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UG :- - Not Required
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No of position :- ( 1 )
Post :- 15th Mar 2024
Overall project manager for C&Q team.
• Will be responsible for managing workload/assignments, planning, scheduling, and reporting on C&Q scope throughout the project. This person should have a successful track record of leading C&Q efforts for large scale green builds in the life sciences space (preferably cell & gene therapy).
• Project Management support to drive and identify areas of project improvement within the following domains:
o CQP generation
o QRAES generation
o Leading the C&Q/Automation team for documentation and execution activities for FAT, IV, ICO, ACO, FT, and validation
• PM in manufacturing space
• Manage project, cross functional teams, and all tasks for timely delivery and budget of a given project
• Manage the internal project scope of work, budget, timeline, and change orders.
• Manage the equipment and resources needed on the project(s).
• Develop and maintain a detailed project schedule and work plan
• Understand Lifecycle management for Quality Applications, processes for protocol development and execution.
• Manage internal and/or client management activities for assigned projects
• Identify and address complex technical issues and resourcing
• Support team members; acting as the liaison to the client for discussing changes in scope of work, timeline, or budget
• Provide frequent/ clear concise project updates to internal/external customers
• Problem solve skills to drive solutions to equipment/process issues, includingFMEA and root cause analysis methodology
• Interface with vendors, when necessary, to ensure vendors will deliver parts, materials, components and equipment on-time, on-budget and to technical specifications
• Must be willing to work onsite in Portsmouth, NH
• Bachelor’s Degree or equivalent required
• Proficiency using PC and Microsoft Office tools
• Outgoing personality with strong ability to communicate effectively with peers in clear, concise terms
• Ability to work as part of a team
• Strong problem-solving and critical thinking skills
• Excellent organizational and time management skills
• Strong attention to detail
• GMP and Good Documentation Practice
• Intermediate skills with WORD (authoring/editing large technical documents with styles, tables, TOCs, track changes)