Summary

The role will be responsible for maintaining a high standard of quality in labelling to enhance Linguistics AI model accuracy and drive continuous enhancement

Responsibilities

• Conduct daily sampling tasks for one or multiple projects in your designated language.
• Perform comprehensive data analysis, identify issues, manage appeals, and offer feedback to enhance labeling quality.
• Analyze and provide feedback on guideline updates, identifying areas for improvement and potential gaps.
• Collaborate closely with labeling teams, Project POC (Point of Contact), and Project QA (Quality Assurance) to ensure adherence to labeling quality standards.
• Participate in calibrations with Labeling teams, alongside Project QA, or provide additional details through offline methods when necessary.
• Collaborate with Model Training or Product teams to align and improve labeling guidelines based on language-specific features.
• Engage with various cross-functional teams.
• Contribute to the development of quality inspection standards and continually optimize the process and system platform.

Requirements

• Bachelor's Degree or equivalent education/experience; an advanced degree in linguistic, literature, philosophy, journalism, or political science is preferred.
• Excellent written and spoken English language skills.
• Attention to detail and proficiency in using data analysis to identify trends.
• Strong aptitude for learning, effective cross-department communication, and collaboration skills.
• Ability to work independently with minimal supervision and a well-developed logical and common-sense approach to job tasks.
• Familiarity with office software such as Excel and Word, with a preference for experience in data processing and other data analysis capabilities.

To Apply

If you're interested in this role, click 'apply now'
All Applications will be treated will with strictest confidence.
Samuel Tse
Senior Consultant - Technology
Gateway Search
DID:+65 6727 6129
www.gateway-search.com
EA Licence No: 19C9807 | Registration No: R1223789

Commissioning, Qualification & Validation (CQV) Engineer

12 months contract

About the Company:

Our client is a US healthcare and a leading global biopharmaceutical company. They have a revenue of US $40.1 billion, with more than 69,000 employees across 140 countries with a heritage of more than 125 years. Our client is committed to provide patients and customers with a reliable supply of high-quality, safe, and effective medicines and vaccines. Their global supply strategy relies on manufacturing capabilities and expertise to achieve this mission.

Job descriptions:

• Perform Commissioning, Qualification, Validation team activities with a direct regard for Safety.
• Generate Commissioning & Qualification (C&Q) Procedures for projects.
• Review/qualify lab equipment – Isolator experience is advantageous.
• Writes, review and revise a variety of Installation, Operation and Performance qualification/verification related documents, including any of all of the following: SOPs, validation/verification master plans, guidelines and execution plans
• Facilitate scoping / planning of commissioning spares and consumables.
• Deliver the C&Q activities as required to meet the schedule
• Track progress of C&Q activities as required.
• Execution of Design reviews, shakedown, commissioning, Factory Acceptance Test (FAT's), Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) activities.
• Coordinate with project contractors and equipment vendors to execute required tests.
• Allocate project resources for efficient execution of project deliverables.
• Coordinate support during C&Q execution

Job Requirements:

• Min 6 years of Computer System validation, qualification, and commissioning experience
• Experience with validation of equipment controlled by PLCs, BAS/BMS systems, DeltaV, and other typical automated system platforms preferred.
• Experience in the pharmaceutical industry

Reg No: R22104540

EA License no: 94C3609

· Perform the duty of Environmental Control Officer in accordance to Environmental Public Health Act

· Maintain ECO registration by NEA

· Full Time ECO - For contract sum exceeding 50 million

· Submission of site environmental control program and site environmental control report

· Attend to all feedback on such irregularities and inform the Occupier immediately

· Inspect the construction site to ensure all facilities and equipment relevant to the maintenance of environmental health are in proper working condition and do not pose any environmental health hazard;

· Point out and discuss environmental health irregularities such as mosquito and fly breeding, rodent infestation, noise/ dust/ smoke/ water pollution, poor housekeeping, earth littering, poor refuse management, poor maintenance of sanitary facilities, etc. with the occupier of the construction site and recommend measures to rectify such irregularities;

· Ensure workplace is in compliance with Workplace Safety and Health Act and its subsidiary regulations that is relevant to its nature of work

· Monitoring of the WSH Management System implementation procedures on site

· Conducting regular site inspections and corrective actions

· To enforce and monitor safety conduct on site

· Carry out investigations and reporting on all incidents, inclusive of accidents, near misses and dangerous occurrences as necessary

· Oversee safe project execution & lead the subcontractors to ensure compliance to all WSH matters

· Liaise closely with project team to provide assistance in any WSH matters

· Recommend the employer of the worksite to implement such reasonably practicable measures to remedy the unsafe condition or unsafe work practice

· Assist in implementation of safety measurement on the worksite

· Identify any unsafe condition in the worksite or unsafe work practice which is carried out in the worksite

· To inspect and report any safety infringement

· Updating & maintaining of all Safety Health & Environmental documentations and legal registers.

