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Document Controller/Tech Writer III
Document Controller/Tech Writer IIIBureau Veritas Group • Indianapolis, Indiana, US
Document Controller / Tech Writer III

Document Controller / Tech Writer III

Bureau Veritas Group • Indianapolis, Indiana, US
30+ days ago
Job type
  • Permanent
Job description

Overview :

Business Title : Business support III

Position Title : Technical Writer Document Controller III

Division : Consumer Products Services

Entity : ATL

Location : Plainfield, IN

Reports to : ATL Manager

FLSA : Non-exempt

Hours Worked : Typically, Monday through Friday 7 : 00 AM – 4 PM

However, must be flexible to meet business needs and overtime requested

Position Summary :

The Technical Writer Document Controller III is responsible for providing a wide range of clerical, organizational, and administrative support to the organization through a combination of technical skills, problem-solving abilities, and a client-centric mindset.

Duties and Responsibilities :

It is everyone’s responsibility to live out our Values and Absolutes by Shaping a World of Trust while ensuring responsible progress.

  • Provide general administrative and clerical support, such as filing, photocopying, and organizing documents
  • Answer and direct incoming internal and external communications
  • Schedule appointments and maintain calendars
  • Assist with basic data entry and record-keeping tasks
  • Provide support for meeting preparation
  • Perform basic research and information gathering as needed
  • Performs work in coordination with clients, coworkers, and supervision from management
  • Able to troubleshoot with N+1 for any client issues or questions with the aim of enhancing client satisfaction and improving client relations.
  • Perform data entry and report project updates
  • Report equipment and system technical issues to the appropriate contacts.
  • Maintain supplies, workstation cleanliness, and equipment, as required.
  • Maintain up to date knowledge of current procedures.
  • Follow the guidelines set forth with clients and in the Bureau Veritas Consumer Products Services, Inc Quality, Health, Safety, Security and Environmental policies and procedures.
  • Comply with clients and Bureau Veritas Consumer Products Services, Inc management systems in accordance with appropriate regulatory agencies.
  • Follows the guidelines set forth in by clients and the Bureau Veritas Consumer Products Services, Inc Quality Manual and Safety / Chemical Hygiene Plan.
  • Adhere to the requirements of the BV-CPS Quality System.
  • Other duties as defined by Manager, department needs and workload
  • Serves as secondary support in multiple additional areas.
  • Resolve escalated and high-profile client requests and issues.
  • Is a subject matter expert (SME) in assigned area and maintains up to date knowledge of current regulations / industry standards, and protocols.
  • Manage and prioritize multiple projects simultaneously
  • Interprets information from multiple sources and provides analysis.
  • Identify, troubleshoot and solve escalated technical issues.
  • Provide enhanced guidance and technical training to internal staff.
  • Write or edit procedure as requested including developing training materials
  • Act in partnership with clients and management to support process improvement development
  • Develop and implement administrative policies and procedures to enhance efficiency
  • Collect, create, maintain and track progress of projects through visualization tools (example PowerBi, Excel, PowerPoint or Dashboards) to manage status and progression of defined project improvements / key initiatives.
  • Gather, track and complete governance documents related to project improvements, department agendas and key initiatives across several department functions (progression of current and / or new additions).
  • Author technical documents related to change management, intra-company issues with the use of systems such as Trackwise / Veeva Vault.
  • As Document Controller / Editor ensure technical procedural revision review and approval workflows are achieved.
  • Monitor, update and look for trends in documentation and reports related to clinical supply chain, clinical trial kit distribution, pharma labeling and device manufacturing (Regulatory, FDA, TSA or GMP environment)
  • Lead team meetings to present projects progress, data and up action items (PowerPoint)
  • Be the subject matter expert for deviations, procedure and technical documentation progress and tracking
  • Follow the guidelines set forth with clients and in the Bureau Veritas Consumer Products Services, Inc Quality, Health, Safety, Security and Environmental policies and procedures.
  • Comply with clients and Bureau Veritas Consumer Products Services, Inc management systems in accordance with appropriate regulatory agencies.
  • Other duties as defined by manager, department needs and workload.

Skills & Proficiencies :

  • Strong organizing / multi-tasking skills, document tracking and naming conventions
  • Strong clear communicator speaking in large groups
  • Project management and project coordination experience
  • High level of attention to detail
  • Knowledge of documentation control and practice
  • Ability to lead meetings (PowerPoint), present and collect data as well as follow up action items
  • Ability to get along with others with excellent interpersonal communication and networking skills
  • Demonstrated strong written and verbal communication skills
  • Ability to work well in a team environment and resolve issues quickly
  • Proficiency with computer systems for example PowerBi, PowerPoint, Tableau, Trackwise, Excel, Veeva Vault etc.
  • Positive attitude
  • Adheres to Company Values
  • Education and Experience :

  • Bachelor’s Degree and 3-5 years’ experience in a project management or quality related field
  • Minimum of 3 year(s) of experience in a cGMP quality warehouse environment or closely related field
  • An equivalent combination of education and experience may be accepted in lieu of above.

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