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

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

... LIMS, Analytical Chemistry, Drug Product, Manufacturing, Validation Benefits Medical, Dental ... leaders in delivering outsourced services and workforce solutions across North America. We help ...

Lead Camstar Developer

Raritan, NJ · On-site

$60.50 - $79/hr

... LIMS, Equipment, HMI. * Fair understanding of computer system and manufacturing validations process. * Proficiency in SQL. * Essential skill: CAMSTAR (EIS). * Skills: Camstar (Siemens Opcenter)

Technical Product Manager

Rahway, NJ · On-site

$169K - $195K/yr

LIMS (e.g., Labware), ELN (e.g., Benchling), Apache Kafka, Spark, Databricks, or similar ... without a valid written search agreement in place for this position will be deemed the sole ...

STARLIMS v12 Senior Developer - Remote

Hazlet, NJ · On-site

$56.25 - $74.25/hr

... LIMS solutions in regulated lab environments. The ideal candidate has a track record of extending ... Knowledge of GxP/CSV, validation documentation, and audit readiness. * Exposure to CI/CD, automated ...

... LIMS, spreadsheets, databases - to Uncountable * Write Python scripts and tooling to parse, validate, and transform scientific data files in a wide variety of formats * Work directly with customer ...

Sr Research Scientist 1

Bedminster, NJ · On-site

$110K - $130K/yr

Significant experience in the validation of test methods both from a design and execution ... Experience with electronic data systems (ELN, LIMS) preferred but not required. * Understanding of ...

Showing results 41-60

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?

For In Lims Validation jobs in Edison, NJ, the most frequently searched job titles are:

What job categories do people searching In Lims Validation jobs in Edison, NJ look for?

The top searched job categories for In Lims Validation jobs in Edison, NJ are:

What cities near Edison, NJ are hiring for In Lims Validation jobs?

Cities near Edison, NJ with the most In Lims Validation job openings:

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.

POMS MES Techno-Functional SME

United Airlines

Manhattan, NY

$73K - $174K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 9 days ago


United Airlines rating

7.9

Company rating: 7.9 out of 10

Based on 342 frontline employees who took The Breakroom Quiz

7th of 26 rated airlines


Job description

At Capgemini Engineering, the world leader in engineering services, we bring together a global team of engineers, scientists, and architects to help the world's mostinnovative companies unleash their potential. From autonomous cars to life-saving robots, our digital and software technology experts think outside the box as theyprovide unique R&D and engineering services across all industries. Join us for a career full of opportunities. Where you can make a difference. Where no two days arethe same. 

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Location: Albany, New York OR Remote with travel on need basis

Job Description:

Capgemini is seeking an experienced POMS MES Techno-Functional SME with deep expertise in Manufacturing Execution Systems (MES) within a GxP-regulated pharmaceutical manufacturing environment. The ideal candidate will serve as a trusted advisor and bridge between business stakeholders, manufacturing operations, quality organizations, validation teams, and technical delivery teams to support, enhance, configure, and implement POMS MES solutions across manufacturing sites.

This role requires a combination of strong functional knowledge of pharmaceutical manufacturing processes, hands-on POMS MES expertise, and familiarity with CSV validation and regulatory compliance requirements.

Your Role:

 

Business & Functional Responsibilities:

  • Collaborate with Manufacturing, Quality, Validation, and IT stakeholders to gather, analyze, and document business requirements.
  • Translate business requirements into MES functional specifications, solution designs, and implementation strategies.
  • Lead requirements workshops, discovery sessions, fit-gap analyses, design reviews, and user acceptance testing (UAT).
  • Partner with manufacturing teams to optimize production workflows and leverage POMS MES capabilities to improve operational performance.
  • Drive alignment between MES solutions, manufacturing processes, business objectives, and regulatory requirements.
  • Support process harmonization initiatives across manufacturing sites.
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MES Technical Responsibilities:

  • Configure, support, and enhance POMS MES workflows, electronic batch records (EBR), recipes, and manufacturing execution processes.
  • Support MES module configuration, troubleshooting, and issue resolution activities.
  • Perform root cause analysis and corrective actions for production support issues.
  • Support and review MES integrations with enterprise systems such as ERP, LIMS, Historians, Automation/SCADA, and other manufacturing applications.
  • Review technical specifications, configuration documentation, and implementation deliverables.
  • Assist with system deployments, upgrades, migrations, and release management activities.
  • Provide expertise in electronic batch record execution, deviations management, manufacturing investigations, and exception handling.

