369 Product Validation jobs in Singapore
Quality Assurance
Posted today
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Purpose:
To operationalise efforts that ensures the company's products and solutions complies/exceeds the regulatory requirements, provides assurance(s) in quality to meet/exceed set specifications, and promotes the growth of the business in Asia.
Main Duties:
- To operate and support the objectives and duties of the Regulatory Affairs & Quality Assurance department in enhancing and assuring the products and solutions meets/exceeds the regulatory requirements, standards of quality, and promotes customers' satisfaction.
- To support and fulfil the enquiries, documentation, declarations, and requirements of institutions / authorities enforcing standards and regulations in the region, as per department manager direction.
- To identify, research, review, facilitate and support the department manager on addressing issues pertaining to certification, quality and standards of the company's products and solutions (e.g. Good Manufacturing Practices (GMP), Halal certification, International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH),etc.).
- To liaise, facilitate and support the end-to-end movements of raw materials, processes, and final products, through the provision of accurate documentation/reporting (e.g. declarations, technical papers, dossier, product instructions, etc.) as required by other departments (e.g. logistic, sales, etc.) and different offices of PLUMINO Group. Also, to liaise with relevant external parties that requires assurances in the products through delivery of technical documentation, presentations or other appropriate methods.
- To liaise and work with relevant parties (internal and external parties) in obtaining, documenting, reviewing and recording technical documents (e.g. product specifications/instructions, MoA, CoA, MSDS, packing specification, SDS, etc.); and ensuring quality, methodologies, analysis and outcomes meets/exceeds current established requirements.
- To review, report, record, update and action to achieve the company's internal regulatory affairs activities, customer's technical/specification enquiries (including Pharmacopeia compliance) and the company's response, quality assurance efforts, and any other initiatives that impacts the products' quality, standard and stated assurances, as per department manager direction.
- Schedule, support/manage, and execute internal/external audit(s) on the quality/standards in new/old products, raw material(s), preparation/manufacturing methods and processes, packaging of materials and products, storage, and transportation of the goods, to ensure compliance to the company's, regulators and standards bodies/institutions' requirements. Also, to assess, record, and report to the department manager on areas that pose current or potential risk(s) and shortcoming(s), and possible Corrective and Preventive Actions (CAPA).
- To investigate, analyse, and report to department manager of internally/externally established challenges on quality (e.g. product efficacy, cargo damage, product complaints, certification, etc.) or non-conformity to assured standards. Also, establish resolution with department manager in addressing experienced challenges while meeting the company's objective(s) and established standards/requirements.
- To document, report, record and update internal records of customer requests or complaints, audit results, quality incidents/issues (with evidence/observation and resolution included), technical requirements/updates to be accessible and reviewed by the department manager.
- To collaborate closely with other departments and the management to protect the value offering of the company and to support the achievement of the company's planned objectives.
General Responsibilities:
- To establish, maintain, and continuously improve the company's quality management system to ensure compliance with local regulations in Singapore, as well as GMP, GDP, and relevant regulatory requirements.
- To Review and approve quality-related documents, including quality agreements, SOPs, change control, and deviation handling
- To support the ongoing efforts of the organization to achieve aspired and planned goals/outcomes.
- To support fellow employees and leaders of the organization to achieve positive business outcomes.
- To work and operate within the boundaries of legal regulations, the values of the organization, and the standards established by the company and industry.
Relationships:
- Reporting to and actively supporting the Regional Regulatory Affairs & Quality Assurance Manager of HQ.
- Work closely with 'Sales' department to support customers' enquiries.
- Work closely with 'Accounting' department for financial matters.
- Work with 'Logistic' department (both locally and globally) for logistic and warehousing arrangements, audits, and documentation.
- Work with the company's global manufacturing plants on to secure the company's product quality and standards, and to facilitate precise policing and reporting.
- Work with regulatory bodies to update and comply with regulatory requirements when needed.
Qualifications:
- A minimum of a Bachelor's degree in a related subject.
- A minimum of 1-3 year of Quality Assurance / Regulatory Affairs experience in a company manufacturing of pharmaceutical, or nutraceutical products.
- Strong ability to write technical documentations and reports.
- Good interpersonal skills that support a small and highly interdependent team.
- Strong ability to communicate clearly with others of varied levels and culture, to achieve main responsibilities.
- Confident command of English and Chinese.