Requirements:

· Candidate must be a Registered Environmental Control Officer with National Environmental Agency

· At least 2 years of working experience in related field is required

· Possess Advance Certificate in WSH or Safety Coordinator Training Certificate

· Minimum 2 years of relevant working experience in Building Construction or LTA Projects

· Manage working at Height

· Lifting Supervisor

· Confined Space Safety Assessor

• Establish new and maintaining existing relationships with customers.
• Manage and interpret customer requirements and calculate quotations for clients.
• Perform pre-sales technical assistance and product education.

Requirements:

• Diploma in Electronic, Mechanical/Mechatronics Engineering
• At least 2 years of sales experience in cleanroom environment/semiconductor industry

If you are keen to apply for the position, kindly email your detailed resume in MS Word to [email protected]

Please note that only shortlisted candidates will be notified.

For more job opportunities, please visit our website at www.recruit-expert.com

EA Licence: 19C9701

Registration: R1326740

Summary: The Credit Control department is responsible for the expeditious collection of revenue from all customers within the credit terms and period. This includes customers paying from Europe, Americas, etc and any other areas which may be allocated to the Credit Controller. The Credit control department also liaise with some Asia agents on collections they make on our behalf. They are also responsible for recording of disputes and following up on the resolution of these disputes.

Reports to: Credit Control Manager

Role and Responsibilities:

• Timely collection of payments;
• Following up on disputes on invoices and queries and ensuring they are attended to promptly;
• Provide prompt updates on customers’ accounts;
• Preparing of Statement of Accounts for customers and reports for agents;
• Submission of payment details in system when payments are credited in the account;
• Report collections forecast;
• Management reporting;
• Working with internal and external parties – Business units, Revenue Process team, Sales & Marketing teams, customers and agents.

Requirements:

Education, Knowledge & Working Experience

• Minimum Diploma in Finance or related field;
• Min 3 years of experience in credit and control function ideally in a shipping environment;
• Knowledge of credit risk analysis;
• Computer literate, excellent in MS Excel.

Personal characteristics

• Good interpersonal and communication skills, spoken and written;
• Able to multitask, prioritize, and manage time efficiently;
• Possesses creative problem-solving and negotiation aptitude;
• Goal-oriented, organized team player;
• Self-motivated and self-directed.

about the company

My client is a specialised manufacturer serving the machinery/equipment market. They are a Chinese MNC and with their innovating technology, this is a great brand to join at an exicting time in their development. The role needs the candidate to be based permanently in Hanoi, Vietnam

about the job

• Leader of the Quality Department
• Work with a cross-functional team to manage quality issues in New Production Introductions (NPI) program, resolving issues in material or process to successfully reach mass production
• Work with Purchasing and Engineering Team to develop local sourcing and manage supplier quality issues
• Establish control plans based on customer requirements and PFMEA for incoming, in process, outgoing and reliability inspection
• Drive the implementation of process control in critical process that will impact product quality
• Initiate activities and programs for continuous improvement on product quality and manufacturing processes
• Manage field returns and complaints

skills & experience required

• Master / Degree in Electrical / Mechanical / Manufacturing Engineering or equivalent
• Minimum 10 years of experience in contract manufacturing / services (EMS) environment
• Prior NPI manufacturing experience will be a plus
• Extensive Experience in supplier & product quality management
• Six sigma certified / lean manufacturing / continuous improvement techniques a plus
• Have good understanding of PPAP, and quality tools like MSA, SPC & FMEA
• Will be based in Hanoi, Vietnam permanently

If you are interested in the position , kindly send your CVs in to yitwei.kwan(@)randstad.com.sg
Please include your availability, expected salary and reason for leaving current job.
We regret that only shortlisted candidates will be contacted
EA: 94C3609 / Reg: R1325913

1. Support the implementation of quality measures for nursing homes, which includes:Planning and organizing engagements with nursing homes to share the purpose and details of the quality measures.

• Presenting (using Tableau) and analysing the data for the quality measures.
• Preparing reports for CCOs and AIC management.
• Addressing questions from CCOs with regards to the quality measures.

2. Support the development of quality measures for other eldercare services, which includes:

• Reviewing local service/regulatory requirements, good practices, international practices to identify potential quality measures for home nursing care and other community-based care services.
• Conducting a preliminary analysis and presenting the findings.
• Liaising with other AIC Divisions to support the team’s quality measurement work.
• Organising meetings with the appointed workgroup, who will deliberate and select the quality measures for the sector.

3. Assist in the implementation of other key quality initiatives such as:

• Facilitating discussions with nursing homes to develop action plans with the aim of improving the safety culture in their organisations.
• Supporting the implementation of a quality assurance programme involving nursing homes and home nursing care providers.

