Bureau Veritas - Indianapolis, IN

posted 4 months ago

Full-time - Entry Level
Indianapolis, IN
251-500 employees
Professional, Scientific, and Technical Services

About the position

The Project Coordinator and Technical Writer role at Bureau Veritas is a vital support position that involves providing project support across various functions including Operations, Customer Service, Facilities, and Compliance. The primary responsibility of this role is to facilitate, author, and edit quality-related documents while managing change controls. The successful candidate will work closely with the lead team and other personnel to gather input necessary for the progression of key initiatives. This position is integral to ensuring that documentation is accurate, up-to-date, and compliant with industry standards, particularly in a cGMP environment. In this role, you will be tasked with collecting, creating, maintaining, and tracking the progress of projects using visualization tools such as Power BI, Excel, PowerPoint, or dashboards. You will assist in supporting the gathering, tracking, and completion of governance documents related to project improvements and departmental agendas. Additionally, you will serve as a technical writer, supporting documentation related to change management and intra-company issues using Trackwise. As a Document Controller/Editor, you will help facilitate procedural revision reviews and approval workflows as needed, ensuring that all documentation related to clinical supply chain, clinical trial kit distribution, pharma labeling, and device manufacturing is accurate and compliant. This position requires strong organizational and multi-tasking skills, as well as a keen attention to detail. You will need to demonstrate excellent interpersonal and networking skills, along with strong written and verbal communication abilities. Proficiency in various computer systems, including Power BI, PowerPoint, Tableau, Trackwise, Excel, and Veeva Vault, is essential for success in this role. A positive attitude and the ability to work well in a team environment are also critical attributes for this position.

Responsibilities

  • Collect, create, maintain, and track progress of projects using visualization tools like Power BI, Excel, and PowerPoint.
  • Assist in supporting, gathering, tracking, and completing governance documents related to project improvements and departmental agendas.
  • Serve as a technical writer to support documentation related to change management and intra-company issues using Trackwise.
  • Act as Document Controller/Editor to support procedural revision review and approval workflows as needed.
  • Work with documentation and reports related to clinical supply chain, clinical trial kit distribution, pharma labeling, and device manufacturing in a cGMP environment.

Requirements

  • Bachelor's Degree in a related field.
  • Minimum of one (1) year of experience in a cGMP environment.
  • Strong organizing and multi-tasking skills, document tracking, and naming conventions.
  • Strong attention to detail.
  • Knowledge of documentation control and document change control.
  • Excellent interpersonal and networking skills.
  • Demonstrated strong written and verbal communication skills.
  • Ability to work well in a team environment.
  • Proficiency with computer systems such as Power BI, PowerPoint, Tableau, Trackwise, Excel, and Veeva Vault.

Nice-to-haves

  • PMP certification or strong proven project coordination and management skills.
  • Experience in a cGMP environment.

Benefits

  • 401(k)
  • 401(k) matching
  • Dental insurance
  • Disability insurance
  • Employee assistance program
  • Employee discount
  • Flexible spending account
  • Health insurance
  • Health savings account
  • Life insurance
  • Referral program
  • Retirement plan
  • Vision insurance
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service