Total 2,628 quality assurance specialist job vacancies in Quality Assurance / Control category in Singapore

Role Summary

The job holder is responsible for applying a local Quality Assurance program for the R&D Test Facility in alignment with Good Laboratory Practice (GLP), other applicable regulations and company best practices. This is to assure Test Facility Management (TFM) and management that the facilities and studies are in compliance with Good Laboratory Practice regulations.

Additionally, the incumbent supports the implementation of applicable standards pertinent to non-clinical research and/or toxicological assessments in order to verify that the studies are performed in accordance with the applicable regulatory frameworks, QMS requirements and best practices.

The incumbent also supports the quality oversight of suppliers and contract laboratories for pre-clinical research and/or toxicological assessments, as well as to identify opportunities for quality and process improvements in pre-clinical development.

Responsibilities

• Plan, perform and report QA inspections and suppliers audits to assure TFM and management that procedures/standards are in compliance with relevant national and international requirements for GLP for both internal and external entities. Monitor and follow up on corrective actions and preventive actions (CAPAs) reporting in response to internal audits and regulatory inspections.
• Support the monitoring of pre-clinical studies throughout their conduct and reporting for compliance with the GLP principles.
• Support R&D Test Facility for inspection readiness, participating in regulatory inspections/accreditations, and managing the corrective and preventive actions (CAPAs) reporting in response to internal audits and regulatory inspections
• Provide administrative support for the QMS document/record/training management system, including QA review of records such as QMS documents (SOPs/WKIs/Forms), Training, Nonconformance (NC), Corrective Action Preventive Action (CAPA) and Lab Change Request (LCR) for key QMS processes. Provide regular training on the systems and QMS (e.g. Good Documentation Practice, GLP) for new and existing staff.
• Manage the archival process in accordance with established SOP and GLP principles
• Monitor and report quality Key Performance Indicators (KPI) during Quality Management Review (QMR)
• Perform QA review of equipment/instrument qualification plans, reports and related documentation for GLP activities, to assure that the laboratory equipment/instrument are suitable for their intended purposes
• Continue to be developed as an expert in understanding GLP compliance on a global basis including local compliance enforcement experience with Health Authorities

Requirement

• Bachelor degree in scientific discipline (Life Sciences, Biology, Chemistry etc) or equivalent
• Minimum 3 years of work experience in a laboratory environment (chemical/biologic analyses) and participation in quality assurance related to activities in tobacco, food, pharmaceutical or similar industry and/or at least 3 years experience as a specialist in a relevant area of activity. Experience in another quality standards eg. ISO 17025 would be an advantage
• Working knowledge of OECD principles of Good Laboratory Practice, knowledge of other quality systems such as FDA GLP Principles, cGMP, ISO, GCP and AAALAC is an advantage

• Perform checks on food products, storage, and processing facilities to ensure quality guideline in the vicinity.
• Conduct daily inspections and implement of the factory's food safety, quality, sanitation, and hygiene in accordance with ISO & HACCP requirement.
• Collaborate with the export coordinator to determine the operational needs for export shipments of the food products

Requirements:

• Diploma in Food Technology or equivalent
• At least 2 years of QA/QC experience in food manufacturing sector.
• Familiar with ISO standards for Quality and Food Safety

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: R24120303

Overview: -

• 5 Days (Monday to Friday), Office Hours
• East - Loyang
• Monthly Base Salary: $2700 - $3500 (Based on working experience)
• AWS (13th Month) + Variable Bonus

Your Responsibilities: -

• Maintain and update documents and records related to ISO 9001, ISO 14001, and ISO 13485 systems
• Establish and maintain proper documentation control and distribution
• Conduct internal and external audits
• Liaise with external auditors and certification bodies
• Generate monthly reports
• Review and update Quality Management System procedures
• Ensure system compliance
• Manage internal and external corrective action reports
• Plan and conduct periodic system audits
• Maintain and regularly review calibration and preventive maintenance for instruments and equipment
• Direct and head internal audit programs and recommend improvements for internal audit policies and procedures

Requirements: -

• Minimum 2 years of working experience in QMS and ISO 9001 audit, preferably in manufacturing industries
• Good knowledge of ISO 9001, ISO 14001, and ISO 13485 quality system
• Knowledge in preparing FMEA and Control Plans

Interested applicants may click "Apply Now" or email to [email protected] to submit your application.

By submitting your personal data and/or resume, you will be deemed to have agreed and consented to us collecting, using, retaining, and disclosing your personal information to prospective employers for their consideration.

We regret to inform that only shortlisted candidates would be notified. We wish you the best of luck!

