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Jobs that require r&d skill

R&D Manager – Ref: NSJ
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R&D Manager  – Ref: NSJ

Responsible for development of new tests/capabilities, as well as management of R&D Projects / ad-hoc Projects
Responsible for the department's safety performance and awareness; spearheads and manages initiatives that drive a culture of safety first
Under the direction of the Operations Manager and / or General Manager, helps lead the efficient operation and growth of the assigned department
Plan, assign and schedule work for designated staff
Assists in    Read more

the engineering and coordination of projects from start to finish
Works to assure quality, timeliness, consistency and accuracy of test reports
Demonstrate knowledge of capabilities, processes and expertise to be able to clearly explain the benefits of Element testing services
Represents the highest levels of integrity and professionalism at all times
Responsible for promoting and ensuring the quality assurance and safety program initiatives are executed upon
Responsible and accountable to assigned staff decisions to include hiring, performance management, performance review decisions and execution, and approval of overtime and time cards
Work with assigned staff to ensure work schedules are maintained and balanced
Maintain an environment of respect and dignity within the department covering employee interactions and problem solving while ensuring work rules are known and followed
Manages a team with fairness and consistency and takes interest in the development of direct reports
Provide general administrative functions as required (invoicing, job list upkeep, supply report data for creation)
Review testing services and promote additional capacity and process improvement
Translate technical requirements of the client into providing pricing, timing and technical knowledge for quoting and commercial efforts

To apply, please email your detailed CV in MS Words format to: Sarah Jumain,
Sarah Binte Mohamed Jumain (CEI: R1981588)
Recruit Express Pte Ltd
EA license Number: 99C4599

Process Engineer / Validation Engineer (Office Hrs 5D, cGMP, Pharma MNC)
Recruitexpress   via Recruitexpress


Under general supervision, reviews specifications and determines the critical aspects of facilities, utilities, computer systems and manufacturing equipment with regard to product and process quality, writes qualification protocols for operating systems and records related test results. prepares final reports that identify the results of protocol testing and the conditions of release.

Essential Job Functions:

• Carries out responsibilities in accordance with the organization's policies, procedures, and state, federal and local    Read more

> • Writes protocols that challenge the critical parameters related to installation, operation, and performance of the related facility, utilities, computer systems, or equipment.
> • Assures that protocols are approved through proper channels; writes and revises validation protocols.
> • Executes validation and qualification protocols per related SOPs and assures that acceptance criterion related to validation and qualification protocols are met.
> • Analyzes new and existing equipment, recommends equipment modifications as needed for validation optimization.
> • Assures that all test data is gathered and recorded in accordance with cGMP requirements.
> • Analyzes data to ascertain if it meets related protocol acceptance criteria; writes deviation reports as required upon failures to meet protocol acceptance criteria.
> • Writes final reports and assures that they are approved through proper channels.
> • Performs necessary equipment and system IQ, OQ, and PQ's to assure compliance in all manufacturing and support areas.
> • Develops and communicates project timelines and status.
> • Complies with all GMP and safety requirements, SOP's and Company policies and procedures.
> • Performs related duties as assigned.
> • Work in self-directed manner and must be able to work on problems of a complex scope where analysis of data requires and in-depth evaluation of various factors
> • Ability to exercise judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results
> • Demonstrated understanding and use of statistical methods in experiment design, data analysis, validation, and process monitoring

