Total 22 job vacancies by T0ss-ex S Pte. Ltd.

The Job

• Work with various teams and Project managers (for applications) to plan, update and review infra setup and delivery plans.
• Review and advise in technical resource planning, risk management of infra technical delivery plans and activities to meet regulatory requirements and IT standards/guidelines.
• Manage and coordinate with Vendor to complete the required setup/projects.
• Identify and coordinate other team's resources (eg. e2P) for project execution and/or infra setup activities.
• Proactively plan and track the delivery schedule.
• Promote teamwork and skills transfer between staffs.
• Prioritise delivery of assigned tasks.
• Meet agreed timelines.
• Delegate and distribute work effectively.
• Manage the deployment of hardware/software and support activities on new and existing infrastructure systems.
• Supervise vendor technical RE/SE in the system support and maintenance activities for DR related activities.
• Promote teamwork and motivate project team members.
• Distribution works and monitor progress.
• Identify manpower requirements, and recommend recruitment on relevant team members.
• Project activities deployment to support smooth technical operations.

Requirements

• Diploma/Degree in computer science or related field with working experience of at least 5 – 8 years or more depending on standard of qualification.
• Relevant experience and knowledge in IT Infra Project Implementation and Operations.
• 6 - 10 years’ relevant working experience in Financial Institutions.
• 1 - 2 years’ experience or exposure to a Dev Ops project implementation.
• Technical skills in IT infrastructure (network, servers, database, application servers).
• Technical skills in Cloud Architecture/Service, DevOps platform.
• Strong technical and analytical skills.
• Good analytical and trouble shooting skills.
• Good communication skills – written and verbal.
• ITIL, IT Operations, Project Methodology & Tools (e.g. PMP/PRINCE2).
• Knowledge in Agile Methodology in Project Management.
• Knowledge in Internet technology and web/mobile based applications..

Job Description

The SAP ABAP Developer is responsible for the gathering of SAP requirements and specifications, analyzing, designing, documenting, coding, testing, configuring, deploying, implementing and maintaining systems and applications.

Duties and Responsibilities

• Participate and collaborate with the users, business analyst, quality assurance/quality control analyst in the gathering of user requirements and specifications.
• Analyze technical and business requirements and translate these into basic and detailed technical design.
• Participate and conduct feasibility study, research and development, prototyping and proof of concept (PoC) in implementing new/existing systems, solutions and processes.
• Participate in the technical and project documentation such as but not limited to functional, system and technical design, requirements and specifications.
• Develop, customize, enhance, fix and maintain codes, applications and systems.
• Create test scenarios and data and conduct or participate in non-functional and functional testing (e.g., unit testing, system testing, integration testing, etc.).
• Document, analyze and report test results.
• Develop and review codes, programs and configurations to verify consistency and conformance with established programming and industry standards, guidelines, policies and practices.
• Conduct incident and problem analysis, data gathering, investigation and resolution of issues, and provide technical consultancy, assistance and support.
• Deliver the required systems/applications/solutions on time and based on agreed budget and specifications.
• Identify, assess and recommend opportunities for application and process improvement.
• Prepare reports, manuals and other documentation on the status, operation and maintenance of software.
• Provide regular and effective progress updates to the project manager/team lead/supervisor/immediate manager.
• Actively participate in and lead the peer review and status meeting to communicate progress and escalate risks and roadblocks.
• Prepare training materials and provide assistance in conducting the training to users or other members of the team.
• Responsible for the information security by protecting confidential information from unauthorized access, ensuring the integrity of the information and information system, taking appropriate measures to manage security risks and following and complying with the laws, legislations and terms of contracts.
• Perform other duties as assigned, if necessary.

