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Labware Lims Developer Jobs (NOW HIRING)

AMRI

LIMS Master Data Specialist III

Rensselaer, NY · On-site

$100K - $125K/yr

Associate's or Bachelor's degree in Life Sciences, Engineering, or a related STEM field. * Minimum ... Experience with major LIMS platforms such as LabVantage (preferred), LabWare, or STARLIMS. * Soft ...

Curia, Inc.

LIMS Master Data Specialist III

Rensselaer, NY · On-site

$100K - $125K/yr

Associate's or Bachelor's degree in Life Sciences, Engineering, or a related STEM field. * Minimum ... Experience with major LIMS platforms such as LabVantage (preferred), LabWare, or STARLIMS. * Soft ...

Curia, Inc.

LIMS Master Data Specialist III

Rensselaer, NY · On-site

$100K - $125K/yr

Associate's or Bachelor's degree in Life Sciences, Engineering, or a related STEM field. * Minimum ... Experience with major LIMS platforms such as LabVantage (preferred), LabWare, or STARLIMS. * Soft ...

Syensqo

Lab Technician

Mount Pleasant, TN · On-site

$65K - $70K/yr

... MS Excel, LabWare LIMS, and data collection software. * Participate in the development and ... Interacts regularly with production employees, including Operations Engineers, Operations Manager ...

Syensqo

Lab Technician

Mount Pleasant, TN · On-site

$65K - $70K/yr

... MS Excel, LabWare LIMS, and data collection software. * Participate in the development and ... Interacts regularly with production employees, including Operations Engineers, Operations Manager ...

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Labware Lims Developer information

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$11K

$88.2K

$135.5K

How much do labware lims developer jobs pay per year?

As of Aug 20, 2026, the average yearly pay for labware lims developer in the United States is $88,166.00, according to ZipRecruiter salary data. Most workers in this role earn between $32,000.00 and $120,000.00 per year, depending on experience, location, and employer.

What is a LabWare LIMS developer?

A LabWare LIMS Developer is responsible for configuring, customizing, and maintaining the LabWare Laboratory Information Management System (LIMS) to support laboratory workflows and data management. They work closely with scientists, quality teams, and IT staff to develop and enhance system functionalities, including scripting, reporting, and database management. Their role often involves troubleshooting system issues, integrating LIMS with other enterprise systems, and ensuring compliance with industry regulations. Strong programming skills, knowledge of laboratory operations, and experience with LabWare LIMS are essential for success in this role.

What are the main challenges a LabWare LIMS developer typically faces on the job?

Labware LIMS Developers often face challenges related to integrating the LIMS with a wide variety of laboratory instruments, managing complex data workflows, and ensuring system compliance with industry regulations such as GLP or GMP. They may encounter rapidly evolving project requirements as scientific and operational needs change, requiring adaptability and ongoing collaboration with IT, QA, and lab personnel. Effective troubleshooting and clear communication with end-users are crucial for addressing issues promptly and maintaining consistent system performance. Despite these challenges, the role offers the opportunity to make a direct impact on laboratory efficiency and data integrity.

What are the key skills and qualifications needed to thrive in the LabWare LIMS developer position, and why are they important?

To thrive as a Labware LIMS Developer, you need expertise in software development, database management, and laboratory informatics, typically supported by a degree in computer science, information technology, or a related field. Familiarity with the LabWare LIMS platform, scripting languages (such as SQL, JavaScript, or Python), and relevant certifications like LabWare Certified Professional are highly beneficial. Strong problem-solving abilities, attention to detail, and effective communication skills help developers work across interdisciplinary teams. These skills ensure tailored, reliable lab informatics solutions that support both scientific and regulatory requirements in laboratory environments.

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Labware Lims Developer jobs near you
Infographic showing various Labware Lims Developer job openings in the United States as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $88,166 per year, or $42.4 per hour.

System Level Review (SLR) & Audit Trail Review (ATR) Consultant - GxP Laboratory Systems

Alphanumeric Systems Inc.

