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Lims Developer Jobs in Colorado (NOW HIRING)

Agilent

Principal Automation Engineer

Frederick, CO · On-site

$146K - $229K/yr

Join a growing team with this exciting new opportunity for a Principal Automation Engineer in our ... Exposure to CSV/MES/DCS/PCS/SCADA/PLC/LIMS/EBR/QMS/PDH * Tools: Agile PLM, MS Project/Smartsheet ...

Biodesix

Business Systems Analyst III

Louisville, CO · On-site

$96K/yr

... DevOps, Jira, Bugzilla), preferred * Experience in regulated software environments, with exposure to labs, medical businesses, or LIMS, preferred WHAT YOU'LL GET: * Annual Base Salary Range Starting ...

New

Eli Lilly

Data Architect, Data Foundry

Louisville, CO · On-site

$66.50 - $85.75/hr

Everything the software engineering team builds--pipelines, APIs, prototypes--depends on the data ... Familiarity with LIMS, ELN systems (e.g., Benchling), and laboratory instrument data integration.

Philip Morris International

Laboratory Analyst

Aurora, CO · On-site

$88K - $110K/yr

Quality Control Engineer - Aurora, CO Be a part of a revolutionary change! At Philip Morris ... Advanced knowledge of LIMS, preferably LabVantage. * Well-developed IT skills (Office) and project ...

Agilent

Principal Automation Engineer

Frederick, CO · On-site

$146K - $229K/yr

Exposure toCSV/MES/DCS/PCS/SCADA/PLC/LIMS/EBR/QMS/PDH * Tools: Agile PLM, MS Project/Smartsheet,RAM CMMS, TMS DCS * Demonstrate the Agilent core values ofintegrity, trust, respect, teamwork ...

Cni

Hazardous Waste Personnel

Denver, CO

$22.75 - $27.50/hr

... Engineering, Health, Manufacturing, Public Safety, Consulting, and Transportation) for the federal ... Samples receipt and data entry for LIMS tracking following detailed instructions. * Samples ...

Eurofins

Quality Control Specialist

Centennial, CO · On-site

... validation engineering techniques and procedures. * Support training efforts for laboratory ... Demonstrate proficiency with LIMS and electronic analysis and tracking systems. * Ensure compliance ...

Lockheed Martin

Quality Receiving Inspector

Littleton, CO · On-site

$47K - $83K/yr

... engineering specifications and drawings - Confident usage of SAP across multiple transactions Desired skills - Quality Notifications - LIMS - EDSS - 2+ years experience performing quality inspections ...

Lockheed Martin

Quality Receiving Inspector

Littleton, CO · On-site

$41K - $72K/yr

Desired skills - SAP - LIMS - EDSS - 1 year experience performing quality inspections -Quality Notifications - Familiarity analyzing and interpreting engineering specifications and drawings EEO ...

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Lims Developer information

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How much do lims developer jobs pay per hour?

As of Jun 28, 2026, the average hourly pay for lims developer in Colorado is $55.56, according to ZipRecruiter salary data. Most workers in this role earn between $42.45 and $67.98 per hour, depending on experience, location, and employer.

What is LIMS and why is it used?

A LIMS (Laboratory Information Management System) is software used by Lims Developers to manage and track laboratory data, samples, and workflows. It helps ensure data accuracy, compliance, and efficiency in laboratory operations, often requiring knowledge of database management and programming skills.

Is LIMS an ERP system?

A LIMS (Laboratory Information Management System) is not an ERP (Enterprise Resource Planning) system; it is specialized software designed to manage laboratory data, samples, and workflows. While both systems handle data management, ERPs are broader and focus on overall business processes, whereas LIMS is tailored for laboratory operations. LIMS developers often work with database management and automation tools to customize laboratory solutions.

What are examples of LIMS?

Examples of Laboratory Information Management Systems (LIMS) include commercial platforms like LabWare, STARLIMS, and Thermo Fisher SampleManager. These systems are used to manage laboratory data, track samples, and automate workflows, often requiring knowledge of database management and laboratory processes.

