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Research & Development jobs

ABBOTT LABORATORIES
08Jul
Administrator
ABBOTT LABORATORIES   via Indeed

Primary Function:
Perform administrative support and secretarial duties for a department or group.
Prepare correspondence, presentations and reports.
Compose routine correspondence.
Maintain confidential records and information.
Responsibilities:
Screens telephone calls and visitors, and resolves inquiries and requests.
Schedules and maintains calendar of appointments, meetings and travel itineraries, and coordinate related arrangements.
Tracks operational data in a database, including financial and other reporting metrics.
Uses software tools to compile data into presentation format.
Maintains accurate schedule of activities of    Read more

the executive(s) supported, including complex meeting coordination and extensive travel arrangements.
Independently prepare presentations and recurring reports.
Prepares and manages correspondences and collation of reports/documents to meet business timeline.
Organizes a variety of local meetings, corporate events as and when called upon.
Maintain a systematic filing system.
Any other duties as assigned by supervisor.
Requirements:
Diploma in related discipline or GCE "O" with minimum 3 years of experience.
Minimum 1 year of relevant experience in an administrative role (e.g. team/department admin)
Proficient with Microsoft Office required
Experienced in handling customer visits with great confidence.
Experience using CTE for travel desk support, travel claims or SAP for purchasing is advantageousPosition is based in Tuas (Singapore)

Skills
Abbott
07Jul
Administrator
Abbott   via Glassdoor

JOB DESCRIPTION:

Primary Function:

Perform administrative support and secretarial duties for a department or group.

Prepare correspondence, presentations and reports.

Compose routine correspondence.

Maintain confidential records and information.

Responsibilities:

Screens telephone calls and visitors, and resolves inquiries and requests.

Schedules and maintains calendar of appointments, meetings and travel itineraries, and coordinate related arrangements.

Tracks operational data in a database, including financial and other reporting metrics.

Uses software tools to compile data into presentation format.

Maintains accurate schedule of activities    Read more

of the executive(s) supported, including complex meeting coordination and extensive travel arrangements.

Independently prepare presentations and recurring reports.

Prepares and manages correspondences and collation of reports/documents to meet business timeline.

Organizes a variety of local meetings, corporate events as and when called upon.

Maintain a systematic filing system.

Any other duties as assigned by supervisor.

Requirements:

Diploma in related discipline or GCE "O" with minimum 3 years of experience.

Minimum 1 year of relevant experience in an administrative role (e.g. team/department admin)

Proficient with Microsoft Office required

Experienced in handling customer visits with great confidence.

Experience using CTE for travel desk support, travel claims or SAP for purchasing is advantageous

*Position is based in Tuas (Singapore)

JOB FAMILY:

Administrative Support

DIVISION:

ANSC Nutrition Supply Chain

LOCATION:

Singapore > Singapore : SN01

ADDITIONAL LOCATIONS:

WORK SHIFT:

Standard

TRAVEL:

No

MEDICAL SURVEILLANCE:

Not Applicable

SIGNIFICANT WORK ACTIVITIES:

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)

Skills
Agilent Technologies, Inc.
03Jul
Customer Operations Specialist
Agilent Technologies, Inc.   via Indeed

Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek - so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com.

Be the lynchpin in the team that propels Agilent    Read more

forward. In our organization, where altitude is combined with critical thinking and tenacity, you will overcome headwinds with laser-focused determination. Hone your skills in Account Management, Customer Relationship Management and Project Management. Poise yourself for the next level of your career.
Be the Go-To person that delivers Trusted Answers in a dynamic and forward-looking organization. You will make a difference in the lives of millions of people through your work at Agilent.

Primary Responsibilities:-
Ensure the highest level of quality service is rendered to customers by providing them accurate information, solving problems and serve in a variety of pre and post sales functions via calls and emails.
Account management of quote to cash cycle, generation and conversion of quotes to orders where accuracy and responsiveness are critical
Coordinate and responsible for end to end order management which includes order fulfillment, shipment coordination, 3rd party requisitions, returns and payment liaison with both internal and external stakeholders.
Work closely with both internal and external stakeholders to fulfill customer orders in a timely and accurate manner, ensuring orders are align with Agilent's policies, processes and legal requirements.
Ensure close follow-up of outstanding orders and issue with proactive communication to customers.
Keeping up to date on sales discount and marketing, promotional programs and to administer these accordingly.
Responsible for customer's journey and manage sensitive issues with poise and professionalism, escalate when necessary
Provide support in business projects related to process improvement, customer experience, etc.
Performing on miscellaneous duties and projects as assigned.
Opportunities to be engaged in global and regional initiatives and projects, collaborating with other cross functional teams within Agilent to achieve goals as needed.
Key Deliverables:-
Effective customer account management and deliver an exceptional customer experience
To understand and resolve customers' concerns by applying appropriate skills and meet customers requirement in effective way.
Timely response to internal and external customers' enquiries and emails
Accurate and timely processing of orders within turnaround time
Ensure every order is always compliant to Agilent's policies and processes
Prompt follow-up on order management to ensure revenue recognition
Keeping customers informed about order status.
Maintaining post order entry responsibilities using control related reporting to ensure compliance
Consistent contribution to achieve department key performance indicators
Maintain amicable work atmosphere by communicating and acting in a collaborative manner with stakeholders to resolve customer issues and deliver trusted answers

