Senior CQV Project Manager - GMP Validation & Commissioning

IPS-Integrated Project Services; Lexington (KY); Remote; USD 90,000 - 120,000; Full time

Benefits offered by this job

Competitive salary

Travel opportunities

Professional development programs

Job summary

A leading project services firm seeks a Project Manager of CQV in Lexington, KY to manage complex commissioning and compliance projects in the pharmaceutical and biotech sectors. Ideal candidates will possess a Bachelor's degree in Engineering, with over 7 years of relevant experience. The role demands strong client relations and project management skills, a risk-based approach, and familiarity with regulatory compliance. This position involves significant travel, requiring flexibility and commitment to high-quality standards.

Qualifications

• 7+ years of experience in Pharmaceutical, Biotech, or related field.
• Experience with Risk-Based Approaches to Commissioning.
• Strong understanding of regulatory requirements.

Responsibilities

• Lead and deliver commissioning and compliance projects.
• Coordinate project activities and manage client relationships.
• Develop project schedules and deliverable tracking reports.

Skills

Project Delivery

Commissioning

Validation

Client Communication

Education

Bachelor’s degree in Engineering or related discipline

Tools

GMP Regulations

cGMP Compliance

Job description

A leading project services firm seeks a Project Manager of CQV in Lexington, KY to manage complex commissioning and compliance projects in the pharmaceutical and biotech sectors. Ideal candidates will possess a Bachelor's degree in Engineering, with over 7 years of relevant experience. The role demands strong client relations and project management skills, a risk-based approach, and familiarity with regulatory compliance. This position involves significant travel, requiring flexibility and commitment to high-quality standards.