Project Engineers
- North America, East Coast
- Contract
- CAPEX Projects
Our client, a global pharmaceutical manufacturing organization are looking for a talented Project 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.
Essential Duties and Responsibilities for this role include, but are not limited to:
- Report to the CQV Program Manager
- Engineering administration and tasks
- Part of CCC (care, custody and control) process team . Our current teams are fully focused on executions
- To help drive closure of Construction punches, troubleshooting punches, change controls (PCC or TW), ACA’s (Automation change assessments), CTOP/VTOP/VDR readiness etc. These individuals must have demonstrated experience with cross-functional collaboration, driving for action and closure.
- Supporting the Project Manager in scope development activities & change management.
- Close out reports across the CQV disciplines
- Help the CQV teams close out executions
- Drive and support the readiness of CCC deliverables by facilitating regular meetings with key stakeholders
- Provide updates to project leadership team
- 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
- Coordinating with Constructability, Commissioning & Qualification and Validation.
- Supporting the development of a detailed schedule for all engineering and technical discipline activities.
- Extensive Project Engineering experience within BioPharma or Pharma Project
- Engineering / Construction / Capex experience.
- Experience with liaising with other departments and building PMs/leads
- Experience with project / engineering databases
- Willingness to take action in a proactive manner for driving progress
- Strong communication skills
- BA/BS in a related field and experience in 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
- Emphasis for this hire is on attitude (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
#LI-NR1
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 QCS Staffing for seven years now and have always received a professional service. QCS Staffing'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 QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
I have always received a highly professional & personable service from the team at QCS Staffing. 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
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