System Administrator

Neurotech Pharmaceuticals, Inc.

Cumberland, Northern (RI, KY)

Hybrid

USD 130,000 - 140,000

Full time

5 days ago
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Job summary

Neurotech Pharmaceuticals, Inc. in Cumberland, RI is seeking a System Administrator to lead maintenance planning and CMMS administration (Blue Mountain RAM).

This role ensures regulatory compliance, data integrity, and efficient site operations, coordinating with technicians, engineers, and contractors to optimize PM and calibration programs. The ideal candidate has 7–10 years in maintenance planning or CMMS administration, with GMP/regulatory experience and strong analytical, documentation, and

Qualifications

  • 7–10 years in maintenance planning, CMMS administration or facilities operations.
  • Experience in GMP-regulated environments (biotech/pharma) preferred.
  • Direct CMMS administration experience, Blue Mountain RAM preferred.
  • Experience with maintenance planning, calibration programs, and contractor coordination.
  • Strong documentation, analytical and communication skills.

Responsibilities

  • Own the Maintenance Planning and Scheduling System, including weekly and long-range scheduling of all preventive, corrective, and calibration activities.
  • Lead the development and maintenance of PM and calibration programs in alignment with asset criticality and regulatory requirements.
  • Provide end-to-end ownership and governance of the Blue Mountain CMMS (BMRAM) including system administration, asset lifecycle data, and reporting.
  • Serve as the primary owner of Facilities KPIs, responsible for performance metrics and informed decision-making.
  • Manage CMMS user administration, including new user setup, role-based access, and training.
  • Create, maintain, and modify maintenance job plans for equipment and instruments.
  • Maintain data integrity and audit readiness of all CMMS records for GMP compliance.
  • Coordinate with internal technicians, engineers, and external contractors to minimize disruption.
  • Monitor maintenance backlog and schedule adherence; adjust per priorities.
  • Own and track calibration compliance for regulatory requirements (GMP, FDA).
  • Review equipment performance and work order history to support reliability improvements.
  • Support RCA efforts and continuous improvement initiatives in maintenance.
  • Review project requests and vendor proposals; assist in prioritization and planning.
  • Coordinate facilities-related projects, repairs, and upgrades with stakeholders.
  • Maintain documentation to ensure GMP, OSHA, EPA compliance.
  • Prepare and deliver Facilities KPIs and dashboards (PM, calibration, downtime, W.O. performance).
  • Adhere to safety policies, GMP requirements.

Skills

Maintenance planning
CMMS administration
Facilities operations
Regulatory compliance
Calibration programs
Data analysis
Vendor coordination
Documentation control
Safety awareness
Root cause analysis

Education

GMP/regulatory training

Tools

Blue Mountain RAM (BMRAM)
IBM Maximo

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

System Administrator

Full Time Cumberland, RI, US

8 days ago Requisition ID: 1125

Salary Range: $130,000.00 To $140,000.00 Annually

Neurotech Pharmaceuticals, Inc.is a private biotech company located in Cumberland, RI and Needham, MA,. Since our inception more than 20 years ago, our focus has been on developing and commercializing transformative therapies for chronic eye diseases. The core platform technology, Encapsulated Cell Therapy (ECT), is a first-in-class drug delivery platform designed to slow the progression of chronic eye diseases. Neurotech’s first commercial product, ENCELTO TM (revakinagene taroretcel-lwey), is approved in the United States for the treatment of adults with idiopathic Macular Telangiectasia Type 2 (MacTel). Encapsulated cell-based gene therapy is designed to provide long-term, sustained delivery of therapeutic proteins for the treatment of chronic eye diseases.

We are seeking a System Administratorto support Facilities management and site operations by leading the planning, scheduling, and coordination of maintenance and calibration activities. This role is responsible for ownership and administration of the CMMS system (Blue Mountain RAM – BMRAM) and plays a critical role in ensuring efficient operations, regulatory compliance, and equipment reliability.


Responsibilities

  • Own the Maintenance Planning and Scheduling System, including weekly and long-range scheduling of all preventive, corrective, and calibration activities.
  • Lead the development and maintenance of preventive maintenance (PM) and calibration programs in alignment with asset criticality and regulatory requirements.
  • Provide end-to-end ownership and governance of the Blue Mountain CMMS, serving as the primary Subject Matter Expert responsible for system administration, asset lifecycle data, preventive maintenance programs, calibration management, workflow configuration, reporting, compliance, and user support.
  • Serve as the primary owner of all Facilities and Maintenance KPIs, responsible for establishing, maintaining, analyzing, and communicating performance measures that drive operational excellence and informed decision-making
  • Manage CMMS user administration, including new user setup, role-based access assignments, account maintenance, and end-user training to ensure effective system utilization and compliance with established processes
  • Create, maintain, and modify maintenance job plans specific to various equipment and instruments of varying complexities.
  • Maintain data integrity and audit readiness of all CMMS records to support GMP compliance.
  • Coordinate and schedule work with internal technicians, engineers, and external contractors to ensure efficient execution and minimal disruption to operations.
  • Monitor and manage maintenance backlog and schedule adherence, making adjustments based on operational priorities.
  • Own and track calibration compliance, ensuring all activities meet regulatory requirements (GMP, FDA, etc.) and addressing overdue or at-risk items.
  • Perform review and analysis of equipment performance and work order history to support reliability improvements and downtime reduction initiatives.
  • Support root cause analysis (RCA) efforts and continuous improvement initiatives related to maintenance effectiveness.
  • Review project requests and vendor proposals; assist in prioritization and execution planning.
  • Coordinate facilities-related projects, repairs, and upgrades with contractors and internal stakeholders.
  • Maintain all required documentation and records to ensure compliance with GMP, OSHA, EPA, and local regulatory requirements.
  • Prepare and deliver Facilities KPIs and dashboards, including PM compliance, calibration compliance, downtime, and work order performance metrics.
  • Adhere to all safety policies, procedures, and GMP requirements.

Education & Experience

  • 7- 10 years of experience in maintenance planning, CMMS administration, or facilities operations.
  • Experience working in a GMP-regulated environment (biotech, pharmaceutical, or similar) preferred.
  • Direct experience administering a CMMS, with Blue Mountain RAM (BMRAM) strongly preferred due to its use as the organization's primary system. Experience with comparable systems, including IBM Maximo or similar enterprise platforms, is acceptable.
  • Experience with maintenance planning, calibration programs, and contractor coordination. Strong working knowledge of CMMS systems and maintenance planning processes.
  • Understanding of preventive maintenance, calibration practices, and asset reliability concepts.
  • Ability to maintain accurate, compliant documentation in a regulated environment.
  • Strong analytical skills with the ability to interpret data and identify improvement opportunities.
  • Effective organizational and time management skills; ability to manage multiple priorities.
  • Strong written and verbal communication skills.
  • Ability to work independently and collaboratively within cross-functional teams.
  • Demonstrated commitment to safety, quality, and continuous improvement.

Neurotech Pharmaceuticals provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

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