Job Requirements:

• Degree in any discipline with 1 to 3 years of working experience. Entry-level candidates will also be considered
• Experience in data collection, analysis, visualisation and reporting; and knowledge of the community care sector would be an advantage
• Familiarity with analytics and statistical software e.g., Tableau, Stata would be an advantage
• Effective interpersonal, engagement and follow-up skills
• Strong written and verbal communication skills
• Passion for quality and ageing issues
• Resilient and results-oriented

Responsibilities:

• Prepare annual credit reviews and credit assessments on new and existing cases
• Prepare the necessary documents and perform the periodic risk reports
• Perform the periodic risk reports and monitor the submission of annual credit reviews
• Assist in market risk and liquidity risk management
• Reviewing KYC and CDD duties
• Perform ad-hoc assignments assigned by the Bank

Requirements:

• Degree holder with at least 5 years of risk control and monitoring experience in Banks
• Effectively bilingual (to review credit document in both English & Chinese due to Head Office requirement in China)
• Proficient in MS Excel, PowerPoint, and Word
• Only Singaporeans

Please state your availability, currentand expected salary in the resume.

Qualified or interested candidates, please visit our GMP website at

www.gmprecruit.com to apply for this position with GMP Job Code: 23766

We regret that only shortlisted candidates will be notified.

GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | Paris Low | Registration No: R22106109

General

• Manage and maintain quality documents/ procedures/ records in compliance with regulations and SOPs.
• Complete training on time and before carrying out the assigned tasks.
• Actioning assigned change controls, change actions, deviations, NCRs and CAPAs.
• Carry out the assigned tasks in compliance to GMP and SOPs and in alignment with defined timeframes and business needs.
• Notify and escalate issues related to tasks to reporting manager for potential issues which may risk the business activities.
• Quality oversight of contract manufacturers including: DOS/NCR/Deviation and CAPA, Change Control and routine stability testing monitoring. On time and in compliance to GMP and applicable standards
• No recalls or Critical product quality issue on product in the market due to batch release oversight.
• Release timeframe within target timeframe
• Oversight and management of change control process.
• Change Controls and tasks to be actioned within the defined target dates and in compliance to GMP and SOPs.
• Artwork review according to requirement
• Oversight and management of process.
• Deviations to be completed in compliance with GMP SOPs and SOPs with timeframes of business needs
• No recalls or Critical product quality issue on products in the market due to due diligence oversight.
• Work with internal departments and 3rd party suppliers to maintain oversight of the complaints process to ensure complaints are managed according to compliance requirements.
• Complaints resolved within required timeframes as defined in SOPs and according to the compliance requirements of regulations and SOPS.
• Timely reporting of complaints.
• Maintain and implement the quality risk management process
• Support in annual management review
• Participate in due diligence checks for new suppliers/ products and support in supplier audit management.
• Other projects of duties as per assignment

Requirement

• Min. Degree / Diploma in Chemistry / Pharmacy or other engineering
• Min. 1 year of experience in Pharmaceutical / medical device industry with at least 1 year of QA or GMP environment
• Experience in Supply chain quality , manufacturing quality or quality organisation in commercial needs
• Good knowledge of deviation management , CAPA ,change control and document management in pharma / medical device industry

If interested, please email your resume to [email protected]

➖

Alex Goh Hock Leong

(CEI.No: R1763413 l Recruit Express Pte Ltd (Healthcare & Life Science) | 99C4599)

Roles & Responsibilities

Roles and Responsibility

· Able to read and interpret technical and fabrication drawings

· Able to review Documents (BOM, ITP, Procedures, etc) and Drawings as per specification requirements

· Piping, Steel Structure and raw materials verification and inspection

· Liaises with Vendors on work schedule and activities (Load-Test, NDE, Painting, etc)

· Able to use measuring, technical instrument, including micrometer, weld-gauges etc

· Ensure Welding is performance according to the approved WPS

· Conduct in-line machined, Fit up and visual inspection (with reports) according to require standards, specification, PRINT prior to delivery or customer inspection

· Assist in compilation of Quality documents prior customer acceptance

· Compliance to HSE regulations and requirement at all time.

· Monitor in-progress activities with effective coordination among respective team for updates

· Report to QC Engineer on Work activities and Job status

· Liaises with QC admin on reports and documents status for submission.

· Willing to perform other ad-hoc work scope when assigned

Qualification

· Diploma in engineering, CSWIP 3.1 certificate

· Good knowledge in ISO 9001:2009, ISO45001:2018 requirements

· Minimum 3 years of relevant working experience in offshore platform/ oil and gas industry

· Knowledgeable in reading, understanding engineering drawings and specification requirements

· Understand piping fabrication/installation inspection and testing requirements

· Knowledgeable in welding inspection and quality control system

· Familiar with basic conventional NDT methods

· Computer literate and familiar in using basic Microsoft office programs

· Good/corrected vision

· Good team player and able to work independently

· Good communication and interpersonal skill

· Willing to perform overtime, shift work when required

Core Responsibilities:

• To perform quality assurance functions with regard to the product (jet engine components), process and maintain quality management system while ensuring compliance with all related government agencies, aviation authorities and customers’ requirements and regulations.
• Establish quality procedures and quality control instructions.
• Liaise with customers / vendors / suppliers on non-conformance activities, perform root cause analysis and determine effective corrective actions to reduce or eliminate the cost of poor quality.
• Perform internal audits to evaluate quality system, products and processes (ISO9001 / AS9100 / NADCAP).
• Perform vendors’ and on-site audits as required.
• Uphold customers’ and regulatory authorities’ requirements.
• To carry-out other QA functions as required.

