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Signal Inspector Jobs in Boston, MA (NOW HIRING)

BETA GROUP INC

Senior Traffic Engineer

Norwood, MA · On-site

$106K - $160K/yr

Proficiency with traffic signal design * Must be able to collect field data and measurements including but not limited to roadway, sidewalk, and utility assets; and perform asset inspections * Must ...

BETA Group, Inc

Senior Traffic Engineer

Norwood, MA · On-site

$106K - $160K/yr

Proficiency with traffic signal design * Must be able to collect field data and measurements including but not limited to roadway, sidewalk, and utility assets; and perform asset inspections * Must ...

BETA Group, Inc.

Senior Traffic Engineer

Norwood, MA · Hybrid

$106K - $160K/yr

Proficiency with traffic signal design * Must be able to collect field data and measurements including but not limited to roadway, sidewalk, and utility assets; and perform asset inspections * Must ...

Massgeneralbrigham

Licensed Electrician

Boston, MA · On-site

$49.80/hr

What You'll Do - Install and maintain circuits for heat, power, lighting, motors, signals, and alarm systems. - Perform inspections and testing of motors, signal and alarm systems, electrical ...

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All JobsSignal Inspector JobsSignal Inspector Jobs in Boston, MA

Signal Inspector information

See Boston, MA salary details

$22

$49

$67

How much do signal inspector jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for signal inspector in Boston, MA is $49.78, according to ZipRecruiter salary data. Most workers in this role earn between $45.29 and $66.78 per hour, depending on experience, location, and employer.

What is a signal inspector?

A Signal Inspector is responsible for inspecting, testing, and maintaining railroad or transit signal systems to ensure they operate safely and comply with regulations. They examine signal equipment, wiring, switches, and related components for defects or malfunctions. Their duties often include troubleshooting issues, performing routine maintenance, and documenting inspections. Signal Inspectors work closely with maintenance and engineering teams to ensure the reliability of signaling systems. This role is critical for ensuring the safe and efficient movement of trains or transit vehicles.

What are the typical daily responsibilities of a signal inspector?

Signal Inspectors typically spend their days inspecting, testing, and maintaining railway signaling equipment such as switches, relays, and track circuits. They ensure all systems are functioning correctly and in compliance with safety standards, often working outdoors in various weather conditions and locations along the rail network. Collaboration with maintenance crews, engineers, and supervisors is common, as is the need to keep detailed records of inspections and repairs. This hands-on role can require travel and irregular hours, but it offers the satisfaction of playing a critical role in transportation safety.

What are the key skills and qualifications needed to thrive as a signal inspector, and why are they important?

To thrive as a Signal Inspector, you need a strong understanding of railway signaling systems, safety regulations, and electrical/mechanical troubleshooting, often supported by relevant vocational training or certification. Familiarity with signal testing equipment, diagnostic tools, and compliance with industry-specific safety protocols like FRA regulations is essential. Attention to detail, problem-solving abilities, and clear communication are vital soft skills that set top candidates apart. These skills ensure the reliability and safety of train operations, helping prevent accidents and costly downtime.

What are popular job titles related to Signal Inspector jobs in Boston, MA?

For Signal Inspector jobs in Boston, MA, the most frequently searched job titles are:

What job categories do people searching Signal Inspector jobs in Boston, MA look for?

The top searched job categories for Signal Inspector jobs in Boston, MA are:

Signal Inspector jobs near you
Infographic showing various Signal Inspector job openings in Boston, MA as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $103,546 per year, or $49.8 per hour.

Director, Drug Safety & Pharmacovigilance Scientist

Waltham, MA • On-site

Dyne Therapeutics
Biotechnology Research and Development • 11 - 50 employees
Learn more about Dyne Therapeuticsexternal

Full-time

Posted 25 days ago

Job description

Role Summary:

The Director, Drug Safety & Pharmacovigilance Scientist provides strategic and scientific leadership for safety surveillance, signal detection, benefit-risk evaluation, and risk management activities across Dyne's development programs. This role characterizes and communicates the safety profiles of investigational therapies, contributes to regulatory safety strategies and submissions, and ensures pharmacovigilance activities are conducted in compliance with applicable global regulations and company procedures. The Director collaborates across Clinical Development, Clinical Operations, Regulatory Affairs, Medical Affairs, Biostatistics, Data Management, Quality, and external partners to support proactive safety oversight and informed program decision-making. The role applies expert scientific judgment to complex safety data, drives continuous improvement of pharmacovigilance processes, and contributes to a culture focused on patient safety, scientific excellence, and operational rigor.
 