What does a typical workday look like for a Lims Developer?

A typical workday for a Lims Developer involves analyzing laboratory workflow requirements, designing and configuring LIMS solutions, and developing or customizing modules to meet specific user needs. You may spend time troubleshooting system issues, collaborating with scientists or lab staff to gather feedback, and deploying software updates or integrations with laboratory instruments. Regular meetings with project managers or stakeholders are common, ensuring alignment with broader organizational goals. The role often requires balancing technical problem-solving with effective communication to deliver practical, user-friendly solutions for laboratory environments.

What is a Lims Developer job?

A LIMS (Laboratory Information Management System) Developer is responsible for designing, developing, and maintaining software solutions that support laboratory workflows. They customize and integrate LIMS platforms to streamline data management, improve efficiency, and ensure compliance with industry regulations. This role requires programming skills, database knowledge, and an understanding of laboratory processes. LIMS Developers often collaborate with scientists, IT teams, and quality assurance professionals to optimize system functionality.

How can I learn LIMS?

To learn LIMS as a developer, you can start with online courses, tutorials, and vendor-specific training programs offered by LIMS providers. Gaining knowledge of database management, scripting, and laboratory workflows is essential, and familiarity with tools like SQL, Python, or Java can be beneficial. Practical experience through internships or projects helps build proficiency in customizing and maintaining LIMS systems.

What are the key skills and qualifications needed to thrive in the Lims Developer position, and why are they important?

To thrive as a Lims Developer, you need strong programming skills, knowledge of laboratory workflows, and experience with Laboratory Information Management Systems (LIMS), often supported by a degree in computer science or a related field. Familiarity with database management systems, scripting languages (such as Python or Java), and certifications in relevant platforms like STARLIMS or LabWare are valuable assets. Attention to detail, strong problem-solving ability, and effective communication help Lims Developers excel when working with lab personnel and IT teams. These skills and qualities are essential for ensuring accurate, efficient data management and seamless integration of laboratory processes within the organization.

What are popular job titles related to Lims Developer jobs in Colorado? For Lims Developer jobs in Colorado, the most frequently searched job titles are:
What job categories do people searching Lims Developer jobs in Colorado look for? The top searched job categories for Lims Developer jobs in Colorado are:
Lims Developer jobs near you
Infographic showing various Lims Developer job openings in Colorado as of June 2026, with employment types broken down into 80% Full Time, 8% Part Time, and 12% Contract. Highlights an 82% Physical, 4% Hybrid, and 14% Remote job distribution, with an average salary of $115,567 per year, or $55.6 per hour.
Sr Quality Automation and CSV Engineer (Onsite)

Sr Quality Automation and CSV Engineer (Onsite)

Tolmar

Windsor, CO • On-site

Full-time

Posted 26 days ago

Job description

Core Hours: Monday - Friday, 8:00 am - 5:00 pm
Purpose and Scope
The Senior Automation CSV Engineer will lead the design, implementation, and validation of automated systems and new technology solutions within a sterile injectable pharmaceutical manufacturing environment. This role ensures compliance with regulatory requirements (FDA, EMA, ICH) and company standards for computerized systems, automation platforms, and AI-enabled technologies used in production, quality control, and data analytics.
Essential Duties & Responsibilities
  • Automation and Computer System Validation:
    • Develop and execute validation strategies for automated systems, robotics, and AI-based tools in compliance with GAMP 5, 21 CFR Part 11, FDA's CSA for Production and Quality System Software, Annex 11, Annex 22, and PIC/S.
    • Perform risk assessments and ensure data integrity
    • Author and review validation documentation (URS, FS, DS, IQ/OQ/PQ protocols, reports).
  • System Lifecycle Management:
    • Oversee system implementation, upgrades, and change control for automation and computer systems.
    • Collaborate with IT, Engineering, and Quality teams to maintain validated state of systems.
  • Regulatory Compliance:
    • Ensure adherence to cGMP, FDA, EMA, and global regulatory guidelines for sterile injectable manufacturing.
    • Support audits and inspections by providing validation evidence and technical expertise.
  • Innovation & Continuous Improvement:
    • Identify opportunities to integrate new technologies and advanced analytics for process optimization and predictive maintenance.
    • Drive digital transformation initiatives.
  • Quality Oversight & Approval:
    • Provide independent quality oversight for automation and computer system validation activities.
    • Review and approve validation protocols, reports, and change control documentation to ensure compliance and data integrity.
    • Act as a quality representative during system implementation and qualification phases.
  • Adhere to company and departmental timelines with high accuracy and quality.
  • Maintain an atmosphere of teamwork, cordiality, and respect towards co-workers.
  • Performs other duties as assigned.