Qualifications:

• At least 2-3 years’ of relevant experience in Aerospace QA environment.
• Good analytical, communication and interpersonal skills.
• Meticulous attention to details, able to multi-task and commit to job.
• Familiar with ISO9001 / AS9100 Quality Management System requirements.
• Experience in using problem-solving tools including fishbone diagrams, FMEA and 5-whys methodology.
• Able to interact effectively with other functional departments such as Engineering and Production to resolve issues relating to products and processes.
• Familiarity with audit covering special processes including heat treatment, plasma coating, NDT would be a plus
• Experience in metallurgical laboratory evaluations would be advantageous

Education Requirements:

• Degree / Diploma in Mechanical / Aeronautical Engineering

My client a well established Pharma company is looking out for a competent QA Associate, this following are the requirements:

Responsibilities

• Contract/External Manufacturer Quality Oversight: Monitor quality aspects of contract manufacturers, including handling OOS/NCR/Deviation and CAPA, Change Control, and routine stability testing. Ensure compliance with GMP and relevant standards, meeting timelines for actions.
• Releases of products : Oversee batch release to prevent recalls or critical quality issues in the market.
• Change Control: Address individual change controls promptly and efficiently. Manage the change control process, ensuring compliance with GMP and company SOPs. Execute change control tasks within defined timeframes.
• Artwork Review: Conduct artwork reviews to meet requirements.
• Manage deviations, NCR, CAPA: Prevent recalls or critical quality issues related to due diligence.
• Customer Complaints: Collaborate with internal departments and suppliers to oversee the complaints process.
• Document Management:Update SOPs/WIs/FGS as per role responsibilities.
• Internal and External Auditing: Conduct and faciliate resolution audits within specified timeframes, adhering to regulations and SOP and follow up on NCR/CAPA outcomes.

Key Requirements

• Possesses BSc in chemistry, pharmacy, or related field.
• 1 to 3 years of QA experience in pharmaceutical/medical device industry
• Strong familiarity with Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP)
• Experience in supply chain quality, manufacturing quality, or quality management in commercial settings.
• Proficient in deviation management, CAPA, change control, and documentation within pharmaceutical/medical device sectors.
• Auditing experience is desirable.
• High level of attention to details

How to Apply:

Interested applicants may apply by sending in your updated résumé (in MS Word format) to my email or apply directly:

Consultant: Tan Jun Jie

EA personnel reg. no.R1878852

EA License No. 17C8502

Job Description

• Industry/ Organization Type: Manufacturing
• Position Title: Control (Software) Design Engineer / Automation Engineer
• Working Location: Pioneer (Close to Joo Koon MRT)
• Working Hours: 5 days (Mon – Fri, 8.30 am – 6.00 pm)
• Salary Package: Up to $4,000 + AWS + Performance Bonus
• Duration: Permanent Role

Key Responsibilities

• Project Management including scheduling, Budget control & other project-related matters
• Responsible for hardware and software (PLC) design for customized machine / total system
• To supervise, test and commission projects both in Singapore and/or overseas
• Project presentation & documentation
• To work with third-party engagement wherever necessary for project-related matters

APPLY NOW!!!

• Diploma / Degree
• Min 5 years of relevant experience
• Proficient in PLC programming is compulsory

Please apply through ANY of the following methods:

• Submit your application by clicking the APPLY button;
• Email your resume to Job(at)anradus.com.sg. Please indicate #65637 on the email subject.

Anradus Application Policy: We value each application and ensure every resume is reviewed. Our process is efficient, typically concluding within 3 working days. If you do not receive communication from us within this timeframe, it's likely that your application has not been shortlisted by our client. In such cases, we recommend continuing your job search to maximize your opportunities.

Anradus Pte Ltd | EA License No. 20C0161 | Rachael Lee | EA Reg No.: R2093131

Job Description

• Industry/ Organization Type: Manufacturing
• Position Title: QA Engineer / Quality Assurance Engineer
• Working Location: Serangoon
• Working Hours: 5 days (Monday to Friday, 8.30 AM - 6 PM)
• Salary Package: Basic Salary up to $5,500 + OT + Variable Bonus
• Duration: Permanent

Key Responsibilities

• Ensure that ISO13485 and FDA 21 CFR Part 820 systems are adequately maintained, and continuous improvements are implemented
• Coordinate with various functions to ensure awareness and understanding of the Quality Management System.
• Plan and coordinate gap analysis exercises and provide advice on bridging the gap
• Manage and oversee quality audits by plan and ensure quality audits findings and recommendations are rectified and implemented
• Apprise management of quality audit findings and corrective actions taken
• Ensure that the procedures and processes prescribed by the Quality Management System are in place and implemented per requirement
• Review the Quality Management System periodically to assess continued suitability and areas of possible improvement
• Arrange for ISO13485, ISO14971 and FDA 21 CFR Part 820 awareness training and further refresher training as needed
• Coordinate and plan work of external audit such as Customer, ISO certification and Regulatory bodies
• Ensure that systems and procedures are in compliance with ISO13485, ISO14971, FDA 21CFR Part 820, and GDP requirements
• Mentor / supervise as assigned and ensure timely and accurate completion of quality projects
• Support Plant wide audit/ inspection activities and special projects, as assigned
• Able to travel for suppliers/customers visits
• Any other ad-hoc duties as assigned

APPLY NOW!!!

