Senior Auditor, Quality Assurance
- Bangalore, Manila, Bengaluru, Kuala Lumpur
- Quality Assurance
- ICON Full Service & Corporate Support
- Remote or Office
Talent Acquisition Business Partner
- Full Service Division
About the role
Senior Auditor, Quality Assurance
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a Senior Auditor, Quality Assurance at ICON, you will ensure the quality and compliance of clinical trials, interpreting regulatory requirements, and contribute to the advancement of innovative treatments and therapies.
What You Will Do:
You will lead on quality assurance and compliance tasks requiring technical depth, with a focus on quality and continuous improvement.
Key responsibilities include:
- Managing Quality Issue during its entire life cycle
- Development of CAPA for Quality Issues
- Collaborating with cross-functional teams to identify areas for improvement in quality assurance processes and practices.
- Providing expert guidance and recommendations to stakeholders on quality assurance best practices and regulatory requirements.
- Contributing to the continuous improvement of quality assurance programs and initiatives.
- May need to support regulatory inspections and Sponsor audits of ICON
Your Profile:
You will have a strong foundation in quality assurance and compliance, with the experience to work independently and guide others.
Required qualifications and experience:
- Bachelor's degree in a relevant discipline
- Minimum of 5 years of experience in quality assurance within the pharmaceutical, biotechnology, or CRO industry, with at least 2 years in a leadership or senior role.
- Deeper understanding of Quality Issues and CAPA
- Deeper understanding of Quality Management System in CRO environment
- In-depth knowledge of regulatory requirements and guidelines governing clinical trials (e.g., ICH-GCP, FDA regulations).
- Strong analytical and problem-solving skills, with the ability to identify and address complex quality issues.
- Excellent communication and interpersonal skills, with the ability to effectively interact with internal and external stakeholders at all levels.
- Willingness to travel as required, though very minimum
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON 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.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply
Explore more about ICON
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
Career ProgressionContent type
BlogsPublish date
02/28/2022
Summary
Around 268,000 people are employed by the UK life sciences industry and as one of the fastest-growing sectors, this number is expected to continue rising. Life sciences is a flourishing job mark
Similar jobs at ICON
Salary
Location
UK, Reading
Department
Full Service - Quality Assurance
Location
Reading
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Quality Assurance
Job Type
Temporary Employee
Description
We are currently seeking a Principal Auditor Quality Assurance to join our diverse and dynamic team on a 1 year fixed term contract in Client Relationship Quality Assurance (CRQA). As a Principal Audi
Reference
JR147274
Expiry date
01/01/0001
Author
Caroline LockAuthor
Caroline LockSalary
Location
Romania, Bucharest
Location
Sofia
Prague
Warsaw
Bucharest
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Quality Assurance
Job Type
Permanent
Description
AI Compliance ManagerAs a Responsible AI & Compliance Manager at ICON, you will be responsible for ensuring that all AI products, agents, and services are developed and deployed in line with ethical s
Reference
JR153283
Expiry date
01/01/0001
Author
Jonathan CunliffeAuthor
Jonathan CunliffeSalary
Location
Poland, Warsaw
Department
Full Service - Quality Assurance
Location
Sofia
Dublin
Warsaw
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Quality Assurance
Job Type
Permanent
Description
The EU Audit Defense team are seeking an individual to join them as a QA Manager position. QA Manager will have People Leader responsibilities for oversight of the EU Audit Defense Team. This is a sp
Reference
JR149266
Expiry date
01/01/0001
Author
Maya KatsarskaAuthor
Maya KatsarskaSalary
Location
Regional United States (PRA)
Location
Multiple US Locations
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Quality Assurance
Job Type
Permanent
Description
As a Senior Manager, Quality Assurance at ICON, you will ensure the quality and compliance of clinical trials, interpreting regulatory requirements, and contribute to the advancement of innovative tre
Reference
JR150666
Expiry date
01/01/0001
Author
Brandon PupekAuthor
Brandon PupekSalary
Location
US, Lenexa KCIB (PRA)
Location
Lenexa
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Quality Assurance
Job Type
Permanent
Description
As a Manager, Quality Control at ICON, you will be responsible for overseeing the quality control processes and ensure that all products meet the required quality standards and specifications.What You
Reference
JR152534
Expiry date
01/01/0001
Author
Sasha BrownAuthor
Sasha BrownSalary
Location
US, Portland, OR
Department
Full Service - Quality Assurance
Location
Portland
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Quality Assurance
Job Type
Permanent
Description
Due the business function alignment of this role, there is a requirement for the individual to be onsite at the Laboratory 3 out of 5 days. The role: We are looking for a Quality Assurance Auditor to
Reference
JR151868
Expiry date
01/01/0001
Author
Kris CostelloAuthor
Kris Costello