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Lims Project Manager Jobs in Indiana (NOW HIRING)

Novartis

Supervisor, QC Chemistry

Indianapolis, IN

$88K - $132K/yr

Collaborate with other groups to drive project success. * Troubleshoot method challenges. * Manage ... Experience with LIMS. Commitment to Diversity and Inclusion: Novartis is committed to building an ...

INCOG

Senior MES Engineer

Fishers, IN

$97K - $134K/yr

... and ongoing management of Manufacturing Execution System (MES) platforms to ensure seamless ... Project Support SME for implementation of technology, automation, and OT infrastructure projects.

INCOG

QC Chemistry Technician, 3rd Shift

Fishers, IN

$18.50 - $23.50/hr

Be team oriented and willing to act as both a facilitator of special projects and a contributor to ... data management and/or data analysis systems (LIMS, JMP, Minitab, etc.) Additional Preferences:

INCOG BioPharma Services

Senior MES Engineer

Fishers, IN

$94K - $129K/yr

... and ongoing management of Manufacturing Execution System (MES) platforms to ensure seamless ... Project Support · SME for implementation of technology, automation, and OT infrastructure projects ...

INCOG BioPharma Services

Senior MES Engineer

Fishers, IN · On-site

$97K - $134K/yr

... and ongoing management of Manufacturing Execution System (MES) platforms to ensure seamless ... Project Support • SME for implementation of technology, automation, and OT infrastructure ...

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Lims Project Manager information

What are the key skills and qualifications needed to thrive as a LIMS Project Manager, and why are they important?

To thrive as a LIMS Project Manager, you need a strong background in laboratory processes, project management experience, and a relevant degree in science or IT. Familiarity with Laboratory Information Management Systems (LIMS), project management software, and often certifications like PMP or Six Sigma are typically required. Excellent communication, leadership, and problem-solving skills help manage cross-functional teams and client expectations effectively. These skills and qualifications are crucial to ensure timely, successful LIMS implementations that meet organizational and regulatory requirements.

What are some common challenges faced by LIMS Project Managers during system implementation, and how can they be addressed?

LIMS Project Managers often encounter challenges such as aligning system functionality with diverse laboratory workflows, managing stakeholder expectations, and ensuring data integrity during migration. Effective communication with lab staff and IT teams, thorough documentation of requirements, and phased implementation strategies can help mitigate these issues. It's also important to provide robust training and prioritize user feedback during the rollout to ensure successful adoption.

What is the difference between Lims Project Manager vs Laboratory Technician?

AspectLims Project ManagerLaboratory Technician
CredentialsBachelor's in Life Sciences, Project Management CertificationAssociate's or Bachelor's in Science, relevant lab certifications
Work EnvironmentOffice-based, overseeing projects in labs or biotech companiesLaboratory setting, performing tests and sample analysis
Industry UsageUsed in biotech, pharmaceutical, and clinical labs for project oversight

The Lims Project Manager focuses on planning, coordinating, and managing laboratory information system projects, ensuring timely delivery and compliance. In contrast, a Laboratory Technician performs hands-on testing and sample analysis. While both roles work within laboratory environments, their responsibilities and required skills differ significantly.

What are LIMS Project Managers?

LIMS Project Managers are professionals who oversee the implementation and maintenance of Laboratory Information Management Systems (LIMS) within organizations. Their responsibilities include coordinating between laboratory staff, IT teams, and vendors to ensure the system meets the needs of the laboratory. They manage project timelines, budgets, and ensure compliance with industry regulations. LIMS Project Managers also handle troubleshooting, training, and post-implementation support to ensure the system operates efficiently and effectively.
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What job categories do people searching Lims Project Manager jobs in Indiana look for? The top searched job categories for Lims Project Manager jobs in Indiana are:
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Lims Project Manager jobs near you
Infographic showing various Lims Project Manager job openings in Indiana as of June 2026, with employment types broken down into 89% Full Time, 7% Part Time, 1% Temporary, and 3% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution.
Lab Supervisor - Bioanalytical (Ligand Binding Assays)

Lab Supervisor - Bioanalytical (Ligand Binding Assays)

B2S Life Sciences

Franklin, IN • On-site, Remote

Full-time

Posted 13 days ago

Key responsibilities

  • Supervise and coordinate daily bioanalytical lab activities supporting ligand binding assay workflows.

