LIMS Engineer Job at BillionToOne (Union City)

LIMS Engineer

We are looking for a LIMS Engineer to join our Automation team in support of cli...

Location

United States , Austin

Salary:

168585.00 - 170201.00 USD / Year

BillionToOne

Expiration Date

Until further notice

Requirements

Bachelor's degree with Biological or Computational focus
Expert in Python
3+ Years Experience bench work experience
3+ Years Experience with developing LIMS, apps, or customer-facing tools
Ability to troubleshoot and diagnose advanced technical issues
Experience developing scripting solutions to automation problems, especially in a fast paced environment (startup experience a plus)
Strong attention to detail and ability to work flexibly and well under accelerated timeframes
Highly organized, strong written and verbal communication skills
Creative problem-solver who enjoys a variety of daily tasks

Job Responsibility

Develop LIMS workflows end-to-end: requirements gathering, Python development, interaction and collecting feedback, testing, and QA validation
Develop standalone applications that utilize Clarity API to add new self-service features
Oversee monitoring of LIMS servers and databases, identify bottlenecks, and optimize performance to support rapid scaling
Assist in triaging, investigating, and resolving operational LIMS issues for the CLIA lab
Participate in performing LIMS code reviews, verifications, and validations
Ensure compliance to all relevant corporate and regulatory requirements

What we offer

Working alongside brilliant, kind, passionate and dedicated colleagues, in an empowering environment, toward a global vision, striving for a future in which transformative molecular diagnostics can help millions of patients
Open, transparent culture that includes weekly Town Hall meetings
The ability to indirectly or directly change the lives of hundreds of thousands patients
Multiple medical benefit options
employee premiums paid 100% of select plans, dependents covered up to 80%
Extremely generous Family Bonding Leave for new parents (16 weeks, paid at 100%)
Supplemental fertility benefits coverage
Retirement savings program including a 4% Company match
Increase paid time off with increased tenure
Latest and greatest hardware (laptop, lab equipment, facilities)

Fulltime

LIMS Integration Engineer

Our Integration Engineers play a critical role in designing, implementing, and m...

Location

United Kingdom , Manchester or London

Salary:

Not provided

Magentus

Expiration Date

Until further notice

Requirements

Integration experience in one or more NHS settings e.g., national, acute, community social care, primary care
Experience in working with healthcare interoperability and integration technologies (e.g., HL7 v2, ASTM, FHIR)
Strong interpersonal skills with the ability to communicate in a technical and non-technical language
The ability to meet tight deadlines, balancing competing priorities and responding to client needs
The ability to build effective relationships with co-workers and clients
A continuous improvement mindset

Job Responsibility

Designing, configuring, and maintaining HL7 interfaces and integration solutions connecting our systems with other healthcare systems including PAS, order comms and reporting systems
Documenting laboratory analyser interfaces and specific requirements for each customer laboratory needs
Collaborating with cross-functional teams to design and document HL7 interfaces and data mappings, adhering to industry standards and best practice
Conducting thorough testing and validation of HL7 interfaces to ensure data accuracy, message integrity, and system interoperability
Diagnosing and resolving issues related to data exchange, interface connectivity, and data transformation
Implementing security measures to safeguard patient data and ensure compliance with relevant healthcare regulations, such as GDPR and NHS Digital standards
Maintaining comprehensive documentation of integration solutions, including interface specifications, configuration settings, and troubleshooting procedures
Collaborating with internal teams, external vendors, and healthcare providers to gather requirements, assess integration needs, and provide technical expertise
Providing training and support to end-users and technical staff on the usage of integrated systems and interfaces
Providing input and recommendations for improvements for internal processes to drive efficiency and effectiveness

What we offer

25 days annual leave (increases with length of service up to 4 days) plus 8 bank holiday
Holiday purchase scheme via salary sacrifice
An extra day annual leave for your birthday
Enhanced Maternity Leave
Enhanced Paternity Leave
Religious holiday swap programme
Up to two days paid Volunteering days
Paid time off during the working day to donate blood
Pawrental Leave
Litmos learning

Fulltime

New

Laboratory Technician II

Laboratory Technician II performs essential laboratory duties including wet chem...

