Total 86 Quality Assurance / Control job vacancies in D22 Jurong, Jurong Island, Tuas

Job Description & Requirements

Key Goal:

Responsible for performing quality inspections, documenting results, assist in corrective actions, prepare for audits, and aid in the training of new technicians.

Duties and Responsibilities

Customer Relationship Management

• Interacting with customers and dealing with their queries and complaints appropriately
• Provide excellent customer satisfaction experience to client
• Attend monthly clients meeting where required

Day to Day Operations Management

• Conduct QC inspection at clients’ properties.
• Conduct Survey request from Sales Department.
• Monthly report submission to client
• Manage Technician’s performance via Scorecard
• Assist with identification of pest specimens
• Assist Operations Department on repetitive pest issues at client property

Mentoring & Department Management

• Mentor and develop Workers/Technicians/Supervisors and nurture an environment where they can excel through encouragement, empowerment and knowledge
• Advise Operations team on issues that require their immediate attention

Reporting & Analytics

• Provide QC Audit reports to client on a timely manner (pictorial reports)
• Prepare weekly and monthly reports and surveys to Clients and or Sales Department.
• Prepare Monthly Analytics reports

Ad-Hoc / Project Work

• Assist with ad hoc tasks assigned by superior.
• Assist with ensuring international best practices are implemented.
• Champion new processes, software and other infrastructure changes to improve internal practices and the customer experience

Academic Education & Knowledge Requirements

• Tertiary education or equivalent
• ITE-NEA Pest Management Course
• Work-at-Height, Building Construction Safety Supervisor (BCSS) (advantageous)
• Mirkan Application, IPM Square / Other Technology (advantageous)
• Advanced knowledge in pest control practices, chemicals, equipment and pest biology (advantageous)
• Working knowledge of regulatory and quality system requirements (including Risk Assessments, ISO9001, ISO14001 and ISO45000)

Work Experience Requirements

• Minimum of 3 years of relevant work experience in pest control industry.
• Minimum 2 year of driving experience/ driver’s license

Skills Requirements

• Well verse in pest management process and procedures.
• Proficient in MS Office (Word, Excel, Power point), Microsoft SharePoint, ClickUp, Jira, etc
• Report writing skills in English and required speaking skills in English.
• Problem solving and people management skills
• Proactive and high attention to detail

Be part of something altogether life-changing!

Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.

Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.

The Quality Control Analyst for Cytiva is responsible for sampling and inspection on raw materials, in-process materials, and finished products to ensure that product specifications and company and regulatory requirements are met, and release on a timely basis to meet on time delivery to our customers.

This position is part of the Quality Control team located in Global Life Sciences Solutions Singapore Pte Ltd, 25 Tuas South Street 1, Singapore 638034 and will be working on-site. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.

In this role, you will have the opportunity to:

• Upkeeping and maintaining 5S and housekeeping in QC laboratory
• Performing raw materials inspection and sampling
• Inspecting or performing testing on raw materials, finished products conforming to production specifications in compliance with documented procedures and in accordance to stipulated deadlines
• Discarding or rejecting finished products and raw materials that do not meet approved specifications
• Performing environmental monitoring in the manufacturing facility
• Reporting inspection and testing results with those responsible for products, materials and/or facilities, and recommend necessary corrective actions where necessary
• Maintaining accurate paper and electronic records
• Updating or creating of laboratory procedures if required
• Assisting in non-routine analysis, laboratory investigation, change control, deviation report writing, as well as non-conformance management
• Assisting the development and validation of new lab equipment or test methods
• Developing and maintaining specialized technical expertise in order to provide support for existing products and ongoing GxP operations as required
• Driving continuous improvement projects as required
• Participating in EHS program (e.g. safety inspection) and complying with EHS regulations & policies

The essential requirements of the job include:

• Diploma with reasonable work experience OR equivalent relevant laboratory work experience. Fresh graduates with a degree in Science are welcome to apply
• Extremely detail and accuracy-oriented with good written and verbal communication skills
• Computer literate (Word, Excel, Oracle database, Electronic Documentation System) to create spreadsheets, e-mail, memos, graphic, and technical writing skills (create and edit procedures)

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

• Knowledge and experience of a GxP environment or other regulated industry
• Ability to write clear technical documentation

JOB DESCRIPTION

• Conduct inspection of incoming, in-process and final inspection on machined parts, weldments and assemblies as per technical drawings, customer’s specifications and requirements through the use of various types of inspection equipment set up
• Perform dimension check on parts, components and tools using micrometers, calipers, comparators, indicator, CMM & CREAFOAM
• Perform visual, mechanical and functional check on components.
• Report non-compliance parts to QA Engineer
• Performs visual and dimensional inspection of incoming and outgoing components/parts
• Understand current specifications involving inspection tolerances, limitations, and procedures.
• Responsible for conducting inspection in accordance with approved technical data.

