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Remote Batch Monitoring Jobs in Massachusetts (NOW HIRING)

Sr. Engineer, Drug Product

Cambridge, MA · On-site +1

$130K - $150K/yr

... monitoring, and leading technical assessments for deviations, investigations, and process ... Review executed batch records, deviations, process data, and analytical results to confirm process ...

Data Engineer with AI - Remote

Boston, MA · On-site +1

$124K - $149K/yr

What you'll do * Design, build, and maintain batch/streaming pipelines in Python + PySpark on ... MLflow , feature stores, model deployment/monitoring; familiarity with LLM workflows (embeddings ...

Data Engineer (Remote)

Canton, MA · On-site +1

$121K - $145K/yr

Implement monitoring, alerts, and testing of data pipeline performance, data quality metrics, and ... batch/real-time scoring) * Continually improve ongoing reporting and analytics, automating or ...

Data Engineer (Remote)

Canton, MA · On-site +1

$121K - $145K/yr

Implement monitoring, alerts, and testing of data pipeline performance, data quality metrics, and ... batch/real-time scoring) * Continually improve ongoing reporting and analytics, automating or ...

Systems Integration Architect

Lakeville, MA · On-site +1

$104K - $143K/yr

We are open to remote candidates. The Systems Integration Architect is responsible for designing ... event-based, batch) • Develop detailed technical designs, specifications, and interface ...

Systems Integration Architect

Lakeville, MA · On-site +1

$104K - $143K/yr

We are open to remote candidates.The Systems Integration Architect is responsible for designing ... event-based, batch) • Develop detailed technical designs, specifications, and interface ...

Systems Integration Architect

Lakeville, MA · On-site +1

$104K - $143K/yr

We are open to remote candidates. The Systems Integration Architect is responsible for designing ... based, batch) Develop detailed technical designs, specifications, and interface documentation ...

... g., batch inference, quantization) to ensure models run efficiently in production environments ... Monitor Production Performance: Help build and maintain dashboards to monitor model health, data ...

... g., batch inference, quantization) to ensure models run efficiently in production environments ... Monitor Production Performance: Help build and maintain dashboards to monitor model health, data ...

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Showing results 1-20

Remote Batch Monitoring information

What is the difference between Remote Batch Monitoring vs Remote Data Entry Clerk?

AspectRemote Batch MonitoringRemote Data Entry Clerk
Required CredentialsBasic technical skills, familiarity with monitoring softwareHigh school diploma, data entry experience
Work EnvironmentMonitoring systems, analyzing batch processes remotelyInputting data into databases or spreadsheets remotely
Industry UsageManufacturing, logistics, ITHealthcare, finance, administrative sectors
Common Search IntentMonitoring batch processes remotelyEntering data from home

Remote Batch Monitoring involves overseeing and analyzing batch processes in real-time using specialized software, primarily in manufacturing or logistics. In contrast, Remote Data Entry Clerks focus on inputting data into systems from home, often in administrative or healthcare settings. While both roles are remote and require attention to detail, they differ in technical requirements and industry applications.

What are the key skills and qualifications needed to thrive as a Remote Batch Monitoring Specialist, and why are they important?

To thrive as a Remote Batch Monitoring Specialist, you need strong analytical skills, attention to detail, and a basic understanding of IT operations, often supported by a degree in computer science or related experience. Familiarity with batch processing tools such as IBM Tivoli Workload Scheduler, Control-M, or Automic, as well as ticketing systems like ServiceNow, is typically required. Excellent problem-solving abilities, clear communication, and the ability to remain calm under pressure are crucial soft skills. These skills and qualifications are vital to ensure timely issue resolution, minimize system downtime, and maintain the smooth operation of critical business processes.

What are some common challenges faced in a Remote Batch Monitoring role, and how can they be managed?

One of the main challenges in Remote Batch Monitoring is responding promptly to system alerts and resolving issues without direct access to on-site resources. Effective communication with IT teams and clear documentation of incidents are essential in this remote environment. Familiarity with monitoring tools, strong analytical skills, and the ability to prioritize tasks help manage multiple batch jobs efficiently. Building a routine for regular status checks and collaborative problem-solving ensures smoother operations and minimizes downtime.

