LIMS Engineer Jobs

New

LIMS Engineer

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

Location

United States , Union City

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

OneLIMS Lead

We are looking for a highly skilled OneLIMS Lead for a hybrid role based in Toro...

Location

Canada , Toronto

Salary:

Not provided

Amaris Consulting

Expiration Date

Until further notice

Requirements

Degree in Life Sciences, Pharmacy, Chemistry, Engineering, Information Systems, or related field
8+ years of experience in pharmaceutical or biotech environments, including 4+ years in LIMS implementation or major LIMS upgrades
Experience working in Quality Control lab operations—ideally Raw Materials testing and release
Strong knowledge of Computer System Validation in GMP/GLP context: GAMP5, Annex 11, 21 CFR Part 11
Proven experience as a functional lead, business analyst, or project manager on laboratory informatics projects, preferably multisite
Demonstrated ability to coordinate cross-functional teams and external vendors, influence decisions, and manage stakeholders
Excellent communication skills with the ability to translate between business and technical teams
Strong documentation skills and high attention to detail
Proven experience with QC or laboratory master data: materials, specs, analytical methods, limits, and static data structures
Hands-on involvement in at least one data migration or large-scale master data harmonization project including mapping, cleansing, and reconciliation

Job Responsibility

Act as the primary interface between QC laboratories, Manufacturing & Supply, Quality, IT, and external suppliers for the OneLIMS Raw Materials scope
Lead planning and execution of the Raw Materials deployment, including scope definition, timeline, risks, interdependencies, and status reporting
Translate Raw Materials and Quality Control processes into OneLIMS configuration and workflows, ensuring harmonization across sites
Oversee master data requirements gathering, pilots, and configuration for ~600 Raw Materials records and associated analytical methods
Supervise the build and verification of LIMS calculations, limits, and business rules, ensuring regulatory compliance and data integrity
Coordinate data migration, cutover, and hypercare activities for the Raw Materials scope
Define and manage User Acceptance Testing and validation strategy in alignment with GMP, GLP, GAMP5, Annex 11, and 21 CFR Part 11
Review and approve UAT scripts, validation plans and protocols, ensuring full traceability
Ensure high-quality configuration documentation and detailed specifications
Support SOP red-lining and updates to align laboratory processes with the new system

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

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

Safety Director - Industrial Maintenance

Lead and manage the industrial maintenance safety program to ensure a safe, comp...

Location

United States , Little Rock

Salary:

Not provided

Lexicon, Inc

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Safety, Engineering, Industrial Hygiene, Environmental Science, or related field preferred
8+ years of EHS experience in heavy industrial/manufacturing/process environments
3–5 years leading maintenance safety programs or teams
CSP, CIH, CRSP, OHST, CHST or relevant safety certifications preferred
Strong understanding of mechanical, electrical, and process safety principles
Strong leadership, coaching, project management, investigative (root cause) skills
Excellent communication/ presentation abilities
Proficient with incident management and safety management software
Safety-first mindset, decisive, collaborative, influential
Must be legally authorized to work in the United States for our company without the need for current or future visa sponsorship

Job Responsibility

Develop, implement, and maintain the maintenance safety management system, policies, procedures, and work controls
Ensure compliance with OSHA, EPA, NFPA, local regulations, industry standards, and company EHS policies
Oversee and continuously improve preventive programs
Lead safety strategy for maintenance activities
Direct and deliver safety training and competency programs for maintenance staff and contractors
Manage incident investigation and root cause analysis for maintenance-related events
Conduct regular audits, inspections, and risk assessments of maintenance operations
Champion good catch, near-miss reporting, and safety culture initiatives
Coordinate with operations, engineering, reliability, procurement, and contractors to integrate safety
Oversee contractor safety prequalification, orientation, monitoring, and enforcement

What we offer

Health Insurance
HSA with Employer contributions
Dental Insurance
Vision Insurance
Life Insurance
Disability Income Benefits
Paid Holidays
Paid Vacation
401 (k)

Fulltime

Mes Project Leader

As an MES Project Leader, you will oversee the full project lifecycle — from ini...