Process Engineer 

• Coordinates all work related to Process Engineering deliverables on scheduled projects needed to meet the deadlines developed by Plant Capital Plan, New Product Introductions, and New Process Technology Developments.
> • Responsible for manufacturing engineering support, the development of new process technologies, and the support of new product introductions/tech transfers.
> • Organizes testing associated with the development of new process technologies and the support of new product introductions/tech transfers and works closely with the overall Tech Transfer team.
> • Works closely with technical services to develop and confirm Critical and Key Process Parameters needed for Equipment and Process Validation. Develops and delivers presentations to communicate project timelines and milestone completions.
> • Serve as the Subject Matter Expert for equipment and processes within area of responsibility and thereby serving as the SME for investigations, design reviews, equipment/process troubleshooting , Capital Project planning , change control and other related activities for the site.
> • Able to work well in cross functional TEAMS, good communication and presentation skills, strong technical understanding, general automation knowledge, multi-tasking and time management
> • Work effectively with others from diverse backgrounds and demonstrate capability to adapt to new, different, or changing requirements. Display strong moral principles and work ethics while demonstrating initiative. Maintain a professional presence and display responsible behaviors.
> • Develops conceptual strategies, processing schemes, feasibility studies, PFD’s, and detailed scopes of work.
> • Identify and execute projects to increase safety, reduce product cost, improve product quality, improve yield, and reduce material usage.
> • Work on several different projects and be able to prioritize these projects.
> • Assists in developing control strategy and instrument process design, including emergency and shutdown procedures, instrument specification sheets, control ranges, alarm points, and automation strategy.
> • Authors, updates, reviews, and approves area procedures and master batch records to ensure correct content and compliance with Good Manufacturing Practices.
> • Designs studies, executes experiments and perform data analysis.
> • Writes study proposals, progress reports, development reports, and various technical memo’s.
> • Evaluates new technologies to improve the commercial production process.
> • Supports scale up activities from R&D to production.
> • Provides miscellaneous overhead support of facility.
> • Supports the assurance of a robust manufacturing process for the current registered process as experience is gained post launch.
> • Sets up robust process for trouble shooting.
> • Acts as an effective change agent.
> • Acts as a key player for the expansion of projects as needed to increase scale of manufacture.
> • Investigate deviations from standards of manufacturing process using effective root cause analysis tools. Recommending and implementing effective corrective and preventative actions.
> • Generating, evaluating, and implementing innovative and creative solutions.
> • Assist as subject matter expert for technical projects.
> • Capable of generating a project scope and cost plan to effectively draft a capital request.
> • Develops product and process knowledge in multiple process train areas.
> • Contributes to equipment URS development and retrofit. Participates in equipment FAT’s, SAT’s, etc.
> • Participate in Quality Risk Assessments and process hazards analysis activities.

Job skills & knowledge:

• Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements.
> • Pharmaceutical principles, practices and applications.
> • Principles of mathematical and statistical computations.
> • Interpreting software and ladder logic diagrams and flowcharts.
> • Interpreting electrical and mechanical blue prints and specifications including HVAC systems and. construction plans.
> • Solving practical problems and considering a variety of concrete variables in situations where only limited standardization exists.

Basic Qualifications

• Min 5 years experience working in a regulated environment
> • Working knowledge of Standard Operating Procedures and Protocols/Reports
> • Understanding of validation/qualification strategies
> • Knowledge of applicable quality regulations and standards
> • Quality or quality support experience in a regulated environment (GLP, cGMP, ISO)
> • 3 years quality assurance or quality control experience in cGMP pharmaceutical or drug development organization
> • Working knowledge of facility equipment commissioning and qualification
> • Working knowledge of process and cleaning validation
> • Working knowledge of Computer System Validation
> • Quality assurance or quality control experience in a cGMP pharmaceutical setting
> • Education: B.S. in an Engineering discipline, or Life Science degree
> • Required: 3-5 years quality or quality support experience in a cGMP pharmaceutical setting
> • Desired: 4-7 years facility, equipment, and/or cleaning validation experience in a cGMP manufacturing setting
> • Sound working knowledge of processing equipment used to manufacture APIs
> • Knowledge of clean room standards

Professional Skills, Qualifications and Experience:
• Strong ability to manage multiple priorities, self-starter attitude, good oral and writing skills and the ability to work independently and as a team in an efficient manner.
> • Ability to utilize GDP during document creation and review.
> • Working knowledge of current regulatory guidelines and standards.
> • Ability to apply and incorporate pharmaceutical standards, rules and guidances. (e.g. FDA, EU, ISO, ICH, ISPE, etc.)
> • Comfortable in a fast-paced environment with the ability to adjust to changing priorities.
> • Flexible and accountable.
> • Detailed oriented work standards.
> • Office Hours 5 Days

Interested candidates please send a copy of your resume to Subject: Validation / Process Engineer – Leon

Leon Leong De Cong
Recruit Express Pte Ltd (Healthcare & Lifesciences Division)
EA License: 99C4599

Design Engineer (MNC) – Ref: NSJ
Recruitexpress   via Recruitexpress

Design Engineer (MNC)  – Ref: NSJ

To design and develop new model assigned by the Project Leader;
To ensure the design of new product/model meeting the specification and cost;
Responsible for the release of the test evaluation data and drawings;
To coordinate and support new product transfer from R&D to production