Recruit Lync Pte. Ltd. | EA Licence Number: 22C1000

Jonathan Chang Sing Erh | EA Personnel Licence: R22110541

Responsibilities

• Perform incoming/ outgoing / in process quality checks and control
• Perform daily inspection on sanitation, hygiene, food safety and quality aspects to ensure good manufacturing and good hygiene practise at work.
• Conduct routine microbial and shelf life testing
• Provide production staff training in GMP, GHP, and CCP.
• Endure adherence to SFA requirements and ISO&HACCP documents are properly carried out
• Develop and recommend improvements of facilities, equipments and procedures to enhance safety, quality and efficiency
• Handle internal/ external audit and liaise with SFA for import and export inspection
• Any other ad hoc duties as assigned.

Requirement:

• Candidate must possess at least Diploma, equivalent or above in Food Science
• Bilingual in English and Chinese to liaise suppliers from China
• Preferably 1 year(s) of working experience in the related field is required for this position.
• Knowledge in food safety & quality audits will be an advantage
• Able to work independently, self-motivated, initiative and able to communicate effectively with all levels

Quality Inspector (Jurong East)

base salary + OT pay + 1 month AWS + company shuttle bus

Focal point for inspection queries and scheduling of inspection activities. Ensures conformance of materials, purchased parts and manufactured parts in alignment with quality control plans, specifications, processes and standards. Adds value by ensuring products and services are delivered in compliance with customer expectations.

Job Responsibilities:

• Unboxing, unwrapping and preparing of items for inspection.
• Execute in process and/or final inspection of materials, purchased parts and manufactured parts to ensure conformance with quality control plan, procedures, documentation and standards.
• Review and ensure manufacturing work orders and associated documentation is completed and processed correctly in a timely and efficient manner.
• Monitor and ensure callibration of equipment, work areas are kept clean and appropriate PPE and best practice lifting practices are adhered to at all times.
• Prioritise inspection activities in alignment with delivery objectives.
• Effectively communicate non conformance issues to engineering / production expedites solutions as necessary to support delivery objectives.
• Attending production meetings.
• Completing of non scheduled urgent inspection tasks within the completions business.

SKILLS & QUALIFICATIONS:

• Comfortable working at Penjuru, Jurong East area. Company shuttle service provided
• Min NDT/ NDE/ SPM/ secondary education level
• 1-2 years' experience in manufacturing facility/ quality inspection/ industrial/ engineering
• Experience in manufacturing workshop processes and controls.
• Competent is reading and understanding engineering drawings, processes and procedures.

• Develop and implement procedures for inspecting, testing, and evaluating the quality in accordance with the industry and company's standards.
• Set up Project Quality System, implement and maintain in accordance with Singapore standards.
• Track all legal and regulatory compliance requirements and performance and identify preventive programs to mitigate any potential non-compliance.
• Evaluate the implementation of Quality Plans and Quality Control Plans at sites to ensure that the project Quality Plan adheres to specifications and contract requirements.
• Conduct periodic site visits to perform detailed and documented quality, process, and safety checks, ensuring that quality meets industry and company standards.

Requirements:

• ISO 9001: 2015 Lead Auditor Certified
• Degree in Engineering or equivalent
• At least 8 years of implementation and management of quality systems experience in Construction 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: R21100996

Location: Kranji, Singapore (with travel to different sites as needed)
Salary: Up to SGD 6,500 (commensurate with experience)

Job Responsibilities:

• Lead the Quality Control (QC) team (1 QA Executive and 8 QC Inspector) to ensure continuous improvement and compliance with quality standards, safety regulations, and customer expectations.
• Support all operational quality-related activities, including reviewing quality requirements and ensuring adherence to ISO 9001 standards.
• Develop and implement quality control procedures and act as the Management Representative (MR) for ISO audits in manufacturing and quality processes.
• Conduct regular audits and inspections of products and processes to identify areas for improvement.
• Collaborate with production staff to resolve quality control issues and perform root cause analysis, including the formulation of 8D, corrective, and preventive actions.
• Develop and maintain quality control documentation, including equipment calibration records.
• Ensure all products meet quality and safety standards before release.
• Identify and implement process improvements to enhance efficiency and reduce costs.
• Work closely with other departments to integrate quality control procedures across all business functions.
• Provide training and guidance to QA/QC staff on quality control procedures and best practices.
• Manage customer feedback and provide timely responses to maintain high levels of customer satisfaction.

Requirements:

• Minimum Diploma/Degree in Mechanical Engineering or related fields.
• At least 5 years of experience in a quality control role, preferably in a manufacturing environment.
• Strong knowledge of ISO 9001:2015 quality control procedures and standards.
• Certified Internal Quality Auditor (ISO 9001:2015).
• Great attention to detail and a result-driven approach.

