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Zenith Technologies is firmly estalished as one of the worlds leading independent Enterprie Performance Solution Providers. Delivering automation, process ocntrol ad MES excellence to theLife Sciences sector globally. Founded in 1998, we have grown to be a global force across the world. With headquarters in Ireland, and with a network of 14 offices located at strategic locations, we combine a local aspect with a global vision in all our locations.

Our primary focus is in the highly regulated pharmaceutical & biotechnology sectors where automation & compliance are intrinsic requirements of the manufacturing process. Our core expertise is centered on two critical levels our our customers' infrastructure, namely production control and Enterprise Management. At both these levels, we possess an extensive track record in successfully meetng the expectations of our global blue chip client base. Multiple platform Process Control capabilities and a broad range of experience in the Manufacturng Execution Systems (MES) arena provide customers with point solutions or full trnkey syems whichmeet their specific needs.

Zenith Singapore has been established since 2002 and has been involved in some of the leading life science projects locally and regionally and continues to seek out the best engineering & science talent to join the growing Zenith team.


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CSV Engineer

$6000 to $9000 (Monthly)

Zenith Technologies (A Cognizant company) is one of the leading Automation Engineering companies, providing innovative, reliable and technically-advanced process measurement, automation and MES Product and Services to the Life Sciences industries. Zenith is a progressive company with offices located in UK, UK, USA, Germany, Belgium, Singapore, India and China.

Position : CSV Engineer/ Senior CSV Engineer

Responsibilities :

- Responsible for preparing and executing test documentation for GMP computerized systems as well as providing support in the troubleshooting of issues during test execution.

- You should have excellent understanding of 21 CFR Part 11, ICH standards, EMA and FDA (GxP) regulations, and GAMP methodologies.

- Coordinate with multi-disciplinary validation team and be responsible for the validation of automated equipment and/or control systems

- Create and modify validation documentation including but not limited to:

· User Requirements Specifications (URS)

· Design Reviews (DR)

· Criticality assessments

· CSV protocols (SAT, IQ, OQ, PQ) which verify if the system is compliant to regulatory and client requirements

· Reports which summarize the results of the protocol executions

· Exception reports which identify defects or issues during test execution

· Review vendor documentation

· Continuous improvement on validation process and procedure

· Assist or coordinate generation of Standard Operating Procedures (SOPs)

· Follow the proper site safety practices; wearing adequate safety equipment when required

Job Requirements

- Degree in Engineering or Science discipline. Preferably in Electrical Engineering, Computer Science/Information Technology, or Chemical/Biochemical/Mechanical Engineering.

- Minimum 2 years of experience in Pharmaceutical Industry

- Proven track record in promoting safety practices in related role

- Demonstrated proficiency of written and verbal communication skills (including technical writing and presentations) with ability to communicate and collaborate effectively with technical and senior management staff

- Proactive, self-starter and capable of working alone or in a team environment.

- Familiar with Microsoft office suite of applications

- Ability to interpret and operate within defined schedules managing available resources to achieve project milestones

- Previous DCS (DeltaV), WinCC, SIEMENS and Rockwell automation systems testing experience an advantage.

- Experienced in developing automation protocols an advantage.

- Good knowledge of cGMP, GAMP, GDP, 21CFR Part 11 and ICH Q10 guidelines

- Knowledge of ASTM 2500E risk-based approaches

- To be aware and supportive of the project’s requirement for flexibility in working hours/shift patterns through the differing phases of the project’s life cycle

- Experience with Quality Change Control is desirable.

Please email your resume to

10 months ago
Senior MES Engineer

$6000 to $10000 (Monthly)

Zenith Singapore is looking to hire a MES Senior Engineer to join our MES team working at our client site, a pharmaceutical MNC. The selected candidate will be required to provide consultation and engineering service to the execution phase of the project. He/she will also be involved in the generation and ownership of IQ/OQ/PQ documentation and the GoLive Support.

Main Responsibilities

· Troubleshoot and provide solutions for MES & ERP problems in recipe execution and recipe authoring.

· Liaise with QA to provide approved change control documentation for all MES system changes.

· Design, create, write and execute to a high-quality standard, test and validation protocols, risk assessments, and system documentation.

