Essential Duties and Responsibilities:

• Demonstrates and promotes the company vision
• Regular attendance and punctuality
• Applies GMP/GLP in all areas of responsibility, as appropriate
• Learns to conduct routine analyses in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines
• Learns how to document work and maintain study documentation and laboratory records
• Learns how to use laboratory equipment and software appropriate for assigned tasks
• Attends and participates in project meetings
• Learns to perform peer review of data
• Learns to plan assigned workload on a daily basis and effectively schedule multiple assignments
• Contributes to a cohesive team environment
• Plans individual workload in coordination with team members
• Maintains a clean and safe laboratory work environment
• Conducts all activities in a safe and efficient manner
• Performs other duties as assigned

Job Requirement:

• Candidate must possess at least Diploma in Food Science, Chemistry, Science or equivalent
• Interacts with operational personnel, scientific personnel, and department management
• May work with potentially hazardous materials
• Overtime and weekend work as required
• Work requires some standing and sitting for long periods of time, including working within a laboratory hood and standing at a bench top
• Work requires use of PPE (personal protective equipment)
• Will be exposed to potential food allergens
• Entry level are welcome

Responsibilities:

• Responsible for conducting Gas Chromatography (GC) using GC techniques and instruments.
• Perform calibration, troubleshooting and maintenance of GC instruments.
• Develop and validate analytical methods using GC.
• Analyze samples to determine the composition of various substances.
• Interpret chromatograms to identify peaks and quantify compounds.
• Interpret and report results accurately and timely, maintain detailed records of all analysis performed including raw data.
• Complete all laboratory reports as applicable.
• Provide training to laboratory analysts following the standard of ASTM, IP, ISO methods.
• Ensure compliance with safety protocols, quality control procedures, and regulatory guidelines.
• Understand and keep updated with all laboratory safety, reporting techniques and analysis methods.
• Perform all other duties and responsibilities as assigned.

Requirements:

• Diploma / Degree in Science / Chemistry or related field.
• Equivalent work experience in OGC industry.
• Understand ASTM standards and procedures.
• Protocol, procedure, and safety oriented.
• Ability to perform analytical tasks.
• Must be able to differentiate colors accurately by sight.
• Ability to work effectively under pressure, while directing numerous projects concurrently with different deadlines.
• High tolerance for job pressure.
• Ability to verify and check results during and after office hours.eekend, and holidays, based on customers’ requirements.
• Ability to verify and check results during and after office hours.
• Position requires a dependable and reliable individual whose daily presence adds to the success of the department.
• Able to work independently and a good team player.
• Ability to work and communicate with people of diverse personalities and backgrounds.

Additional Information

• Qualified or interested candidates, please submit your updated resume in MS Word / PDF format to [email protected]

We regret to inform you that only shortlisted candidates will be notified.

Please include the following in your resume (if any): -

• Last drawn / current and expected salary.
• Reason(s) for leaving previous / current company.
• Education background.
• Work experience in point forms.

Essential Duties and Responsibilities:

• Demonstrates and promotes the company vision
• Regular attendance and punctuality
• Applies GMP/GLP in all areas of responsibility, as appropriate
• Learns to conduct routine analyses in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines
• Learns how to document work and maintain study documentation and laboratory records
• Learns how to use laboratory equipment and software appropriate for assigned tasks
• Attends and participates in project meetings
• Learns to perform peer review of data
• Learns to plan assigned workload on a daily basis and effectively schedule multiple assignments
• Contributes to a cohesive team environment
• Plans individual workload in coordination with team members
• Maintains a clean and safe laboratory work environment
• Conducts all activities in a safe and efficient manner
• Performs other duties as assigned

Job Requirement:

• Candidate must possess at least Diploma in Food Science, Chemistry, Science or equivalent
• Interacts with operational personnel, scientific personnel, and department management
• May work with potentially hazardous materials
• Overtime and weekend work as required
• Work requires some standing and sitting for long periods of time, including working within a laboratory hood and standing at a bench top
• Work requires use of PPE (personal protective equipment)
• Will be exposed to potential food allergens
• Entry level are welcome

a) Assist supervisor with formulations.

b) Develop and formulate products according to project briefs.

c) Optimize existing formulations for improved performance, stability, or compliance with regulatory changes.

d) Source and evaluate new or alternative raw materials when required.

e) Perform necessary tests, including but not limited to stability testing, packaging compatibility testing, and performance evaluations.

f) Support and troubleshoot product quality issues.

g) Provide technical support during scale-up, pilot batches, and production.

h) Ensure that formulations comply with regulatory standards.

i) Work closely with other departments such as product development, regulatory, sales, QA/QC and production.

j) Maintain a good document control system for formulation and other technical information.

k) Ensure GMP and regulatory requirement.

l) Any other adhoc work assigned by the supervisor.

