What Qa Tester Jobs are in Singapore?

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher's ( 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.
You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System ( which makes everything possible.
The QA Operations Coordinator is responsible for supporting the Quality Assurance (QA) function by coordinating daily QA operations with various functions, ensuring product quality compliance and on-time release of product. The QA Operations Coordinator is responsible for managing, updating, controlling and archiving quality records and SOPs. Functions as a bridge between various functions to ensure timely completion of training, and document accuracy.
This position reports to the QA Manager and is part of the QA team located in Singapore Tuas site and will be an on-site role.
What you will do:
+ Filing and archiving cGMP documents as directed, ensuring that the procedures, forms and records are reviewed and revised according to schedule, performing record archival and ensuring that cGMP records are organized and retained according to record retention periods.
+ Ensuring that product labels are printed in accordance with approved product specifications and supporting batch record management by facilitating and coordinating the flow of batch records across different functions.
+ Supporting training program by liaising closely with various functions to ensure timely completion of training, and other quality-related activities such as customer audits, ensuring that records and documents required are being consolidated as a form of audit preparation process.
Who you are:
+ High School Diploma, GED or local equivalent
+ Computer literate (Word, Excel, Oracle database, Electronic Documentation System) to create spreadsheets, e-mail, memos, graphic, etc. and technical writing skills (create and edit complex procedures)
+ Possess effective time management and organizational skills; able to balance multiple priorities and having the ability to interact and communicate effectively with both internal and external stakeholders
It would be a plus if you also possess previous experience in:
+ An industry in a manufacturing/lab environment with cGMP exposure
Cytiva , a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job.
#LI-TW1
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .

**Manager Quality Control (Micro and Sample Management)**
**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 a **Manager Quality Control (Micro and Sample Management)** in **Amgen Singapore Manufacturing.**
**Live**
**What you will do**
In this vital role, you will be responsible for QC Microbiology Shift teams. Responsibilities include leading and supervision of staff, maintenance of the weekly lab schedule and prioritization of daily work tasks. Providing Quality oversight to ensure that processes are followed in accordance to current Good Manufacturing Practices (cGMP). The Manager will ensure that facilities, equipment, materials, organization, processes, procedures and products align with cGMP practices and other applicable regulations. Perform review, approval and tracking of cGMP processes, procedures, documents and records, including but not limited to nonconformance records and CAPAs.
Under minimal supervision, the Manager Quality Control will be responsible for overseeing day to day activities in microbiology (including but not limited to routine environmental & utilities monitoring; raw material and product testing such as bioburden, microbial limits test, endotoxin, qPCR, microbial ID; media, reagent and culture qualification such as growth promotion; etc.), sample management and stability (including but not limited to sample logging, receipt and processing, sample aliquoting, movement and storage of samples, stability initiations and time point pulls, etc.). The Manager Quality Control will collaborate with the global Amgen QC network and provide on-site support and collaboration for both biologics and small molecule manufacturing.
Additional Responsibilities:
+ Responsible for presenting the QC Microbiology lab area during audits and inspections
+ Functional Area Owner for microbiology testing, stability processing and shipment deviations
+ Oversight of Microbiology laboratory investigations
+ Lead laboratory troubleshooting and problem-solving exercises
+ Manage Contract Test Lab sample lifecycle (purchase orders to results)
+ Oversight of LIMS Lot Authorization and on-time lot disposition deliverables
+ Responsible for ensuring compliance with safety guidelines, cGMPs and other applicable regulatory requirements.
+ Support staff training, career development and performance management.
+ Support site and global initiatives
+ Support the implementation of new equipment and technologies
+ Supports Continual Improvement and LEAN initiatives, programs and projects
+ Ensures that changes that could potentially impact product quality are assessed according to procedures
+ Ensures that deviations from established procedures are investigated and documented per procedures
+ Ensures that records are complete, accurate, and documented according to written procedures and cGMP requirements
+ Collaborates cross functionally as needed to ensure the Quality Management System processes are executed in accordance with established procedures
+ Alerts senior management of quality, compliance, supply and safety risks
+ Represents the quality unit during audits and inspections
+ Supports internal/external audits and inspections as part of the audit/inspection management team
**Win**
**What we expect of you**
**Basic Qualifications**
+ Doctorate degree OR
+ Master's degree and 2 years of Quality or Operations related experience OR
+ Bachelor's degree and 4 years of Quality or Operations related experience OR
+ Diploma and 8 years of directly related experience
+ Strong knowledge and understanding of microbiology testing methodology and strategy for contamination control
+ Knowledge and experience with general GMP laboratory operations, data integrity requirements and associated laboratory equipment
+ Experience with computerized laboratory information management systems, electronic laboratory notebooks and other QC analytical equipment
+ Ability to lead diverse teams
+ Good communication skills (technical writing and verbal communication/presentation)
+ Ability to work in cross-functional and multisite teams
+ Interact effectively with variety of communication and working styles
+ Problem solving skills with the ability to apply logic and assess data to reach decisions and solutions related to compliance and product quality.
**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
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.
**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.