• Bachelor’s Degree in Quality Management or Electronics Engineering
• At least 3 years of working experience in Quality Management Systems, and in a manufacturing environment
• Excellent hands-on knowledge of Quality Management Systems primarily in ISO 13485 and FDA 21 CFR Part 820
• Lead, mentor and facilitate problem-solving and quality improvements
• Establish controls system required in ISO13485 & FDA registered facility
• Strong communication and interpersonal skills
• FDA Inspection experience preferred

Kindly apply through ANY of the following methods:

• Submit your application by clicking the APPLY button;
• Email your resume to Job(at)anradus.com.sg. Please indicate #65191 on the email subject.

Anradus Application Policy: We value each application and ensure every resume is reviewed. Our process is efficient, typically concluding within 3 working days. If you do not receive communication from us within this timeframe, it’s likely that your application has not been shortlisted by our client. In such cases, we recommend continuing your job search to maximize your opportunities.

Anradus Pte Ltd | EA License No. 20C0161 | Adelin Chong | EA Reg No.: R1875641

Job Description

• Industry/ Organization Type: Manufacturing/ Prefabricated Steel
• Position Title: Assistant Quality Engineer
• Working Location: Jurong West
• Working Hours: 5 days, Mon - Fri (8 am – 5 pm)
• Salary Package: Basic Salary Up to $3,500 + AWS + Variable Bonus
• Duration: Permanent Role

Key Responsibilities

• Conduct internal audits and supplier audits to evaluate compliance with quality standards.
• Participate in product and certification audits.
• Assist in the establishment and maintenance of procedures, work instructions, and document control.
• Analyze test reports and collaborate with relevant teams to identify areas for improvement.
• Address potential quality issues and work with cross-functional team members to implement follow-up actions.
• Collaborate with the relevant team to investigate root causes, develop Corrective and Preventive Actions for non-conformance or procedural failures.
• Support the preparation of Quality Assurance/Quality Control (QA/QC) plans.
• Formulate QC checklists, inspections, and procedures related to QA/QC.
• Compile monthly reports to track quality and compliance performance.
• Maintain documentation related to certifications.
• Assist the QA/QC department in areas of Health, Safety, and Environment (HSE) by participating in hazard assessments, incident investigations, and risk assessments when necessary.
• To support and engage in other activities or new project development as and when required

APPLY NOW!!!

• Min Diploma in Engineering or other relevant fields
• More than 2 years' experience in QA/QC and audits
• Independent and self-motivated

Kindly apply through ANY of the following methods:

• Submit your application by clicking the APPLY button;
• Email your resume to Job(at)anradus.com.sg. Kindly indicate #65806 on the email subject.

Anradus Application Policy: We value each application and ensure every resume is reviewed. Our process is efficient, typically concluding within 3 working days. If you do not receive communication from us within this timeframe, it's likely that your application has not been shortlisted by our client. In such cases, we recommend continuing your job search to maximize your opportunities.

Anradus Pte Ltd | EA License No. 20C0161 | Angel Lim | EA Reg No.: R1769781

Job Description

• Industry/ Organization Type: Precision Engineering
• Position Title: QA Engineer
• Working Location: Defu Lane
• Working Hours: 5.5 days, Mon – Fri (8 am – 5 pm), Sat (8 am – 12 pm)
• Salary Package: Basic Salary + Variable Bonus
• Duration: Permanent

Key Responsibilities

• Be involved in supporting Internal and External Audit.
• Inspect Mechanical parts, detect welding and mechanical appearance defects.
• Use measuring equipment such as Trimos, Profile projector, Hexagonal Arm. Height gauges, Vernier calipers, etc.
• Read and interpret all drawing symbols and welding symbols.
• Liaise with external customers and internal teams.
• Provide technical advice and the best method for improving production work.
• Support Acceptance Test Plan / Process Management Plan and conduct training.
• Perform FA, Incoming, In-process and Outgoing inspection to meet the delivery schedule.
• Ensure all measuring equipment is calibrated.
• Ensure maintenance record and Production in-process record is updated on time.
• Ensure the implementation of corrective actions/preventive action as a result of weekly Source inspection by customers.
• Compiling Outgoing Inspection reports to support documents in the customer portal, Microsoft Office and Outlook.
• Assist with Document Control - To ensure all drawings are latest and filed in a proper manner.
• Assists/performs other non-routine duties as assigned by QA Manager

APPLY NOW!!!

