Sr QA Specialist

Job Description

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.

Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together. Job Description

Key Responsibilities :

• Apply critical thinking and risk-based judgment to address routine and complex manufacturing challenges, and ensuring continuous improvement.
• Review and approve documentation and records related to drug substance manufacturing activities, including batch records, materials management, cleaning, and analytical data.
• Provide support for manufacturing investigations, including deviations, CAPAs, and change controls associated with production processes.
• Participate in authoring, reviewing, and approving SOPs, forms, and controlled documents to ensure compliance with GMP requirements.
• Provide QA oversight during manufacturing operations and collaborate with cross-functional teams to resolve issues promptly.
• Support internal and external audits, inspection readiness, and continuous improvement initiatives at the site.
• Actively participate in Quality System improvement and harmonization activities, including electronic system implementation.
• Engage in Quality Risk Management activities to assess and mitigate risks in site operations.
• Provide guidance and mentorship to others in the Quality group.

Qualifications :

Preferred Qualifications :

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