experience in the use of an electronic document management system, preferably in a GxP environment.
  • Experience with Visio, SharePoint, or Veeva (or similar EDMS) is a plus.
Seniority level

Associate

Employment type

Contract

Job function

Quality Assurance and Other

Pharmaceutical Manufacturing

Medical insurance

Vision insurance

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Remote GxP Document Control & Compliance Specialist
Remote GxP Document Control & Compliance Specialist

GForce Life Sciences • Princeton (NJ)

Hybrid
USD 60,000 - 80,000
Document Control, Senior Specialist
Document Control, Senior Specialist

Scorpion Therapeutics • United States

On-site
USD 110,000 - 150,000
Document Control Specialist
Document Control Specialist

BioPhase • United States

Remote
Sr. QA Document Control Specialist
Sr. QA Document Control Specialist

EPM Scientific • Boston (MA)

On-site
USD 90,000 - 130,000
Senior QA Specialist, Global Document Control Management
Senior QA Specialist, Global Document Control Management

Scorpion Therapeutics • California (MO)

On-site
USD 90,000 - 130,000
Document Control Specialist
Document Control Specialist

Orion Group • New Jersey

Hybrid
Quality Specialist III, Document Control and Training
Quality Specialist III, Document Control and Training

Scorpion Therapeutics • Madison (WI)

On-site
USD 78,000 - 98,000
Excellent benefits package
Competitive salary
Documentation Specialist
Documentation Specialist

Scorpion Therapeutics • Pennsylvania

On-site
USD 65,000 - 95,000
Senior Document Control Specialist - Veeva EDMS & GxP Expert
Senior Document Control Specialist - Veeva EDMS & GxP Expert

BioPhase • United States

Remote
USD 60,000 - 80,000
Document Controller
Document Controller

Medasource • United States

On-site
USD 50,000 - 70,000
Vision insurance
Medical insurance