  • Ensure studies are executed on time and according to approved protocols, SOPs, and client expectations.

  • Provide subject matter expertise in ligand binding assay platforms and assist with method qualification, validation, and sample analysis.

Job description

Position Summary
The Lab Supervisor, Bioanalytical (Ligand Binding Assays), is responsible for overseeing the daily operations of a regulated bioanalytical laboratory supporting ligand binding assay (LBA) studies within a Contract Research Organization (CRO). This role ensures high-quality, compliant execution of immunoassays (e.g., ELISA, MSD) used in pharmacokinetic (PK), immunogenicity (ADA), Neutralizing Antibody (Nab) and biomarker analysis in support of preclinical and clinical programs.
The supervisor provides technical leadership, staff development, and operational oversight to ensure delivery of accurate, timely, and regulatory-compliant data in accordance with GLP, GCP, and applicable regulatory guidance.
Key Responsibilities
Laboratory Operations & Supervision
  • Supervise and coordinate daily bioanalytical lab activities supporting LBA workflows.
  • Ensure studies are executed on time and according to approved protocols, SOPs, and client expectations.
  • Monitor assay performance, troubleshoot issues, and ensure data integrity.
  • Allocate resources (staff, instruments, reagents) to meet study timelines and priorities.
  • Maintain a safe and efficient laboratory environment.
  • Provides support for laboratory operations by addressing and resolving issues that may arise.
  • Other duties as assigned.

Technical Leadership (LBA Focus)
  • Provide subject matter expertise in ligand binding assay platforms (ELISA, ECL/MSD, etc.).
  • Assists with method qualification, validation, and sample analysis.
  • Review assay data, identify trends, and guide troubleshooting/root cause investigations.
  • Ensure adherence to regulatory expectations for assay performance (accuracy, precision, sensitivity, selectivity).

Quality & Compliance
  • Ensure compliance with GLP, GCP, 21 CFR Part 11, and relevant regulatory guidance (FDA, EMA).
  • Serves as Test Site Management for reports, audits, and investigations, as applicable. Support audits (internal, client, regulatory inspections) and address findings with appropriate CAPAs.
  • Ensure proper documentation practices and data integrity standards.

Staff Management & Development
  • Supervise, coach, and mentor bioanalytical scientists and technicians.
  • Conduct performance reviews, training plans, and career development initiatives.
  • Ensure staff are trained and qualified on applicable methods, instrumentation, and SOPs.
  • Foster a collaborative, high-performance, and accountable team environment.

Continuous Improvement
  • Identify and implement process improvements to increase efficiency, quality, and throughput.
  • Support adoption of new technologies and automation within LBA workflows.
  • Contribute to SOP development, revision, and standardization.

Requirements
Education
  • Bachelor's degree in Biology, Biochemistry, Immunology, or related field (Master's preferred).

Experience
  • 5-8+ years of experience in bioanalytical laboratory environments, preferably within a CRO.
  • 2+ years of supervisory or team leadership experience.
  • Strong hands-on experience with ligand binding assays (ELISA, MSD, Gyrolab).

Technical Skills
  • Deep understanding of LBA method development, validation, and sample analysis.
  • Experience with PK, ADA (screening, confirmatory, titer), and biomarker assays.
  • Familiarity with laboratory data systems (e.g., LIMS, Watson, SoftMax Pro, Discovery Workbench).
  • Strong data analysis and troubleshooting skills.

Regulatory Knowledge
  • Working knowledge of GLP/GCP and regulatory guidance for bioanalytical methods (ICH, FDA, EMA).
  • Experience supporting audits and inspections.

Preferred Qualifications
  • Experience in large molecule bioanalysis, ligand binding assays (monoclonal antibodies, biologics).
  • Exposure to automation platforms or high-throughput assay systems.
  • Experience with electronic lab notebooks and data integrity best practices.
  • Management, supervisory experience preferred.

Key Competencies
  • Leadership & team development
  • Technical expertise in bioanalysis
  • Problem-solving & critical thinking
  • Strong communication & stakeholder management
  • Attention to detail & data integrity focus
  • Organizational and time management skills

Work Environment
  • Laboratory-based role within a regulated CRO environment.
  • May require occasional extended hours to meet study deadlines.
  • Interaction with cross-functional teams, including QA, project management, and clients.

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