REQUIREMENT

• GCE ‘O’ / ‘A’ Level with minimum 2 year working experience or
• Diploma in Mechanical / Manufacturing / Quality Management with minimum 1 year working experience.
• Good interpersonal skill and ability to communicate with all levels.
• Good understanding of technical drawing
• Familiar with all inspection methods and techniques
• Basic understanding of General Dimension & Tolerance control
• Proficient in the use of various types of inspection equipment and visual inspection aids

• NIGHT SHIFT
• 1 WEEK OFF 1 DAY SUNDAY NIGHT
• CAN ACCEPT WET MARKET ENVIRONMENT
• AREA : JURONG FISHERY PORT
• SELLING SEAFOOD
• PURCHASE SEAFOOD
• ARRANGE JOB TO STAFF
• CHECKING STAFF'S JOB
• RESPOND CUSTOMER
• NEED A LORRY LICENSE - SOMETIME NEED DELIVERY
• PACKING ITEM
• TEACHING STAFF
• EVERY DAY DO A REPORT TO BOSS
• SOMETIME NEED GO CUSTOMER'S WET MARKET SURRVEY

We are looking for a QA Engineer (Manual Testing) to join a software company working on latest Web3.0 technologies.

• International software company in the FinTech/ gaming industry using web-based application
• Salary package up to $4,000 + AWS + VB (approx. 2-3 months bonus)
• Dynamic working environment

Responsibilities

• Review requirements, specifications and technical design documents to provide timely and meaningful feedback.
• Create detailed, comprehensive and well-structured test plans and test cases.
• Perform thorough regression testing when bugs are resolved.
• Stay up-to-date with new testing tools and test strategies.
• Coordinate with development team/project management team for smooth SIT/UAT.

Requirements

• Tertiary education in IT related field.
• Min. 2 years of working experience in Software Testing (Web Application/Mobile Application).
• Strong knowledge of software quality assurance methodologies, tools and processes.
• Candidates without prior experience in software testing are welcomed to apply.

Interested candidates may apply via email to spml@scientecpersonnel.com (indicating Job ID J44549 for faster processing). All job applications will be processed with strict confidence and only shortlisted candidates will be contacted.

Lee Wen Ying (Mattias) - R23112909

ScienTec Consulting Pte Ltd - 11C5781

Summary of Job Scope:

Responsible for technical enhancement of quality control and analytical development in QC Laboratory functions.

• Work allocation and arrangement for daily QC routine work
• Finish Product Quality Control
• Checking Report of "In-Process control of Tablet"
• In process quality control of intermediates (IPQC)
• Review and evaluation of Analyst test report and data to ensure test result is up-to date and accurate.
• Review and ensure QC Records and BMR are up-to-date, complete and accurate.
• Supervision of quality control check on raw material dispensing
• Management, Monitering and testing on sample.
• Monitor retained samples and waste of tested sample of intermediates and finished products.
• Environment monitoring and recording for retention sample room.
• Supervision and training of laboratory technicians and laboratory assistant and chemist in carrying out their duties.
• Responsibe to revise of SOP for IPQC and FPQC and relevant section.
• Verify and approve test result in absence of QC Manager.
• Calibration of laboratory equipment and apparatus.
• Ensure Good Laboratory Practice (GLP) & Lab Safety.
• Optimization of usage of laboratory equipment.
• Support in the investigation and management of product complaints.
• Participate in process and cleaning validation.

