MES Designer Job at Accenture (Cork)

MES Designer

Are you a motivated Systems Engineer with Manufacturing Execution Systems (MES) ...

Location

Ireland , Cork; Dublin

Salary:

Not provided

Accenture

Expiration Date

Until further notice

Requirements

Manufacturing Execution Systems (MES) experience within Life Science, Pharmaceutical or Biotech industry
hands-on MES design experience

Job Responsibility

Partner with technical leads and clients to support the design, development, documentation, and implementation of Manufacturing Execution Systems (MES) for a growing client base
Collaborate with business clients and internal teams to determine appropriate solutions and deliver on multiple large-scale projects
Work collaboratively with business users to define the needs and design solutions that add value
Gather user requirements in relation to controlling and recording manufacturing activities
Design, author, develop and configure Electronic Batch Records (EBR)
Implement MES solutions and integrate with ERP and control equipment
Document MES configuration and validation of EBRs

Fulltime

Software Development Advisor

We are currently seeking a Software Development Advisor to join our team in CDMX...

Location

Mexico , CDMX

Salary:

Not provided

NTT DATA

Expiration Date

Until further notice

Requirements

10+ years of deep expertise in .NET, C#, VB.NET
Bachelor's degree in Computer Science, Software Engineering, or a related Engineering discipline
7+ years of professional object-oriented programming experience heavily focused on C# and VB.NET
5+ years of experience working in discrete or continuous manufacturing environments
Deep understanding of MES workflows, batch processing, and industry standards
Expert-level capability with MS SQL Server, SSIS, SSRS, and/or Oracle databases
Hands-on experience with OPC DA/UA, REST/SOAP APIs, message queues (MSMQ), and connecting MES platforms to ERP systems
Experience with Visual Studio, Git, and Azure DevOps for CI/CD environments

Job Responsibility

Architect and build advanced MES modules using C# and .NET
Safely modernize and migrate legacy, factory-critical VB.NET and ASP applications into modern .NET frameworks
Design robust integration layers connecting the MES layer with ERP (SAP/Oracle), SCADA, PLCs, and WMS (Warehouse Management Systems) using APIs and Web Services
Develop software that interacts with hardware controls, machine interfaces, and OPC servers to automate real-time data collection on the factory floor
Architect and optimize complex T-SQL queries, stored procedures, and triggers using MS SQL Server and/or Oracle databases to ensure high data integrity
Act as the technical lead on MES projects, reviewing code, writing technical specifications, and mentoring junior developers on engineering best practices
Provide tier-3, on-call support for critical production issues, minimizing equipment downtime and ensuring 24/7 system reliability

Fulltime

Sr Associate SAP Architect, Order to Cash - Clinical

Let’s do this. Let’s change the world. In this vital role you will be responsibl...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree OR Master’s degree in computer science or STEM majors and 1 to 3 years of SAP implementation experience in SAP S/4 SD OR Bachelor’s degree in computer science or STEM majors and 3 to 5 years of SAP implementation experience in SAP S/4 SD OR Diploma in computer science or STEM majors and 7 to 9 years of IT or years of SAP implementation experience in SAP S/4 SD
Strong hands-on experience configuring and customizing sales, delivery & billing document types and Item categories, contracts and pricing, ATP, export controls, output determination, credit Management, EDI/IDOC integration with 3PL’s, Inter and Intra company STO’s. Experience with S/4HANA Advance intercompany STO and Sales process
Good understanding of SAP Fiori, ABAP and BTP technologies
Ability to design and implement solutions based on business requirements, including debugging and root cause analysis
Experience in creating detailed documentation, including functional specifications, test cases, and compliance reports
SAP Certified Application Associate in SAP S/4 Hana Sales and Distribution
Strong analytical and problem-solving abilities
Excellent communication and collaboration skills
Ability to work effectively with cross-functional teams and stakeholders
Detail-oriented with a focus on accuracy and compliance

