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Lims Data Entry Jobs in Worcester, MA (NOW HIRING)

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Lims Data Entry information

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$11

$19

$28

How much do lims data entry jobs pay per hour?

As of Aug 31, 2026, the average hourly pay for lims data entry in Worcester, MA is $19.43, according to ZipRecruiter salary data. Most workers in this role earn between $16.30 and $21.83 per hour, depending on experience, location, and employer.

What is a LIMS Data Entry?

A LIMS Data Entry job involves entering, updating, and managing data within a Laboratory Information Management System (LIMS). Professionals in this role are responsible for accurately inputting laboratory test results, sample information, and other relevant data to ensure the integrity and traceability of laboratory records. They often work closely with laboratory staff and may also help in verifying data, generating reports, and maintaining compliance with regulatory standards. Attention to detail, familiarity with laboratory processes, and strong computer skills are essential for success in this position.

What are the key skills and qualifications needed to thrive as a LIMS Data Entry specialist?

To thrive as a LIMS Data Entry specialist, you need strong attention to detail, data accuracy, and familiarity with laboratory information management systems (LIMS), often supported by a high school diploma or relevant experience. Proficiency in LIMS software, basic database management, and Microsoft Office Suite is typically required. Excellent organizational skills, time management, and effective communication help ensure smooth workflow and collaboration with laboratory staff. These skills are essential for maintaining data integrity, supporting laboratory operations, and ensuring compliance with regulatory standards.

What are some common challenges faced by LIMS Data Entry professionals and how can they be effectively managed?

LIMS Data Entry professionals often encounter challenges such as managing large volumes of data, ensuring high levels of accuracy, and keeping up with strict deadlines. To effectively manage these, it is important to develop a systematic workflow, regularly double-check entries, and utilize built-in validation tools provided by the LIMS platform. Collaboration with laboratory staff and IT teams can also help resolve discrepancies quickly and maintain data integrity.

What is the difference between Lims Data Entry vs Laboratory Technician?

AspectLims Data EntryLaboratory Technician
CredentialsHigh school diploma or equivalent; familiarity with LIMS softwareHigh school diploma or associate degree; technical training in lab procedures
Work EnvironmentOffice or computer-based setting within labsLaboratory setting performing tests and experiments
Job ResponsibilitiesEntering, updating, and managing data in LIMS systemsConducting tests, preparing samples, and recording results

While both roles support laboratory operations, Lims Data Entry focuses on managing data within Laboratory Information Management Systems, whereas Laboratory Technicians perform hands-on testing and sample analysis. Understanding these differences helps in choosing the right career path or job search focus.

What are popular job titles related to Lims Data Entry jobs in Worcester, MA?

For Lims Data Entry jobs in Worcester, MA, the most frequently searched job titles are:

What job categories do people searching Lims Data Entry jobs in Worcester, MA look for?

The top searched job categories for Lims Data Entry jobs in Worcester, MA are:

What cities near Worcester, MA are hiring for Lims Data Entry jobs?

Cities near Worcester, MA with the most Lims Data Entry job openings:

Lims Data Entry jobs near you
Infographic showing various Lims Data Entry job openings in Worcester, MA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 84% In-person, and 16% Remote job distribution, with an average salary of $40,416 per year, or $19.4 per hour.

Scientist I, Analytical Development and Quality Control

Kailera Therapeutics, Inc.

Waltham, MA

Full-time

Re-posted 10 days ago

Job description

What You'll Do:

The Scientist I, Analytical Development and Quality Control is an experienced scientist within the Analytical Development and Quality Control (AD/QC) organization, with a primary focus on analytical quality control, method validations, stability programs, and data integrity. This role applies broad knowledge of analytical principles and QC practices to support release and stability testing, data trending, and lifecycle management of analytical methods.

The Scientist I is responsible for analyzing and interpreting stability and release data, identifying trends and potential quality risks, and applying a foundational understanding of degradation pathways to ensure product quality over time. This individual contributes to the maintenance and integrity of analytical data systems, including LIMS and stability databases, and ensures compliance with regulatory expectations and internal quality standards.

 

Required location: Waltham, MA (hub-based, onsite 3-4 days per week)

 

Responsibilities:

  • Analyze and trend release and stability data to identify variability, shifts, and emerging quality risks, and communicate findings to departmental leadership and project teams
  • Review release and stability test results to ensure accuracy, completeness, and compliance with specifications, procedures, GMP requirements, and overall data integrity
  • Execute and support registration stability programs, including protocol implementation, sample management, and data evaluation across timepoints
  • Apply scientific understanding of degradation pathways to interpret analytical data for trending purposes, and support investigations (OOS, OOT, deviations) and CAPA analysis
  • Maintain and ensure integrity of data within LIMS and stability databases, ensuring accurate data entry, traceability, and audit readiness
  • Conduct data integrity reviews and assessments in alignment with ALCOA+ principles, identifying gaps and supporting remediation actions as needed
  • Author and review analytical reports and regulatory documentation, including sections supporting stability, specifications, and method performance
  • Design and execute analytical experiments to support method lifecycle activities, including development, qualification/validation, transfer, or troubleshooting
  • Collaborate with cross-functional teams to communicate data insights, support investigations, and contribute to project milestones and regulatory submissions
  • Experience with data analysis tools (e.g., Excel advanced functions, JMP, or statistical software) for trending and visualization
  • Working knowledge of ICH guidelines and regulatory expectations for analytical methods and stability programs
  • Evaluate temperature excursions for stability and release samples, assessing potential impact on product quality using scientific judgment, stability data, and relevant regulatory/technical guidance

 

Required Qualifications:

  • 8+ years of hands-on experience with analytical techniques (e.g., HPLC/UHPLC, LC-MS, GC, compendial tests) supporting release and/or stability testing
  • Experience trending and interpreting stability and QC data, with a working understanding of degradation pathways and stability-indicating methods
  • Proficiency with LIMS and laboratory data systems, along with a strong understanding of data integrity principles (ALCOA+) and regulatory expectations
  • Strong technical writing and communication skills, including experience reviewing analytical data and contributing to reports or regulatory documentation
  • Demonstrated collaboration and problem-solving skills, with the ability to manage multiple priorities in a fast-paced, quality-focused environment

Preferred Qualifications:

  • Experience supporting regulatory submissions (e.g., IND, NDA, BLA) with analytical or stability sections
  • Familiarity with stability program design and lifecycle management in a pharmaceutical or biotechnology setting
  • Experience participating in or supporting regulatory inspections and audits
  • Exposure to method development, qualification/validation, or transfer activities within Analytical Development or QC
  • Advanced degree preferred

Education:

  • Bachelor's, Master's, or Ph.D. in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a related discipline within a GMP-regulated environment

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