Interested candidates please apply online or send your latest CV to [email protected]

AlwaysHired Pte Ltd

Reg No: R1549345

EA: 24C2293

• Serve as the Test Manager, comprehensively understanding business requirements for the Core Banking System, Fund Transfer, and other related banking systems, ensuring all testing in alignment with the requirements
• Responsible for conducting IT software testing
• Collaborate closely with various stakeholders to ensure effective and efficient teamwork throughout the testing process.
• Key stakeholders include: End users, system development teams, and back-office departments from the head office Test support teams from other IT vendors and Offshore vendors

Qualifications:

• Bachelor’s degree in Information Technology, Computer Science, or a related field with a minimum of 5 years of experience supporting IT project test phases within the banking sector.
• Experience in IT software testing, with prior experience as an IT professional in a banking or financial institution will be advantageous.
• Lead the creation of test plans and test definitions for banking IT systems, demonstrating knowledge in software quality management including software testing methodologies, including the creation of test plans, test documentation, execution of test cases, and analysis of test results.
• Experience in managing risk and control processes, including timely escalation and resolution of significant issues to management.
• Proven experience in collaboration, teamwork, and strong leadership in managing stakeholder relationships.
• Demonstrated project engagement skills, including the preparation and presentation of regular reports and documentation, effective communication of project status and progress to stakeholders and IT teams, and alignment with business priorities.

Work location: Changi Business Park (One@ Changi City)

To apply, please visit www.gmprecruit.com and search for Job Reference: 24771

To learn more about this opportunity, please contact Gia Grace at [email protected]

We regret that only shortlisted candidates will be notified.

GMP Technologies (S) Pte Ltd | EA License: 11C3793 | EA Personnel: Bautista Gia Grace De Guzman | Registration No: R23111973

Your Job

The primary purpose of your role is to work closely with the Product Development team to develop and maintain a Quality Plan. This plan is crucial in managing and mitigating project risks to ensure a flawless product launch that meets the customer's cost, quality, and delivery requirements.

Our Team

You will be reporting to the AQP Manager.
Internal: Product Design Engineers, Manufacturing / Process / Tooling Engineers, Project Management, Manufacturing Plants, Product Management & Sales / Marketing

External: Customers, Suppliers

What You Will Do

• Quality Plan Development: Ensures the project Quality Plan for new products and product modifications are focused on the voice of customer and all project quality deliverables are completed in a timely manner.
• Risk Analysis: Facilitation during front-end product / tool / assembly design or process reviews, design & process FMEA reviews by providing inputs on internal and external quality history, lessons learned and through active critical thinking / questioning. Reviews and approved reliability test plan.
• Metrology / Qualification of New / Modified Parts: Facilitate the development of measurement plans / methods and lead the disposition of new products at FOT (First Off Tool) and Qualification. Ownership of gauges & necessary inspection fixtures, perform Measurement System Analysis, Capability Studies & any necessary statistical analysis with goal of Tool / Process Qualification.
• Flawless Launch: Work with Manufacturing AQP or QE to conduct Safe Launch exercise. Perform process audits and reverse (go & see) FMEA’s to qualify new production processes, and to ensure compliance to documented control plans for new products.
• Customer Approval: Ensures customer required documentation relating to customer acceptance of new products and product modifications are completed.
• Supplier Approval: Reviews and approves supplier product specific documentation on new and modified purchased components. Works with supplier quality engineer to ensure compliance.
• Problem Solver: Lead in the problem solving (8D’s), analysis, and resolution of new product related customer complaints or internal quality complaints during launch. Support efforts for prevention of repeat issues & systemic improvements to the Product Development Processes to reduce New Products QNs.
• Principle Based Management & Quality Systems: Understand & practice the KOCH 5 dimensions & guiding principles, Lean / Six Sigma, International Standards Organization (ISO) and Environmental, and/or Health and Safety (EH&S) Management Systems by following stated policies and procedures.
• Perform other related duties as assigned by management.