Skills
Advanced Technology Research Centre (ATREC) Pte Ltd
03Jul
R&D Engineer - Ref:ATREC/KKH
Advanced Technology Research Centre (ATREC) Pte Ltd   via Advanced Technology Research Centre (ATREC) Pte Ltd

Job Description:
>To conduct R&D in advanced energetic materials. Job scope include:
>
Materials synthesis/crystallisation and scale up including process design, quality control and test/characterization of materials.
Assist in coordination of infrastructure development with contractors.
Sourcing and procurement of materials including inventory management.
Equipment maintenance including preventive maintenance.
Documentation of materials processes for compliance with quality management system.

Job Requirements:

Degree in Chemical Engineering.
Relevent working experience in R&D will be an advantage.
Good knowledge in chemistry, especially in    Read more

synthesis and process scale-up, crystallization and drying of solids.
Experience in operation of process analytical tools will an advantage. E.g. RC-1, FBRM, ReactIR, microscope analysis, chromatographic analysis (GC or HPLC, IC), DSC and TGA.
Good technical report writing skills
Good team player with the ability to work cross-functionally with other team members
Possess good learning attitude
Good communication skills
Singaporeans need apply

Skills
ABBOTT LABORATORIES
03Jul
Operational Excellence Specialist
ABBOTT LABORATORIES   via Indeed

Primary Function:
Successfully drives and facilitate the Business Process Improvement approach within Abbott Manufacturing Singapore site through the deployment of Business Process Improvement Systems, related tools and thought processes.
Acts as a subject matter expert regarding process improvement initiatives.
Presents recommendations and progress reports to senior site leadership.
Provides support and project management leadership to team members within a business unit and functional level.
Responsible for creating an environment and assisting leadership and    Read more

customers in the timely and successful completion of cost effective, strategic project and business improvement opportunities.
Serves as project leader while implementing constructive long-term change initiative.
Responsibilities:
Implement process improvement projects in the plant to streamline workflow.
Perform data collection and job re-design for standard work implementation at the shop floor.
Perform data collection and analysis on long term production issues and perform root cause analysis to resolve the problem.
Support and run cost improvement projects such as performing trials, engineering studies, flushing reduction projects.
Help manage and maintain current process such as visual factory, RCA in the operations area.
Any other duties as assigned by supervisor.
Requirements:
Bachelor Degree any discipline or Diploma with minimum 3 to 5 years of experience.
3 to 6 years of Operations experience in a manufacturing environment.
Experienced in Lean Six Sigma preferred, certification is advantageous
Well-versed in using Microsoft Word, Excel and PowerPoint.
Experience in implementing improvement ideas/ projects.
Strong communication skills and interpersonal skills.

Skills
NITTO DENKO ASIA TECHNICAL CENTRE PTE. LTD.
02Jul
Ra/Qms Specialist
NITTO DENKO ASIA TECHNICAL CENTRE PTE. LTD.   via JobsCentral

Job Description:


Collects documentation and coordinates with cross-functional teams to prepare regulatory submissions to regulatory agencies (or commercial partners).
Creates and maintains regulatory submission timelines and track deliverables to ensure company goals are met.
Supports overall organizational regulatory strategies
Provides strategic input and regulatory advice to project teams on development programs including new product development and changes to existing products.
Keeps abreast of current regulatory landscape for medical device globally, e.g., FDA guidance    Read more

documents, Medical Device Regulations (MDR), EU guidance documents, IEC 62304, ISO 13485.
Develops and communicates recommendations regarding new/emerging regulations to management and project teams.
Identifies potential project issues proactively to allow implementation of appropriate regulatory strategies to mitigate risks.
Reviews quality systems processes and serves to improve awareness, visibility, and communication on quality initiatives to support assigned quality goals and priorities.
Support QMS team in development of procedures, other quality documentations as applicable.
To translate new and complementary standards’ requirements into documents (QM, SOPs, Forms) and define the applicability of the requirements for the different types of businesses. E.g., EU IVDR, GDPMD, IEC 62304 and etc.
Support process improvement for Regulatory Affairs function
Monitors FDA, HSA and other agency laws and regulations, and provides recommendations and assistance to ensure company compliance
Brings QMS/Regulatory Affairs questions/issues to the attention of management
Work closely with product development team to support any troubleshooting activities as applicable.

