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Project Manager III

Hopewell, NJ 08534

Posted: 02/07/2024 Employment Type: Contract Job Category: Clinical Development and Operations Job Number: 596403 Is job remote?: No Country: United States

Job Description


Responsible for coordination, implementation, executive, control and completion of the project while remaining aligned with the strategy, commitments and goals of the organization. providing schedule oversight for the qualification, validation, manufacturing activities for equipment, utilities, and facilities.

Essential Functions of the job:
  • Plan and implement projects
  • Help define project scope, goals and deliverables
  • Define tasks and required resources
  • Collect and manage project team
  • Manage the project budget
  • Allocate project resources
  • Create a project schedule and timeline
  • Support and direct team
  • Lead quality assurance
  • Report on the project status
  • Present to stakeholders reports on progress as well as problems and solutions
  • Implement and manage changes when necessary to meet project deliverables
  • Evaluate and assess the result of the project

Skills:

*Biopharma process experience required

  • Excellent communication skills and leadership skills
  • Project planning, risk management, and time management
  • Project management qualification (PMP), Certified Associate in Project Management (CAPM), or equivalent experience as a project manager
  • Experience in strategic planning, risk management and/or change management
  • Scientific degree (ideally: pharmaceutical sciences, engineering, chemistry, or related discipline).
  • 5+ years’ experience in validation, biological quality assurance and/or quality control in an FDA-regulated biotechnology or pharmaceutical company with progressive levels of responsibility.
  • Track record and skills/experience gained within a similar position and level.
    • Good collaboration and project management skills.
    • Credible and confident communicator (written and verbal).
    • Customer focused
    • Strong analytical and problem-solving ability.
    • Hands-on approach, with a ‘can do’ attitude. Able to work under minimal supervision.
    • Ability to prioritize with good time management skills.
    • Excellent attention to detail, with the ability to work accurately in a demanding environment.
    • Self-motivated, with the ability to work proactively using own initiative.
    • Committed to learning and development.
    • Preferred:
      • Good IT skills e.g., Microsoft Office (Word, Excel, PowerPoint, Project and Outlook).
      • Significant contacts
        • Manufacturing, Validation, Site Automation, Engineer, Quality Control, and Global Technical Operations (GTS) associates.
  • BS Degree in a related scientific discipline
  • Strong PC literacy; MSOffice skills; knowledge of SAP QM module
  • Ability to work on a computer for extended periods of time
  • Must be willing to travel approximately 5-10%
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Although this hasn't been an issue at The Planet Group, the staffing industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly and never provide banking information during the application process. Candidate safety is a top priority at The Planet Group.

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