Who You Are (Basic Qualifications)

• BS Degree in Engineering or other related field
• Experience in Quality Engineering or Automotive related field
• Strong organizational skill to anticipate, plan, organize and self-monitor workload
• Good communication skill and presentation skill
• Good interpersonal skills for effective leadership and team facilitation
• Solid Knowledge & understanding of metrology and GD&T
• Knowledge of statistics - experience using Minitab or other software
• Experience in using MS Office (Excel, Word, Power Point)
• Able to travel (domestic and international) 20%

What Will Put You Ahead

• Training in Capability Analysis (CPK) , SPC, AIAG VDA FMEA, Lean / Six Sigma, reliability test plans , VDA19 , VDA5
• Experience in Quality engineering in a new-product introduction environment
• Experience performing PFMEA/DFMEA and using other Advanced Quality Planning tool
• Experience working as customer interface (including Automotive OEMs and Tier1/2 suppliers)
• Working knowledge of testing, molding, stamping, plating and assembly processes
• Good knowledge of IATF 16949, VDA 6.3, AIAG core tools (APQP, PPAP, FMEA, MSA, SPC)
• Quality System (ISO 9001 or IATF 16949) and Supplier Auditing experience, Gage and Fixture design
• Knowledge of VDA 5, VDA19 , AIAG-VDA FMEA
• Experience working with European automotive customers

At Koch companies, we are entrepreneurs. This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions. Any compensation range provided for a role is an estimate determined by available market data. The actual amount may be higher or lower than the range provided considering each candidate’s knowledge, skills, abilities, and geographic location. If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.

Who We Are

As a Koch company, Molex is a leading supplier of connectors and interconnect components, driving innovation in electronics and supporting industries from automotive to health care and consumer to data communications. The thousands of innovators who work for Molex have made us a global electronics leader. Our experienced people, groundbreaking products and leading-edge technologies help us deliver a wider array of solutions to more markets than ever before.

At Koch, employees are empowered to do what they do best to make life better. Learn how our business philosophy helps employees unleash their potential while creating value for themselves and the company.

Additionally, everyone has individual work and personal needs. We seek to enable the best work environment that helps you and the business work together to produce superior results.

Quality Control Engineer - Supplier Quality | SPQP | Exp in CMM | Up to $4.5k | 5 Days |

Work Location: Yishun Industrial Park A [Canberra MRT] / Have company transport

Salary: $4000 to $4500 depends on experience

Working Days: 5 Days // 8am/8.30am - 5.30pm/6pm

Requirements

• Degree/Diploma with minimum 5years experience in Mechanical
• Must be from mechanical engineering background
• Preferably one or two process knowledge such as machining, sheet metal, plastics, and Moulding process
• Familiar with advanced GD&T + Auditing skill
• Calibration of simple tools and familiar with calibration standards
• Metrology skill that includes hands on experience in CMM, Smart scope (CMM knowledge is a must, preferably Zeiss CMM)
• Able to travel to JB for supplier visit or to our factory, when required
• Plastic injection molding knowledge is preferred

Job scope

• CMM Programming and training the other site Engineer and technicians
• Manage supplier part qualification process (SPQP) to ensure the quality of the delivery from supplier to comply to the processes.
• Complaint management that includes preliminary failure analysis, containment coordination, disposition coordination with supplier, RTV arrangement, follow up on 8D, and repair order delivery.
• Perform audits at supplier site for NPI pilot production process qualification, 8D implementation.
• Perform first article inspection at supplier site to ensure supplier have the measurement capability in terms of equipment and supplier technicians have the skill set required.
• Develop inspection plan/instruction for incoming inspection. ISO 8015 expert, conduct training to supplier on the common GD&T tools.
• Calibration management to ensure the equipment calibrated on schedule and also advance planning for measurement equipment for NPI parts.
• Material review board (MRB) management

The Supreme HR Advisory Pte Ltd | 14C7279

Ong Boon Kiet (Travys) | R22104769

Senior Recruitment Consultant

Responsibilities:

• Perform product inspection and/or audits of quality assurance in the production line, restaurants, events etc
• Perform packaging line and manufacturing inspection
• Ensures raw materials, in-process and finished products meet company standards
• Conduct Food Hygiene Audit checks at production line, restaurants, events etc and ensure any non-compliance are reported to management and resolved swiftly
• Responsible for spot check and inspection of finished goods to comply with specification and customer requirements
• Any other ad-hoc duties as assigned by the Company

Requirements:

• Candidate must possess at least a Diploma, Advanced/Higher/Graduate Diploma, Food & Beverage Services Management, Food Technology/Nutrition/Dietetics or equivalent
• Comfortable to handle administrative work in HACCP and/or other Food Safety Audits
• Relevant experience in Food & Beverage industry is an advantage

Whatsapp 91834574 for more information

As an Officer, Quality Distribution under Singapore Replenishment Centre, you are tasked to oversee quality system for the warehousing & repackaging operations that is responsible for our global manufacturing sites.