Job Responsibility

Design, configuration, and implementation of SAP S/4 HANA Clinical OTC processes (Order management, billing, invoice management, distribution and logistics)
Ensure seamless integration between SAP S/4 modules (MM, FI, PP, TM, ATTP, GTS, EAS, Ariba, and EWM) as well as non-SAP systems for planning, quality and manufacturing (Example - MES, IRT, IVRS and Anaplan)
Conduct architectural reviews and assessments to identify potential risks and recommend mitigation strategies
Creation and maintenance of critical documentation such as technical assessments, configuration specs, functional designs, test cases, and user manuals. Ensure compliance with pharmaceutical industry standards and regulations
Participate in ERP implementation projects, including blueprinting, gap analysis, testing, go-live, and post-production support
Participate in sprint planning, reviews, and retrospectives to deliver and sustain Amgen's S/4HANA ecosystem utilizing the Scaled Agile Framework (SAFe)
Develop innovative solutions that drive speed to value via AI/ML and leading practices

Fulltime

Control Systems Software Designer

As a member of a highly motivated, multidisciplinary team, you will design and d...

Location

Canada , Woodbridge

Salary:

36.54 - 54.81 USD / Hour

ATS Automation Tooling Systems Inc.

Expiration Date

Until further notice

Requirements

A post-secondary degree specializing in Mechatronics, Systems, Electrical or Computer Engineering
3 years of experience programming Programmable Logic Controllers (PLC), and Human/Machine Interfaces (HMI) using Allen Bradley (Rockwell Studio 5000 Logix Designer) or Siemens (TIA Portal) software
3 years of experience in a hands-on automation/controls environment working on Supervisory Control and Data Acquisition (SCADA) and Manufacturing Execution Systems (MES) systems
Proficiency in understanding programs written in structured test (i.e. Visual Basic, C#, Python, languages). Strong programming, mechanical and electrical problem-solving skills
Experience with configuration/troubleshooting of instrumentation (power supplies, meters, sensors, safety switches, etc.) using vendor software and interfaces
Experience working in Just-In-Time environments and on mission critical systems
Ability to communicate effectively, both orally and in writing
Understanding of robotics, control systems and machine operation with hands-on experience is required
A self-starter with the ability to work as part of a team in a fast-paced environment with minimal supervision

Job Responsibility

Design and develop software programs (PLC and/or PC based) specific to customer and project requirements based on standard ATS programming methods (ATS Global Code Standard)
In depth programming in environments mainly using PLC Ladder logic (Rockwell / Siemens platforms), and structured test (i.e. shell scripting, Visual Basic, C#, Python)
Ability to reverse-engineer and write PLC code from scratch
Select, test and integrate hardware and software components such as robots, I/O, analog devices, motion controllers, sensors, vision systems and lasers
Debug and commission control systems at our facility, during the system integration stage and then at the customer's site during installation. Travel to both domestic and international customer locations for SAT (up to 20% travel per year)
Work with other members of the control systems design department and other groups to continuously improve methods of integrating controls technology, with the goals being enhanced safety, enhanced functionality and reduced cost
Work with customers, project managers, designers, toolmakers and electricians to solve problems to provide the customer with a complete, functional automation system
Provide thorough testing of machine functionality to verify software program completeness
Provide accurate documentation for each project and training specific to their current project (i.e. machine operation, programming principles and program structure)
Improve the knowledge and capability of other members of the department through mentoring. Responsible for meeting Team Member level KPIs as assigned. (Budget, Schedule, Quality, CI)

What we offer

Eligible for Annual Incentive Bonus
Stock Purchase Plan
3 Weeks Vacation
Health Care Benefits + $600 Health Care Spending Account
Employee Engagement Events (Employee BBQ’s and lunches, weekly snack day, etc.)
Employee Development Programs
Overtime pay
RSP matching
Employee Referral Bonuses
Educational Reimbursement Program

Fulltime

New

Senior Software Development .NET C# VB.NET

We are currently seeking a Senior Software Development- .NET, C#, VB.NET to join...

