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In Lims Validation Jobs in Edison, NJ (NOW HIRING)

IBX

Cell Services Supervisor - Second Shift

Piscataway, NJ · On-site

$15 - $19/hr

... in the lab for clients and other stakeholders o Help build, validate and implement SOPs for new ... LIMS. o Ordering supplies and ensuring that stock inventories are maintained for all essential ...

Teachercool

Veeva Quality Lead

Jersey City, NJ · On-site

... system validation activities (URS, IQ, OQ, PQ) in accordance with 21 CFR Part 11 and Annex 11 ... visibility LIMS & Laboratory Quality ● Apply working knowledge of Laboratory Information ...

Inteldot

Sr MES Engineer - PAS-X

Raritan, NJ · On-site +1

$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 ...

Inteldot

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 ...

Inteldot

Sr MES Engineer - PAS-X

Raritan, NJ · On-site

$140 - $200/hr

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

Inteldot

Sr MES Engineer - PAS-X

Raritan, NJ · On-site +1

$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 ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

... LIMS, Analytical Chemistry, Drug Product, Manufacturing, Validation Benefits (via System One ... leaders in delivering outsourced services and workforce solutions across North America. We help ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

... LIMS, Analytical Chemistry, Drug Product, Manufacturing, Validation Benefits (via System One ... leaders in delivering outsourced services and workforce solutions across North America. We help ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

... LIMS, Analytical Chemistry, Drug Product, Manufacturing, Validation Benefits (via System One ... leaders in delivering outsourced services and workforce solutions across North America. We help ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

... LIMS, Analytical Chemistry, Drug Product, Manufacturing, Validation Benefits (via System One ... leaders in delivering outsourced services and workforce solutions across North America. We help ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

... LIMS, Analytical Chemistry, Drug Product, Manufacturing, Validation Benefits (via System One ... leaders in delivering outsourced services and workforce solutions across North America. We help ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

... LIMS, Analytical Chemistry, Drug Product, Manufacturing, Validation Benefits (via System One ... leaders in delivering outsourced services and workforce solutions across North America. We help ...

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Showing results 21-40

All JobsIn Lims Validation JobsIn Lims Validation Jobs in Edison, NJ

In Lims Validation information

See Edison, NJ salary details

$23

$53

$80

How much do in lims validation jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for in lims validation in Edison, NJ is $53.83, according to ZipRecruiter salary data. Most workers in this role earn between $40.82 and $65.43 per hour, depending on experience, location, and employer.

What is the difference between In Lims Validation vs Laboratory Technician?

AspectIn Lims ValidationLaboratory Technician
CertificationsGMP, GLP, Validation certificationsTypically relevant certifications include Lab Technician or related training
Work EnvironmentQuality assurance, validation labs, regulated industriesLaboratories performing tests and experiments
Job FocusEnsuring LIMS systems meet regulatory standardsPerforming tests, recording data, maintaining lab equipment

In Lims Validation professionals focus on validating Laboratory Information Management Systems to ensure compliance with industry standards, while Laboratory Technicians perform routine testing and data collection. Both roles are essential in regulated labs but differ in scope and responsibilities.

How to validate a LIMS system?

Validating a LIMS (Laboratory Information Management System) involves developing a validation plan, performing installation and operational qualification, and documenting each phase to ensure the system meets user requirements and regulatory standards. It typically includes testing data integrity, system security, and functionality, often supported by validation protocols and traceability. Familiarity with regulatory guidelines such as 21 CFR Part 11 is essential for compliance.

What are popular job titles related to In Lims Validation jobs in Edison, NJ?

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In Lims Validation jobs near you
Infographic showing various In Lims Validation job openings in Edison, NJ as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 8% Part Time, 3% Temporary, and 5% Contract. Highlights an 84% Physical, 5% Hybrid, and 11% Remote job distribution, with an average salary of $111,965 per year, or $53.8 per hour.

QMS & SAP Validation Analyst (Contract)

Kashiv Biosciences LLC

Piscataway, NJ • On-site

$65 - $75/hr

Contractor

Re-posted 19 days ago

Job description

Job Type
Contract
Description
Position Type: Contractor / Consultant - FTC (6-9 Months with possible extension)
Location: Piscataway, NJ (onsite - physical presence required) - OR - Chicago, IL (onsite - physical presence required)
Reports To: Sr. Director of IT
Rate: $65-$75/hour, not overtime eligible
Work Authorization: Must be authorized to work in the U.S. without sponsorship, now or in the future
Position Summary
We are seeking a Validation Analyst to support validation of our Quality Management System (MasterControl) and SAP implementation (QM, Materials Management, Production modules). This role works under the direction of a senior validation lead and partners with Quality, IT, and business functions to deliver validation artifacts in compliance with 21 CFR Part 11, GxP, and EMA expectations.
Essential Duties & Responsibilities
  • Support validation of MasterControl QMS - authoring and executing IQ/OQ/PQ protocols, traceability matrices, and validation summary reports
  • Support SAP implementation and validation activities across QM, MM, and PP modules, including test script authoring and execution under senior oversight
  • Contribute to risk assessments, data integrity assessments, and change control documentation
  • Liaise with QA, IT, business process owners, and external SAP implementation partners
  • Support periodic review and maintenance of validated state for assigned systems
  • Assist in audit and inspection readiness for MasterControl and SAP

Requirements
Position Requirements and Qualifications
  • Bachelor's degree in Life Sciences, Engineering, IT, or a lab-based role in life sciences with 3+ years of relevant experience; OR Master's degree with 1-2 years of relevant experience
  • Prior exposure to CSV activities in a GxP-regulated environment
  • Working understanding of 21 CFR Part 11, EU Annex 11, and EMA guidance
  • Experience authoring or executing validation protocols

Experience:
  • Exposure to MasterControl QMS (validation, administration, or end-user)
  • Exposure to SAP (any module, ideally QM, MM, or PP) in a GxP environment
  • Familiarity with GAMP 5 principles
  • Experience with ALCOA+ data integrity principles
  • Prior experience supporting enterprise system implementations in pharma, biotech, or medical device

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
  • Prior experience and acting as a liaison across IT, Quality, Lab, and ERP (SAP Preferred) and related systems.

Work Environment & Physical Demands: •
  • This is an on-site position at our Piscataway, NJ location - OR - Chicago, IL location•
  • 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.

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