 

Validation & Compliance Responsibilities:

  • Support Computer System Validation (CSV) activities throughout the system lifecycle.
  • Author, review, and maintain validation documentation including:
    • User Requirements Specifications (URS), Functional Requirements Specifications (FRS), Design Specifications (DS), Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ)
    • Validation Summary Reports (VSR)
    • Ensure compliance with FDA 21 CFR Part 11, GAMP 5 Guidelines, GMP.
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Your Skills and Experience: 

  • Bachelor's degree in Engineering, Computer Science, Information Technology, Life Sciences, or a related field.
  • 8-12 years of experience in Life Sciences, Pharmaceutical, or Biotech manufacturing environments.
  • 5+ years of hands-on experience supporting or implementing POMS MES solutions.
  • Strong understanding of MES concepts, electronic batch records (EBR), batch execution, manufacturing operations, and production workflows.
  • Experience working in GxP-regulated environments.
  • Solid understanding of pharmaceutical manufacturing processes, validation methodologies, and quality systems.
  • Experience supporting MES implementations, enhancements, upgrades, and production support activities.
  • Ability to review and interpret functional and technical documentation.
  • Strong troubleshooting and analytical problem-solving skills

Preferred Qualifications:

  • Experience with large-scale MES implementation or site rollout programs.
  • Exposure to system integrations involving ERP, LIMS, Historian, SCADA, or automation platforms.
  • Knowledge of ISA-95 manufacturing standards and digital manufacturing architectures.
  • Experience supporting global manufacturing organizations.

The base compensation range for this role in the posted location is $73,000 - $174,000/year.

Capgemini provides compensation range information in accordance with applicable national, state, provincial, and local pay transparency laws. The base compensation range listed for this position reflects the minimum and maximum target compensation Capgemini, in good faith, believes it may pay for the role at the time of this posting. This range may be subject to change as permitted by law.

The actual compensation offered to any candidate may fall outside of the posted range and will be determined based on multiple factors legally permitted in the applicable jurisdiction.

These may include, but are not limited to: Geographic location, Education and qualifications, Certifications and licenses, Relevant experience and skills, Seniority and performance, Market and business consideration, Internal pay equity.

It is not typical for candidates to be hired at or near the top of the posted compensation range.

In addition to base salary, this role may be eligible for additional compensation such as variable incentives, bonuses, or commissions, depending on the position and applicable laws.

Capgemini offers a comprehensive, non-negotiable benefits package to all regular, full-time employees. In the U.S. and Canada, available benefits are determined by local policy and eligibility and may include: 

  • Paid time off based on employee grade (A-F), defined by policy: Vacation: 12-25 days, depending on grade, Company paid holidays, Personal Days, Sick Leave
  • Medical, dental, and vision coverage (or provincial healthcare coordination in Canada)
  • Retirement savings plans (e.g., 401(k) in the U.S., RRSP in Canada)
  • Life and disability insurance
  • Employee assistance programs
  • Other benefits as provided by local policy and eligibility

Important Notice: Compensation (including bonuses, commissions, or other forms of incentive pay) is not considered earned, vested, or payable until it becomes due under the terms of applicable plans or agreements and is subject to Capgemini's discretion, consistent with applicable laws. The Company reserves the right to amend or withdraw compensation programs at any time, within the limits of applicable legislation.

Disclaimers

Capgemini is an Equal Opportunity Employer encouraging inclusion in the workplace. Capgemini also participates in the Partnership Accreditation in Indigenous Relations (PAIR) program which supports meaningful engagement with Indigenous communities across Canada by promoting fairness, accessibility, inclusion and respect.  We value the rich cultural heritage and contributions of Indigenous Peoples and actively work to create a welcoming and respectful environment. All qualified applicants will receive consideration for employment without regard to race, national origin, gender identity/expression, age, religion, disability, sexual orientation, genetics, veteran status, marital status or any other characteristic protected by law.

This is a general description of the Duties, Responsibilities and Qualifications required for this position. Physical, mental, sensory or environmental demands may be referenced in an attempt to communicate the manner in which this position traditionally is performed. Whenever necessary to provide individuals with disabilities an equal employment opportunity, Capgemini will consider reasonable accommodations that might involve varying job requirements and/or changing the way this job is performed, provided that such accommodation does not pose an undue hardship. Capgemini is committed to providing reasonable accommodation during our recruitment process. If you need assistance or accommodation, please reach out to your recruiting contact.

Please be aware that Capgemini may capture your image (video or screenshot) during the interview process and that image may be used for verification, including during the hiring and onboarding process.

Click the following link for more information on your rights as an Applicant in the United States.  http://www.capgemini.com/resources/equal-employment-opportunity-is-the-law

Capgemini is a global business and technology transformation partner, helping organizations to accelerate their dual transition to a digital and sustainable world, while creating tangible impact for enterprises and society. It is a responsible and diverse group of 340,000 team members in more than 50 countries. With its strong over 55-year heritage, Capgemini is trusted by its clients to unlock the value of technology to address the entire breadth of their business needs. It delivers end-to-end services and solutions leveraging strengths from strategy and design to engineering, all fueled by its market leading capabilities in AI, generative AI, cloud and data, combined with its deep industry expertise and partner ecosystem.


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About United Airlines

Sourced by ZipRecruiter

United Airlines is embarking on an exciting journey to become the best airline in aviation history. Our purpose, "Connecting People, Uniting the World," extends beyond transportation, emphasizing our commitment to uplift and create opportunities in the places we serve. With a global presence and diverse workforce, we value inclusivity and are dedicated to hiring tens of thousands of individuals across various roles. Our comprehensive benefits package, including perks like space available travel, parental leave, and 401k, aims to support your well-being and growth.

Industry

Aviation

Company size

10,000+ Employees

Headquarters location

Chicago, IL, US

Year founded

1926

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