Director, Quality Control Microbiology- Biologics​/Molecules

Director, Quality Control Microbiology
- Biologics/Small Molecules 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, 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.

The QC Microbiology Director is a vital role for the success of Clinical and Commercial Biologics and Small Molecule Quality Control. This individual provides strategic leadership and oversees daily microbiological operations. Responsibilities include leading the microbiology QC team supporting both clinical and commercial programs for biologics and small molecule sectors.

• Lead the development and implementation of end‑to‑end QC microbiological strategies for Gilead’s biologics and small molecules products, including setting up specifications for cell banks, product, raw materials, environmental monitoring/facilities, etc. Ensure that these strategies are effectively applied across all stages of the product life‑cycle.
• Lead and develop teams. Provide leadership, guidance, and motivation to direct reports and project teams. Focus on developing strong leaders within the QC department, ensuring they are equipped to make critical decisions and meet project timelines.
• Proactively manage daily internal and external business, including interactions with internal teams, CMO project leads, and management to plan, develop, and coordinate activities to set up, review, track and trend adventitious agent testing such as sterility, endotoxins, bioburden, micro‑biological identification, particulate matter, and environmental monitoring.
• Develop and implement innovative technologies, methods, and processes for microbial analysis.
• Ensure all laboratory activities (internal and external) are conducted in compliance with relevant regulations and guidelines.
• Provide scientific leadership and technical expertise to the laboratory teams.
• Drive qualification, implementation and execution of micro USP methods for biological and small molecule products, including in‑process, release and stability.
• Support microbiology quality events.
• Author and/or review microbiology procedures, including protocols and reports.
• Manage sample submission to third parties for microbial identification.
• Manage and develop microbiology personnel and work closely with internal and external teams.
• Work closely with quality on defining and implementing aseptic techniques and cross‑contamination controls.
• Future management and oversight of the day‑to‑day operations of the microbiology laboratory, including sample processing, data analysis, and reporting. Undertake facility environmental trend reporting.
• Work with accuracy, urgency and a continuous improvement perspective.
• Represent Gilead as a microbiology subject‑matter expert. Interface with regulatory agencies as required, representing Gilead to authorities and regulatory inspectorates in matters relating to GxP.

• PhD with 8+ years of relevant experience in the pharmaceutical industry.
• Master’s degree with 10+ years of relevant experience in the pharmaceutical industry.
• Bachelor’s degree with 12+ years of experience in the pharmaceutical industry.
• Associate’s degree with 14+ years of experience in the pharmaceutical industry.
• High School…