Location

United States , Friendswood, TX

Salary:

Not provided

Airswift Sweden

Expiration Date

Until further notice

Requirements

Polytechnic diploma or technical certification in Chemical Engineering, Process Engineering, or related Technical fields
Demonstrated computer literacy and ability to learn laboratory information management systems (LIMS)
Experience with QA/QC systems preferred
Strong understanding of safety protocols, especially related to chemical handling, H2S, and NORM testing
Ability to work independently with moderate supervision in a fast-paced environment
Strong organizational, communication, and problem-solving skills

Job Responsibility

Sample Handling & Preparation: Receive, inspect, inventory, and prepare incoming field samples for testing
Retrieve samples from storage and ensure accurate sample tracking
Perform sample purging to remove H2S
Prepare samples via centrifugation, aliquoting, weighing, and packaging for shipments
record weights and dimensions (DIMS)
Analytical Testing: Conduct H2S testing on small-volume samples (SAR not required) and log results
Perform H2S testing on large-volume samples (SAR required)
Execute NORM testing using a Geiger counter
Conduct API Gravity measurements
Perform Total Sulfur analysis

Fulltime

Technician Materials Science Engineering

Position is required to coordinate sample preparation and analytical testing nee...

Location

United States , Latrobe

Salary:

Not provided

Kennametal

Expiration Date

Until further notice

Requirements

Technical degree (science, math, computer) or high school diploma and 3-5 years practical experience in a technical function
Attention to detail
Excellent communications skills
Proactive approach for safety and continuous improvement
Collaboration with trust and respect in a diverse team environment
Ability to address high volume workload while maintaining standards for safety and quality
Focus on exceptional customer experience
Basic PC skills in spreadsheets and word processing

Job Responsibility

Actively manage sample flow to include receiving samples from submitters, confirming correct identification and test plan, resolving questions on requests by communication with submitters and analysts, routing samples to labs for analysis, communicating special requirements or timelines to team members
Coordinate return, disposal or storage for samples upon request completion
Consult with analytical lab engineers to develop strategy for complex projects and to establish priorities and timelines
Generate summaries to facilitate tracking for open requests
Provide set up and training for new LIMS users
Order equipment and consumables needed for laboratory operation as requested by team members
Perform routine sample preparation and analytical testing. Requires appropriate PPE (may include safety glasses, gloves, lab coat, safety shoes, dust mask). Report results in LIMS
Strictly adhere to standard procedures developed at the Technology Center
Follow all EHS practices
Maintain work area in a neat and orderly fashion

Assistant Manager – R&D Processing, Home Care Bars

To lead the process design strategy for Home Care (HC) Bars, focusing on innovat...

Location

India , Mumbai

Salary:

Not provided

Unilever

Expiration Date

Until further notice

Requirements

Bachelor’s degree in chemical engineering (BE/B.Tech/)
5–7 years of experience in Research and Development, preferably in NSD Bars formulation and processing
Proficiency in digital tools for data modeling, process efficiency, and measurement
Strong knowledge of process control and mechanical instrumentation
Experience with HAZOPs and safety approval systems
Skilled in MS Office (Excel, PowerPoint, Word), SAP, and SCADA
Demonstrated project management and problem-solving capabilities
Understanding of consumer action standards and process parameter optimization

Job Responsibility

Develop and execute Design of Experiments (DoE) to define material handling protocols and processing routes for innovation and cost-saving initiatives
Provide timely technical inputs across critical project workstreams
Lead manufacturing design lock for key technologies and ensure alignment with strategic objectives
Define safety foundations and proactively eliminate risks in accordance with the Safety in Manufacture and Supply Approval System (SIMAS) to secure project approvals
Drive capability building initiatives at AMC-Bars
Oversee installation and commissioning of plant equipment, author operating manuals, and conduct initial operator training
Collaborate with Supply Chain to evaluate and enhance return on investment (ROI) for projects
Ensure product quality through close coordination with Supply Chain teams
Conduct standard trials and tests for soaps and NSD bars at lab and pilot scales, supported by physical-chemical analysis
Plan, execute, and report main plant trials with comprehensive data analysis and technical documentation

Fulltime

Manager, Quality Systems (QMS)

As the Manager, Quality Systems, you will support the design, implementation, an...

