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Project Coordinator II

Exela Pharma Sciences
Lenoir, NC Full Time
POSTED ON 12/19/2024 CLOSED ON 2/3/2025

What are the responsibilities and job description for the Project Coordinator II position at Exela Pharma Sciences?

Position Summary

The Project Coordinator II manages small pharmaceutical projects independently and supports larger, more complex projects under the guidance of a Project Manager. The Project Coordinator is responsible for being in compliance with all safety policies, cGMPs, and SOPs.

Job Responsibilities

  • Independently manage small projects and support larger projects under supervision.
  • Develop project schedules, track budgets, and coordinate cross-functional team efforts.
  • Identify and report potential risks while facilitating issue resolution.
  • Provide detailed project status reports and communicate updates to stakeholders.
  • Maintain personal training compliance status and work in compliance with applicable SOPs, cGMPs, regulatory requirements, safety, environmental and company policies.
  • Perform other duties as assigned.

Required Skills

  • Proficiency in project management methodologies (e.g., Agile, Waterfall).
  • Strong analytical and problem-solving skills.
  • Familiarity with project management software (e.g., MS Project, Smartsheet).
  • Proficiency in Microsoft Office Suite.
  • Ability to prioritize tasks and manage competing deadlines.
  • Perform other duties as assigned to support project and team objectives.
  • Must display sound judgment, ability to seek guidance, and follow directions.
  • Strong analytical, listening, verbal/written communication, achieve accuracy without being rushed, efficient time-management, problem-solving, attention to detail, prioritization, organization, interpersonal, computer and conflict management skills.

Education and Experience Requirements

  • Bachelor’s degree in a related field.
  • 2–3 years of project coordination experience. Experience in a regulated industry (e.g., pharmaceuticals) preferred.
  • An appropriate mix of education and experience in a cGMP manufacturing environment may be considered in lieu of a formal degree.
  • Experience with pharmaceutical manufacturing processes and cGMP practices preferred.
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