Core Values
This position is expected to operate within the framework of Tolmar's Core Values:
  • Center on People:We commit to support the well-being of our patients. We are committed to treating our employees and those we serve as valued partners. By placing people at the heart of our actions, we actively engage, invigorate, acquire knowledge, and grow together.
  • Are Proactive & Agile:We embody a culture of engagement and action. With a hands-on approach, we fearlessly adapt to change. We anticipate, respond swiftly and efficiently to ignite a spirit that propels us towards extraordinary outcomes.
  • Act Ethically:We are committed to consistently conducting our business in an ethical, compliant, and socially aware manner, in line with our purpose of positively impacting lives. We actively cultivate diversity, equity, inclusion & sustainability in our workplace.
  • Constantly Improve:We are committed to a collaborative & proactive effort to improve our products, systems, processes, and services by reducing waste, increasing efficiency & improving quality.
  • Are Accountable:We think, act, and communicate with honesty, transparency, and clarity in alignment with our core values. We don't compromise our values for near term gain. We take accountability & ownership of our work, actions, successes, and setbacks. We strive to deliver our best as we shape the future.

Knowledge, Skills & Abilities
  • Excellent organizational and project management skills.
  • Excellent oral and written communication skills.
  • Ability to work independently with minimal supervision and as part of a cross-functional team.
  • Advanced knowledge of Automation and CSV/CSA principles, industry guidance, regulatory requirements, cGMP practices, and ICH guidelines.
  • Strong project management and cross-functional leadership skills.
  • Ability to author strong technical reports free of errors.
  • Advanced knowledge with Microsoft Office Suite, and various GMPS systems such as Veeva eQMS, Maximo CMMS, BMS, LIMS, CDS, and ERPs.
  • Familiarity with SCADA, PLC, MES, and AI platforms from simple context analysis tools to large language modeling, prompt engineering and the role of human interaction for process engineering and establishment of trustworthy data.
  • Advanced troubleshooting and problem-solving skills.
  • Ability to manage multiple projects concurrently and under tight time constraints.

Education & Experience
  • Bachelor's degree in Engineering, Computer Science, Pharmaceutical Sciences, or related field required
  • Master's degree in Engineering, Computer Science, Pharmaceutical Sciences, or related field preferred
  • Minimum of 8 years' experience in pharmaceutical automation and computerized system validation.
  • Strong knowledge of sterile injectable manufacturing processes and aseptic techniques.
  • Expertise in GAMP 5, 21 CFR Part 11, Annex 11 and knowledge of Annex 22 compliance.
  • Proficiency in risk-based validation and data integrity principles.

Working Conditions
  • Working conditions include general office environment.
  • Business demands may require working extended hours.

Compensation and Benefits
  • Annual pay range $125,000 - $135,000 depending on experience
  • Bonus Eligible
  • Benefits information: https://www.tolmar.com/careers/employee-benefits

Tolmar compensation programs are focused on equitable, fair pay practices including market-based base pay and a strong benefits package. The final compensation offered may vary from the posted range based on the selected candidates qualifications and experience.
Tolmar is an Equal Opportunity Employer. We do not discriminate on the basis age 40 and over, color, disability, gender identity, genetic information, military or veteran status, national origin, race, religion, sex, sexual orientation or any other applicable status protected by state or local law. It is our intention that all qualified applicants be given equal opportunity and that selection decisions are based on job-related factors.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
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About Tolmar

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Fort Collins, CO, US

Year founded

2006

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