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Labware Lims Developer Jobs (NOW HIRING)

Johnson Matthey

Laboratory Team Lead

Devon, PA · On-site

$84.83K/yr

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

$84.83K/yr

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 ...

New

VTI Life Sciences

VTI Life Sciences (VTI) is seeking forward-thinking, ambitious engineers looking to accelerate ... Support system integration activities across related laboratory and enterprise systems (e.g., LIMS ...

supremesoft

CSV Validation QC Engineer

Jersey City, NJ · On-site

Preferred Skills • Experience in Labware, Empower LIMS systems • Experience in validating Lab equipments Job Roles/Responsibilities • Act as Validation and Qualification Lead on a large global ...

Merck & Co.

Bachelor's degree in engineering, information technology, or a related field.Preferred Skills ... Hands-on experience with Laboratory Information Management Systems (LIMS), Chromatography Data ...

Periodic Labs

Laboratory Technician

Menlo Park, CA · On-site

$100K - $130K/yr

This role is for someone with a science or engineering background who enjoys working with ... Participate in test runs and validation of new labware, equipment, or experimental methods

Hemlock Semiconductor

Testing Technician

Hemlock, MI · On-site

These panels allow solar project developers and owners to lower the embodied carbon of their ... Entering data into the LIMS system. Lab Maintenance: * Cleaning analytical labware. * Managing ...

Air Liquide

Laboratory Technician I

Taylor, TX

$22 - $23/hr

Our highly-skilled chemists assist other scientists and engineers from companies in these fields to ... Sample login and management using LIMS * Analysis of semiconductor grade chemicals for trace ...

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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 May 31, 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 job?

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 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.

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.
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What are the most commonly searched types of Labware Lims Developer jobs? The most popular types of Labware Lims Developer jobs are:
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Labware Lims Developer jobs near you
Infographic showing various Labware Lims Developer job openings in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $88,166 per year, or $42.4 per hour.
QC Specialist, Master Data

QC Specialist, Master Data

Genentech, Inc.

Hillsboro, OR • On-site

Full-time

Posted 15 days ago

Genentech rating

9.0

Company rating: 9.0 out of 10

Based on 21 frontline employees who took The Breakroom Quiz

6th of 70 rated pharmaceutical

Job description

Hillsboro Technical Operations (HTO) is a drug product & finished goods manufacturing organization responsible for the reliable delivery of Roche's commercial portfolio & pipeline products. The Operations organization at HTO is divided into three value streams, which combine to produce millions of units of life-saving medicine every year to patients around the world.
The Opportunity:
Do you have a passion for consistent data and understand how this can be achieved through clear and consistent Master Data? Are you a problem solver that believes most or all issues can be linked to a process flaw? Then you may be the person we are looking for. The HTO Quality Control (QC) Team is looking for an individual interested in managing simple to moderately complex sets of Master Data that support QC operations. This role will collaborate with internal and external departments (e.g. QC Operations, Database System Developers, Business Analysts, Manufacturing, Packaging, External Quality, Control System Scientists, Product Technical Leads etc.) to maintain and improve contemporary relevance of QC Master Data. This role will gain a deeper understanding of how the master data is utilized and how it can be improved as they own/perform activities that support/improve lab operations using Good Manufacturing/Laboratory Practices. These activities will include conducting minor deviation investigations, owning Corrective and Preventive Actions (CAPAs), owning Change Request Actions, performing periodic reporting, data review and generation of certificates of test/analysis, direct material release, and analytical equipment administration.
  • You will create, update, test various sets of Master Data and end-user defined system settings that enables consistent execution, collection, transaction, storage, analysis, and reporting of analytical/microbiological tests and activities performed by Quality Control Operations. Supported Software Systems include: Labware LIMS, Biovia, Molecular Devices SoftMax Pro, SAP, Mettler Toledo LabX, Waters Empower Chromatography Data System, Veeva, and ValGenesis.
  • You will be the site representative on System Enhancement Teams and User Communities of Practice Teams, communicate system changes and best practices to local system users and coordinate initial and maintain continuous end user training materials/content for supported systems.
  • You will perform Direct Material Release and review / generate Drug Product Certificates of Analysis, as needed.
  • You will lead or participate in minor Quality Control Investigations (e.g.: Out of Specifications, Out of Expectations, Over Action Limits, local and global process deviations) using established Root Cause Analysis tools and generating data-based impact assessments within established timelines.
  • You will collaborate with key stakeholders to identify and execute Corrective and Preventive Action Plans, completing assigned actions through self or others with tact and effective communication skills.
  • You will author, review, and/or approve various business process & compliance related documents such as, standard operating procedures, work instructions, monitoring protocols, monitoring reports, gap assessments, and risk assessments.
  • You will participate in cross functional teams that ensure safety, quality, delivery, engagement and cost objectives are sustained / exceeded. You will own, delegate and/or drive actions that result from these teams.

Who You Are
  • You hold a Bachelor's of Science degree with 4-7 years of experience in the pharmaceutical industry, quality control and/or database management or 8+ years of experience with an Associates/Vocational Degree. 3 years of experience working in a cGMP or similarly regulated environment is required.
  • You possess a working understanding of database management/relational tables, Operational Excellence tools, cGMP regulations and industry guidelines related to biological processing. You consistently apply this understanding when executing your tasks. We would be even more delighted, if you have experience building reporting tools such as tableau dashboards.
  • You work independently within standard operating procedures, guidelines, and policies to execute role based accountabilities and have the judgment / discretion to escalate matters of significance in a timely manner, ensuring efficient operations and regulatory compliance.
  • You are able to assess various changes/issues related to quality control or database management to define/determine next actions required to bring about a desired outcome or mitigate risks associated with these changes/issues to the QC organization.
  • You have strong verbal and written communication skills with ability to summarize minor to moderate problems that drive timely informed decisions and completion of simple to moderate actions.
  • You have a curious open mindset and continuously share information with others as a means to foster effective cross functional teams

Work Environment/Physical Demands/Safety Considerations
  • You will be working on site in a flexible open space work environment with random visits to a QC laboratory environment that requires laboratory gowning (lab coat, goggles, gloves)
  • You will work on/interact with computerized systems/screens for long periods of time (6-8 hours)
  • You may be required to lift up to 25lbs
  • You may have to work with hazardous materials and chemicals

Relocation benefits are available for this position.
The expected salary range for this position based on the primary location of Oregon is $77,770 to $144,430. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.
Benefits
Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

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About Genentech

Sourced by ZipRecruiter

A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry for more than 40 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. Genentech has multiple therapies on the market for cancer & other serious illnesses. Please take this opportunity to learn about Genentech where we believe that our employees are our most important asset & are dedicated to remaining a great place to work.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

South San Francisco, CA, US

Year founded

1976

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