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Freelance Labware Lims Developer Jobs in Pennsylvania

Novartis

Quality Control Specialist II

Morrisville, PA · On-site

$89K - $166K/yr

... MS&T, Engineering, and Validation teams. This is an exciting opportunity to help build the ... with LabWare LIMS and Empower CDS is preferred. * Proven experience in analytical method ...

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 ...

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 ...

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Freelance Labware Lims Developer information

What is a freelance Labware LIMS developer?

A Freelance Labware LIMS Developer is an independent professional who specializes in designing, customizing, and maintaining LabWare Laboratory Information Management Systems (LIMS) for laboratories. They work on a contract basis to help labs implement, configure, and optimize LabWare LIMS software to manage samples, workflows, and data efficiently. Their responsibilities often include system integration, scripting, troubleshooting, and user training to ensure that the LIMS meets the specific needs of the organization.

What skills and qualifications are needed to thrive as a freelance Labware LIMS developer?

To thrive as a Freelance Labware LIMS Developer, you need strong programming skills (particularly in Java and SQL), a solid understanding of laboratory workflow processes, and experience with Labware LIMS configuration or implementation. Familiarity with tools such as Labware LIMS, REST/SOAP APIs, and relevant certifications like Labware Certified Professional are highly beneficial. Excellent problem-solving abilities, effective communication, and the ability to work independently are standout soft skills for this role. These competencies ensure the development of robust, user-friendly LIMS solutions that meet client requirements and industry standards.

What are common challenges freelance Labware LIMS developers face when working with multiple clients?

Freelance Labware LIMS developers often encounter challenges such as adapting quickly to diverse client environments, each with unique workflows and data management needs. Balancing multiple projects requires strong organizational skills to manage timelines, requirements, and communication across different stakeholders. Additionally, freelancers must stay current with Labware updates and integration requirements, as clients may use varying versions or have custom configurations. Building strong client relationships and clear documentation practices also help ensure smooth handovers and ongoing support.

What is the difference between Freelance Labware Lims Developer vs Laboratory Information Systems (LIS) Specialist?

AspectFreelance Labware Lims DeveloperLaboratory Information Systems (LIS) Specialist
CredentialsIT or software development background, certifications in Labware LIMSHealthcare or laboratory IT certifications, LIS-specific training
Work EnvironmentFreelance projects, client sites, remote workLaboratories, healthcare facilities, IT departments
Industry UsagePharmaceutical, biotech, research labsClinical labs, hospitals, diagnostic centers
Search & Comparison IntentDeveloping or customizing LIMS softwareManaging and supporting LIS systems

While both roles involve laboratory information systems, Freelance Labware Lims Developers focus on customizing and developing LIMS software, often working independently. LIS Specialists typically manage, support, and optimize existing LIS systems within healthcare or clinical environments. The roles overlap in technical skills but differ in scope and work setting.

What are the most commonly searched types of Labware Lims Developer jobs in Pennsylvania?

The most popular types of Labware Lims Developer jobs in Pennsylvania are:

What are popular job titles related to Freelance Labware Lims Developer jobs in Pennsylvania?

For Freelance Labware Lims Developer jobs in Pennsylvania, the most frequently searched job titles are:

What job categories do people searching Freelance Labware Lims Developer jobs in Pennsylvania look for?

The top searched job categories for Freelance Labware Lims Developer jobs in Pennsylvania are:

What cities in Pennsylvania are hiring for Freelance Labware Lims Developer jobs?

Cities in Pennsylvania with the most Freelance Labware Lims Developer job openings:

Freelance Labware Lims Developer jobs near you
Infographic showing various Freelance Labware Lims Developer job openings in Pennsylvania as of August 2026, with employment types broken down into 77% Full Time, 8% Part Time, and 15% Contract. Highlights an 81% Physical, 4% Hybrid, and 15% Remote job distribution.

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

Collegeville, PA

Alphanumeric
Health Care and Social Assistance • 51 - 200 employees
Learn more about Alphanumericexternal

$70 - $85/hr

Contractor

Medical, Dental, Vision, Retirement, PTO

Re-posted 7 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.

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.
Education:Employment Type: CONTRACTOR

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