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Maximo Project Manager Jobs in Edison, NJ (NOW HIRING)

Develop and lead upgrade projects, managing all aspects from concept justification to final ... Experience with CMMS, preferably Maximo. * D esirable * Preferably a third level qualification in ...

ARM, Maximo, SAP, Oracle WAM, etc.) * 3 years' experience writing functional / technical design ... Knowledge of Project Management basics. * Demonstrated ability to work in teams and cross ...

LTE Engineer

Warren, NJ ยท On-site

... components (Maximo objects, TRM Rules, Java extensions, etc) based on detailed design. Performs ... Manages the interrelationships among various projects or work objectives

Change Control Manager

Livingston, NJ ยท On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... project coordination, or a similar operational role, ideally in a data center, critical facilities ... Familiarity with CMMS/EAM platforms (e.g., Maximo, Upkeep, or similar) or ITSM change management ...

... project coordination, or a similar operational role, ideally in a data center, critical facilities ... Familiarity with CMMS/EAM platforms (e.g., Maximo, Upkeep, or similar) or ITSM change management ...

... and Maximo * Manage scope, schedule, and budget of work assigned. * Perform functional tasks ... conduit projects in dense urban environments, work permit development, easements, and ROW ...

Distribution Engineer

Trenton, NJ ยท On-site

$59K - $106K/yr

  • Medical

  • Retirement

  • PTO

... and Maximo * Manage scope, schedule, and budget of work assigned. * Perform functional tasks ... conduit projects in dense urban environments, work permit development, easements, and ROW ...

Distribution Engineer, Electrical Utility

Trenton, NJ ยท On-site

$59K - $106K/yr

  • Medical

  • Retirement

  • PTO

... and Maximo * Manage scope, schedule, and budget of work assigned. * Perform functional tasks ... conduit projects in dense urban environments, work permit development, easements, and ROW ...

Showing results 21-40

Maximo Project Manager information

See Edison, NJ salary details

$46.1K

$100K

$159.9K

How much do maximo project manager jobs pay per year?

As of Aug 15, 2026, the average yearly pay for maximo project manager in Edison, NJ is $99,964.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,600.00 and $117,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Maximo Project Manager?

To excel as a Maximo Project Manager, you need a strong background in project management, asset management principles, and hands-on experience with IBM Maximo software, typically supported by a relevant degree and project management certification (such as PMP). Mastery of Maximo modules, system integration tools, and understanding of EAM (Enterprise Asset Management) practices are essential, as well as familiarity with related IT infrastructure. Excellent communication, leadership, and problem-solving abilities help in managing cross-functional teams and engaging stakeholders effectively. These skills ensure successful project delivery, system optimization, and alignment with organizational goals.

What are the most common challenges faced by Maximo Project Managers, and how are they typically addressed?

Maximo Project Managers often encounter challenges such as managing complex system integrations, aligning diverse stakeholder expectations, and ensuring user adoption of new processes. These obstacles are typically addressed by conducting thorough requirement gathering, maintaining clear and regular communication with all parties, and providing robust training and support for end users. Strong project planning skills and a proactive approach to risk management also help anticipate and resolve issues before they impact project timelines. Collaboration with IT teams, business units, and external vendors is key to overcoming these challenges and achieving successful project outcomes.

What is a Maximo Project Manager?

A Maximo Project Manager oversees the implementation, customization, and optimization of IBM Maximo, an enterprise asset management (EAM) system. They coordinate project timelines, manage stakeholders, and ensure the system meets business requirements. Responsibilities include system configuration, data migration, user training, and workflow enhancements. They also collaborate with IT teams, vendors, and end-users to ensure seamless deployment and ongoing support. Strong project management, technical expertise, and industry-specific knowledge are essential for success in this role.

What are popular job titles related to Maximo Project Manager jobs in Edison, NJ?

For Maximo Project Manager jobs in Edison, NJ, the most frequently searched job titles are:

What job categories do people searching Maximo Project Manager jobs in Edison, NJ look for?

The top searched job categories for Maximo Project Manager jobs in Edison, NJ are:

What cities near Edison, NJ are hiring for Maximo Project Manager jobs?

Cities near Edison, NJ with the most Maximo Project Manager job openings:

Infographic showing various Maximo Project Manager job openings in Edison, NJ as of July 2026, with employment types broken down into 85% Full Time, 12% Part Time, 1% Temporary, and 2% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $99,964 per year, or $48.1 per hour.

Engineer II, Process Equipment Engineer Small Molecule (Hopewell, NJ)

BeiGene, Inc.

