CQV Project Coordinator
- East Coast
- Contract
- Commissioning, Qualification and Validation
Our client, a global Pharmaceutical manufacturing organization are looking for a talented CQV Project Coordinator 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:
- In coordination with CQV, process engineering and other project teams, drive coordination of daily, weekly, and monthly activities for your assigned area. Focus will be on execution, staffing coordination and area availability.
- Manage schedule execution of selected work packages (exact packages to be defined in coordination with the candidate).
- Drive and support the readiness and availability of materials for startup and commissioning execution.
- Take on critical projects at the request of, and reporting to, the CQV leadership team.
- Actively engage with PMs/Coordinators in other teams to ensure alignment and sharing of best practices.
- Work with project trouble shooting and EHS teams for field coordination activities
- Adopt the “one team approach” acting as a partner with our EPCM firm to remove hurdles.
Requirements
- Minimum 10 years Project coordination experience on Large Scale Projects
- Minimum 5 years relevant field / greenfield project experience
- Experience with liaising with other departments and building PMs/leads, ensuring streamlined FAT deliverables for all buildings.
- Willingness to take action in a proactive manner for driving progress
- Strong communication skills
- BA/BS in a related field and 5+ years’ experience successfully executing complex projects in a Pharm/cGMP environment
- Experience with coordinating field activities bringing together multi-functional teams in a dynamic yet visible way
- Positive Can-Do attitude and strong collaboration.
- Excellent analytical and problem-solving capabilities
- Lean / Six Sigma capabilities highly recommended
- Acts with detail-driven ownership and follow through
If this role is of interest, please apply now.
#LI-MC1
I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
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