· Design, create, write and/or make all required changes to MES & ERP Recipes, worksheets, equipment and material spec's including phase transition logic to a high-quality standard.

· Design, create, write and/or make all required changes to ensure cleaning, equipment and product procedures are aligned to MES processes and vice versa.

· Design, create, write and provide training for all other site personnel on their related MES roles and arrange system access.

· Participate in MES knowledge exchanges, MES Governance meetings and manage issues, work-around and fixes identified.

· Work closely with IT regarding upgrades, patching, hardware support, security and system access and provide technical expertise in implementing upgrades and patching.

· Liaise with Global MES on required system improvements.

· Provide support to other MES system users as required to ensure business continuity.

· Participate in MES projects from initiation to ensure MES system or hardware requirements are taken into consideration.

· Ensure maintenance/replacement of MES hardware, printers, scales, scanners and bar-code labelers. Review for upgrades periodically.

· Keep other MES Team Members up to date on MES changes Documentation of all activities in line with cGMP requirements.

· Cross training within the team and training of new team members.

· Participation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems.

· Adheres to and supports all health and safety standards, procedures and policies.

· SME desired Experience working on projects in the pharmaceutical and/or biotechnology industries knowledge of GAMP lifecycle and quality management processes employed in the pharmaceutical sector Excellent communication skills and collaborative with team members and external groups

· Self-starter who can get the job done despite obstacles

· Requires a Bachelor’s degree or foreign equivalent in Computer Science, IT, Technologies, Chemical Engineering or Biologics related field

· Minimum 5 years’ experience as an MES Software Engineer with Simatic IT experience.

Please email your resume to

a year ago
Project Management Manager

$8000 to $10000 (Monthly)

Responsibilities :

  • To manage on-time, on-budget multiple process control system projects to customer expectations as the leader of the project management and engineering management team. Supervise staff in delivering the project implementations, problem and change management, issue resolution and manage multiple large projects simultaneously.

  • To provide technical and project management contributions to pre-sales team efforts to bid solutions to RFPs/tender specification.

  • Plan and organize project resources

  • Prepare and obtain approval on projects/department budgets

  • Track billing milestones/payment collections for projects

  • Establish project workplan, schedule, milestones, resources requirement, project budget, project organisation, work breakdown structure, scope, cost and risk management

  • Manage the sub-contractors/suppliers

  • Liaise with senior client management

  • Manage the daily project tasks with project leads/team members.

Requirements :

  • 8 to 10 years working experience with at least 3 to 4 years project management experience in technology projects preferably in Pharmaceutical Manufacturing

  • Possess maturity, stewardship and leadership qualities with strong problem resolution skills and excellent customer relationship management skills

  • Good negotiation and presentation skills

  • Good oral and written communication skills

  • Possess the drive to do what it takes to deliver results and exceed customer expectation

  • Knowledge and experience in manufacturing Automation Systems , MES & Historian, Lab Systems and IT-OT will be an advantage.

  • Responsible for profitability of assigned projects and subsequent cross-selling.

Please email your resume to

a year ago
Trainee Automation Engineers

$3200 to $4000 (Monthly)

Zenith Technologies, now a Cognizant Company is a world leader in delivering digital transformation solutions to Life Sciences Manufacturing. Through our knowledge and expertise in Digital, Manufacturing execution systems & process Automation, we deliver manufacturing systems that are optimised to improve operational efficiencies, whilst maintaining compliance. Our specialist engineering teams have the aptitude to deliver and support Pharma 4.0 architectures and solutions covering all IT, OT and IoT applications, infrastructures and services.

Operating across 5 continents and with over 900 skilled employees, Zenith partners with the leading Life Sciences companies globally to provide performance improvements, reduced costs and improve time to market. We are a single end to end partner for consultancy, design implementation, optimisation and support for all applications in the Pharmaceutical and Biotechnology Manufacturing.

What will I gain from a career with Zenith?

