LIMS Integration Engineer Job at Magentus (Manchester or London)

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

LIMS Support Engineer

The LIMS Support Engineer will provide essential application support for Laborat...

Location

United States , Morris Plains

Salary:

87120.00 - 181500.00 USD / Year

NTT DATA

Expiration Date

Until further notice

Requirements

8+ years of LIMS support or development experience
8+ years of hands-on skills in LabVantage (Java/Groovy) or LabWare (LADL, LIMS Basic)
8+ years of strong SQL skills (Oracle/SQL Server/PostgreSQL)
Understanding of QC/R&D workflows and regulated environments
Strong problem-solving and communication skills

Job Responsibility

Provide L2/L3 incident resolution for LIMS applications (LabVantage or LabWare)
Diagnose and resolve configuration issues, workflow errors, sample lifecycle problems, and data inconsistencies
Conduct detailed root-cause analysis and implement permanent fixes
Maintain LIMS master data, workflows, templates, and stability modules
Support version upgrades, patches, and environment maintenance
Assist laboratory users with operational questions, access issues, and data troubleshooting
Support integrations between LIMS and instruments, SAP/ERP, middleware, and APIs
Troubleshoot interface failures (REST/SOAP APIs, ETL jobs, instrument connectors)
Support CSV documentation, change control, IQ/OQ/PQ impact checks, and audit readiness
Ensure compliance with GxP, 21 CFR Part 11, and ALCOA+

Fulltime

Solution Architect

We are a leading provider of IT, engineering and consulting services. We are loo...

Location

Poland , Warsaw

Salary:

Not provided

Astek

Expiration Date

Until further notice

Requirements

Hold a Bachelor’s degree in Computer Science, Information Systems, Engineering, or have equivalent practical experience
Bring 7–10 years of experience as a Solution Architect in a regulated or highly structured environment
Have hands-on knowledge of SQL databases, relational data structures, and reporting systems
Possess proven experience in system integration projects (MES, ERP, LIMS, PLM, or related)
Communicate clearly and collaborate effectively in a cross-functional, global team setup
Are able to de-escalate discussions, maintain productivity, and keep focus on outcomes
Demonstrate expertise across multiple technology domains (e.g., networks, systems, databases, security)
Quickly understand the functions and capabilities of new technologies
Keep yourself up to date with trends and emerging technologies
Can develop and articulate a clear vision for one or more technology areas

Job Responsibility

Design and document solution architectures for Emerson PKM (core application), integrations across MES, LIMS, ERP, and PLM systems, as well as reporting capabilities, ensuring data consistency and interoperability
Define data models, interface specifications, and integration patterns that connect business requirements with technical implementation across all solution domains
Create architecture decision records and detailed technical documentation for PKM configurations, integration solutions, and reporting needs
Facilitate alignment between business stakeholders and technical teams to ensure shared understanding of the architectural design, data flows, and system capabilities
Lead architecture reviews, support solution validation activities, and assist in testing related to PKM, integrations, and reporting deliverables
Drive continuous improvement of solution standards, architectural patterns, and best practices across the Enterprise Recipe Management program

What we offer

Long-term collaboration
Technical training, certifications, and skills development
Competence Center mentoring – being a member of the Competence Center community from day one is an opportunity to develop your skills, participate in various conferences, and share knowledge and experience with people who face the same challenges every day
Clear career path
Employee benefits package (Multisport, private healthcare, life insurance, subsidized city card)
Friendly working atmosphere, team-building events, and team-building meetings

New

Director, Technical Development Operations

We are seeking an execution-driven, scientifically-grounded leader to establish ...

Location

United States , Norwood

Salary:

167000.00 - 300700.00 USD / Year

Moderna

Expiration Date

Until further notice

Requirements

Degree in Life Sciences, Chemistry, Engineering, Pharmaceutical Sciences, or related technical discipline
15 years of relevant experience with Bachelor’s degree or 10 years of relevant experience with a PhD.