To apply, please email your detailed CV in MS Words format to: Sarah Jumain,
Sarah Binte Mohamed Jumain (CEI: R1981588)
Recruit Express Pte    Read more

EA license Number: 99C4599

Technical Manager (Chemical)/East/ $10000 - $12000
Recruitexpress   via Recruitexpress

Overall Job Purpose
Research and development of new finishing and chemicals 
Job Responsibilities

Provide support and resolves issues pertaining to processes and finishing products in the domain of Quality, Product development, and operating procedures
Responsible for managing a technical testing laboratory and ensuring compliance with local regulations
Liaise with customers on technical requirements
Source and liaise with companies on new chemical development in the market to support product development/finishing
Provide technical support on new product    Read more

recipes, improvement on existing recipes, design processes for recipes production
Liaise with various department from testing to implementation of recipes
Projects as needed

Job Requirements

Bachelor of chemical engineering/chemistry with minimum 8 years’ of relevant experiences in chemical related industry especially in quality function
Strong in technical expertise, quality standards and processes
Possess technical knowledge and be adapt at all phases of the manufacturing process
Relevant experience in product development and quality control
Resourceful with strong problem-solving skills and leadership capabilities

Research & Development Admin Assistant Director - HEALTHCARE
Recruitexpress   via Recruitexpress

Responsible for the development and implementation of key research strategy on Research Manpower Development
Oversee day to day operations of the units
Responsible for collating, monitoring, analyzing and reporting of institutions research KPIs through the Research Performance Dashboard.
Assist Director (Education & Research), on all other strategic development aspects of Research Manpower Development.
Oversee the development & implementation of programmes, initiatives and schemes
Responsible for the collation, monitoring, analyzing and reporting of institutions    Read more

research KPIs through the Research Performance Dashboard System


Minimum a Bachelor’s Degree, preferably in Science/Life Sciences/Health Sciences
Experience with Clinician Scientists/researchers’ management
Familiar with NMRC’s talent management schemes

Qualified and interested candidates please email your resume to
Subject heading: R&D Admin AD

Michelle Lee Ser Min
Recruit Express Pte Ltd
EA Licence No. 99C4599

Quality Assurance Specialist (Office Hours 5 Days, Pharma MNC)
Recruitexpress   via Recruitexpress

Essential Functions 

The Quality Assurance Specialist is an adept technical writer/editor and the use of desktop Office applications.
The QA Specialist must become familiar with site databases and proficient in the retrieval and presentation of information.
The QA Specialist will trend this information using the graphical features of Microsoft Excel and display these in Microsoft Word reports. A major example is the Annual Product Review (APR). 
In addition the QA Specialist will    Read more

lead in Change Control decisions and work with other departments to identify and solve issues that impact the product validation or the regulatory state.
The QA Validation Specialist not only works with all site departments but supports Corporate Regulatory and R&D needs as well.
The QA Specialist will support Regulatory Affairs with technical writing as pertaining to equipment and processes for product submissions and Request for Information (RFI).
The QA Specialist will provide project support for the New Product launches and utilize Microsoft Project to organize site deliverables. 
Additional responsibilities may include assisting with validation activities associated with equipment and/or processes.
The job may require travel to vendor sites to complete Factory Acceptance Testing in order to accept equipment for the site. Expect travel of less than 10%.


Min Diploma / Degree in Chemical Process Technology, Foodscience, Biotechlonogy, Biology, Biomedical Sciences, Science or its equivalents
No Experience Needed, Full training/ on the job guidance will be provided
Able to start immediately
Location : West

If you are interested in any of the positions, do kindly drop your most updated resume to   (Attn: QA Specialist- Leon)

Thank You.
Leon Leong De Cong
> R1551708
Recruit Express Pte Ltd (Healthcare & Lifesciences Division)
> EA License: 99C4599