In this role, a typical day will include:

• Meet quality objectives set by management & comply to Alcon, QMS and Safety requirements.
• Support, perform and/or lead internal audits, supplier audits and external/regulatory audits, including updating and maintenance of system related to audits. Responsible for audit finding closure, as required.
• Responsible for supplier quality management (selection, qualification, and monitoring) and is the primary quality interface with the suppliers.
• Work with internal stakeholders and suppliers on resolving of quality issues to closure for all incoming & production rejects through supplier action request (SAR) process.
• Support site impact / gap assessment and remediation against new/revised External Standards and Corporate SOPs.
• Coordinate/Manage Management Review, consolidate monthly data and prepare monthly summary report for site quality metrics reporting into Global Platform.
• Timely initiation of NCRs and product on-hold activities.
• Conduct and support investigations for non-conformances, FAAs and customer complaints.
• Trend, analyze and monitor key performance indicators, suggest improvements, and escalate to supervisor/management as necessary.
• Identify improvement opportunities and lead/support the implementation activities to improve performance and efficiency.
• Review and approve distribution activities, such as change request, nonconformance, CAPA, escalation, SAR and customer complaints.
• Work with cross-functional teams to resolve operational quality issues.
• Performs any other duties as assigned by Supervisor according to business needs.
• Complies with all policies and standards.

WHAT YOU’LL BRING TO ALCON:

• Diploma, preferably in Science, Life Science, Engineering or other appropriate education and experience in pharmaceutical, medical device, or supply chain industry.
• 1-3 years of relevant experience in Quality Management system
• Added knowledge or experience with ISO 13485/ GMP standards would be highly advantageous but not a must

HOW YOU CAN THRIVE AT ALCON:

• Good team player
• Enjoy working with various cross functional team across manufacturing sites
• Comfortable to be based at Tanjong Penjuru (pickup from Jurong East MRT)

Alcon Careers

See your impact at alcon.com/careers

Job Descriptions:

- To support in ensuring the product quality in satisfying company and customer need and requirements

- To support in ensuring quality control through documentation such as maintaining of QC report, SOP specifications and test methods are available.

- Perform internal and external audit to compliance with QMS requirement.

- Support Production on all quality-related activities, including working closely with supplier and Engineering

- Participate in investigations and ensure CAPA findings, risks, recommendations, Non-Conformances reporting and outcomes are appropriate and are clearly documented and communicated

- Oversee implementation and improvement of IQC, IPQC, OQC process related to customer's products in a timely, efficient, and effective manner.

Requirement : -

- Ability to work under pressure

- Experience in Quality control under semi-conductor manufacturing equipment.

- Able to work independently

- Minimum Diploma qualification

- Able to work late if require.

Job Responsibilities:

· Review and approve documentations and ensure compliance to company standards

· Ensure adherence to quality procedures and regulatory requirements

· Maintaining of current system and identify trends/observations

· Conduct of internal audits to ensure internal controls are in place

· Facilitate and prepare regulatory submissions and attend to queries

· Adhoc tasks and projects as assigned

Job Requirements

· Minimum Diploma in a related discipline

· Minimum 4 years of quality assurance experience

· Experience within the Pharmaceutical industry would be an added advantage

· Able to start immediately or within short notice

Interested candidates, kindly email your detailed resumes in MS word format to [email protected]

Attention to Joseph Koh Wei Jie (R1873431)

Shortlisted candidates will be notified

www.ambition.com.sg

EA Registration Number: R1873431

Data provided is for recruitment purposes only

Business Registration Number: 200611680D. License Number: 10C5117

Location: Woodlands

Mon to Fri 8.30am to 5.30pm

Industry: Semicon Manufacturing

Salary: $3000-$4500

Job Description

• Manage customer complaints, corrective and preventive action programs.
• Work closely with customers, production and suppliers to meet the quality requirements.
• Responsible for product quality management, implement quality plans, drive quality improvement projects and prepare quality report to identify problem areas and work on problem resolutions
• Interface with and handle customers/vendors on quality issues.
• Issue and closure of CAR for customer (RMA) and Supplier issue – External
• RMA receipt and disposition of RMA in Macola – External.
• Work with QA department and Engineering on customer related issues e.g. RMA

Requirements:

• Degree / Diploma in Engineering (Electrical Engineering, Mechanical Engineering, etc).
• Knowledge of CMM, profile projector, and measuring equipments.

Please submit your updated resume in MS format by using the APPLY NOW BUTTON.

Alternatively, you may also email your resume to us at [email protected]

Emily Fong

Senior Talent Specialist

Atomrecruit Pte. Ltd. | MOM EA License No.: 15C7443

EA Personnel Reg No.: R1768368

AlwaysHired is representing our established client in the early childhood education space to recruit for a Quality Assurance Executive for Regulatory & Standards responsibilities. This position will be supporting their team onsite at their HQ office.