Requirement:

· Diploma / Bachelor’s degree in Chemistry, Cosmetic Science, or a related field.

· Minimum 1 to 2 years of experience in personal care formulation or related field. Fresh graduates are welcome to apply.

· Strong understanding of raw materials, and formulation techniques.

· Familiarity with GMP and regulatory guidelines.

· Good team player, passionate and patient.

· Meticulous and organized.

• Daily calibration of Equipment’s
• Daily Monitoring of cleaning and recoding the same.
• Water sampling and analysis as per the schedule.
• Environment monitoring of listed areas in lab and plant as per SOP.
• MLT of finished product as and when received for analysis.
• Update documents in raw data sheet for all analysis.
• Release of test reports to the concerned at the end of analysis.
• Zone of Inhibition testing for antibacterial projects at R&D (KRC &KBC).
• Antibacterial Efficacy studies of in-house /market formulation.
• Biochemical assay for irritation evaluation of formulated samples.
• Culture Maintenance and Sub culturing of Bacteriological and fungal cultures (Inoculated cultures using spreading, streaking and pour plate techniques)
• Growth Promotion Test for Culture Media, Environmental Monitoring, Sampling of Products- FG, RM, Testing of Disinfectant by Efficacy Test.
• Responsible for EMS and QMS activity.
• Preparation of QA SOPs and review of other department SOPs as and when required.
• Responsible for verification of packing records, labels, COAs, containers etc. for dispatch activity and maintaining the dispatch related documents.
• Ensuring the marketing samples are packed properly, labeled, COAs, container and it is delivered correctly to the marketing requirement based on the sample advice not/sample request and approval of COA.
• Responsible for Issuance/distribution of controlled documents of BPCRs/formats/log books/SOPs/protocols etc.
• Responsible for Filling customer questionnaires as and when required.
• Supporting regulatory/marketing/sales department as and when required.
• Reviewingand approval of analytical documents before batch release.
• Reviewing and approval of product dossiers.
• Coordinating with HR department for making annual training planner and conducting training programms as per schedule.
• Responsible for preparation of self-inspection schedule and coordinating with team for execution as per the schedule.
• Responsible for review and approval of Equipment/Instrument qualification.
• Responsible for all external audits (Customer, regulatory and ISO audits) as and when required.
• Handling of change control, deviation, market complaints, returned goods, product recall, self inspection and corrective and preventive actions.
• Responsible for daily monitoring of all department functions and record the observations and issuing of non confirmity to department.
• Responsible for review and approval of stability protocols and summary reports.
• Responsible and assure for follow up of individual department for calibration & preventive maintenance of laboratory equipment and laboratory instruments are conducted as per schedule.
• Responsible for applying drug licencees and supporting to maintains the legal documents properly.
• Approving all specifications and master production instructions, Test methods, Qualifications.
• Responsible for review and approval of executed BPCRs and equipment cleaning records.

• Safely and effectively carry out routine synthetic organic chemistry techniques (Reactions, recrystallizations, chromatography) /Biochemistry/ Fermentation technogies/ natural extracts etc..
• Be able to conduct routine chemistry reactions / formulations with procedures supplied and discussed by supervisor.
• Sound chemistry knowledge and good process development skills at Small & Large Scale.
• Have basic understanding of the reactivity and functional group compatibility of the chemical target, intermediates, and reagents employed.
• Will follow all safety requirements strictly inside the lab.
• Should have good communication skills
• Hands on experience with common laboratory instruments like GC
• Will maintain the lab record books on day-to-day basis.
• Will report / note down all the observations made while doing the experiments.
• Will send samples to analytical department with the consent of the group leader.
• Hands on experience in handling mg scale to kg level reactions
• Will maintain all reports in order.
• Will maintain the chemicals used with proper labeling and in the right way.
• The chemists should be aware of environmental impacts of the chemicals used / discarded (should have the MSDS of chemicals that he / she is using)
• Will submit the signed lab record copies on regular basis.
• Will carry out other works that is being allotted by the higher authorities.
• Qualification: M. Sc chemistry with 1-10 years’Experience in a chemical laboratory.

