Total 987 Quality Assurance / Control job vacancies in D22 Jurong, Jurong Island, Tuas

Job Description & Requirements

Our team is looking for a Plant Inspector (Oil and Gas / Refinery) with experience in inspecting Cooling Towers and Boilers. As a Plant Inspector, you will be responsible for assistance in implementation of Testing & Inspection programs.

Roles & Responsibilities:

· Work as a member of the technical team to provide process engineering support for operations in the refinery.

· Provide technical advice / support to daily operational issues.

· Perform unit optimization, troubleshooting, de-bottlenecking studies.

· Lead/participate in safety initiatives including risk assessments and HAZOP reviews

· Support on-going reliability improvements and equipment strategy development

· Analyze complex technical issues, identify key drivers, propose strategy / recommendations to support decision-making/resolution of technical issues

· Responsible for the development/execution of margin improvement ideas/projects.

· Coordinate NDT activities, Inspection activities relevant to the API and Refinery owner standards.

· Review RT films, witnessing NDT activities to get unique results.

· Experience in CUI, CUPS programs.

· Interpret the rests of UTG/PAUT and do the fracture analysis and remaining life calculations.

· Ensure quality of inspected items to meet project requirements and refinery standards.

· Inservice inspections in refineries / Oil and Gas / Petrochemical industries, such as corrosion under pipe support (CUPS), corrosion under insulation (CUI), Injection & Mix points inspections.

· Read, understand project related ITP, procedures, specification requirements.

· Review documents and drawings as per specification • Knowledge / experience about Piping Isometrics, P & ID, general arrangement drawings, Structural drawings, Weld Maps, welding symbols, Cutting Plans, Quality control procedures, Base Materials, and welding consumables.

· Inspection, review of mill certificates, Material verification, Inspection of Pipes, Fittings, Flanges, valves, nipples, plate tubes as per respective materials specifications, Codes, Standards & Client Specifications. Inspection / Witness & Review Stage wise activities earlier stage of spool fabrication

· Fit-up Inspection and welding inspection, visual inspection

· Monitor and record welding parameter during welding as per WPS.

· Carry on & witness ferrite test inspection with Client after welding duplex / super duplex pipe spools weld joints.

· Witness for post weld heat treatment and review the reports. line check inspection, Pneumatic Testing, Hydro test, hot oil flushing, Chemical cleaning, Flood test, flushing & reinstatement, till the final stage of colour coding and valve tagging.

CRITERIA

· Graduate / Diploma Engineers with > 5 years of relevant experience.

· Relevant Engineering Degree or Diploma in Mechanical, Petroleum/Oil/Gas, Civil, Chemical or Industrial Engineering are acceptable.

· API 510 / 570 / 653, QAQC Qualified CSWIP 3.1 Welding inspector / Certified QAQC Inspector / Certified QA QC Engineer and NDT Level I & II.

· Expereince in inspecting Cooling Towers and Boilers is must.

· Experience in piping line walk, reinstatement inspections according to Isometric drawings.

· Knowledge in Non-Destructive Testing methods.

· Knowledge/experience in welding inspection, structural fabrication, piping Isometric drawing and piping materials.

· Work Independently and can work in Singapore and other countries.

· Master Microsoft Office include Excel, PowerPoint and Words.

· Fluent Reading, Speaking and Writing in English.

· Willing to commit 24 months contract/ project completion.

· Hardworking, Fast Learner, Mobile and Able to Work Long Hours/Public Holidays (OT Compensated) To Ensure Timely Completion of Tasks.

· Team Worker, Mature, Meticulous, Pro-Active Work Attitude & Work Independent.

Energetic & Result Orientated.

No Deviation is a provider of patient-centric solutions for the pharmaceutical industry, and we are currently seeking individuals who are passionate about joining our team. Our areas of expertise include engineering consultancy, Commissioning Qualification Validation (CQV), as well as Quality, Compliance, and Regulatory services.