Qualifications:

Preferred Degree in Chemical Engineering, Chemistry, Biomedical Science.
At least 3 years prior experience in medical device industry is preferred.
Understanding of Medical device software development is desired.

 
Interested applicants, please apply via the "Apply Now" button with your updated CV. Kindly include current salary, expected salary and notice period.
We regret that only shortlisted candidates will be notified.

Skills
NITTO DENKO ASIA TECHNICAL CENTRE PTE. LTD.
30Jun
Product Engineering Manager
NITTO DENKO ASIA TECHNICAL CENTRE PTE. LTD.   via JobsCentral

Lead and manage full lifecycle of product from design/development to scalable cost-effective mass production. Drive cross functional initiatives which include, but not limited to, establishing and managing supply chains, lead the design/development of front-end and back-end production process, works with contract manufacturers on verification/validation of production line as regulated by medical devices standards, establishing good manufacturing practices and quality control system, and manage post-sales engineering services
Work closely with    Read more

management to identify/recruit/secure technical/manpower resources to successfully execute the project within budget.
Responsible for leading, planning, monitoring, tracking and prioritizing engineering team’s product development projects across multiple functional organizations in facilitating successful, on-time and within budget execution.
Lead Design Control activities. Provide/Seek technical expertise pertaining to the design and development of new products in alignment with applicable internal procedures, and external regulations and standards.
Participate in Risk management activities. Provide/Seek technical expertise pertaining to the identification and mitigation of design and use risks.
Ensure project status / outcomes are properly documented and presented quantitatively with scientific & engineering discipline and be responsible to integrate and maintain project related documents and information, and collaborate with internal document control.
Review and analyze project activities and costs to determine progress toward stated goals and objectives. Implements appropriate countermeasures to ensure successful outcomes.
Ensure clear and smooth communication of the team and provide proper regular reporting to the management.
Supports the product development process and is a proponent of continuous process improvement.
Determine patentable ideas throughout the work and carry out activities relating to the patent filing procedure, along with IP department
Oversee & follow though certification procedure & testing for Consumer Electronics & Medical Device  

 
Requirements:

5 to 10 years of manufacturing experience in the medical device and/or consumer electronics industry.
Bachelor's in Engineering, Electrical, Mechanical, Chemical, or equivalent technical degree.
Extensive knowledge of the medical device and/or consumer electronics manufacturing process.
Experience in product development process from concept development to prototyping and design/documentation release to manufacturing.
Experience in managing contract manufacturers is preferred.
Experience with cGMP, ISO 9001 operations is required.
Experience with ISO 13485 operations is advantageous.
Ability to multitask, possess good leadership and manage multiple stakeholders.

Interested candidates, kindly send in your CV with current salary, expected salary & commencement date.
 
We regret to inform that only shortlisted candidates will be notified.

Skills
NITTO DENKO ASIA TECHNICAL CENTRE PTE. LTD.
30Jun
Senior Software Engineer
NITTO DENKO ASIA TECHNICAL CENTRE PTE. LTD.   via JobsCentral

Key Responsibilities

Work closely with electrical, firmware and software engineers to develop software architecture documentation.
Collaborate with stakeholders to write firmware and software requirements and develop software requirements specifications.
Lead software risk management, software verification and validation activities.
Own and write medical device software life cycle development processes and procedures.
Work closely with firmware QA and testing teams either from Contract manufacturer or Software consultant.
Work closely with design assurance, quality systems and regulatory    Read more

teams to achieve company goals.

 Qualifications

5+ years of experience working on Class II and Class III medical devices (Preferably software classification A and B )
BS, MS in computer science. 
Demonstrated applied expertise in FDA requirements (21 CFR 820)( Preferably)   and medical device regulations including ISO 13485, ISO 14971, IEC 60601, IEC 62366, and IEC 62304. 
Solid understanding of medical device cyber security and privacy guidelines and regulations (e.g, GDPR).
Experience working on connected medical devices (mobile and cloud supported devices).
Solid experience in preparing technical files for supporting regulatory submissions (including CE mark, US FDA).
Strong working knowledge of support tools (e.g., Jira, Github)
Good written and oral communication skills and experience writing SRS, software architecture documents, test protocols and reports.