Job Description

• To ensure ongoing compliance with the PIC/S Guideline for GMP.
• To achieve quality assurance operational objectives by contributing information and analysis to strategic plans and reviews; preparing and completing action plans; implementing production, productivity, quality, and customer-service standards; identifying and resolving problems; completing audits; determining system improvement; implementing change.
• Develops and implements a practical system for Quality Management System activities to facilitate smooth, timely workflows in the performance of job function.
• To provide guidance, interpretation, information on regulations, laws and industry guidance that affect pharmaceutical industry.
• Serve as a SME in matters relating to quality assurance and cGMP.
• Ensure facility follows applicable quality management directives such as SOPs, manuals, policies, procedures, work instruction, etc.
• Responsible for reviewing, trending and investigating excursions of environmental monitoring and supportive utilities data.
• The inspection and investigation of product recalls and product complaints to look into factors which has affect product quality.
• Acts as the Authorized Person to perform batch release and ensure each batch of medicinal products are manufactured and checked in compliance with the laws in force in the country and in accordance with the requirements of the Marketing Authorization.
• Reviews, approves or authorizes written procedures and other documents, including amendments.
• Oversees various quality management systems and analyze trending.
• Reviews and approves deviations and CAPA.
• Review, approves and implement changes according to established Change Control procedure.
• Coordinates and participates in quality risk management activities.
• Initiates investigation for product complaints, reviews and approves corrective/preventive actions associated.
• Coordinates product recalls, associated reconciliation, documentation and investigations.
• Reviews, approves and monitors suppliers of materials.
• Reviews, approves and monitors contract manufacturers and providers of other GMP related outsourced activities.
• Ensures validation and qualification are carried out according to schedule.
• Provides training or ensures appropriate training is provided to QA staffs.
• Monitors compliance of the organization with the requirements of Good Manufacturing Practice via Internal Audit.
• Coordinates management reviews of process performance, product quality and Pharmaceutical Quality
• System and advocates continual improvement
• Ensures timely and effective communication and escalation process exists to raise quality issues to appropriate levels of management.

Requirements

• ISO/GMP in Pharmaceutical Experience will be prioritize
• At least bachelor degree, post graduate diploma in any science, or others filed related to pharmaceutical
• Minimum 7-8 years experience
• Well versed in computer skill especially in excel and other Microsoft office skills and knowledge in Navision is preferred.
• Close attention to details is essential
• Must be able to perform each essential duty satisfactory and in timely manner
• Independent & communication skills

Job Summary:

Support in the daily business operations for drop shipment activities, including packing, quality check and preparation of delivery of pharmaceutical and nonpharmaceutical products for orders. Assist in drug stock management activities.

Core Responsibilities:

• Assist in the implementation of quality assurance and quality improvement projects and activities to meet the Good Distribution Practice and Good Distribution Practice Medical Device Singapore (GDP & GDPMDS) standard
• Assist in internal audits, record checking and implementation of post-audit corrective actions
• Support in preparing document, forms, chart and SOPs.
• Assist pharmacists in product recalls
• Assist in inventory management of pharmaceutical and nonpharmaceutical products
• Ensure proper storage and handling of drug stock
• Highlight equipment failures and unusual activities to pharmacists/supervisors
• Maintain the proper functioning of facilities
• Suggest improvements to workflows and procedures
• To carry out any additional job-related duties that may be assigned from time to time

Job Requirements:

• Diploma in Pharmaceutical Science or equivalent
• Experience in the pharmaceutical sector or Quality Management Systems specific to Good Distribution Practices (GDP or GDPMDS) preferred
• Organised, meticulous and pay attention to details.

Job Description

• Perform as the Company nominated QC representative daily quality inspections on the various disciplines for the Company’s sub-contracted site activities: boiler welding, mechanical erection of process equipment, piping, painting, structural steel erection.
• Perform receipt inspections of goods and equipment at delivery to check completeness and to report about eventual transport damages. Monitor the storage and preservation conditions on site.
• Monitor the implementation of the approved site Inspection and Test Plans
• Verify that the quality related site activities are in accordance with the applicable codes and standards.
• Monitor and perform spot-wise inspections on all non-destructive testing on site.
• Monitor subcontractor’s work tools calibration.
• Monitor level of training and qualification of all subcontractor personnel.
• Register, follow-up and monitor handling of non-conformities.
• Monitor and review that all sub-contractor QC documentation is available, compliant and complete according to the specification and ITP and in accordance to the actual progress on site.
• Coordinate exchange of relevant QA/QC documentation to and from site subcontractors and third parties (including Notified Body).
• Ensure that all sub-contractor QC documentation is hand-over as-built and complete at pre-defined inspection milestones.
• Liaise with the Company’s relevant discipline project engineers and vendor QC inspectors about quality related matters.
• Assist to site meetings with customer, sub-contractors or vendors about quality-related matters.
• Organise and chair weekly QC site meetings with main subcontractor QC personnel. Draft meeting reports and distribute to all participants, the QC Manager, the Site Construction Manager and other stakeholders.
• Invite and accompany the customer representative and third parties (including notified body) for witness and hold point activities according ITP.
• Coordinate with and report to the Company’s Site Construction Manager on all quality and safety-related issues.