We strongly uphold our core values of Empathy, Integrity, and Transparency, and we strive to create a collaborative, innovative, and inclusive work environment that fosters personal growth and development.

No deviation is seeking a dedicated and detail-oriented QC IPC Chemist for a 1 year Night shift only (8pm-8am) contract role in a leading pharmaceutical company. The ideal candidate will play a key role in ensuring the quality and compliance of products by supporting chemical analysis and testing according to regulatory standards. This is an excellent opportunity for a junior-level professional looking to gain valuable experience in the pharmaceutical industry.

By joining our team, you will have the opportunity to make a meaningful impact in the pharmaceutical industry while advancing your career.

Key Responsibilities:

• The IPC Chemist is responsible for ensuring that the manufacturing process remains consistent and meets predefined quality standards throughout the various stages of production. They perform tests and checks on samples taken during production to ensure that the intermediate stages align with quality specifications before the final product is manufactured.
• Conducts analytical testing using methods like HPLC, GC, FTIR, UV-Vis spectrometry, titrations, and other chemical assays to analyze the potency, purity, and identity of drug substances.
• Performs stability studies to assess how the quality of a drug substance or product changes over time under various environmental conditions.
• Tests for impurities, residual solvents, and microbial content to ensure compliance with regulatory guidelines.
• Prepares and maintains lab documentation, such as test results, standard operating procedures (SOPs), and analytical reports.
• Works in a controlled laboratory environment, following Good Laboratory Practices (GLP) and regulatory standards such as those from the FDA or EMA.

Qualifications and Experience:

• Diploma in Chemistry, Pharmaceutical Science, or a related field.
• Basic knowledge of analytical techniques such as HPLC, GC, UV, and wet chemistry.
• Familiarity with GMP, GLP, and relevant regulatory guidelines.
• Strong attention to detail, problem-solving skills, and ability to work independently.
• Excellent organizational skills and ability to maintain accurate documentation.
• Effective communication skills and a team-oriented mindset.
• Preferred Experience:
• Prior experience in a pharmaceutical or chemical laboratory setting is advantageous, but fresh graduates are welcome to apply.
• Contract Duration: 1 year, with potential for extension based on performance and business needs.

COMPANY DESCRIPTION

Located on Jurong Island, the petrochemical hub of Singapore, SRC operates a refinery that is capable of processing 290,000 barrels of crude oil per day to produce fuel products and chemical feedstocks that are supplied to domestic markets and overseas export markets under the brand labels of its shareholders.

RESPONSIBILITIES

(Annual Gross Salary: S$46,000 to S$50,000)

• Perform testing of petroleum products, refinery intermediate, process and effluent water
• Conduct sampling and testing of gases and LPG streams
• Perform QC/QA work including calibration and maintenance of equipment
• Perform stock-taking and reordering of chemicals and consumables

• Diploma in Science & Technology / Engineering or NITEC in Chemical Process Technology / Chemical & Life Science

Purpose of Position

• Provide maintenance and engineering support for process control systems to ensure safe and reliable operation of the plant.
• Provide technical and engineering support for projects and modifications related to control system to achieve business and operational objectives.

Principle Responsibilities

• Responsible for the maintenance and engineering of all process control systems which may be installed in the plant or externally at customers' site.
• Perform fine-tuning, troubleshooting, modification and programming of the Control System as needed to improve system performance and optimize process operation needs.
• Response to 24-hour emergency call-out and provide night-shift support during plant startup, shutdown and as requested by Operation Team.
• Work closely with the Instrument Team to troubleshoot and resolve instrumentation problems.
• Work with the Project Team to develop requirements and/or specifications of control system for projects and modifications; supervise & implement the project works according to the schedule and requirements.
• Plan and execute preventive and corrective maintenance works for plant turnaround.
• Perform strategy planning for control system expansion, upgrading and renewal.