Qualifications:

• Minimum 8 years of experience with SAP ABAP design and development.
  • R: Report programming.
  • I: Interface programming (Dataset, RFC, IDoc)
  • C: Conversion programs (LSMW, BDC, BAPI)
  • E: Enhancement programs (Explicit/Implicit enhancement points, Customer/User Exit, BTE, BAdI, Modification).
  • F: Forms (SAP Script, SMARTFORMS. ADOBE form knowledge is an advantage)
• Fiori scripting is an advantage (SAPUI5 framework).
• BI knowledge is an advantage.
  • Identify creative ways to improve reporting efficiency and effectiveness by streamlining processes and systems
  • Activate business content/BW extractors
  • Modelling and handling various types of SAP extractors in modelling
  • Write ABAP Code for BW extractors, Transformations
• Proven understanding of SAP ABAP development concepts, guidelines and SAP architecture
• Knowledge of ERP systems in any kind of industry
• Knowledge of business processes in SAP modules such as FICO, SD, MM, PE is an added advantage.

Skills:

• Analytical skills
• Problem-solving
• Basic knowledge of SAP modules FI/CO, SD, PP, MM, PE
• Communication
• Interpersonal skills
• Teamwork
• Leadership
• Research skills

• 10+ yrs. of strong experience in years of programming experience in RPG, Free RPG and CL in an AS/400 environment.
• Experience in JDA MMS (AS400) is added advantage
• Strong understanding of Software Development Life cycle and ability to work as the primary liaison between Business users and Developers. Excellent analytical and Problem solving skills, leadership and management abilities and team spirit.
• Strong verbal, written, and interpersonal communication skills with both technical and non-technical audiences.
• Systems integration, AS400 systems, SQL, DB2 database concepts.
• Knowledge of Retail and Warehouse Management System.
• Production Support background
• Experience in onsite-offshore model in managing large projects involving multiple teams across globe

Responsibilities:

• Design and deliver DeltaV systems on-site, ensuring seamless integration and functionality.
• Lead the design, development, and implementation of automation solutions aligned with S88 standards for plant operations.
• Manage and guide a team of engineers in the execution of automation projects.
• Lead the development, review, and delivery of System Development Life Cycle (SDLC) documents, ensuring compliance with site standards.
• Serve as a Subject Matter Expert, overseeing the development of system architecture, specifications, control strategies, and sequence of operations throughout all project phases.
• Establish and maintain trusted client relationships to ensure project alignment and customer satisfaction.

Requirements:

• Strong technical expertise in control systems, with hands-on experience in control panels, networking, panel/field wiring, and PLC control systems.
• Extensive experience in the automation sector, preferably in the pharmaceutical and/or biotechnology industries.
• Proven experience in the design and commissioning of DeltaV Distributed Control System (DCS) projects for GMP manufacturing environments.
• In-depth knowledge of Batch S88 standards, including concepts such as Control Modules (CM), Equipment Modules (EM), Phases, Recipes, and Units.
• Familiarity with GAMP lifecycle and quality management processes within the pharmaceutical industry.
• Proficiency in Microsoft Office tools including Excel, SharePoint, Word, and PowerPoint.
• Strong communication and customer service skills, with a focus on building positive client relationships.
• Leadership skills with the ability to effectively lead engineering teams to deliver automation projects.
• Hands-on experience in operations support on-site.
• Strong analytical and problem-solving abilities, with a solution-oriented approach.

Job Purpose
The Commissioning & Validation Engineer provides specialized scientific and technical support for the validation, revalidation, and requalification of laboratory equipment and computerized systems. These activities are performed in strict adherence to current Good Manufacturing Practices (cGMPs), Standard Operating Procedures (SOPs), and regulatory guidelines, with a continuous focus on enhancing quality and operational efficiency.

Key Responsibilities

Validation & Documentation

• Protocol Development & Execution: Develop validation protocols based on comprehensive Validation Plans. Execute validations, revalidations, and requalifications for lab equipment, including computerized systems, in compliance with internal and external standards.
• Reporting & Documentation: Author validation summary reports, ensuring accuracy, technical soundness, and adherence to all regulatory requirements. Review and approve validation documentation to maintain compliance.
• Maintenance & Requalification: Regularly perform validation maintenance reviews and requalification of lab equipment to ensure sustained compliance with GMP standards.
• Equipment Decommissioning: Support the decommissioning process for lab equipment, ensuring proper documentation and compliance throughout.

Collaboration & Investigation

• Cross-Functional Coordination: Work cross-functionally with relevant stakeholders to ensure timely and accurate execution of validation projects.
• Discrepancy Management: Investigate and resolve any discrepancies encountered during validation and qualification processes.
• Vendor Protocol Review: Review and provide input on vendor validation protocols and reports, including managing discrepancy investigations.

