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Lims Remote Jobs in New York (NOW HIRING)

Sr MES Engineer - PAS-X (Remote)

Raritan, NJ · Remote

$106K - $137K/yr

Support system integration with ERP, LIMS, automation (PLC/SCADA), historians, and other manufacturing systems. * Participate in FAT, SAT, commissioning, qualification, and validation activities to ...

Lims Remote information

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$91.4K

$139K

$187.1K

How much do lims remote jobs pay per year?

As of Aug 17, 2026, the average yearly pay for lims remote in New York is $138,976.00, according to ZipRecruiter salary data. Most workers in this role earn between $119,200.00 and $157,000.00 per year, depending on experience, location, and employer.

What is a Lims Remote?

A LIMS Remote job involves working with a Laboratory Information Management System (LIMS) while operating remotely. LIMS professionals manage, configure, and support software used by laboratories to track samples, manage workflows, and ensure compliance. Responsibilities may include data analysis, system customization, troubleshooting, and user training. These roles are common in pharmaceutical, healthcare, environmental, and food testing industries. Remote LIMS jobs require strong technical, analytical, and communication skills to collaborate with onsite teams.

What does a Lims Remote do?

A typical day for a LIMS Remote professional involves monitoring and troubleshooting laboratory information systems, responding to user support requests, configuring system settings, and ensuring data integrity and regulatory compliance. You will often coordinate with on-site lab staff, IT departments, and sometimes software vendors to resolve issues and implement new features. Most of your communication and collaboration will be done via remote tools such as email, video calls, and ticketing systems. This remote format provides flexibility while requiring strong self-management and clear communication skills to maintain productivity and positive relationships with team members.

What are the key skills and qualifications needed to thrive in the Lims Remote position, and why are they important?

To thrive as a LIMS Remote specialist, you need expertise in laboratory workflows, data management, and a solid understanding of Laboratory Information Management Systems (LIMS), often supported by a degree in life sciences, IT, or a related field. Familiarity with major LIMS software platforms (such as LabWare, STARLIMS, or Thermo Fischer), database management, and relevant industry certifications is highly advantageous. Strong problem-solving, remote communication skills, and attention to detail are essential soft skills for this position. These skills ensure efficient remote support, accurate data handling, and effective collaboration with laboratory and IT teams across various locations.

What are the most commonly searched types of Lims jobs in New York?

The most popular types of Lims jobs in New York are:

What are popular job titles related to Lims Remote jobs in New York?

For Lims Remote jobs in New York, the most frequently searched job titles are:

What cities in New York are hiring for Lims Remote jobs?

Cities in New York with the most Lims Remote job openings:

Infographic showing various Lims Remote job openings in New York as of August 2026, with employment types broken down into 85% Full Time, 5% Part Time, 1% Temporary, 8% Contract, and 1% Nights. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $138,976 per year, or $66.8 per hour.

Sr MES Engineer - PAS-X (Remote)

Inteldot

Raritan, NJ • Remote

$106K - $137K/yr

Full-time

Posted 18 days ago


Job description

Position Overview

We are seeking an experienced Senior MES Engineer with extensive expertise in Werum PAS-X Manufacturing Execution System (MES) implementations within regulated pharmaceutical and biotechnology manufacturing environments. This role will be responsible for designing, configuring, deploying, and supporting PAS-X solutions that enable digital manufacturing, electronic batch records (EBR), and compliant shop floor execution while ensuring alignment with business, manufacturing, and regulatory requirements.

Key Responsibilities
  • Lead the design, configuration, implementation, and support of Werum PAS-X MES solutions for pharmaceutical manufacturing operations.
  • Collaborate with Manufacturing, Process Engineering, Quality, Validation, Automation, and IT teams to translate business and process requirements into MES functional solutions.
  • Configure PAS-X Master Batch Records (MBRs), workflows, electronic forms, material management, equipment integration, and process parameters.
  • Support end-to-end MES deployment activities, including requirements gathering, solution design, configuration, testing, commissioning, and production support.
  • Develop and review functional specifications, design documents, configuration specifications, and technical documentation.
  • Troubleshoot MES issues, perform root cause analysis, and implement sustainable corrective actions.
  • Support system integration with ERP, LIMS, automation (PLC/SCADA), historians, and other manufacturing systems.
  • Participate in FAT, SAT, commissioning, qualification, and validation activities to ensure regulatory compliance.
  • Ensure MES solutions comply with GxP requirements, 21 CFR Part 11, Annex 11, and Data Integrity principles.
  • Lead change requests, system enhancements, software upgrades, and continuous improvement initiatives.
  • Provide technical leadership during technology transfers, new product introductions, and commercial manufacturing support.
  • Mentor junior engineers and provide technical guidance to project teams and business stakeholders.
Required Qualifications
  • Bachelor's degree in Engineering, Computer Science, Information Technology, or related technical discipline.
  • 7+ years of experience implementing and supporting Manufacturing Execution Systems within regulated pharmaceutical or biotechnology environments.
  • 5+ years of hands-on experience with Werum PAS-X MES, including system configuration and deployment.
  • Strong understanding of pharmaceutical manufacturing processes, electronic batch records (EBR), and digital manufacturing concepts.
  • Experience configuring PAS-X Master Batch Records (MBRs), workflows, process logic, and manufacturing recipes.
  • Working knowledge of GAMP 5, FDA 21 CFR Part 11, Annex 11, and Data Integrity requirements.
  • Experience supporting commissioning, qualification, validation, and production go-live activities.
  • Strong analytical and problem-solving skills with the ability to troubleshoot complex MES issues.
  • Excellent communication, documentation, and stakeholder management skills.
  • Ability to manage multiple priorities in a fast-paced manufacturing environment.
Preferred Qualifications
  • Experience supporting biologics, sterile manufacturing, cell & gene therapy, or vaccine production.
  • Experience integrating PAS-X with SAP ERP, LIMS, DeltaV, PI Historian, OPC, or other manufacturing systems.
  • Knowledge of ISA-95 manufacturing integration standards.
  • Experience with software development lifecycle (SDLC), Agile, Waterfall, or Hybrid project methodologies.
  • Previous participation in global or multi-site PAS-X implementations.
  • Experience supporting regulatory inspections and customer audits.
  • Knowledge of serialization, track-and-trace, and digital manufacturing initiatives.
  • Experience with cloud or hybrid manufacturing IT architectures is a plus.