Job Requirements

• Familiar and hand-on with the engineering tools and programming languages of control systems (Honeywell, Siemens PCS7 and Triconex), able to make program modifications and configuration changes confidently.
• Experienced and familiar with various phases of project works such as engineering, fabrication & construction and commissioning.
• Knowledge and experience with computer system networking, server/client and virtualization architectures.
• Degree in Electronics/Electrical Engineering, major in Control is preferred.
• Minimum 5 years relevant experience working and maintaining Honeywell DCS, Siemens PCS7, Triconex PLC and etc.

Job Description

The Quality Assurance Engineer is responsible to ensure that all products, processes, methods and equipment are validated and is the quality representative in Quality improvement projects. He/She handles external customer complaints and change management business processes. The QA Engineer expected to lead and drive cross functional team in day-to-day issues, global bench marking activities, internal process robustness and automations. He/She must be inclined to have hands-on understanding of tool and product functionality and production.

In this role, you will have the opportunity/responsibility to:

• Continuous improvement of Core Value Drivers and KPI’s in support of quality and business growth through the rigorous deployment of DBS tools
• Manage CAPA & 8D processes; assure root cause analysis and effectively implement robust CAPA in a timely manner. Follow-up and verification of CAPAs to assure no recurrence. Adhere to corporate escalation and reporting guidelines
• Strong focus on variation reduction using data driven approach and automotive core tools such PFMEA, Capability analysis/SPC. MSA etc.
• Proactively identify leading key Indicators and provide Manufacturing Quality Trend Charts/Analysis and suggest/implement improvements based on the trends.
• Support QMS to meet ISO 9001 requirements. Perform Internal Audits per the annual audit schedule, prepare report, follow-up and verification of completion of actions initiated from audit(s)
• Evaluates work methods, procedures and policies. Tracks progress of qualification status and reliability results & determine disposition of non-conforming processes.
• Lead and Support People engagement initiatives both site and global
• Drive efficiency, automation and digitalization in production & QM methods

The essential requirements of the job include:

• Minimum Bachelor’s degree in Engineering/Science
• Min 5 years relevant working experience in manufacturing with 3 years in Quality Control/Assurance in Semiconductor, Electronics or Automotive Manufacturing.
• Solid understanding of quality tools and methods. (FMEA, Control Plan, SPC, 5Why, FTA, 8D, 6 Sigma, Minitab/JMP)
• Certified Quality Engineer or Certified Lead auditor with thorough understanding of ISO 9001 2015 requirements
• Excellent English communication and Interpersonal skills.

It would be a plus if you also possess previous experience in:

• Previous exposure to the Manufacturing sector.
• Excellent problem-solving and analytical skills.
• Analytical and data visualization skills eg Tableau, Qlikview
• Lean / Kaizen proficiency/ black belt proficiency a plus

We are looking for QA Automation Engineer to join a FinTech company in Singapore!

• Exciting opportunity to work with a team of professionals to deliver high quality software applications
• Salary up to $4,500 + AWS + Bonuses (attractive employment benefits)
• Permanent position, opportunity to work on Blockchain/FinTech/Trading platform related projects

Responsibilities:

• Design, develop, and maintain automation frameworks for software & Hardware testing, process automation, and data integration
• Create detailed test cases, test plans and maintain salable automation frameworks to support continuous integration and delivery processes
• Execute automated test cases and analyze test results to identify defects, performance issues, and areas for improvement
• Integrate automated tests with CI/CD pipelines
• Identify areas where automation can improve operational efficiency and reduce manual intervention
• Document automation processes, test cases, and results for reference and auditing purposes
• Stay up-to-date and continuously improve the software testing process with new testing strategies, automation testing tools and methodologies
• Maintain strong verbal and written communication skills
• Support manual testing when needed and perform other duties as assigned

Requirements:

• Singaporean only
• Min 3 years of experience in automation testing using Selenium/Python/Appium
• Strong in Python scripting
• Experience in API automation, test automation and integrating it into CI/CD pipelines
• Domain knowledge in FinTech/Blockchain industry will be an added advantage

