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Lims Developer Jobs in Massachusetts (NOW HIRING)

MES Engineer Location : Boston Area (On site in Norwood, MA) Department: Internal DP Operations ... LIMS, and automation platforms, using industry-standard protocols like OPC or RESTful APIs. o ...

... LIMS, and automation platforms, using industry-standard protocols like OPC or RESTful APIs. o ... Engineering, Computer Science, or a related technical field. · Experience: o 2-4 years of ...

MES Engineer

Foxboro, MA · On-site

$110K - $151K/yr

They are seeking a Senior Engineer to support Manufacturing Execution Systems (MES) and enhance ... VBS/VBA, C# or similar, VMware, MATLAB, SQL, LIMS (various), Reporting Systems (XSLT, Crystal ...

CSV Specialist

Lexington, MA · On-site

$45 - $52/hr

Hyrbrid - 3 days a week in person (Lexington, MA) Pay: $45-52/hr 6month contract The CSV Engineer ... Familiarity with MODA, LabWare, or other QC/LIMS platforms preferred. * Proficient in Microsoft ...

MES Engineer

Foxboro, MA · On-site

$110K - $151K/yr

They are seeking a Senior MES Engineer to support Manufacturing Execution Systems (MES) and related ... VBS/VBA, C# or similar, VMware, MATLAB, SQL, LIMS (various), Reporting Systems (XSLT, Crystal ...

Showing results 41-60

Lims Developer information

See Massachusetts salary details

$18

$57

$89

How much do lims developer jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for lims developer in Massachusetts is $57.71, according to ZipRecruiter salary data. Most workers in this role earn between $44.09 and $70.62 per hour, depending on experience, location, and employer.

What does a Lims developer do?

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?

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.

What skills and qualifications are needed to be a Lims developer?

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.

Infographic showing various Lims Developer job openings in Massachusetts as of August 2026, with employment types broken down into 79% Full Time, 3% Part Time, and 18% Contract. Highlights an 81% Physical, 4% Hybrid, and 15% Remote job distribution, with an average salary of $120,030 per year, or $57.7 per hour.

Other

Posted 6 days ago


Job description

Position Title: MES Engineer
Location: Boston Area (On site in Norwood, MA)

Department: Internal DP Operations Systems Regulatory Relevance: GxP

Primary System: Apprentice Tempo MES


Role Overview:

The MES Engineer will play a critical role in supporting the design, development, implementation and management of the Manufacturing Execution Solutions (MES) within the organization''s Drug Product manufacturing area. This role involves translating manufacturing processes into robust MES solutions, ensuring compliance with GxP standards, and integrating MES with other enterprise systems and automation platforms to streamline operations.


Key Responsibilities:

·       MES Support and Development:

o   Assist in the design and configuration of Tempo MES solutions, including electronic batch records (eBRs), under the guidance of senior engineers.

o   Contribute to the development of modular, scalable, and reusable MES recipe templates based on ISA 88/95 standards.

o   Perform impact assessments for recipe modifications and system updates, ensuring adherence to GxP requirements.

o   Collaborate with cross-functional teams to gather user requirements and define functional specifications for MES functionalities.

o   Assist in recipe design and authoring electronic batch records (eBR) to develop modular, scalable and reusable MES recipe and equipment workflow templates following ISA 88/95 standards.

o   Perform root cause analysis and resolve MES issues related to system configuration, recipe design, or integration failures.

·       System Integration and Analytics:

o   Support efforts to integrate MES with other enterprise systems, such as ERP, LIMS, and automation platforms, using industry-standard protocols like OPC or RESTful APIs.

o   Assist in the development of data visualization tools and reporting dashboards to support operational decision-making.

o   Possess technical knowledge in DCS, automation, and systems integration, including the design and management of data dashboards, label management systems, and reporting tools.

·       Operational Support:

o   Provide day-to-day technical support for MES system users, assisting in troubleshooting and resolving recipe or system-related issues.

o   Participate in technical transfer activities to ensure smooth onboarding of new products and processes into manufacturing.

o   Support off-hours manufacturing operations as needed to address critical MES-related issues.

·       Compliance and Documentation:

o   Ensure compliance with Good Documentation Practices (GDP), GxP regulations, Data Integrity guidelines and company policies during all MES-related activities.

o   Participate in validation activities to support the implementation and ongoing maintenance of MES systems.


Required Qualifications:

·       Education:

o   Bachelor’s degree in Engineering, Computer Science, or a related technical field.

·       Experience:

o   2-4 years of experience with MES systems, preferably some in Drug Product manufacturing in pharmaceutical or biotechnology environments.

o   Basic understanding of GxP regulations, GAMP guidelines, and Computer System Validation (CSV).

·       Technical Skills:

o   Exposure to MES platforms such as Tempo, Syncade, or equivalent systems is preferred.

o   Familiarity with basic programming concepts or languages like SQL, Python, or C#.

o   General knowledge of manufacturing processes, automation systems, and systems integration principles.


Additional Competencies:

  • Strong problem-solving and analytical skills with a willingness to learn and adapt quickly.
  • Effective communication and collaboration abilities to work in cross-functional teams.
  • Commitment to maintaining compliance with regulatory and internal standards.