MSD   via Indeed

Job Description
Join us in our mission to INVENT the future. Let’s be part of our team of dedicated, energetic individuals who are committed to be the most trusted supplier of pharmaceuticals and health products worldwide. Apply and join us now as Microbiologist to be based in our Manufacturing Division in Tuas, Singapore.
Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants    Read more

with a “Safety First, Quality Always” mindset striving for continuous improvement. We work in the local plant connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates and finished products.
Support testing/ monitoring functions pertaining to aseptic manufacturing and microbiological testing of Raw materials, Excipient, In-process materials, semi finished and finished products manufactured in the API, DPI, Biotech, Tablets and R&D facilities.
Responsible for testing of developmental and clinical products as required.
Participate in analytical developmental activities as required.
Perform routine/non-routine quality monitoring, sampling and testing of Utility systems inclusive of Purified water, Water for Injection, Pure steam. Compressed air and Nitrogen systems.
Perform the routine/non-routine environmental monitoring for all required plants, facilities, clean rooms, hygienic areas and labs, inclusive of particle monitoring test.
Perform personnel qualification and re-qualification and also to lead qualification and re-qualification of the clean rooms, when necessary.
Provide testing support to plant validation activities
Perform in-process and release samples testing of excipient/ packaging components for the different drug products, semi finished drug product and drug substances. i.e., Sterility test, Bacterial endotoxin test, Bioburden test, Microbial Limits Test, etc., as appropriate.
Perform routine and Batch related Environmental monitoring in clean rooms and other production areas and laboratory.
Perform Media Receival, Sterility check and Growth Promotion Tests for media used for testing.
Perform initial Quality Control check and regular QC checks on ready-to-use cultures and maintenance of cell cultures.
Perform microbial identification (Bacteria, mold and yeast) in water, environment and product samples.
Perform periodic review of closed out Validation Document packages and Standard Operating Procedures.
Extend documentation support to the department by participating in writing/revising of SOPs, protocols, Test reports and any other work assigned by the Senior, Lead Microbiologist, Sr/ Manager, Microbiology.
Support investigations
Prepare/Support Trend Reports
Liaise with external vendors on instrument calibration and maintenance.
Solicit quotations of laboratory consumables.
Maintain continuous supply of laboratory consumables
Participate in SHE, Business Compliance, cGMP and all other compliance-related matters, where applicable.
Supervise and oversee Third Party Contractors, where applicable.
Need to co-ordinate with Quality, respective Plant Operations, Projects and Engineering & Maintenance.
Liaise with other department for training needs and technical support
Liaise with vendor and service engineers/ESPs for equipment validation, calibration and maintenance work.
Need to coordinate with suppliers of microbiological media and other equipment.
Any other duties as assigned by the Supervisor / Manager.
Degree in Microbiology / Biotechnology.
0 to 3 years’ experience in pharmaceutical industry is preferred. No working experience can also be considered.
Good understanding of Safety and cGMP practices
Experience in operating laboratory equipment and lab computer systems is very desirable.
Analytical development mindset in research and commercialization activities
Our Manufacturing & Supply Division is committed to be the most trusted supplier of bio-pharmaceuticals worldwide. Our facilities, along with our external contractors, suppliers, and partners, create an interdependent global manufacturing network that’s committed to delivering a high quality, reliable supply to customers and patients on time, every time.
Who we are …
Merck & Co., Inc., Kenilworth, New Jersey, USA is known as “Merck” in the United States, Canada & Puerto Rico. We are known as “MSD” in Europe, Middle East, Africa, Latin America & Asia Pacific. We are a global biopharmaceutical leader with a diverse portfolio of prescription medicines, oncology, vaccines and animal health products.
We are driven by our purpose to develop and deliver innovative products that save and improve lives. With 69,000 employees operating in more than 140 countries, we offer state of the art laboratories, plants and offices that are designed to Inspire our employees as we learn, develop and grow in our careers. We are proud of our 125 years of service to humanity and continue to be one of the world’s biggest investors in Research & Development.
What we look for …
In a world of rapid innovation, we seek brave Inventors who want to make an Impact in all aspects of our business, enabling breakthroughs that will affect generations to come. We encourage you to bring your disruptive thinking, collaborative spirit and diverse perspective to our organization. Together we will continue Inventing For Life, Impacting Lives while Inspiring Your Career Growth.
We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively for the common good. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Kenilworth, NJ, USA, also known as Merck Sharp & Dohme Corp., Kenilworth, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
No relocation
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Valid Driving License:
Hazardous Material(s):
Number of Openings:

Requisition ID:R52464

Exhibition Imagineer, Exhibitions & Projects
Confidential   via Indeed

Position Overview

Science Centre Singapore is dedicated to the promotion of interest, learning and creativity in science & technology through imaginative and enjoyable experiences, and to contribute to the nation's development of its human resource.