CAPA
Quality Control
Quality Management
Quality Assurance
Interpersonal Skills
Regulatory Affairs
Oncology
ISO
GMP
Raw Materials
Assurances
Compliance
Packaging
Audits
Change Control
Regulatory Requirements
Manufacturing
Audit
Quality Assurance
Posted today
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Job Description
Location: Tuas (Walking distance from MRT)
Working hours: Monday to Friday (8.00 am to 5.15 pm)
Salary: $4,000 - $5,000
Main Duties:
- Responsible for collaborating with all Business Units' (BUs) to collate and analyze monthly data for performance trend analysis and prioritize quarterly governance action plans
- Working together with BUs' on external audits, Request For Change (RFC), quality risk assessment, to identify continuous improvement areas, with aim to promote food safety culture within the organization
- Act as leader for GTQM Resource Database
- Maintain and update resource documents for Group TQM and BUs as per company's requirements.
- Support to create Group R&D policies, guidelines, and procedures aligned with international standards.
- New / alternative vendor qualification for ingredient (RM), Packaging (PM)
- Activities include document review, supplier liaison, technical assessment, and audits to meet standards before listing on the Approved Vendor List.
- New lines / change of equipment Process Qualification PQ, which involves sterility test plan designing and execution; cleaning and sanitation (CIP) and Hygiene verification to meet requirements
- To develop and maintain Quality Plan program for all Business Units, coordinate and engage BUs' key stakeholders for Quality Plans alignment for implementation
- Any other assignments /projects that assigned by superior, to meet business needs
Requirement
- Min. Degree holder in Food Technology, Food Science or related Science / Engineering fields
- Has minimum 5 years QA/QC working experience in dairies / beverage industry
- Willing to travel for business purposes
- Possess knowledge and experience in food packaging qualification, certified lead auditor are added advantages
If interested, please send me your most updated resume to WA: or email me at:
All candidates' information will be treated with the strictest confidence
Katherine Carlen
CEI.No: R
Recruit Express Pte Ltd
EA Licence No: 99C4599
Tell employers what skills you haveVerbal Communication
Risk Assessment
Food Safety
Quality Assurance
Release Management
Sanitation
Test Cases
Trend Analysis
Auditor
TQM
Food Technology
Packaging
General Insurance
Audits
Food Science
Document Review
Quality Assurance
Posted today
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Job Description
Eterna Indonesia is a leader in technology development with a special focus on pioneering web and software solutions. Our commitment to innovation and excellence motivates us to grow our team. We are currently seeking a highly skilled and motivated QA to manage our CRM project for solar energy initiatives and ensure the highest quality standards.
Role Overview:
The QA will work from a virtual office server in Discord, overseeing project management tasks and quality assurance processes. This role involves working as an outsourced agent for a pioneering tech company based in the USA, adhering to working hours from 3 PM WIB to 12 AM WIB.
Key Responsibilities:
Project Management:
Plan, execute, and finalize projects according to deadlines.
Coordinate the efforts of team members and senior management to deliver projects according to plan.
Define project scope, goals, and deliverables that support business goals in collaboration with senior management and stakeholders.
Develop full-scale project plans and associated communications documents.
Effectively communicate project expectations to team members and stakeholders in a timely and clear fashion.
Manage project dependencies and critical path.
Track project milestones and deliverables.
Quality Assurance:
Develop and execute test plans to ensure product quality.
Test new features built by the team to ensure they function as intended with no bugs or issues.
Identify, record, document thoroughly, and track bugs.
Perform thorough regression testing when bugs are resolved.
Collaborate with developers and product managers to identify system requirements.
Stay up-to-date with new testing tools and test strategies.
Mandatory Qualifications:
Proven working experience in project management and quality assurance in the information technology sector.
Familiarity with Atlassian tools, including Jira.
Solid technical background with understanding and/or hands-on experience in software development and web technologies.
Strong familiarity with project management software tools, methodologies, and best practices.
Experience with quality assurance methodologies, tools, and processes.
Excellent client-facing and internal communication skills.
Excellent written and verbal communication skills in English.
Strong organizational skills including attention to detail and multitasking skills.
Ability to work from 3 PM WIB to 12 AM WIB.
Preferred Qualifications:
Any certifications in Project Management (e.g., PMP, PMI-ACP) and Quality Assurance (e.g., ISTQB, CSTE).
Familiarity with programming and the tech stack of our client's app.
Experience working in virtual office environments and using Discord for daily communications.
Familiarity with all the tools needed for this role.
Join Our Team:
Eterna Indonesia offers a dynamic work environment, opportunities for growth, and the chance to be part of an innovative team. If you have a passion for project management and quality assurance, and a dedication to excellence, apply now!
