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Senior Labware Lims Developer Jobs in Philadelphia, PA

MSD

Technical Product Manager

West Point, PA · On-site

$161K - $187K/yr

Bachelor's degree in Life Sciences, Biomedical Engineering, Chemical Engineering, Computer Science ... LIMS (e.g., Labware), ELN (e.g., Benchling), Apache Kafka, Spark, Databricks, or similar.

Johnson Matthey

Laboratory Team Lead

Devon, PA · On-site

Bachelor's degree in Chemistry, an Engineering discipline or a related field and 2 years of related ... Laboratory Information Management System (LIMS) Labware version 6. To submit your application ...

Johnson Matthey

Laboratory Team Lead

Devon, PA · On-site

Bachelor's degree in Chemistry, an Engineering discipline or a related field and 2 years of related ... Laboratory Information Management System (LIMS) Labware version 6. To submit your application ...

Matthey

Laboratory Team Lead

Devon, PA

Bachelor's degree in Chemistry, an Engineering discipline or a related field and 2 years of related ... Laboratory Information Management System (LIMS) Labware version 6. To submit your application ...

Merck & Co.

Technical Product Manager

West Point, PA · 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 ...

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Senior Labware Lims Developer information

See Philadelphia, PA salary details

$25.2K

$81K

$165K

How much do senior labware lims developer jobs pay per year?

As of Aug 22, 2026, the average yearly pay for senior labware lims developer in Philadelphia, PA is $81,017.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,900.00 and $103,900.00 per year, depending on experience, location, and employer.

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.

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 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 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 are the most commonly searched types of Labware Lims Developer jobs in Philadelphia, PA?

The most popular types of Labware Lims Developer jobs in Philadelphia, PA are:

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For Senior Labware Lims Developer jobs in Philadelphia, PA, the most frequently searched job titles are:

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The top searched job categories for Senior Labware Lims Developer jobs in Philadelphia, PA are:

Senior Labware Lims Developer jobs near you

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

Alphanumeric

Collegeville, PA • On-site

$70 - $85/hr

Contractor

Medical, Dental, Vision, Retirement, PTO

Posted 16 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.
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.

Job Requirements
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.

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