Construction Project Manager

Construction Project Manager Employer GenScript Location Piscataway, New Jersey Start date Apr 25, 2026 categoriesView less categories Job Details Company Job Details About GenScript GenScript Biotech Corporation (

Stock Code:

1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.

Job Title:

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 done.

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.

Reporting and Improvement:

Regularly report project progress, 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. #LI-EB1 #GS 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.

Please note:

Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform. Company GenScript Biotech Corporation (HK.1548) is an important technology and service provider in the world for life science R D and manufacture. Built upon its solid DNA synthesis technology, GenScript Biotech comprises four major business units: a life-science services and products business unit, a biologics contract development and manufacturing organization (CDMO) business unit, an industrial synthetic products business unit, and an integrated global cell therapy company. GenScript Biotech was founded in New Jersey, USA in 2002 and listed on the Hong Kong Stock Exchange in 2015. The company's business operations span over 100 countries and regions worldwide with legal entities located in the U.S., China, Japan, Singapore, Netherlands, Ireland, the United Kingdom, Korea, Belgium and Spain. GenScript Biotech provides premium, convenient and reliable services and products for over 200,000 customers. As of June 30, 2024, GenScript Biotech had more than 6,900 employees globally, and 103,600 peer-reviewed journal articles worldwide had cited GenScript Biotech's services and products. In addition, GenScript Biotech owns a number of intellectual property rights, including over 300 patents, over 900 patent applications and great numbers of know-how secrets. Driven by the corporate mission of "make people and nature healthier through biotechnology", GenScript Biotech strives to become the most trustworthy biotech company in the world. Company info Location Piscataway NJ United States