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Quality Assurance
Posted 4 days ago
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Job Description
- Oversee incoming, IPQC, outgoing inspection.
- Establish & maintain SOP and Work Instruction (WI).
- Perform daily, weekly & monthly QA reports.
- Analyze and trouble-shooting production quality issues.
- Handle customers’ complaint (CAR) with effective corrective actions and close 8D on time.
- Provide training to QC inspectors.
- Perform QC inspectors’ job assignment.
- Conduct regular line audit and drive for quality improvement.
- Conduct internal ISO audit and manage external customer audit.
Job Requirements:
- At least 2 years of experience in quality assurance.
- Able to read engineering drawing.
- Knowledge in GD&T and basic measuring equipment.
- Those with experience in using CMM will be considered favorably.
- Knowledge of ISO 9001:2015 Quality Management System.
- Knowledge in MS Excel.
- Able to communicate in Mandarin, in order to liaise with Mandarin speaking associate
Quality Assurance Manager
Posted 6 days ago
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Job Description
Quality Assurance Manager
Job Responsibilities:
+ Provide specialized technical knowledge of quality systems and tools and management expertise in support of project Quality programs
+ Establish and implement QA/QC in the engineering design environment and in support of procurement activities
+ Develop, maintain and improve quality procedures to meet project specific requirements
+ Plan and implement quality induction and training for project personnel as well as internal Quality audits across a multi discipline engineering design team
+ Make recommendations for corrective and preventive action strategies
+ Apply quality tools for problem solving and verify contractually required standards for project execution are met
+ Interface with Class society and Independent Verification bodies to support project regulatory compliance requirements.
+ Interface closely with engineering to establish quality requirements for equipment packages / materials. Provide Quality inputs to technical bid evaluation work process.
+ Monitoring the project works and update performance matrices and status reports.
+ Accountable, under general direction, for the performance and results of the project Quality discipline
+ Lead and manage QA team including Lead / Senior Quality specialists
Job Requirements:
+ Possess tertiary qualifications in Quality Management, Engineering or Project Management
+ Have at least 10 years of related work experience including:
- developing Quality programs that meet ISO9001 and ISO 45001requirements for engineering design and procurement support; and
- design projects for Offshore (FPSO/Platforms) and Onshore (Refineries, LNG facilities, Storage terminal etc)
+ Those with recognized Lead Auditor qualification (ISO 9001), Lead Auditor Qualification (ISO14001 and OHASA18001) would be highly regarded
+ Strong understanding and familiarity with industry codes & regulations
+ Substantial offshore oil and gas experience, including recent experience in quality management within a multi-discipline engineering business
+ Previous track record in leading and managing a team
+ Possess a high level of resilience and positive work attitude
+ High level of accuracy and attention to detail
+ Excellent project management and coaching skills
+ Strong analytical and problem-solving skills
+ Strong people-oriented mindset
+ Possess the confidence and maturity to deal with professionals at all levels
+ Willingness to learn and deliver timely and quality results to internal stakeholders
Associate Quality Assurance
Posted 6 days ago
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Job Description
**Amgen Singapore Manufacturing**
**HOW MIGHT YOU DEFY IMAGINATION?**
Amgen is one of the world's leading independent biotechnology companies. For over 4 decades, Amgen has pioneered biotechnology breakthroughs, to bring state-of-the-art medicines from laboratory to the patient. Amgen has not only discovered and developed innovative human therapeutics, but has invested in cutting edge manufacturing capability and support services to deliver these exciting therapies to medical teams around the world. Japan and Asia Pacific (JAPAC) is the fastest growing region in Amgen. Now we are hiring an **Associate Quality Assurance** in **Amgen Singapore Manufacturing** .
**Live**
**What you will do**
The Incoming Quality Assurance (IQA) Associate position will provide support for the IQA team, which is part of the Lot Disposition group of the Quality Assurance function. The role will be based out of Amgen Singapore Manufacturing (ASM) or one of its partner 3rd Party Logistics Service Provider (LSP) and will work under the general supervision of the hiring manager.
The IQA team provides expertise in performing inspection, sampling and testing of incoming materials to meet Amgen specifications and ensure a constant supply of raw materials for ASM. The team provides these crucial services to ensure only the highest quality raw materials are used to create products for our patients.
Main Responsibilities:
+ Comply with safety guidelines, cGMPs (Good Manufacturing Practices) and other applicable regulatory requirements
+ Complete required assigned training prior to execution of required tasks
+ Perform raw material inspection, sampling and rapid ID testing in accordance to written SOPs and Methods.
