Senior GMP Project Manager – Life Sciences & FDA Compliance

cGMP Consulting Inc.; Cincinnati (OH); On-site; USD 85,000 - 100,000; Full time

Benefits offered by this job

Medical

Dental

Vision

PTO

401K

Job summary

cGMP Consulting Inc. is seeking a senior project manager to lead engineering activities for GMP-compliant pharmaceutical projects. You will drive project plans, timelines, budgets and resource allocation, while ensuring regulatory alignment and client satisfaction across multiple concurrent initiatives.

Ideal candidates bring extensive GMP/FDA exposure, strong cross-functional leadership, and a proven track record in delivering complex programs on time and within budget.

Qualifications

• Bachelor's degree in Engineering, Science, or related field.
• 4+ years in a GMP manufacturing environment leading deliverables.
• Familiar with FDA regulatory requirements.
• Project management certification (PMP, CAPM) or equivalent.

Responsibilities

• Develop and oversee project plans, timelines, deliverables and resource allocation.
• Monitor progress, manage risk and coordinate resources across multiple projects.
• Serve as main point of contact for client projects and ensure clear communication.

Skills

PMP certification

Project management

Stakeholder management

Cross-functional leadership

Regulatory compliance

Risk management

Communication

Education

Bachelor's degree in Engineering/Science

Tools

MS Project

Jira

Job description

cGMP Consulting Inc. is seeking a senior project manager to lead engineering activities for GMP-compliant pharmaceutical projects. You will drive project plans, timelines, budgets and resource allocation, while ensuring regulatory alignment and client satisfaction across multiple concurrent initiatives.

Ideal candidates bring extensive GMP/FDA exposure, strong cross-functional leadership, and a proven track record in delivering complex programs on time and within budget.