 
Interested candidates, kindly send in your CV with current salary, expected salary & commencement date.
 
We regret to inform that only shortlisted candidates will be notified.

Skills
NITTO DENKO ASIA TECHNICAL CENTRE PTE. LTD.
30Jun
Senior Product Development Engineer
NITTO DENKO ASIA TECHNICAL CENTRE PTE. LTD.   via JobsCentral

Job Description:
>
Be part of the cross-cultural team driving Product Development of Medical devices from concept to production, including translation of product requirements to technical specifications, definitions of product hardware architecture, review and selection of key technologies, performing design reviews to assess robustness, product debug and validation and resolving issues.
Conduct Hardware and Electronic development to meet design requirements in terms of functionality, reliability, cost and compliance to industry standards.    Read more

Must be sensitive to cost during the architecture phase and able to propose trade-offs between cost, quality and functionality. Plan schedule, estimate level of effort and man hour.
Responsible for design, implementation, integration, debugging, verification and validation testing of hardware modules for product development. Conduct prototype design simulation using suitable software platforms. Create test plan and test cases for Hardware verification. Create validation requirements documents, generate and execute high/low level unit/integration test plans.
Responsible for the software development life cycle (project planning, software test requirements/strategy definition, software verification/validation and software quality assurance)
Software verification/validation testing – create test plan and test cases. Generate and execute high/low level unit/integration test plans. Review the test result and lead the root cause analysis in troubleshooting activities. Support continuous improvement in the software validation process and methods.
Support Software quality assurance – Perform code reviews. Outline corrective action for given issues and problems. Ensure the software meets Project requirements. Ensure Regulatory compliance is fully met with proven design solutions and design practices.

 
Skills/Qualification:
>
Degree or Master in Electrical & Electronic Engineering or equivalent experience.
At least 3 years working experience in Product development for Medical device
Design experience in complex electromechanical products is an advantage. Other relevant experience include Optical sensor components (Light Emitting Diode/Photo detector), Electro-mechanical components and embedded system design.
Possess IEC61010, IEC62304 and ISO138485 knowledge.
Able to handle laser class 3b equipment.
Strong EMC knowledge and design countermeasure.
Working knowledge of CAD tools, including Altium Designer, PCB design and layout tools.
Conversant with DFx and quality concepts including designing for manufacturability, verification and reliability testing and regulatory requirements.
With hands on experience on hardware prototyping (testing & evaluation)
Familiar with firmware development on embedded systems using C/assembly.
A committed, competent and self-motivated team player with outstanding analytical and problem solving skill, strong verbal, written communication and excellent communication/presentation skills for interfacing with other Project team members.

 
Interested candidates, kindly send in your CV with current salary, expected salary & commencement date.
 
We regret to inform that only shortlisted candidates will be notified.

Skills
NITTO DENKO ASIA TECHNICAL CENTRE PTE. LTD.
30Jun
Senior Embedded Software Engineer
NITTO DENKO ASIA TECHNICAL CENTRE PTE. LTD.   via JobsCentral

Job Description:
>
Develop reliable software with high quality and easy to maintain source code
Perform software design, testing and documentation for PC application.
Create and execute software for computer interfacing via USD and Bluetooth
Support team members by developing functional testing software
Interact with other teams (requirements gathering/transferring, development, Q&A and etc.) to deliver effective result.
Lead the Classification of the software for UP project to comply ISO13485 and CE marking.
Review and manage the    Read more

source code development activities for main module and test module in ACT and lead the Verification and validation activities.
Conduct a software verification/validation testing –perform verification and validation tests with standard/customized test tools, as well as self-developed test application. Generate test reviews and test reports. Continuous improvement in the software validation process and methods.

 
Skills/Qualification:
>
Master/Bachelor’s Degree in Computer Engineering, Computer Science or related field.
Minimum 2-year experience in PC based application development using VB.Net or C#.Net
Experience in computer interfacing or signal processing
Experience in code optimization, debugging and checking for memory leaks, etc
Knowledge in database (MS SQL, MySQL, NoSQL) and Linus server is a plus

 
Interested candidates, kindly send in your CV with current salary, expected salary & commencement date.
 
We regret to inform that only shortlisted candidates will be notified.

Skills