Manager, Quality Assurance

As a Manager, Quality Assurance at ICON, you will ensure the quality and compliance of clinical trials, interpreting regulatory requirements, and contribute to... Manager, Quality Assurance job in Turkey, Ankara | ICON JUMP TO CONTENT Manage your application Shortlist 0 Search Careers in ICON Careers We encourage our people to seize the opportunity to bring flexibility, innovation and determination to every situation. By doing this, our people build exciting and rewarding careers, deliver results to help bring life-changing medicines and devices to market and maintain ICON’s success as an industry leader. View jobs at ICON About Icon Overview of Service Lines Job Categories ICON Full Service Full Service Full-service roles offer the opportunity to work on projects and programmes on behalf of the world’s most innovative pharma, biotech and medical device companies. View roles Recruitment Process Accellacare Biometrics Clinical Operations Commercialisation and Outcomes Early Clinical and Bioanalytical Solutions Global Logistics Division Laboratory Medical Affairs & Scientific Affairs Project Management ICON Strategic Solutions (FSP) ICON Strategic Solutions Our Strategic Solutions team is embedded in our clients’ businesses, helping to deliver cutting edge research. View roles Recruitment Process Biometrics Clinical Operations Clinical Research Associate Medical Affairs & Medical Writing Project Management Regulatory Affairs/ Drug Safety/ Quality Assurance Global Business Services Global Business Services Global Business Services functions are the backbone of the organisation, providing support services in areas including Finance, IT, HR, Sales, QA, Facilities & Administration, Legal & Procurement. Commercial roles offer opportunities to be involved in the exciting world of proposals, sales and marketing. View roles Recruitment Process Inside ICON About ICON Our Culture & Our People Our Mission & Values Overview of Service Lines Full Service Strategic Solutions (FSP) Global Business Services Accellacare Site Network ICON Biotech ICON Leadership Our Locations Our Locations With headquarters in Dublin, Ireland, ICON has employees in 119 locations across 53 countries. View roles Global Office Locator Ireland Asia Pacific Australia China India Japan Korea Malaysia Taiwan Europe, Middle East & Africa Belgium Bulgaria Germany Hungary Italy Netherlands Poland Romania Slovakia South Africa Spain Türkiye United Kingdom United States Latin America Argentina Brazil Chile Colombia Mexico Global Office Locator Why ICON? Why ICON? No matter what part of ICON you work in, you are contributing to solving some of the most complex healthcare challenges and are helping to deliver new medicines and devices that are impacting millions of peoples’ lives, right across the world. 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Quality Assurance Manager At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a 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 treatments and therapies. What You Will Do: Your focus will be on coordinating quality assurance and compliance delivery, resolving issues, and developing team capability. Key responsibilities include: Developing and implementing quality assurance strategies and processes to support clinical trial activities. Conducting quality assessments and audits to ensure compliance with regulatory standards and guidelines. Collaborating with project teams to identify and address quality issues and implement corrective actions as needed. Providing guidance and support to staff regarding quality assurance policies, procedures, and best practices. Contributing to the development and maintenance of quality management systems and documentation. Your Profile: You will have solid quality assurance and compliance experience, with the ability to manage competing priorities and develop your team. 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. 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 resolve quality issues effectively. Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and stakeholders. Willingness to travel as required (approximately 35%) 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 Share: Hi, I am Tuba and I manage this role Talent Acquisition Business Partner Icon Strategic Solutions View my profile Email [email protected] View my other roles Send me a message First Name * Last Name * Email address * Enquiry * Send Cancel Get Job Alerts! Sign up to receive job updates tailored to your interests. Sign Up Not Ready to Apply? Join our Talent Community for future alerts. Sign up Explore more about ICON About ICON Explore Global Office Locator Explore Benefits & Rewards Explore Inclusion & Belonging Explore Career Pathways Explore Environmental, Social & Governance Explore List #1 Day in the life How to write an outstanding CV for a life sciences job Teaser label Career Progression Content type Blogs Publish 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 Teaser label Learn expert tips on crafting an outstanding CV for life sciences jobs, from highlighting relevant skills and experience to tailoring your resume. 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