CQV Program Manager - GMP Manufacturing Leader

Pharmatek; Mount Vernon (IN); On-site; USD 90,000 - 120,000; Full time

Job summary

A pharmaceutical company in Indiana is seeking a Mid-Senior level Project Manager to oversee capital projects in Oral Solid Dosage manufacturing. The ideal candidate will have 7–10 years of experience in pharmaceutical manufacturing and possess strong skills in project management, budgeting, and cross-functional collaboration. This full-time role is essential for ensuring project alignment with corporate goals and requires onsite work at a GMP facility.

Qualifications

• 7–10 years of experience in pharmaceutical manufacturing focusing on Oral Solid Dosage.
• Proven track record in managing multiple capital projects.
• Strong understanding of GMP processes and validation protocols.

Responsibilities

• Lead and manage full lifecycle of capital projects.
• Oversee engineering activities for projects.
• Develop and maintain accurate project budgets and forecasts.

Skills

Capital project management

Leadership

Budgeting

Communication

Attention to detail

Education

Bachelor’s degree in Engineering

Advanced degree preferred

Tools

Microsoft Project

Job description

A pharmaceutical company in Indiana is seeking a Mid-Senior level Project Manager to oversee capital projects in Oral Solid Dosage manufacturing. The ideal candidate will have 7–10 years of experience in pharmaceutical manufacturing and possess strong skills in project management, budgeting, and cross-functional collaboration. This full-time role is essential for ensuring project alignment with corporate goals and requires onsite work at a GMP facility.