• Must possess a minimum of a Diploma in mechanical engineering or equivalent.
• Min. 2 years relevant experience in QA.
• Experience in Machining, Metal stamping, fabrication and related secondary processes (such as welding, plating, and powder coating) industry will be preferred.
• Good knowledge of auditing skills for ISO9001 and Qualified Internal Auditor experience.
• Good problem-solving skills and analytical skills i.e. good skills in 5S, 8D methodology, 5-why analysis
• Must be able to read and interpret technical drawings.

Please apply through ANY of the following methods:

• Submit your application by clicking the APPLY button;
• Email your resume to Job(at)anradus.com.sg. Please indicate #65696 on the email subject.

Anradus Application Policy: We value each application and ensure every resume is reviewed. Our process is efficient, typically concluding within 3 working days. If you do not receive communication from us within this timeframe, it's likely that your application has not been shortlisted by our client. In such cases, we recommend continuing your job search to maximize your opportunities.

Anradus Pte Ltd | EA License No. 20C0161 | Adelin Chong | EA Reg No.: R1875641

Job Description

• Industry/ Organization Type: Freight Forwarding/ Warehousing
• Position Title: Trade & Compliance Executive
• Working Location: Cecil Street
• Working Hours: 5 days (Mon to Fri, 9 am – 6 pm)
• Salary Package: Basic + Performance Bonus
• Duration: Permanent Role

Key Responsibilities

• Collaborate with cross-functional teams to enhance internal processes related to quotation speed, relevant shipping documents, inventory management (oversees WH), and supply chain planning in general.
• To assist in quotation matters.
• To liaise with partners on compliance matters.
• To ensure compliant coordination between pricing and operations team.
• To foster a culture of continuous learning and professional development within the team.
• Other necessary tasks as assigned.

APPLY NOW!!!

• Minimum Diploma holder.
• Critical Thinking & Problem-Solving skills.
• Ability to work independently and with initiative.
• MS Office skills.
• Candidates without experience are welcome to apply; training will be provided.

Kindly apply through ANY of the following methods:

• Submit your application by clicking the APPLY button;
• Email your resume to Job(at)anradus.com.sg. Please indicate #65644 on the email subject.

Anradus Application Policy: We value each application and ensure every resume is reviewed. Our process is efficient, typically concluding within 3 working days. If you do not receive communication from us within this timeframe, it's likely that your application has not been shortlisted by our client. In such cases, we recommend continuing your job search to maximize your opportunities.

Anradus Pte Ltd | EA License No. 20C0161 | Adelin Chong | EA Reg No.: R1875641

Job Description

• Industry/ Organization Type: Food Manufacturing
• Position Title: QC Assistant
• Working Location: Woodlands (Nearest MRT: Admiralty)
• Working Hours: Tuesday to Saturday, 7.30 am-4.30 pm/8.30 am-5.30 pm (Alternate between these shifts on a weekly basis)
• Salary Package: Up to $2,800 + AWS + Bonus
• Duration: Permanent

Key Responsibilities

• Plant hygiene control & factory checking.
• To perform QC check such as microbial check, sensory, & visual checks on raw materials and all finished products produced by the seasoning manufacturing line.
• To do in-house verification/ calibration on the equipment.
• To maintain QC laboratories.
• Any other work as shall be assigned by the Company from time to time.

APPLY NOW!!!

• At least NITEC with 1 year of related working experience.
• Able to start immediately or in short notice.

Please apply through ANY of the following methods:

• Submit your application by clicking the APPLY button;
• Email your resume to Job(at)anradus.com.sg. Please indicate #65768 on the email subject.

Anradus Application Policy: We value each application and ensure every resume is reviewed. Our process is efficient, typically concluding within 3 working days. If you do not receive communication from us within this timeframe, it's likely that your application has not been shortlisted by our client. In such cases, we recommend continuing your job search to maximize your opportunities.

Anradus Pte Ltd | EA License No. 20C0161 | Adelin Chong | EA Reg No.: R1875641

Qualifications and Profile

• Good Knowledge of programming languages like Java, JavaScript and HTML
• Good to have knowledge on Banking or Finance.
• Expertise in automation testing tools like Selenium, Auto IT, Rest Assured, Cypress and Cucumber
• Takes initiative to chase down answers.
• Hands on knowledge of desktop based app and its automation
• Able to adapt to changing business and project priorities.
• Proactive in bringing solutions to observed gaps in requirements and process.
• Proactive in test planning, able to identify and breakout tasks based on a test plan.
• Able to prioritize and execute QA tasks with minimal supervision.
• Execute tasks from QA lead or above.
• Mentor and guide junior level Associate QA Engineers and QA Engineers.
• Perform root cause analysis.
• Install and/or configure tests for systems.
• Optimize test cases for higher efficiency, especially for specific changes in code or features.
• Test client-server interaction.
• Test user behavior analytics.
• Analyze and test UI and UX requirements.
• JIRA and Confluence