Location

Canada , Vancouver

Salary:

94880.00 - 118600.00 CAD / Year

AbCellera Biologics

Expiration Date

Until further notice

Requirements

5+ years of experience managing quality systems in a GxP-regulated environment, with demonstrated application of global CMC/GMP requirements and relevant regulations and guidance
Bachelor’s degree in a relevant scientific or engineering discipline with 8+ years of industry experience in biotechnology, pharmaceuticals, or life sciences
Strong understanding and hands-on experience with quality management systems and continuous improvement principles, including their application to QC laboratory operations and regulated environments
Solid understanding of drug development processes from discovery through CMC development, with the ability to translate business and regulatory requirements into practical, compliant solutions
Experience supporting, configuring, or owning QC laboratory electronic systems (e.g., LIMS, LES, CDS) in a GMP-regulated environment, including system lifecycle management and change control
Proactive in identifying opportunities for improvement, with strong critical thinking and problem-solving skills

Job Responsibility

Establishing, supporting, maintaining, monitoring, and continuously improving the QC Quality Management System (QMS) framework and associated quality system processes in compliance with applicable global CMC/GMP requirements
Supporting the operation, administration, and lifecycle management of QC laboratory electronic systems (eSystems), ensuring they effectively support sample management, analysis, data acquisition, data review, and result reporting in compliance with global GMP, data integrity, and regulatory requirements
Contributing to the design, implementation, and evolution of the QC data architecture, identifying eSystem capabilities needed to support QC workflows, data integrity (ALCOA++), and phase-appropriate compliance
Serving as the Business Process Owner (BPO) for QC laboratory systems (e.g. LIMS, LES, CDS), overseeing system changes, enhancements, and upgrades throughout the system lifecycle
Overseeing and maintaining QC eSystems master data, including user roles, permissions, system configurations, and controlled data objects
Developing, reviewing, and maintaining GMP procedures, work instructions, controlled documentation, and training materials governing the compliant and effective use, administration, and data management of QC eSystems, including delivery of end-user training sessions
Providing QC eSystem support for investigations, deviations, and CAPAs, including data retrieval, audit trail review, and system impact assessments
Supporting qualification and computer system validation activities for QC systems (e.g., protocol and risk assessment review, validation deviations/exceptions, and lifecycle documentation)
Managing QC eSystem licensing, user access, vendor relationships, and budgeting/forecasting for QC digital infrastructure
Collaborating cross-functionally with QC, Quality Systems, IT, Engineering, Validation, and external vendors to ensure QC eSystems are fit-for-purpose, compliant, and aligned with laboratory and business processes

What we offer

Equity
Annual bonus dependent on team and company performance
6% (non-match) RRSP contribution
CAD $1,500 annual Active Lifestyle Allowance
Annual vacation
Professional development opportunities
Comprehensive health benefits
Scientific and technical mentorship
Teams and social groups to build community and connections

Fulltime

Pharmaceutical Business Analyst

Are you a detail-oriented professional with strong analytical skills and a passi...

