Note: The job is a remote job and is open to candidates in USA. Curium Pharma is the world’s largest nuclear medicine company with extensive experience in developing and distributing radiopharmaceutical products. The Senior Project Manager will collaborate across various functions to implement strategic initiatives and manage projects within the North American Operations team.
Responsibilities
- Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, DEA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.)
- 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
- Improve integrated risk management across NPD, MOB and Strategic Business projects
- Coordinate MOB and Strategic Business Initiatives to be integrated, where necessary, in escalation and governance process where critical projects are managed and reported
- Lead 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
Skills
- Bachelor lever degree in engineering or related sciences or equivalent experience
- 5+ 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
- Strong in computer skills and experience with Microsoft Word, PowerPoint, Excel, Visio, MS Project and experience with Project Management software
- This position may require limited travel
- Experience in manufacturing operations preferred
- PMP certification preferred
- Experience in ERP/data base management a plus
- Lean or Six Sigma trained/certified a plus
Company Overview