Associate Project Manager - Fully Onsite

Job Description

When you’re part of the team at Thermo Fisher Scientific, you’ll do important work like helping customers in finding cures for cancer, protecting the environment, and finding new ways of developing abuse deterrent drug technologies. Your work will have impact, and you’ll be supported in achieving your career goals.

*** This role is Fully Onsite at our Cincinnati facility.***

Cincinnati / Pharma Services Group / Drug Product Division / North America

How will you make an impact?

Our Cincinnati site is a Center of Excellence for specialized oral solid dose commercial manufacturing and drug development within our Pharma Services Group (PSG). By joining Thermo Fisher Scientific, you will have the opportunity to impact the lives of our customer's patients in the local community and worldwide. The Associate Project Manager supports the Project Manager on daily tasks to ensure flawless project execution. Performs day-to-day client project and business tasks that support development products. Manages cross functional deliverables and communication to enhance key project milestones. This is a great development opportunity that can align with your career aspiration whether you are looking to build experience in the development pharmaceutical space.

What will you do?

• Supports Project Managers with project and account activities including but not limited to batch readiness execution, batch release execution, managing proposal introduction into Changepoint (PM software), writing small proposals, and project kickoff support.
• Serves as customer logistics coordinator for the site including customer hosting and batch observations, logistics support, ordering catering for customer visits, and coordinates customer office assignments.
• Assists Project Managers in change of scope writing and managing small projects.
• Responsible for generating internal forms required for ongoing projects and newly awarded projects

How will you get here?

• High school or GED, Bachelors degree preferred
• 1 year of experience required, or equivalent combinations of education, training, and relevant work experience may be considered

Knowledge, Skills & Abilities:

• General knowledge of the pharmaceutical industry and practical knowledge of GMPs.
• Advanced communication skills and ability to solve problems, make decisions independently, and coordinate projects.
• Strong proficiency in Microsoft Outlook, Word, Excel and Powerpoint.
• Ability to work and communicate well with employees in multiple areas and job levels.
• Effective written and interpersonal skills.
• Ability to work on multiple projects simultaneously.