What are the responsibilities and job description for the Pharmaceutical Project Management Expert position at MMR Consulting?
Job Summary
MMR Consulting is seeking a skilled Senior Biopharmaceutical Manager CQV to lead projects in the design, commissioning & qualification, start-up and project management of various processes, systems and facilities within the pharmaceutical/biotech industry. This role requires a strong understanding of cGMP operations and previous PM experience.
Key Responsibilities
- Provide technical guidance into engineering assessments, design, project management, commissioning and start-up of equipment and facilities.
- Lead or support project execution from feasibility through to project completion/handover, including all project stages such as feasibility assessments, concept design, procurement, construction/installation, project controls, commissioning & qualification.
- Prepare business cases, manage stakeholders, review technical documentation, integrate safety into design and execution, prepare/review automation sequences, facilitate project management tools, coordinate meetings, travel may be required occasionally.
Required Skills and Qualifications
- 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.
Benefits
MRR Consulting offers equal employment opportunities, celebrates diversity, committed to creating an inclusive environment for all employees.
MMR Consulting is seeking a skilled Senior Biopharmaceutical Manager CQV to lead projects in the design, commissioning & qualification, start-up and project management of various processes, systems and facilities within the pharmaceutical/biotech industry. This role requires a strong understanding of cGMP operations and previous PM experience.
Key Responsibilities
- Provide technical guidance into engineering assessments, design, project management, commissioning and start-up of equipment and facilities.
- Lead or support project execution from feasibility through to project completion/handover, including all project stages such as feasibility assessments, concept design, procurement, construction/installation, project controls, commissioning & qualification.
- Prepare business cases, manage stakeholders, review technical documentation, integrate safety into design and execution, prepare/review automation sequences, facilitate project management tools, coordinate meetings, travel may be required occasionally.
Required Skills and Qualifications
- 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.
Benefits
MRR Consulting offers equal employment opportunities, celebrates diversity, committed to creating an inclusive environment for all employees.
