What are the responsibilities and job description for the Senior Project Manager (GMP, Quality Systems) position at Planet Pharma?
Job Description :
- Essential Duties & Responsibilities
- Provides analytical support to the Project Management Office under minimal supervision.
- Proactively participates in processes and makes recommendations for system refinements within the Project Management Office.
- Support Planning Sessions as documentation lead and / or workstream lead.
- Performance Management Participates in the evaluation and feasibility process for potential projects.
- Provides clear direction on project requirements to meet expectations of external customers and business stakeholders.
- Interacts through program and / or project updates and reviews with all levels of management.
- Drives implementation of projects by establishing strategy, schedules, budgets, and financial analysis.
- Drives use of Project Management Methodology throughout projects.
- Approves team deliverables for project completion.
- Risk Management Leads team in risk management approaches and systems.
- Responsible for making decisions regarding the appropriate risk when there is substantial project or program impact.
- Administration
- Ensures appropriate linkages of this information to the project prioritization and / or portfolio process.
- Maximizes business results through continuous improvement in organization's ability to execute projects and programs from initiation to completion and production scale-up.
- Owning SharePoint site, tracking and execution of scope and financial deliverables and associated reporting.
- Finance Management Provides financial analysis and justification for new projects or programs.
- Monthly financial updates (submitted via SharePoint)
- Issue Resolution
- Eliminates or minimizes barriers to progress.
- Anticipates potential conflict situations, identifies and acts on proactive solutions.
- May perform other duties as assigned.
- Communication Weekly and monthly SharePoint updates of Initiative and Milestone
- Status Participation, including presenting updates / escalated items and fielding questions, in the standing global Master Planner meeting
- Escalation of issues, risks, and changes via established Integration Management Office (IMO) and Quality Workstream communication mechanisms
- Utilizing and enhancing standard reporting and communication tools to ensure appropriate and timely communication and reporting from multiple projects and quality / regulatory Core Team members
- Meeting participation / facilitation
- Quality Management Systems
- Execution to completion of harmonized process / quality system element roll-out.
- This will require collaboration with the Manufacturing Integration team
- Execution of outstanding process / quality system element assessments.
- This will include coordinating document owners and SMEs to ensure harmonized end state / content / IT tools; working with Manufacturing Integration team to develop change plans, and completing issuance / roll-out of processes
- Participation in and execution of elements of the Quality Integration Workstream Core Team and Communication Plan
Qualifications :
Education and / or Experience :
MBA / MS or Bachelors with equivalent plus 7 years project management experience and 10 years of demonstrated success leading multi-site, global or enterprise-wide programs in the medical products industry