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Liew Chien Hui - R2090138

ScienTec Consulting Pte Ltd - 11C5781

Job Title: DCS Engineer

Work Location: Jurong Island

Expected Start Date: 01 January 2025

Responsibilities for this position may include but not limited to:

• Provides engineering design, troubleshooting and maintenance of Distributed Control System (DCS)
• Troubleshoot day-to-day process problems related to process control applications, controller tuning and batch receipes execution
• Supports Process Hazard Analysis and implements process changes through a Management of Change Process
• Maintains up-to-date documentations for the DCS
• Conducts training programs for operators on DCS & Batch Receipes
• Initiates and manages DCS hardware life cycle, software and process control network upgrades
• Leads / supports development and execution of control system pojects, and greenfield projects

Required Qualifications

• Bachelor's Degree in Electrical / Electronics / Instrumentation and Control / Chemical from an accredited university
• Minimum 5 years of related work experience in DCS in the refinery, petrochemical or checmical industry
• Strong analytical / trouble-shooting skills
• Good interpersonal and communication skills
• Able to work independently in a team and in a diverse enviroment.

Preferred Qualification:

• Knowledge and work experience in Honeywell DCS System (TPS/EPKS DCS and Experion Batch)
• Knowledge in SQL Programming / Power BI, Process Controls Domain & Network adminstration.

Intersted candidates, do drop me your resume @ evonong@davyomega.com

Job Responsibilities:

• Support continuous improvement efforts in QMS.
• Support in root cause analysis and implementation of corrective/ preventive actions for process related concerns.
• Analyze and provide timely respond to customer complaints.
• Interface with Customer and Operations to ensure new product transfer to manufacturing are in accordance with approved requirements.
• Prepare Quality performance metrics and reports.

Requirements:

• Diploma in Mechanical Engineering, Quality, or equivalent.
• Minimum 2 years work experience in Quality Management System in manufacturing environment.
• Good knowledge of ISO 9001. Knowledge of API Q1 is preferred.
• Strong command of English language, both oral & writing.
• Knowledge of metal working industry is preferred.
• Knowledge of risk assessment principles and methods.
• Knowledge of SAP is preferred.
• Positive & proactive attitude.

Role Objective:

Coordinates all activities related to Quality Control. Analysing and reporting of quality performance.

Job Responsibilities:

· Responsible for the quality control during the production stage in accordance with the ISO standard

· Ensure compliance with ISO9001:2008 quality standards

· Assist in document control and maintenance of ISO 9001 quality management system

· Coordinate daily QC Activities to ensure inspections are carried out appropriately

· Analyzing and reporting of quality performance

· Document and quality data control

· Other duties as assigned from time to time

Job Description:

• Ensure the machine is working correctly, and calibrating the machine to ensure proper measuring.
• Perform incoming, in-process and final inspection as per customer requirement.
• Maintain calibration record of measuring equipment.
• Document inspection results by completing reports and logs.
• Maintain safe and healthy working environment by following standards and procedures.
• Raise non-conformance report if necessary.

Job Requirements:

• NITEC/Higer NITEC in Precision Engineering.
• 2 -3 years of relevant QC experience in a manufacturing environment and knowledge.
• Able to interpret technical/mechanical drawings of geometrical dimensioning and tolerance.
• Able to perform CMM measurement; preferably with Wenzel or Zeiss.

Posted Job Advert

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

Did you know that we are the 1st biologics contract manufacturer in Singapore? We offer you exposure to upcoming biotech and established pharmaceutical companies and to the manufacturing technology needed to produce mammalian treatments and cell therapies of tomorrow. Our global manufacturing network is recognized for its reliable, high-quality services, regulatory track record, global footprint, innovative technology platforms and extensive experience – we, in Singapore are proud to be part of this global network.

The Senior QA Specialist will support day-to-day Quality Assurance activities in accordance with approved SOPs / Policies for a multi-product, cGMP contract manufacturing facility.

