Position: Project Manager
Location: Columbus, OH
Duration: 12 Months
Job Overview:
We are seeking a skilled Project Manager for a 12-month onsite assignment based in Columbus, OH. The role requires a commitment of at least three days per week onsite. The ideal candidate will have a strong background in project management with previous experience in scientific, non-GMP environments.
Responsibilities:
Oversee project planning, development, scheduling, and execution for cross-functional teams including Process Development, Analytical Development, Quality Control, and Operations.
Manage project timelines, budgets, invoicing, scope, and alignment with team priorities.
Develop and maintain RAID Logs and Gantt charts for project tracking.
Lead and manage multiple projects simultaneously, with a focus on meeting deadlines and delivering results.
Client Overview:
Our client, a gene therapy CDMO specializing in viral vector process and analytical development, is looking for a Project Manager to support their team. This role is essential to the smooth execution of various projects within the organization.
Required Qualifications:
Bachelor’s degree or higher.
At least 5 years of experience in project management within biotech or pharmaceutical industries.
Proven track record managing cross-functional teams, particularly in biotech or pharmaceutical settings.
Previous experience working with non-GMP teams (e.g., Process Development, Analytical Development, Quality Control, and Operations).
Strong communication, negotiation, and interpersonal skills.
Proficiency in Microsoft Office and project management software, particularly Smartsheet.
Preferred Qualifications:
Experience with Adeno-associated virus (AAV) vectors, Biologics, or Gene Therapy.
Background in scientific research or lab work.
Experience with SAP systems.
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