CQV PLANNER

CQV Planner - Pharmaceuticals - North Carolina - 15-Month Contract  Our client, a global Pharmaceutical manufacturing organization are looking for a talented CQV Engineer to join their expanding team.
With continued organizational growth and considerable investment across their portfolio and capital programs this is an extremely exciting opportunity to contribute towards their brand-new manufacturing facility on the East Coast of the United States.
Responsibilities.
Planning of CQV phase of project with a focus on the qualification of the drug substance building and process areas.
Develop toolset to enable execution level planning and scheduling of CQV phase scope for project Interface with EPCM planning on the front-end of schedule, and with PQ planning on the back-end of schedule.
Lead CQV planning meetings for the functions associated with the qualification of the drug substance manufacturing buildings Work with these groups to ensure end-to-end schedule visibility and strategic alignment.
Provide support to leadership and PM’s to achieve overall project goals Requirements.
Minimum of 5 years of planning experience including experience with design and construction projects for biopharmaceutical manufacturing facilities.
Minimum 5years experience on CQV Team Experience with CIP commissioning planning Experience with complex projects and working in or around operating facilities.
Ability to keep work pace and meet deadlines.
Good organizing and planning skills.
Demonstrated proficiency communicating and collaborating at a variety of levels with customers, vendors, equipment suppliers and operations staff.
Proven success working well in a team environment with flexibility to react to changing business needs.
Strong leadership and communication skills.
Problem solver with a focus on achievement of overall project goals.
Computer skills (Spreadsheets, Word Processing, Visio, Microsoft Project) If this role is of interest to you, please apply now!    #LI-NR1