Key Responsibilities:

• Oversee daily Quality Assurance (QA) operations in line with approved SOPs and policies within a multi-product, cGxP contract manufacturing environment.
• Demonstrate strong motivation and exceptional expertise across all relevant job functions.
• Competently review and approve SOPs, protocols, reports, and records.
• Participate as an active member of cross-functional site teams handling various projects and issues.
• Coordinate multiple activities across departments, ensuring seamless communication and workflow.
• Exhibit excellent troubleshooting abilities, identifying process pathways and developing strategic improvements.
• Possess advanced knowledge of cGMP topics.
• Contribute to regulatory inspections or customer audits as needed.
• Lead or support improvement initiatives and strategic process developments.
• Quickly adapt to leadership roles in various process areas as required.
• Assume supervisory responsibilities in the absence of the direct supervisor.
• Comprehend and communicate the company’s business strategy while maintaining a wide-ranging perspective on operational trends and changes.
• Provide QA oversight to QC/DS lab services, Engineering, and Validation activities, reviewing documents and Trackwise records outside routine operations. Documents may include, but are not limited to, PQR, BLA content, new product introductions, qualification/validation strategies, gap assessments, and customer suspension/decommissioning processes.
• Actively participate in or lead complex investigations into deviations, change controls, CAPA proposals, and discrepancy reports using Root Cause Analysis tools to ensure timely and effective resolution.
• Oversee the proper implementation and timely closure of CAPA related to deviations.
• Support regulatory inspections or customer audits, confidently representing the company as a subject matter expert in QA oversight.
• Offer QA oversight for site-wide improvement projects, collaborating across departments to ensure clear communication and updates.
• Lead or assist in resolving complex process and project issues.
• Mentor and coach junior team members, fostering their development.
• Formulate and present solutions to internal and external teams and management.
• Represent QA Validation/Technical Compliance in decision-making processes during internal and external cross-functional meetings.
• Complete any additional tasks as assigned by the supervisor.

Key Requirements:

• Bachelor's degree or higher in Life Sciences or Pharmaceuticals, with significant experience in Validation and Quality roles within the Biopharmaceutical industry.
• A team player with 5+ years of relevant experience in a similar industry or role.
• Thorough understanding of regulatory requirements and local codes and standards (e.g., FDA, EMEA, ICHQ7).
• Practical and theoretical experience in quality management systems within GM facilities.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

Did you know that we are the 1st biologics contract manufacturer in Singapore? We offer you exposure to upcoming biotech and established pharmaceutical companies and to the manufacturing technology needed to produce mammalian treatments and cell therapies of tomorrow. Our global manufacturing network is recognized for its reliable, high-quality services, regulatory track record, global footprint, innovative technology platforms and extensive experience – we, in Singapore are proud to be part of this global network.

As a QC Expert you will be responsible for the supervision of all testing techniques and scheduling of testing with coordinating with the other departments delivering samples to ensure timely delivery of results. This role is also required to supervise the review of laboratory data (both internal and external) and the closeout of deviations.

Responsibilities

• Supervising the review of laboratory data (both internal and external) and the closeout of deviations
• Author and review Change Controls, Deviations/Investigation as well as Test Methods, Specifications and SOPs
• Perform report writing (Example: Deviations/Investigations/Trending)
• Maintains knowledge of new technologies
• Strong ability to manage multiple priorities and lead projects.
• Customer and regulatory agency interaction as required
• Problem solving of analytical/ microbiological methods as well as troubleshooting of equipment as applicable.
• Manage/perform equipment qualification and validation maintenance review
• Lead/ execute method transfers and validation/ qualification.
• Lead or participate in initiatives aimed at continuously improving quality processes and outcomes e.g. Lean Six Sigma methodologies, cost-cutting solutions, idea-box, etc
• Collect and analyze data related to quality metrics e.g. using statistical tools to identify trends, patterns, and potential areas for improvement
• Participate in Risk Assessment
• SME in 1 or more areas as aligned with training plan and known as go to person for technical advice.
• Able to make decision on the area of expertise
• Coach and train junior team member
• Participate and support in audit
• Any other duties as assigned by your manager

