Browse by job sector

Consultant in PMO

  1. North America, United States
Raleigh
  1. Contract
Competitive
  1. Life Sciences
33432
Apply to this job Save job
Consultant in PMO - Raleigh, North Carolina - 15-Month Contract 

Our client, a global Pharmaceutical manufacturing organization are looking for a talented Consultant in PMO to join their expanding team. With continued organizational growth and considerable investment across their portfolio and capital programs this is an extremely exciting opportunity to contribute towards their brand-new manufacturing facility on the East Coast of the United States.


Responsibilities: 

Drive the identification, prevention, and remediation of risks to cGMP operations readiness for a greenfield large scale Biopharmaceutical facility focused on the manufacture of monoclonal antibody drug substance and drug product. This includes responsibility for the following areas in partnership with both full-time employees and other consultants on the project:
  • Project management plans and delivery for the risk management portion of the larger operations readiness project.
  • Communication plans regarding risk management for operations readiness.
  • Drive prospective weekly gemba and deep dive for key milestone objectives within the operations readiness plans.
  • Drive response and action plans to significant issues impacting the delivery of on-time high-quality cGMP operations readiness for the facility.
Requirements: 

Experience and contacts;
  • Proven experience in biopharmaceutical cell culture, purification, and fill finish facility operations. This would also include experience with support areas within the facility such as laboratories, warehouse, maintenance, utilities etc.
  • Proven experience delivering cGMP operations readiness for a greenfield drug substance and drug product cell culture facility.
  • Proven experience driving prospective and reactive processes for risk identification, prevention, and remediation.
  • Mature skills leading cross functional teams and providing project management, communications (oral, written, and powerpoint), risk management and gemba consulting services.
  • Subject matter expert for cGMP and operations expectations to start up a new greenfield biopharmaceutical cell culture manufacturing site that has drug substance, drug product and all support operations on site.
  • Natural positive attitude and ways of working to inspire the best in team performance. This must be paired with ability to find and call out gaps and risks in team plans and performance. We need a person to come in and challenge teams to continuously improve plans and delivery.

If this role is of interest to you, please apply now! 

 #LI-MC1
Apply to this job Save job
Save as a job alert
List #1

Similar Jobs

Electromechanical Project Manager

Salary

Competitive

Location

Antwerpen

Salary

Competitive

Sector

CAPEX Projects

Job type

Contract

Location

Belgium

Brussels

Description

Electromechanical Project Manager - Belgium - 9 Months Contract Do you want to work with a world leader in material technology? This opportunity is currently available to a Electromechanical

Reference

36736

Expiry Date

01/01/0001

Craig Thornton

Author

Craig Thornton
Craig Thornton

Author

Craig Thornton
Read more
Read more
Senior Project Manager

Salary

Competitive

Location

Capelle Les Grands

Salary

Competitive

Sector

CAPEX Projects

Job type

Contract

Location

France

Description

Senior Project Manager - France - 12 Months Contract How would you like the opportunity to work with in one of the largest biopharmaceutical projects in the country? If yes, then this is the

Reference

36650

Expiry Date

01/01/0001

Suraj Chauhan

Author

Suraj Chauhan
Suraj Chauhan

Author

Suraj Chauhan
Read more
Read more
Quality Technician

Salary

Competitive

Location

Galway

Salary

Competitive

Sector

Compliance / Quality Assurance

Job type

Contract

Location

Ireland

West

Description

Quality Technician - Galway, Ireland - 6 Months Contract Are you a Quality Technician looking for your next pharmaceutical role? Our client is a global medical technology leader dedicated to

Reference

36732

Expiry Date

01/01/0001

James Smithson

Author

James Smithson
James Smithson

Author

James Smithson
Read more
Read more

Insights

Living and working in Ireland
Read more

03/12/2025

QCS Staffing | What does a commissioning manager do?

What does a Commissioning Manager do?
Read more

02/20/2025

Day In the Life of a Commissioning Engineer Jobs

Day in the Life of a Commissioning Engineer

Read more

11/03/2024

VIEW ALL

Send us your CV

Our candidates are the cornerstone of our organisation and we are always looking to connect with new professionals who are seeking their next contract assignment or career opportunity.

Send your CV
Upload your CV