Job Responsibility

Build, lead, and develop a high-performing multidisciplinary bioassay operations team, including scientists, automation technologists, analysts, and supervisors
Oversee execution of critical assay types such as IVRPE, IVRPA, and REDA supporting stability, release, and characterization
Define and own key operational metrics (e.g., throughput, TAT, % automation coverage, assay reproducibility, cost per result) and drive continuous improvement
Implement and govern GxP-ready infrastructure across SOPs, ELN templates, LIMS integration, barcoding, and sample chain-of-custody workflows
Execute workforce planning, recruiting, and training strategies aligned to the scale and complexity of automated operations
Serve as bioassay and operations lead in the design, build, and launch of the centralized Bioassay CoE, including facility input, equipment selection, FAT/SAT planning, validation, and Go-Live
Lead cross-functional integration with Quality, Facilities, Automation Engineering, Analytical Development, IT, Supply Chain, and EHS to ensure scope alignment, risk mitigation, and on-time delivery
Develop and implement the operating model that supports flexible deployment of GMP and non-GMP testing within shared lab space
Collaborate with automation and digital teams to embed next-generation tools, including opportunities to incorporate Generative AI capabilities for smarter lab operations and enhanced data analytics.

What we offer

Best-in-class healthcare coverage, plus voluntary benefit programs
Holistic approach to well-being, with access to fitness, mindfulness, and mental health support
Family planning benefits, including fertility, adoption, and surrogacy support
Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
Savings and investment opportunities
Location-specific perks and extras

Fulltime

Solutions Architect

We are seeking an experienced SAP Solution Architect to spearhead the Plan to De...

Location

United States

Salary:

152000.00 - 209000.00 USD / Year

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Business, Information Technology, Engineering, or a related field
advanced degree preferred
7+ years of experience as an SAP Business Analyst, with at least 3 years in a lead role supporting Plan to Produce processes
Expertise in SAP modules such as PP (Production Planning), QM (Quality Management), and MM (Materials Management)
experience with SAP S/4HANA is a plus
Proven experience integrating SAP with LIMS, WMS, MES, and QMS in a manufacturing or life sciences environment
Strong understanding of GxP regulations (e.g., 21 CFR Part 11, GMP) and their application to manufacturing and quality processes
Experience with in-house and contract manufacturing workflows, including batch management and material traceability
Excellent project management skills, with proficiency in tools like MS Project, Jira, or similar
Strong analytical, problem-solving, and communication skills to bridge business and technical teams

Job Responsibility

Solution Design, Implementation & Integration: Responsible for designing, describing, and managing SAP solution design of SAP modules (e.g., PP, QM, MM) to support end-to-end Plan to Deliver processes, including production planning, shop floor execution, quality management, and material management
Facilitate integration between SAP and boundary applications (LIMS, WMS, MES, QMS) to ensure data consistency, process alignment, and real-time visibility across manufacturing, quality operations, and warehouse processes
Collaborate with cross-functional teams and business stakeholders to map and optimize business processes, ensuring compliance with GxP standards and regulatory requirements (e.g., FDA, EMA) and upholding “fit to standard” design principles in alignment with organizational goals
Develop and maintain functional specifications, process flows, integration plans and system configurations to ensure PTD processes scalability, reliability, and performance
Review configurations and deployments to maintain quality standards
Create clear, concise decision rationale documents balancing innovation with practicality, considering factors like cost, support, and compatibility with global end to end designs
Effectively communicate complex technical concepts to non-technical stakeholders and multifaceted business processes to technical stakeholders
Manufacturing Support: Support both in-house and contract manufacturing operations by configuring SAP solutions to manage production schedules, capacity planning, and material traceability
Ensure SAP configurations align with manufacturing workflows, including batch management, shop floor control, and contract manufacturing processes
Quality Control & Assurance: Oversee the implementation of SAP Quality Management (QM) module to support quality control and assurance processes in a GxP environment

What we offer

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

Fulltime

Sr. Quality Systems Engineer

Beacon Technologies is seeking a Sr. Quality Systems Engineer for our client par...