+ Generate complete and accurate documentation using electronic or handwritten systems.
+ Review records to ensure raw materials are tested and inspected according to specification and SOPs
+ Perform business operations related to inspection/sampling/testing (i.e updating dashboards, relevant metrics, housekeeping, inventory management, audit support)
+ Support site/network Continual Improvement initiatives
+ Ensures facilities, equipment, materials and procedures comply with cGMP practices and other applicable regulations
+ Alert management of quality, compliance, supply and safety risks in a timely manner
+ Participate in raw material issues or deviations
+ Performs additional duties as specified by management
All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional tasks and responsibilities.
**Win**
**What we expect of you**
**Basic Qualifications**
+ Bachelor's Degree and 2 years of directly related experience OR
+ Associate's Degree and 4 years of directly related experience OR
+ High School Diploma / GED and 6 years of directly related experience
+ 2 years of experience in regulated environment
+ Experience and basic troubleshooting skills with laboratory and process equipment
+ Experience with LIMS, SAP, TrackWise
+ Ability to understand, apply and evaluate basic chemistry
+ Ability to adhere to regulatory requirements, written procedures and safety guidelines
+ Ability to evaluate documentation/data according to company and regulatory guidelines
+ Ability to interact with inspectors (internal and external)
+ Ability to interpret and apply Good Manufacturing Practice (GMP) knowledge
+ Ability to organize work, handle multiple priorities and meet deadlines
+ Detail oriented as well as flexible and adaptable to changing priorities and requirements
+ Ability to perform computer operations, such as ability to navigate in MS Office and complete Computer Based Training (CBT)
+ Ability and willingness to work any shift in support of operations, which may include the occasional night or weekend shift, as required.
+ Ability to handle first tier problem solving that may involve cross functional interactions
+ Pass eye exam (corrected or uncorrected) in order to be qualified to perform visual inspection of raw materials. Failing these disqualifies a staff member from performing essential activities for the role.
+ Color Vision: Normal via Ishihara testing methods.
+ Stereo Depth Perception: (corrected or uncorrected) Stereo Depth less than or equal to 100 Arc Seconds.
+ Near Vision: (corrected or uncorrected) of 20/20, both eyes together.
Your selection for this role will be subject to fulfilling the medical requirements of this job scope. If so, you will be informed of the medical check(s) that you may need to undergo. All medical related expenses incurred from this medical check shall be borne by the company.
**Thrive**
**What you can expect of us**
As we work to develop treatments that take care of others, so we work to care for our teammates' professional and personal growth and well-being.
+ Vast opportunities to learn and move up and across our global organization
+ Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
+ Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
**Apply now**
**for a career that defies imagination**
In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.
**careers.amgen.com**
**Equal Opportunity Statement**
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.
Quality Assurance Intern
Posted today
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**Description**
The candidate will be working directly with the Quality Assurance Team in Singapore to support present improvement projects that overlook the day-to-day business operations and processes by performing data analytics, trend interpretation and execute applied forecasting for the business operations. Through on-the-job training, he/she will assist to develop and monitor various performance metrices and support business transformation activities that aim to rapidly detect and resolve potential anomalies, provide agile and transparent reporting, optimize capture performance, and thus improve business efficacy and efficiency. Additionally, with excellent data management and visualization, strong attention to detail, and critical thinking skills, the incumbent will provide strategic and data-driven business insights to allow for the direct improvement of the organization's operations and attainment of business objectives.
**JOB DESCRIPTION:**
**1.** **Modelling & Analytics**
**a.** Collect, process, and analyze data to identify anomalies and patterns in Quality Indicators.
**b.** Draw valid inferences, prepare insights in both narrative and visual formats, such as a dashboard.
**2.** **Business Intelligence**
**a.** Conduct statistical analysis pertaining to the day-to-day operations and processes to support business growth, optimization, and strategy development.
**b.** Develop and maintain refined analytic dashboards and models that allows for enhanced visualization and easy real-time data access to encourage operational efficiency and efficacy.
**3.** **Applied Forecasting**
**a.** With the use of business analytic tools, categorize and analyze quality and operational issues.
**b.** Track data and apply quantitative and qualitative forecasting methods to determine patterns and encourage better decision making.
**4.** **Special Projects**
**a.** Develop and maintain various records, dashboards, and visual automations as part of digital transformation to increase analytical accuracy, efficacy, and efficiency.
**b.** Deep dive into data management and architecture to identify gaps and justify the need for improvements, as part of continuous improvement projects. **5.** **Others**
**a.** Support the MRO Team & Operations' activities and projects.
**b.** Support the Quality Assurance team in the development and execution of new initiatives and projects.
**Qualifications**
**JOB REQUIREMENTS:**
* Major in Engineering or Data Science is preferred.