We are looking for a dynamic candidate to join the Exhibitions department as Exhibition Imagineer. You will be responsible for the content development of Permanent and Temporary Exhibitions to deliver meaningful, interactive and engaging exhibition    Read more

experiences for Science Centre’s visitors. By blending creativity and innovative technological advancements, the Imagineer produces distinctive experiential storytelling of science through our exhibition galleries.

Essential Job Functions

As an Exhibition Imagineer, you will conduct research and development in Science and social science content for an Exhibition. You are responsible for scoping the content and developing the story and experience design for an exhibition. You are responsible for following through with project management, development of scripts and education programmes accompanying the exhibition in collaboration with our Education Programmes Division.


The ideal candidate should have a good knowledge in Science. Knowledge in Exhibition curation for Museums / Science Centres or knowledge in Design, Educational Technology or equivalent practical experience in a related field is also advantageous. He/She should have experience in collaborating with multidisciplinary teams of Designers, Researchers, Engineers and Content Strategists throughout the design process. Having worked in designing experiences across multiple platforms is an added advantage. Knowledge in science communication, creative storytelling, experience design and project management are advantageous.

The candidate should be passionate about science, has the ability to translate concepts into experiences and to lead and ideate products from scratch. Candidate should be self-driven and creative with good organizational and communications skill, and processing a good aesthetic and/or design sense.

He/She should possess excellent people and negotiation skills as well as problem-solving skills.

Sport Singapore
Sport Physiologist #SGUnitedTraineeships #PublicService
Sport Singapore   via Indeed

Roles & Responsibilities
At Sport Singapore, we aspire to transform the nation through an active lifestyle designed around innovative, fun and meaningful sporting experiences.

Sport has the unique ability to bring people together through play, regardless of age, gender, race, ability or social status. It imparts life values, nurtures character and builds resilience. It inspires and evokes the Singapore spirit through shared experiences and strengthens our national identity. We help    Read more

Singaporeans Live Better Through Sport.

Sport Singapore is constantly on the lookout for individuals who are passionate about what they do.

Anchored in our values of Passion for Sport, Strength through Teamwork and Care for People, we believe in working and playing, not just as a team, but as a family.


You will be part of the team to;

Conduct needs assessments for development of support proposals to sport programmes
Individualised laboratory- and field-based testing
Report and interpret testing results to coaches and athletes for practical applications
Develop new testing protocols where appropriate, to enhance the process of monitoring athletes’ physiological adaptations and sport performance.
Advice on optimal training protocols to enhance athletes’ physiological adaptations and sport performance
Build R&D work into ongoing support and service delivery to sport programmes
Conduct applied research to answer targeted questions by sport programmes
Conduct exercise and health related R&D work that will impact the larger Singapore community (i.e. general public)
Educate coaches, athletes and students.
Identify knowledge gaps and resources to bridge these gaps
Implement a career pathway based on best practices and international standards
Engage the pool of expertise in Singapore


We are looking for self-motivated individuals who value integrity, teamwork and take pride in going the extra mile to provide excellent service to stakeholders and the community. This individual should be a sport advocate through living an active lifestyle and staying active.

In addition, you should possess

Background in Sport Science/Physiology or its equivalent
Good background knowledge and understanding of other exercise/sport science disciplines such as nutrition, psychology, strength & conditioning, and biomechanics.

Only shortlisted applicants will be notified

Food Technologist #SGUnitedTraineeship
Confidential   via Indeed

Roles & Responsibilities
Main Duties and Responsibilities

Support research and development of new products and/or processes, including:

New product development.
Sourcing and evaluating new / alternate raw materials.
Participation in trial runs, commercial runs and troubleshooting.
Conducting sensory evaluation.
Maintenance of laboratory, equipment and pilot plant.


Bachelor degree in Science, Food Science and Technology or related disciplines.
Trained in food technology and science, including chemistry knowledge / calculations and product development.
Possess laboratory skills and a keen interest    Read more

in research.
Self-driven, proactive and able to multitask.
Team player with strong interpersonal and collaborative skills.

Note: Traineeship will be for a period of 12 months.