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Senior Labware Lims Developer Jobs in New York (NOW HIRING)

supremesoft

CSV Validation QC Engineer

Jersey City, NJ · On-site

Preferred Skills • Experience in Labware, Empower LIMS systems • Experience in validating Lab equipments Job Roles/Responsibilities • Act as Validation and Qualification Lead on a large global ...

Merck & Co.

Technical Product Manager

Rahway, NJ · On-site

$117 - $184.20/hr

Bachelor's degree in Life Sciences, Biomedical Engineering, Chemical Engineering, Computer Science ... Experience with tools like LIMS (e.g., Labware), ELN (e.g., Benchling), Apache Kafka, Spark ...

Cellares

Senior Process Engineer

Bridgewater, NJ · On-site

$90K - $210K/yr

Position Summary We are seeking an innovative and highly motivated Senior Process Engineer on our ... LIMS * Work with our software team to provide feedback on internal software solutions * Provide ...

Cellares

Senior Process Engineer

Bridgewater, NJ · On-site

$90K - $210K/yr

Position Summary We are seeking an innovative and highly motivated Senior Process Engineer on our ... LIMS * Work with our software team to provide feedback on internal software solutions * Provide ...

Cellares

Senior Process Engineer

Bridgewater, NJ · On-site

$90K - $210K/yr

Position Summary We are seeking an innovative and highly motivated Senior Process Engineer on our ... LIMS * Work with our software team to provide feedback on internal software solutions * Provide ...

Weston Solutions

Senior Laboratory Chemist

Edison, NJ · On-site

$88K - $110K/yr

Weston is seeking an experienced Senior Laboratory Chemist to support the EPA Response Engineering ... Experience working with Laboratory Information Management Systems (LIMS) * Understanding of ...

PDI (NY)

Senior R&D Data Scientist

Woodcliff Lake, NJ · On-site

Chemistry or Chemical Engineering * Computational Chemistry/Physics * Bioinformatics Required ... Experience with LIMS, ELN, or scientific informatics platforms * Knowledge of 21 CFR Part 11, audit ...

PDI

Senior R&D Data Scientist

Woodcliff Lake, NJ · On-site

Chemistry or Chemical Engineering * Computational Chemistry/Physics * Bioinformatics Required ... Experience with LIMS, ELN, or scientific informatics platforms * Knowledge of 21 CFR Part 11, audit ...

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Senior Labware Lims Developer information

What are the typical collaboration points between a Senior Labware LIMS Developer and laboratory staff during system enhancements?

A Senior Labware LIMS Developer frequently collaborates with laboratory staff to gather requirements, validate workflows, and ensure that system enhancements align with actual lab processes. This involves conducting user interviews, participating in design reviews, and providing training or support during user acceptance testing. Regular communication helps bridge gaps between technical capabilities and lab needs, resulting in solutions that improve efficiency and data integrity within the lab environment.

What are the key skills and qualifications needed to thrive as a Senior Labware LIMS Developer?

To thrive as a Senior Labware LIMS Developer, you need expertise in software development, database management, and extensive experience with LabWare LIMS, often supported by a degree in computer science, bioinformatics, or a related field. Proficiency in LabWare scripting, SQL, JavaScript, and familiarity with laboratory workflows and compliance standards like GxP are typically required, along with relevant certifications. Strong analytical thinking, problem-solving, and effective communication skills enable you to translate complex lab requirements into robust technical solutions. These competencies are essential for delivering reliable, scalable LIMS implementations that support scientific operations and regulatory compliance.

What is the difference between Senior Labware Lims Developer vs Labware Lims Analyst?

AspectSenior Labware Lims DeveloperLabware Lims Analyst
CredentialsTypically requires a degree in life sciences, computer science, or related field; certifications in Labware LIMS are commonOften holds similar degrees; certifications in Labware LIMS may be preferred but less emphasized
Work EnvironmentFocuses on software development, customization, and integration within laboratory settingsPrimarily analyzes data, supports system users, and ensures data integrity in labs
Employer & Industry UsageUsed by biotech, pharma, and clinical labs for system development and maintenanceEmployed in similar industries for data analysis and system support roles

The Senior Labware Lims Developer primarily focuses on developing and customizing LIMS software, while the Labware Lims Analyst concentrates on data analysis and system support. Both roles require relevant certifications and work within laboratory environments, but their core responsibilities differ significantly.