Quality Assurance

• Lifecycle Documentation: Participate in multi-disciplinary project teams for writing, executing, and reviewing validation lifecycle documentation, ensuring it meets all scientific and safety standards.
• Protocol Compliance: Ensure validation protocols are executed according to study plans and regulatory expectations.

Requirements

• Experience: Minimum of 3 years in pharmaceutical manufacturing, with a strong foundation in cGMPs and validation practices.
• Regulatory Knowledge: Familiarity with FDA, EMEA, GAMP, ICHQ7, and other relevant regulatory guidelines.
• Lab Equipment Qualification (LEQ): Extensive hands-on experience with lab equipment validation and qualification, preferably in the biotech sector.
• GMP Expertise: Experience in a GMP-compliant environment with thorough knowledge of GMP regulations.
• Validation & QA: Proven experience in validation procedures and quality assurance,with a focus on maintaining high scientific quality in all validation activities.
• Project Management & Communication: Strong project management, multitasking, and independent working skills. Excellent communication and teamwork abilities, with an emphasis on safety, quality, and meeting deadlines.

Job Purpose
Cognizant is seeking an experienced Siemens PLC Engineer to support a range of upcoming automation projects. This role focuses on designing, coding, and testing Siemens PLC systems using the TIA portal, with an emphasis on pharmaceutical industry applications. The ideal candidate should bring expertise in Building Management Systems (BMS) or Process Control Systems (PCS), with experience in pharmaceutical environments being highly preferred.

Key Responsibilities

PLC System Design & Development

• Design,Code, and Test Siemens PLC Systems: Utilize the TIA portal to design, program, and test Siemens PLC systems, ensuring compliance with project specifications, industry standards, and pharmaceutical regulatory requirements.
• Hardware Design: Engineer and design hardware components for PLC systems, ensuring they meet project-specific needs and operational reliability standards.
• System Integration & Interface: Ensure seamless integration of PLC systems with other automation platforms, such as SCADA, HMI, and various control systems.

Pharmaceutical Industry Expertise

• Regulatory Compliance: Apply deep understanding of pharmaceutical industry regulations to ensure all PLC solutions adhere to cGMP and other regulatory standards, enhancing operational compliance and efficiency.

Building & Process Control Systems

• Desigo CC System: Work with Desigo CC to implement and manage building automation systems.
• BMS/PCS Expertise: Leverage expertise in Building Management Systems (BMS) and/or Process Control Systems (PCS) to execute various project tasks, ensuring proper integration with other operational systems.

Project Management & Execution

• Project Oversight: Lead and manage PLC projects from planning through execution, ensuring timely delivery within budget and meeting quality standards.
• On-Site Support: Provide on-site support for system installation, commissioning, and troubleshooting, quickly addressing technical issues to ensure smooth operation.

Requirements

• Experience: 4-6 years of hands-on Siemens PLC engineering experience, specifically within the pharmaceutical industry.
• Technical Expertise: Proficiency with the TIA portal for designing, coding, and testing PLC systems. Experience with Desigo CC and BMS/PCS is highly preferred.
• Problem-Solving Skills: Strong troubleshooting abilities to provide effective on-site support during installation, commissioning, and system operation.
• Communication & Collaboration: Excellent communication skills, with the ability to engage effectively with clients, project teams, and stakeholders.
• Project Management: Proven ability to manage PLC projects, ensuring successful delivery on time and within budget.
• Certifications: Relevant certifications in Siemens PLC systems, BMS, or PCS.
• Pharmaceutical Industry Knowledge: In-depth knowledge of regulatory requirements, cGMP, and best practices in the pharmaceutical sector.

Availability: Ability to start on short notice

Key Responsibilities

DeltaV System Design & Implementation

• Design & Deliver DeltaV Systems: Lead the design and implementation of DeltaV application systems for the site, ensuring alignment with project requirements and GMP standards.
• S88 Standards Compliance: Develop and implement automation solutions in compliance with ISA S88 standards, including control modules, equipment modules, phases, recipes, and units.
• System Architecture & Controls Strategy: Collaborate with the development team to define system architecture, specifications, controlstrategies, and sequence of operations, ensuring all stages are accounted for in the design and development plan.