* Background in Aviation is a plus.
* Result-driven and passionate about building value-added deliverables for the company.
* Keen interest in data visualization, data management, business analysis, and strategic thinking.
* Excellent analytical, critical thinking, and problem-solving skills.
* Data-driven individual with attention to detail and accuracy.
* Entrepreneurial mindset and willingness to go the extra-mile is a plus.
* Initiative and self-motivated individual.
* Excellent interface with Microsoft Suite
* Experience in PowerBI, Tableu, Visual Basic, Excel Macros, and programming is a plus.
* Fluent in English (written and oral).
* Fluency in a 2ndlanguage (written and oral) is a plus
**Recruiting Company:** Bell Textron Inc.
**Primary Location:** Singapore-Singapore
**Job Function:** Quality
**Schedule:** Full-time
**Job Level:** Individual Contributor
**Job Type:** Internship / Co-Op
**Shift:** First Shift
**Job Posting:** 08/22/2025, 6:06:18 AM
**Job Number:**
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Quality Assurance Professional
Posted today
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Job Description:
">We are seeking a highly skilled Quality Management Specialist to join our team. In this role, you will be responsible for collaborating with Business Units to analyze monthly data, identify trends and prioritize quarterly governance action plans.
">Key Responsibilities:
">- Work closely with Business Units on external audits, Request For Change (RFC), quality risk assessment to improve processes.
- Lead the GTQM Resource Database and maintain resource documents.
- SUPPORT document maintenance and user access requests.
- Create Group R&D policies, guidelines and procedures aligned with international standards.
- New vendor qualification for ingredients, packaging and equipment.
Qualifications:
">- Degree in Food Technology, Food Science or related field.
- 4-5 years QA/QC experience in dairy/beverage industry.
- Certified lead auditor an advantage.
What We Offer:
">A dynamic work environment, opportunities for growth and development, and a competitive compensation package.
Quality Assurance Professional
Posted today
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Job Description
We are seeking a highly skilled Quality Assurance Specialist to join our team.
The successful candidate will be responsible for ensuring the highest quality of work in our projects, from planning to completion. This involves conducting regular inspections, reviewing technical documents, and collaborating with various stakeholders to identify and address potential issues.
In this role, you will have the opportunity to work on complex projects, develop your expertise in quality assurance, and contribute to the growth and success of our organization.
We offer a dynamic and supportive work environment, opportunities for professional development, and a competitive compensation package.
To be considered for this position, please submit your resume and a cover letter outlining your qualifications and experience.
Quality Assurance Specialist
Posted today
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Job Description
This role involves ensuring compliance with various regulations, federal, state, and local, as well as corporate policies to avoid business disruptions. The incumbent will communicate identified compliance and quality risks to their supervisor.
- Conduct compliance assessments of sites and cross-site Quality Systems, including process inspections, facility inspections, equipment reviews, record checks, and training records.
- Review SOPs, protocols, batch records, reports, and quality records for accuracy and compliance with applicable regulations and internal policies.
- Participate in the development of recommendations for corrective and preventative actions to respond to client visit and regulatory inspection findings.
- Perform site-wide applicable regulations or standards (ISO/GLP/GMP) training sessions, as developed and approved by senior Quality Systems team members.
- Assist in the preparation of support during regulatory inspections, as required.
- Maintain written and signed records of all audits and inspections, and may sign records documenting audit performance and reporting to management.
Responsibilities Continues
- Facilitate facility and equipment record and logbook reviews.
- Approve customer test reports and participate in reagent release activities to support laboratory operations.
- Assist in correcting regulatory risk areas identified by Senior Quality Systems team members.
- Inspect and audit subcontractors, vendors, and suppliers of products and services.
- Support the analysis and collection of site Quality Metrics via QMS.
- Support preparations for Quality Management Review (QMR).
- Implement process improvements for dashboard analysis and analyze metric data for QMS.
- Support Quality Assurance projects.
- Deliver basic regulatory training to operations personnel.
- Respond promptly to Customer inquiries to support qualification and regulatory requests.
To be successful in this role, you should possess:
- A min Bachelor's degree or equivalent, preferably in a life science.
- A minimum of 2 years of experience in a Quality Assurance role.
- Strong attention to detail and writing skills are essential.
We offer a comprehensive benefits package that includes:
- Professional growth opportunities
- Ongoing training and development programs
- A collaborative work environment