Job Requirements

• Degree/Diploma in Engineering (Mechanical, Chemical preference) or equivalent.
• A minimum of 5 years experience in QC inspection on welding, NDT and mechanical erection activities.
• A sound working knowledge of EN standards and PED for (boiler) welding, piping, coating, NDT and pressure testing. Demonstrated working experience with steam boiler erection and pressure equipment.
• Good understanding of mechanical erection activities, their possible problems and to act pro-actively to prevent them from happening.
• The ability to work in a team as part of the Company and to communicate with colleagues (on and off-site), enforce resolution by the sub-contractor and to follow-up related communication.
• Any certification related to QC activities (welding, NDT, painting/coating inspection, audit etc) is a plus.
• Willing to work in Tuas, shift and weekend.
• Preferable with local driving license.

PURPOSE AND SCOPE

• Responsible for the scheduled & corrective maintenance of instrumentation & control system and equipment

KEY ROLES AND RESPONSIBILITIES

• Performing scheduled maintenance (Preventive/Predictive Maintenance) programs and corrective maintenance (CM) of all the analyzer and instruments in the plant and prepare reports
• Preparation of MSRA for all maintenance works to be carried out
• Calibrating analyzer, instruments, components, CEMS and systems.
• Installing, configuring, calibrating and maintaining control, measurement and indicating instrumentation (pneumatic, analog & digital).
• Installing and terminating pneumatic and fluid connections.
• Inspecting and testing the operation of instruments and systems to diagnose faults
• Removing, repairing, adjusting and replacing components of control valve & actuators, positioner, transmitters and switches
• Maintaining backup and revision documentation for control systems and instrumentation.
• Coordination with 3rd party vendors for maintenance work and spare parts ordering
• Raising and closing permits in CMMS/ SAP system for maintenance work
• Successful candidate can be appointed as part of the Company Emergency Response Team (CERT) (training will be provided)

QUALIFICATIONS & EXPERIENCE

• Diploma in Instrumentation or equivalent Engineering discipline
• Minimum 3-5 years of experience in controls and instrumentation
• Knowledgeable and experience in PLC and DCS systems
• Experience working in the Incineration plant / process Power plant industry is an advantage

RESPONSIBILITIES:

• Handle daily NDE inspection for LPI, MPI and UT.
• Operation of NDE equipment such as UT, LPI, MPI.
• Prepare reports for NDE inspection.
• Able to interpret BOM and Quality Plan requirements.
• Able to do UT scan plans and review NDE specifications as needed.
• Maintain HSE standards at the work station.

REQUIREMENTS:

• Minimum 3 years experience in Oil & Gas Industry.
• ASNT level 2 certification for LPI, MPI and UT.
• ISO 9712 (Multi-Sector) certification for LPI, MPI and UT will be an advantage.
• Able to work independently.

Responsibilities:-
• Perform non-destructive tests (NDT) and determines product acceptability to the authorized limits of the NDT level obtained in accordance with the prescribed methods and procedures
• Perform NDT Inspection duties in support of customer parts
• Record, organize and evaluate test results and generate NDT reports
• Perform verification of In-coming / In-process dimensional inspection
• Perform Final Dimensional and Visual Inspection
• Maintain all measuring equipment in QA Department
• Ensures compliance to all radiation safety rules and regulations and provides protections to self and others during testing
• Dispose of hazardous waste in accordance with Environmental Regulations
• Maintain all NDT equipment, assure all calibration and maintenance has been performed
• Buy off and maintain NDT consumables and ensure inventory is up to date
• Coordinates NDT Inspection workload according to priorities, efficiency and cost
• Participate and drive any projects assigned
• Take on any task assigned by superior

Requirements:

• Minimum Technical Certificate/NITEC in Engineering (Mechanical/Precision) or equivalent
• At least two years working experience in related field
• Able to perform measurement using micrometer, surface roughness, bore gauge and NDT Level II (At least LPI, MPI & UT)
• Required language(s): English (both spoken and written)
• Must be computer literate
• Positive working attitude & self motivated

Job Description

Responsibilities:

• To carry out daily routine inspections
• Assist in all laboratory work including sampling, analysis and quality control.
• To conduct on-line and goods return inspection.
• To check on the quality for all in-coming raw materials.
• Any other duties as assigned by the superior.
• To implement, monitor, review of QA management system
• To confers with Management Team to solve work-related problems
• To keep all documents in a systematic filing

Requirements:

• Diploma and/or above in the related field
• Preferably relevant working experience in food Industry
• Experience in ISO/halal certification
• Proficient in Microsoft Office (Word, Excel & PowerPoint)
• Bilingual
• Able to work independently with minimum supervision

Responsibilities:

• Responsible for monitoring and ensuring the quality of all the operation aspects of the facility according to the established SOP, GMP, GDP and GLP practices and regulatory requirements
• Responsible to brief the new operators on the GMP and hygiene briefing
• Responsible to brief the relevant maintenance, quality control personnel on the GMP and hygiene briefing that require to entering the dispensing area and production area
• Investigation of Product Complaints
• Review of BMR
• Initiation & follow up of Change Control and Deviations
• Perform qualifications, the process and cleaning validation
• Any ad-hoc duties as assigned by the superior

Requirements:

• Bachelor’s Degree
• 3+ years’ experience
• Demonstrate experience and skills in conduct audit, supplier management and site inspection readiness
• Strong knowledge and understanding of Quality System functions, manufacturing / packaging processes, validation, engineering drawings and basic statistical processes
• Good technical writing skills and communication as well as presentation skills
• Working knowledge of Microsoft Office, Microsoft Project, Statistical Software

We are a logistics courier delivery company based in Toh Guan Road, Jurong, and looking for an experienced Trade Compliance Officer.

Responsibilities:

• Play a critical role in protecting the company from regulatory risks and ensuring its continued success in the global marketplace.
• Develop and implement comprehensive trade compliance programs, including policies, procedures, and training materials.
• Conduct thorough risk assessments and audits to proactively identify and mitigate potential compliance issues.
• Stay current on changes in international trade regulations and laws and provide updates and guidance to relevant stakeholders. Include monitoring regulatory changes related to import/ export and freight forwarding business activities for Asia Pacific Market.
• Monitor the development of trade legislation and regulations and provide analysis and recommendations to sourcing and supply chain management on the potential impact.
• Represent the company in interactions with government agencies to resolve trade compliance issues, such as export license applications and customs audits.
• Provide training and support to employees on trade compliance matters, including import/export controls and customs regulations.
• Work closely with cross-functional teams to integrate trade compliance into all aspects of the company's operations globally.
• Subject matter expert in Trade Compliance matters and managing flags from trade compliance management tool.
• Perform verification and checks on import and export classification codes to ensure proper classification is managed and done.
• Work with the Company Global Trade Services team to execute trade compliance strategies, drive and enforce global import processes, seek automation opportunities, and leverage new technologies such as e-screening platforms.
• Drive scalable business solutions with the business stakeholders to ensure compliance with global trade regulations
• Work with vendors to set up effective import/export and freight forwarding processes that scale to support businesses
• In-depth understanding of import/ product license classification methodology
• Sound decision making skills and proactive problem solving abilities
• Develop and maintain the project plan (using MSProject)
• Identify, analyze and implement robust compliance systems in collaboration with the Company's IT professionals
• Support global sites in internal assessments, desk audits, completing post audit follow up actions, and developing programs that proactively identify common themes and address compliance issues across sites and other entities in Asia Pacific regions.
• Manages communication and relationships with US Customs and Border Protection (CBP) or other applicable authorities
• Oversees First Sale program to include vendor assessments and filings with CBP
• Primary owner of the customs compliance manual and process updates based on changes in company operations, product mix, and changes in the regulatory requirements

Requirements:

• Bachelor's degree in international trade, international trade, supply chain management, business or other related fields
• 3-5+ years of experience in trade compliance, with a focus on global trade
• Extensive knowledge of international trade regulations and laws, including import and export controls, trade sanctions, anti-boycott regulations, and customs regulations
• Strong analytical and problem-solving skills, with the ability to think creatively and develop innovative solutions
• Excellent written and verbal communication skills, with the ability to effectively communicate with stakeholders at all levels
• Ability to work independently and as part of a team in a fast-paced, deadline-driven environment
• Experience with trade compliance management software programs, such as OCR Global Trade Management, is preferred
• Fluency in Korean language (both spoken and written) is required as the role involves communication with Korean counterparts in other countries.

Please submit your updated resume through the Apply Now link.