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LGC Group

Sells oligos, probes, primers, viral materials

MES Application Engineer

Enterprise ApplicationsConfirmed live in the last 24 hours
Full-timePetaluma, CA, USA

About the Job

Requirements

  • A bachelor's degree in computer science, engineering, manufacturing systems, biotechnology, or a related technical discipline, or an equivalent combination of education and relevant experience.
  • Three or more years of experience in manufacturing systems, manufacturing execution systems, industrial automation, application development, or a comparable technical environment.
  • Experience configuring or developing applications on Tulip or a comparable low-code manufacturing platform, and ability to translate process requirements into maintainable workflows.
  • Working knowledge of SQL, relational data concepts, APIs or web services, structured data exchange, and system troubleshooting.
  • Ability to gather requirements, document solutions, test changes, resolve production issues, and communicate effectively with cross-functional stakeholders.
  • Proficiency with standard Microsoft 365 applications and disciplined technical documentation practices.
  • Build effective working relationships with manufacturing users, technical teams, quality partners, vendors, and stakeholders at multiple organizational levels.
  • Collaborate effectively in cross-functional teams and influence decisions through clear evidence, practical recommendations, and respectful challenge.
  • Work autonomously, take ownership, and recognize when stakeholder engagement, technical escalation, or quality review is required.
  • Apply structured problem-solving skills to analyze data, isolate root causes, and implement sustainable solutions.
  • Adapt to evolving customer, process, and technology requirements while managing multiple priorities in a dynamic manufacturing environment.
  • Deliver commitments reliably while balancing speed, quality, maintainability, compliance, and business value.
  • Promote cooperation, knowledge sharing, and user ownership to achieve successful deployment and adoption.
  • Maintain an internal-customer focus and respond appropriately to production support needs.
  • Demonstrate curiosity and persistence when addressing complex manufacturing-process and systems problems.
  • Communicate complex technical information clearly to technical and non-technical audiences.
  • Exercise professional judgment, tact, diplomacy, and appropriate care when handling confidential or proprietary information.
  • Current U.S. work authorization is required; the employer cannot sponsor or assume sponsorship for temporary visas.

Responsibilities

  • Develop, configure, test, deploy, and maintain Tulip applications supporting oligonucleotide manufacturing operations and customer-specific production workflows.
  • Translate process requirements into digital solutions, following approved architecture, validation, and change-control practices.
  • Deliver hands-on application configuration, integration, testing, documentation, production support, and continuous improvement across project and operational work.
  • Partner with Manufacturing, Quality, Process Engineering, Automation, IT, program teams, equipment suppliers, and Tulip specialists to design and implement solutions.
  • Document requirements, designs, test evidence, change records, troubleshooting outcomes, training materials, and user guidance for technical and non-technical audiences.
  • Own the application lifecycle for assigned Tulip solutions, including requirements, configuration, version control, testing, release, monitoring, support, and controlled updates.
  • Serve as the site subject-matter expert for Tulip application development, operator workflow design, electronic records, data collection, and manufacturing-system interfaces.
  • Identify and implement opportunities to reduce manual entry, improve usability and traceability, strengthen error prevention, and increase manufacturing workflow efficiency and reliability.
  • Configure dashboards and reporting; monitor application performance, data quality, adoption, support issues, and workflow effectiveness using agreed measures.
  • Work primarily at a computer and regularly on the manufacturing floor for observation, testing, deployment, user support, and equipment-interface activities.
  • Follow applicable quality, safety, cybersecurity, data-integrity, documentation, validation, and change-control requirements, including ALCOA+ principles where applicable.
  • Support integrations between Tulip and approved databases, cloud services, APIs, enterprise systems, and manufacturing or laboratory equipment, including file generation, file parsing, and data exchange where in scope.
  • Perform other duties as required or assigned by management to meet business needs.

Desired Qualifications

  • Direct experience developing and supporting Tulip MES applications in a production environment.
  • Experience in life sciences, diagnostics, biotechnology, pharmaceutical, or other regulated manufacturing environments.
  • Experience with Python, AWS services, databases, and integration patterns supporting calculations, data processing, or file-based instrument workflows.
  • Familiarity with validation, change control, GMP or ISO quality systems, cybersecurity, and ALCOA+ data-integrity expectations.
  • Experience integrating manufacturing or laboratory equipment, ERP systems, analytical instruments, or automation platforms such as liquid handlers and synthesizers.

About the Company

LGC Group

Sells oligos, probes, primers, viral materials

LGC Group provides life sciences tools and solutions, including oligo components, probes, primers, and recombinant viral materials, plus proficiency-testing schemes for areas like food safety. Its products support detection and development in healthcare through mass spectrometry, immunoassays, and nucleic acid chemistry for vaccines, diagnostics, and therapies. The company differentiates itself with a broad portfolio and global testing services that help customers from diagnostics to vaccine development. Its goal is to improve healthcare outcomes and public safety by enabling accurate testing and high-quality scientific tools.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
London, United Kingdom
Founded
1841

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