Biopharma Project Manager - Construction

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

 

Location: Clayton NC

Travel: up to 20%

 

The Project Engineer will be responsible for the oversight of projects for an industry leading biological therapeutic product manufacturer, as a member of the Grifols Engineering Team. The position will be stationed in Cayton, NC. Projects will include responsibilities for managing projects related to Blood Plasma processing equipment, utilities, and HVAC systems, electrical, automation systems and renovations involving facilities and equipment. Candidate must be willing to adjust working hours to meet the needs of the project(s), including some weekend work when required to match the schedule of project crafts. Some travel will be required.

 

Role responsibilities to include, but not limited to:

• Manage partial scope of a large project or complete scope for plasma product manufacturing building, equipment, utilities, HVAC, electrical, automation systems and renovations involving facilities, equipment, and infrastructures
• Responsibilities includes developing scope of work by working with multidisciplinary team
• Incorporate IT, Environmental and process safety, and Process Controls methodology in scope of work
• Manage project from concept to hand-over, to include budgeting, estimating, forecasting, schedule tracking and status updates
• Develop and evaluate bid packages for all scope of work
• contract management depending on scope of work   
• Work with multidisciplinary team including A&E companies, contractors and supplier, local authorities
• Effectively read, verify, and redline field drawings such as CSA plans, electrical schematics, P&IDs, and piping plans
• Work with internal customers to obtain permission to proceed and hand-over area / system after completion of work
• Field supervision of contractors to ensure the following:  safety of personnel and property, quality & efficiency, security & environmental policies are followed, confirmation of construction schedule
• Track progress of construction per design, anticipate and resolve field issues to avoid rework
• Start-up equipment and systems
• Provide input to future projects as to the practicality of budget, schedule, and project plans

 

Candidate should possess the following:

• Biotech, pharmaceutical or other regulated industry experience favorable, but not required
• Experience interacting with municipalities that have local jurisdiction favorable but not required
• Experience with pharmaceutical utilities and manufacturing processes favorable but not required
• Candidate must have good communication skills, good interpersonal skills, leadership skills and be a strong team contributor
• Candidate must be a self-starter and independent study
• Candidate must have strong problem-solving skills and meticulous attention to details
• Proficiency with Microsoft Office Suite (Word, Excel, PowerPoint)
• Proficiency with MS Project or other scheduling software
• AutoCAD and/ or Revit experience is a plus

 

Education and Experience requirements based on level:

Staff Engineer Level:

• Minimum Education: Bachelor's Degree in Engineering or related field.
• Professional registration and/or certifications as appropriate.
• Minimum of 5 years of related experience. Experience in Biotech, Pharmaceutical or Chemical Industry preferred.