Pintail Solutions


CQV Project Manager - BioPharma

Project Management

Full Time

Phoenix, United States

Posted this week

About the Job

Salary - $92000 - $120000/Year

Full-time2 hours ago
Full Job Description
Job Description

Job Title

Pharmaceutical CQV Project Manager

Position Type

Full Time


Phoenix, AZ

Travel Required

Some travel may be required

External Posting URL

Applications Accepted By

Audra Miller

Audra Miller

Pintail Solutions, Suite 104

12172 Visionary Way

Fishers, IN 46038

Job Description


Pintail Solutions is a niche management advisory firm focused on partner business growth by engaging companies in developing and deploying new business strategies, delivering on key programs, and enabling overall project and portfolio delivery. Pintail Solutions also has expertise in leading change initiatives, large and small, that often get ignored in both the strategy and execution setting. Pintail Solutions offers a dynamic work environment, grounded in the entrepreneurial offices of Launch Fishers in central Indiana.

The project manager will work with project teams at client sites to inspect, test and troubleshoot bio-pharma manufacturing, packaging, and utility systems and equipment. This person is responsible for identifying and coordinating activities for commissioning and qualification and creating engineering and qualification protocols and reports. They will also manage the resources (people and budget) for the same. The successful candidate will interact with client personnel. They will both oversee and execute upon the work.

Roles and Responsibilities

Lead the CQV of process equipment for pharmaceutical projects through basic design, detailed design, construction and CQV phases for process equipment and supporting systems.
Lead planning and allocation of resources to meet CQV Project requirements
Scope work and generate project proposals & cost estimates
Have an excellent understanding of CQV execution methodologies for GMP pharmaceutical facilities

Qualifications and Education Requirements

BS in a science or engineering field or equivalent experience
10+ years experience commissioning and qualifying bio-pharma systems equipment and systems
Experience with risk assessments, qualification protocols, commissioning plans/test scripts and summary reports is desired.
Experience in lyophilization and bioprocessing

Additional Notes

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Posted this week

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