Commissioning & Qualification (C&Q)

• C&Q Protocol Development: Develop commissioning and qualification protocols based on C&Q plans, ensuring alignment with GMP regulations.
• System Testing & FAT: Supervise and execute Factory Acceptance Testing (FAT) to ensure system functionality and regulatory compliance.

System Development Life Cycle (SDLC)

• SDLC Deliverables: Create, review, and maintain SDLC documentation in accordance with site standards, ensuring that all deliverables meet quality and compliance requirements.
• Data Flow & Process Design: Define and document processes and data flow that support project needs, optimizing system performance and compliance.

Automation Strategy Compliance

• Automation Strategy: Ensure that the project’s automation strategy is followed, guaranteeing a streamlined approach to system development and integration.

Requirements

• Industry Experience: Experience in a similar role, ideally in pharmaceutical and/or biotechnology industries, with a focus on automation solutions for GMP manufacturing.
• DeltaV Expertise: Proficiency in Emerson DeltaV DCS, with extensive experience in DeltaV Batch systems, including commissioning, qualification, and design.
• Technical Proficiency: Strong technical skills in control systems, including control panels, networking, PLC systems, panel/field wiring, and system integration.
• Batch S88 Standards: In-depth understanding of Batch S88 standards, including control modules, equipment modules, phases, recipes, and units.
• GAMP & Quality Management: Familiarity with GAMP lifecycle standards and quality management processes commonly used in the pharmaceutical industry.
• Teamwork & Collaboration: Ability to work effectively within a team, collaborating with cross-functional teams to achieve project goals.
• Testing & Troubleshooting: Experience conducting system testing, particularly Factory Acceptance Testing (FAT), and resolving technical issues.
• Software Proficiency: Advanced skills in Microsoft tools (Excel, SharePoint, Word, and PowerPoint).
• Communication Skills: Strong communication and customer orientation skills, with the ability to explain technical details clearly.
• Problem-Solving Skills: Excellent analytical and problem-solving abilities to address challenges during project execution.

Job Purpose

As the use of Manufacturing Execution Systems (MES) grows within the life sciences sector, we are looking for an experienced Senior Systems Engineer to join our expanding MES team. The candidate will be based on-site at a pharmaceutical multinational corporation (MNC) and will play a critical role in the execution phase of MES projects. Responsibilities include providing engineering support, troubleshooting, managing validation documents (IQ/OQ/PQ), and offering GoLive support to ensure seamless system integration and operation.

Key Responsibilities

MES System Troubleshooting & Support

· MES & ERP Troubleshooting: Identify and resolve issues in recipe execution and recipe authoring within MES and ERP systems.

· Change Control Documentation: Collaborate with QA to ensure approved change control documentation is in place for all MES system updates and modifications.

System Design, Testing & Validation

· Design & Validation: Design, write, and execute high-quality test and validation protocols, risk assessments, and system documentation, ensuring compliance with cGMP standards.

· Recipe Creation & Modifications: Create and update MES and ERP recipes, worksheets, and equipment/material specifications, including phase transition logic, to ensure alignment with system processes.

· Process Alignment: Ensure MES processes are properly aligned with equipment, cleaning, and product procedures.

Training & Knowledge Sharing

· MES Training: Provide comprehensive training to site personnel on MES-related roles, including system access, and ensure cross-training within the MES team.

· Governance & Issue Management: Participate in MES knowledge exchanges and governance meetings, managing issues, workarounds, and fixes as they arise.

System Upgrades & Maintenance

· System Upgrades: Collaborate with IT to manage MES system upgrades, patching, and hardware support, including system security and access.

· Hardware Support: Ensure maintenance and periodic upgrades of MES hardware such as printers, scales, scanners, and barcode labelers to maintain operational efficiency.

Continuous Improvement & Documentation

· Continuous Improvement: Contribute to continuous improvement initiatives aimed at enhancing the quality, safety, environmental, and production systems on-site.

· Documentation & Compliance: Ensure all activities and changes are thoroughly documented in compliance with cGMP and industry standards.