Nice to have

• Automation test result analysis and investigation of failures.
• Perform change impact analysis.
• Perform risk-based test analysis.
• Bonus skills and tools knowledge:
• GitHub and Bitbucket
• Docker
• Postman
• Jenkins CI
• Node.js & Selenium WebDriverIO
• JavaScript
• Kubernetes
• Xray test case management tools

• 1-year renewable contract
• Must have experience in building and writing on test scenario/cases and functional testing (manual & automation)
• Strong communication and experience in managing various stakeholders (internal & external)
• Knowledge in agile and waterfall methodology

Job Description

• Translate requirement into test scenarios and test cases
• Liaise with key stakeholders to confirm on the test coverage
• Getting sign-off for all test deliverables to close-off the testing cycle
• Execute manual and automation test cases
• Point of contact of the QA related matters and enquiries for the project
• Lead the discussions during QA activities such as test coverage walkthrough, SIT/UAT execution
• Assist PM to formulate QA strategy for the project as necessary

• Diploma in Computer Science or Testering or equivalent work experience
• Minimum 2 years of working experience in QA
• Experience in working with stakeholders, conducting architecture reviews, and consensus building
• Knowledge in CI/CD pipeline tool such as Ship & Hat would be an added advantage
• Thirsty for knowledge and keen to explore new technologies
• Excellent communication skills and strong analytical and conceptual skill
• Knowledge in agile and waterfall methodology
• Experience in using JIRA and SharePoint

Triton AI Pte Ltd

Registration Number: R23118389

EA: 21C0661

• Renewable contract; convertible to perm
• Medical Coverage
• Bonus

• Establish new and maintaining existing relationships with customers.
• Manage and interpret customer requirements and calculate quotations for clients.
• Perform pre-sales technical assistance and product education.

Requirements:

• Diploma in Electronic, Mechanical/Mechatronics Engineering
• At least 2 years of sales experience in cleanroom environment/semiconductor industry

If you are keen to apply for the position, kindly email your detailed resume in MS Word to [email protected]

Please note that only shortlisted candidates will be notified.

For more job opportunities, please visit our website at www.recruit-expert.com

EA Licence: 19C9701

Registration: R1326740

Work Location: Central

Working Hours: 5days (9am to 6pm)

Responsibilities:

• To be responsible for the implementation and monitoring of any laws and regulations regarding compliance
• To provide advice and guidance on compliance policies and procedures relevant to the applicable rules and regulations of the company
• To provide advisory and manage any Anti-Money Laundering (AML) queries
• To conduct due diligence checks and account/profile reviews at Client onboarding or periodically
• To conduct screenings and investigations on accounts or relationships
• To identify and mitigate client relationships and/or account activities that may present sanctions risk

Requirements:

• Degree with minimum of 5 years’ compliance experience in EAM or Private Bank
• Proficient in MS office, Word, and Excel

Please state your availability, current and expected salary in the resume.

Qualified or interested candidates, please visit our GMP website at

www.gmprecruit.com/current_jobs/posting.aspx to apply for this position with GMP Job Code: 23563

We regret that only shortlisted candidates will be notified.

GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | Paris Low | Registration No: R22106109

The QA Officer is a key appointment in the department and takes the lead in the development, monitoring, and review of QA procedures. The QA Officer is also responsible for ensuring the administration and accurate and appropriate recording and storage of QA records and associated documentation. He / She will also provide administrative support to the department and the QA structures of HWA as required.

This is a position of responsibility that requires the ability to work autonomously and the confidence to provide sound direction and guidance to colleagues, both junior and senior, concerning quality assurance requirements and procedures.

Job Descriptions:

• Support quality assurance and enhancement activities throughout the School
• Play an active role in ensuring that quality assurance and enhancement issues are appropriately considered throughout the School
• Manage the production of relevant quality assurance literature, reports, and other documentation
• Prepare executive summaries of all relevant internal and external documentation and outputs, as required by management and other audiences
• Prepare reports and other forms of assurance for the Academic Board and the Governing Body
• Assist management and staff on developments within the fields of quality assurance and enhancement
• Any other relevant duties assigned by the School

Requirements:

• Bachelor's degree with 1-2 years of related work experience.
• Knowledge of Law or Quality Assurance will be an added advantage.
• Self-motivated, versatile, resourceful, and result-oriented.
• Able to work in a fast-paced environment, multitask, and work independently with minimal supervision.
• Proficient in MS Office.

POSITION SUMMARY:

The Compliance function is a trusted partner in promoting and supporting an ethical work environment and a culture of ethics, integrity and compliance with the ultimate aim to pursue Menarini Group’s mission and protect its reputation. The Compliance function pursues its mission though designing Compliance Programs and facilitating their implementation and oversight, through education, advice and monitoring, thereby enabling a risk-informed decision making and supporting management and employees to make the right decisions always.