Location

Singapore

Salary:

Not provided

Amaris Consulting

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Engineering (Chemical, Industrial, Manufacturing), Computer Science, Information Systems, or related field
8+ years in pharmaceutical, biotech, or regulated manufacturing
5+ years of hands-on experience with MES platforms (e.g., Siemens OpCenter, Werum PAS-X, Rockwell MES)
Solid understanding of GMP operations and digital manufacturing processes
Experience managing end-to-end technology or transformation projects
Familiarity with system integration (ERP, SCADA, LIMS) and validation lifecycle (IQ/OQ/PQ)
Excellent communication, leadership, and client-facing skills

Job Responsibility

Lead MES Implementation Projects: Manage project scope, timelines, resources, budgets, and risks
Drive Cross-Functional Collaboration: Coordinate with digital, quality, manufacturing, and IT stakeholders
Client Engagement: Act as the main point of contact, facilitating workshops, requirement sessions, and steering meetings
Business Analysis: Map manufacturing workflows, identify process gaps, and translate them into system requirements
System Configuration & Testing: Oversee MES configuration, UAT execution, and integration with ERP, LIMS, SCADA, or DeltaV
Compliance & Documentation: Ensure deliverables meet GMP, FDA 21 CFR Part 11, EU Annex 11, and ALCOA+ standards
Continuous Improvement: Support clients in digital transformation initiatives and best practice adoption

What we offer

Global Diversity: Be part of an international team of 110+ nationalities
Trust and Growth: 70% of our leaders starting at entry-level
Continuous Learning: Internal Academy and over 250 training modules
Vibrant Culture: Regular afterworks, team-building events
Meaningful Impact: CSR initiatives, including the WeCare Together program

New

Manufacturing associate

This is a contract role: ***Shift schedule rotating 12-hour night shift from 6PM...

Location

United States , Novato

Salary:

15.00 - 30.00 USD / Hour

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Strong communication skills—verbal and written
Ability to work in a team environment which includes good conflict resolution and collaboration
Displays good initiative to identify areas for improvement and implement solutions
Bachelor’s degree in science related area or engineering
Associate’s degree in science related area or Biotech certificate with 2+ years of experience in a biotech manufacturing environment or other regulated industry

Job Responsibility

Understanding of process theory and equipment operation
Ability to learn biopharmaceutical manufacturing processes including mammalian cell culture, depth filtration, tangential flow filtration, column chromatography, centrifugation, protein purification, and formulation of bulk drug substance
Support initiatives for process optimization
Identify and elevate processing issues and support solutions
Gain experience with automation systems (LIMS, MES, PI, etc.)
Provide feedback and/or suggested changes to operational procedures
Assist in the incorporation of new technologies, practices, and standards into procedures
Capable of writing and reviewing process documents
Understanding of cGMPs as related to Commercial Operations
Ability to utilize Quality systems (Deviations, CAPAs, Change Requests, Action/Alert Reports, etc.)

What we offer

discretionary annual bonus
discretionary stock-based long-term incentives
paid time off
company-sponsored medical, dental, vision, and life insurance plans

Fulltime

New

EMR Integrations Manager

BillionToOne is seeking a EMR Integrations Manager to lead the operational deliv...

Location

United States

Salary:

147841.00 - 168961.00 USD / Year

BillionToOne

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Health Informatics, Information Systems, or related field preferred
5+ years of experience in lab systems, EMR integration, interoperability, or healthcare IT operations
5+ years of experience with clinical systems, LIMS, and Salesforce
Hands-on experience with HL7, FHIR, and integration platforms (Redox, Mirth, or similar)
Proven ability to manage integration projects end-to-end, including planning, testing, and production support
Excellent problem-solving, organizational, and communication skills

Job Responsibility

Manage day-to-day EMR integration operations, ensuring accurate and timely order and result transmissions across partner systems
Oversee HL7 integrations, including setup, validation, testing, and ongoing monitoring of connections through Redox and other vendors
Lead manual EMR order associations and triage—investigating and resolving missing or misrouted orders and results
Improve and maintain automation processes (bots) for EMR order matching and reduce manual touchpoints
Coordinate manual testing workloads for EMR integrations, ensuring end-to-end data validation and compliance
Work with Software engineering to ensure the scalability of our EMR integrations
Serve as the project manager for EMR integrations across all business units, coordinating between Sales, Engineering, Product, and external partners
Manage the intake and approval process for new EMR integration requests, ensuring alignment with business priorities and feasibility
Represent EMR Operations on hospital and clinic integration calls, providing technical and workflow expertise
Collaborate with Engineering and Product teams to resolve issues, drive continuous improvement, and manage release readiness

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 Engineer

BillionToOne

Location:
United States , Austin

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.

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Location:United States , Austin

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.

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Contract Type:
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Job Posted:
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