This position is based in Waltham, MA.

Primary Responsibilities Include:

Safety Surveillance, Signal Detection & Risk Management
  • Conduct and lead safety surveillance activities for assigned clinical development programs, including ongoing review of aggregate safety data and identification of emerging safety trends.
  • Lead signal detection, signal evaluation, risk classification, benefit-risk assessment, and risk management activities across the product lifecycle.
  • Review, analyze, and interpret safety information from clinical studies, individual case safety reports (ICSRs), nonclinical studies, scientific literature, and other relevant sources.
  • Support medical and scientific review of ICSRs, including evaluation of case narratives, MedDRA coding, causality assessments, expectedness determinations, company comments, and follow-up activities.
  • Develop safety monitoring strategies and risk mitigation plans that support effective benefit-risk evaluation.
Safety Reporting, Documentation & Regulatory Support
  • Author and contribute to safety signal assessment reports, aggregate safety reports, and safety analyses, including DSURs, PSURs/PBRERs, and responses to health authority safety inquiries.
  • Contribute to safety-related sections of clinical and regulatory documents, including protocols, informed consent forms, investigator brochures, reference safety information, clinical study reports, integrated safety summaries, briefing documents, and regulatory submissions.
  • Prepare and present safety data, analyses, recommendations, and risk management strategies to cross-functional teams and governance committees.
  • Maintain complete, accurate, and inspection-ready documentation of safety surveillance activities, safety decisions, and associated deliverables.
Cross-Functional Leadership & Safety Governance
  • Partner with Clinical Development, Clinical Operations, Regulatory Affairs, Medical Affairs, Biostatistics, Data Management, Quality, and external vendors to integrate safety considerations into study conduct and program strategy.
  • Participate in safety governance forums and cross-functional program teams, providing scientific insight and recommendations to support decision-making.
  • Influence safety-related discussions across development programs through clear communication of complex safety data and benefit-risk considerations.
  • Foster a culture of collaboration, accountability, scientific excellence, and continuous improvement across Drug Safety & Pharmacovigilance and the broader organization.
Pharmacovigilance Operations, Compliance & Continuous Improvement
  • Develop, maintain, and enhance pharmacovigilance SOPs, work instructions, templates, and processes in alignment with global regulatory requirements and industry best practices.
  • Provide pharmacovigilance training and guidance to internal colleagues and cross-functional partners on safety surveillance, reporting requirements, documentation practices, and inspection readiness.
  • Support pharmacovigilance vendor oversight activities, including review of deliverables, quality assessments, issue escalation, and process improvements.
  • Monitor evolving pharmacovigilance regulations, guidance, and industry standards and implement appropriate process enhancements to ensure continued compliance and operational effectiveness

Education and Skills Requirements:

  • Advanced degree in life sciences, health sciences, pharmacy, medicine, nursing, or a related discipline required; MD, PharmD, PhD, or equivalent advanced degree preferred.
  • 10+ years of relevant pharmacovigilance, drug safety, clinical development, or related biotechnology or pharmaceutical industry experience.
  • Demonstrated expertise in safety surveillance, signal detection, signal evaluation, aggregate safety review, benefit-risk assessment, and risk management for clinical-stage development programs.
  • Experience authoring or contributing to DSURs, PSURs/PBRERs, safety signal assessments, regulatory safety responses, and safety-related sections of clinical or regulatory documents.
  • Deep knowledge of global pharmacovigilance regulations and guidance, including FDA, EMA, ICH, GVP, GCP, and applicable safety reporting requirements.
  • Experience reviewing, analyzing, and interpreting clinical and safety data, including ICSRs, aggregate datasets, safety listings, tables, figures, and data visualizations.
  • Working knowledge of safety databases, MedDRA coding, ICSR workflows, safety management plans, and pharmacovigilance vendor oversight practices.
  • Demonstrated ability to apply sound scientific and medical judgment to complex safety information and communicate implications effectively to diverse stakeholders.
  • Strong analytical, problem-solving, technical writing, presentation, and project management skills.
  • Ability to manage multiple priorities and deliver high-quality work in a dynamic, fast-paced environment.
  • Proven success collaborating within matrixed organizations and influencing stakeholders without direct authority.
  • Strong attention to detail, accountability, integrity, and commitment to patient safety.
  • Experience in rare disease, neuromuscular disease, or clinical-stage biotechnology is preferred.

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