Location

Mexico , Guadalajara

Salary:

Not provided

NTT DATA

Expiration Date

Until further notice

Requirements

Bachelor's degree in Computer Science, Software Engineering, or a related Engineering discipline
7+ years of professional object-oriented programming experience heavily focused on C# and VB.NET
5+ years of experience working in discrete or continuous manufacturing environments
Deep understanding of MES workflows, batch processing, and industry standards
Expert-level capability with MS SQL Server, SSIS, SSRS, and/or Oracle databases
Hands-on experience with OPC DA/UA, REST/SOAP APIs, message queues (MSMQ), and connecting MES platforms to ERP systems
Experience with Visual Studio, Git, and Azure DevOps for CI/CD environments

Job Responsibility

MES Development & Modernization: Architect and build advanced MES modules using C# and .NET. Safely modernize and migrate legacy, factory-critical VB.NET and ASP applications into modern .NET frameworks
System Integration: Design robust integration layers connecting the MES layer with ERP (SAP/Oracle), SCADA, PLCs, and WMS (Warehouse Management Systems) using APIs and Web Services
OT/IT Convergence: Develop software that interacts with hardware controls, machine interfaces, and OPC servers to automate real-time data collection on the factory floor
Database & Reporting: Architect and optimize complex T-SQL queries, stored procedures, and triggers using MS SQL Server and/or Oracle databases to ensure high data integrity
Technical Leadership & Mentorship: Act as the technical lead on MES projects, reviewing code, writing technical specifications, and mentoring junior developers on engineering best practices
Support & Maintenance: Provide tier-3, on-call support for critical production issues, minimizing equipment downtime and ensuring 24/7 system reliability

New

Senior Director Research & Development

The Single-Use Technologies Division (SUD) is a global leader in the design and ...

Location

United States , Plainville

Salary:

212000.00 - 317000.00 USD / Year

myGwork - LGBTQ+ Business Community

Expiration Date

Until further notice

Requirements

Bachelor's degree in engineering, physical sciences, or chemistry required
Master's degree or Ph.D. preferred
10+ years of progressive R&D leadership experience, preferably within bioprocessing, bioproduction, or regulated medical device environments
Demonstrated success leading global, multi-site teams and delivering complex products from concept through commercialization
Strong background in bioprocess systems and equipment
experience with single-use technologies strongly preferred
Experience with digital and data-enabled systems (automation, control systems, MES, ERP, historians, analytics) preferred
Ability to influence across functions and operate effectively in a matrixed, fast-paced environment
Ability to travel up to 25% domestically and internationally

Job Responsibility

Serve as an integral member of the SUD leadership team, representing R&D in strategic planning (STRAP), portfolio prioritization, and Annual Operating Plan (AOP) processes
Own and execute the global R&D and product development strategy aligned with the business and market needs
Partner closely with Product Management, Market Development, Manufacturing Engineering, Operations, Quality, and Commercial teams to drive end-to-end lifecycle execution
Engage directly with customers and commercial teams on complex technical programs
Partner with the Bioproduction Group Innovation team, other business groups, and the Corporate Innovation Council to develop next-generation products, platforms, and differentiated intellectual property
Drive technology collaboration across divisions and business units to accelerate innovation and leverage enterprise capabilities
Translate customer and market requirements into differentiated products that meet cost, quality, performance, regulatory, and time-to-market expectations
Lead the advancement of digitalization, automation, and data-enabled technologies within single-use and bioprocessing systems
Champion all aspects of regulated product development, ensuring compliance with design control and quality system requirements
Serve as process owner for New Product Introduction (NPI), Engineer-to-Order (ETO/customization), and product improvement processes

What we offer

A choice of national medical and dental plans, and a national vision plan, including health incentive programs
Employee assistance and family support programs, including commuter benefits and tuition reimbursement
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
Variable annual bonus based on company, team, and/or individual performance results

Fulltime

New

Project Manager - MES (Medical Devices / Life Sciences)

We are currently seeking a Project Manager - MES (Medical Devices / Life Science...