Job Responsibilities:

General Responsibilities

• Ensure that all services offered through the centres meet or exceed internal and quality assurance guidelines.
• Conduct audits on regulatory compliances, internal processes, procedures and potential highrisk
  non-compliances areas as per Regulatory Standards.
• Involved in initiatives to implement quality measures to raise the standard of early childhood
  care and education in child care centres.
• Ensure centres’ adherence and conformity to corporate identity and guidelines.
• Ensure the team provide a safe and nurturing environment for children that encourage their
  social, emotional, physical and intellectual development.
• To escalate issues and concerns to management in a timely manner.

Licensing and SPARK certification

• Familiar with ECDC Act
• Familiar with SPARK QRS-U.
• Ensure that the centres adhere and compliance to the regulatory standards.
• Develop action plan to meet Licensing & SPARKS criteria

Policies and Procedures

• To oversee, track and monitor centre’s corrective action responses, ensuring that centre’s
  principals, supervisors and staffs follow through all corrective action plans and review the
  effectiveness of such responses.
• Motivate the team to achieve operational effectiveness, ensuring ongoing organisational
  capabilities without compromising quality standards.

Requirements:

• Diploma in Early Childhood Care & Education (ECCE) or related discipline.
• At least 3 year(s) of working experience in the related field is required for this position
• Knowledge of quality/compliance management as well as regulations and standards in Early
  Childhood
• Experience with quality improvement systems
• Aptitude for reviewing data, strong analytical skills and meticulous
• Proficient in Microsoft applications such as Word, Excel and PowerPoint
• Preferably Junior Executive specialized in Quality Control/Assurance or equivalent.

We regret to inform that only shortlisted candidates will be contacted.

AlwaysHired Pte Ltd (24C2293) | Ong Jian Fu (Keith) (R1327244)

Job Description

• Industry/ Organization Type: Manufacturing/Production
• Position Title: Quality Technician/ Technician
• Working Location: North East (Transport provided).
• Working Hours: Monday – Friday, 8.30 am – 6 pm
• Salary Package: Up to $2300 + AWS
• Duration: Permanent Role

Key Responsibilities

• Ensure that the products being manufactured are up to both company and consumer quality standards.
• Inspect and evaluate materials and components provided by suppliers.
• Responsible for testing and identifying the frequency at which continuous or random tests are undertaken.
• Support in carrying out investigations on products that need enhancements based on customer specifications.
• Any other task as assigned by the Superior.

APPLY NOW!!!

• Minimum NITEC qualification in an Engineering field.
• Hands-on experience with measuring equipment such as vernier callipers and micrometer.
• Familiar with CMM programming like PC-DMIS.
• Flexible to work beyond the normal working hours should the need arise.

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 #67086 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 Objectives

Be Part of Process Assurance Team (PAT) supporting bank’s Project, Development and Service Delivery teams to ensure process compliance to System Development Methodology (SDM) process

The team acts as a quality gate for SDM major milestones to ensure entry & exit criteria are met and is responsible to review the quality of the artefacts such as functional & design specification, testing documents and others project deliverables.

The successful candidate will be working with Project and Technical Delivery managers to ensure high quality of
deliverables.

Key Responsibilities

• Establish controls and compliance checks on System development methology processes
• Design, formulate and enforce governance & compliance process improvement.
• Conduct quality gate review for SDM major milestones (analysis, design, build, test and deployment)
• Perform walkthroughs and interviews with project and application delivery managers to drive process adherence
• Report findings and provide consulting support in ensuring compliances with procedures
• Aside from day-to-day duties, there will be requirements to undertake other responsibilities such as management
reporting & other centrally driven project initiatives as needed

Key Requirements

• Degree in computer science/engineering or related disciplines
• At least 6 to 9 years of relevant experience in IT process compliance audit or Project Management
• Excellent written and verbal communication, interpersonal, organization and analytical skills a MUST
• Strong working experience with MS Office (Word, Excel, PowerPoint), MS Visio, MS Project and SharePoint
• Prior experience in IT risk management and security will be added advantage

About Air Liquide Advanced Materials (ALAM)

Air Liquide Advanced Materials (ALAM) is transforming the science of electronics and technology. Every day, breakthroughs are making technologies – from micro-processors, memory chips and flat panels to photovoltaic cells – even smaller and more powerful, opening up countless new possibilities in how the world lives, works and connects We innovate with atomic scale engineering to open up countless new possibilities in how the world lives, works and connects. Today, our ALOHATM and Voltaix® products are critical to the manufacture of the newest computer chips required for Big Data and the Internet of Things. To enhance our execution from discovery to delivery we are adding talented people to our team.