Requirements

· MES Expertise: Hands-on experience with MES systems such as Werum PAS-X, Aspen, Syncade, Siemens MES (Camstar, Opcenter, Simatic IT), including full application configuration and interfacing with SAP and automation systems.

· Pharmaceutical Process Knowledge: In-depth understanding of pharmaceutical business processes, including chemical manufacturing (W&D, solid bulk manufacturing, packaging) and biopharma operations.

· Batch Record Creation: Experience creating Master Batch Records within Werum PAS-X.

· Industry Standards: Strong knowledge of S88 and ISA S95 industry standards, as well as experience with GAMP lifecycle and pharmaceutical quality management processes.

· Communication & Collaboration: Excellent communication skills with the ability to collaborate effectively with internal teams and external groups.

· Project Experience: Demonstrated experience working on projects in pharmaceutical or biotechnology environments.

This role offers an exciting opportunity to be at the forefront of MES development in the life sciences industry while contributing to the success of critical manufacturing projects.

DeltaV System Design & Development

• Design & Implement DeltaV Systems: Lead the design and delivery of Emerson DeltaV DCS applications, ensuring system performance and compliance with industry standards and GMP regulations.
• S88 Standards Compliance: Develop automation solutions adhering to S88 batch control standards, including control modules (CM), equipment modules (EM), phases, recipes, and units.
• System Modifications: Work with cross-functional teams to design and develop system modifications, ensuring effective integration of system architecture, control strategies, and sequences of operation.

System Development Life Cycle (SDLC)

• SDLC Deliverables: Create and review System Development Life Cycle deliverables, ensuring that they align with the site’s technical and compliance standards. Define processes and data flow that meet project needs.

Commissioning & Testing

• System Testing & FAT: Supervise and execute Factory Acceptance Testing (FAT) and other system tests, ensuring DeltaV systems meet operational and regulatory standards.
• System Commissioning: Participate in system commissioning efforts, ensuring seamless system integration and operation in a GMP manufacturing environment.

Collaboration & Automation Strategy

• Team Collaboration: Collaborate with project teams to ensure that automation systems are designed, developed, and implemented effectively.
• Automation Strategy: Ensure adherence to the project’s automation strategy, driving efficient execution and regulatory compliance throughout the system lifecycle.

Requirements

• Industry Experience: Proven experience in a similar role, ideally within the pharmaceutical or biotechnology industries, with expertise in automation for GMP manufacturing.
• DeltaV Expertise: Extensive experience with Emerson DeltaV DCS systems, including DeltaV Batch control systems.
• System Design & Commissioning: Strong background in designing and commissioning DeltaV DCS projects for GMP sites.
• Technical Proficiency: Deep knowledge of control systems, including control panels, networking, panel/field wiring, and PLC systems.
• S88 Batch Standards: Comprehensive understanding of Batch S88 standards, particularly control modules, equipment modules, phases, recipes, and units.
• GAMP Knowledge: Familiarity with GAMP lifecycle guidelines and quality management processes used in the pharmaceutical industry.
• Teamwork & Leadership: Strong teamwork skills, with experience leading system testing and commissioning activities.
• Testing & Troubleshooting: Proven ability to supervise and conduct system testing, including FAT, and resolve technical issues.
• Software Proficiency: Proficient in Microsoft tools such as Excel, SharePoint, Word, and PowerPoint.
• Communication & Problem-Solving: Excellent communication skills, with strong customer orientation, analytical, and problem-solving abilities.

Automation Strategy Compliance: Ensure that all development activities align with the project's overall automation strategy.

The primary function is to design and develop solutions for critical business processes residing in Oracle E-Biz/Fusion suite: Manufacturing Suite.

He/she has to analysis, troubleshoot E-Biz and/or business process issue/inefficiencies and provide sound business enhancement/ solution/ alternative that is based on Oracle E-Biz/Fusion standard capability and functionality.

He/she has to provide documentation on Application Architectural design, As-Is and To-Be business processes, function and technical design, application setup and configuration, Test scenarios, System Testing, Issue logging, root cause analysis and resolution, and provide deliverable update to management.