What is remote batch monitoring?

Remote batch monitoring involves overseeing and managing batches of automated processes or jobs from a location outside of the physical data center, usually via secure online tools. Professionals in this role monitor the execution of scheduled tasks, check for errors or delays, and ensure the smooth running of critical business operations. This job is essential for organizations with complex IT environments that rely on batch processing for tasks like data backups, report generation, and large-scale data transfers.
What are popular job titles related to Remote Batch Monitoring jobs in Massachusetts? For Remote Batch Monitoring jobs in Massachusetts, the most frequently searched job titles are:
What cities in Massachusetts are hiring for Remote Batch Monitoring jobs? Cities in Massachusetts with the most Remote Batch Monitoring job openings:

Sr. Engineer, Drug Product

Sail Biomedicines

Cambridge, MA • On-site, Remote

$130K - $150K/yr

Other

Posted 18 days ago


Job description

Position Summary

We are seeking an Engineer / Scientist to support drug product process development, process characterization, technology transfer, and manufacturing support for targeted lipid nanoparticle (tLNP) drug product processes. This role will focus on transferring complex LNP manufacturing processes to CDMOs, building and maintaining process models, supporting scale-up and process performance monitoring, and leading technical assessments for deviations, investigations, and process improvements.

The ideal candidate has hands-on experience with biologics, nanoparticle, RNA, sterile drug product, or advanced therapy manufacturing processes and is comfortable working across process development, analytical data, manufacturing execution, and quality systems.

Key Responsibilities

Process Development

  • Support process optimization and characterization activities for LNP formulation, TFF, mAb sterile filtration, and final fill.
  • Support definition and refinement of CPPs, KPPs, CMAs, IPCs, IPTs, and release-relevant process controls.
  • Collaborate with Analytical Development, Quality, Manufacturing, Supply Chain, Regulatory, and external partners to ensure process knowledge is captured and applied consistently.

Technology Transfer to CDMOs

  • Lead LNP/tLNP drug product unit operations to external manufacturing partners, including formulation, TFF/UF-DF, conjugation, sterile filtration, and final fill.
  • Role will communicate and align internal process knowledge to CDMO's through development of process descriptions and ensure alignment on CPPs, KPP, CMAs, equipment fit, single-use assembly design, and hold times. Review documentation from CDMOs surrounding batch execution at all relevant scales.
  • Review executed batch records, deviations, process data, and analytical results to confirm process performance and identify improvement opportunities.
  • Provide person-in-plant or remote technical support

Process Modeling & Data Analysis

  • Develop and maintain process models for mass balance, IPCs/IPTs, and process parameters. Use process models to support scale-up, tech transfer, batch planning, deviation impact assessments, and manufacturing readiness.
  • Support continued process verification by identifying trends, process drifts, and relationships between process inputs and product quality attributes.

Required Qualifications

  • BS with 6+ years of relevant experience or MS with 4+ years of relevant experience. Advanced degree in Chemical Engineering, Bioengineering, Pharmaceutical Sciences, or related field.
  • Experience in process development, manufacturing sciences, technical operations, or GMP manufacturing support.
  • Experience with biologics, RNA, LNPs, nanoparticles, sterile drug product, vaccines, cell/gene therapy, or other complex parenteral products.
  • Experience supporting CDMO manufacturing campaigns, engineering runs, GMP batches, GLP tox batches, or clinical supply manufacturing.
  • Ability to analyze process data and build mass balance or process models using Excel, JMP, Python, MATLAB, Spotfire, or similar tools.
  • Strong technical writing skills with experience authoring technical reports, deviation assessments, process descriptions, or transfer documentation.
  • Ability to work cross-functionally with internal teams and external CDMOs in a fast-paced development environment.

Preferred Qualifications

  • Experience with process risk assessments, FMEA, continued process verification, process characterization, or control strategy development.
  • Familiarity with GMP documentation, change control, CAPA, deviation systems, and regulatory expectations for biologics or sterile drug products.

Salary Range: $130,000 - $150,000

Sail Biomedicines is an Equal Opportunity Employer. Sail does not discriminate based on race, religion, color, sex, gender identity, sexual orientation, age, national origin, veteran status, or any other status protected under federal, state, or local law.