
Construction Project Manager
GenScript, Piscataway, NJ, United States
Construction Project Manager
Location: Piscataway, NJ (Fully onsite)
Reports to: Director of US Site Operations
Compensation: The estimated salary range is $120,000 - $150,000, based on experience.
Overview
GenScript is seeking a talented, detail-oriented and self-driven individual to join the Operations Department, contributing to the planning, design, construction, commissioning, validation, and engineering process systems development for our facilities in Piscataway, NJ. This position is valid for at least 1-2 years with the opportunity to transition to facility manager after the construction projects are completed.
Job Responsibilities
Project Planning and Execution:
Develop comprehensive project plans ensuring projects proceed according to set objectives, including requirement gathering, feasibility analysis, risk assessment, and solution formulation.
Manage cost estimation for all project phases and create cost control plans.
Procurement and contract management.
Oversee bidding and procurement for project design, construction, and long-lead equipment.
Manage contract signing and execution with suppliers and contractors, ensuring compliance with terms, quality, and deadlines.
Compliance and Regulatory Affairs:
Plan and execute government and third-party procedures to ensure project compliance with US regulations.
Plan and manage government permits applications.
Project Management:
Manage technical, quality, safety, and timeline aspects of projects, ensuring timely resolution of technical issues, compliance with quality standards, and implementation of safety measures.
Coordinate with construction firms, supervisory, and contracting units to manage internal and external project relationships.
Commissioning and Validation: Organize factory acceptance tests, commissioning, and validation to ensure systems meet user requirements.
Project Completion:
Lead the final inspection, handover, documentation review, and project settlement activities, ensuring successful project completion and handover.
Report project progress regularly, compile project reports, analyze lessons learned, and suggest improvements.
Qualifications and Requirements
Education and Experience:
Bachelor’s degree or higher in Mechanical/Electrical, Chemical Engineering, Biomedical Engineering, or related fields.
10+ years of experience in biopharmaceuticals with substantial project management and facility operations experience.
Hands-on experience in managing construction, experience in executing projects from business requirement collection through to design, construction, commissioning, validation, and final settlement is preferred.
Skills:
Strong management and reporting capabilities, clear management vision, able to handle high-pressure work environments.
Solid technical expertise combined with engineering knowledge.
Demonstrated skills in problem solving, root cause analysis with result-driven thought process.
Additional Considerations:
Proficient in project management software (e.g., Procore, Microsoft Project, Primavera P6).
Familiarity with construction estimating and scheduling tools.
Understanding of US building codes, zoning laws, safety regulations, and biopharmaceutical industry standards.
Equal Employment Opportunity
GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company’s policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
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Location: Piscataway, NJ (Fully onsite)
Reports to: Director of US Site Operations
Compensation: The estimated salary range is $120,000 - $150,000, based on experience.
Overview
GenScript is seeking a talented, detail-oriented and self-driven individual to join the Operations Department, contributing to the planning, design, construction, commissioning, validation, and engineering process systems development for our facilities in Piscataway, NJ. This position is valid for at least 1-2 years with the opportunity to transition to facility manager after the construction projects are completed.
Job Responsibilities
Project Planning and Execution:
Develop comprehensive project plans ensuring projects proceed according to set objectives, including requirement gathering, feasibility analysis, risk assessment, and solution formulation.
Manage cost estimation for all project phases and create cost control plans.
Procurement and contract management.
Oversee bidding and procurement for project design, construction, and long-lead equipment.
Manage contract signing and execution with suppliers and contractors, ensuring compliance with terms, quality, and deadlines.
Compliance and Regulatory Affairs:
Plan and execute government and third-party procedures to ensure project compliance with US regulations.
Plan and manage government permits applications.
Project Management:
Manage technical, quality, safety, and timeline aspects of projects, ensuring timely resolution of technical issues, compliance with quality standards, and implementation of safety measures.
Coordinate with construction firms, supervisory, and contracting units to manage internal and external project relationships.
Commissioning and Validation: Organize factory acceptance tests, commissioning, and validation to ensure systems meet user requirements.
Project Completion:
Lead the final inspection, handover, documentation review, and project settlement activities, ensuring successful project completion and handover.
Report project progress regularly, compile project reports, analyze lessons learned, and suggest improvements.
Qualifications and Requirements
Education and Experience:
Bachelor’s degree or higher in Mechanical/Electrical, Chemical Engineering, Biomedical Engineering, or related fields.
10+ years of experience in biopharmaceuticals with substantial project management and facility operations experience.
Hands-on experience in managing construction, experience in executing projects from business requirement collection through to design, construction, commissioning, validation, and final settlement is preferred.
Skills:
Strong management and reporting capabilities, clear management vision, able to handle high-pressure work environments.
Solid technical expertise combined with engineering knowledge.
Demonstrated skills in problem solving, root cause analysis with result-driven thought process.
Additional Considerations:
Proficient in project management software (e.g., Procore, Microsoft Project, Primavera P6).
Familiarity with construction estimating and scheduling tools.
Understanding of US building codes, zoning laws, safety regulations, and biopharmaceutical industry standards.
Equal Employment Opportunity
GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company’s policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
#J-18808-Ljbffr