About The Business Line

https://electronics.airliquide.com/offer-brands/our-offer/electronics-advanced-materials

Work Location

Tuas west Avenue

Responsibilities:

• Lead and oversee a team of quality control technicians responsible for analyzing and managing raw materials, in-process materials, and finished goods.
• Champion a culture of safety and quality, ensuring adherence to company safety procedures and standards.
• Responsibilities include assigning work, implementing policies and procedures, and driving improvements in safety, analytical methods, equipment, and working conditions.
• Focus on enhancing employee relations, coaching and developing staff, resolving issues, and striving for continuous improvement in all areas.
• Manage department priorities, oversee training programs, resolve non-conformance issues, update standard operating procedures (SOP), and investigate root causes of contamination and quality issues.
• Review product Statistical Process Control (SPC)/ Statistical quality control (SQC) alerts, perform investigation as needed and respond with corrective and preventive actions.
• Responsible for providing regular reports, completing required training, evaluating employee competency, and ensuring compliance with safety protocols and plant documentation.

Requirements:

• Diploma / Bachelor Degree in Chemical Process Technology or equivalent qualification.
• Possesses more than 2 years of leadership experience, preferably in a quality related function or chemical manufacturing environment.
• Experience with gas chromatography (GC), Fourier-Transform Infra-Red (FTIR) and other on line analyzer equipment and sampling systems.
• Knowledge of analytical techniques used for characterization of trace impurities in chemicals.
• Proficient in Automation and control systems and is capable of implementing programming techniques and configurations.
• Strong leadership, team player, problem solving, interpersonal, organizational, and communication skills.
• Ability to manage multiple priorities satisfactorily.
• This position may be required to work on rotating shifts, and along with being flexible to changing schedules and shifts as needed.

**We thank you for your interest in Air Liquide. Interested applicants are encouraged to send in a detailed resume, including reasons for leaving for past employment. Please be informed that only shortlisted candidates would be notified.**

Job Info:

• Entitle AWS & VB
• Monday to Friday, 9 am to 6 pm
• Boon Lay, West Region

Key Responsibilities:

• Provide support to functional departments in ensuring food quality and safety during daily operations.
• Plan, organize, and coordinate to ensure the QA Department runs efficiently daily.
• Align with the company’s business objectives and collaborate with department leads to adjust responsibilities in line with GM’s strategic plans.
• Prepare monthly reports, such as Complaint Log, HACCP Objectives Summary, Demerit Point System Records, and GMP audits, for management submission.
• Gather and analyze data for trend analysis on non-conformities and improvement initiatives.
• Plan lab testing based on FG sensitivity levels to manage department expenses and stay within budget.
• Participate in and support quality system implementations, including audits by government agencies, certification bodies, and customers.
• Collaborate with all functional departments on process improvements, standards, and procedures documentation.
• Lead short-term projects, initiatives, or training programs and ensure timely completion.
• Report non-conformance issues related to food quality or safety to the relevant coach.
• Perform additional projects as assigned.

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RK Recruitment Pte Ltd | EA License No.: 20C0280
Chan He Guang | EA Personnel No.: R23117560

1. Perform analytical equipment lifecycle management as per current regulatory requirements / SOP.

2. Involve in equipment qualification, writing URS, reporting and implementing SOP’s for system operation and maintenance, monitoring performance of the equipment and decommissioning of equipment.

3. Support and / or perform maintenance / calibration of laboratory equipment in compliance with established schedules.

4. Liaise with vendors/service providers for PM / Calibration in a timely manner.

5. Responsible for maintenance / calibration planning of equipment within QC Department.

6. Ensure real time documentation, maintain data integrity and appropriate traceability.

7. Responsible for the accurate, timely and compliant execution of assigned projects and related documentation.

8. Assist / perform method validation and transfer as required.

9. Conduct QC Department equipment operation and maintenance training to QC staff as required.

10. Perform and / or support in maintaining the asset register for equipment in the QC Department.

11. Initiate CAPEX for equipment purchase.

12. Responsible for QC lab and equipment/instrument cleanliness.

13. Any other activities as and when assigned by the Superior.

KEY DUTIES AND RESPONSIBILITES:

• Preparation and review of qualification documents e.g., User requirement specification, DQ, IQ, OQ and PQ protocol for equipment, utilities & facility in compliance with the regulatory guidelines.

• Execution of qualification and validation activities including process, cleaning, computer system, equipment, utilities, and facility.

• Candidate must have knowledge and experience of qualification/validation principles and their practical application.

• Preparation and review of process and cleaning validation protocols and reports.

