CQV Project Manager

The ideal candidate will be responsible for planning, coordinating, and implementing projects within the decided-upon budget, timeline, and scope. They will also effectively monitor and present project updates to relevant stakeholders, clients, or project team members.

Responsibilities:

• Generation, Execution / Approval of Qualification Life Cycle documents from SLIA through to PQ and Final Summary Reporting for Direct Impact Systems.
• Generation of Commissioning Test documents for No Impact Systems.
• Implementation of Change Controls on the change management system to support project activities as applicable.
• The role requires someone to coordinate and manage all elements of commissioning & qualification of large and small scale projects.
• If assigned a budget for project execution: Monitor budgets closely reporting on funding committed, expenditure forecasting and progress.
• Coordinate and supervise third party suppliers / vendors , service providers and sub-contractors as necessary.

Qualifications

• Degree in Engineering or related discipline is a necessary requirement for this position with project management experience.
• 5 years’ experience in projects in the Pharmaceutical or Biotech /Medical devices sector or Major project environment.
• Can demonstrate a knowledge of Systems and Equipment and engineering design.
• Ability to communicate clearly and in a timely manner to keep Company/Contractor personnel abreast of on-going changes and potential changes.
• Proven ability to adapt in a changing environment and changing methods of working and project requirements / priorities.