  • Experience in a range of technologies including: SCADA, DCS, PLC, Instrumentation, DeltaV, Machine Vision and MES

  • Experience with the following software vendors: Emerson Process Management / Siemens / GE / Wonderware / ABB / Allen Bradley / Rockwell Automation / Werum / OSI Soft / Aspentech

  • Experience working with top Life Science companies and engineers

  • An initial 12 week intensive Graduate Programme

  • Excellent salary & benefits

  • Continuous training and mentoring

  • Career development opportunities

  • Experience in exciting and challenging projects

  • Global career opportunities

Position : Trainee Automation Engineers

We are now hiring fresh degree graduates from the following disciplines:

  • Pharmaceutical Engineering

  • Bioengineering

  • Process and Chemical Engineering

  • Chemical and Biopharma / Biotech Engineering

  • Electronic & Electrical Engineering

  • Automation and Process Control

  • Computer Systems Engineering / Software Engineering

  • Business Information Systems / Information Technology

Please email your resume to

a year ago
DeltaV Automation Engineer or Senior Engineer

$4500 to $8000 (Monthly)

Position : DeltaV Automation Engineer

Automation Engineer/Senior Engineer will be involved in the design, configuration, implementation, testing, coding, commissioning and validation of client projects as well as day today support and maintenance of the client automation systems.

The successful candidates would be required to have a minimum of 3 to 8 years of Emerson DeltaV DCS batch experience. These long-term roles offer an excellent opportunity to grow within Zenith Technologies.

· Good knowledge of GAMP lifecycle and quality management processes employed in the pharmaceutical and biotechnology sectors

· Experience implementing Emerson DeltaV automation solutions for clients in the Pharmaceutical and/or Biotechnology industries

· Experience with design, development, coding and testing of DeltaV DCS.

· Preparation of functional specification and design specification documentation, and testing of automation systems

· Advanced understanding of S88 / Batch Proficiency & Biotech Conversant

· Advanced understanding on all Project Lifecycle phases and tasks

· Configuration and programming experience, CMs, EMs, Unit Classes, Recipes, Controllers and Graphics

· Knowledge of virtualization is added advantage

· Experience in supporting client/sites for NC, CAPA, Root cause analysis and automation Change control management

· Good analytical & problem-solving skills

· Excellent communication skills

· Must work well in a team environment

· Self-starter who can get the job done despite obstacles

· Requires a Bachelor degree or foreign equivalent in Chemical, Electrical or Bio-Process Engineering, or related field

· 3 to 8 years of progressive experience as an Automation Engineer, DCS Software Engineer or related occupation.

Please email your resume to

a year ago
Automation Project Manager

$8000 to $10800 (Monthly)

Position : Automation Project Manager


· Manage all commercial aspects of all ZT (Zenith Technologies) related work including budget reporting and traceability, Hours Trackers, purchase orders, timesheets, invoicing, invoice tracker, rates.

· Support Client’s Automation Manager in delivery of non ZT Task’s/Projects as requested.

· Responsible for Business World maintenance i.e. timesheets, expenses, projects hours’ report; new project/workorder set up, addition of resources to projects, price lists, activity codes etc.

· External contractor management as required by Client Automation Manager.

· Interfacing/Quarterly reviews with Site Operations Managers/EPCM Group.

· Ensure ZT team complete all Mandatory Training and maintain training records.

· Responsible for Managed Service Budget and control of the Capital spends.

· Organise & Lead the Monthly Managed Service meetings and generate monthly reports.

· Agree and Deliver KPI's developed for measurement of ZT performance in conjunction with Client and ZT including issuing a yearly performance survey to Client based customers.

· Issue Monthly Managed Service progress report (dashboard) outlining Spends versus Budgets per Area as well Projects work in progress.


· Suitability degree qualified, experienced senior project engineer with over 10 years’ pharmaceutical/biotech manufacturing experience.

· Experience with DCS Systems, preferably Delta V or MES or background in automation.

· Strong interpersonal and communication skills with a strong ability to motivate.

· Successful experience in heading high level projects, managing priorities, budgeting, tasks and resources.

· Strong problem solving and technical innovation skills.

· Excellent presentation and facilitation skills.

· Ability to work independently and efficiently to meet deadlines.

· Ability to multi-task multiple priorities in a fast-paced environment.

· Self-motivated, detail-oriented and excellent organizational and time management skills.

· Team player with a ‘can-do’ positive attitude.

Please email your resume to

2 years ago