Job Description

• Demonstrates and promotes the company vision
• Regular attendance and punctuality
• Applies GMP/GLP in all areas of responsibility, as appropriate
• Organizes and conducts routine analyses independently and in compliance with applicable methods, protocols, SOPs and regulatory agency guidelines
• Documents work and maintains study documentation and laboratory records
• Independently able to use and perform basic troubleshooting of laboratory equipment and software appropriate for assigned tasks, while learning to perform routine and non-routine maintenance
• Provides input and participates in project meetings
• Performs peer review and QC review of data
• Performs assigned workload on a daily basis and effectively completes multiple assignments.
• Contributes to a cohesive team environment and maintains a positive attitude. Plans individual workload in coordination with team members.
• Maintains a clean and safe laboratory work environment
• Understands data generated, and history of methods.
• Recognizes deviations from normal results and inform Study Director, Principal Investigator, and/or management of any problems and/or deviations that may affect the integrity of the data and participates in corrective action of problems.
• Identifies problems, determines appropriate actions, and implements solutions with support or independently as appropriate.
• Able to adapt to new procedures or particular needs as directed.
• Able to identify critical steps in an assay.
• Leads process improvement initiatives.
• Completes all required training courses.
• Trains and assists less experienced staff
• May assist in optimizing and validating methods for a variety of matrices
• Participates in client visits or calls as needed
• Learns to write text for reports, methods and, or protocols
• Knowledge of departmental procedures and policies
• Viewed as a resource within their team
• Conducts all activities in a safe and efficient manner
• Performs other duties as assigned

Job Requirements

• Bachelor’s Degree in relevant field (Laboratory experience may be substituted for degree)
• May work with potentially hazardous substances and/or radio labeled
  materials
• Mandatory immunizations and screening as required
• Expected to understand the process for handling hazardous wastes and receive on-the-job training for handling specific waste types in their job
  area
• Will be exposed to food allergens (ex. Milk, tree nuts, peanuts, fish,
  shellfish, etc.)
• Work requires some standing and sitting for long periods of time, including working within a laboratory hood and standing at a bench top.
• Work requires use of PPE (personal protective equipment).
• Overtime and weekend work as required.
• Will be exposed to potential food allergens.

Role Summary

• Analytical Chemist in a team with a broad technical portfolio of technics such as chromatography (i.e. GC, LC0, and mass spectrometry (i.e. LC-MS/MS, GC-MS/MS). The role will aim at building functional capability and capacity for efficient execution of in vivo toxicology and studies at the facility. In addition, this role will ensure scientific and technical rigor in the responsible areas to support Company's science and innovation pipelines
• This role will be part of a team where he/she will have to work jointly with operators having different levels of expertise. Communication, proactiveness, and self-management will be essential in order to deliver functional execution of in vivo studies on time and on budget whilst ensuring compliance with pertinent guidelines and scientific standards (i.e. OECD GLP, ISO, AVA, AAALAC, OECD TGs and USFDA)
• This role will also have to (1) plan resources and timelines; (2) update and maintain equipments, workflows, and laboratory information systems; and (3) develop and implement new assays, test methods, equipment workflows and systems

Responsibilities

• Lead the organization's effort on test method development / optimization and validation focusing on chromatographic systems (i.e GC, LC) and mass spectrum (i.e LC-MS/MS, GC-MS/MS) for the identification and quantification of chemical constituents and metabolic biomarkers in complex matters
• Provide technical leadership to the Bioanalytics department in the relevant technical domain; conduct training to the junior analysts and new hires; provide first-line technical support to day-to-day smooth quality testing. Act as a study director for GLP studies in the Bioanalytics department. Ensure the methods, equipment, systems and workflows are fit for purpose, up-to-date and efficient
• Keep track with the technological advancement in the field, assess, adopt and provide expertise for developing and implementing new / innovative techniques, assays, methods, capabilities that will enable / accelerate Company's scientific project portfolio execution in particular for scientific substantiation of RRP products and exploration of adjacent therapeutic areas
• Represent the functions to coordinate and liaise with cross-functional units and stakeholders (HODs, SDs, Sponsors, global counterparts) on the planning, resourcing, execution, data analysis and reporting of in vivo (and ex vivo, in vitro) pre-clinical studies within R&D. Foster a culture of collaboration and enable frequent technical exchange across the network.
• Ensure the day-to-day laboratory operation is smooth and efficient, devise and implement continuous improvement projects to keep up the laboratory operation and systems to the best practices
• Participate in establishing and maintaining an adequate, current and effective QMS system and assume ownership roles for the business area, systems, equipment and SOPs when applicable. Support quality / compliance inspections and audits conducted by both internal and external parties
• Back-up to the department manager to review and approve test results, and assist on study planning for the Bioanalytics department in work flow optimization, resourcing, procurement etc