Location

Puerto Rico , San Juan

Salary:

Not provided

NTT DATA

Expiration Date

Until further notice

Requirements

10+ years of strong proficiency in: C#, ASP.NET, .NET Core, SQL Server, WPF or Blazor (for HMI/Dashboard development)
5+ years of experience with MES architecture and shop floor system integration (PLCs, SCADA)
Proven experience managing MES implementations in: Life Sciences, Medical Devices (Class II/III preferred)
PMP (Project Management Professional) OR Certified Scrum Master (CSM)
Strong understanding of Quality Management Systems (QMS)
Familiarity with: FDA 21 CFR Part 11, GAMP standards, ISO 13485, FDA Design Controls
Hands-on experience with Computer System Validation (CSV)
Strong documentation and audit readiness experience
Strong leadership and stakeholder management
Excellent communication and reporting skills

Job Responsibility

Define project scope, objectives, and deliverables in collaboration with senior management and key stakeholders
Develop comprehensive project plans including timelines, milestones, and resource allocation
Drive end-to-end execution of MES implementation projects, ensuring alignment with organizational goals
Forecast project requirements and manage budgets effectively
Track project expenses and identify/mitigate variances proactively
Optimize resource utilization across teams and project phases
Lead cross-functional teams including software engineers, automation specialists, and QA teams
Delegate tasks effectively, ensuring accountability and high performance
Drive delivery using Agile or hybrid SDLC methodologies
Identify and mitigate project risks, issues, and bottlenecks

Fulltime

Systems Administrator, Cell Manipulation Core Facility

The System Administrator III will work internal to the Cell Manipulation Core Fa...

Location

United States , Boston

Salary:

106000.00 - 123500.00 USD / Year

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

Knowledge of lab safety and infection control
Knowledge of cell therapy processing, medical, hematologic, oncologic and scientific terminology
Knowledge of Web publishing, ODBC/JDBC interfaces and SQL
Knowledgeable of BOE template builder and ability to collaborate/train on the builder
Ability to assess workload and prioritize and delegate tasks
Ability to accommodate schedule adjustments, as well as off-shift and weekend assignments as workload dictates
Excellent customer service skills and demonstrated ability to develop effective internal working relationships with a diverse employee population
Strong project management skills
Demonstrated competence in managing system projects
Demonstrated competence in writing and executing validation plans

Job Responsibility

The System Administrator III will work internal to the Cell Manipulation Core Facility to manage systems across the Cell Therapy (CT) Networks by implementation and validation of computer systems impacting the department and CT program. The System Administrator III works in conjunction with the project teams from Partners Healthcare System and CMCF technical staff as well as working with DFCI and Partners IS on enterprise systems such as Epic and Sunquest. Systems will include, but are not limited to Partners Order Entry System for Biological Products (BOE/BPAA), Eceptionist, Sunquest, REES Environmental Monitoring systems, Internal Server systems, CMCF FileMaker Databases, FreezerWorks Bio-Repository system selected MES, and other internal systems such as Microsoft Access and Filemaker databases
Demonstrates knowledge of CMCF, clinical and laboratory workflow to incorporate and propose design consideration for CMCF applications
Examines existing business models and flows of data in CT and assists to implement and support the IT manufacturing solutions for the CMCF
Performs thorough data and system analyses and develops a risk-based analysis understanding
communicates the consequences that erroneous data could have on patient care
Creates and maintains the procedures for system use, maintenance, and validation documents for upgrades and continuity of care during down time
Identifies critical data and coordinating / consolidation of existing data systems into the appropriate secure database
Manages all internal computer systems used by the facility and assists in the compilation of relevant data as required for ongoing analysis and quality improvement
Manages the team that submits data to the CIBMTR either via OTTR registry agent or formsnet3
Assists in the implementation / management of software needs for various transfusion management activities for DF clinical lab and teams

Fulltime

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MES Designer

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