Collegeville, PA • On-site

$70 - $85/hr

Contractor

Medical, Dental, Vision, Retirement, PTO

Posted 13 days ago

Job description

System Level Review (SLR) & Audit Trail Review (ATR) Consultant – GxP Laboratory Systems
 
Location: Collegeville, PA (100% Onsite)
Pay: $70–85/hour W2 (depending on experience)
Benefits: Medical, Dental, Vision, 401(k), PTO, Paid Holidays, and more.
 
About the Opportunity:
Alphanumeric is seeking an experienced System Level Review (SLR) & Audit Trail Review (ATR) Consultant to support a leading global pharmaceutical organization at its Collegeville, PA campus.
This role is ideal for a Computerized System Validation (CSV) professional with hands-on experience supporting laboratory equipment and computerized systems in a regulated GxP environment. The successful candidate will perform System Level Reviews, Audit Trail Reviews, and Data Integrity assessments while ensuring laboratory systems remain compliant, inspection-ready, and aligned with FDA regulatory expectations.

Candidates with experience performing Periodic Reviews, Computerized System Reviews, or equivalent laboratory system compliance assessments are encouraged to apply.
 
What you’ll be doing:
  • Perform System Level Reviews (SLRs) for laboratory equipment and computerized systems.
  • Execute Audit Trail Reviews (ATRs) to evaluate system compliance, electronic records, and data integrity.
  • Assess laboratory systems for compliance with GxP, FDA 21 CFR Part 11, and applicable regulatory requirements.
  • Review audit trails, electronic records, user access, security controls, system configurations, and lifecycle documentation.
  • Identify data integrity risks, compliance gaps, and opportunities for remediation.
  • Author and review validation documentation, including risk assessments, validation plans, protocols, reports, periodic reviews, and change controls.
  • Support Computerized System Validation (CSV) activities throughout the system lifecycle.
  • Partner with Quality Assurance, Validation, Laboratory Operations, Engineering, and IT teams to ensure systems remain in a validated state.
  • Support internal audits, regulatory inspections, and inspection readiness initiatives.
  • Ensure validation deliverables meet established quality standards and project timelines.
 
Required Qualifications:
  • Bachelor's degree in Engineering, Computer Science, Chemistry, Biology, Life Sciences, or a related technical discipline.
  • Minimum 5 years of experience supporting GxP-regulated pharmaceutical, biotechnology, or life sciences environments.
  • Hands-on experience performing Computerized System Validation (CSV).
  • Experience conducting System Level Reviews (SLRs), Periodic Reviews, and/or Audit Trail Reviews (ATRs) for laboratory equipment or computerized systems.
  • Strong knowledge of:
    • GxP
    • FDA 21 CFR Part 11
    • Data Integrity (ALCOA+)
    • Electronic Records and Electronic Signatures
    • Change Control and Risk Assessment
  • Experience supporting laboratory computerized systems and laboratory equipment.
  • Strong technical writing, documentation, and communication skills.
 
Preferred Experience: Experience with one or more of the following systems is highly desirable:
  • Waters Empower
  • LabWare LIMS
  • LabVantage
  • Chromeleon
  • OpenLab
  • Electronic Laboratory Notebooks (ELN)
  • Veeva
  • Kneat
  • ValGenesis

Preferred Skills:
  • Computerized System Validation (CSV)
  • Data Integrity
  • Audit Trail Reviews
  • System Level Reviews
  • Laboratory Compliance
  • Risk Assessment
  • CAPA
  • Change Control
  • Root Cause Analysis
  • GAMP 5
  • Good Manufacturing Practice (GMP)
  • Laboratory Information Management Systems (LIMS)
 
Why Join Us?
This is an opportunity to support highly visible compliance initiatives within a global pharmaceutical organization. You'll work alongside cross-functional Quality, Validation, Engineering, and Laboratory teams on projects that directly impact regulatory compliance, data integrity, and inspection readiness.
 
Please Note: This is a 100% onsite position located in Collegeville, PA. Candidates must be authorized to work in the United States on a W2 basis. We are unable to accept third-party candidates or provide sponsorship now or in the future.