**Specialist Quality Assurance**
**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 a **Specialist Quality Assurance** in **Amgen Singapore Manufacturing.**
**Live**
**What you will do**
Responsible for providing oversight and leadership for quality systems execution and operations support, the Specialist Quality Assurance will support manufacturing operations and IPC testing through presence on the floor, and support of complex manufacturing investigations, change control, and unexpected result investigations.
Main Responsibilities:
+ Provide Quality oversight to plant operations, ensuring appropriate application and execution of GMP compliance requirements and Amgen Quality Management System in plant operations through phases of commissioning, process qualification, regulatory approval and market supply
+ Support routine GMP documentation review activities (e.g. electronic batch records, SOPs, logbooks, work orders, batch production reports and validation protocols etc.) and ensure key performance indicator met targeted metrics
+ Co-lead and support the deployment of Amgen quality systems, including management review, validation, change control and CAPA and ensure that the systems are managed in compliance with cGMP expectations
+ Participate in complex root cause investigations for deviations
+ Review and approve deviation investigations, change controls, and other quality records (with focus on highly complex records)
+ Provides Quality Assurance support in New Product Introduction (NPI) team
+ Coach site Quality Assurance professionals on resolution of complex problems
+ Participate in regulatory inspections, and interact directly with regulatory inspectors
+ Supporting other Quality Assurance initiatives/activities such as continuous improvement projects, supplier quality, stability program, product quality review, customer complaint investigation.
**Win**
**What we expect of you**
**Basic Qualifications**
+ Doctorate degree OR
+ Master's degree and 2 years of directly related experience OR
+ Bachelor's degree and 4 years of directly related experience OR
+ Diploma and 8 years of directly related experience
+ 8 years related work experience (manufacturing, process development, or quality assurance) in the pharmaceutical / biologics industry with progressively increasing responsibility and demonstrated experience in project management, quality assurance, and quality systems.
+ Direct experience with bulk manufacturing of biopharmaceuticals/API preferred.
+ Demonstrated proficiency of written and verbal communication skills (including technical writing and presentations) with ability to communicate and collaborate effectively with technical and senior management staff.
+ Experience with regulatory audits and inspections
+ Problem solving skills with the ability to apply logic and assess data to reach decisions and solutions related to compliance and product quality.
**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
**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.**
**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.

**Senior Associate Quality Assurance**
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 a **Senior Associate Quality Assurance** in **Amgen Singapore Manufacturing.**
**What you will do**
The Senior Associate QA will be required to perform 12-hour shift (rotational night and day, or full night shift as required due to business needs).
Main Responsibilities:
+ Quality Professional with background and experience in commercial production of Biological drug substance to oversee night shift or day shift operations as required.
+ Conduct Quality Assurance activities related to quality floor support for solution and equipment preparation, cell culture and product purification & Drug Substance Filling operations.
+ Support of electronic batch record review and approval, change control, investigations and product release
+ Work in a cross functional team with Process Development, Manufacturing, Supply Chain, Engineering and Facilities to ensure product quality and market supply
+ Role may include participation in new product introductions, additional equipment, installation commissioning, qualification.
+ Support continuous improving initiatives
**Win**
**What we expect of you**
**Basic Qualifications**
+ Masters Degree OR
+ Bachelor's Degree and 2 years of directly related experience OR
+ Associate's Degree and 6 years of directly related experience OR
+ High School Diploma / GED and 8 years of directly related experience
+ Preferred 5+ years of relevant work experience in the commercial manufacturing environment within the pharmaceutical / biologics industry and understanding of GMP pharmaceutical production, biological drug substance experience and operation
+ Experience with batch record review, and quality record support
+ Experience in pharmaceutical equipment operation, design and control including GMP change control
+ Experience in providing floor support, troubleshooting unit operations, and resolving and documenting investigations to support cGMP production
+ Understanding of equipment log review and continuous monitoring requirements
+ Good communication skills (technical writing and verbal communication/presentation)
+ Interacts effectively with variety of communication and working styles
+ Experience with regulatory audits and inspections
+ Problem solving skills with the ability to apply logic and assess data to reach decisions and solutions related to compliance and product quality
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.