Location

Canada , Toronto

Salary:

Not provided

Amaris Consulting

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Business, Life Sciences, Engineering, or related field
Proven experience as a Business Analyst in the pharmaceutical or biotech industry
Strong understanding of GxP, regulatory compliance, and pharmaceutical manufacturing processes
Experience working with ERP, MES, LIMS, or other life sciences digital systems
Excellent communication, documentation, and stakeholder management skills
Ability to work independently and collaboratively in a fast-paced environment

Job Responsibility

Gather, analyze, and document business requirements from stakeholders across departments
Translate business needs into functional specifications and user stories
Collaborate with cross-functional teams including IT, QA, Manufacturing, and Regulatory Affairs
Support system implementation and process improvement initiatives
Perform gap analysis and recommend solutions to enhance operational efficiency
Assist in validation documentation and ensure compliance with industry regulations (GxP, FDA, EMA)

What we offer

An international community bringing together more than 110 different nationalities
An environment where trust is central: 70% of our leaders started their careers at the entry level
A strong training system with our internal Academy and more than 250 modules available
A dynamic work environment that frequently comes together for internal events (afterworks, team buildings, etc.)

Fulltime

Senior Director of Process Engineering

Are you motivated to participate in a dynamic, multi-tasking environment? Do you...

Location

United States

Salary:

196000.00 - 324000.00 USD / Year

NeoGenomics Laboratories

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Engineering, Life Sciences, or related field required or equivalent work experience required
Master’s degree preferred
12 or more years of experience in process engineering, laboratory automation, or technology transfer within clinical diagnostics or biotechnology, including 7 or more years in a leadership role required
Ability to travel up to 50% of the time
Proven expertise in technology transfer and laboratory automation
Strong knowledge of Lean Six Sigma and operational excellence methodologies
Experience navigating systems for laboratory workflows, including LIMS
Ability to lead cross-functional teams and manage complex projects
Knowledge of regulatory requirements for clinical laboratories (CLIA, CAP, FDA)
Excellent communication, leadership, and problem-solving skills

Job Responsibility

Provide strategic leadership for engineering projects and initiatives within the laboratory, and manage engineering teams, contractors, and external vendors to ensure on-time, on-budget project delivery
Drive operational excellence through best practices in process optimization, quality, and efficiency
Manage multiple complex projects simultaneously, overseeing resource allocation and providing strategic guidance on priorities
Identify, develop and execute automation strategies that enhance laboratory workflows, reduce turnaround times, and increase reliability in a cost-effective manner
Lead internal and external technology transfer initiatives across all clinical modalities
Identify opportunities for continuous improvement and cost optimization while supporting automation strategies that drive efficiency and scalability, leveraging Lean Six Sigma principles
Collaborate with QA and Compliance teams to ensure all deliverables meet regulatory and quality standards
Ensure compliance with CLIA, CAP, NYSDOH, and other relevant regulations
Apply product development life cycle processes to design and implement new solutions for laboratory operations
Partner with R&D, Lab Operations, QA, and IT to align technology transfer and automation objectives with organizational goals

What we offer

Career coaches internally
Many training opportunities
Highly competitive benefits with a variety HMO and PPO options
Company 401k match
Employee Stock Purchase Program
Tuition reimbursement
Leadership development
Start employees off with 16 days of paid time off plus holidays
Wellness courses
Highly engaged employee resource groups

Fulltime

LIMS Engineer

BillionToOne

Location:
United States , Union City

Category:
IT - Software Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
December 26, 2025

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for LIMS Engineer

LIMS Engineer

LIMS Integration Engineer

Laboratory Technician II

Technician Materials Science Engineering

Assistant Manager – R&D Processing, Home Care Bars

Manager, Quality Systems (QMS)

Pharmaceutical Business Analyst

Senior Director of Process Engineering

LIMS Engineer

BillionToOne

Location:United States , Union City

Category:IT - Software Development

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:December 26, 2025

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for LIMS Engineer

LIMS Engineer

LIMS Integration Engineer

Laboratory Technician II

Technician Materials Science Engineering

Assistant Manager – R&D Processing, Home Care Bars

Manager, Quality Systems (QMS)

Pharmaceutical Business Analyst

Senior Director of Process Engineering

Location:
United States , Union City

Category:
IT - Software Development

Contract Type:
Not provided

Job Posted:
December 26, 2025