He/ she has to understand and comply with company policy and procedure, ITGC (Governance Control) and SOX requirements. He// She has to Uphold IT operation efficiency and SLA.

RESPONSIBILITIES:

• Lead in user requirements gathering and analysis
• Drive user discussions and conduct workshops to facilitate information gathering
• Perform feasibility study to ascertain area of automation
• Document user requirements into user specifications (functional & technical)
• Lead in system design and development of functionality according to the agreed user specifications
• Develop test plan & scripts
• Conduct testing on developed functionality to ensure compliance to user specifications and internal quality assurance requirements
• Lead in user training & user acceptance testing
• Provide periodic reports to reporting manager on project progress
• Handle issues resolution in accordance to SLA

Experience:

Bachelor in Computer Science, Information Technology or above

· Minimum 5 years in in High-Tech manufacturing- Has gone through

at least 1 round of Oracle Implementation cycles

· Experience with Scrum agile methodology

· Hands-on experience Oracle Apps ERP Application System |

(functionality, database schema, architecture, etc)

· Experience in setups and technically competent.

· Strong expertise in with software development lifecycles &

methodologies

o Experience in Oracle Supply and Demand Planning, Bills Of Materials, Cost Management, Engineering, Quality modules

Responsibilities:

• Lead Integration Team that supports customers integration

components

• Partner with customer’s technology team to design, build and

maintain integration tools, products and applications

• Build, Maintain and Support customer’s ETL (Informatica BDM,

Java)

• Build, Maintain and support customer’s integration tools and

applications using Informatica MFT, Axway MFT, Mulesoft and

AWS API Manager

• Design, build and maintain integration with external banks, data

vendors to customer’s core accounting and investment platforms

• Develop and maintain SOPs, best practices, service catalogs in an

around Integration CoE

• Lead team to support audit, compliance and governance for

applications managed by the team.

• Proactively identify improvements/automation and work with

customer and implement

• Ensure production stability and incident resolution as per the

agreed turnaround time and SLA

• Develop and nurture top performing team both onsite and

offshore

Responsibilities:

• Telecom Domain experience in E2E BSS, experience in digital and

UX based design

• Strong knowledge on designing E2E customer journeys and

processes across FAB (Fulfillment, Assurance and Billing)

• Provide E2E solution for business capabilities

• Identify E2E reusable pattern and optimize the product catalog,

inventory objects

• Validates E2E architecture and integration points proposed by

solution architects

• Ensures futuristic/right first-time and product agnostic solution

design

• Support the data migration with entity mapping and

transformation rules validation

• Evaluate component level solutions to ensure solutions are

complete and feasible to implement

• Participate solution design workshops, reviews and ensure E2E

solution aligns to the requirement

• Coordinate interactions with various component

teams/stakeholders, walk-through the E2E solution design and

sign offs

• Collaborate with delivery PMs to drive dates/plan and support

implementation team with project activities to ensure solution

design is properly understood and implemented

• Review project deliverables for completeness/done criteria,

quality, and compliance defined as part of the design

Responsibilities:

o Technically manage projects to deliver on time, within budget,

and meet the business requirements.

o Coordinate interactions with various component

teams/stakeholders, walk-through the E2E solution design and

sign offs

o Collaborate with developers to drive dates/plan and support

implementation team with project activities to ensure solution

design is properly understood and implemented.

o Review project deliverables for completeness/done criteria,

quality, and compliance defined as part of the design.

o Co-ordinate with end user for providing regular updates on

project deliverables and get final sign-off from them.

o Flag any risks/dependencies identified for the projects and co-

ordinate on the project delivery timelines.

