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    LG

    LGC Group

    Life Sciences

    Automation Engineer

    Petaluma, United StatesOn-SiteFull-time3+ yrs experience$112.2k / yearPosted 2d ago
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    Job description

    This is a 12-month contract position.

    The Automation Engineer designs, configures, tests, implements, and sustains automation solutions for formulation, DNA synthesis, manufacturing workflows, and production data systems at the Petaluma site. The role partners with Manufacturing, Quality, Operational Technology, Enterprise Information Technology, and external vendors to deliver reliable, maintainable, and compliant automation solutions. This position combines hands-on equipment and workflow support with software development, MES/LIMS integration, scheduling and batching automation, production data capture, and practical deployment of automation technologies that improve productivity, data integrity, operational efficiency, and manufacturing scalability.

    To perform this job successfully, an individual must be able to capably perform each of the following essential duties:

    • Develop, configure, test, troubleshoot, and verify assigned automated liquid handling workflows on Dynamic Devices, Tecan, and other production equipment, including methods, deck layouts, consumables, plates, scripts, workflow verification, and integration with related manufacturing processes
    • Develop, modify, test, troubleshoot, and document automation and scheduling software scripts for assigned workflows using C#, Python, instrument specific programming languages, and other approved technologies
    • Support DNA synthesis automation and workflow integration activities involving sample tracking, batch tracking, instrument status, barcode identifiers, labels, and data flow between manufacturing processes and digital systems
    • Configure and test MES and LIMS workflows that support traceability including operator tasks, station activities, production records, instrument events, and batch status visibility
    • Contribute to the design, implementation, configuration, and improvement of scheduling and batching automation solutions for assigned workflows, including run sequencing, dispatching, queue management, and hands-off workflow initiation, to reduce manual batching decisions and improve process consistency
    • Execute dry runs, wet runs, process simulations, user acceptance testing, issue triage, and operational readiness testing in collaboration with Manufacturing, Quality, Process Design, and Operational Technology teams
    • Author or contribute to work instructions, automation requirements, risk assessments, test protocols, traceability documentation, deviation records, and validation or computer software assurance deliverables in support of controlled implementation, quality review, and compliant system sustainment.
    • Identify and communicate workflow bottlenecks, manual handoff risks, data integrity gaps, batching inefficiencies, and automation improvement opportunities for evaluation by senior engineering, quality, or management stakeholders
    • Partner with internal stakeholders and external vendors to resolve automation issues, verify workflow performance, and ensure solutions are usable by operators and sustainable by site teams
    • Adhere to company policies, procedures, safety expectations, quality requirements, data integrity practices, and engineering standards
    • Perform other duties as assigned

    Essential Knowledge and Qualifications:

    • Bachelor’s degree in automation engineering, electrical engineering, mechatronics, robotics, computer science/engineering, manufacturing technology, or a related technical discipline with at least 1 year of automation experience; or associate degree or technical certificate in a related technical discipline with at least 3 years of automation experience; or an equivalent combination of relevant education and hands-on automation experience
    • Working knowledge of software development and scripting using C# and Python, including the ability to read, troubleshoot, modify, test, and document code used for instrument control, workflow automation, data processing, system integration, and manufacturing support
    • Hands-on experience supporting liquid handlers, laboratory automation, workflow integration, manufacturing automation, instrument integration, or automated laboratory or manufacturing systems
    • Working knowledge of liquid handling workflows, plate-based processing, sample tracking, batch tracking, barcode-driven workflows, instrument setup, basic method troubleshooting, and manufacturing data capture requirements
    • Experience configuring, operating, supporting, or troubleshooting automated liquid handling systems such as Tecan, Lynx, Hamilton, Beckman, or comparable platforms
    • Experience supporting automated workflows that include instruments, consumables, plates, labels, barcode identifiers, data capture, and structured operator or system handoffs
    • Experience documenting automation configurations, test results, troubleshooting outcomes, work instructions, training materials, and operational handoff information
    • Ability to follow controlled procedures, execute testing, document technical changes, and communicate issues clearly across Manufacturing, Quality, Engineering, Operational Technology, Enterprise Information Technology, and vendor teams
    • Demonstrated written and verbal communication skills, including the ability to communicate technical information to both technical and non-technical stakeholders
    • Strong attention to detail, practical troubleshooting skills, and comfort working in active manufacturing or laboratory environments
    • Ability to work independently on assigned tasks while escalating risks, blockers, and technical decisions appropriately
    • Working knowledge of Microsoft Office applications including Outlook, Word, Excel, PowerPoint, and Teams