Experience:

• Bachelor’s or Diploma in a relevant science field or equivalent.
• Minimum of 10 years of experience in GMP (Good Manufacturing Practice) Quality.
• Relevant work experience, preferably in a laboratory setting, within the biotech or medical field.
• Individual contributor, high level understanding of QC activities and lab function

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

Did you know that we are the 1st biologics contract manufacturer in Singapore? We offer you exposure to upcoming biotech and established pharmaceutical companies and to the manufacturing technology needed to produce mammalian treatments and cell therapies of tomorrow. Our global manufacturing network is recognized for its reliable, high-quality services, regulatory track record, global footprint, innovative technology platforms and extensive experience – we, in Singapore are proud to be part of this global network.

The QA Specialist will be responsible for performing day-to-day tasks of the QA Department in a GMP facility manufacturing clinical and commercial pharmaceutical products.

Key responsibilities:

• Monitor day-to-day Quality Assurance activities in accordance with approved SOPs / Policies for a multi-product, cGxP contract manufacturing facility
• Highly motivated individual and have superior skills in all areas relevant to the job
• Review executed batch records and logbooks efficiently to ensure compliance with cGMP per written procedures
• Compile lot genealogy
• Participate actively and approve deviation investigations, utilizing Root Cause tools to enable effective and timely closure of deviation investigations
• Provide oversight to ensure correct implementation of CAPA based on deviation raised and ensure timely closure of CAPA
• Timely escalation of quality events on the floor based on knowledge of defined SOPs and policies
• Support changeover activities and QA on Call
• Provide training to new members and Participate in walkdown/ QA on Shopfloor and provide feedback to member of cross functional site team(s) on projects / issues
• Superior ability to troubleshoot; able to identify process pathway and work to develop improvement in strategy site team(s) on projects/ issues
• Understanding of advanced topics pertaining to cGMP
• Participate in Regulatory Inspections or Customer Audits as required.
• Identify process pathway and work to develop improvement in strategy
• Help/Transfer and quickly assimilate to leadership role in other process areas
• Assume Supervisory responsibility in absence of supervisor
• Any other tasks as and when assigned by supervisor

Key requirements:

• Bachelor Degree with relevant work experience in Quality Assurance in the Biopharmaceutical industry.
• Relevant QA Operations background from the Biopharma environment.
• Hands-on experience coordinating & interacting with internal departments on manufacturing activities.
• Fair knowledge and experience of the practical and theoretical requirement of quality management system in a GMP facility.
• Familiarity with Regulatory requirements and local Codes & Standards (e. g. , FDA, EMEA, andlCHQ7).
• Meticulous and Systematic.
• Team player, with strong focus on safety, quality and timelines.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

School of Physical and Mathematical Sciences (SPMS)

Nanyang Technological University, Singapore

Associate Prof / Full Professor in Optimization, Control, and Scientific Computing

Young and research-intensive, Nanyang Technological University (NTU Singapore) is ranked among the world’s top universities. The College of Science seeks a diverse and inclusive workforce and is committed to equality of opportunity. We welcome applications from all and recruit on the basis of merit, regardless of age, race, gender, religion, marital status, family responsibilities, or disability.

The School of Physical and Mathematical Sciences at NTU offers multidisciplinary academic programs that provide students with a wide-ranging and up-to-date education. They offer undergraduate training leading to BSc (Hons) and graduate training leading to MSc and PhD degrees.

We invite applications for an Associate / Full Professor position specializing in Optimization, Control, and Scientific Computing. We are looking for world-class candidates with expertise in the computational aspects of algorithmic design and a strong focus on applying these skills to real-world problems. The successful candidate will be expected to teach both undergraduate and postgraduate courses in applied mathematics, conduct high-quality research in computation-specific areas of optimization and its interactions with other domains, such as scientific computing and scientific machine learning, and promote interdisciplinary collaboration among the disciplines of mathematics, computer science, and engineering. Candidates with strong academic portfolios are encouraged to apply. We are particularly interested in candidates who have extensive experience in consulting and collaborating with data-related industries such as AI and cloud computing.

