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Principal Project Manager

Curium Pharma
Maryland, MO Full Time
POSTED ON 10/24/2024 CLOSED ON 11/22/2024

What are the responsibilities and job description for the Principal Project Manager position at Curium Pharma?

Job description: Summary of Position

This Principal Project Manager role provides a unique opportunity to collaborate across the different functions including Regulatory Affairs, Research and Development (R&D), Operations, Quality, Supply Chain, Finance, Legal, HR, Engineering, Marketing and Commercial. This individual will work closely with the Vice President – North American Project Management Office – and the Director Project Manager – Maintenance of Business (MOB) projects – to implement Curium’s strategic initiatives and projects.  This position requires effective communication on program status to senior leadership across the company. 

Essential Functions
  • Coordinate and align multiple shared services (i.e., QC, Validation, Operations) activities between board approved New Product Development (NPD)and MOB-related initiatives.   
  • Provide Project Management Services for North America Strategic Business Initiative projects that are classified as NPD or MOB.  
  • Facilitate key meetings, including core and designated sub-team meetings.  
  • Coordinate MOB and Strategic Business Initiatives to be integrated, where necessary, in escalation and governance process where critical projects are managed and reported.
  • Support efforts in improving and enhancing the PMO process/governance structure and systems initiatives. Areas of focus could include resource management across all functional groups for NPD, MOB, and other Strategic Business issues; optimizing the financial forecasting process; supporting PMO portfolio software implementations; Assisting with execution of stage gate process for all projects.
  • Provide PM Services, when necessary, to ensure business continuity within the PMO.    
  • Present project status/issues/risks to the Project Review Committee team members and provide recommendations on project direction.
  • Work with the PMO group during concept phase to provide scoping, scheduling, and cost information for requirements.
  • Provide PM services/support for elements of Integration activities for M&A.
  • Through Project Management systems, capture and share information from each project to drive continuous improvement and best practices.
  • All other responsibilities as assigned with or without accommodation.
Requirements
  • Bachelor level degree in engineering or related sciences or equivalent experience.
  • 8 or more years of experience in pharmaceutical industry and leading cross-functional projects
  • Technical understanding of the pharmaceutical processing  
  • Knowledge/experience in aseptic/terminally sterile operations; isolator technology a plus
  • Knowledge/experience in radiopharmaceutical industry and operations a plus
  • Experience in manufacturing operations preferred.
  • Team member and Team Leader experience.
  • Strong evidence and mastery of being a Team contributor.
  • Demonstrates strong interpersonal skills, including ability to maintain composure and professionalism under pressure.
  • Allocate resources effectively across multiple projects and appropriately set priorities.
  • Work well under tight and conflicting deadlines.
  • Excellent written and oral communication skills.
  • Strong interpersonal and negotiation skills, conflict management, priority setting, strategic agility, building effective teams, managing vision and purpose.
  • Strong management, time-management, and organizational skills.
  • PMP certification preferred.
  • Strong in computer skills and experience with Microsoft Word, PowerPoint, Excel, Visio, MS Project and experience with Project Management software.  Experience in ERP/data base management a plus.
  • Lean or Six Sigma trained/certified a plus.
  • This position may require limited travel.

 

Working Conditions:

  • Willingness to work in plant producing radioactive materials and requiring all employees to participate in safety programs designed to minimize potential and/or actual exposure levels.
  • Standard office environment, coupled with approximately 5% or less time in radiopharmaceutical manufacturing and laboratory environments.
  • Must be willing to wear a variety of personal protective equipment.  
  • Responsibilities also include the ability to lift, walk, bend, stoop, push, pull, reach, and climb stairs with or without accommodation.
  • May be required to work weekends and holidays to support operations. 
Project Estimator and Project Manager
Tri-State Equipment -
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