**Who We Are**
Applied Materials is a global leader in materials engineering solutions used to produce virtually every new chip and advanced display in the world. We design, build and service cutting-edge equipment that helps our customers manufacture display and semiconductor chips - the brains of devices we use every day. As the foundation of the global electronics industry, Applied enables the exciting technologies that literally connect our world - like AI and IoT. If you want to push the boundaries of materials science and engineering to create next generation technology, join us to deliver material innovation that changes the world.
**What We Offer**
Location:
Singapore,SGP
You'll benefit from a supportive work culture that encourages you to learn, develop, and grow your career as you take on challenges and drive innovative solutions for our customers. We empower our team to push the boundaries of what is possible-while learning every day in a supportive leading global company. Visit our Careers website to learn more.
At Applied Materials, we care about the health and wellbeing of our employees. We're committed to providing programs and support that encourage personal and professional growth and care for you at work, at home, or wherever you may go. Learn more about our benefits ( .
**Key Responsibilities**
1. Performs inspection of purchased parts, materials, components, and/or equipment. Confirm accuracy and follow inspection methods of manufactured parts.
2. Assists in determining methods, sequences, and procedures used for inspection. And will perform basic inspections.
3. Utilizes drawings, specifications, and sketches, adapting inspection measuring devices and procedures when necessary. Read and interpret basic technical drawings and specification requirements.
4. Collaborate with Cross Functional Teams to resolve quality issues
5. Populate standard reports, test results, and quality problems.
6. Conduct Intermediate Problem Solving to identify root causes and solutions.
7. Use basic precision measuring inspection tooling, gauges, and equipment.
8. Assists in determining, audit methods, sequences, and procedures used for inspection. In addition, perform basic audits.
**Functional Knowledge**
+ Has developed analytical skills and application of scientific methods to perform a variety of activities
**Business Expertise**
+ Has good understanding of how the team integrates with others
**Leadership**
+ Has no supervisory responsibilities
**Problem Solving**
+ Recognizes and solves typical problems that can occur in own work area without supervisory approval; evaluates and selects solutions from established operating procedures and/or scientific methods
**Impact**
+ Impacts the quality of own work
**Interpersonal Skills**
+ Uses communication skills to exchange of information
**Additional Information**
**Time Type:**
Full time
**Employee Type:**
Assignee / Regular
**Travel:**
**Relocation Eligible:**
No
Applied Materials is an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, national origin, citizenship, ancestry, religion, creed, sex, sexual orientation, gender identity, age, disability, veteran or military status, or any other basis prohibited by law.