The candidates are expected to:

· Establish a world-class research programme.

· Enhance the College’s visibility as an international leader in education and research.

· Secure research funding from competitive grants and industry partnerships.

· Mentor and supervise graduate students and postdoctoral researchers.

· Collaborate with interdisciplinary teams within the university and with external partners.

· Deliver engaging and effective teaching to both undergraduate and graduate students.

· Undertake essential administrative responsibilities within the Schools.

Requirements:

· PhD in mathematics or a related subject.

· Strong research record and relevant publications in reputable peer-reviewed international journals and conferences.

· A good track record of supervising research staff, postdocs, students, and interns in relevant fields

· Experienced in cross-disciplinary research initiatives and collaboration.

· Demonstrated excellence in research, evidenced by a strong publication record in reputable journals

· Recognition in the research community, such as invited talks, awards, or memberships in professional societies.

· Proven ability to secure research funding.

Application Procedure

Required application documents:

· Cover letter.

· Curriculum Vitae, including a full publication list.

· Statement of current and future research interest.

· Teaching statement.

· Names of at least four referees.

For any enquiries, please contact Bernhard Schmidt, bernhard@ntu.edu.sg.

School of Physical and Mathematical Sciences (SPMS)

Nanyang Technological University, Singapore

Associate Prof / Full Professor in Optimization, Control, and Scientific Computing

Young and research-intensive, Nanyang Technological University (NTU Singapore) is ranked among the world’s top universities. The College of Science seeks a diverse and inclusive workforce and is committed to equality of opportunity. We welcome applications from all and recruit on the basis of merit, regardless of age, race, gender, religion, marital status, family responsibilities, or disability.

The School of Physical and Mathematical Sciences at NTU offers multidisciplinary academic programs that provide students with a wide-ranging and up-to-date education. They offer undergraduate training leading to BSc (Hons) and graduate training leading to MSc and PhD degrees.

We invite applications for an Associate / Full Professor position specializing in Optimization, Control, and Scientific Computing. We are looking for world-class candidates with expertise in the computational aspects of algorithmic design and a strong focus on applying these skills to real-world problems. The successful candidate will be expected to teach both undergraduate and postgraduate courses in applied mathematics, conduct high-quality research in computation-specific areas of optimization and its interactions with other domains, such as scientific computing and scientific machine learning, and promote interdisciplinary collaboration among the disciplines of mathematics, computer science, and engineering. Candidates with strong academic portfolios are encouraged to apply. We are particularly interested in candidates who have extensive experience in consulting and collaborating with data-related industries such as AI and cloud computing.

The candidates are expected to:

· Establish a world-class research programme.

· Enhance the College’s visibility as an international leader in education and research.

· Secure research funding from competitive grants and industry partnerships.

· Mentor and supervise graduate students and postdoctoral researchers.

· Collaborate with interdisciplinary teams within the university and with external partners.

· Deliver engaging and effective teaching to both undergraduate and graduate students.

· Undertake essential administrative responsibilities within the Schools.

Requirements:

· PhD in mathematics or a related subject.

· Strong research record and relevant publications in reputable peer-reviewed international journals and conferences.

· A good track record of supervising research staff, postdocs, students, and interns in relevant fields

· Experienced in cross-disciplinary research initiatives and collaboration.

· Demonstrated excellence in research, evidenced by a strong publication record in reputable journals

· Recognition in the research community, such as invited talks, awards, or memberships in professional societies.

· Proven ability to secure research funding.

Application Procedure

Required application documents:

· Cover letter.

· Curriculum Vitae, including a full publication list.

· Statement of current and future research interest.

· Teaching statement.

· Names of at least four referees.

For any enquiries, please contact Bernhard Schmidt, bernhard@ntu.edu.sg.