Quality Control Analyst I
About the role
This vacancy has now expired. Please click here to view live vacancies.
At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.
Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That's our vision. We're driven by it. And we need talented people who share it.
If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.
ICON plc, a leading Contract Research Organisation employing approximately 14,000 employees across 97 offices in 38 countries, seeks a highly motivated QC Analyst to join its Global Quality Team in the Singapore Laboratory.
The successful candidate will join a professional and experienced team focused on making an impact globally and supporting ICON's mission - to help its clients accelerate the development of drugs and medical devices that save patient lives and improve their quality of life.
The Role
Based in the Singapore laboratory, the successful candidate will join the global QC team and will be responsible to work locally and globally within the quality monitoring system. The successful candidate will be responsible for the processing, maintenance, and improvement of global quality control data accumulated within the global quality and harmonization monitoring system to ensure the production of the highest quality data sets. The successful candidate needs to possess some knowledge in areas such as method validation, and laboratory clinical laboratory systems and equipment.
Due to the nature of this position it may be required for the employee to travel.
Role responsibilities include:
Sustaining the global quality control program for all ICON Laboratories including data entry, data management, data analysis, action plan development, and corrective action monitoring.
Fluent knowledge of the global quality control system, skills to endure and successfully participate in internal, regulatory, and client audits with respect to the global quality control system.
Support the Biorad Unity Quality Control System, and related activities.
Prepare and present quality control summaries to Senior Management.
Facilitate discussions, and contribution of advanced troubleshooting techniques that will provide opportunities to improve performance.
Review and contribute cumulative knowledge to improve correlative performance between laboratories.
Drive the laboratory correlation data analysis, and feedback process towards real time processing.
Ensure compliance with all regulatory requirements domestic, and internationally.
Experience & Knowledge Requirements:
Bachelor's Degree for Academy trained or ASCP Certified Technologists
Masters or PhD. in Clinical Laboratory Science or related field for uncertified applicants
Quality Certification / Six Sigma Certification preferred.
3 - 6 years of prior relevant clinical laboratory experience with some in a supervisory capacity.
Academy trained or ASCP Certified Medical Technologists preferred
Strong verbal and written communication skills.
Knowledge of CAP regulatory requirements including proficient testing.
Proven track record of contributing to quality, and process improvements.
Ability to liaise, and develop a collaborative work environment with laboratory personnel including management.
Strong understanding of statistical concepts with the ability to interpret the trends, and predict future performance.
Ability to remain composed in stressful situations, performing effectively despite shifting priorities, work load, and external pressures.
Accomplished action oriented self-starter actively seeking out improvements, and team development
Mandarin-speaking ability is preferred.
Benefits of Working in ICON:
ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career.
We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.
Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package - a dedicated recruiter will discuss this with you at interview stage. We care about our people as they are the key to our success. We provide an open, friendly and dynamic working environment where we empower people and provide opportunities to develop long term careers.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish date
03/16/2026
Summary
Driving Study Start-Up: James Pereira's Journey at ICON James Pereira's career in clinical research has been shaped by a single driving question: how do we get studies started faster? From his earl
Teaser label
Inside ICONContent type
BlogsPublish date
03/15/2026
Summary
Who's Who In a Clinical Trial Team Clinical trials rely on large, cross functional teams working together across countries, time zones and specialisms. For those new to the industry, the number of
Teaser label
IndustryContent type
BlogsPublish date
02/16/2026
Summary
What Sponsors, CROs, and Sites Each Do Clinical research brings together many organisations, each with a specific role in delivering a clinical trial. For those new to the industry, the relationsh
Similar jobs at ICON
Salary
Location
Spain, Madrid
Location
Dublin
Warsaw
Barcelona
Madrid
Reading
Swansea
Blue Bell
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Data Scientist Lead
Job Type
Permanent
Description
The COA Lead is accountable for the definition of COA endpoint strategies and responsible for the conduct of related activities in relation to specific programs, assets or indications. The scope evolv
Reference
JR147332
Expiry date
01/01/0001
Author
Clodagh FinneganAuthor
Clodagh FinneganSalary
Location
Ireland, Dublin
Department
Full Service - Corporate Support
Location
Dublin
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Accounting & Finance
Job Type
Permanent
Description
We are currently seeking an Investigator Payments Coordinator to join our diverse and dynamic team. As an Investigator Payments Coordinator at ICON, you will play a key role in managing and processing
Reference
JR147329
Expiry date
01/01/0001
Author
Clodagh FinneganAuthor
Clodagh FinneganSalary
Location
China, Beijing
Location
Beijing
Chengdu
Guangzhou
Shanghai
Wuhan
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Study Start Up
Job Type
Permanent
Description
Job Advert PostingWe are currently seeking a Site Specialist I/II/Sr to join our diverse and dynamic team. As a Site Specialist I/II/Sr at ICON, you will play a pivotal role in designing and analyzing
Reference
JR141473
Expiry date
01/01/0001
Author
Allen HaoAuthor
Allen HaoSalary
Location
Hungary, Budapest
Location
Budapest
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and a
Reference
JR147200
Expiry date
01/01/0001
Author
Orsolya BerkeAuthor
Orsolya BerkeSalary
Location
UK, Reading
Location
Reading
Remote Working
Remote or Office
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
Here at the ICON FSP group, we are in partnership with one of the world’s leading Independent Biotechnology companies and we’re looking for experienced, UK-based Clinical Research Administrators to co
Reference
JR146112
Expiry date
01/01/0001
Author
Dominic BradyAuthor
Dominic BradySalary
Location
France, Paris
Location
Paris
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
We are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsible for overseeing the planning, execution, and successfu
Reference
JR146498
Expiry date
01/01/0001
Author
Serena MilanesiAuthor
Serena Milanesi