What are the responsibilities and job description for the Senior Biopharmaceutical Manager CQV position at MMR Consulting?
About the Role
This is an outstanding opportunity to join MMR Consulting's growing team, working with engineers involved in the design, commissioning & qualification, start-up and project management of various processes, systems and facilities. The successful candidate will work out of client's facilities, typically in the Bradley, IL area (1.5 hrs drive from Chicago).
Responsibilities
- Work on client sites, requiring compliance with the client's safety rules, including mandatory vaccination policies for COVID-19 where applicable.
- Supervise contractors during critical installations of process equipment and associated utilities.
- Visit construction and installation sites, wear necessary safety PPE, engage and coordinate with other engineering disciplines and cross-functional departments.
- Facilitate project management tools throughout the execution of projects, provide technical guidance, lead/support project execution, prepare business cases, manage stakeholders, review technical documentation, integrate safety, prepare/review automation sequences.
Requirements
- 10 years of experience in engineering/project management of various equipment and facilities within the pharmaceutical/biotech industry, with knowledge of requirements for a cGMP operation.
- Previous PM experience is required.
- Possess leadership skills, able to take initiative to lead projects involving multiple stakeholders, departments, varying complexity.
- Basic knowledge of AutoCAD, engineering degree, preferably in Mechanical, Chemical, Electrical Engineering, certification in Project Management would be an asset, ability to travel to the US would be an asset.
What We Offer
MRR Consulting offers equal employment opportunities, celebrates diversity, committed to creating an inclusive environment for all employees.
This is an outstanding opportunity to join MMR Consulting's growing team, working with engineers involved in the design, commissioning & qualification, start-up and project management of various processes, systems and facilities. The successful candidate will work out of client's facilities, typically in the Bradley, IL area (1.5 hrs drive from Chicago).
Responsibilities
- Work on client sites, requiring compliance with the client's safety rules, including mandatory vaccination policies for COVID-19 where applicable.
- Supervise contractors during critical installations of process equipment and associated utilities.
- Visit construction and installation sites, wear necessary safety PPE, engage and coordinate with other engineering disciplines and cross-functional departments.
- Facilitate project management tools throughout the execution of projects, provide technical guidance, lead/support project execution, prepare business cases, manage stakeholders, review technical documentation, integrate safety, prepare/review automation sequences.
Requirements
- 10 years of experience in engineering/project management of various equipment and facilities within the pharmaceutical/biotech industry, with knowledge of requirements for a cGMP operation.
- Previous PM experience is required.
- Possess leadership skills, able to take initiative to lead projects involving multiple stakeholders, departments, varying complexity.
- Basic knowledge of AutoCAD, engineering degree, preferably in Mechanical, Chemical, Electrical Engineering, certification in Project Management would be an asset, ability to travel to the US would be an asset.
What We Offer
MRR Consulting offers equal employment opportunities, celebrates diversity, committed to creating an inclusive environment for all employees.