What is a Senior Labware LIMS Developer?

A Senior Labware LIMS Developer is an experienced software professional who specializes in designing, developing, and maintaining Laboratory Information Management Systems (LIMS) using LabWare software. They work closely with laboratory staff and IT teams to customize and optimize LIMS solutions, ensuring efficient data management and compliance with industry regulations. These developers often lead complex projects, troubleshoot technical issues, and mentor junior team members to enhance laboratory workflows.
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What are popular job titles related to Senior Labware Lims Developer jobs in New York? For Senior Labware Lims Developer jobs in New York, the most frequently searched job titles are:
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Senior Labware Lims Developer jobs near you
Infographic showing various Senior Labware Lims Developer job openings in New York as of June 2026, with employment types broken down into 74% Full Time, and 26% Contract. Highlights an 100% In-person job distribution.

Computer System Validation (CSV) Engineer

Kashiv Biosciences LLC

Piscataway, NJ • On-site

Full-time

Re-posted 8 days ago

Job description

Job Type
Full-time
Description
Position Type: Full-time Employee (FTE)
Location: Piscataway, NJ (onsite - physical presence required)
Reports To: Sr. Director of IT
Work Authorization: Must be authorized to work in the U.S. without sponsorship, now or in the future
Position Summary
We are seeking an experienced CSV Engineer to support validation activities across a broad portfolio of regulated systems, including laboratory instrumentation, engineering and manufacturing equipment, and enterprise platforms. This role serves as a liaison across Quality, IT, Laboratory, and Manufacturing functions, ensuring systems are validated and maintained in compliance with 21 CFR Part 11, GxP, and EMA requirements.
Essential Duties & Responsibilities
  • Plan, author, and execute validation deliverables (VP, URS, FS, DS, IQ/OQ/PQ, Traceability Matrix, Validation Summary Reports) across assigned systems
  • Support CSV activities across lab instruments (HPLC, GC, spectrophotometers, balances, etc.), engineering and manufacturing equipment, and enterprise systems including Caliber LIMS, SAP, and BMRAM
  • Partner with system owners, QA, and IT to maintain systems in a validated state through change control and periodic review
  • Execute risk assessments and data integrity assessments aligned with ALCOA+ principles
  • Support audits, inspections, CAPA investigations, and deviations related to computerized systems
  • Collaborating with senior validation leads and SMEs to drive consistent practices across sites

Requirements
Position Requirements and Qualifications
  • Bachelor's degree in Life Sciences, Engineering, or IT; OR equivalent laboratory experience in a life sciences environment
  • Minimum 5 years of CSV experience in a GxP-regulated environment
  • Working knowledge of 21 CFR Part 11, EU Annex 11, and EMA guidance
  • Hands-on experience authoring and executing IQ/OQ/PQ protocols
  • Experience validating at least two of: laboratory instruments, engineering/manufacturing equipment, LIMS, SAP, or CMMS/calibration platforms (e.g., BMRAM)

Experience:
  • Minimum 5 years of CSV experience in a GxP-regulated environment
  • Working knowledge of 21 CFR Part 11, EU Annex 11, and EMA guidance
  • Hands-on experience authoring and executing IQ/OQ/PQ protocols
  • Experience validating at least two of: laboratory instruments, engineering/manufacturing equipment, LIMS, SAP, or CMMS/calibration platforms (e.g., BMRAM)

Specialized Knowledge and Skills:
  • Familiarity with GAMP 5 principles and risk-based validation
  • Exposure to Caliber LIMS
  • Exposure to SAP (QM, MM, PP) in a GxP context
  • Experience with BMRAM or equivalent CMMS/calibration systems
  • Prior experience acting as a liaison across IT, Quality, Lab, and Manufacturing teams

Work Environment & Physical Demands:
  • This is an on-site position
  • Must be able to work extended hours or weekend hours, as may be required.

Noise:
  • No extraordinary noise levels.

Standing/Lifting:
  • Very unlikely, but can be able to lift at least 20 lbs.

Visual:
  • No extraordinary requirements.

Stress:
  • High-paced demanding environment to meet ambitious project goals.

Travel:
  • Moderate domestic travel may be required.

Apply