Location

United States , El Segundo

Salary:

Not provided

Beacon Technologies

Expiration Date

Until further notice

Requirements

5+ years of experience in systems engineering on compliance systems, or regulatory technology environments
Bachelor’s degree in Engineering, Computer Science, Information Technology, or related technical field
Understanding of U.S. import compliance requirements related to CPSC, CBP, ACE, and electronic Certificate of Compliance filings are a plus
Experience working with integrated systems such as LIMS, data warehouses, and document management platforms
Trained in Veeva vault configuration and administration is preferred
Proven ability to translate regulatory and business requirements into clear technical specifications
Experience working cross-functionally with IT teams, external partners, and business stakeholders
Strong communication skills, comfortable leading meetings, training sessions, and discussions with both technical and non-technical audiences
Experience supporting external customers or retail partners in compliance-related processes is a plus
Project management experience with system implementations or enhancements

Job Responsibility

Act as the global subject matter expert for Certificate of Conformance (COC) processes related to U.S. imports
Own and continuously improve the end-to-end eCOC workflow, including integrations across Laboratory Information Management Sytem (LIMS), Google Big Query (GBQ), and Veeva
Partner with IT to define business and system requirements for enhancements impacting COC generation, metadata, test report management, and CSV full message set creation
Ensure alignment of system functionality with CPSC Portal and CBP ACE eFiling requirements
Collaborate with laboratories to ensure test reports and supporting documentation are accurately generated and transmitted through the system landscape
Support retailers performing direct import by gathering their eFiling requirements, providing guidance on CSV file creation, and troubleshooting submission issues
Lead business-side project management activities for system implementations, upgrades, and regulatory-driven changes
Oversee configuration, testing, validation, and user acceptance testing for eCOC-related system updates
Support the Organizational Change Management and training team ensuring training are developed and delivered to internal and external users to understand how to download test reports, generate COCs, and create compliant CSV files
Monitor regulatory updates and proactively assess impacts to systems and processes

What we offer

career advancement opportunities
extensive training
excellent benefits including paying for health and dental premiums for salaried employees

Fulltime

New

Manager, QC Systems

As the Manager, QC Systems, you will support the design, implementation, and ong...

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

Fulltime

Analytical Lab Manager

As the Analytical Lab Manager, you will oversee the daily operations of Valvolin...

Location

United States , Lexington

Salary:

Not provided

Valvoline

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Chemistry, Chemical Engineering, or a related scientific discipline (Master’s preferred)
5+ years of experience in an analytical or lubricant testing laboratory, with at least 2 years in a leadership or supervisory capacity
Demonstrated expertise with ASTM D-series test methods for oil and lubricant analysis
Experience managing laboratory equipment calibration and certification programs
Proficiency with analytical instruments including ICP, FTIR, viscometers, Karl Fischer titrators, and other industry specific equipment
Working knowledge of ASTM standards and quality assurance systems
Experience with LIMS platforms and data integrity protocols
Strong leadership and communication skills with the ability to mentor, motivate, and develop team members
Excellent analytical and troubleshooting abilities
High attention to detail, organizational strength, and commitment to operational excellence

Job Responsibility

Lead and develop a team of laboratory professionals focused on oil and lubricant analysis
Coordinate testing schedules, priorities, and resources to meet customer and operational goals
Review, validate, and approve analytical data to ensure consistency and compliance with ASTM and Valvoline standards
Oversee calibration and certification of analytical instruments (e.g., ICP, FTIR, viscometers, Karl Fischer titrators, and other industry specific equipment)
Maintain and manage equipment calibration schedules, documentation, and traceability in alignment with corporate quality systems
Support the development, implementation, and improvement of laboratory SOPs and testing methodologies
Ensure all laboratory activities meet safety, environmental, and quality requirements
Act as the technical point of contact for oil analysis programs, method troubleshooting, and customer inquiries
Drive continuous improvement initiatives, leveraging data and process insights to enhance accuracy and efficiency
Stay current with evolving ASTM test methods, emerging technologies, and best practices in lubricant testing and equipment calibration

What we offer

Health insurance plans (medical, dental, vision)
Health Savings Account (with employer base deposit and match)
Flexible spending accounts
Competitive 401(k) with generous employer base deposit and match
Incentive opportunity
Life insurance
Short and long-term disability insurance
Paid vacation and holidays
Employee Assistance Program
Employee discounts

LIMS Integration Engineer

Magentus

Location:
United Kingdom , Manchester or London

Category:
IT - Software Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
December 10, 2025

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