Hopewell, NJ โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago


Job description

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
General Description:
BeOne Medicines is seeking highly motivated and organized engineer, to join our team at the Hopewell, NJ site. The successful candidate will be responsible for supporting a new Small Molecule manufacturing facility and maintaining a stable, qualified, GMP manufacturing facility in close collaboration with the manufacturing and quality teams. The individual ensures reliable operation and state of compliance for a 24x7 commercial manufacturing facility. This role works independently, with minimal supervision and direction and will provide technical direction, Project Management support, Commissioning and SME expertise in the areas of oral solid dose manufacturing including blending, granulation, compression and encapsulation. Projects may often require independent decision making and exercising judgment. This role will be based in Hopewell NJ and report to the Senior Director Engineering.
Responsibilities:
  • Provide SME input into Equipment, Facility for Small Molecule project.
  • Provide SME input for the commissioning, qualification and validation of responsible systems.
  • Develop and maintain technical, operational procedures, preventative maintenance plans for responsible systems.
  • Work in cross functional team with Global Engineering to hit project milestones and KPI's.
  • Work with external partners as required.
  • Manage the assets of buildings & facility. Experience with small molecule drug product manufacturing equipment. With a focus on downstream equipment. For example, Tablet Press, Tablet Coating Machines, etc.
  • Solicit and respond to user input with the team members and maintain positive relationships with all internal and external stakeholders.
  • Directly support operations with troubleshooting and issue resolution with respect to equipment, facilities, and utilities.
  • Participate and lead in fault analysis and remediation.
  • Requires working in an industrial manufacturing environment including gowning.
  • Other duties as assigned.

Required Skills/Experience:
  • BS or higher in engineering and/or related discipline.
  • Minimum of 4 + years of equipment and facility support in a GMP environment. Strong understanding of Quality in GMP environment including Good Documentation Practices, Deviation and Capa management.
  • Excellent communication and interpersonal skills, with the ability to collaborate across functional teams.
  • Proven ability to manage multiple complex priorities simultaneously under tight timelines.
  • Analytical problem-solving skills and proactive decision-making.
  • Ability to summarize and present project information clearly to management.
  • Bachelor's degree in Engineering, Life Sciences, or related field with 4+ years of GMP pharmaceutical experience required, or Masters degree with 2+ years required.
  • Experience with CMMS, Metrology, and facility maintenance is required.
  • People leadership, direct supervision required.
  • The ability to operate self-sufficiently and to motivate oneself is crucial for the success of this position. In addition, the ability for this person to develop and maintain transparent communication between departments is essential.

Preferred Skills/Experience:
  • OE and/or LEAN Methodologies

Physical Requirements:
  • Ability to work in an office environment, construction site, and laboratory or manufacturing areas.
  • Must be able to sit, stand, and use standard office equipment for extended periods.

Computer Skills:
  • Proficiency in Microsoft Office Suite (Excel, PowerPoint, Word, Outlook).
  • Proficiency with CMMS, Maximo preferred.
  • Experience with project management tools such as Microsoft Project, Autocad, Smartsheet.
  • Familiarity with data management and visualization tools (e.g., SharePoint, Teams, Power BI).
  • Ability to create and maintain Gantt charts, dashboards, and tracking templates.
  • Comfortable working within document management systems (e.g., Veeva Vault, eQMS, or similar).

Other Qualifications: Demonstrates strong accountability, communication, and ability to build trust in a fast-paced, regulated environment
Travel: May require domestic travel up to 5% travel
Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
  • Fosters Teamwork
  • Provides and Solicits Honest and Actionable Feedback
  • Self-Awareness
  • Acts Inclusively
  • Demonstrates Initiative
  • Entrepreneurial Mindset
  • Continuous Learning
  • Embraces Change
  • Results-Oriented
  • Analytical Thinking/Data Analysis
  • Financial Excellence
  • Communicates with Clarity

Salary Range: $95,600.00 - $130,600.00 annually
BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com.

BeiGene logo

About BeiGene

Sourced by ZipRecruiter

BeiGene (NASDAQ: BGNE; HKEX: 06160; SSE: 688235) is a global, science-driven biotechnology company focused on developing innovative and affordable medicines to improve treatment outcomes and access for patients worldwide. With a broad portfolio of more than 40 clinical candidates, we are expediting development of our diverse pipeline of novel therapeutics through our own capabilities and collaborations. We are committed to radically improving access to medicines for two billion more people by 2030. BeiGene has a growing global team of over 8,200 colleagues across five continents. For more information, please visit www.beigene.com .

Industry

Health care and social assistance

Company size

5,001 - 10,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

2010

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