Reporting directly to Corporate Compliance Director, Corporate Compliance Support Director (CCSD) APAC will partner with regional and country based management and resources to support and facilitate the implementation of Corporate Compliance Programs across the 13 markets of the Asia-Pacific (China, Indonesia, Thailand, Malaysia, Philippines, Singapore, Vietnam, South Korea, Taiwan, Hong Kong, Australia, New Zeeland and India) in a consistent and harmonious manner.

The CCSD will communicate, counsel, train and monitor implementation of the Corporate Compliance Programs and initiatives across the markets, also ensuring such initiatives and programs are aligned with Menarini’s Global Compliance Framework and related Global Policies over time.

The CCSD is also expected to support the design and enforcement of Corporate Compliance Education and Training Programs across the region, including tight monitoring and taking direct responsibility over appropriate and timely delivery and tracking of such programs over time.

KEY RESPONSIBILITIES:

• Support the development and implementation of a robust, word-class Corporate Compliance Framework that enhances the reputation of Menarini and minimizes its risk of non-compliance with all applicable laws, regulations and self-regulation that affect the Company’s operations.
• Develop a thorough understanding of, and familiarity with, the Company’s business, its organization, markets, facilities, customers and competitors, in order to identify trends and design and implement appropriate programs, plans and strategies.
• Clearly communicate throughout the Company a culture of ethics, integrity and compliance, including personal accountability at all levels.
• Support Corporate Compliance in the implementation of the Company’s Global Code of Conduct, Ethics and Integrity Policies, Global Anti-Corruption Program and any other relevant global policy and procedural document; improve and recommend updates to the policies, procedures and programs at the division, and at the regional and country level.
• Perform independent reviews aimed to ensure that Regional Compliance Officer, Country Officers/Liaisons at country/market level are implementing and monitoring country/market specific compliance programs, in alignment with Menarini’s Global Compliance Programs and Policies.
• Apply project management skills to ensure effective monitoring over implementation of programs, trainings and initiatives, also meeting high quality standard, deadlines and expectations of stakeholders.
• Proactively collaborate with business to promote whistleblowing and reporting channels, and continually improve the process to encourage the management of issues for early, proactive resolution in order to mitigate greater risks.
• Support the development education and training programs related to Global Compliance initiatives for the APAC countries/markets, to ensure appropriate training and communication contents are delivered to appropriate targets, with the established frequencies.
• Support the delivery, as needed, of global compliance training and communication initiatives, also providing assurance over the appropriate tracking and evaluation of trainings, with ultimate aim to explain and reinforce management’s commitment to ethical standards integrity and compliance.
• Support Regional and Country Compliance Officers in implementing requirements deriving from global licensors’ due diligence and other contractual obligations.
• In partnership with regional business leadership and Regional/Country Compliance Officers, facilitate and contribute to Regional Compliance Committees and support related recommendations and action plans.
• Lead, in coordination with Corporate Compliance, regional compliance risk assessments; manage communication of resulting reports/ recommendations and support any required business remediation plans / corrective actions.
• Establish and maintain key contact relationships with management at Regional/Country level and various functional area(s) of responsibility to support the Corporate Compliance Director and Regional/Country Compliance Officers in assessing and mitigating risks across the organization.
• Continuously report to Corporate Compliance Director any significant matters regarding the market compliance programs and ensures regional alignment on compliance strategic initiatives and programs

KEY REQUIREMENTS:

• A Master’s Degree from a globally recognized institution is preferred
• Candidates should have at least 12 years’ experience in compliance, preferably from the healthcare industry (pharmaceutical or medical device)
• Intimate knowledge of anti-bribery, anti-corruption, healthcare compliance and trade control legislation is essential
• Compliance experience across APAC countries and markets is also highly desirable
• Excellent project management skills
• Demonstrated leadership and strong professional presence are key
• Ability to influence up, down and sideways in the organization
• Coaching skills are advantageous
• Excellent presentation skills and a strong communicator, ie able to breakdown and explain complex issues simply
• Commercial mind-set and solid understanding of business drivers
• Good written and verbal skills
• Self-starter, hands-on, resourceful, tactful
• Strong emotional quotient and culturally adept
• Well organized, timely and flexibility to adapt to changing priorities
• Team player with ability to work independently

Responsibilities

• Liaison with customer / supplier on production quality issues, drive improvements;
• Establish Quality Inspection Procedures ;
• Perform internal audits to meet AS9100 & NadCap requirements;
• Analyse process capabilities (cpk) and recommend areas of improvements;
• Perform Gage R&R, calibration of CNC and quality jigs & other instruments

Requirements

• Degree in Mechancial / Production Engineering or other educational background with relevant working experience;
• Familiar with ISO/ QS/ AS Quality Management system, Qualified internal auditor;
• Must be well verse in interpreting mechanical drawings (ISO, GD&T)
• Experience in Coordinte Measuremnt Machine (CMM) Programming an advantage;
• Good analytical knowledge and sense for technical details & precision
• Passion to innovate and improve, willingness to learn & adapt to challenges
• Good team player, ability to communicate well within all levels of the organization