• Coordinate with the cross functional team and external service provider to meet qualification & validation schedules and maintain equipment, systems, and processes in validated state.

• Review equipment and process related change control; perform Risk Assessment to determine criticality of the proposed changes.

• Write, review, and revise validation SOPs in compliance with regulatory guidelines.

• QA oversight and/or review during the validation process.

• Manage incidents and deviations related to validation & qualification.

• Perform compliance reviews of all applicable deviations, investigations, and CAPAs related to qualification and validation.

• Review and suggest continuous improvements to the Validation Master Plan, current quality system practices, validation protocols and procedures for newly installed equipment, and overall validation strategies.

• Cross train and develop expertise in other areas of validation.

• Must be able to interact and lead effectively in a team-based environment.

• Familiarity with regulatory/compliance environment.

EDUCATION & EXPERIENCE

• Degree a scientific discipline or equivalent.

• Experience in a regulated industry preferred.

• A minimum of 5-7 years’ relevant experience in pharmaceutical manufacturing environment.

• Proficient in the use of Microsoft Word, Excel, Access, PowerPoint, and Explorer.

KEY DUTIES AND RESPONSIBILITIES

1. Preparation, execution and review of computer system validation protocols and reports.

2. Preparation and management of CSV deliverables for laboratory instruments and systems, manufacturing equipment, utility systems, IT, and enterprise systems.

3. Ensure the Computer System Validation is in alignment with the Validation Master Plan for Computer Systems.

4. Ensure timely completion of all validation related activities including computer system, equipment, utilities, and facility with compliance.

5. Perform assessment of vendor documents for CSV deliverables.

6. Conduct risk assessments to identify potential risks associated with computerized systems, including data integrity, security, and regulatory compliance.

7. Preparation and review of standard operating procedures to establish and maintain the quality system of the organization.

8. Participate in CFT meeting related to IT systems and ensure the completion of pending actions.

9. Periodic Review of IT application and systems implemented and compilation of reports.

Education and Experience

Diploma or Degree in IT or equivalent.

A minimum of 5-7 years’ relevant experience in pharmaceutical manufacturing environment.

Experience in electronic validation system, QMS, ERP system, SCADA, is preferred.

Proficient in the use of Microsoft Word, Excel, Access, PowerPoint, and Explorer.

Job Scope

• Responsible to review and approve master batch records and subsequent batch records
• Review and approve cleaning records and procedures and ensure compliance with set
• Review and approve GMP documentation Ensure adherence to quality procedures, regulatory requirements and cGMPs.
• Review and approve deviations according to the site procedures
• Handle product complaints.
• Ensure complaints are investigated thoroughly with CAPAs effective to prevent recurrence.
• Coordinate with cross-functional team to prepare Annual Product Reviews, discuss trends and atypical observations and recommend improvement actions.
• Conduct internal and external audits
• Maintain inspection readiness and support inspections from regulatory agencies and customers.
• Actively participate in GMP walk downs to ensure site operation and facility maintained in inspection ready state.
• Support the maintenance of validated stated of GMP systems and processes.
• Facilitate and prepare regulatory submissions and attend to regulatory queries in a timely manner

Requirements

• A Bachelor Degree in Science / Chemical Engineering or equivalent with relevant pharmaceutical experience.
• Minimum 1-3 relevant years of experience in QA/QC and GMP Compliance
• Familiar with manufacturing operations applications; six sigma and lean principles and process improvement tools.
• Thorough knowledge of GMP compliance regulations, ICH Q7a Guidelines, Good Documentation Practices and other applicable regulations.
• Proven track record of continuous improvement in quality operations or manufacturing.

All qualified applicants, please send in your resume to:
[email protected]

Tricia Celestine Goh (R1981653)
Recruit Express Pte Ltd | Company Reg. No. 199601303W | EA License Number: 99C4599

Responsibilities:

• Perform product inspection and/or audits of quality assurance in the production line, restaurants, events etc
• Perform packaging line and manufacturing inspection
• Ensures raw materials, in-process and finished products meet company standards
• Conduct Food Hygiene Audit checks at production line, restaurants, events etc and ensure any non-compliance are reported to management and resolved swiftly
• Responsible for spot check and inspection of finished goods to comply with specification and customer requirements
• Any other ad-hoc duties as assigned by the Company

Requirements:

• Candidate must possess at least a Diploma, Advanced/Higher/Graduate Diploma, Food & Beverage Services Management, Food Technology/Nutrition/Dietetics or equivalent
• At least 2 years relevant experience
• Comfortable to handle administrative work in HACCP and/or other Food Safety Audits
• Relevant experience in Food & Beverage industry is an advantage

Whatsapp 91834574 for more information