Requirements

• Bachelor's degree in scientific discipline
• PhD in Chemistry, Life Sciences or related technical/scientific discipline is preferred
• Minimal 5 years' relevant experience with technical and scientific knowledge with focus on analytica and bioanalytical method development, validation and laboratory operations, with a CRO, R&D unit within pharmaceutical or healthcare industries, or translational academic research organizations
• In-depth knowledge preferably with hands-on experience on broad range of analytical and bioanlytical platforms and work flows in toxicology studies and life science research, i.e. LC/GC, LC-MS/MS, and other characterization tools for chemical entities
• Good understanding of regulatory guidelines such as FDA, ICH, OECD GLP and TGs related to in vivo toxicology study and method validation is preferred
• Excellent communication and influencing skills

Job Responsibilities:

• Perform various analytical tests and ensure all samples are tested and completed on time using the appropriate test methods.
• Conduct methodological research by evaluating procedures, techniques, and instrumentation. Stay up-to-date on food and pharmaceutical testing, analytical instrumentation and method development.
• Verify, validate, and/or perform the transfer of analytical methods.
• Identify and resolve issues with test method performance.
• Investigate problematic laboratory samples.
• To support maintaining the standard of testing activities and assist in any improvement plans and executions.

Job Requirements:

• Degree in Food Science/ Chemistry.
• Minimum 5 years of laboratory experience in chemical analysis of food.
• Experience in operating HPLC, GC, LC-MS/MS and UV-Vis spectrophotometers preferred.
• Familiarity with ISO/IEC 17025 and quality management system.

One of our European based MNC client is looking for an Application Chemist.

Key Responsibilities:

• Provide application formulation and field support to the Performance Coatings industry in the East Asia Pacific Region for different segments i.e. Automotive, Synthetic, Industrial and Fabric Coatings
• Perform day-to-day lab duties and conduct related applications testing in laboratory
• Assist R&D with new products development
• Maintain a well-organized lab and cleanliness of equipment, operate safely in laboratory environment by maintaining high level of SHE standard.
• Create good internal communications within Singapore team and global experts.

Requirements:

• Degree in Chemistry, Material Science or Chemical Engineering.
• Several years of working experience in coatings industry including coating formulation, properties testing and coating application process.
• Experience in soft substrates coating is an added advantage.
• Knowledge in polymer is an added advantage.
• After internal training finished able to work on multi projects independently (from start to technical approval by customer)
• Strong willingness to learn, proactive attitude, good interpersonal skills, creative thinking, analytical mindset, diligent and with a high level of tenacity.

Assistant Laboratory Chemist

Purpose & Scope:

Work closely with R&D Manager in a laboratory setting to conduct research on new or existing paint formulas with minimal supervision. Typical projects the Chemist may work on are new product development or modification of existing products, raw material evaluations, benchmarking studies, sample preparations, color matching, batch process review and specification testing. The Laboratory Chemist is expected to design and document all projects be familiar with all QC test procedures and factory processes. He may be required to scale-up batches and work in QC as needed.

Reports To: Research & Development Manager

Duties:

• Work in the R&D laboratory.
• Interact with the R&D Manager, Technical Director, sales, marketing, and vendors to develop new products or modify existing products.
• Design benchmarking studies of products and interprets the results to clearly communicate advantages and disadvantages.
• Evaluate raw materials to make recommendations on their potential use.
• Interact with production to solve manufacturing/scale-up issues.
• Conduct investigations of product complaints.
• Perform testing from standard procedures.
• Develop and writes test methods as needed.
• Record and organize projects in an electronic format.
• Enter or modify formulas into the formula database as needed for production.
• Work in QC as needed.
• Maintain a clean and safe work environment.
• Complete any additional assignments as directed.
• Report to R&D Manager.

Requirements:

• A four-year degree in Organic Chemistry / Polymer Chemistry / Industrial Chemistry
• 2 to 4 years formulating / testing experience in Paint / Coating Field
• Knowledge of paint / coating testing, including the methods used, equipment and systems.
• Ability to work in an industrial laboratory setting
• If necessary need to go out to the field for application support or trouble shooting.
• Possess ability to follow standard operating procedure.

· Good level of IT literacy with the ability to use MS office including Outlook, Word & Excel.

• Possess safety habits & awareness required as a condition of employment.
• Possess skills to accurately record and communicate research results to others both orally and in writing.
• Follow prescribed policies & procedures.

Interested applicants are invited to apply directly at the NUS Career Portal.