**Audit and Inspection Coordinator** **- VIE Contract**
+ Location: Singapore, Singapore
+ Target start date: 01/11/2026
iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.
PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.
PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide. Therefore, only applications that are submitted in English will be considered. Please make sure to apply with your personal email address.
**About the job**
_As_ **_Audit and Inspection Coordinator_** **_VIE_** _within our Pharmacovigilance (PV) Quality team, you'll work with global teams to integrate quality standards and initiatives. Your routine activities will be PV audit preparations and follow up, health authority PV inspections support, audit and inspection findings trending and oversight of CAPA implementation, and the projects include tools / digital initiatives and process improvements._
_Join the engine of Sanofi's mission - where deep immunoscience meets bold, AI-powered research. In R&D, you'll drive breakthroughs that could turn the impossible into possible for millions._
_Ready to get started?_
**About Sanofi**
_We're an R&D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system - and innovative pipeline - enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives._
**Main responsibilities:**
+ Support AIR (Audit and Inspection readiness) team activities for audits and inspections, i.e. support the management of pre-requests, participation in the back room, follow up of CAPAs, and other.
+ Contribute to deliver metrics for the Quality Forum, AIPG (Audit/inspection PV Governance) Meeting, PSPV (Patients Safety Pharmacovigilance) quarterly reports and monthly reports.
+ Support the management of PV Service Providers and Business Partners audits
+ Support in the preparation of country office audits and inspections, definition of root-cause analysis and Corrective & Preventive Actions (CAPA) follow-up.
+ Support country office to pull ICSR compliance data at time of audits and inspections and for routine monitoring.
+ Work with PV Compliance team to identify missing investigations and / or trends related to local ICSR Compliance.
+ Provide analysis of PV findings trends across regions for audits and inspections.
+ Provide support for the maintenance of the Pharmacovigilance System Master File (PSMF).
+ Lead and support AIR apprentice in the launch of the survey for the lessons learned from the PV inspections and support the preparation of the action plan based on the results.
+ Provide support for completion of survey for global process audits.
+ Engage in development and implementation of training materials related to process improvement initiatives.
+ Contribute in joint projects between Audit and inspection readiness team and PV compliance team.
**About you**
**Experience:**
+ Experience in Pharmacovigilance / Medical Affairs / Regulatory Affairs or Quality Assurance.
+ Experience in CAPA (Corrective and Preventive Actions) management.
**Soft and technical skills:**
+ Good interpersonal communication and networking skills.
+ Able to work transversally and to network with key stakeholders.
+ Goal oriented.
+ Dependability, independent yet willing to incorporate feedback.
+ Organized and detail oriented, efficient at time management.
+ Effective problem-solving skills, quick learner, analytic thinker.
+ Understanding of Pharmacovigilance regulatory requirements.
+ Tech-savvy, knowledge of MS office (proficient use of Excel and PowerPoint).
**Education:**
+ Pharmaceutical Degree or Master's Degree in Human Health Sciences.
**Languages:**
+ Fluent in English - verbal and written.
**Why choose us?**
+ Be part of a pioneering biopharma company where patient insights shape drug development.
+ Work at the forefront of AI-powered science that accelerates discovery and improves outcomes.
+ Collaborate beyond your expertise, sparking new ideas with diverse, multidisciplinary teams.
+ Help improve the lives of millions of people globally by making drug development quicker and more effective.
+ Join a workplace where diversity, equity, and inclusion are at the core, with Employee Resource Groups and leadership programs that celebrate every voice.
+ Achieve genuine work-life balance in a supportive R&D environment.
iMove is a unique program tailored for European youth interested in challenging themselves with meaningful assignments across the globe. At Sanofi we have a strong ambition to invest in young talents who will drive the success of Sanofi tomorrow.
Sanofi's Work Abroad Program, iMove, offers jobs-assignments with actual responsibilities and a perspective to grow. We provide those opportunities in various functions such as: marketing, finance, regulatory, supply chain, clinical trials, production, etc. and in more than 40 countries. Sanofi unites people who are passionate about solving healthcare needs across the world. Joining our iMove Work Abroad Program is a unique opportunity to make a difference through your work.
\#LI-EUR
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
We are an R&D driven, AI-powered biopharma company committed to improving people's lives and creating compelling growth. Our team is guided by one purpose: we chase the miracles of science to improve people's lives.
We want to build a healthier, more resilient world, and turn the impossible into the possible by discovering, developing, and delivering medicines and vaccines for millions of people around the world.
Discover more about us visiting or via our movie We are Sanofi ( a career that makes a difference.
Reinvention is in our DNA. It's what drove our evolution from a small French enterprise to one of the world's leading biopharma companies. Whether it's using AI to shorten drug-discovery times or building trust in healthcare, you could be helping our teams make life better for patients, partners, and communities.
This is where you grow your career. We open the door for you to explore new opportunities, push your limits, and connect with people who are driven by a shared purpose: we chase the miracles of science to improve people's lives.

