Sr. Project Manager / Pharma
- Overall responsibility for the technical/commercial delivery and project execution.
- Implementing Quality Plans.
- Define scope of work and how the project will be delivered within the budget.
- Develop the project execution strategy in alignment with the Project Team and Customer.
- Monitor the effectiveness of the project execution strategy and modify as necessary to accommodate changing circumstances throughout the life of the project.
- Identify resource needs, timing and organize with resource owners.
- Coordinate the design between all disciplines.
- Obtain PO from the Client, agree to invoicing details, track payments, etc.
- Prepare Project Monthly Project Reports and ensure early notification of any significant project issues with potential commercial risks.
- Manage Customer agreement and sub-consultant agreements/contracts.
- Develop and agree project schedule(s): track/report progress and implement controls.
- Develop project budgets and then monitor and report on them regularly.
- Set up the project change management log: prepare change orders, identify and record changes, and review regularly with the Client.
- Ensure compliance with local statutory and regulatory authorities.
- Monitor and enforce compliance with AtkinsRéalis and/or Customer procedures.
Review contract risks, organize appropriate reviews and take appropriate steps to mitigate. - Develop and maintain good Customer relationships.
- Set up appropriate communications and reporting structures (meeting, reports etc.) and follow up on any Customer complaints or issues.
- Lead the proposal effort: develop the execution strategy, commercials for proposal and lead the presentation to the Client.
- Motivate and direct the project team, including sub consultants.
- Close out of projects including certification, handover, close-out review/report, project metrics, capturing "Lessons Learned" and filing/archiving.
- Bachelor's degree in Engineering, Architecture, or relevant work experience.
- Professional Engineering (PE) licensure is strongly preferred.
- 10 + Years of design experience in a design firm setting (preferably in the Pharmaceutical, Biopharmaceutical, Cell & Gene Therapy sectors).
- Experience managing large capital projects.
- Knowledge of cGMP Manufacturing standards.
- Good commercial awareness and business acumen.
- Good understanding of all disciplines.
- Excellent organizational skills with an ability to produce quality work and achieve project deadlines within budget.
- Strong work ethic, self-driven, results-oriented with a positive outlook, and a clear focus on high quality.
- A forward planner who identifies and resolves project issues.
- Ability to critically assesses own performance and the performance of others.
- The ability to travel as needed for client and project development.
- Excellent communication skills (both verbal and written).
- Excellent commercial skills with the ability to manage projects to budget man-hours and commercial return targets.
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