Live opening · Posted 1 day ago
At a glance
The key details from the original listing.
About the role
Description supplied by the original job listing.
The associate will review operational activities and data for accuracy, identify deviations and potential risks, and collaborate with cross-functional teams to implement corrective and preventive actions. Day-to-day tasks include preparing quality reports, supporting process improvements, maintaining quality records, and communicating quality-related findings to stakeholders. The role requires proactive engagement, attention to detail, and consistent follow-up to ensure continuous improvement and adherence to established quality management systems.
Qualifications
Strong foundation in Quality Assurance and Quality Control, with experience applying these principles in a regulated or clinical development environment.
Proficiency in Quality Management practices, including documentation, audits, corrective and preventive actions, and adherence to standards such as ISO 9001 and related frameworks.
Demonstrated Analytical Skills for reviewing data, identifying trends or deviations, and supporting evidence-based decision-making.
Effective Communication skills, including clear written and verbal reporting, and the ability to collaborate with cross-functional and remote teams.
Bachelor’s degree in life sciences, pharmacy, engineering, quality management, or a related field; equivalent relevant experience may be considered.
Familiarity with clinical trials, medical devices, or pharmaceutical supply chains is highly beneficial.
Strong organizational skills, attention to detail, and the ability to manage multiple tasks in a remote work setting.
Work arrangement
Yes
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