    Desired Knowledge and Qualifications:

    • Direct experience with Lynx and/or Tecan liquid handlers in a biotechnology, diagnostics, pharmaceutical, life science, or advanced manufacturing environment
    • Experience supporting DNA synthesis, oligonucleotide manufacturing, plate-based workflows, reagent delivery workflows, sample preparation, or high-throughput laboratory automation
    • Experience with Tulip Manufacturing Execution System workflows, Laboratory Information Management Systems, electronic batch records, production data capture, operator guidance systems, or station-based digital work instructions
    • Experience with scheduling software, batch scheduling logic, run sequencing, dispatching tools, production planning systems, optimization algorithms, or rules-based workflow automation
    • Exposure to artificial intelligence (AI)-assisted batching, algorithmic scheduling, automated queue management, hands-off workflow initiation, or decision-support tools for manufacturing or laboratory operations
    • Familiarity with structured query language (SQL), Python, scripting, representational state transfer (REST) application programming interfaces (APIs), OPC Unified Architecture (OPC-UA), barcode systems, label printing systems, instrument event capture, database integrations, or manufacturing data pipelines
    • Experience supporting Good Manufacturing Practice (GMP), International Organization for Standardization (ISO), regulated, or quality-controlled environments, including commissioning, computer software assurance testing, change control support, and data integrity practices

    What we offer (US based-employees):

    • Competitive compensation with strong bonus program
    • Comprehensive medical, dental, and vision benefits for employees and dependents
    • FSA/HSA Pre-tax savings plans for health care, childcare, and elder care
    • Deductible Buffer Insurance and Critical Illness Insurance
    • 401(k) retirement plan with matching employer contribution
    • Company-paid short- and long- term disability, life insurance, and employee assistance program
    • Flexible work options- 8, 10 and 12 hour shifts available with option of day, swing and night shifts.
    • Pet Insurance for our furry friends
    • 8 weeks of Parental Leave for qualifying life events
    • PTO that begins immediately
    • Full week paid off during the holidays
    • Town Hall monthly meeting onsite/virtual, Cheer program where employees are recognized for outstanding work, Companywide social events, frequent catered lunches and much more!

    The typical pay range for this role is: Salary Range: $112,211 (Minimum) - $168,316 (Maximum)

    This range represents the low and high end of the anticipated salary range for the California -based position.  The actual base salary will depend on several factors such as: experience, skills, and location.

    This position requires current U.S. work authorization. We are unable to sponsor or assume sponsorship for temporary visas (including H‑1B, H‑2B, OPT, O‑1, TN)

    ABOUT LGC:

    LGC is a leading, global life science tools company, providing mission-critical components and solutions into high-growth application areas across the human healthcare and applied market segments. Its high-quality product portfolio is comprised of mission-critical tools for genomic analysis and for quality assurance applications, which are typically embedded and recurring within our customers’ products and workflows and are valued for their performance, quality, and range.

    OUR VALUES

    • PASSION
    • CURIOSITY 
    • INTEGRITY
    • BRILLIANCE
    • RESPECT

    EQUAL OPPORTUNITIES 

    LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, pregnancy or maternity, religion, or belief. Short listing, interviewing and selection will always be carried out without regard to gender, sexual orientation, marital status, color, race, nationality, ethnic or national origins, religion or belief, age, or trade union membership.

    For more information about LGC, please visit our website www.lgcgroup.com

    #scienceforasaferworld

    Science for a Safer World

    LGC Group is a global life science‑based organisation delivering measurement science, standards, and assurance solutions across healthcare, pharma, and food sectors.

    Job details are sourced from the employer's original posting.

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    About the company

    LGC Group

    LGC Ltd ( www.lgcgroup.com ) is an international life sciences company working with customers in the government, academic, pharmaceutical, agricultural biotechnology, food, environment, security and sports sectors. LGC’s Grant Management Group (GMG) manages a number of research funding programmes on behalf of government departments and other large national health bodies, to improve NHS patient health and care. At the National Institute for Health and Care Research (NIHR) we enable and deliver world-class research that transforms people’s lives, promotes economic growth and advances science. We manage public investment in excess of £550 million per annum and provide bespoke expertise to charitable and commercial organisations to get the most out of their research funding. The NIHR Central Commissioning Facility (CCF) in Twickenham, based at LGC Ltd ( www.lgcgroup.com ), is one of NIHR’s Coordinating Centres and manages a number of research funding programmes on behalf of NIHR and the Department of Health and Social Care (DHSC). This role is based in the Systems Team at Twickenham.

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