**Date Posted:**

**Country:**
Singapore
**Location:**
SG-01-SINGAPORE-010 ~ 10 Loyang Cres ~ 10 LOYANG CRES-010, Phase 1
**Position Role Type:**
Onsite
Pratt & Whitney, an RTX business, is a world leader in the design, manufacture and service of aircraft engines and auxiliary power units for commercial, military and business aircraft. Through industry-leading businesses - Collins Aerospace, Pratt & Whitney, and Raytheon - RTX pushes the limits of technology and science to redefine how we connect and protect our world.
We are advancing aviation, engineering integrated defense systems, and developing next-generation technology solutions and manufacturing to help global customers address their most critical challenges. Make a difference with a career at Pratt & Whitney.
**What You Will Do**
+ Perform detailed inspection of engines parts & components per manuals and technical work publications.
+ Perform dimensional inspection using various precision measuring instruments such as bore gauges, computer measuring machine and borescope equipment.
+ Perform engine level inspection per manuals and technical work publications.
+ Interpret technical work instructions such as Service Bulletins or equivalent work instructions.
+ Perform daily work tasks per Quality work procedures and guidelines.
+ Support and participate in EH&S, Quality, Ethics and Continuous Improvement projects and initiatives.
+ Perform various other duties as assigned by Workshop Engineer/Manager.
**Qualifications You Must Have**
+ Minimum NITEC or Higher NITEC in Precision /Aerospace/ Electrical/ Mechanical Engineering or any other related discipline.
+ Possess high level of integrity and accountability with a strong drive towards Quality.
+ Able to work on weekly rotating shifts.
**Qualifications We Prefer**
+ Candidates with Diploma will be advantageous
+ 2 years of relevant working experience as detailed inspector / visual and dimensional inspection within the aviation industry.
+ Good working knowledge in Microsoft Office applications and SAP.
**What We Offer**
+ Career and skills development opportunities.
+ Employee scholarship program for further education.
+ Comprehensive health, medical and dental benefits.
+ On-the-job training and in-house/external certifications.
+ Competitive remuneration package.
+ Allowance and overtime benefits where applicable.
+ Company transport provided.
_RTX adheres to the principles of equal employment. All qualified applications will be given careful consideration without regard to ethnicity, color, religion, gender, sexual orientation or identity, national origin, age, disability, protected veteran status or any other characteristic protected by law._
**Privacy Policy and Terms:**
Click on this link ( to read the Policy and Terms
Raytheon Technologies is An Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age or any other federally protected class.

**Date Posted:**

**Country:**
Singapore
**Location:**
SG-01-SINGAPORE-005 B1 ~ 5 Tuas Dr 2 ~ 5 TUAS DR 2-005 B1
**Position Role Type:**
Onsite
Pratt & Whitney, an RTX business, is a world leader in the design, manufacture and service of aircraft engines and auxiliary power units for commercial, military and business aircraft. Through industry-leading businesses - Collins Aerospace, Pratt & Whitney, and Raytheon - RTX pushes the limits of technology and science to redefine how we connect and protect our world.
We are advancing aviation, engineering integrated defense systems, and developing next-generation technology solutions and manufacturing to help global customers address their most critical challenges. Make a difference with a career at Pratt & Whitney.
**What You Will Do**
+ Perform visual and dimensional inspection on aircraft engine components.
+ Inspect aircraft components and ensure conformance against the technical drawings, work instructions and specification requirements.
+ Responsible for receiving inspection, in-process and final inspection of repairable parts/components channelled into the cell.
+ Understand the specifications involving inspection tolerances, limitations and procedures established by the manufacturer of the product being inspected.
+ Participate in audits and inspections as and when required.
+ Participate in the EH&S programs and takes personal responsibility to ensure safety adherence.
+ Support the continuous improvement programs, CORE (Customer Oriented Results & Excellence) activities and additional tasks assigned by the supervisor.
**Qualifications You Must Have**
+ Diploma in Engineering or relevant technical qualifications. 
+ Non-diploma holders may be considered based on relevant work experience.
+ Min 2 years of relevant experience in visual inspection and the use of various inspection equipment.
+ Candidates with no prior experience but a strong interest in the aerospace industry, including mid-career switchers, are welcome to apply.
+ Ability to pass vision exam (Jaeger #1 test chart at not less than 12 inches) and color blindness test.
+ A positive and learning mindset with keen interests to learning new technology.
+ Ability to understand basic technical drawing and standard operation procedures (SOP).
+ Willing to work on rotating shifts (Day & Night) and overtime on need basis.
**Qualifications We Prefer**
+ Relevant aerospace, manufacturing or precision engineering.
+ Basic working knowledge of MS office application and SAP.
**What We Offer**
+ Career and skills development opportunities.
+ Employee scholarship program for further education.
+ Comprehensive health, medical and dental benefits.
+ On-the-job training and in-house/external certifications.
+ Competitive renumeration package.
+ Allowance and overtime benefits where appliable.
+ Company transport provided.
_RTX adheres to the principles of equal employment. All qualified applications will be given careful consideration without regard to ethnicity, color, religion, gender, sexual orientation or identity, national origin, age, disability, protected veteran status or any other characteristic protected by law._
**Privacy Policy and Terms:**
Click on this link ( to read the Policy and Terms
Raytheon Technologies is An Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age or any other federally protected class.