o Responsible to create detailed design and develop java-based

application solution including front-end and back-end

implementation

o Manage internal & External Audit to drive closure signoff

o Manage resource capacity Planning

o Ensure 100% delivery SLA compliance

o Develop/troubleshoot built for a telecom client

o Understand the requirements (both functional and non-

functional) with inputs from business analysts and participate in

creating high level estimate

o Create systems requirements document and participate in the

design, development, and testing phases

o Do impact analysis, participate in high level design, create design

specifications as per the high-level design, create unit test plans

o Work with interface teams for designing and developing APIs

o Understand various application that needs interface and data

exchange, various stakeholders of application consumers and

arrive multiple alternate solutions, trade off best solution after

assessing the pros and cons of all the alternatives

o Develop and review Artifacts (Code, Documentation, Unit test

scripts, etc)

o Support the test validation activities (Functional, Integration,

system, UAT) and fix/resolve reported defects within the agreed

SLA

o Participate in retrospective meeting and work on continuous

improvement to improve the delivery quality and timeline with

defect reduction / automation / re-use artifacts

o Participate in deployment planning and support go-live, provide

warranty support

o Support Major incidents, provide quicker resolution as required

for reported issues and minimize the impact to end users

Job Description:

DCS Automation Engineer (DeltaV)

We are seeking an experienced DeltaV DCS Engineer with 8-10 years of relevant experience, ideally in the Pharmaceutical or Biopharmaceutical industry.

The ideal candidate will have a strong background in designing and commissioning DeltaV Distributed Control Systems (DCS) for GAMP manufacturing sites, with a deep understanding of Batch S88 standards.

Key Responsibilities:

• Design and commissioning of DeltaV DCS projects for GAMP manufacturing sites.
• Ensure compliance with Batch S88 standards, including Control Modules (CM), Equipment Modules (EM), Phases, Recipes, and Units.
• Collaborate with cross-functional teams to understand and optimize pharmaceutical and biopharmaceutical processes.
• Work with automation hardware and networking technologies to support system implementation.
• Manage and coordinate automation information across multiple stakeholders.
• Follow Software Development Life Cycle (SDLC) and quality management processes specific to the pharmaceutical industry.

Required Skills and Experience:

• Minimum of 8-10 years of experience in a similar role, with a focus on DeltaV DCS in the Pharmaceutical or Biopharmaceutical industry.
• In-depth knowledge of DeltaV DCS Batch systems.
• Strong understanding of GAMP standards and regulatory requirements in the pharma sector.
• Familiarity with Batch S88 standards for process automation.
• Experience with automation hardware and networking technologies.
• Excellent communication skills and the ability to work both remotely and onsite as needed.
• Ability to thrive in a team-oriented environment, managing multiple stakeholders effectively.

Preferred Qualifications:

• Hands-on experience with quality management processes in the pharmaceutical industry.

a) Drive business process transformation and ensuring that the

system has the capabilities to support various business functions

by working closely with our business partners (vendors) and

various divisions, to understand the needs of our stakeholders;

b) Collaborate with stakeholders to gather requirements, understand

and document business needs and objectives related to public

services, particularly on the vehicle registration and licensing sys.

c) Review business rules and service journeys, gathering requirement

specifications, engaging stakeholders, creating user journey maps

and wireframes, and providing support on updates to management;

d) Develop user stories, specifications, acceptance criteria, and create

detailed process maps to visualise, understand and streamline

current workflows and business processes;

e) Participate in daily stand-up meetings, sprint planning, sprint

reviews & retrospective sprints, and assisting in project

management matters; and

f) Conduct and facilitate User Acceptance Test (UAT) and trainings for

users, and providing support services throughout the project. This

includes preparation of test cases and documenting the expected

and actual results for each test scenario in a clear and concise.

Qualifications and skill sets:

a) Minimum 5 years of work experience as business analyst or

equivalent position. Handled large scale front-facing projects, with

experience in stakeholder engagement and comms management;

b) Bachelor’s degree in Business, Management of Information

Systems, Information/ Infocom Technology, or related discipline;

c) Proven and hands-on experience with IT project implementation,

specifically on user requirements gathering, IT business analysis,

application solutioning, UI/UX design and using testing software;

d) Experience in AGILE methodologies and Cloud platform projects,

preferably in using Jira, Figma, MS Visio, and Tricentis Tosca;

e) Strong analytical and problem-solving skills;

f) Have a positive attitude and good interpersonal skills, able to work

and communicate effectively with stakeholders to ensure business

needs are met;

g) Possess strong communication skills with an excellent command of

the English language;

h) Must be organised and able to work with minimal supervision to

ensure tasks are well completed and project is on schedule; and

i) Experience in end user service journey design projects, and

implementing government projects would be an added advantage.