Audit Operational Specialist
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 Quality Assurance Specialist II at ICON, you will support the implementation and execution of supplier quality activities for GMP suppliers and provides support of the Quality Management lifecycle workstream, monitoring the compliance of R&D GMP suppliers
What You Will Do: You will contribute to quality assurance and compliance activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
Primarily focuses on supplier quality management, compliance, and quality assurance support
Manage Supplier Notifications of Change (SNCs), supports New Supplier Requests (NSRs) and supplier audits, ensures quality records are completed on time and remain inspection-ready,
Proactively identifies and mitigates risks, monitors key quality metrics
Medical Device Batch Release activities
Supports executions of GMP audits and supplies identification and selection process
Your Profile: You will bring relevant quality assurance and compliance experience, along with the following qualifications and skills.
Required qualifications and experience:
Bachelor's degree in a related field (e.g., Life Sciences, Regulatory Affairs, or Compliance).
Working knowledge of current Good Manufacturing Practice requirements for the biopharmaceutical and medical device industries
Experience in supplier quality management and auditing GMP suppliers (e.g., CMOs)
Experience with risk management strategies and general project management
Proven success in identifying and implementing continuous improvement initiatives
Minimum of 5 years professional working experience in the field of healthcare products or related activitiessuch aspharmaceuticalor devicemanufacturing, Quality Control or Quality Assurance including at least 4 years in GMP Quality or Compliance.
Experience working in a global organization and effectively collaborating across functions, geographies, and cultures.
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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.
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
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Quality Compliance & Systems Operational Specialist in Warsaw – pracodawca: KCR Placement
KCR Placement to globalna organizacja zajmująca się badaniami klinicznymi, która stawia na wartości takie jak integralność, współpraca i inkluzyjność. Pracownicy mają możliwość rozwoju zawodowego w dynamicznym środowisku, które sprzyja innowacjom i doskonałości. Oferowane są różnorodne ścieżki kariery oraz stabilne zatrudnienie w międzynarodowym zespole.
