Pharma Project Manager – Client-Facing & Cross-Functional

Piramal Pharma Ltd

Lexington (KY)

On-site

USD 70,000 - 95,000

Full time

14 days+

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Job summary

Piramal Pharma Solutions, Lexington, is seeking a Project Manager to serve as the primary interface with clients across development and manufacturing projects. You will coordinate cross-functional teams to drive project success according to scope, timeline, and budget.

Reporting to the Director of Project Management, you will oversee meetings, timelines, risk management, and revenue-related activities while maintaining strong client relationships and adherence to FDA guidelines.

Qualifications

  • Bachelor’s degree in applicable scientific field is required.
  • One to three years of Project Management experience desired.
  • Minimum two years in pharmaceutical industry experience desired; CM or CRO experience preferred.
  • Good working knowledge of cGMP Guidelines and FDA regulations; understand SOPs and Safety/OSHA policies.
  • Proficiency with SmartSheet (or equivalent PM software) and MS Office suite.

Responsibilities

  • Serve as the main point of contact for internal and external clients throughout the manufacturing process.
  • Lead role in determining specific client requirements.
  • Ensure client expectations are managed and met.
  • Negotiate scope changes with clients.
  • Manage project scope, timeline and budget of multiple complex projects.

Education

Bachelor’s Degree in applicable scientific field
Advanced degree (preferred)

Tools

SmartSheet
Excel
Word
PowerPoint

Job description

Piramal Pharma Solutions, Lexington, is seeking a Project Manager to serve as the primary interface with clients across development and manufacturing projects. You will coordinate cross-functional teams to drive project success according to scope, timeline, and budget.

Reporting to the Director of Project Management, you will oversee meetings, timelines, risk management, and revenue-related activities while maintaining strong client relationships and adherence to FDA guidelines.

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