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
IndustryContent type
BlogsPublish date
04/03/2026
Summary
Understanding Central Monitoring vs On Site Monitoring Monitoring is a core component of clinical trial oversight. It ensures that studies are conducted in line with the protocol, that data is re
Teaser label
Our PeopleContent type
BlogsPublish date
03/26/2026
Summary
Why Francis returned to ICON: building a long-term career in clinical research Francis Kayamba is a Clinical Research Associate based in Johannesburg, South Africa. He first joined ICON in February
Teaser label
Our PeopleContent type
BlogsPublish date
03/24/2026
Summary
Career paths are rarely straightforward, especially in the fast moving world of clinical research. For many professionals, gaining experience across organisations can provide valuable perspectiv
Similar jobs at ICON
Salary
Location
Brazil, Sao Paulo
Location
Sao Paulo
Mexico City
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Drug Safety
Job Type
Permanent
Description
We are currently seeking a Pharmacovigilance Associate to join our diverse and dynamic team. As a Pharmacovigilance Associate at ICON, you will play a vital role in monitoring and ensuring the safety
Reference
JR148124
Expiry date
01/01/0001
Author
Florencia PistolesiAuthor
Florencia PistolesiSalary
Location
Argentina, Buenos Aires
Location
Buenos Aires
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc. As a key member of our research department, you will be responsible for overseeing and coordina
Reference
JR145113
Expiry date
01/01/0001
Author
Florencia PistolesiAuthor
Florencia PistolesiSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Study Start Up
Job Type
Permanent
Description
Job Description Summary:Support preparation, process and tracking of regulatory and site level critical documents and of site activation tasks required for study site activation in accordance with ICO
Reference
JR140536
Expiry date
01/01/0001
Author
Florencia PistolesiAuthor
Florencia PistolesiSalary
Location
US, Downers Grove, IL
Location
Downers Grove
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical
Reference
JR145071
Expiry date
01/01/0001
Author
Melissa BennerAuthor
Melissa BennerSalary
Location
US, Blue Bell (ICON)
Department
Full Service - Symphony Health
Location
Raleigh
Blue Bell
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Analyst
Job Type
Permanent
Description
We have an incredible opportunity for an MDM Data Steward & Operations Analyst to join ICON’s Symphony Health team. The MDM Data Steward & Operations Analyst is responsible for the timeliness, accurac
Reference
JR142909
Expiry date
01/01/0001
Author
Tallulah PierreAuthor
Tallulah PierreSalary
Location
Brazil, Sao Paulo
Department
Full Service - Corporate Support
Location
Sao Paulo
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Talent Acquisition
Job Type
Permanent
Description
We are currently seeking a Talent Sourcing Recruiter to join our diverse and dynamic team. As a Talent Sourcing Recruiter at ICON, you will focus on building strong talent pipelines for critical roles
Reference
JR145976
Expiry date
01/01/0001
Author
Florencia Borello TaianaAuthor
Florencia Borello Taiana