Your application will be processed only if you apply via NUS Career Portal.

We regret that only shortlisted candidates will be notified.

Job Description

The National University of Singapore invites applications for Research Assistant/ Research Associate (QC Analytical Chemist) in the Department of Clinical Imaging Research Centre (CIRC) Yong Loo Lin School of Medicine. CIRC is a dedicated molecular imaging research centre. It is equipped with on-site capability for the preparation of PET radiopharmaceuticals in a state-of-the-art GMP-certified facility. CIRC is positioned to support both academic and commercially led clinical research programs, with dedicated clinical imaging facilities area advanced modalities of PET-CT and PET-MRI. For more details on what we do, do visit https://medicine.nus.edu.sg/circ/. Appointments will be made on a two-years contract basis with the possibility of extension.

Purpose of the post

The QC Analytical Chemist will be responsible to, and work closely with Head of QC, to ensure the successful and safe release of radiopharmaceuticals manufactured at CIRC. The QC Analytical Chemist’s principal role will be to perform all quality control tests required by pharmacopeia. Alongside with maintaining the inventory of raw materials, maintenance of equipment and all the necessary documentation required for the QC laboratory in compliance to PIC/S GMP.

Main Duties and Responsibilities

The QC Analytical Chemist will be able to:

• Perform analytical chemistry methods (HPLC, GC, radioTLC etc) for ensuring that the radiopharmaceutical is safe for clinical use.
• Perform environmental monitoring as required by PIC/S GMP in the cleanrooms (environmental monitoring, airborne particle monitoring)
• Manage routine microbial tests such as microbial plate incubation, sterility testing, bioburden testing, etc and liaising with third party contractors if required.
• Handle raw materials management, including maintaining inventory status, purchase and receiving of raw materials.
• Establish, develop and validate QC Test Methods for the radiopharmaceutical QC release testing.
• Assist in writing Standard Operating Procedures (SOPs), Work Instructions (WIN), Recordsheets (REC), etc and fill in Batch Manufacturing Records (BMR).
• Ensure that the appropriate documentation is in place.
• Support in managing of QC equipment and metabolite laboratory equipment, including qualifications, operations maintenance, cleaning, calibration and re-qualification.
• Maintain cleanliness in the QC laboratory and the cyclotron facility.
• Handle chemical and biohazard waste disposal.

Main Duties and Responsibilities

• Adhere to good safety and health practices from the university guidelines.
• Cross training to Production routine manufacturing of radiopharmaceuticals
• Any adhoc duties as required for this role

Physical Demands and Work Environment

Personnel should be comfortable with:

• exposure to radiation when handling radioactive samples.

• handling of chemicals for QC testing (flammables, acids, and bases).

• Handling chemical and biohazard wastes

• Occasion lifting of heavy objects such as lead shield containment (lead pots)

• Flexible working hours with occasionally over time

Qualifications

The applicant should:

1. Have a minimum of BSc degree in Chemistry, Biochemistry, pharmacy or a related field;
2. Good knowledge and experience on GMP (Good Manufacturing Practice) or GLP (Good Laboratory Practice);
3. Preferably hands-on experience with operating and maintaining analytical instruments such as HPLC, GC, TLC and also aseptic isolator for sterility testing.
4. Have good analytical processing skills, as well as,
5. Have good critical thinking and proactiveness at work.

Remuneration will be commensurate with the candidate’s qualifications and experience.

Formal application: Please submit your application, indicating current/expected salary, supported by a detailed CV (including personal particulars, academic and employment history, complete list of publications/oral presentations and full contacts of two (2) referees to this job portal.

Scope and Responsibilities

• Prepare quality audit plan for ISO 17025 SAC Singlas and client’s audit
• Calibrate and maintain Gas Chromatography instruments, test methods in accordance with standard methods such as ASTM, IP, UOP, etc
• Prepare chemical stock solutions and reagents
• Standardize reagent/equipment
• Conduct Test Method Assessment
• Initiate, investigate and review quality improvement/corrective and preventive action
• Maintain SQC program
• Should have indepth knowledge in GC , GC-MS - able to maintain the instruments independently
• Setup new methods in accordance with standard methods
• Training new analyst on the new methods/instruments
• Upkeep the cleanliness of work areas, apparatus and equipment
• Perform any tasks as assigned by Laboratory Management

Requirements

• Candidate must possess at least Diploma/Advanced/Higher/Graduate Diploma in Chemistry or equivalent
• At least 3 years experience operating and maintaining GC and GC-MS
• Good spoken English and communication skills
• Computer Literate